Intestinal Innate Antiviral Immunity and Immunobiotics: Beneficial Effects against Rotavirus Infection
- 1Immunobiotics Research Group, Tucuman, Argentina
- 2Laboratory of Immunobiotechnology, Reference Centre for Lactobacilli (CERELA-CONICET), Tucuman, Argentina
- 3Food and Feed Immunology Group, Laboratory of Animal Products Chemistry, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan
- 4Faculty of Medicine, INSIBIO (UNT-CONICET), National University of Tucuman, Tucuman, Argentina
- 5Livestock Immunology Unit, International Education and Research Center for Food and Agricultural Immunology (CFAI), Graduate School of Agricultural Science, Tohoku University, Sendai, Japan
The mucosal tissues of the gastrointestinal tract are the main portal entry of pathogens such as rotavirus (RV), which is a leading cause of death due to diarrhea among young children across the globe and a major cause of severe acute intestinal infection in livestock animals. The interactions between intestinal epithelial cells (IECs) and immune cells with RVs have been studied for several years, and now, it is known that the innate immune responses triggered by this virus can have both beneficial and detrimental effects for the host. It was demonstrated that natural RV infection in infants and experimental challenges in mice result in the intestinal activation of pattern recognition receptors (PRRs) such as toll-like receptor 3 (TLR3) and striking secretion of proinflammatory mediators that can lead to increased local tissue damage and immunopathology. Therefore, modulating desregulated intestinal immune responses triggered by PRRs activation are a significant promise for reducing the burden of RV diseases. The ability of immunoregulatory probiotic microorganisms (immunobiotics) to protect against intestinal infections, such as those caused by RVs, is among the oldest effects studied for these important group of beneficial microbes. In this review, we provide an update of the current status on the modulation of intestinal antiviral innate immunity by immunobiotics and their beneficial impact on RV infection. In addition, we describe the research of our group that demonstrated the capacity of immunobiotic strains to beneficially modulated TLR3-triggered immune response in IECs, reduce the disruption of intestinal homeostasis caused by intraepithelial lymphocytes, and improve the resistance to RV infections.
One of the leading causes of children mortality is preventable infectious diseases (1, 2). Rotavirus (RVs), calicivirus, astrovirus, and adenovirus account to the viral etiologic agents of gastroenteritis in humans (3, 4). RV, a naked double-strand RNA (dsRNA) virus, is the most common cause of severe dehydrating diarrhea in children (5, 6). The main symptoms of RVs gastroenteritis are nausea, low-grade fever, vomit, and acute watery diarrhea. Even though two oral vaccines containing attenuated live viruses are being used globally, Rotarix (GlaxoSmithKline) and RotaTeq (Merck), the epidemic in the developing world is far from being controlled (6, 7). Vaccine effectiveness is reduced in developing areas, and some possible reasons are children infected at an early age, high viral challenge loads, and the lack of transferred maternal antibodies (8, 9).
Some lactic acid bacteria (LAB) strains are able to impact on human and animal health by modulating the mucosal and systemic immune systems. Those immunoregulatory probiotic LAB, known as immunobiotics, provide protection against viral infections by modulating innate and adaptive antiviral immunity. Thus, several reports have shown that immunobiotic LAB shorten the duration of diarrhea, reduce the number of episodes, diminish RVs shedding, normalize gut permeability, and increase the production of RVs-specific antibodies (10–12).
The purpose of this review is to provide an update of the current status on the modulation of intestinal antiviral innate immunity by immunobiotics, and their beneficial impact on RVs infection. We also highlight some results of our group, which demonstrate the capacity of immunobiotic strains to beneficially modulate toll-like receptor (TLR)-3-triggered immune response in intestinal epithelial cells (IECs), reduce the disruption of intestinal homeostasis caused by intraepithelial lymphocytes (IELs), and improve the resistance to RVs infection.
Intestinal Antiviral Innate Immune Response and Rotavirus
Upon RVs internalization, the capsid uncoats loosing VP4 and VP7, the outer surface proteins, and yielding a transcriptionally active double-layered particle. The eleven segments of dsRNA viral genome are transcribed directing the synthesis of structural and non-structural proteins and serving as templates for the complementary strand of genomic RNA (13). The IEC senses viral dsRNA through pattern recognition receptors (PRRs), such as TLR3, retinoic acid-inducible gene-I (RIG-I), and melanoma differentiation-associated gene-5 (MDA-5), and cellular signaling cascades are activated to react to viral infection (14–16) (Figure 1). One of the major innate responses against dsRNA viruses relies on the activation of those PRRs, which leads to the production of cytokines and chemokines by IECs and immune cells. Thus, RVs dsRNA triggers the production of IL-8, IP-10, IL-6, TNF-α, and IL-15 in IECs via the TLR3-, RIG-I-, and MDA5-activated pathways inducing recruitment and activation of macrophages and NK cells and stimulating adaptive B- and T-cell immune responses. As a result of PRRs activation, interferons (IFNs) and IFN-regulated gene products are also produced and they play a key role in establishing an antiviral state for virus clearance and restriction of spread (Figure 1). Type I and III IFNs limit RV infection in vitro, and their levels are augmented in RVs-infected children and animals (17–19). Both families of IFN are immediately produced upon RV infection, elicit responses on different types of receptors, and temporally and spatially regulated in the gastrointestinal tract (20). Another evidence suggesting that IFNs are crucial to limit RV infection relies on the fact that this virus has evolved mechanisms to manipulate IFNs signaling such as the type I IFNs damping NSP1 protein (21). While TLR3 mainly recognizes viral components such as viral nucleic acid in endosomal compartments, RIG-I and MDA-5 recognize cytoplasmatic dsRNA. These pathways converge at the level of IFN regulatory factor-3 (IRF3) (18, 22, 23). Upon IRF3 phosphorylation, antiviral responses initiate the activation of type I IFN, which in turn induces the synthesis of interferon-stimulated genes (ISGs), secretion of proinflammatory cytokines, and activation and maturation of antigen-presenting cells (APCs) (Figure 2).
Figure 1. Innate immune response against rotavirus in intestinal epithelial cells (IECs). Rotavirus double-strand genomic RNA activates toll-like receptor 3 (TLR3), retinoic acid-inducible gene-I (RIG-I), and melanoma differentiation-associated gene-5 (MDA-5), which are pattern recognition receptors (PRRs) expressed in IECs. Cellular signaling cascades are activated and converge at the level of interferon (IFN) regulatory factor-3 (IRF3) that upregulate the expression of type I (IFN-α, IFN-β) and type III (IFNλ1, IFNλ2/3) IFN, which in turn induces the synthesis of IFN-stimulated genes with antiviral activities (MxA, Mx1, RNase L, OAS, PKR). Antiviral PRRs also activate nuclear factor κB (NF-κB) pathway and induce the secretion of proinflammatory cytokines and chemokines (IL-6, IL-8, MCP-1, CXCL10). Those effects could be imitated in vitro and in vivo by administration of the dsRNA synthetic analog poly(I:C).
Figure 2. Innate immune response against rotavirus in intestinal mucosa. Rotavirus double-strand genomic RNA activate toll-like receptor 3 (TLR3), retinoic acid-inducible gene-I (RIG-I), and melanoma differentiation-associated gene-5 (MDA-5), which are pattern recognition receptors (PRRs) expressed in intestinal epithelial cells (IECs) and dendritic cells (DCs). Activation of antiviral PRRs in the intestinal mucosa increases the production of type I IFN (IFN-α, IFN-β), IFN-γ, and proinflammatory cytokines and chemokines (TNF-α, IL-6, IL-8, IL-12, MCP-1), which improves the antiviral state in IECs, induces the recruitment and activation of immune cells and the maturation of DCs. Those effects could be imitated in vitro and in vivo by administration of the dsRNA synthetic analog poly(I:C).
Poly(I:C), a synthetic analog of dsRNA, when administered intraperitoneally to mice mimics the local intestinal immune response elicited by an enteric viral infection (24, 25). Both purified RVs dsRNA and poly(I:C) are able to induce severe mucosal damage in the gut via TLR3 activation including villous atrophy, mucosal erosion, and gut wall attenuation (24). IELs, which are mostly T cells distributed as single cells within the epithelial cell layer, play a critical role in disrupting epithelial homeostasis caused by abnormal TLR3 signaling (Figure 3) (24). Due to their key location at the interface between the inner intestinal tissue and the lumen, these specialized immune cells are important as a first line of defense against microbes and in maintaining the epithelial barrier homeostasis. The majority of IELs are CD8+ being simply classified as CD8αα+ or CD8αβ+. The CD8αβ+ IELs bear the hallmarks of adaptive immune cells, whereas the CD8αα+ IELs are considered innate immune cells (26). When TLR3 is abnormally activated by poly(I:C) and RVs, genomic dsRNA, IL-15, and CD3+NK1.1+CD8αα+ IELs are involved in the disruption of epithelial homeostasis. In addition, it was demonstrated that TLR3 activation in IECs induces the expression of retinoic acid early inducible-1 (RAE1), which mediates epithelial destruction and mucosal injury by interacting with the NKG2D receptor expressed on IELs (27) (Figure 3).
Figure 3. Inflammatory damage of the intestinal mucosa induced by rotavirus in a toll-like receptor 3-deppendent manner. Both purified rotavirus double-strand genomic RNA and poly(I:C) induce severe mucosal intestinal damage via TLR3 activation and intestinal epithelial cells (IECs) and intraepithelial lymphocytes (IELs) interaction. Activation of TLR3 in IECs increases the expression of proinflammatory cytokines and chemokines (MCP-1, IL-8, IL-15) and retinoic acid early inducible-1 (RAE1). IL-15 produced by IECs induce the recruitment of CD3+NK1.1+CD8αα+ IELs, which mediates epithelial destruction and mucosal injury by the NKG2D receptor expressed on these cells that is able to recognize RAE1. This intestinal TLR3-IECs-IELs interaction induces villous atrophy, mucosal erosion, and gut wall attenuation.
Thus, increasing our understanding of how PRRs such as TLR3 are activated and regulated in immune cells and IECs may help designing effective therapies for the prevention and/or treatment of viral diseases.
Beneficial Effects of Immunobiotics in Rotavirus Infection
Several studies have demonstrated that immunobiotics are able to improve the outcome of RV infection in human and livestock animals.
Effects of Immunobiotics in Humans
Lactobacillus rhamnosus GG is probably the most studied probiotic bacteria in the context of intestinal viral infections. Isolauri et al. (28) first described for more than 20 years, a protective effect of L. rhamnosus GG strain in RVs gastroenteritis in infants and children. In this study, the patients who received either a L. rhamnosus GG-fermented milk product or a L. rhamnosus GG freeze-dried powder after oral rehydration presented a significantly shorter duration of diarrhea when compared to the placebo group. Later, Majamaa et al. (29) conducted a study, in which 6- to 35-month-old children with RVs gastroenteritis received either L. rhamnosus GG, Lactobacillus acidophilus or a combination of Streptococcus thermophilus with L. delbrückii subsp. bulgaricus twice daily for 5 days. Only children who received L. rhamnosus GG had shorter diarrhea duration. The protective effect was related to augmented intestinal and serum IgA concentration, and a higher number of specific antibody-secreting cells to RVs. Additional studies showed that the consumption of L. rhamnosus GG is able to shorten the diarrheal phase in children suffering from RVs infection, an effect that was associated with increased concentrations of IgA antibodies as well (28–33). Furthermore, meta-analysis showed that the administration of L. rhamnosus GG to hospitalized children reduced the overall incidence of health care-associated diarrhea, including symptomatic RVs gastroenteritis (34). In spite of this evidence, it is important to notice that the shortening of diarrhea already at day 3 after probiotic treatment strongly suggests that the main therapeutic effect involves innate immune responses rather than the modulation of adaptive immunity (35).
Another example of probiotic treatment for alleviating RVs gastroenteritis was the use of Lactobacillus reuteri, which has been daily administered to hospitalized children with acute diarrhea for the length of hospitalization (up to 5 days). L. reuteri shortened both the duration of RVs diarrhea and the disease severity, when compared to the placebo group (36). L. sporogenes daily administered to newborns during 1 year, prevented the incidence and also diminished the duration of acute RVs diarrhea (37). Fang et al. (38) demonstrated that a minimal effective dose of L. rhamnosus significantly reduced fecal shedding RVs concentration in pediatric patients. Although the administration of lyophilized Lactobacillus paracasei strain ST11 daily for 5 days had a clinically significant benefit in the management of non-RVs-induced diarrhea, ST11 treatment against severe RVs diarrhea was ineffective (39). Children with RV infection who received milk-based formula supplemented with either B. animalis Bb12 alone or combined with S. thermophilus had fewer RVs infections (40).
In Argentina, mucosal infections such as bronchitis and diarrhea are the most common infectious diseases in children (41–43). In a randomized controlled trial conducted by Villena et al. (44), L. rhamnosus CRL1505 (administered in a yogurt formulation) improved mucosal immunity and reduced the incidence and severity of intestinal and respiratory infection in children. Hence, the incidence of infectious events was reduced from 66% in the placebo group to 34% in the group that received the probiotic yogurt. Furthermore, there was also a significant reduction in the occurrence of indicators of disease severity such as fever and the need for antibiotic treatment in children receiving the probiotic yogurt (44). Therefore, the results of this trial suggested that consumption of yogurt containing L. rhamnosus CRL1505 was helpful to reduce the burden of common childhood morbidities, especially those associated to viral infections including RVs (44).
Effects of Immunobiotics in Livestock Animals
Apart from the beneficial effects of immunobiotics on humans, some studies have evaluated their antiviral and anti-inflammatory activities in animals. Zhang et al. (45) reported that probiotic administration to gnotobiotic pigs challenged with RVs did not yielded differences in virus titers with respect to the placebo group. Nonetheless, LAB administration downregulated the recruitment of viral-activated monocytes/macrophages into the intestinal tract thereby limiting the inflammation induced by the virus (45).
In another study, it was shown that systemic monocyte/macrophage and APCs responses were modulated by immunobiotics in the context of a RV infection (45). Probiotic LAB induced strong TLR2-expressing APCs responses in blood and spleen, RVs induced a TLR3 response in spleen, and TLR9 responses were induced by RVs (as measured in immune cells isolated from spleen) and LAB (as determined in blood circulating immune cells). Immunobiotics and RVs had an additive effect on TLR2- and TLR9-expressing APCs responses, consistent with the adjuvant effect of LAB. Immunobiotics augmented IFN-γ and IL-4 levels in serum, but suppressed TLR3- and TLR9-expressing APCs responses in spleen and the serum IFN-α response induced by virulent RVs (46).
During RVs infections in weaned pigs, there is evidence of disruption of the barrier function as evidenced by the decreased villus height and crypt depth, lower levels of IgA, IL-4, and mucin 1 as well a reduced transcription of ZO-1, occludin, and Bcl-2 in jejunal mucosa (47). Some of these effects have been partially associated with alterations of transforming growth factor (TGF)-β production (48). Azevedo et al. (48) demonstrated that immunobiotic LAB further enhanced the Th1 and Th2 cytokine responses to RV infection as indicated by significantly higher concentrations of IL-12, IFN-γ, IL-4, and IL-10 in RVs-infected gnotobiotic pigs. LAB also helped to maintain immunological homeostasis during RV infection by regulating TGF-β production. It was also shown that treatment of pigs with L. rhamnosus GG modulated TGF-β and promoted the enhancement of intestinal epithelial tight junctions, which may contribute to the preservation and restoration of the gut homeostasis after RV infection (11). Further evidence was reported by Maragkoudakis et al. (12) demonstrating that Lactobacillus casei Shirota and L. rhamnosus GG protected porcine and goat epithelial cells from RVs and other transmissible gastroenteritis viruses.
Cellular and Molecular Mechanisms of Immunobiotics Actions
The interactions of IECs with luminal antigens and with immune cells play a central role in determining the type of immune response triggered by intestinal microorganisms (5, 6). A critical and virtually universal early innate response of host cells to viral infection is the secretion of factors belonging to the IFN family. The secretion of IFN results in the expression of several ISGs products with antiviral activities.
We showed in different studies that the originally established porcine intestinal epithelial cell line (PIE cells) is a useful tool for studying IFN response triggered by TLR3, RIG-I, and/or MDA-5 activation. These cells are permissive to porcine RVs and also respond to dsRNA and its synthetic analog poly(I:C) (49, 50). Furthermore, co-cultures of PIE cells with immune cells isolated from porcine Peyer’s patches (PPs) provide an in vitro system to study the transduction of the signal from its detection by IECs to the effect on the under laying immune cells.
The response of PIE cells to poly(I:C) challenge was evaluated, and it was found that MCP-1, IL-8, TNF-α, IL-6, and both IFN-α and IFN-β were upregulated in PIE cells after stimulation (49). We also showed that after stimulation of co-cultures with poly(I:C), there was an upregulation of IFN-α, IFN-β, IFN-γ, IL-2, and IL-12p40 in immune cells (49). TLR3 was the receptor involved in the recognition of the luminal stimulus and the responsible to trigger the expression and release of cytokines, which in turn activated the underlying APCs and effector lymphocytes.
Rotavirus infection stimulates IFN-β and early antiviral gene expression by a signaling pathway that requires MAVS, an adaptor protein that is recruited to signaling complexes following activation of RIG-I or MDA-5 (51, 52). In addition, both RIG-I and MDA-5 are involved in recognizing RVs infection, as proven by the reduction of IFN-β induction when these factors are lost (51, 52). Taking into account those facts, we evaluated the suitability of PIE cells and co-cultures as models for studying this signaling pathway after RVs infection. Our results showed that PIE cells have functional TLR3, RIG-I, and MDA-5 receptors, which signal via IRF3 and NF-κB, inducing IFN-β and the upregulation of the ISGs MxA and RNase L (50), which are important antiviral effectors of IFN pathway.
We used PIE cells for the screening of immunobiotic LAB strains taking into consideration their ability to enhance IFN-β production upon poly(I:C) stimulation (49, 53). Thus, L. casei MEP221106 was selected because of its potential to impact on viral intestinal infections. L. casei MEP221106 had the highest capacity to improve IFN-β production in poly(I:C)-challenged PIE cells. Moreover, in vitro co-culture experiments showed that L. casei MEP221106 was able to improve not only the production of IFN-β but also the levels of other cytokines including IFN-α, TNF-α, MPC-1, and IL-6. In co-cultures of PIE cells with immune cells, we demonstrated that L. casei MEP221106 improved the production of inflammatory and antiviral cytokines by PPs cells when compared with control cells (49).
The PIE system was also used to screen bifidobacteria strains with anti-RVs effect (50). Bifidobacterium infantis MCC12 and Bifidobacterium breve MCC1274 were selected in the screen because they significantly upregulated IFN-β in response to poly(I:C) challenge. In addition, both MCC12 and MCC1274 strains significantly increased PIE cells resistance to RV infection (Figure 4), while other strains with moderate or no effect in IFN-β production did not have any influence on RVs replication (50). As a result of the enhanced IFN-β levels, there was a concomitant upregulation of the ISGs MxA and RNase L. These effectors of antiviral immunity have different mechanisms of action: RNase L degrades dsRNA and the resulting RNA fragments activate RLRs to amplify IFN production and induce apoptosis on virus infected cells (54), while MxA hijacks newly synthesized viral proteins into perinuclear complexes. Then, the upregulation of MxA, RNase L, and probably other ISGs induced by MCC12 and MCC1274 strains through IFN-β would be related to the lower RVs replication found in bifidobacteria-treated PIE cells. This is supported by the fact that IFN-β is a key factor for improving defenses against RVs since viral replication is restricted in permissive cells when they are pretreated with IFN-β (55). Accordingly, IFN-β treatment of newborn calves and piglets prior to RV infection reduces virus replication and disease severity (56).
Figure 4. Beneficial effects of immunobiotic bifidobacteria on the innate immune response against rotavirus in intestinal epithelial cells (IECs). Rotavirus double-strand genomic RNA activates toll-like receptor 3 (TLR3), retinoic acid-inducible gene-I (RIG-I), and melanoma differentiation-associated gene-5 (MDA-5), which are pattern recognition receptors (PRRs) expressed in IECs. Cellular signaling cascades mediated by interferon (IFN) regulatory factor-3 (IRF3) upregulate the expression of type I (IFN-α, IFN-β), and type III (IFNλ1, IFNλ2/3) IFN, which in turn induces the synthesis of IFN-stimulated genes with antiviral activities (MxA, Mx1, RNase L, OAS, PKR). Antiviral PRRs also activate nuclear factor κB (NF-κB) pathway and induce the secretion of proinflammatory cytokines and chemokines (IL-6, MCP-1, CXCL10). Preventive treatment of IECs with Bifidobacterium infantis MCC12 or Bifidobacterium breve MCC1274 reduce the expression of A20, increase the activation of IRF3, improve the production of the antiviral factors IFN-α, IFN-β, MxA, and RNase L, and differentially regulate the expression of IL-6, MCP-1, and CXCL10.
Several cytokines are induced via NF-κB signaling as a result of RVs infection, including IL-8, RANTES, GM-CSF, GRO-α, MIP-1β, and IP-10 (57), as observed in both cell lines and histological intestinal samples. Secreted cytokines initiate an important primary line of host defense, but if this response lasts too long or is dysregulated, it may lead to tissue damage and epithelial barrier dysfunction. In this regard, we have reported that efficient regulation of inflammatory response induced by immunobiotic bacteria is essential to achieve full protection against pathogens (58, 59). In line with this, we also showed that bifidobacteria strains MCC12 and MCC1274 differentially modulated the production of proinflammatory mediators in RVs-infected PIE cells (Figure 4) (50).
Toll-like receptor negative regulators play key roles in maintaining intestinal hemostasis by regulating TLR signaling. The zinc-finger protein A20, due to its deubiquitinase and ubiquitinase E3 ligase activities, is capable to terminate TLR signaling that results in inhibition of NF-κB activation and reduction of inflammatory induced cytotoxicity (60). Saitoh et al. (61) reported that IRF3 activation is suppressed by A20. The A20 protein is able to induce the suppression of the IFN-mediated immune response and IFN-promoter-dependent transcription by physically interacting with IKK-i/IKKϵ and inhibiting dimerization of IRF3 following engagement of TLR3 by dsRNA. Moreover, A20 knock down results in enhanced IRF3-dependent transcription triggered by the stimulation of TLR3 or virus infection. Human monocyte-derived dendritic cells (DCs) stimulated with poly(I:C) upregulate A20. When A20 is downregulated in DCs, they showed higher activation of NF-κB and AP-1, which resulted in increased and sustained production of IL-6, IL-10, and IL-12p70. Furthermore, DCs enhanced their T cell stimulatory capacity (62). Negative regulators involved in TLR signaling can be modulated by immunobiotic strains in human intestinal cell lines (63). In this regard, we also reported that both B. infantis MCC12 and B. breve MCC1274 significantly reduced the expression of A20 in RVs-infected PIE cells (Figure 4) (50), which is in line with the capacity of both strains to improve IRF3 activation and IFN-β production. In line with our findings, MacPherson et al. (64) also studied the effect of probiotics in the modulation of poly(I:C) induced inflammatory response in HT-29 cells. Stimulating HT29 cells with poly(I:C) alone increased the expression of A20, but the co-stimulation with poly(I:C) and probiotics significantly reduced A20 expression levels.
We also used these porcine in vitro systems to attain deeper knowledge into the mechanisms involved in the immunomodulatory effect of L. rhamnosus CRL1505 and concentrated our attention in the crosstalk between the immunobiotic strain and porcine IECs and APCs, in order to explain its capacity to reduce viral diarrhea episodes in children (44). Moreover, we performed comparative studies with another immunobiotic strain, Lactobacillus plantarum CRL1506, that is able stimulate intestinal immunity in animal models (65). Studies comparing the immunobiotic strains L. rhamnosus CRL1505 and L. plantarum CRL1506 in co-cultures of PIE cells and APCs, stimulated with poly(I:C), showed that both strains improved the production of type I IFNs in response to poly(I:C) challenge (66). In addition, CRL1505 and CRL1506 strains modulated the expression of proinflammatory and regulatory cytokines and influenced activation and maturation of APCs (Figure 5). However, L. rhamnosus CRL1505 had a stronger effect both when applied alone or combined with a posterior poly(I:C) challenge. The improved Th1 response induced by immunobiotic lactobacilli was evidenced by the augmented expression of MHC-II, IL-1β, IL-6, and IFN-γ in DCs (66, 67). Those studies gave scientific basis for explaining the protection against intestinal viral infections achieved by L. rhamnosus CRL1505 in children.
Figure 5. Beneficial effects of immunobiotic lactobacilli on the innate immune response against rotavirus in intestinal mucosa. Rotavirus double-strand genomic RNA or poly(I:C) activate toll-like receptor 3 (TLR3), retinoic acid-inducible gene-I (RIG-I), and melanoma differentiation-associated gene-5 (MDA-5), which are pattern recognition receptors (PRRs) expressed in intestinal epithelial cells (IECs) and dendritic cells (DCs). Activation of antiviral PRRs increases the production of IFN-α, IFN-β, IFN-γ, and proinflammatory cytokines and chemokines (TNF-α, IL-6, IL-8, IL-12, MCP-1), which improves the antiviral state in IECs, induces the recruitment and activation of immune cells and the maturation of DCs. In addition, both purified rotavirus genomic dsRNA and poly(I:C) activate TLR3 in IECs increasing the expression of IL-15 and retinoic acid early inducible-1 (RAE1). IL-15 produced by IECs induces the recruitment of CD3+NK1.1+CD8αα+ intraepithelial lymphocytes (IELs), which mediates epithelial destruction and mucosal injury by the NKG2D receptor expressed on these cells that is able to recognize RAE1. Preventive treatments with Lactobacillus rhamnosus CRL1505 or Lactobacillus plantarum CRL1506 improve the production of type I IFN and IFN-γ in the intestinal mucosa enhancing the antiviral state and differentially regulate the expression of inflammatory cytokines and chemokines reducing the intestinal damage, especially associated with the TLR3–IECs–IELs interaction.
The receptors, which are activated by the immunobiotics strains with antiviral capabilities MEP221106, MCC12, MCC1274, CRL1505, and CRL1506 strains in PIE cells to reduce A20, improve IRF-3 activation and increase IFN-β production remains to be uncovered. Bifidobacteria strains with a high capacity to stimulate TLR2 such as B. longum BB536 and B. breve M-16V were able to increase the expression of A20 in PIE cells and reduce TLR4-mediated inflammatory response (68, 69). On the contrary, strains with low capacity of stimulating TLR2 did not modify the expression of the ubiquitin-editing enzyme A20 in PIE cells challenged with TLR4 agonists. In our experiments, we were unable to block the increase of IFN-β induced by the lactobacilli and bifidobacteria by using anti-TLR2 or anti-TLR9 antibodies, suggesting that other receptor(s) are involved in the immunobiotic activity (66). Further studies are needed in order to find the PRRs involved in the recognition of lactobacilli and bifidobacteria leading to A20 and IFN-β modulation in PIE cells.
Recently, we confirmed in vivo the differential antiviral immunomodulatory activities triggered by L. rhamnosus CRL1505 and L. plantarum CRL1506 (65). Both strains increased the production of IFNs, the CRL1505 treatment being the most effective for increasing the levels of IFN-γ. Then, our results suggest that these two lactobacilli strains have potential to be used to improve the outcome of viral gastrointestinal disease. This is also supported by the human clinical trial demonstrating the capacity of L. rhamnosus CRL1505 to improve the infectious disease rates in children (70). Recently, Zhang et al. (71) proposed the activation of innate immunity with flagellin as a preventive and therapeutic strategy against RVs infection. They demonstrated that intraperitoneal flagellin injection reduced severity and shedding of RVs RNA in acute and chronic infected mice via TLR5/NLRC4 activation, which resulted in secretion of IL-22 and IL-18 by different effector cells. Although the mechanism of action of flagellin administration is substantially different to the mechanisms elicited by immunobiotics, both approaches rely on the principle of combating viral infection by enhancing innate immune defenses.
Lactobacillus rhamnosus CRL1505 and L. plantarum CRL1506 also reduced TLR3-induced small intestinal injury by regulation of proinflammatory cytokines production and IECs–IELs interaction (65) (Figure 5). IECs and IELs are the first line of defense against pathogens including viruses, and their interaction is essential for maintaining an appropriate immunological homeostasis. IECs produce a variety of cytokines and chemokines, including IL-6, IL-7, IL-8, IL-15, TNF-α, TGF-β, and GM-CSF. IL-15 functions as a mediator of TLR3-induced small intestinal injury (24). Abnormal TLR3 signaling results in elevated levels of IL-15, which regulates IECs apoptosis by activating perforin-mediated killing by CD3+NK1.1+ IELs (70). Moreover, IL-15 is able to enhance the cytotoxic activity of human IELs (72). Blocking the α receptor of IL-15 partially protected mice from poly(I:C)-induced small intestinal injury, including less villous atrophy, and mucosal erosion (24). Autologous ligands released by cells stress and infection are recognized by the NKG2D receptor in NK cells. NKG2D ligands expression is downregulated by gut microbiota, as demonstrated in germ-free mice, which had increased surface expression of these ligands (73). RAE1, a high affinity NKG2D ligand, which is minimally detected in normal cells, is upregulated upon TLR3 activation. In fact, blockade of NKG2D–RAE1 interaction avoids the cytotoxic effect of IELs on IECs and prevents acute small intestinal injury in mice challenged with dsRNA (27). Therefore, TLR3 signaling stimulates IECs to express IL-15 and RAE1 and induces CD3+NK1.1+CD8αα+ IELs to express NKG2D through IEC-derived IL-15. In our hands, poly(I:C) treatment of mice increased intestinal injury in a IL-15- and CD8αα+NKG2D+-dependent manner (65). Poly(I:C) induced inflammatory-mediated intestinal tissue damage through the increase of CD3+NK1.1+ and CD8αα+NKG2D+ cells as well as proinflammatory mediators (TNF-α, IL-1β, IFN-γ, IL-15, RAE1, IL-8). Mice pretreated with immunobiotic lactobacilli before TLR3 activation responded with reduced levels of TNF-α, IL-15, RAE1, CD3+NK1.1+, CD3+CD8αα+, and CD8αα+NKG2D+ cells (Figure 5). The beneficial effect of these lactobacilli improved mice health as reflected by a significant reduction of body weight loss and intestinal tissue damage after poly(I:C) challenge (65).
It is well known that commensal bacteria in the gut are able to modulate IELs function. Furthermore, IELs are significantly reduced in germ-free mice (74, 75) underlying gut microbiota importance in the maintenance of IELs. These specialized lymphocytes are very important players in mucosal protection; they seem to occupy a unique temporal niche from which they are able to detect and limit bacterial penetration already in the first hours after pathogen attack (76). Ismail et al. (76) showed that IEL antibacterial response depends on bacterial stimulation in a MyD88-dependent signaling. Later, Jiang et al. (77) investigated the role of NOD2 signaling in the maintenance of IELs and found that NOD2 maintained IELs via recognition of gut microbiota. They demonstrated that stimulation of IEL requires activation of PRRs signaling in neighboring IECs (76, 77).
Therefore, it was shown that commensal bacteria establish a regulatory milieu in a healthy gut, with increased expression of immuno-inhibitory cytokines such as TGF-β and IL-10, which in turn downregulate NKG2D ligand surface expression (78, 79). This is in line with our findings for the immunomodulatory strains L. rhamnosus CRL1505 and L. plantarum CRL1506, which reduced expression of RAE-1 and increased levels of intestinal IL-10. Whether the immunomodulatory effects of L. rhamnosus CRL1505 and L. plantarum CRL1506 are induced by direct action on the IECs (indirectly on IELs) and/or a direct effect on IELs is an open question, which we propose to address in the near future.
The detailed characterization of the cellular and molecular mechanisms underlying the intestinal innate defense against RV infection achieved in the past years has opened new ways for developing strategies to preventing and treating this viral induced diarrhea. In this sense, the use of immunobiotic bacteria to beneficially modulate IFN and inflammatory signaling pathways in IECs and immune cells is an attractive target for preventive or therapeutic intervention against RVs infection. Furthermore, the advances in the knowledge of the molecular crosstalk between immunobiotics and the gut innate immune system have provided light into the microorganism-sensing signals that allow these beneficial microorganisms to improve intestinal immune responses. This new molecular information might be helpful to improve the development of functional foods and/or pharmabiotics using immunobiotics aimed to reduce mortality and severity of RVs disease.
JV, MV-P, and HK designed, wrote, and revised the review article.
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.
This study was supported by a Grant-in-Aid for Scientific Research (B) (2) (No. 16H05019), Challenging Exploratory Research (No. 16K15028), and Open Partnership Joint Projects of JSPS Bilateral Joint Research Projects from the Japan Society for the Promotion of Science (JSPS) to Dr. HK. This study was supported by an ANPCyT–FONCyT Grant PICT-2013 (No. 3219) to Dr. JV.
1. Bryce J, Black RE, Walker N, Bhutta ZA, Lawn JE, Steketee RW. Can the world afford to save the lives of 6 million children each year? Lancet (2005) 365(9478):2193–200. doi: 10.1016/S0140-6736(05)66777-3
4. Tran A, Talmud D, Lejeune B, Jovenin N, Renois F, Payan C, et al. Prevalence of rotavirus, adenovirus, norovirus, and astrovirus infections and coinfections among hospitalized children in northern France. J Clin Microbiol (2010) 48(5):1943–6. doi:10.1128/JCM.02181-09
7. Tate JE, Patel MM, Cortese MM, Lopman BA, Gentsch JR, Fleming J, et al. Remaining issues and challenges for rotavirus vaccine in preventing global childhood diarrheal morbidity and mortality. Expert Rev Vaccines (2012) 11(2):211–20. doi:10.1586/erv.11.184
10. Basu S, Paul DK, Ganguly S, Chatterjee M, Chandra PK. Efficacy of high-dose Lactobacillus rhamnosus GG in controlling acute watery diarrhea in Indian children: a randomized controlled trial. J Clin Gastroenterol (2009) 43(3):208–13. doi:10.1097/MCG.0b013e31815a5780
11. Liu F, Li G, Wen K, Bui T, Cao D, Zhang Y, et al. Porcine small intestinal epithelial cell line (IPEC-J2) of rotavirus infection as a new model for the study of innate immune responses to rotaviruses and probiotics. Viral Immunol (2010) 23(2):135–49. doi:10.1089/vim.2009.0088
12. Maragkoudakis PA, Chingwaru W, Gradisnik L, Tsakalidou E, Cencic A. Lactic acid bacteria efficiently protect human and animal intestinal epithelial and immune cells from enteric virus infection. Int J Food Microbiol (2010) 141(Suppl 1):S91–7. doi:10.1016/j.ijfoodmicro.2009.12.024
14. Frias AH, Jones RM, Fifadara NH, Vijay-Kumar M, Gewirtz AT. Rotavirus-induced IFN-beta promotes anti-viral signaling and apoptosis that modulate viral replication in intestinal epithelial cells. Innate Immun (2012) 18(2):294–306. doi:10.1177/1753425911401930
15. Frias AH, Vijay-Kumar M, Gentsch JR, Crawford SE, Carvalho FA, Estes MK, et al. Intestinal epithelia activate anti-viral signaling via intracellular sensing of rotavirus structural components. Mucosal Immunol (2010) 3(6):622–32. doi:10.1038/mi.2010.39
17. Sen A, Rothenberg ME, Mukherjee G, Feng N, Kalisky T, Nair N, et al. Innate immune response to homologous rotavirus infection in the small intestinal villous epithelium at single-cell resolution. Proc Natl Acad Sci U S A (2012) 109(50):20667–72. doi:10.1073/pnas.1212188109
20. Lin JD, Feng N, Sen A, Balan M, Tseng HC, McElrath C, et al. Distinct roles of type I and type III interferons in intestinal immunity to homologous and heterologous rotavirus infections. PLoS Pathog (2016) 12(4):e1005600. doi:10.1371/journal.ppat.1005600
21. Barro M, Patton JT. Rotavirus NSP1 inhibits expression of type I interferon by antagonizing the function of interferon regulatory factors IRF3, IRF5, and IRF7. J Virol (2007) 81(9):4473–81. doi:10.1128/JVI.02498-06
22. Loo YM, Fornek J, Crochet N, Bajwa G, Perwitasari O, Martinez-Sobrido L, et al. Distinct RIG-I and MDA5 signaling by RNA viruses in innate immunity. J Virol (2008) 82(1):335–45. doi:10.1128/JVI.01080-07
25. Araya RE, Jury J, Bondar C, Verdu EF, Chirdo FG. Intraluminal administration of poly I:C causes an enteropathy that is exacerbated by administration of oral dietary antigen. PLoS One (2014) 9(6):e99236. doi:10.1371/journal.pone.0099236
26. Shires J, Theodoridis E, Hayday AC. Biological insights into TCRgammadelta+ and TCRalphabeta+ intraepithelial lymphocytes provided by serial analysis of gene expression (SAGE). Immunity (2001) 15(3):419–34. doi:10.1016/S1074-7613(01)00192-3
27. Zhou R, Wei H, Sun R, Zhang J, Tian Z. NKG2D recognition mediates toll-like receptor 3 signaling-induced breakdown of epithelial homeostasis in the small intestines of mice. Proc Natl Acad Sci U S A (2007) 104(18):7512–5. doi:10.1073/pnas.0700822104
28. Isolauri E, Juntunen M, Rautanen T, Sillanaukee P, Koivula T. A human Lactobacillus strain (Lactobacillus casei sp strain GG) promotes recovery from acute diarrhea in children. Pediatrics (1991) 88(1):90–7.
29. Majamaa H, Isolauri E, Saxelin M, Vesikari T. Lactic acid bacteria in the treatment of acute rotavirus gastroenteritis. J Pediatr Gastroenterol Nutr (1995) 20(3):333–8. doi:10.1097/00005176-199504000-00012
31. Kaila M, Isolauri E, Soppi E, Virtanen E, Laine S, Arvilommi H. Enhancement of the circulating antibody secreting cell response in human diarrhea by a human Lactobacillus strain. Pediatr Res (1992) 32(2):141–4. doi:10.1203/00006450-199208000-00002
32. Shornikova AV, Casas IA, Mykkanen H, Salo E, Vesikari T. Bacteriotherapy with Lactobacillus reuteri in rotavirus gastroenteritis. Pediatr Infect Dis J (1997) 16(12):1103–7. doi:10.1097/00006454-199712000-00002
33. Guarino A, Canani RB, Spagnuolo MI, Albano F, Di Benedetto L. Oral bacterial therapy reduces the duration of symptoms and of viral excretion in children with mild diarrhea. J Pediatr Gastroenterol Nutr (1997) 25(5):516–9. doi:10.1097/00005176-199711000-00005
34. Szajewska H, Wanke M, Patro B. Meta-analysis: the effects of Lactobacillus rhamnosus GG supplementation for the prevention of healthcare-associated diarrhoea in children. Aliment Pharmacol Ther (2011) 34(9):1079–87. doi:10.1111/j.1365-2036.2011.04837.x
35. Vlasova AN, Kandasamy S, Chattha KS, Rajashekara G, Saif LJ. Comparison of probiotic lactobacilli and bifidobacteria effects, immune responses and rotavirus vaccines and infection in different host species. Vet Immunol Immunopathol (2016) 172:72–84. doi:10.1016/j.vetimm.2016.01.003
36. Shornikova AV, Casas IA, Isolauri E, Mykkanen H, Vesikari T. Lactobacillus reuteri as a therapeutic agent in acute diarrhea in young children. J Pediatr Gastroenterol Nutr (1997) 24(4):399–404. doi:10.1097/00005176-199704000-00008
37. Chandra RK. Effect of Lactobacillus on the incidence and severity of acute rotavirus diarrhoea in infants. A prospective placebo-controlled double-blind study. Nutr Res (2002) 22:65–9. doi:10.1016/S0271-5317(01)00367-0
38. Fang SB, Lee HC, Hu JJ, Hou SY, Liu HL, Fang HW. Dose-dependent effect of Lactobacillus rhamnosus on quantitative reduction of faecal rotavirus shedding in children. J Trop Pediatr (2009) 55(5):297–301. doi:10.1093/tropej/fmp001
39. Sarker SA, Sultana S, Fuchs GJ, Alam NH, Azim T, Brussow H, et al. Lactobacillus paracasei strain ST11 has no effect on rotavirus but ameliorates the outcome of nonrotavirus diarrhea in children from Bangladesh. Pediatrics (2005) 116(2):e221–8. doi:10.1542/peds.2004-2334
40. Phuapradit P, Varavithya W, Vathanophas K, Sangchai R, Podhipak A, Suthutvoravut U, et al. Reduction of rotavirus infection in children receiving bifidobacteria-supplemented formula. J Med Assoc Thai (1999) 82(Suppl 1):S43–8.
41. Bardach A, Ciapponi A, Garcia-Marti S, Glujovsky D, Mazzoni A, Fayad A, et al. Epidemiology of acute otitis media in children of Latin America and the Caribbean: a systematic review and meta-analysis. Int J Pediatr Otorhinolaryngol (2011) 75(9):1062–70. doi:10.1016/j.ijporl.2011.05.014
42. Edmond K, Scott S, Korczak V, Ward C, Sanderson C, Theodoratou E, et al. Long term sequelae from childhood pneumonia; systematic review and meta-analysis. PLoS One (2012) 7(2):e31239. doi:10.1371/journal.pone.0031239
43. Gentile A, Bardach A, Ciapponi A, Garcia-Marti S, Aruj P, Glujovsky D, et al. Epidemiology of community-acquired pneumonia in children of Latin America and the Caribbean: a systematic review and meta-analysis. Int J Infect Dis (2012) 16(1):e5–15. doi:10.1016/j.ijid.2011.09.013
44. Villena J, Salva S, Núñez M, Corzo J, Tolaba R, Faedda J, et al. Probiotics for everyone! The novel immunobiotic Lactobacillus rhamnosus CRL1505 and the beginning of Social Probiotic Programs in Argentina. Int J Biotechnol Wellness Ind (2012) 1:189–98. doi:10.6000/1927-3037/2012.01.03.05
45. Zhang W, Wen K, Azevedo MS, Gonzalez A, Saif LJ, Li G, et al. Lactic acid bacterial colonization and human rotavirus infection influence distribution and frequencies of monocytes/macrophages and dendritic cells in neonatal gnotobiotic pigs. Vet Immunol Immunopathol (2008) 121(3–4):222–31. doi:10.1016/j.vetimm.2007.10.001
46. Wen K, Li G, Bui T, Liu F, Li Y, Kocher J, et al. High dose and low dose Lactobacillus acidophilus exerted differential immune modulating effects on T cell immune responses induced by an oral human rotavirus vaccine in gnotobiotic pigs. Vaccine (2012) 30(6):1198–207. doi:10.1016/j.vaccine.2011.11.107
47. Mao X, Gu C, Hu H, Tang J, Chen D, Yu B, et al. Dietary Lactobacillus rhamnosus GG supplementation improves the mucosal barrier function in the intestine of weaned piglets challenged by porcine rotavirus. PLoS One (2016) 11(1):e0146312. doi:10.1371/journal.pone.0146312
48. Azevedo MS, Zhang W, Wen K, Gonzalez AM, Saif LJ, Yousef AE, et al. Lactobacillus acidophilus and Lactobacillus reuteri modulate cytokine responses in gnotobiotic pigs infected with human rotavirus. Benef Microbes (2012) 3(1):33–42. doi:10.3920/BM2011.0041
49. Hosoya S, Villena J, Shimazu T, Tohno M, Fujie H, Chiba E, et al. Immunobiotic lactic acid bacteria beneficially regulate immune response triggered by poly(I:C) in porcine intestinal epithelial cells. Vet Res (2011) 42(1):111. doi:10.1186/1297-9716-42-111
50. Ishizuka T, Kanmani P, Kobayashi H, Miyazaki A, Soma J, Suda Y, et al. Immunobiotic bifidobacteria strains modulate rotavirus immune response in porcine intestinal epitheliocytes via pattern recognition receptor signaling. PLoS One (2016) 11(3):e0152416. doi:10.1371/journal.pone.0152416
51. Sen A, Pruijssers AJ, Dermody TS, Garcia-Sastre A, Greenberg HB. The early interferon response to rotavirus is regulated by PKR and depends on MAVS/IPS-1, RIG-I, MDA-5, and IRF3. J Virol (2011) 85(8):3717–32. doi:10.1128/JVI.02634-10
52. Broquet AH, Hirata Y, McAllister CS, Kagnoff MF. RIG-I/MDA5/MAVS are required to signal a protective IFN response in rotavirus-infected intestinal epithelium. J Immunol (2011) 186(3):1618–26. doi:10.4049/jimmunol.1002862
53. Hosoya S, Villena J, Chiba E, Shimazu T, Suda Y, Aso H, et al. Advanced application of porcine intestinal epithelial cells for the selection of immunobiotics modulating toll-like receptor 3-mediated inflammation. J Microbiol Immunol Infect (2013). 46:474–81. doi:10.1016/j.jmii.2012.04.005
55. Papp H, Laszlo B, Jakab F, Ganesh B, De Grazia S, Matthijnssens J, et al. Review of group A rotavirus strains reported in swine and cattle. Vet Microbiol (2013) 165(3–4):190–9. doi:10.1016/j.vetmic.2013.03.020
56. Arnold MM, Sen A, Greenberg HB, Patton JT. The battle between rotavirus and its host for control of the interferon signaling pathway. PLoS Pathog (2013) 9(1):e1003064. doi:10.1371/journal.ppat.1003064
57. Casola A, Estes MK, Crawford SE, Ogra PL, Ernst PB, Garofalo RP, et al. Rotavirus infection of cultured intestinal epithelial cells induces secretion of CXC and CC chemokines. Gastroenterology (1998) 114(5):947–55. doi:10.1016/S0016-5085(98)70314-2
58. Chiba E, Villena J, Hosoya S, Takanashi N, Shimazu T, Aso H, et al. A newly established bovine intestinal epithelial cell line is effective for in vitro screening of potential antiviral immunobiotic microorganisms for cattle. Res Vet Sci (2012) 93(2):688–94. doi:10.1016/j.rvsc.2011.10.002
59. Zelaya H, Tsukida K, Chiba E, Marranzino G, Alvarez S, Kitazawa H, et al. Immunobiotic lactobacilli reduce viral-associated pulmonary damage through the modulation of inflammation-coagulation interactions. Int Immunopharmacol (2014) 19(1):161–73. doi:10.1016/j.intimp.2013.12.020
61. Saitoh T, Yamamoto M, Miyagishi M, Taira K, Nakanishi M, Fujita T, et al. A20 is a negative regulator of IFN regulatory factor 3 signaling. J Immunol (2005) 174(3):1507–12. doi:10.4049/jimmunol.174.3.1507
62. Breckpot K, Aerts-Toegaert C, Heirman C, Peeters U, Beyaert R, Aerts JL, et al. Attenuated expression of A20 markedly increases the efficacy of double-stranded RNA-activated dendritic cells as an anti-cancer vaccine. J Immunol (2009) 182(2):860–70. doi:10.4049/jimmunol.182.2.860
63. Seifert S, Rodriguez Gomez M, Watzl B, Holzapfel WH, Franz CM, Vizoso Pinto MG. Differential effect of Lactobacillus johnsonii BFE 6128 on expression of genes related to TLR pathways and innate immunity in intestinal epithelial cells. Probiotics Antimicrob Proteins (2010) 2:211–7. doi:10.1007/s12602-010-9055-2
64. Macpherson C, Audy J, Mathieu O, Tompkins TA. Multistrain probiotic modulation of intestinal epithelial cells’ immune response to a double-stranded RNA ligand, poly(i.c). Appl Environ Microbiol (2014) 80(5):1692–700. doi:10.1128/AEM.03411-13
65. Tada A, Zelaya H, Clua P, Salva S, Alvarez S, Kitazawa H, et al. Immunobiotic Lactobacillus strains reduce small intestinal injury induced by intraepithelial lymphocytes after toll-like receptor 3 activation. Inflamm Res (2016) 65(10):771–83. doi:10.1007/s00011-016-0957-7
66. Villena J, Chiba E, Vizoso-Pinto MG, Tomosada Y, Takahashi T, Ishizuka T, et al. Immunobiotic Lactobacillus rhamnosus strains differentially modulate antiviral immune response in porcine intestinal epithelial and antigen presenting cells. BMC Microbiol (2014) 14(1):126. doi:10.1186/1471-2180-14-126
68. Kandasamy S, Vlasova AN, Fischer D, Kumar A, Chattha KS, Rauf A, et al. Differential effects of Escherichia coli Nissle and Lactobacillus rhamnosus strain GG on human rotavirus binding, infection, and B cell immunity. J Immunol (2016) 196(4):1780–9. doi:10.4049/jimmunol.1501705
69. Tomosada Y, Villena J, Murata K, Chiba E, Shimazu T, Aso H, et al. Immunoregulatory effect of bifidobacteria strains in porcine intestinal epithelial cells through modulation of ubiquitin-editing enzyme A20 expression. PLoS One (2013) 8(3):e59259. doi:10.1371/journal.pone.0059259
70. Kinoshita N, Hiroi T, Ohta N, Fukuyama S, Park EJ, Kiyono H. Autocrine IL-15 mediates intestinal epithelial cell death via the activation of neighboring intraepithelial NK cells. J Immunol (2002) 169(11):6187–92. doi:10.4049/jimmunol.169.11.6187
71. Zhang B, Chassaing B, Shi Z, Uchiyama R, Zhang Z, Denning TL, et al. Viral infection. Prevention and cure of rotavirus infection via TLR5/NLRC4-mediated production of IL-22 and IL-18. Science (2014) 346(6211):861–5. doi:10.1126/science.1256999
73. Hansen CH, Holm TL, Krych L, Andresen L, Nielsen DS, Rune I, et al. Gut microbiota regulates NKG2D ligand expression on intestinal epithelial cells. Eur J Immunol (2013) 43(2):447–57. doi:10.1002/eji.201242462
74. Kawaguchi M, Nanno M, Umesaki Y, Matsumoto S, Okada Y, Cai Z, et al. Cytolytic activity of intestinal intraepithelial lymphocytes in germ-free mice is strain dependent and determined by T cells expressing gamma delta T-cell antigen receptors. Proc Natl Acad Sci U S A (1993) 90(18):8591–4. doi:10.1073/pnas.90.18.8591
75. Suzuki H, Jeong KI, Itoh K, Doi K. Regional variations in the distributions of small intestinal intraepithelial lymphocytes in germ-free and specific pathogen-free mice. Exp Mol Pathol (2002) 72(3):230–5. doi:10.1006/exmp.2002.2433
76. Ismail AS, Severson KM, Vaishnava S, Behrendt CL, Yu X, Benjamin JL, et al. Gammadelta intraepithelial lymphocytes are essential mediators of host-microbial homeostasis at the intestinal mucosal surface. Proc Natl Acad Sci U S A (2011) 108(21):8743–8. doi:10.1073/pnas.1019574108
77. Jiang W, Wang X, Zeng B, Liu L, Tardivel A, Wei H, et al. Recognition of gut microbiota by NOD2 is essential for the homeostasis of intestinal intraepithelial lymphocytes. J Exp Med (2013) 210(11):2465–76. doi:10.1084/jem.20122490
78. Serrano AE, Menares-Castillo E, Garrido-Tapia M, Ribeiro CH, Hernandez CJ, Mendoza-Naranjo A, et al. Interleukin 10 decreases MICA expression on melanoma cell surface. Immunol Cell Biol (2011) 89(3):447–57. doi:10.1038/icb.2010.100
Keywords: immunobiotics, rotavirus, inflammation, TLR3, intestinal epithelial cells, intraepithelial lymphocytes
Citation: Villena J, Vizoso-Pinto MG and Kitazawa H (2016) Intestinal Innate Antiviral Immunity and Immunobiotics: Beneficial Effects against Rotavirus Infection. Front. Immunol. 7:563. doi: 10.3389/fimmu.2016.00563
Received: 12 September 2016; Accepted: 22 November 2016;
Published: 05 December 2016
Edited by:Amy Rasley, Lawrence Livermore National Laboratory, USA
Reviewed by:Benoit Chassaing, Georgia State University, USA
Karl William Boehme, University of Arkansas for Medical Sciences, USA
Copyright: © 2016 Villena, Vizoso-Pinto and Kitazawa. 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.