Bovine Immune Factors Underlying Tick Resistance: Integration and Future Directions
- Department of Genetics, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa
The mechanisms underlying tick resistance within and between cattle breeds have been studied for decades. Several previous papers on bovine immune parameters contributing to tick resistance discussed findings across DNA, RNA, protein, cellular, and tissue levels. However, the differences between bovine host species, tick species and the experimental layouts were not always taken into account. This review aims to (a) give a comprehensive summary of studies investigating immune marker differences between cattle breeds with varying degrees of tick resistance, and (b) to integrate key findings and suggest hypotheses on likely immune-regulated pathways driving resistance. Experimental issues, which may have skewed conclusions, are highlighted. In future, improved experimental strategies will enable more focused studies to identify and integrate immune markers and/or pathways. Most conclusive thus far is the involvement of histamine, granulocytes and their associated pathways in the tick-resistance mechanism. Interestingly, different immune markers might be involved in the mechanisms within a single host breed in contrast to between breeds. Also, differences are evident at each tick life stage, limiting the level to which datasets can be compared. Future studies to further elucidate immune molecule dynamics across the entire tick life cycle and in-depth investigation of promising markers and pathways on both molecular and cellular level are in dire need to obtain a scientifically sound hypothesis on the drivers of tick resistance.
The economic importance of ticks and the need to control them was realized alongside the discovery of their potential as vectors of harmful parasites, particularly to livestock (Hunter and Hooker, 1907; Theiler, 1911). The variability in the degree to which cattle display resistance to ixodid ticks was first suggested by Johnston and Bancroft (1918). It is known that tick resistance in cattle varies from more tick-susceptible Bos taurus taurus (B. t. taurus) to more tick-resistant B. t. indicus breeds, between bovine crosses as well as within a single cattle breed (George et al., 1985; Rechav et al., 1991b; Mattioli and Cassama, 1995; Mwangi et al., 1998; Mattioli et al., 2000; Nascimento et al., 2011). However, the biological factors underlying bovine resistance to tick infestation are still poorly understood. Tick resistance is a multi-factorial trait suggested to involve host-related factors such as sex, age, lactation, grooming behavior, skin composition and host surface area, coat length and environmental factors (Wharton et al., 1970; Seifert, 1971; Doube and Wharton, 1980; Binta and Cunningham, 1984; Ali and de Castro, 1993; Meltzer, 1996; Norval et al., 1996; Mattioli, 1998; Martinez et al., 2006; Kongsuwan et al., 2010). It is also well established that the tick-resistance phenotype is heritable, as is evident from breed-specific resistance patterns. Furthermore, it was proposed that tick attachment sites on resistant cattle rapidly become unsuitable for feeding due to host immune responses (Roberts, 1968b). The majority of studies indicate that resistance is acquired through exposure to ticks (Wagland, 1975, 1980; George et al., 1985; Momin et al., 1991) and that resistance is acquired sooner and to a higher degree in B. t. indicus than in B. t. taurus breeds (Riek, 1962; Wagland, 1978, 1980; Rechav et al., 1990). This phenotype only becomes apparent after subsequent (and not initial) tick exposure in B. t. taurus, B. t. indicus and mixed breed cattle (Roberts, 1968a; Wagland, 1975; Hewetson and Lewis, 1976).
To further elucidate potential mechanisms underlying differences in tick resistance, several studies have investigated host immune responses toward ticks on a cellular and molecular level. Gaining an understanding of the molecular mechanisms underlying tick-resistance mechanism will be advantageous in the identification of specific genomic alterations or specific markers that could lead to the ability to screen cattle for their potential resistance status without prolonged tick-infestation trials or counts. This would be helpful in breeding more tick-resistant cattle. In this regard, it was shown that although host-resistance to tick infestation and product yield does not correlated in Holstein-Friesian cattle (Jonsson et al., 2000), but carriers of both B. t. taurus and B. t. indicus genes may suffer from a trade-off between animal-derived product yield and tick resistance (Wang et al., 2007). A clear understanding of tick-resistance mechanisms would also be beneficial to vaccine trials, where a difference in the resistance status of individual animals could skew results and therefore make accurate data interpretation more difficult. Furthermore, more effective vaccine formulations could be devised as vaccine efficacy is hindered by the modulation of host immune responses through tick saliva (Kazimírová and Štibrániová, 2013). Knowledge regarding molecular mechanisms underlying tick resistance could allow for the optimal selection of appropriate adjuvant/vaccine formulation strategies to provide a cross-breed protective response.
This review therefore provides a summary of studies performed up to date in cattle blood and skin tissue, with critical evaluation of findings followed by hypotheses on key role players, possible immune-regulated pathways as well as improvements for consideration when planning future experiments. Several recent studies were published pertaining to genetic associations with regards to the tick-resistance phenotype (Mota et al., 2016a,b, 2017; Junqueira et al., 2017; Sollero et al., 2017), however, these are outside the scope of this summary. This review should provide readers with the basic knowledge and a critical evaluation of findings to date to make informed decisions for future studies investigating the tick-host-interface with a focus on resistance. Due to differences in experimental layouts, which might skew data interpretation and comparisons such as tick life stage, tick species and type of bovine comparison (between or within breeds), are provided in Supplementary Table 1.
Immune cells originate from hematopoietic stem cells in the bone marrow with naïve and mature forms of these cells circulating in the blood and lymphatic systems. Here, they encounter foreign molecules that lead to their proliferation, differentiation and maturation (Janeway et al., 2001). However, due to the constant circulation and changing dynamics of immune response components, experimental designs (especially time points) must be chosen carefully. Various gene expression, translational and cytological studies have investigated blood to elucidate immune responses linked to tick resistance/susceptibility in cattle and these are described in the next section.
Gene Expression Studies in the Blood of Tick-Infested Cattle
Gene expression studies of peripheral blood mononuclear cells identified transcripts for IL-2, IL2Rα, TNFα, and CCR1 to be significantly upregulated in resistant cattle relative to susceptible cattle, while a significantly higher expression of CXCL10 was detected in susceptible Holstein-Friesian compared to resistant Brahman cattle (Piper et al., 2009). Pathway analysis indicated that genes that are more highly expressed in the resistant breed are associated with the hematopoietic cell lineage and cytokine-cytokine receptor interaction pathways. Another study found a significant upregulation of CD25, IL10, FoxP3, and CXCL10 in samples from cattle infested with larvae compared to samples obtained from uninfested animals. In susceptible animals, CXCL8 was downregulated in susceptible animals 24 and 48 h after infestation compared to samples from uninfested animals (Domingues et al., 2014). Although CXCL10 was identified in both studies as differentially regulated, major differences in the study designs hindering any direct comparisons. Piper et al. (2009) obtained blood samples at the peak of tick infestation without reference to a specific time point after infestation and found significantly higher chemokine expression in susceptible compared to resistant cattle breeds. Domingues et al. (2014) on the other hand compared tick-infested versus tick-uninfested cattle of the same breed and identified an increase in CXCL10 in resistant animals 48 h and an increase in susceptible animals 24 h after tick infestation. Therefore, the role of CXCL10 remains to be confirmed in future studies and its contribution to resistance pathways elucidated.
Translational Studies in the Blood of Tick-Infested Cattle
A link between tick resistance and immunoglobulins was proposed in 1987 by Rechav and colleagues who found a positive correlation between tick numbers and total serum gamma globulin levels in naturally infested B. t. taurus and B. t. indicus cattle. During the acquisition of tick resistance, a negative correlation between tick weight and total serum gamma globulin levels was, however, documented in B. t. taurus cattle infested with Rhipicephalus decoloratus (Rechav et al., 1991a). This discrepancy could be a result of differences in experimental design, as the animals studied by (Rechav et al., 1991a) were most likely in the process of acquiring tick resistance as opposed to the more established resistance of cattle studied by Rechav (1987). In this regard, resistance in the former study was supported by reduced tick weights only.
In general, the number of ticks feeding on cattle were found to positively correlate with salivary gland specific IgG levels in previously infested (Sahibi et al., 1998) and naïve (Cruz et al., 2008) B. t. taurus cattle. Cruz et al. (2008) furthermore reported that there was no change in the avidity of antibodies developed by either Rhipicephalus microplus resistant or susceptible animals against salivary soluble extracts (Cruz et al., 2008).
Differences in the IgG1 isotype was observed when comparing cattle breeds displaying varying tick-resistance phenotypes. After multiple infestations of tick-naïve cattle, IgG1 levels (against several tick extracts) were found to be significantly higher in susceptible compared to resistant cattle (Piper et al., 2017), with similar results obtained the studies of Garcia et al. (2017) and Piper et al. (2009). Although no differences were observed for tick-naïve animals at the beginning of the study by Piper et al. (2017), higher tick-saliva specific IgG1 levels were seen before and at the beginning of the first infestation in the tick-resistant cattle breed by Garcia et al. (2017). Yet, Kashino et al. (2005) reported a decrease of IgG1 upon heavy tick infestation in naturally infested susceptible animals, compared to resistant animals (Kashino et al., 2005). As such, the question arises whether studies done under controlled housing conditions and those done under field conditions with natural infestation, and possible co-infections/infestations, can be compared.
In contrast to IgG1 levels, no significant differences were identified for the IgG2 isotype between breeds (Piper et al., 2009, 2017), with similar results seen by Garcia et al. (2017) for resistant animals throughout the study. The latter study does however describe an increase of this isotype in the susceptible breed at the third infestation compared to the baseline. At the same time point, IgG2 levels were significantly higher in susceptible compared to resistant animals. Again, in contrast, Kashino et al. (2005) identified decreased levels of IgG2 in naturally infested susceptible compared to resistant animals during heavy infestation.
Only two studies have investigated IgE levels between resistant and susceptible cattle breeds. Garcia et al. (2017) determined levels of total IgE in the sera of cattle infested with R. microplus. No difference in these levels were noted between resistant and susceptible breeds. Tick-specific IgE antibody levels, however, were shown to be significantly lower in resistant compared to susceptible animals during heavy infestation as well as during subsequent light infestation (Kashino et al., 2005). This difference in IgE levels between cattle breeds seems to be a result of an increase in this immunoglobulin in susceptible animals instead of a decrease in resistant animals. The same trend was seen in some studies investigating IgG isotypes. IgE with associated receptors and cellular responses are believed to have evolved to counter helminths and other parasites that cannot be phagocytosed (Fitzsimmons et al., 2014). In this paper, we propose a role for IgE-dependent responses as one of the drivers of resistance (see sections Dynamics of Granulocytes and Histamine and their Suggested Involvement in the Tick- Resistance Mechanism Over the Tick Lifecycle and Future Directions: Potential Drivers Involved in Tick Resistance), and as such, daily data on the IgE levels throughout the period of tick attachment and subsequent life stages will be of great importance.
Considering the consensus from the majority of studies, resistant animals seem to display a more constant tick-specific immunoglobulin isotype profile with fewer changes observed throughout infestation cycles. Susceptible animals on the other hand show an increase of tick-specific immunoglobulin levels over multiple infestations. Differences in host immune responses are furthermore evident by the observation that a great variation in tick salivary gland extract profiles are recognized between individual cattle sera (Cruz et al., 2008). Furthermore, sera from a resistant compared to a susceptible cattle breed reacted with more tick salivary proteins, which require further investigation (Garcia et al., 2017). On the other hand, differences in tick numbers and thus the amount of tick antigens in different hosts also requires more in-depth studies to determine immune responses independent of varying tick numbers.
Additional host immune components have also been associated with tick resistance to date, including histamine, complement, acute-phase proteins and bovine lymphocyte antigens. Increased histamine and complement levels were found to be associated with lower tick numbers and resistant animals, respectively (Riek, 1962; Wambura et al., 1998; Zhao et al., 2013). Three proteins of the acute-phase response, which is generally initiated in response to tissue damage (Baumann and Gauldie, 1994), were linked to the tick-resistance mechanism by Carvalho et al. (2008). Briefly, susceptible Holstein-Friesian cattle showed a significant increase in haptoglobulin levels resulting from heavy tick infestation as well as constantly higher alpha-1 acid glycoprotein levels compared to resistant Nelore (B. t. indicus) animals. This might be a result of increased tick numbers and the associated increase in tissue damage on susceptible animals. Lastly, only during intense infestation did the more resistant cattle breed show higher levels of serum amyloid A when compared to the more susceptible cattle breed. In two separate studies, a total of 19 bovine lymphocyte antigens were tested in blood collected from a mixed breed cattle population with no overlapping findings. In total, two antigens were significantly associated with tick resistance (W8 and W16) and three with tick-susceptibility (W5, W6, CA31) (Stear et al., 1984, 1989). Additional data is therefore required to resolve knowledge gaps in the pathways associated with the above-mentioned compounds.
Identification of Immune Cell Subtypes in Circulating Blood of Tick-Infested Cattle Using Associated Markers
Identification and quantification of immune cell subtypes in circulating blood has been performed in B. t. indicus, B. t. taurus and mixed breed cattle with the use of associated markers. Piper et al. (2017) did not find any significant differences while Piper et al. (2009) identified significantly higher levels of CD4+, CD25+ activated and WC1+ γδ T-cell populations in more tick-resistant cattle. Significantly higher levels of CD14+ monocyte and MHC II presenting cells were obtained in more tick-susceptible cattle. As these cell subtypes are known to be associated with a variety of immune responses and pathways, linking them to a putative resistance mechanism will only be possible when analyzing them in combination with additional markers (Figure 2).
Identification of Immune Cell Subtypes in Circulating Blood of Tick-Infested Cattle Using Morphological Characteristics
The cellular composition of blood is regarded as an important identifier of the overall health of humans and animals and as such changes in the percentage of different white blood cell populations may be used as an indication of a systemic immune response. Three main studies have relied on the use of different white blood cell population counts (basophils, eosinophils, lymphocytes, total leukocytes, neutrophils, monocytes) in describing the immune response of cattle with varying levels of tick resistance with no differential regulation identified to date (Brown et al., 1984; Rechav, 1987; Rechav et al., 1990). Only blood eosinophil levels were significantly higher in the more susceptible B. t. taurus breed (which carried more ticks) in the study by Rechav et al. (1990). The investigation of cell subtypes in blood represents a daunting task as shown by the lack of identified differential regulation of markers obtained. In contrast, research to date has detected significant differences between hosts with varying tick-resistance status in skin tissue (refer to skin section below). This is the case since the dynamics of immune cells in blood only provide a snapshot of what is occurring at a specific time point. Experimental layouts must thus be considered carefully as studies incorporating and comparing several time points and/or tissues might represent a more realistic view of immune drivers of resistance.
The skin represents the first site of encounter to tick infestation and thus the first line of host immune defense. Upon penetration and successful attachment, ixodid ticks alternate salivation and blood intake every 5–20 min (Francischetti et al., 2009). Numerous salivary components mediate suppression of host responses such as blood coagulation, immunity, inflammation and the ability of the host to develop new blood vessels (Hovius et al., 2008; Kazimírová and Štibrániová, 2013; Kotál et al., 2015). The identification of immunological defense responses at the site of tick infestation have been extensively studied, as evident from the next section.
Gene Expression Studies in the Skin of Tick-Infested Cattle
Based on transcriptional studies in cattle skin, three studies have identified the involvement of the complement cascade in the feeding of ticks in both susceptible and resistant cattle (Wang et al., 2007; Piper et al., 2010; Carvalho et al., 2014). The complement system is composed of a number of molecules and plays a vital part in the immune system for the clearance of foreign cells via a number of mechanisms (Nesargikar et al., 2012). Upregulation of gene expression for complement components in tick-resistant cattle (C1QA) (Wang et al., 2007) and tick-susceptible cattle (complement component 3) (Piper et al., 2010) have been shown, while the general pathway downregulation of complement has also been described in susceptible animals (Carvalho et al., 2014). More in-depth studies are required regarding these components potentially involved in the tick-resistance mechanism. This is due to the various complement components investigated to date combined with differences amongst results reported. Interestingly, all immunoglobulin associated transcripts were identified to be more abundant in less resistant animals (Wang et al., 2007; Piper et al., 2010) which correlates with findings obtained from blood and could be linked to increased tick numbers on these animals. Furthermore, CD14 (on transcriptional level in skin and translational level in blood) was identified in both tissues to be associated with tick-susceptibility (Piper et al., 2008, 2009). CD14 is known to be a marker for monocytes and macrophages and can therefore be involved in several immune response mechanisms (Ziegler-Heitbrock and Ulevitch, 1993).
Other components that were found to be upregulated in susceptible cattle include transcripts for IL13RA1, CD44, CD63, TNFα, IL-1β, IL-10, NFKBp50, CD1a, CCR-1, CCL2, CCL26, TLR9, MyD88, CD14, FTH1, BDA20, and Traf-6 (Wang et al., 2007; Piper et al., 2008; Nascimento et al., 2011). However, no transcript was reported in more than one of these studies and as such all require validation. Most recently, Franzin et al. (2017) reported on a microarray study of skin from uninfested cattle, larvae (2 days after larvae infestation) and nymph (9 days after larvae infestation) life stages fed on B. t. taurus and B. t. indicus breeds. Samples were compared within and between breeds. An observed allergic contact-like dermatitis was found to be delayed in susceptible animals detected by the involvement of IL-6, CXCL-8, CCL-2, HMGB1, ISG15, and PKR which in turn result in the production of chemokines and cytokines involved in the inflammatory response. In another study, downregulation of inflammatory response gene expression was observed within 24 h after tick infestation in susceptible animals, while at the 48-h sampling point genes associated with antigen presentation and oxidative stress were found to be upregulated in resistant cattle (Carvalho et al., 2014). One study identified CXCL-8 expression as being downregulated in resistant cattle between different genetic crossbred cattle groups from which skin and lymph node samples were obtained 9 days after larvae challenge (Regitano et al., 2008). However, it was unclear to which tissue this finding refers to. Differential gene expression was furthermore identified for genes encoding Blimp-1 (Kongsuwan et al., 2010), cathepsin L2 precursor, MHC class antigen I (Nascimento et al., 2011), various adhesion molecules (Carvalho et al., 2010), TNF receptor-associated factor 6, TATA-binding protein, lumican and beta-2 microglobulin (Marima, 2017).
Due to the variation in experimental designs of different studies, caution should be taken when trying to compare results emanating from transcriptional studies, especially with regards to sampling time points. Since gene expression rarely involves absolute quantification and is based on the relative quantification of transcripts between two populations or between transcripts and reference genes under a specific set of conditions, the results generated may be study specific. RNA sequencing would be an alternative approach not yet utilized in this field of study for the obtainment of large-scale results based on absolute quantification which could allow the identification of novel transcripts. In addition to this, studies on a protein and cellular level, to validate potentially relevant findings from gene expression studies, should be undertaken.
Translational Studies and Metabolites in the Skin of Tick-Infested Cattle
Few studies investigated immune factors underlying the tick-resistance mechanism in skin of cattle on the protein or metabolite level. To date, only one paper has focused on proteins. However, no significant findings regarding proteins directly involved in immune response pathways were identified (Kongsuwan et al., 2010). On a metabolite level, higher histamine levels were linked to tick resistance by Schleger et al. (1981) and Willadsen et al. (1979). These findings also correlate with results obtained from studies done on blood (Riek, 1962; Zhao et al., 2013). Histamine is an immunomodulator produced by a variety of cell types including mast cells, basophils, dendritic cells, and T-cells and can regulate both innate as well as adaptive immune response cells (O'Mahony et al., 2011). The expression of the histidine decarboxylase, which results in the decarboxylation of L-histidine and subsequent production of histamine, is influenced by several immune factors including a variety of cytokines. This secondary metabolite regulates, amongst others, antigen-specific Th1 and Th2 cells in addition to antibody isotype responses (Jutel et al., 2006). Histamine seems to be an effector molecule in tick resistance. This is evident from studies showing that histamine injection at tick attachment sites lead to detachment of some tick larvae, indicating a direct involvement of histamine rather than a general inflammatory reaction being the cause of tick rejection (Kemp and Bourne, 1980).
Furthermore, higher tick numbers were observed in cattle treated with an antihistaminic drug (Tatchell and Bennett, 1969). A response localized to the sites of skin damage is generally the first immunological reaction of a body. Histamine is well documented to be involved in proinflammatory responses and the immediate-type hypersensitivity response, characterized by increased vascular permeability, smooth muscle contractions, activation of certain nerves, wheal-and-flare reactions and itch responses (O'Mahony et al., 2011). Acquired resistance was linked to the occurrence of a hypersensitivity reaction to tick salivary gland components (Riek, 1962). The type of hypersensitivity is, however, not known since contradicting results have been obtained (Kemp et al., 1986; Smith et al., 1989; Latif et al., 1991; Bechara et al., 2000; Piper et al., 2010; Prudencio et al., 2011; Marufu et al., 2013).
Identification of Immune Cell Subtypes via Surface Markers at the Site of Tick Attachment
On a cellular level, two potential cell subtypes have been identified across independent studies. Markers used for the identification of γδ T-lymphocytes were found to be present in higher levels in resistant compared to susceptible animals (Constantinoiu et al., 2010; Franzin et al., 2017). Gamma delta T-cells are suggested to function as regulatory T-cells in bovines (Hoek et al., 2009).
The expression of CD3+ T-lymphocytes was found to be increased at different time points in B. t. indicus cattle (compared to B. t. taurus) in two studies (Constantinoiu et al., 2010; Franzin et al., 2017). This could be explained by different infestation protocols. Constantinoiu et al. (2010) made use of naïve cattle which were infested weekly with R. microplus larvae. Samples were taken at 1 day, one, 3 and 7 weeks post-primary infestation. CD3+ T-lymphocytes were found to be more abundant in resistant cattle at 1 day and at 3 weeks. In contrast, Franzin et al. (2017) used naïve cattle, which were challenged only once. Samples were taken at 2 and 9 days post infestation and significantly higher CD3+ T-lymphocyte levels were found in resistant compared to susceptible animals for the later sampling timepoint only. Based on the above studies and the importance of CD3+ T-lymphocytes in innate and adaptive immune responses, these cells are likely involved in the tick-resistance mechanism.
Neutrophils at the Site of Tick Attachment
Although an increase in neutrophil levels at the site of tick attachment is well described and has been related to the number of previous tick exposures (Allen et al., 1977; Binta and Cunningham, 1984; Brown et al., 1984; Gill, 1986; Walker and Fletcher, 1986), no differences have been reported from studies investigating the association of neutrophils to tick resistance. This led to the hypothesis that this cell type is not linked to the tick-resistance mechanism. Latif et al. (1991) found a decrease in the infiltration of neutrophils in less resistant (B. t. indicus and B. t. taurus) animals when compared to resistant Zebu cattle infested with Rhipicephalus appendiculatus nymphs. In contrast, no differences for cattle infested with Amblyomma variegatum nymphs (comparing resistant and more susceptible Zebu animals) were found. Furthermore, no differences in the number of neutrophils at the site of adult R. microplus attachment could be observed between resistant and susceptible breeds by Carvalho et al. (2010). The same results were obtained by Marufu et al. (2014) for naturally infested cattle. It is evident that there is an increase in the number of neutrophils upon larvae and adult tick infestation, where equal numbers of this cell subtype were found to be present irrespective of the resistance classification of the host (Carvalho et al., 2010; Franzin et al., 2017). Although the reaction of neutrophils upon larval maturation to nymphs presents with conflicting results (Latif et al., 1991; Franzin et al., 2017), the lack of differential levels of this granulocyte seen in the larvae and adult life stage may support the hypothesis that this cell subtype remains unchanged across the tick life cycle.
Basophils at the Site of Tick Attachment
The fluctuation in the number of basophils between tick-resistant and tick-susceptible cattle breeds infested with either one- or multi-host ticks have been studied. Interestingly, Latif et al. (1991) again identified a potential variation in host immune responses to different multi-host tick species. At R. appendiculatus nymph attachment sites, significantly fewer basophils were present in more susceptible compared to resistant cattle within and between breeds. In the same study, no significant differences in the number of basophils were identified between tick-susceptible and tick-resistant cattle within the B. t. indicus breed at the sites of A. variegatum nymph attachment. Yet, cattle of intermediate resistance showed the highest numbers of basophils. This can be explained by the study layout as the cattle group of lower resistance had previous exposure to much lower R. appendiculatus numbers compared to A. variegatum. Therefore, animals could be presenting with a higher resistance level against the latter species and thus account for observed discrepancies.
In the one-host tick, R. microplus, basophil infiltration levels were also found to alter between cattle of varying resistance in response to tick infestation (Figure 1). Overall, basophil numbers at the site of adult tick attachment have been shown to be more abundant at tick attachment sites in resistant cattle than in their susceptible counterpart (Carvalho et al., 2010). Similarly, naturally infested cattle were found to have differing levels of basophils at the site of adult female R. microplus attachment, with tick counts negatively correlating with basophil counts (Marufu et al., 2014). The finding that basophil counts increase at the site of tick attachment in cattle was further corroborated by Franzin et al. (2017). This study showed that not only did both tick-resistant and tick-susceptible cattle recruit basophils at the site of R. microplus infestation, but also that upon maturation of R. microplus larvae to their nymph life stage, significantly more basophils were found to be present in resistant compared to susceptible hosts.
Figure 1. Mast cell, basophil, and eosinophil levels identified in the skin of cattle (sections on Basophils, Eosinophils and Mast Cells at the Site of Tick Attachment) with different tick-resistance status and their correlation with blood (section Translational Studies in the Blood of Tick-Infested Cattle) and skin (section Translational Studies and Metabolites in the Skin of Tick-Infested Cattle) histamine levels (based on literature investigating changes as result of R. microplus infestation). Granulocyte and histamine levels are indicated per tick life stage with arrows. An asterix indicates that a specific cell subtype dynamic between life stages was confirmed by literature as per relevant skin and blood section. Where dynamics were obtained from within breed comparisons the asterix was placed in brackets. Resistant and susceptible animals are abbreviated with “R” and “S”, respectively. Graphical representations correspond to the key of Figure 2.
In summary, upon tick attachment basophil levels seem to increase in all cattle. The rate and level of increase is however dependent on the number of previous tick infestations and the level of tick resistance in the respective cattle breed. An increase in the number of infestations of a less susceptible breed to multi-host adult tick species not only showed an association with increased time taken to recruit basophils, but also increased number of basophils compared to previous tick infestations (Allen et al., 1977; Brown et al., 1984; Walker and Fletcher, 1986). Increased levels of this cell subtype in the nymph and adult life stages were found to be higher in resistant animals, with no difference identified between cattle breeds infested with tick larvae (Latif et al., 1991; Carvalho et al., 2010; Marufu et al., 2014; Franzin et al., 2017). These results suggest that it is not necessarily the difference in immune response pathway between cattle breeds that play a part in resistance but rather the level and reaction time of such immune responses.
Eosinophils at the Site of Tick Attachment
Between breed comparisons of eosinophil levels
Altered patterns of eosinophil regulation were identified across different tick life stages, and will hence be discussed accordingly. Three conclusions can be drawn regarding the attachment of larvae on cattle. Firstly, upon tick larvae attachment, there was an overall increase in the number of eosinophils at the site of tick attachment in all cattle breeds. Susceptible cattle did, however, display a higher influx of eosinophils compared to their tick-resistant counterparts (Figure 1; Moorhouse and Tatchell, 1969; Piper et al., 2010; Franzin et al., 2017). Secondly, the infestation history of the host does not seem to play an important role regarding the levels of eosinophils at the larval life stage. This is supported by the observation that a higher influx of eosinophils to the attachment site occurs in susceptible breeds in naïve cattle as well as in cattle that have been repeatedly infested (Piper et al., 2010; Franzin et al., 2017). Lastly, differences are observed amongst larval infestation using different tick species. In the case of Moorhouse and Tatchell (1969) it was found that hours after the attachment of R. microplus larvae to cattle (with previous tick exposure), susceptible cattle presented with a greater number of eosinophils. In contrast, no difference in the influx of eosinophils was observed between resistant and susceptible cattle breeds in response to infestation with the multi-host tick, Haemaphysalis longicornis.
With regards to nymph infestation, Franzin et al. (2017) showed that a reversal of the larval eosinophil response is observed, where upon maturation of tick larvae to nymphs, a greater number of eosinophils occur in resistant breeds (Figure 1). The same trend seen during the nymph life stage continues into the adult life stage (Figure 1). This has been confirmed in studies using Shorthorn-Zebu vs. Shorthorn (Riek, 1962) and Nelore vs. Holstein-Friesian (Carvalho et al., 2010) cattle infested with adult R. microplus. One study did, however, not confirm this observation. Marufu et al. (2014) identified that the more susceptible Bonsmara (B. t. afrikanus) cattle displayed higher eosinophil levels compared to that of the resistant Nguni (B. t. indicus) cattle breed. To date, it is unknown what the cause of this discrepancy could be.
Within breed comparisons of eosinophil levels
In contrast to studies between cattle breeds, no difference in eosinophil levels at the tick larval life stage was found between animals of the same breed (Figure 1). Schleger et al. (1976) showed that in B. t. taurus infested with R. microplus larvae, similar numbers of eosinophils were present between animals of varying resistance. However, eosinophils were more localized to the site of tick attachment in more resistant cattle (Schleger et al., 1976). This is in contrast to what is seen in blood, where eosinophil levels are significantly higher in susceptible cattle, even under conditions of natural infestation (Rechav et al., 1990).
Regarding nymph infestation, differences in the response were observed with regards to what tick species the cattle were infested with. In a study by Latif et al. (1991) Zebu cattle infested with A. variegatum have a greater influx of eosinophils as opposed to cattle infested with R. appendiculatus. However, upon conducting intra-breed comparisons, Zebu cattle that displayed resistance to R. appendiculatus had lower eosinophil levels while no difference in eosinophil levels could be detected in A. variegatum susceptible or resistant animals. The latter observation could, however, be due to the presence of higher A. variegatum tick numbers compared to R. appendiculatus before the commencement of this study. As such, the tick species effect on eosinophil biology remains to be validated.
Studies focusing on the effects of multiple infestations (independent of the host-resistance status), indicated that eosinophil and degranulation levels progressively increase with the number of infestations with Hyalomma anatolicum anatolicum (Gill, 1986) and R. appendiculatus (Walker and Fletcher, 1986) adults. In contrast, Allen et al. (1977) showed that all B. t. taurus cattle infested with adult Ixodes holocyclus had increased eosinophil levels, irrespective of whether the animals were previously infested or not. However, the latter study should be confirmed due to the low numbers of biological repeats per cattle group and low tick numbers used.
Discrepancies observed for within a single breed to between different cattle breeds infested with tick larvae could indicate that eosinophils play different roles in the resistance mechanism in genetically more resistant breeds compared to acquired resistance within breeds. Since studies looking at the changes in eosinophil levels within breeds have mainly focused on B. t. taurus cattle, more studies should investigate changes in B. t. indicus animals of various resistance.
Mast Cells at the Site of Tick Attachment
Differences in mast cell numbers have been related to the tick life stage and differences have furthermore been found when comparing results from within and between breed studies. Upon R. microplus larvae attachment, there is an increase in the number of mast cells at the site of tick attachment in all cattle (Figure 1). This increase is intensified in more tick-resistant cattle (B. t. indicus) when compared to more susceptible animals (B. t. indicus) (Franzin et al., 2017) which was not seen in a study investigating effects within a B. t. taurus breed (Schleger et al., 1976; Figure 1).
Yet, upon maturation to nymphs, the number of mast cells are similar for both resistant and susceptible animals while a significant decrease in the number of mast cells in more resistant hosts is seen in cattle infested with nymphs compared to larvae (Figure 1; Franzin et al., 2017). Similarly, no significant changes in the number of mast cells in the skin of resistant and more susceptible animals infested with R. appendiculatus or A. variegatum nymphs was found between and within cattle breeds except for a suggested decrease of cells in less resistant animals within the Zebu breed (Latif et al., 1991).
When ticks reached the adult life stage, a greater number of mast cells at the site of tick attachment in more resistant cattle was observed in all studies (Figure 1; Engracia Filho et al., 2006; Veríssimo et al., 2008; Marufu et al., 2014). In a study by Engracia Filho et al. (2006), Gyr x Holstein cattle were grouped into resistant and susceptible groups based on previous infestations. Upon adult attachment of R. microplus it was shown that the number of mast cells in the more resistant group was greater than in the more susceptible group (Engracia Filho et al., 2006). Furthermore, this was confirmed in a similar study using a wider range of cattle breeds and resistance groups including Nelore, Holstein-Friesian, Brown, Gyr and crossbred animals which showed that in the upper dermis of R. microplus adult infested cattle skin there was a negative correlation between the number of ticks on the animals and the number of mast cells present (Veríssimo et al., 2008). Both tick-susceptible and more tick-resistant cattle skin naturally infested with R. microplus adults also showed a negative relationship between tick counts and mast cell numbers (Marufu et al., 2014).
In addition, investigation of the skin of B. t. taurus cattle infested with adult H. a. anatolicum suggested that irrespective of previous exposure to ticks, there is a negative correlation between the number of mast cells in the skin of cattle and the number of ticks attached to these animals (Gill, 1986). An increased number of mast cells was found at the tick bite lesion of tertiary as compared to primary infested animals. Additionally, degranulation of mast cells was seen in tertiary infested animals as opposed to naïve cattle. Allen et al. (1977) showed that in the case of adult I. holocyclus attachment on European cattle breeds, the number of mast cells in the skin increased upon tick attachment irrespective of previous exposure. It was also shown that mast cell infiltration and mast cell degranulation increased in previously exposed cattle as opposed to naïve cattle (Allen et al., 1977). In contrast, to the above results, B. t. taurus cattle infested multiple times with adult R. appendiculatus showed a decrease of mast cells at the tick attachment site (Walker and Fletcher, 1986).
In summary, as for the dynamic of the eosinophil cell subtype, differences in results were seen within and between cattle breeds. Mast cells were found to be at similar levels in susceptible and resistant cattle within a cattle breed. While between breeds, resistant cattle showed higher mast cell levels for the larval life stage (Schleger et al., 1976; Franzin et al., 2017). Similar results were obtained for studies investigating tick nymph and adult life stages between breeds.
Dynamics of Granulocytes and Histamine and their Suggested Involvement in the Tick-Resistance Mechanism Over the Tick Lifecycle
Changes in histamine and cell infiltration patterns over the life cycle of R. microplus stress the importance of taking the dynamics of cellular changes in response to the maturing tick into account when planning a study (Figure 1). In the case of histamine, it is increased in the tick larval life stage (in resistant animals) pointing toward it acting as an effector molecule within cattle breeds. In addition, we hypothesize that histamine is increased in resistant animals throughout all tick life stages based on four observations. Firstly, a study comparing susceptible and intermediate-resistant cattle identified higher blood histamine levels throughout the tick life cycle for the latter group within a single cattle breed (Riek, 1962). Secondly, higher histamine levels were found at the site of larval attachment of more resistant cattle within the same breed (Willadsen et al., 1979; Schleger et al., 1981). Thirdly, resistant breeds have equal or higher basophil (Carvalho et al., 2010; Marufu et al., 2014; Franzin et al., 2017); and mast cell (Schleger et al., 1976; Engracia Filho et al., 2006; Marufu et al., 2014; Franzin et al., 2017;) levels throughout all life stages compared to susceptible breeds. Lastly, as histamine can be released from mast cells as well as basophils via an IgE and/or eosinophil-dependent mechanism, the presence of these cells correlate with the increase in histamine observed (Ishizaka et al., 1972; Zheutlin et al., 1984; Janeway et al., 2001; Galli et al., 2005; Stone et al., 2010) (Figure 2).
Figure 2. Proposed mechanism, role players and associated pathways in the tick-resistance mechanism. An asterix (*) indicates immune molecules that have not yet been identified to be linked to tick resistance/susceptibility in cattle (based on chosen exclusion criteria indicated in text). Molecules without an asterix have been linked to tick resistance/susceptibility in literature (as per relevant skin and blood section). Arrows indicate a direct or indirect link between molecules.
Comparison of Findings Obtained within a Single Cattle Breed
Although no differences were observed for mast cell and eosinophil levels at the larval life stage, histamine levels were found to be higher in resistant compared to susceptible animals (Figure 1) (Riek, 1962; Willadsen et al., 1979; Schleger et al., 1981). Potentially, histamine is thus released via basophils, however, no study up to date has extensively investigated this cell subtype within a single breed. It should be noted that Riek (1962) only investigated the dynamics of this compound during the larval life stage in a limited study using only one highly resistant animal. Higher histamine levels upon nymph and adult tick attachment in blood were also identified when comparing medium resistant to susceptible cattle (Figure 1; Riek, 1962). If histamine levels were linked to tick numbers as result of tissue damage, it would be expected that higher histamine levels are present in more susceptible animals which is not the case. This indicates that histamine could be involved in the tick-resistance mechanism within cattle breeds. Since not enough data regarding the number of granulocytes are available to date for the nymph and adult life stages, it cannot be hypothesized by which cell subtype histamine may be released. However, increased mast cell numbers in resistant compared to susceptible animals at the adult life stage could indicate a delay in mast cell dependent release of histamine as seen for inter-breed comparisons at the larval life stage (section Comparison of Findings Obtained between Different Cattle Breeds).
Comparison of Findings Obtained between Different Cattle Breeds
Although mast cells increased upon larvae attachment for all cattle breeds evaluated, this cell subtype was found to be more abundant in resistant breeds (Figure 1) (Franzin et al., 2017). This, together with the equal levels of basophils in both resistant and susceptible cattle at the tick larval life stage (Figure 1; Franzin et al., 2017), indicates that histamine might be increased as a result of mast cell degranulation and contributes to the first line of tick defense. The higher eosinophil levels in susceptible compared to resistant cattle breeds at the larval life stage (Figure 1; Moorhouse and Tatchell, 1969; Piper et al., 2010; Franzin et al., 2017) furthermore suggests that the immune response in susceptible cattle increases histamine levels via an eosinophil-dependent mechanism. This mechanism might be less efficient and slower in susceptible cattle due to its involvement in late-phase reactions (Piliponsky et al., 2001). Mast cell levels in the nymph life stage were found to be present at similar levels in resistant and susceptible breeds (Latif et al., 1991; Franzin et al., 2017), while a relatively higher number of mast cells was seen in more tick-resistant cattle in the adult tick life stage (Figure 1). This could be a result of a decrease of this cell subtype in susceptible and not an increase in resistant animals. The apparent decline in the number of mast cells that was observed in the more resistant cattle breed from the larvae to the nymph life stage may thus be delayed and occurring in the more susceptible cattle at the adult life stage. Since the tick-resistance mechanism in B. t. indicus animals results in a generally faster response to tick infestation compared to B. t. taurus cattle (Riek, 1962; Wagland, 1978, 1980; Rechav et al., 1990), resistance within susceptible cattle breeds might be achieved through a delayed histamine release via basophils. This mechanism is suggested to occur at the nymph life stage in resistant cattle breeds (Figure 1). To specifically elucidate this resistance mechanism in depth, especially granulocyte levels for animals within a breed, presenting with varying tick-resistance phenotypes, need to be determined throughout the tick life cycle. Additionally, investigation of histamine within and between cattle breeds at all tick life stages are essential.
Future Directions: Potential Drivers Involved in Tick Resistance
This integrative discussion will give an evaluation of key role players investigated up to date to establish a global view of components potentially involved (directly or indirectly) in the tick-resistance mechanism. It must be kept in mind that some observed immune responses may be a by-product of the effector pathway/molecule or a response to tick infestation without any involvement in the actual resistance mechanism. For example, gene expression results and actual dynamics occurring on protein level often do not correlate due to post-transcriptional, post-translational and degradation regulation (Vogel and Marcotte, 2012). Therefore, results from studies employing gene expression analysis were only included as part of this discussion if their findings have been validated by a second study. Furthermore, since gamma globulin levels, apart from IgE, were generally increased in susceptible cattle, this could be linked to elevated tick numbers. Even though antibody specificity could be a contributing factor, these molecules were thus not included as key role players in this section as evidence remains non-conclusive. Lastly, due to a constant dynamic of immune molecules, identified markers on translational and cellular levels were included if a significant difference (irrespective of the direction) was seen between animals with more and less resistance status. Figure 2 summarizes potential role players and their possible interactions driving resistance, based on findings up to date with the discussion providing an integrative explanation of identified immune marker interactions of the respective components supported by literature. Indicated with an asterix (*) in the text below and in Figure 2, are components that have not yet been identified to be linked to tick resistance/susceptibility in cattle.
During the process of tick attachment, the skin of the host is damaged/pierced, and tick saliva is exposed to sentinel cells, such as granulocytes. Several acute-phase proteins have been shown to be involved at the site of tick attachment (Carvalho et al., 2008). These proteins can be linked to granulocyte (Quaye, 2008; Stone et al., 2010; Eklund et al., 2012) and monocyte (Hochepied et al., 2003) recruitment and/or activation. Furthermore, tick secreted allergens can cross-link to IgE (Galli and Tsai, 2012) and binding of IgE to its high-affinity receptor (FcεRI) on dermal mast cells (and basophils) has been shown to lead to the release of inflammatory mediators (Stone et al., 2010) such as histamine (Galli et al., 2005).
Following activation, mast cells readily secrete IL-5*, IL-13*, and TNFα (Janeway et al., 2001; Stone et al., 2010). In addition, IgE binding leads to the enhancement of CCL2 (monocyte chemoattractant protein 1) transcription that promotes the migration of monocytes (Oliveira and Lukacs, 2001) and T-cells (Oliveira and Lukacs, 2003) to amplify the local inflammatory reaction. Lastly, due to the antigen presenting nature of mast cells, following the uptake of the IgE-antigen complex, the allergen is presented on mast cells on MHC II, which in turn interacts directly with T-cell receptors (containing CD3) and induces antigen-specific clonal expansion of T-cell populations (Mekori and Metcalfe, 1999; Henz et al., 2001).
Basophils also function as antigen presenting cells in response to certain allergens (Sokol et al., 2008, 2009). The binding of the IgE-allergen complex to FcεRI on basophils activates several pathways in the cell resulting in the release of histamine (Ishizaka et al., 1972) and the expression of IL-4 and IL-13* (Stone et al., 2010). These cytokines are important for the promotion of eosinophil trafficking (Stone et al., 2010) and are also secreted by Th2 cells in response to the presentation of allergen via MHC II and IL-4 production (Perrigoue et al., 2009; Yoshimoto et al., 2009) Activated Th2 cells also secrete cytokines (e.g., IL-5*) which increases eosinophil production (Janeway et al., 2001).
Antigen presentation to Th2 lymphocytes by mast cells and/or basophils, provide two essential signals for isotype switching. The first signal is IL-4 and/or IL-13* which bind to the respective receptors on B-cells and activate transcription at the IgE isotype-specific site via STAT6 (Stone et al., 2010). The second signal involves the binding of CD40L (CD154L*) to the relevant T-cell receptors, which in turn activates DNA switch recombination (Stone et al., 2010). Basophils express high levels of CD154* after activation and have been suggested to play a role in polyclonal amplification of IgE production and in the differentiation of Th2 cells (Stone et al., 2010). In addition, the binding of CD23* to CD21+ B-cells may participate in the control of IgE production (Aubry et al., 1992).
Histamine can also be released from mast cells and basophils via an IgE-independent mechanism (Siraganian and Hook, 1976; Piliponsky et al., 2001) utilizing the major basic protein* released from eosinophils (Zheutlin et al., 1984; Janeway et al., 2001). The binding of the allergen-IgE complex to mast cells is suggested to drive the recruitment and activation of additional mast cells and eosinophils (Wong et al., 2009). Mast cells can also induce the release of IL-6*, CXCL8, CCL2 and CXCL1* by eosinophils (Wong et al., 2009).
The development of eosinophilic allergic inflammation and the initiation of Th2-responses is regulated by a T-cell subtype (Zuany-Amorim et al., 1998). Regulatory T-cells are generally known for their ability to suppress putative deleterious activities of Th cells (Corthay, 2009), with IL-2* playing an important role in the survival and proliferation of CD4+CD25+ regulatory T-cells (Létourneau et al., 2009). The exact role of CD4+CD25+ regulatory T-cells in bovines is, however, unknown. It has been proposed that this cell population is neither anergic nor suppressive in cattle, and that their function(s) can to be linked to γδ T-cells (WC1.1+, WC1.2+) (Hoek et al., 2009). Together with the latter cell type, CD14+ monocytes have been linked to immune suppression in ruminants (Hoek et al., 2009). In addition, γδ T-cells bearing the lineage marker WC1 are associated with the production of the proinflammatory cytokine IFNγ (Rogers et al., 2005), that furthers the action of CXCL10 (an INFγ inducible protein, which recruits activated Th1 cells to the site of inflammation) (Dufour et al., 2002). Interferon gamma (Zella et al., 1998) as well as other cytokines such as IL-10* on monocytes (Loetscher et al., 1996; Sozzani et al., 1998) can mediate upregulation of CCR1* expression. The release of IL-10*, IL-4 and TGFβ can result in the proliferation of subsets of γδ T-cells (Guzman et al., 2014). The accumulation of γδ T-lymphocytes during allergic inflammation in turn is orchestrated by the CCR2/CCL2 pathway (Costa et al., 2009; de Oliveira Henriques and Penido, 2012).
Several immune markers associated with the above pathways, such as histamine, have been identified in section Blood and Skin Tissue (Figure 2). To date, histamine levels in the blood and skin were found to be increased in resistant cattle, while little variation was seen in susceptible animals (Riek, 1962; Willadsen et al., 1979; Schleger et al., 1981). Degranulation of both mast cells (Riley, 1953; Mota et al., 1954) and basophils (Pruzansky and Patterson, 1970) is followed by the subsequent release of histamine in an immediate hypersensitivity reaction (Ishizaka et al., 1970, 1972). This reaction is well known to be linked to more frequent and intense grooming (O'Mahony et al., 2011), which was identified to play a role in tick-resistance (Riek, 1956; Snowball, 1956). Future studies are now required to elucidate these predicted pathways in depth, focusing on likely markers not yet investigated (*) and molecular mechanisms/molecules that have resulted in contradicting findings up to date. Since opposing findings could be linked to varying study time points, a dynamic investigation of all potential role players would be valuable and could lead to a better-defined picture of occurrences.
Critical Evaluation and Concluding Remarks
To date, few immune markers have been investigated with sufficient depth to obtain a picture of events involved in the cattle tick-resistance mechanism. Especially large-scale transcriptome studies have identified various components with hardly any overlap of results between studies. One reason for this is the differences in experimental designs which can drastically influence the occurrence of immune events depicted at the chosen time point corresponding to a specific tick life stage(s). In addition, potential markers or pathways should not only be studied on a molecular level but also on a cellular level. The clearest pictures, as obtained for histamine, granulocytes and gamma globulin levels, were identified using markers on both translational and cellular level. In this regard, some immune markers seem to differ for the resistance mechanism within a host breed compared to between breeds as well as between tick life stages (see section Dynamics of Granulocytes and Histamine and their Suggested Involvement in the Tick-Resistance Mechanism Over the Tick Lifecycle and Figure 1). It should be noted that even though the final effector molecules might be the same, different pathways are possibly involved in establishing this mechanism (see section Future Directions: Potential Drivers Involved in Tick Resistance). Several experimental factors should thus be considered when comparing experiments as some of these parameters can potentially skew results and lead to contradicting findings if not addressed correctly (Table 1). This includes important aspects and potential solutions regarding (1) factors relating to the selection and treatment of host animals, (2) factors relating to infestation and sampling protocols, (3) selection of immune markers and (4) data analysis and interpretation.
Table 1. Problem identification and potential solutions for studies evaluating the interplay of cattle immune responses to tick infestation.
To date, the only partially clear picture of immune events involved in the tick-resistance mechanism involves histamine and associated cell subtypes and molecules (Figures 1, 2). This pathway, with its effector molecules and modes of action, still requires additional in-depth investigation before focus is placed on the identification of other contributing mechanisms. The identified cell dynamics between tick life stages furthermore suggest that future studies should concentrate on the dynamics of immune responses at various time points over the complete tick life cycle. This would reduce between study variations in addition to obtaining a temporal overview of events. In general, it is advisable that experiments are standardized as much as possible and more focus should lie on an in-depth investigation of markers/pathways across genetic, translational and cellular levels to successfully validate a response. Only then can one attempt to consolidate all information into a feasible blue print for the identification of major drivers underlying the bovine immune mechanism driving tick-resistance and subsequent postulation of viable and effective tick control strategies.
LR, SR, CM-O: conceptualized manuscript focus, critically revised draft manuscript, approved final manuscript; LR, SR: accumulated data, designed Figures and Tables, wrote first manuscript draft.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcimb.2017.00522/full#supplementary-material
Supplementary Table 1. Summary of studies investigating tick resistance/ susceptibility categorized according to tissue of study.
Bechara, G. H., Morelli, J., and Szabó, M. P. J. (2000). Skin test and tick immune status in susceptible and resistant cattle in Brazil. Ann. N. Y. Acad. Sci. 916, 570–575. doi: 10.1111/j.1749-6632.2000.tb05338.x
Brown, S. J., Barker, R. W., and Askenase, P. W. (1984). Bovine resistance to Amblyomma americanum ticks: an acquired immune response characterized by cutaneous basophil infiltrates. Vet. Parasitol. 16, 147–165. doi: 10.1016/0304-4017(84)90016-5
Carvalho, W. A., Bechara, G. H., Moré, D. D., Ferreira, B. R., da Silva, J. S., and de Miranda Santos, I. K. F. (2008). Rhipicephalus (Boophilus) microplus: distinct acute phase proteins vary during infestations according to the genetic composition of the bovine hosts, Bos taurus and Bos indicus. Exp. Parasitol. 118, 587–591. doi: 10.1016/j.exppara.2007.10.006
Carvalho, W. A., Domingues, R., de Azevedo Prata, M. C., da Silva, M. V. G. B., de Oliveira, G. C., Guimarães, S. E. F., et al. (2014). Microarray analysis of tick-infested skin in resistant and susceptible cattle confirms the role of inflammatory pathways in immune activation and larval rejection. Vet. Parasitol. 205, 307–317. doi: 10.1016/j.vetpar.2014.07.018
Carvalho, W. A., Franzin, A. M., Abatepaulo, A. R., de Oliveira, C. J., More, D. D., da Silva, J. S., et al. (2010). Modulation of cutaneous inflammation induced by ticks in contrasting phenotypes of infestation in bovines. Vet. Parasitol. 167, 260–273. doi: 10.1016/j.vetpar.2009.09.028
Constantinoiu, C. C., Jackson, L. A., Jorgensen, W. K., Lew-Tabor, A. E., Piper, E. K., Mayer, D. G., et al. (2010). Local immune response against larvae of Rhipicephalus (Boophilus) microplus in Bos taurus indicus and Bos taurus taurus cattle. Int. J. Parasitol. 40, 865–875. doi: 10.1016/j.ijpara.2010.01.004
Costa, M. F., Nihei, J., Mengel, J., Henriques, M. G., and Penido, C. (2009). Requirement of L-selectin for γδ T lymphocyte activation and migration during allergic pleurisy: co-relation with eosinophil accumulation. Int. Immunopharmacol. 9, 303–312. doi: 10.1016/j.intimp.2008.12.004
Cruz, A. P., Silva, S. S., Mattos, R. T., Da Silva Vaz, I., Masuda, A., and Ferreira, C. A. (2008). Comparative IgG recognition of tick extracts by sera of experimentally infested bovines. Vet. Parasitol. 158, 152–158. doi: 10.1016/j.vetpar.2008.08.016
Domingues, R., Wohlres-Viana, S., Reis, D. R., Teixeira, H. C., Ferreira, A. P., Guimarães, S. E., et al. (2014). Expression of immune response genes in peripheral blood of cattle infested with Rhipicephalus microplus. Genet. Mol. Res. 13, 4013–4021. doi: 10.4238/2014.May.23.12
Doube, B. M., and Wharton, R. H. (1980). The effect of locality, breed and previous tick experience on seasonal changes in the resistance of cattle to Boophilus microplus (Ixodoidea: Ixodidae). Experientia 36, 1178–1179. doi: 10.1007/BF01976112
Dufour, J. H., Dziejman, M., Liu, M. T., Leung, J. H., Lane, T. E., and Luster, A. D. (2002). IFN-γ-inducible protein 10 (IP-10; CXCL10)-deficient mice reveal a role for IP-10 in effector T cell generation and trafficking. J. Immunol. 168, 3195–3204. doi: 10.4049/jimmunol.168.7.3195
Engracia Filho, J. R., Bechara, G. H., and Teodoro, R. L. (2006). Dermal mast cell counts in F2 Holstein x Gir crossbred cattle artificially infested with the tick Boophilus microplus (Acari: Ixodidae). Ann. N. Y. Acad. Sci. 1081, 476–478. doi: 10.1196/annals.1373.070
Franzin, A. M., Maruyama, S. R., Garcia, G. R., Oliveira, R. P., Ribeiro, J. M., Bishop, R., et al. (2017). Immune and biochemical responses in skin differ between bovine hosts genetically susceptible and resistant to the cattle tick Rhipicephalus microplus. Parasit. Vectors 10, 51. doi: 10.1186/s13071-016-1945-z
Garcia, G. R., Maruyama, S. R., Nelson, K. T., Ribeiro, J. M., Gardinassi, L. G., Maia, A. A., et al. (2017). Immune recognition of salivary proteins from the cattle tick Rhipicephalus microplus differs according to the genotype of the bovine host. Parasit. Vectors 10, 144. doi: 10.1186/s13071-017-2077-9
George, J. E., Osburn, R. L., and Wikel, S. K. (1985). Acquisition and expression of resistance by Bos indicus and Bos indicus X Bos taurus calves to Amblyomma americanum infestation. J. Parasitol. 71, 174–182. doi: 10.2307/3281899
Gill, H. S. (1986). Kinetics of mast cell, basophil and eosinophil populations at Hyalomma anatolicum anatolicum feeding sites on cattle and the acquisition of resistance. Parasitology 93, 305–315. doi: 10.1017/S0031182000051477
Guzman, E., Hope, J., Taylor, G., Smith, A. L., Cubillos-Zapata, C., and Charleston, B. (2014). Bovine γδ T cells are a major regulatory T cell subset. J. Immunol. 193, 208–222. doi: 10.4049/jimmunol.1303398
Hewetson, R. W., and Lewis, I. J. (1976). A comparison of the effect of two regimes of infestation on the development of resistance by cattle to the cattle tick, Boophilus microplus (Can.). J. Pavasitol. 62, 307. doi: 10.2307/3279294
Hochepied, T., Berger, F. G., Baumann, H., and Libert, C. (2003). α1-Acid glycoprotein: an acute phase protein with inflammatory and immunomodulating properties. Cytokine Growth Factor Rev. 14, 25–34. doi: 10.1016/S1359-6101(02)00054-0
Hoek, A., Rutten, V. P., Kool, J., Arkesteijn, G. J., Bouwstra, R. J., Van Rhijn, I., et al. (2009). Subpopulations of bovine WC1(+) gamma delta T cells rather than CD4(+) CD25(high) Foxp3(+) T cells act as immune regulatory cells ex vivo. Vet. Res. 40, 6. doi: 10.1051/vetres:2008044
Ishizaka, T., Ishizaka, K., Orange, R. P., and Austen, K. F. (1970). The capacity of human immunoglobulin E to mediate the release of histamine and slow reacting substance of anaphylaxis (SRS-A) from monkey lung. J. Immunol. 104, 343.
Janeway, C. A. J., Travers, P., Walport, M., and Shlomchik, M. J. (2001). Immunobiology: The Immune System in Health and Disease. The Components of the Immune System. 5th Edn. New York, NY: Garland Science.
Jonsson, N. N., Matschoss, A. L., Pepper, P., Green, P. E., and Ansell, J. (2000). Resistance of Holstein-Friesian cows to infestation by the cattle tick (Boophilus microplus). Vet. Parasitol. 89, 297–305. doi: 10.1016/S0304-4017(00)00213-2
Junqueira, V. S., Cardoso, F. F., Oliveira, M. M., Sollero, B. P., Silva, F. F., and Lopes, P. S. (2017). Use of molecular markers to improve relationship information in the genetic evaluation of beef cattle tick resistance under pedigree-based models. J. Anim. Breed. Genet. 134, 14–26. doi: 10.1111/jbg.12239
Kashino, S. S., Resende, J., Sacco, A. M., Rocha, C., Proenca, L., Carvalho, W. A., et al. (2005). Boophilus microplus: the pattern of bovine immunoglobulin isotype responses to high and low tick infestations. Exp. Parasitol. 110, 12–21. doi: 10.1016/j.exppara.2005.01.006
Kazimírová, M., and Štibrániová, I. (2013). Tick salivary compounds: their role in modulation of host defences and pathogen transmission. Front. Cell. Infect. Microbiol. 3:43. doi: 10.3389/fcimb.2013.00043
Kemp, D. H., Agbede, R. I., Johnston, L. A., and Gough, J. M. (1986). Immunization of cattle against Boophilus microplus using extracts derived from adult female ticks: feeding and survival of the parasite on vaccinated cattle. Int. J. Parasitol. 16, 115–120. doi: 10.1016/0020-7519(86)90096-2
Kemp, D. H., and Bourne, A. (1980). Boophilus microplus: the effect of histamine on the attachment of cattle-tick larvae–studies in vivo and in vitro. Parasitology 80, 487–496. doi: 10.1017/S0031182000000950
Kongsuwan, K., Josh, P., Colgrave, M. L., Bagnall, N. H., Gough, J., Burns, B., et al. (2010). Activation of several key components of the epidermal differentiation pathway in cattle following infestation with the cattle tick, Rhipicephalus (Boophilus) microplus. Int. J. Parasitol. 40, 499–507. doi: 10.1016/j.ijpara.2009.10.013
Kotál, J., Langhansová, H., Lieskovská, J., Andersen, J. F., Francischetti, I. M., Chavakis, T., et al. (2015). Modulation of host immunity by tick saliva. J. Proteomics 128, 58–68. doi: 10.1016/j.jprot.2015.07.005
Latif, A. A., Punyua, D. K., Capstick, P. B., Nokoe, S., Walker, A. R., and Fletcher, J. D. (1991). Histopathology of attachment sites of Amblyomma variegatum and Rhipicephalus appendiculatus on zebu cattle of varying resistance to ticks. Vet. Parasitol. 38, 205–213. doi: 10.1016/0304-4017(91)90130-N
Létourneau, S., Krieg, C., Pantaleo, G., and Boyman, O. (2009). IL-2- and CD25-dependent immunoregulatory mechanisms in the homeostasis of T-cell subsets. J. Allergy Clin. Immunol. 123, 758–762. doi: 10.1016/j.jaci.2009.02.011
Loetscher, P., Seitz, M., Baggiolini, M., and Moser, B. (1996). Interleukin-2 regulates CC chemokine receptor expression and chemotactic responsiveness in T lymphocytes. J. Exp. Med. 184, 569–577. doi: 10.1084/jem.184.2.569
Martinez, M. L., Machado, M. A., Nascimento, C. S., Silva, M., Teodoro, R. L., Furlong, J., et al. (2006). Association of BoLA-DRB3. 2 alleles with tick (Boophilus microplus) resistance in cattle. Genet. Mol. Res. 5, 513–524.
Marufu, M. C., Chimonyo, M., Mans, B. J., and Dzama, K. (2013). Cutaneous hypersensitivity responses to Rhipicephalus tick larval antigens in pre-sensitized cattle. Ticks Tick Borne Dis. 4, 311–316. doi: 10.1016/j.ttbdis.2012.12.001
Marufu, M. C., Dzama, K., and Chimonyo, M. (2014). Cellular responses to Rhipicephalus microplus infestations in pre-sensitised cattle with differing phenotypes of infestation. Exp. Appl. Acarol. 62, 241–252. doi: 10.1007/s10493-013-9723-5
Mattioli, R. C. (1998). Comment on “A possible explanation of the apparent breed-related resistance in cattle to bont tick (Amblyomma hebraeum) infestations” by M.I. Meltzer. Vet. Parasitol. 67, 275–279. Vet. Parasitol. 79, 263–266.
Mattioli, R. C., Pandey, V. S., Murray, M., and Fitzpatrick, J. L. (2000). Immunogenetic influences on tick-resistance in African cattle with particular reference to trypanotolerant N'Dama (Bos taurus) and trypanosusceptible Gobra zebu (Bos indicus) cattle. Acta. Trop. 75, 263–277. doi: 10.1016/S0001-706X(00)00063-2
Meltzer, M. I. (1996). A possible explanation of the apparent breed-related resistance in cattle to bont tick (Amblyomma hebraeum) infestations. Vet. Parasitol. 67, 275–279. doi: 10.1016/S0304-4017(96)01018-7
Momin, R. R., Banerjee, D. P., and Samantaray, S. (1991). Attempted immunisation of crossbred calves (Bos taurus x Bos indicus) by repeated natural attachment of ticks Hyalomma anatolicum anatolicum Koch (1844). Trop. Anim. Heal. Prod. 23, 227–231. doi: 10.1007/BF02357105
Mota, R. R., Lopes, P. S., Tempelman, R. J., Silva, F. F., Aguilar, I., Gomes, C. C., et al. (2016a). Genome-enabled prediction for tick resistance in Hereford and Braford beef cattle via reaction norm models. J. Anim. Sci. 94, 1834–1843. doi: 10.2527/jas.2015-0194
Mota, R. R., Silva, F. F., Lopes, P. S., Tempelman, R. J., Sollero, B. P., Aguilar, I., et al. (2017). Analyses of reaction norms reveal new chromosome regions associated with tick resistance in cattle. Animal 2017, 1–0. doi: 10.1017/S1751731117001562
Mota, R. R., Tempelman, R. J., Lopes, P. S., Aquilar, I., Silva, F. F., and Cardoso, F. F. (2016b). Genotype by environment interaction for tick resistance of Hereford and Braford beef cattle using reaction norm models. Genet. Sel. Evol. 48, 3. doi: 10.1186/s12711-015-0178-5
Mwangi, E. K., Stevenson, P., Ndung, U. J., Stear, M. J., Reid, S. W., Gettinby, G., et al. (1998). Studies on host resistance to tick infestations among trypanotolerant Bos indicus cattle breeds in east Africa. Ann. N. Y. Acad. Sci. 849, 195–208. doi: 10.1111/j.1749-6632.1998.tb11049.x
Nascimento, C. S., Machado, M. A., Guimarães, S. E. F., Martins, M. F., Peixoto, J. O., Furlong, J., et al. (2011). Expressed sequenced tags profiling of resistant and susceptible Gyr x Holstein cattle infested with the tick Rhipicephalus (Boophilus) microplus. Genet. Mol. Res. 10, 3803–3816. doi: 10.4238/2011.November.8.3
Norval, R. A., Sutherst, R. W., and Kerr, J. D. (1996). Infestations of the bont tick Amblyomma hebraeum (Acari: Ixodidae) on different breeds of cattle in Zimbabwe. Exp. Appl. Acarol. 20, 599–605. doi: 10.1007/BF00052810
O'Mahony, L., Akdis, M., and Akdis, C. A. (2011). Regulation of the immune response and inflammation by histamine and histamine receptors. J. Allergy Clin. Immunol. 128, 1153–1162. doi: 10.1016/j.jaci.2011.06.051
Oliveira, S. H., and Lukacs, N. W. (2001). Stem cell factor and IgE-stimulated murine mast cells produce chemokines (CCL2, CCL17, CCL22) and express chemokine receptors. Inflamm. Res. 50, 168–174. doi: 10.1007/s000110050741
Oliveira, S. H., and Lukacs, N. W. (2003). The role of chemokines and chemokine receptors in eosinophil activation during inflammatory allergic reactions. Braz. J. Med. Biol. Res. 36, 1455–1463. doi: 10.1590/S0100-879X2003001100002
Perrigoue, J. G., Saenz, S. A., Siracusa, M. C., Allenspach, E. J., Taylor, B. C., Giacomin, P. R., et al. (2009). MHC class II-dependent basophil-CD4+ T cell interactions promote TH2 cytokine-dependent immunity. Nat. Immunol. 10, 697–705. doi: 10.1038/ni.1740
Piliponsky, A. M., Pickholtz, D., Gleich, G. J., and Levi-Schaffer, F. (2001). Human eosinophils induce histamine release from antigen-activated rat peritoneal mast cells: a possible role for mast cells in late-phase allergic reactions. J. Allergy Clin. Immunol. 107, 993–1000. doi: 10.1067/mai.2001.114656
Piper, E. K., Jackson, L. A., Bagnall, N. H., Kongsuwan, K. K., Lew, A. E., and Jonsson, N. N. (2008). Gene expression in the skin of Bos taurus and Bos indicus cattle infested with the cattle tick, Rhipicephalus (Boophilus) microplus. Vet. Immunol. Immunopathol. 126, 110–119. doi: 10.1016/j.vetimm.2008.06.011
Piper, E. K., Jackson, L. A., Bielefeldt-Ohmann, H., Gondro, C., Lew-Tabor, A. E., and Jonsson, N. N. (2010). Tick-susceptible Bos taurus cattle display an increased cellular response at the site of larval Rhipicephalus (Boophilus) microplus attachment, compared with tick-resistant Bos indicus cattle. Int. J. Parasitol. 40, 431–441. doi: 10.1016/j.ijpara.2009.09.009
Piper, E. K., Jonsson, N. N., Gondro, C., Lew-Tabor, A. E., Moolhuijzen, P., Vance, M. E., et al. (2009). Immunological profiles of Bos taurus and Bos indicus cattle infested with the cattle tick, Rhipicephalus (Boophilus) microplus. Clin. Vaccine Immunol. 16, 1074–1086. doi: 10.1128/CVI.00157-09
Piper, E. K., Jonsson, N. N., Gondro, C., Vance, M. E., Lew-Tabor, A., and Jackson, L. A. (2017). Peripheral cellular and humoral responses to infestation with the cattle tick Rhipicephalus microplus in Santa Gertrudis cattle. Parasite Immunol. 39:e12402. doi: 10.1111/pim.12402
Prudencio, C. R., Rezende Rodrigues, A. A., Cardoso, R., de Souza, G. R. L., Szabó, M. P. J., and Goulart, L. R. (2011). Cutaneous hypersensitivity test to evaluate phage display anti-tick borne vaccine antigen candidates. Exp. Parasitol. 129, 388–392. doi: 10.1016/j.exppara.2011.08.017
Rechav, Y. (1987). Resistance of Brahman and Hereford cattle to African ticks with reference to serum gamma globulin levels and blood composition. Exp. Appl. Acarol. 3, 219–232. doi: 10.1007/BF01270458
Regitano, L. C., Ibelli, A. M., Gasparin, G., Miyata, M., Azevedo, A. L., Coutinho, L. L., et al. (2008). “On the search for markers of tick-resistance in bovines,” in Animal Genomics for Animal Health, eds M.-H. Pinard, C. Gay, P.-P. Pastoret, and B. Dodet (Basel: Karger Publishers), 225–230.
Riek, R. F. (1962). Studies on the reactions of animals to infestation with ticks. VI. Resistance of cattle to infestation with the tick Boophilus microplus (Canestrini). Crop Pasture Sci. 13, 532–550. doi: 10.1071/AR9620532
Roberts, J. A. (1968b). Resistance of cattle to the tick Boophilus microplus (Canestrini). II. Stages of the life cycle of the parasite against which resistance is manifest. J. Parasitol. 54, 667–673. doi: 10.2307/3277017
Rogers, A. N., Van Buren, D. G., Hedblom, E., Tilahun, M. E., Telfer, J. C., and Baldwin, C. L. (2005). Function of ruminant γδ T cells is defined by WC1.1 or WC1.2 isoform expression. Vet. Immunol. Immunopathol. 108, 211–217. doi: 10.1016/j.vetimm.2005.08.008
Sahibi, H., Rhalem, A., and Tikki, N. (1998). Comparison of effects of low and high tick infestations on acquired cattle tick-resistance: Hyalomma marginatum marginatum. Parasite 5, 69–74. doi: 10.1051/parasite/1998051069
Schleger, A. V., Lincoln, D. T., McKenna, R. V., Kemp, D. H., and Roberts, J. A. (1976). Boophilus microplus: cellular responses to larval attachment and their relationship to host resistance. Aust. J. Biol. Sci. 29, 499–512. doi: 10.1071/BI9760499
Seifert, G. W. (1971). Variations between and within breeds of cattle in resistance to field infestations of the cattle tick (Boophilus microplus). Crop Pasture. Sci. 22, 159–168. doi: 10.1071/AR9710159
Smith, R. E., Mwase, E. T., Heller-Haupt, A., Trinder, P. K., Pegram, R. G., Wilsmore, A. J., et al. (1989). Delayed-type hypersensitivity test for assessing tick-immune status of cattle in Zambia. Vet. Rec. 124, 583–584. doi: 10.1136/vr.124.22.583
Sokol, C. L., Chu, N.-Q., Yu, S., Nish, S. A., Laufer, T. M., and Medzhitov, R. (2009). Basophils function as antigen-presenting cells for an allergen-induced T helper type 2 response. Nat. Immunol. 10, 713–720. doi: 10.1038/ni.1738
Sollero, B. P., Junqueira, V. S., Gomes, C. C. G., Caetano, A. R., and Cardoso, F. F. (2017). Tag SNP selection for prediction of tick resistance in Brazilian Braford and Hereford cattle breeds using Bayesian methods. Genet. Sel. Evol. 49, 49. doi: 10.1186/s12711-017-0325-2
Sozzani, S., Ghezzi, S., Iannolo, G., Luini, W., Borsatti, A., Polentarutti, N., et al. (1998). Interleukin 10 increases CCR5 expression and HIV infection in human monocytes. J. Exp. Med. 187, 439–444. doi: 10.1084/jem.187.3.439
Stear, M. J., Newman, M. J., Nicholas, F. W., Brown, S. C., and Holroyd, R. G. (1984). Tick-resistance and the major histocompatibility system. Aust. J. Exp. Biol. Med. Sci. 62, 47–52. doi: 10.1038/icb.1984.4
Stear, M. J., Nicholas, F. W., Brown, S. C., and Holroyd, R. G. (1989). Class I antigens of the bovine major histocompatibility system and resistance to the cattle tick (Boophilus microplus) assessed in three different seasons. Vet. Parasitol. 31, 303–315. doi: 10.1016/0304-4017(89)90080-0
Veríssimo, C. J., Bechara, G. H., Mukai, L. S., Otsuk, I. P., and Pozzi Arcaro, J. R. (2008). Mast cell counts correlate with Rhipicephalus (Boophilus) microplus tick load in different cattle breeds. Braz. J. Vet. Pathol. 1, 81–87.
Wagland, B. M. (1975). Host resistance to cattle tick (Boophilus microplus) in Brahman (Bos indicus) cattle. I. Responses of previously unexposed cattle to four infestations with 20,000 larvae. Crop Pasture. Sci. 26, 1073–1080. doi: 10.1071/AR9751073
Wagland, B. M. (1978). Host resistance to cattle tick (Boophilus microplus) in Brahman (Bos indicus) cattle. III. *Growth on previously unexposed animals. Crop Pasture. Sci. 29, 401–409. doi: 10.1071/AR9780401
Wagland, B. M. (1980). “Tick-resistance in Brahman cattle. in Ticks and tick-borne diseases,” in Proceedings of a Symposium Held at the 56th Annual Conference of the Australian Veterinary Association, Townsville, 14-18 May 1979. Australian Veterinary Association, 55–60.
Walker, A. R., and Fletcher, J. D. (1986). Histological study of the attachment sites of adult Rhipicephalus appendiculatus on rabbits and cattle. Int. J. Parasitol. 16, 399–413. doi: 10.1016/0020-7519(86)90121-9
Wambura, P. N., Gwakisa, P. S., Silayo, R. S., and Rugaimukamu, E. A. (1998). Breed-associated resistance to tick infestation in Bos indicus and their crosses with Bos taurus. Vet. Parasitol. 77, 63–70. doi: 10.1016/S0304-4017(97)00229-X
Wang, Y. H., Reverter, A., Kemp, D., McWilliam, S. M., Ingham, A., Davis, C. A., et al. (2007). Gene expression profiling of Hereford Shorthorn cattle following challenge with Boophilus microplus tick larvae. Anim. Prod. Sci. 47, 1397–1407. doi: 10.1071/EA07012
Wharton, R. H., Utech, K. B. W., and Turner, H. G. (1970). Resistance to the cattle tick, Boophilus microplus in a herd of Australian Illawarra Shorthorn cattle: its assessment and heritability. Crop Pasture Sci. 21, 163–181. doi: 10.1071/AR9700163
Willadsen, P., Wood, G. M., and Riding, G. A. (1979). The relation between skin histamine concentration, histamine sensitivity, and the resistance of cattle to the tick, Boophilus microplus. Parasitol. Res. 59, 87–93. doi: 10.1007/BF00927849
Wong, C. K., Ng, S. S., Lun, S. W., Cao, J., and Lam, C. W. (2009). Signalling mechanisms regulating the activation of human eosinophils by mast-cell-derived chymase: implications for mast cell-eosinophil interaction in allergic inflammation. Immunology 126, 579–587. doi: 10.1111/j.1365-2567.2008.02916.x
Yoshimoto, T., Yasuda, K., Tanaka, H., Nakahira, M., Imai, Y., Fujimori, Y., et al. (2009). Basophils contribute to TH2-IgE responses in vivo via IL-4 production and presentation of peptide-MHC class II complexes to CD4+ T cells. Nat. Immunol. 10, 706–712. doi: 10.1038/ni.1737
Zella, D., Barabitskaja, O., Burns, J. M., Romerio, F., Dunn, D. E., Revello, M. G., et al. (1998). Interferon-gamma increases expression of chemokine receptors CCR1, CCR3, and CCR5, but not CXCR4 in monocytoid U937 cells. Blood 91, 4444–4450.
Zhao, G., Yu, M., Cui, Q. W., Zhou, X., Zhang, J. C., Li, H. X., et al. (2013). Association of bovine Toll-like receptor 4 with tick infestation rates and blood histamine concentration. Genet. Mol. Res. 12, 2783–2793. doi: 10.4238/2013.February.28.21
Zheutlin, L. M., Ackerman, S. J., Gleich, G. J., and Thomas, L. L. (1984). Stimulation of basophil and rat mast cell histamine release by eosinophil granule-derived cationic proteins. J. Immunol. 133, 2180–2185.
Keywords: cattle, tick, resistance, tick resistance, immune factors, parasite, host
Citation: Robbertse L, Richards SA and Maritz-Olivier C (2017) Bovine Immune Factors Underlying Tick Resistance: Integration and Future Directions. Front. Cell. Infect. Microbiol. 7:522. doi: 10.3389/fcimb.2017.00522
Received: 22 June 2017; Accepted: 07 December 2017;
Published: 19 December 2017.
Edited by:Ard Menzo Nijhof, Freie Universität Berlin, Germany
Reviewed by:Jingwen Wang, Yale University, United States
Marinela Contreras Rojo, Instituto de Investigación en Recursos Cinegéticos (CSIC-UCLM-JCCM), Spain
Copyright © 2017 Robbertse, Richards and Maritz-Olivier. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Christine Maritz-Olivier, email@example.com
†These authors have contributed equally to this work.