Abstract
Climate change involves different dramatic phenomena including desertification and wildfires, severe storms such as hurricanes and blizzards, increased sea levels resulting in flooding coastal cities and rise of atmospheric CO2 concentration. The alteration of the climate in a specific region affects the life of indigenous animals and humans. The climate changes influence living beings both directly and indirectly. The immune system of animals dramatically suffers the climate instability, making animals more susceptible to infectious and not infectious diseases. Different species of livestock animals respond with similar mechanisms to global warming, but some of them are more susceptible depending on their age, metabolism, and genetic conditions. The selection and study of autochthonous species and breeds, more easily adapted to specific environmental conditions could be an interesting strategy to face livestock rearing in the future.
Introduction
Climate changes dramatically increased over the past 20 years. First of all, a global warming has caused the increase of 1°C of the Earth's global surface temperature compared to the average in the mid XX century (1). This phenomenon leads to weather anomalies that drastically affect indigenous plant and animal life. The unstable weather patterns lead to desertification and wildfires, severe storms such as hurricanes and blizzards, increased sea levels resulting in flooding coastal cities and rise of atmospheric CO2 concentration (2). The result of all these events is that warm areas of the planet can cross cool seasons and cold areas of the planet can experience very hot temperatures. Plants and animals are able to face unexpected acute modifications of their environment thanks to their resilient ability, but when such a modification becomes chronic, or too extreme, they can be seriously affected. Moreover, the climate change can spread pathogens and pathogen vectors in new areas where plant and animals are not equipped to fight them. Finally, the climate changes and all the following weather anomalies represent a strong stress for the immune system and finally can put at risk the health of humans and animals. The immune system of animals can be affected both directly and indirectly by climate changes. For example, high environmental temperature directly affects the immune system causing an increase of the body temperature and indirectly, causing a reduction of the food intake, limits the energy sources for the immune responses that are known to be very energy consuming. This review aims to update all the knowledge's on immune system alterations caused by different phenomena of the climate change, focusing on the need to consider multi-stressor effects when evaluating climate change impacts upon animal immune system.
Global Warming and Immune System of Mammals and Avian Livestock
Global warming is the main and strongest phenomenon associated to climate change. The Earth's temperature is increasing by 0.2°C per decade and it is estimated that by 2100 it will be increased by 1.4–5.8°C (3). Most of the studies on climate change effects on immune system focus on the increasing temperatures worldwide. In fact, livestock animals are homoeothermic animals, they can maintain a constant body temperature through the exchange of heat produced by their metabolism and the external environment (4). Farm animals have a thermoneutral zone (TNZ) between 16 and 25°C where they manage to maintain a body temperature between 38.4 and 39.1°C. When the external temperature reach values below or above the TNZ, animals have to actively adapt by playing out physiological, morphological and behavioral adaptation mechanisms (5, 6). The majority of the response to heat stress are common to different species of vertebrates.
The first consequence that heat stress has on livestock is the decrease in daily food intake. Indeed, high environmental temperatures negatively affect the hypothalamic appetite center by reducing food intake (7). The reduction of food intake is a mechanism that aims to reduce the production of heat due to the metabolism, both in the polygastric and in the monogastric animals (8, 9).
Among farm animals, goats are the ruminants that better resist to temperature variations (10). Despite the decrease in dry matter intake (DMI) in goats, there is only a slight reduction in milk production (3–10%), compared to other dairy ruminants. The reduction of milk fat is not accompanied by a reduction in glucose levels or an increase of insulin levels as in cows (11, 12). In lactating cows the food intake begins to decrease at an environmental temperature around 25–26°C and the reduction can reach the 40% when it reaches 40°C (13). At these temperatures, the food intake in dairy goats can be reduced by 22–35% (11) and in buffaloes by 8–10% (14). Also in pigs the caloric intake is reduced when they are subjected to thermal stress (9). Heat stress also affects poultry's behavior. At high temperature the time devoted by chickens to nourishment decreases, they drink less, spend more time on the care of their wings, moving, and walking less (15). The nutrients administered with feed to poultry provide the substrates for cell proliferation and differentiation (also leukocytes); moreover, they can act as immunomodulators. Antigens supplied with the diet stimulate the production of immunoglobulin's in the bursa (16–18). Food intake is than necessary for a correct and efficacious immune response (19).
Another common response to heat stress in different farm animal species (cattle, goats, sheep, pig, poultry) is the increase in peripheral cortisol levels (19–22). Indeed, the heat stress causes the activation of the two axes hypothalamic-pituitary-adrenal (HPA) and sympathetic-adrenal-medullar (SAM), with the final release of cortisol and catecholamines that are known to influence the biology of leukocytes. Lymphocytes, monocytes, macrophages, and granulocytes have receptors for cortisol and catecholamines that mediate a negative alteration of their trafficking, proliferation, cytokine secretion, immunoglobulin (Ig) production, and cytotoxic activity (23).
Poultry subjected to heat stress showed a reduction of the volume and weight of lymphoid organs, low levels of circulating, and intestinal Ig and reduced phagocytosis (24–26). The reduced capability of leukocytes to produce proteins (cytokines and Ig) was mainly due to the phosphorylation of EF2 protein that blocks the protein production by altering the elongation phase of translation (21).
In dairy cows the activation of HPA and SAM axes induce the release of glucocorticoids and catecholamines and the following reduction of cytokine levels, particularly IL-4, IL-5, IL-6, IL-12, IFN-γ, and TNF-α (19). High levels of cortisol lead to immune suppression, overall on T cell compartment, cytokine production, and phagocytosis. Also, catecholamines negatively affect the immune system by inhibiting IL-12 production and promotion of IL-10 release, finally promoting a Th2 response. The hyperthermia concurs to the inhibition of Th1 response, favoring the Th2 mediated humoral response (19). Cortisol aggravates the immunosuppression by inhibiting the activation of T cell, the production of cytokines and the phagocytosis (19). In these conditions of immunosuppression vaccination of animals is inefficacious and some latent viruses can reactivate (19). Once cortisol binds to glucocorticoid receptors on the surface of leukocytes, the activation of proinflammatory transcription factors AP-1 and NFkB on the MAPK signaling pathway (19). The immunosuppression involves also the downregulation of complement system component (19). In dairy cows the majority of the data describes after prolonged heat periods an increase of total leukocytes with an altered differential count, where neutrophils increase, recruited from the bone marrow by cortisol, and lymphocytes decrease (19). Cortisol induces a downregulation of L-selectin which, in turn, reduces the activity of neutrophils and upregulates heat shock proteins (HSP) (27–29). It is interesting to note that if the heat stress occurs during the dry off period, the following lactation is compromised and the animal is more susceptible to production diseases, suggesting the existence of a sort of immunologic memory in the innate immune cells, likely mediated by epigenetic mechanisms (29, 30). Moreover, the reduced production of Ig following the heat stress, compromise the passive immunity transfer from the cow to its calf (19).
Another response common in vertebrates after heat stress is the production of HSPs. In poultry the attempt to maintain a correct body temperature induces the production of reactive oxygen species (ROS) and a consequent oxidative stress in the animal. The oxidative stress stimulates the liver of chicken to produce increased levels of HSPs to protect the tissues against the free radicals (31, 32). In dairy cattle increased levels of HSPs have been described (19). HSP70 and HSP90 activate an inflammatory response mediated by TLR4 (19). Dairy ruminants can activate antioxidant pathways to counteract the negative effects due to excessive production of reactive oxygen species (ROS). Indeed, high levels of catalase, superoxide dismutase (SOD), glutathione reductase (GSH) and malondialdehyde (MDA) have been observed in buffaloes and cows in summer months (33, 34). In sheep subjected to heat shock HSPA2, a member of HSP70 family, resulted upregulated. HSPA2 is known to induce the production of IL-1β that through IL-1R1, also upregulated in sheep under heat stress, can trigger an inflammatory response (35). Also, pigs subjected to prolonged heat stress develop signs of inflammation at the hepatic level (36). Indeed, their hepatocytes present an upregulation of HSPs and TLRs genes, signs of oxidative stress (increased GSH:GSSG ratio) and increased apoptosis (upregulation of PDIA3, P4HB, IRF9, VIM, NDGR2) (37, 38). These responses are partly directly induced by the high environmental temperature and partly indirectly by the reduced feed intake (36).
Data on the effect of global warming on the immune system of livestock sometimes are in contrast and this could be due to genetic differences of different breeds under study. For example, in poultry it has been described that different breeds of broilers and hens respond differently to heat stress (15, 39). In general, autochthonous breeds can adapt easily to environmental stress compared to others. Salem Black goats are known to better adapt to high temperature compared to Malabari and Osamabadi goats, showing lower levels of HSP70 after a prolonged period of high environmental temperature compared to the other two breeds (40). On the other hand, autochthonous animals reared in different condition compared to their usual ones, can develop dramatic stress responses. For example, the Tharpakar cow, a dual-purpose breed native to arid zone, shows an immunosuppression with and increase incidence of mastitis cases when reared in hot and humid environment (41). Different studies aimed to improve the resilience of livestock, identified genes associated to heat resistance such as heat shock 27 kD associated protein 1 (HSPBAP1) in goats, an inhibitor of HSP27. SNPs within HSPBAP1 gene were associated to susceptibility/resistance to heat stress (42). Other studies in cattle and chicken identified genes involved in different mechanisms such as immune response (interleukins and cluster differentiation markers), metabolism (NADH), remodeling of mammary gland and central nervous system functions confirmed the complexity of heat shock response in animals (43, 44). All these studies evidence that the resistance to high temperature negatively correlate to the production level of the animals (45).
Global Warming and Immune System of Fish Livestock
Human activities can have a huge impact on climate changes, influencing directly, and/or indirectly not only terrestrial environments but also aquatic ones. In aquatic environments those changes can be chemical (e.g., acidity, salinity, oxygen levels), physical (e.g., temperature), or biological (e.g., algae growth). These modifications of the environment affect the animals, in particular their immune system, impairing their capability of protection against pathogens (46–49).
Motile organisms, like fish, can be tolerant to some environmental changes or can escape from those alterations moving from one place to another, but aquacultured fish raised in sea cages, are not able to relocate in order to avoid ecological alterations. Those changes can be considered stressors, and in natural environments, those do not normally occur alone but in combination (49–51).
Water temperature can deeply affect fish immune system. Acute and chronic changes in temperature have also different impacts on animals, being short term episodes compensated by processes such as heat shock protein response, while chronic temperature variations are less likely to be solved by such responses (52–55).
Some studies suggest that it polarize the immune responses: at low temperatures fish may rely more on innate immune system, while at higher temperatures is the adaptive immunity that is more efficient (56–60). Pattern recognition by glucan binding proteins was predominant in perch (Perca fluviatilis) acclimated at lower temperatures, while, opsonin was more effective at higher temperatures (61).
A common phenomenon associated to the response of immune system to high environmental temperature (water temperature) is the increase of the antibody levels. This has been reported in several studies with different fish species (60, 62–73), where high temperatures seem to boost antibody levels indicating that a potential increment of oceans temperatures could actually help protecting some aquatic species against pathogens (73, 74).
Also, innate immunity of fishes is affected by water temperature; in South Asian carp (Catla catla) Toll Like Receptors (TLRs) and NOD-like receptors are modulated both by cold or warm water. TLR2, TLR4 and NOD2 expression increases with higher water temperatures, while TLR5 and NOD1 expression increases at both high and low temperatures (69).
In three-spined sticklebacks (Gasterosteus aculeatus) granulocyte respiratory burst activity and lymphocyte proliferation were inhibited when maintained for short period at high water temperatures and enhanced at low water temperatures. When the animals were exposed to a ‘heat wave' of 28°C for 2 weeks, long lasting immune disorders occurred resulting in the impairment of the immune system and the following spread of infectious diseases among those fish populations (70).
Temperature in gene expression changes of immune molecules. In farm raised Atlantic cod (Gadus morhua), cold water (up to 16°C) caused an increase of b2-M, MHCI, and IgM mRNA expression; on the contrary warmer raising water induced a downregulation of the same genes, being only IL-1β upregulated at high water temperatures (48). By the other hand, in the skin of Atlantic salmon (Salmo salar) low temperatures induce IL-1β, IL-8, and TNF-α upregulation (73).
Alterations of Salinity and Acidity of Oceans and Immune System of Fish Livestock
The climate change has induced modification of water environment in terms of salinity and pH.
Ocean acidity can change as a result of natural environmental sources (71), but different studies consider anthropogenic activities as the main contributors for water acidification. Approximately one third of the CO2 released since the industrial revolution has been taken up by the oceans (72), leading to the drop of pH (72). Recent studies estimated an average decrease in ocean pH of 0.1 in the last two centuries (75). Atlantic halibut (Hippoglossus hippoglossus) exposed to different water temperatures and pH levels showed signs of inflammatory responses with increased expression of complement component C3 and fibrinogen β chain precursor at high CO2 concentrations (reduced pH), without the influence of the temperature, suggesting that these changes are directly a consequence of the decrease of pH (74, 76).
In some species (Squalius carolitertii and Squalius torgalensis) the combination of low pH and high temperature of the water triggers the downregulation of Interferon-induced guanylate-binding protein 1 (GBP1) gene in liver, an antiviral and antimicrobic factor (49).
The alteration of the salt composition of waters is mainly due to the increased evaporation and strongly influences the life of fishes (77). In turbot (Scophthalmus maximus) Hsp70 and IgM expression was correlated to both temperature and salinity, temperature being the dominant factor (62). Freshwater fish are naturally tolerant to salinity alterations, but in seawater the complex variations of salinity can alter fish immune functionality, especially in stenohaline fish (78). A study developed in Nile tilapia (Oreochromis niloticus), a freshwater fish that prefers brackish waters, demonstrated that slowly increasing salinity in the environment did not have any significant impact on monocyte and lymphocyte number and phagocytotic process, yet a continuous decrease in water salinity was correlated with an increment in leukocyte number and phagocytosis (79, 80). In a different tilapia species (Oreochromis mossambicus), the increased salinity water caused a gain in lysozyme activity in plasma and head kidney homogenate (81).
A study on gilthead sea bream (Sparus aurata), a commonly aquacultured species with a wide range of salinity tolerance, demonstrated that hyper-saline water highly increases IgM production, while a decrease on water salinity do not (82). In another work, pipefish (Syngnathus typhle) kept in high salinity conditions and infected with Vibrio spp. presented significantly higher phagocytosis values compared to controls. When the fishes remained for a longer period in high salinity environment increased energy was required for osmoregulation leading to both lymphocyte and monocyte proliferation reduction, suggesting that during longer high salinity periods animals can be immunocompromised (47).
Water oxygen levels is another important parameter for aquatic animals' survival, and this parameter is clearly related to water temperature, salinity, and ionic concentration. Among the few studies published, hypoxia, and water temperature were investigated on Atlantic cod (Gadus morhua), and the expression of HSP70 was significantly higher in hypoxic conditions and at low temperatures (51). Macrophages of Atlantic salmon in vitro stimulated with poly I:C (TLR ligand) showed a significant increase of IFN-α mRNA levels in non-hypoxic conditions compared to normoxic conditions. This difference suggests that chronic hypoxia can modulate the innate immune response, altering the susceptibility of those animals to infections (83).
Alteration of Water Cycle and Immune System of Livestock Animals
The increased salinity of the oceans has been demonstrated to alter the water cycle of the earth leading to dramatic phenomena such as rainfalls, floods, and dust storms (77). The consequence of the alteration of the water cycle is that “arid regions have become drier and high rainfall regions have become wetter” (84).
So, the climate change, including alteration of water cycle and atmospheric CO2, concurs to the modification of the plant composition and accordingly to the reduction of food quality and quantity (85). The poor quality and low quantity of food negatively influences the immune response of animals, that is highly energy demanding and continuously requires adequate immune stimulation (19, 85). In these conditions, animals are more susceptible to infections and infestations.
Moreover, the alterations of the climate conditions allow the worldwide distribution of vectors of infectious diseases once endemic in specific regions. Burden of vector borne diseases increased in the last years depending on different factors: short life cycle of the vectors, reduction of incubation period, increased number of vector populations and extension of the times of transmission of the pathogen. All this factors are deeply influenced by the environment in particular temperature and water/humidity. Indeed both mosquitos and ticks, the major vectors, are highly susceptible to global warming, floods, and droughts. In particular the increased temperatures favor the spread of mosquitos in Northern latitudes where they find a suitable niche for reproduction and can overwinter, whereas in the tropical areas very high temperatures and the alternation of heavy rainfalls and droughts exacerbate the incidence of vector borne diseases by shortening the life cycle of vectors and promoting the host-pathogen interaction due to the livestock overcrowding at the water pools in dry seasons (86–88). Based on this, prediction models suggest a wide spread of vector borne diseases such as Rift Valley fever and Malaria (89, 90). Regarding tick vectors, their movement toward Northern region has been registered. For example Ixodes ricinus has been documented in Sweden and Russia, whereas Ixodes persulcatus in subarctic regions (91–93). The climate change can also negatively affect the spread of vector borne diseases. Indeed, the excessive temperature rise and prolonged dry period in subtropical and tropical areas can reduce the survival and reproduction rate of specific tick species such as Riphicephalus sanguineus. For the same reason epidemiological models predict that Leishmaniosis will decrease in the future (90).
The spread of vector borne diseases can induce immunosuppression in livestock and humans, favoring a further circulation of diseases (19). This add up to the immunosuppression caused by heat stress and sudden changes of temperatures, aggravating the susceptibility to infections (19, 94).
Pig farming is largely developing in tropical areas where climate change causes very hot and humid summers. These conditions challenge the immune system as previously described by activating the HPA axis and resulting in the immune suppression of the animals. The poor hygiene conditions typical of the tropical areas favor the spread of pathogens such as Salmonella and Isospora among pigs also in northern regions (95, 96).
Finally, the increase frequency of dust storm can impact on animal health. Strong winds transport dust with a complex and variable composition around very wide areas of the world. Dust is mainly made up of silicon dioxide, aluminum oxide, iron and titanium oxides, calcium and magnesium oxides, sodium and potassium oxides (97). It can also contain microorganisms such as bacteria, fungi, and viruses (98–100). The small dimension of the particles (PM 0.1 and PM 2.5) is the main responsible of the tissue damages, causing apoptosis, autophagy, and oxidative stress in the airway cells (101, 102).
Conclusions
Climate change includes several dramatic phenomena such as global warming, rise of atmospheric CO2 concentration, alteration of salinity and pH of oceans, reduction of O2 concentration in waters that lead to desertification and wildfires, severe storms such as hurricanes and blizzards, increased sea levels resulting in flooding coastal cities. All these phenomena are tightly linked to one another (Figure 1). So the climate change should be analyzed as a very complex problem and should be faced by an integrated strategy at different levels. Climate change impacts on production and reproduction of livestock causing important economic losses, being the high yield animals (with an accelerated metabolism and a genetic selection based on production) the less resilient and the most affected by the environment modifications. But it also impacts on the immune system of the animals inducing immune suppression and increasing their susceptibility to infections. The spread of vector borne diseases promoted by climate change also contribute to the impairment of the animal welfare. On the other hand, the intensive farming of livestock contributes to worsen the global warming, mainly by the emission of green-house gases such as CO2, CH4, and N2O (livestock sector concurs directly and indirectly with 18% of green-house gases emissions) (103). Given that climate change will progressively reduce the quantity and the quality of food for humans and animals, one strategy for future livestock management could be the valorization of autochthonous livestock breeds known to be highly resilient and disease resistant, to have low dietary needs (they have good production levels also with a frugal ration) and to produce high quality products (104).
Figure 1
Statements
Author contributions
JF, VH, GC, DV, and FR discussed the organization of the manuscript, drafted the manuscript and commented on the manuscript.
Funding
This work was supported by the Attivare-Cariplo 2017 Project Oltepo Biodiverso.
Conflict of interest
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.
References
1.
NASA. NOAA Analyses Reveal 2019 Second Warmest Year on Record. (2020). Available online at: https://www.nasa.gov/press-release/nasa-noaa-analyses-reveal-2019-second-warmest-year-on-record
2.
MirsaeidiMMotahariHKhamesiMTSharifiACamposMSchraufnagelDE. Climate change and respiratory infections. Annals Am Thoracic Soc. (2016) 13:1223–30. 10.1513/AnnalsATS.201511-729PS
3.
Intergovernmental Panel on Climate Change (IPCC). Climate Change: Synthesis Report. (2007). 10.1017/CBO9780511546013
4.
National Research Council (US) Subcommittee on Environmental Stress. Effect of Environment on Nutrient Requirements of Domestic Animals. (1981). National Academies Press (US). Retrieved from https://www.ncbi.nlm.nih.gov/books/NBK232338/
5.
MountLE. The concept of thermal neutrality. Heat Loss Animals Man. (1974) 425–39. 10.1016/B978-0-408-70652-0.50027-5
6.
RobertshawD. Environmental Physiology. Baltimore, MD: University Park Press (1974).
7.
BaileCAForbesJM. Control of feed intake and regulation of energy balance in ruminants. Physiol Rev. (1974) 54:160–214. 10.1152/physrev.1974.54.1.160
8.
KadzereCMurphyMSilanikoveNMaltzE. Heat stress in lactating dairy cows: a review. Livestock Prod Sci. (2002) 77:59–91. 10.1016/S0301-6226(01)00330-X
9.
SpeakmanJRKrolE. Maximal heat dissipation capacity and hyperthermia risk: neglected key factors in the ecology of endotherms. J Animal Ecol. (2010) 96:726–46. 10.1111/j.1365-2656.2010.01689.x
10.
BernabucciULaceteraNBaumgardLHRhoadsRPRonchiBNardoneA. Metabolic and hormonal acclimation to heat stress in domesticated ruminants. Animal. (2010) 4:1167–83. 10.1017/S175173111000090X
11.
HamzaouiSSalamaAAKAlbanellESuchXCajaG. Physiological response and lactational performances of late-lactation dairy goats under heat stress conditions. J Dairy Sci. (2013) 96:6355–65. 10.3168/jds.2013-6665
12.
SalamaAAKCajaGHamzaouiSBadaouiACastro-CostaAFacanhaDAEet al. Different levels of response to heat stress in dairy goats. Small Ruminant Res. (2014) 121:73–9. 10.1016/j.smallrumres.2013.11.021
13.
RhoadsRPBaumgardLHSuageeJKSandersSR. Nutritional interventions to alleviate the negative consequences of heat stress. Adv Nutrition. (2013) 4:267–76. 10.3945/an.112.003376
14.
HoodaOSinghS. Effect of thermal stress on feed intake, plasma enzymes and blood bio-chemicals in buffalo heifers. Indian J Anim Nutrition. (2010) 27:122–7.
15.
MackLAFelver-GantJNDennisRLChengHW. Genetic variations alter production and behavioral responses following heat stress in 2 strains of laying hens. Poultry Sci. (2013) 92:285–94. 10.3382/ps.2012-02589
16.
SchaffnerTMuellerJHessMWCottierHSordatBRopkeC. The bursa of fabricius: a central organ providing for contact between the lymphoid system and intestinal content. Cell Immunol. (1974) 13:304–12. 10.1016/0008-8749(74)90247-0
17.
EkinoSNawaYTanakaKMatsunoKFujiiHKotaniM. Suppression of immune response by isolation of the bursa of Fabricius from environmental stimuli. Aust J Exp Biol Med Sci. (1980) 58:289–9610.1038/icb.1980.28
18.
JeurissenSHMJanseEMKochGDe BoerGF. Postnatal development of mucosa-associated lymphoid tissues in chickens. Cell Tissue Res. (1989) 258:119–2410.1007/BF00223151
19.
BagathMKrishnanGDevarajCRashamolVPPragnaPLessAMet al. The impact of heat stress on the immune system in dairy cattle: a review. Res Vet Sci. (2019) 126:94–102. 10.1016/j.rvsc.2019.08.011
20.
SejianVBhattaRGaughanJBDunsheaFRLaceteraN. Review: adaptation of animals to heat stress. Animal. (2018) 12:S431–44. 10.1017/S1751731118001945
21.
KamelNNAhmedAMHMehaisenGMKMashalyMMAbassAO. Depression of leukocyte protein synthesis, immune function and growth performance induced by high environmental temperature in broiler chickens. Int J Biometeorol. (2017) 61:1637–45. 10.1007/s00484-017-1342-0
22.
LaraLJRostagnoMH. Impact of heat stress on poultry production. Animals. (2013) 3:356–69. 10.3390/ani3020356
23.
ElenkovIJ. Neurohormonal-cytokine interactions: Implications for inflammation, common human diseases and well-being. Neurochem Int. (2008) 52:40–51. 10.1016/j.neuint.2007.06.037
24.
GhaziSHabibianMMoeiniMMAbdolmohammadiAR. Effects of different levels of organic and inorganic chromium on growth performance and immunocompetence of broilers under heat stress. Biol Trace Element Res. (2012) 146:309–17. 10.1007/s12011-011-9260-1
25.
Quinteiro-FilhoWMRibeiroAFerraz-de-PaulaVPinheiroMLSakaiMSaLRMet al. Heat stress impairs performance parameters, induces intestinal injury, and decreases macrophage activity in broiler chickens. Poultry Sci. (2010) 89:1905–14. 10.3382/ps.2010-00812
26.
BartlettJRSmithMO. Effects of different levels of zinc on the performance and immunocompetence of broilers under heat stress. Poult Sci. (2003) 82:1580–8. 10.1093/ps/82.10.1580
27.
BurtonJLErskineRJ. Immunity and mastitis: some new ideas for an old disease. Vet Clin North Am. (2003) 19:1–45. 10.1016/S0749-0720(02)00073-7
28.
KansasG. Selectins and their ligands: Current concepts and controversies. Blood. (1996) 88:3259–87. 10.1182/blood.V88.9.3259.bloodjournal8893259
29.
Do-AmaralBCConnorEETaoSHaydenMJBubolzJWDahlGE. Heat stress abatement during the dry period influences metabolic gene expression and improves immune status in the transition period of dairy cows. J Dairy Sci. (2011) 94:86–9. 10.3168/jds.2009-3004
30.
NeteaMGSchlitzerAPlacekKJoostenLABSchultzeJL. Innate and adaptive immune memory: an evolutionary continuum in the host's response to pathogens. Cell Host Microbe. (2019) 25:13–26. 10.1016/j.chom.2018.12.006
31.
Felver-GantJNMackLADennisRLEicherSDChengHW. Genetic variations alter physiological responses following heat stress in 2 strains of laying hens. Poultry Sci. (2012) 91:1542–51. 10.3382/ps.2011-01988
32.
GuXHHaoYWangXL. Overexpression of heat shock protein 70 and its relationship to intestine under acute heat stress in broilers: 2. Intestinal Oxidative Stress Poultry Sci. (2012) 91:790–9. 10.3382/ps.2011-01628
33.
LallawmkiriMSinghSUpadhyayRDeS. Impact of vitamin E supplementation on heat shock protein 72 and antioxidant enzymes in different stages of Murrah buffaloes during seasonal stress. Indian J Animal Sci. (2013) 83:909–15.
34.
YatooMDimriMSharmaM. Seasonal changes in certain blood antioxidants in cattle and buffaloes. Indian J Animal Sc. (2014) 84:173–6.
35.
LuZChuMLiQJinMFeiXMaLet al. Transcriptomic analysis provides novel insights into heat stress responses in sheep. Animals. (2019) 9:387. 10.3390/ani9060387
36.
CuiYHaoYLiJBaoWLiGGaoYet al. Chronic heat stress induces immune response, oxidative stress response, and apoptosis of finishing pig liver: a proteomic approach. Int J Mol Sci. (2016) 17:393. 10.3390/ijms17050393
37.
HorowitzM. From molecular and cellular to integrative heat defense during exposure to chronic heat. Compar Biochem Physiol Part A. (2000) 131:475–83. 10.1016/S1095-6433(01)00500-1
38.
ZhangHJXuLDrakeVJXieLOberleyLWKregelKC. Heat-induced liver injury in old rats is associated with exaggerated oxidative stress and altered transcription factor activation. FASEB J. (2003) 17:2293–305. 10.1096/fj.03-0139fje
39.
XuYLaiXLiZZhangXLuoQ. Effect of chronic heat stress on some physiological and immunological parameters in different breed of broilers. Poultry Sci. (2018) 97:4073–82. 10.3382/ps/pey256
40.
AleenaJSejianVBagathMKrishnanGBeenaVBhattaR. Resilience of three indigenous goat breeds to heat stress based on phenotypic traits and PBMC HSP70 expression. Int J Biometeorol. (2018) 62:1995–2005. 10.1007/s00484-018-1604-5
41.
AlhussienMManjariPMohammedSSheikhAAReddiSDixitSet al. Incidence of mastitis and activity of milk neutrophils in Tharparkar cows reared under semi-arid conditions. Trop Anim Health Produc. (2016) 48:1291–5. 10.1007/s11250-016-1068-8
42.
ZidiA.Abo-ShadyH.MolinaA.Menéndez-BuxaderaA.Sánchez-RodríguezM.DíazC.et al. Genome wide association for heat stress tolerance/susceptibility in Florida dairy goats. In: Proceedings, 10 th World Congress of Genetics Applied to Livestock Production, Communication. (Vancouver, BC) (2014). p. 340.
43.
HayesBBowmanPChamberlainAGoddardM. A validated genome wide association study to breed cattle adapted to an environment altered by climatic change. PLoS ONE. (2009) 4:e6676. 10.1371/journal.pone.0006676
44.
CarabañoMJRamónMDíazCMolinaAPérez-GuzmánMDSerradillaJM. Breeding for resilience to heat stress effects in dairy ruminants. A comprehensive review. J Animal Sci. (2017) 95:1813–26. 10.2527/jas.2016.1114
45.
SerradillaJMCarabañoMJRamñnMMolinaADiazCMenéndez-BuxaderaA. Characterisation of Goats' response to heat stress: tools to improve heat tolerance. Goat Sci. (2017) 15:329–47. 10.5772/intechopen.70080
46.
PetersNEMeybeckMChapmanDV. Effects of human activities on water quality. Encyclopedia Hydrol Sci. (2005). 10.1002/0470848944.hsa096
47.
BirrerSCReuschTBHRothO. Salinity change impairs pipefish immune defence. Fish Shellf. Immunol. (2012) 33:1238–48. 10.1016/j.fsi.2012.08.028
48.
Perez-CasanovaJRiseMDixonBAfonsoLHallJJohnsonSet al. The immune and stress response of Atlantic cod to long-term increases in water temperature. Fish Shellfish Immunol. (2008) 24:600–9. 10.1016/j.fsi.2008.01.012
49.
JesusTFMorenoJMRepolhoTAthanasiadisARosaRAlmeida-ValVMFet al. Protein analysis and gene expression indicate differential vulnerability of Iberian fish species under a climate change scenario. PLoS ONE. (2017) 12:e0181325. 10.1371/journal.pone.0181325
50.
MadaroAOlsenREKristiansenTSEbbessonLOENilsenTOFlikGet al. Stress in Atlantic salmon: response to unpredictable chronic stress. J Exp Biol. (2015) 218:2538–50. 10.1242/jeb.120535
51.
MethlingCAluruNVijayanMMSteffensenJF. Effect of moderate hypoxia at three acclimation temperatures on stress responses in Atlantic cod with different haemoglobin types. Compar Biochem Physiol Part A. (2010) 156:485–90. 10.1016/j.cbpa.2010.04.006
52.
VergheseJAbramsJWangYMoranoKA. Biology of the heat shock response and protein chaperones: budding yeast (Saccharomyces cerevisiae) as a model system. Microbiol Mol Biol Rev. (2012) 76:115–58. 10.1128/MMBR.05018-11
53.
ChengSYChenCSChenJC. Salinity and temperature tolerance of brown-marbled grouper Epinephelus fuscoguttatus. Fish Physiol Biochem. (2012) 39:277–86. 10.1007/s10695-012-9698-x
54.
ChoHCKimJEKimHBBaekHJ. Effects of water temperature change on the hematological responses and plasma cortisol levels in growing of red spotted grouper, epinephelus akaara. Dev Rep. (2015) 19:19–24. 10.12717/DR.2015.19.1.019
55.
EldridgeWHSweeneyBWLawJM. Fish growth, physiological stress, and tissue condition in response to rate of temperature change during cool or warm diel thermal cycles. Canadian J Fish Aquat Sci. (2015) 72:1527–37. 10.1139/cjfas-2014-0350
56.
AlcornSWMurrayALPaschoRJ. Effects of rearing temperature on immune functions in sockeye salmon (Oncorhynchus nerka). Fish Shellf Immunol. (2002) 12:303–34. 10.1006/fsim.2001.0373
57.
Le MorvanCTroutaudDDeschauxP. Differential effects of temperature on specific and nonspecific immune defences in fish. J Exp Biol. (1998) 201:165–8.
58.
BlyJEWilliam ClemL. Temperature-mediated processes in teleost immunity: In vitro immunosuppression induced by in vivo low temperature in channel catfish. Vet Immunol Immunopathol. (1991) 28:365–77. 10.1016/0165-2427(91)90127-X
59.
AinsworthAJDexiangCWaterstratPGreenwayT. Effect of temperature on the immune system of channel catfish (Ictalurus punctatus)-I. Leucocyte distribution and phagocyte function in the anterior kidney at 10°C. Compar Biochem Physiol Part A. (1991) 100:907–12. 10.1016/0300-9629(91)90313-2
60.
BowdenTJThompsonKDMorganALGratacapRMLNikoskelainenS. Seasonal variation and the immune response: a fish perspective. Fish Shellf Immunol. (2007) 22:695–706. 10.1016/j.fsi.2006.08.016
61.
MarnilaPLiliusEM. Thermal acclimation in the perch (Perca fluviatilis L.) immunity. J Thermal Biol. (2015) 54:47–55. 10.1016/j.jtherbio.2015.01.002
62.
HuangZHMaAJWangXA. The immune response of turbot, Scophthalmus maximus (L.), skin to high water temperature. J Fish Dis. (2011) 34:619–627. 10.1111/j.1365-2761.2011.01275.x
63.
ChenWHSunLTTsaiCLSongYLChangCF. Cold-stress induced the modulation of catecholamines, cortisol, immunoglobulin m, and leukocyte phagocytosis in tilapia. General Compar Endocrinol. (2002) 126:90–100. 10.1006/gcen.2001.7772
64.
DominguezMTakemureATsuchiyaMNakamuraS. Impact of different environmental factors on the circulating immunoglobulin levels in the Nile tilapia, Oreochromis niloticus. Aquaculture. (2004) 241:491–500. 10.1016/j.aquaculture.2004.06.027
65.
LangstonALHoareRStefanssonMFitzgeraldRWergelandHMulcahyM. The effect of temperature on non-specific defence parameters of three strains of juvenile Atlantic halibut (Hippoglossus hippoglossus L.). Fish Shellfish Immunol. (2002) 12:61–76. 10.1006/fsim.2001.0354
66.
MagnadóttirBJónsdóttirHHelgasonSBjörnssonBJørgensenTØPilströmL. Humoral immune parameters in Atlantic cod (Gadus morhua L.). Compar Biochem Physiol Part B. (1999) 122:181–8. 10.1016/S0305-0491(98)10157-8
67.
JungTSdel CastilloCSJavaregowdaPKDalviRSNhoSWParkSBet al. Seasonal variation and comparative analysis of non-specific humoral immune substances in the skin mucus of olive flounder (Paralichthys olivaceus). Dev Compar Immunol. (2012) 38:295–301. 10.1016/j.dci.2012.06.005
68.
SugaharaKEguchiM. The use of warmed water treatment to induce protective immunity against the bacterial cold-water disease pathogen Flavobacterium psychrophilum in ayu (Plecoglossus altivelis). Fish Shellfish Immunol. (2012) 32:489–93. 10.1016/j.fsi.2011.12.005
69.
BasuMPaichhaMSwainBLenkaSSSinghSChakrabartiRet al. Modulation of TLR2, TLR4, TLR5, NOD1 and NOD2 receptor gene expressions and their downstream signaling molecules following thermal stress in the Indian major carp catla (Catla catla). 3 Biotech. (2015) 5:1021–30. 10.1007/s13205-015-0306-5
70.
DittmarJJanssenHKuskeAKurtzJScharsackJP. Heat and immunity: an experimental heat wave alters immune functions in three-spined sticklebacks (Gasterosteus aculeatus). J Animal Ecol. (2014) 83:744–57. 10.1111/1365-2656.12175
71.
RiceKCHermanJS. Acidification of Earth: An assessment across mechanisms and scales. Appl Geochem. (2012) 27:1–14. 10.1016/j.apgeochem.2011.09.001
72.
SabineCLFeelyRAGruberNKeyRMLeeKBullisterJLet al. The oceanic sink for anthropogenic CO2. Science. (2004) 305:367–71. 10.1126/science.1097403
73.
JensenLBBoltanaSObachAMcGurkCWaagbøRMacKenzieS. Investigating the underlying mechanisms of temperature-related skin diseases in Atlantic salmon,Salmo salarL., as measured by quantitative histology, skin transcriptomics and composition. J Fish Dis. (2015) 38:977–92. 10.1111/jfd.12314
74.
DavalosDAKassoglouK. Fibrinogen as a key regulator of inflammation in disease. Semin Immunopathol. (2011) 34:43–62. 10.1007/s00281-011-0290-8
75.
RavenJCaldeiraKElderfieldHHoegh-GuldbergOLissPSReisbellUet al. Ocean acidification due to increasing atmospheric carbon dioxide. The Royal Society (2005).
76.
Bresolin de SouzaBKJutfeltFKlingPForlinLSturveJ. Effects of increased CO2 on fish gill and plasma proteome. PLoS ONE. (2014) 9:e102901. 10.1371/journal.pone.0102901
77.
DurackPJ. Ocean Salinity and the Global Water Cycle. Oceanography. (2015) 28:20–31. 10.5670/oceanog.2015.03
78.
GonzalezRJ. The physiology of hyper-salinity tolerance in teleost fish: a review. J Compar Physiol B. (2011) 182:321–9. 10.1007/s00360-011-0624-9
79.
ChoiKCopeWGHarmsCALawJM. Rapid decreases in salinity, but not increases, lead to immune dysregulation in Nile tilapia, Oreochromis niloticus (L.). J Fish Dis. (2013) 36:389–99. 10.1111/j.1365-2761.2012.01417.x
80.
KumarVBJiangIFYangHHWengCF. Effects of serum on phagocytic activity and proteomic analysis of tilapia (Oreochromis mossambicus) serum after acute osmotic stress. Fish Shellf Immunol. (2009) 26:760–7. 10.1016/j.fsi.2009.03.005
81.
JiangIFBharath KumarVLeeDNWengCF. Acute osmotic stress affects Tilapia (Oreochromis mossambicus) innate immune responses. Fish Shellfish Immunol. (2008) 25:841–6. 10.1016/j.fsi.2008.09.006
82.
CuestaARLaiz-CarrionRMartín del RíoMPMeseguerJMiguel ManceraJAngeles EstebanM. Salinity influences the humoral immune parameters of gilthead seabream (Sparus aurata L). Fish Shellfish Immunol. (2005) 18:255–61. 10.1016/j.fsi.2004.07.009
83.
KyammeBOGadanKFinne-FridellFNiklassonLSundhHSundellKet al. Modulation of innate immune responses in Atlantic salmon by chronic hypoxia-induced stress. Fish Shellf Immunol. (2013) 34:55–65. 10.1016/j.fsi.2012.10.006
84.
DurackPJWijffelsSEMatearRJ. Ocean salinities reveal strong global water cycle intensification during 1950 to 2000. Science. (2012) 336:455–8. 10.1126/science.1212222
85.
GherlendaANHaighAMMooreBDJohnsonSNRieglerM. Climate change, nutrition and immunity: effects of elevated CO2 and temperature on the immune function of an insect herbivore. J Insect Physiol. (2016) 85:57–64. 10.1016/j.jinsphys.2015.12.002
86.
TabachnickWJ. Challenges in predicting climate and environmental effects on vector-borne disease episystems in a changing world. J Exp Biol. (2010) 213:946–54. 10.1242/jeb.037564
87.
CeccatoPRamirezBManyangadzeTGwakisaPThomsonMC. Data and tools to integrate climate and environmental information into public health. Infectious Dis Poverty. (2018) 7:126. 10.1186/s40249-018-0501-9
88.
AltoBWJulianoSA. Precipitation and temperature effects on populations of Aedes albopictus (Diptera: Culicidae): implications for range expansion. J Med Entomol. (2001) 38:646–56. 10.1603/0022-2585-38.5.646
89.
PowellJRTabachnickWJ. History of domestication and spread of Aedes aegypti - a review. The Memórias do Instituto Oswaldo Cruz. (2013) 108:11–17. 10.1590/0074-0276130395
90.
PurseBVMasanteDGoldingNPigottDDayJCIbañez-BernalSet al. How will climate change pathways and mitigation options alter incidence of vector-borne diseases? A framework for leishmaniasis in South and Meso-America. PLoS ONE. (2017) 12:e0183583. 10.1371/journal.pone.0183583
91.
Dantas-TorresF. Climate changes, biodiversity, ticks and tick-borne diseases: the butterfly effect. Int J Parasitol: Parasites and Wildlife. (2015) 4:452–61. 10.1016/j.ijppaw.2015.07.001
92.
Estrada-PeñaA. Climate change decreases habitat suitability for some tick species (acari: Ixodidae) in South Africa. Onderstepoort J Vet Res. (2003) 70:79–93.
93.
SutherstRWBourneAS. The effect of desiccation and low temperature on the viability of eggs and emerging larvae of the tick, Rhipicephalus (Boophilus) microplus (Canestrini) (Ixodidae). Int J Parasitol. (2006) 36:193–200. 10.1016/j.ijpara.2005.09.007
94.
MoriyamaMIchinoheT. High ambient temperature dampens adaptive immune responses to influenza a virus infection. Proc Natl Acade Sci USA. (2019) 116:3118–25. 10.1073/pnas.1815029116
95.
HautekietVGeertVMarcVRonyG. Development of a sanitary risk index for Salmonella seroprevalence in Belgian pig farms. Preventive Vet Med. (2008) 86:75–92. 10.1016/j.prevetmed.2008.03.005
96.
SkucePJMorganERvan DijkJMitchellM. Animal health aspects of adaptation to climate change: beating the heat and parasites in a warming Europe. Animal. (2013) 7:333–45. 10.1017/S175173111300075X
97.
SchweitzerMDCalzadillaASSalamoOSharifiAKumarNHoltGet al. Lung health in era of climate change and dust storms. Environmental Res. (2018) 163:36–42. 10.1016/j.envres.2018.02.001
98.
ChenPSTsaiFTLinCKYangCYChanCCYoungCYet al. Ambient influenza and avian influenza virus during dust storm days and background days. Environ. Health Perspect. (2010) 118:1211–6. 10.1289/ehp.0901782
99.
GriffinDW. Atmospheric movement of microorganisms in clouds of desert dust and implications for human health. Clini Microbiol Rev. (2007) 20:459–477. 10.1128/CMR.00039-06
100.
MakiTSusukiSKobayashiFKakikawaMToboYYamadaMet al. Phylogenetic analysis of atmospheric halotolerant bacterial communities at high altitude in an Asian dust (KOSA) arrival region, Suzu City. Sci Total Environ. (2010) 408:4556–62. 10.1016/j.scitotenv.2010.04.002
101.
GualtieriMOvrevikJMollerupSAsareNLonghinEDahlmanHJet al. Airborne urban particles (Milan winter-PM2.5) cause mitotic arrest and cell death: effects on DNA, mitochondria, AhR binding and spindle organization. Mutation Res. (2011) 713:18–31. 10.1016/j.mrfmmm.2011.05.011
102.
HuangQZhangJPengSTianMChenJShenH. Effects of water soluble PM2.5 extracts exposure on human lung epithelial cells (A549): a proteomic study. J Appl Toxicol. (2014) 34:675–87. 10.1002/jat.2910
103.
SteinfeldHGreberPWassenaarTCastelVRosalesMde HaanC. Livestock's Long Shadow. Environmental Issue and Options. Livestock, Environment, and Development Initiative. Rome: United Nations Food and Agriculture Organization (2006)
104.
CuroneGFilipeJCremonesiPTrevisiEAmadoriMPolleraCet al. What we have lost: mastitis resistance in Holstein Friesians and in a local cattle breed. Res in Vet Sci. (2018) 116:88–98. 10.1016/j.rvsc.2017.11.020
Summary
Keywords
climate change, livestock, immune system, global warming, inflammatory response
Citation
Filipe JF, Herrera V, Curone G, Vigo D and Riva F (2020) Floods, Hurricanes, and Other Catastrophes: A Challenge for the Immune System of Livestock and Other Animals. Front. Vet. Sci. 7:16. doi: 10.3389/fvets.2020.00016
Received
23 October 2019
Accepted
10 January 2020
Published
31 January 2020
Volume
7 - 2020
Edited by
Robert Paul Rhoads, Virginia Tech, United States
Reviewed by
François J. M. A Meurens, UMR INRA-Oniris 1300 Oniris-Nantes Atlantic National College of Veterinary Medicine, France; Carol Geralyn Chitko-McKown, Agricultural Research Service, United States Department of Agriculture, United States
Updates
Copyright
© 2020 Filipe, Herrera, Curone, Vigo and Riva.
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) and the copyright owner(s) 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: Federica Riva federica.riva@unimi.it
This article was submitted to Veterinary Infectious Diseases, a section of the journal Frontiers in Veterinary Science
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