Evolutionary processes have shaped the vertebrate immune system over time, but proximal mechanisms control the onset, duration, and intensity of immune responses. Based on testing of the hygiene hypothesis, it is now well known that microbial exposure is important for proper development and regulation of the immune system. However, few studies have examined the differences between wild animals in their natural environments, in which they are typically exposed to a wide array of potential pathogens, and their conspecifics living in captivity. Wild spotted hyenas (Crocuta crocuta) are regularly exposed to myriad pathogens, but there is little evidence of disease-induced mortality in wild hyena populations, suggesting that immune defenses are robust in this species. Here we assessed differences in immune defenses between wild spotted hyenas that inhabit their natural savanna environment and captive hyenas that inhabit a captive environment where pathogen control programs are implemented. Importantly, the captive population of spotted hyenas was derived directly from the wild population and has been in captivity for less than four generations. Our results show that wild hyenas have significantly higher serum antibody concentrations, including total IgG and IgM, natural antibodies, and autoantibodies than do captive hyenas; there was no difference in the bacterial killing capacity of sera collected from captive and wild hyenas. The striking differences in serum antibody concentrations observed here suggest that complementing traditional immunology studies, with comparative studies of wild animals in their natural environment may help to uncover links between environment and immune function, and facilitate progress towards answering immunological questions associated with the hygiene hypothesis.
Citation: Flies AS, Mansfield LS, Grant CK, Weldele ML, Holekamp KE (2015) Markedly Elevated Antibody Responses in Wild versus Captive Spotted Hyenas Show that Environmental and Ecological Factors Are Important Modulators of Immunity. PLoS ONE 10(10): e0137679. https://doi.org/10.1371/journal.pone.0137679
Editor: Joy M. Burchell, King's College London, UNITED KINGDOM
Received: April 15, 2015; Accepted: August 19, 2015; Published: October 7, 2015
Copyright: © 2015 Flies et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All data are included in the Supporting Information files.
Funding: This work was supported by Award No.W911NF-08-1-0310 from the Army Research Office, National Institutes of Health grant 1R01GM105042, and National Science Foundation grants IOS1121474 and DEB1353110 to KEH, National Science Foundation Grant IOS0809914 to Stephen Glickman, National Institutes of Health grants K26RR023080 and U10 AI090872 to LSM, Grants-in-Aid-of research from Sigma Xi, Grants-in-Aid of Research from the American Society of Mammalogists, Veterinary Student Scholars grant D12Z0-604 from the Morris Animal Foundation, and an NSF Graduate Research Fellowship to ASF. Custom Monoclonals International Corp contributed antibodies used in this study. Author CKG, president of Custom Monoclonals International Corp, provided advice on experimental design, assay optimization, and assisted in writing the Materials and Methods section of the manuscript. The specific role of this author is articulated in the ‘author contributions’ section.
Competing interests: The authors have the following competing interests. Chris K. Grant is president of Custom Monoclonals International, which contributed antibodies for this research. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.
Abbreviations: nAb, natural antibody; ANA, anti-nuclear antibody; aAb, autoantibody; BKC, bacterial killing capacity; MIC, minimum inhibitory concentration, wild immunity
Evolutionary processes have shaped the vertebrate immune system over time, but proximal socio-ecological factors mediate the activation, duration, and intensity of immune responses [1, 2]. For example, an animal’s sex, diet, sociality, life-history stage, and pathogen pressure can influence its immune function [2–7]. One proximal factor widely believed to shape immune function during ontogenetic development is exposure to potential pathogens, including both microbes and macroparasites. In fact, reduced parasitic helminth exposure has been correlated with the increased prevalence of allergy and autoimmune disease in some human populations (reviewed in ). The hygiene hypothesis was originally proposed as an explanation for the commonly observed pattern of increased occurrence of allergic disease in relatively hygienic environments  and in human populations with access to modern medicine. This hypothesis has been modified many times, but one of its basic tenets remains the idea that reduced exposure to potential pathogens leads to dysregulated development of immune defense pathways, and consequently to increased risk of allergy and autoimmune disease. Although debate about the implications and breadth of the hygiene hypothesis continues, it is clear that environmental exposure to potential pathogens can play a critical role in the development of the immune system [10–12].
Wild-type animals, which are those that putatively represent the normal phenotype for a given species as it occurs in nature, represent a critical component of many laboratory studies, yet few studies have actually examined immune function in wild animals living in their natural environment, and fewer still have compared immune function between wild and captive conspecifics [12–17]. Differences between captive and wild animals with respect to immune activation, duration and intensity can be expected due to regular cleaning of captive facilities, implementation of pathogen control programs, reduced energy expenditure in captive animals, and a more stable environment in captivity than in the wild [6, 18, 19].
A more robust understanding of the effects of ecological variables such as pathogen exposure on immune function might be gained by studying immune function in non-traditional species, and assessing how basic immune defenses differ between wild and captive animals with similar genetic backgrounds. Carnivores are particularly interesting with respect to immune function because they are regularly exposed to pathogens that are capable of infecting both prey and predator. For example, particular Salmonella spp. and Shiga toxin-producing Escherichia coli are commonly found in wildlife carcasses [20, 21] on which carnivores feed. Furthermore, several carnivores in Africa, including spotted hyenas (Crocuta crocuta), regularly test seropositive for anthrax antibodies, yet they show no signs of disease . Wild hyenas are also known to harbor an abundance of parasitic worms of several genera , and survive exposure to a wide array of viral pathogens including but not limited to: rabies virus, canine distemper virus, corona virus, calicivirus, and parvovirus [24, 25]. In the wild, spotted hyenas live in large social groups, which increases the probability of acquiring socially transmitted pathogens . Furthermore spotted hyenas can live more than 20 years, which likely makes their acquired immune system, specifically recall responses, more important than in shorter-lived species, such as mice, that are not re-exposed to the same pathogens over the course of many years . High pathogen exposure rates coupled with low mortality rates from infectious disease suggest that immune function may be particularly robust in wild spotted hyenas.
Our primary objective in this study was to assess differences in immune function between wild spotted hyenas inhabiting a pathogen-rich and highly variable environment in their natural habitat, and captive hyenas inhabiting a more stable captive environment in which efforts were made to minimize the hyenas’ exposure to pathogens. To accomplish this, we used an immune defense component model (Fig 1), modified from Schmid-Hemp and Ebert , to compare immune defenses in wild and captive hyenas along two continua: 1) constitutive to induced defenses, and 2) non-specific to specific defenses. Constitutive defenses are innate defenses that are present in the absence of infection and are functional without prior exposure to a pathogen . Induced defenses can be innate or adaptive and are initiated in response to the recognition of specific molecular patterns that are often associated with threats to physiological homeostasis . Specific defenses are effective against only a limited range of antigens and specificity can be modified during a host’s lifetime. Specific defenses are most effective upon repeated exposure to the same pathogen, because they are maintained after initial infection, allowing a much faster response to subsequent infections. Non-specific defenses target a broader range of antigens but are not modified over time.
Patterns shown here are hypothesized based on existing literature and the locations within the plot were adjusted based on the results of this study. Bacterial killing capacity (BKC) is the least specific defense and also falls at the constitutive end of the x-axis. Specific IgG falls near the induced end of the x-axis, and is the most specific defense represented here. Anti-nuclear antibodies (ANAs) are specific to nuclear proteins and nucleic acids and can be induced following ligation of endosomal pattern recognition receptors. Natural IgG and IgM are non-specific and can be produced independent of CD4 T cell help. The dashed lines represent primary exposure (left) and secondary (right) exposure.
Natural antibodies (nAbs) are germline encoded, undergo little or no somatic hypermutation, and are thus largely non-specific, but can be rapidly induced by the microbiota or infection by pathogens [29–32]. By contrast, specific antibodies produced by B-2 cells, are primarily of the IgG isotype in non-mucosal regions, are produced in response to a strong stimulus, such as an infection, and undergo somatic mutation and affinity maturation . nAbs are primarily of the IgM isotype, but can also be of the IgG and IgA isotypes [33, 34]. Natural IgM makes up the majority of total IgM in mice, and functions in concert with complement to provide first line defenses to inhibit pathogen invasion and replication . Anti-nuclear antibodies (ANA) represent a subset of autoantibodies (aAbs) that bind to intracellular self-antigens, and are commonly derived from nAbs independently of help from T cells, but can also be induced via T cell dependent mechanisms .
Complement, the primary mediator of serum bacterial killing capacity (BKC), is a first-line immune defense that is continually produced at low levels in the absence of pathogenic challenge, and functions to prevent infection [36, 37]. Complement levels can increase quickly following infection, but the duration of the complement pulse is generally short compared to the rise in antibody levels following infection (Fig 1) .
We hypothesized here that higher levels of induced immune defenses (Fig 1: quadrants I and IV) would be observed in a pathogen-rich natural environment than in a relatively clean captive environment. By contrast, we expected that constitutive immune defenses (Fig 1: quadrants II and III), which are less dependent on pathogen exposure and maintained at baseline levels in the absence of such exposure, should be similar in pathogen-rich wild and pathogen-poor captive environments [14, 28]. We measured relative concentrations of total IgG and IgM antibodies, autoreactive IgG (aIgG) and autoreactive IgM (aIgM) that bind nuclear antigens, natural IgG (nIgG) and natural IgM (nIgM) against keyhole limpet hemocyanin (KLH), and complement-mediated bacterial killing capacity (BKC) of serum. Based on these studies we found strikingly different serum antibody concentrations in captive and wild hyenas.
Materials and Methods
Collection of serum samples from captive and wild hyenas
Captive spotted hyenas used in this study were born and housed at the Field Station for Behavioral Research at the University of California, Berkeley (UCB) (37.882843°N, -122.240330°E). The colony was founded by importing 20 infant hyenas from the Talek region of Kenya in 1984–1985 . All hyenas were treated with anti-helminthic drugs prior to importation from Kenya and no parasitic worms have been detected in the colony since its founding, whereas a high diversity and abundance of parasitic worms have been detected in the feces of the wild hyenas . The captive hyena enclosures have cement floors that are hosed down each day with water, and steam cleaned annually. Fecal material is removed from medium-sized external enclosures on a daily basis, and fecal material is removed from large outdoor enclosures on a monthly basis. The captive hyenas used in our study have been in captivity for less than four generations, and were derived directly from the same wild population under study here, located in the Talek region of the Masai Mara National Reserve, Kenya.
No disease outbreaks have ever occurred in the captive population, but many virulent viral, bacterial, and protozoan pathogens have been documented in wild spotted hyenas in East Africa [22, 24, 25, 40–42]. Ticks, fleas, tsetse flies, and other biting insects, any of which are capable of transmitting pathogens to hyenas, are commonly observed on wild hyenas, but not on captive hyenas. Additionally, the captive hyenas are fed only USDA approved meat and standard carnivore chow (Nebraska Brand, USA), whereas the wild hyenas feed on fresh ungulate carcasses and rotting carrion .
The captive hyenas exhibit most of the same behaviors as wild hyenas, including scent marking, establishment of dominance hierarchies, greeting ceremonies, and mating , but social group size is much smaller in the captive group than in the wild group. Pathogen transmission is often positively correlated with host density, and the effect becomes more pronounced in species that live in large aggregations . Wild hyenas live in social groups that can include more than 100 individuals . By contrast, captive hyenas are housed in groups of two or three. The low number of hyenas in each enclosure reduces the possibility of direct transmission of pathogens among group members via social interactions. Interspecific pathogen transmission between captive hyenas and wild local animals is probably rare because wild animals seldom stray into the hyena enclosures. Wild hyenas are regularly observed feeding on carcasses from which lions, jackals, and vultures, have also fed, and wild hyenas often engage in fierce battles with other carnivores.
The Institutional Animal Care and Use Committees at both the University of California, Berkeley and Michigan State University approved this study, under approval numbers # R091-0609R and # 07/08-099-00, respectively. Captive hyenas were immobilized with blow dart-delivered intramuscular injections of ketamine (4–6 mg/kg) and xylazine (1 mg/kg). Blood was drawn from the jugular vein and serum was aliquoted, and frozen at -80°C until use. Sera from wild spotted hyenas in the Maasai Mara, Kenya (-1.44290°N, 35.20731°E), were collected as part of the long-term Michigan State University Hyena Research Project, which has continuously monitored and recorded demographic information about the wild hyena clan since 1988. Research on wild hyenas was approved by the Kenya Wildlife Service and carried out under Research Permit # NCST/RRI/12/1/BS-011/24 from the Kenyan National Council for Science, Technology & Innovation. Hyena tissue samples were exported under the Genetic Materials Access Permit #0004 from the National Environment Management Authority of Kenya. Wild spotted hyenas were immobilized using dart-delivered intramuscular injections of Telazol (6.5 mg/kg; Zoetis, USA) in a plastic dart fired from an air rifle (Telinject Inc., USA) . Serum was collected as described above, but was snap frozen in liquid nitrogen in the field, then transported to Michigan on dry ice, and stored at -80°C until use.
Quantification of total IgG and IgM
Total IgG and IgM were quantified using sandwich ELISAs. Checkerboard 2-fold dilutions of sera and detection antibodies were used to determine optimal dilutions for assays. First, capture antibodies (IgG: Bethyl Labs # A20-117A; IgM: Custom Monoclonals International # CM7) were diluted into coating buffer (0.05 M carbonate-bicarbonate, pH 9.6) at 10 μg/ml, aliquoted into 96-well plates. The plates were then washed twice with TBST and non-specific binding was then blocked 1% BSA in TBS. All standards, sera, and detection antibodies were diluted in 1% BSA in TBST. We used pooled sera from both captive and wild hyenas to create a standard curve on each plate. Standard curves were run in duplicate on each plate. The starting dilutions of the pooled sera standard curve were 1:10,000 and 1:100 for total IgG and IgM, respectively, and 12 doubling dilutions were performed. Serum samples were diluted 1:100,000 for IgG and 1:1,000 for IgM and 100 μl were aliquoted into each well and incubated for 60 minutes. All samples were tested in triplicate. The plates were washed three times with TBST before adding 100 μl of horseradish peroxidase (HRP)-conjugated anti-IgG (Kirkegaard & Perry Laboratories # 04-20-02) or anti–IgM (Kirkegaard & Perry Laboratories # 04-20-03) detection antibodies to the plates at concentrations of 0.2 μg/ml and 0.25 μg/ml, respectively. The plates were then incubated 60 minutes and washed four times. 100 μl/well of 3,3',5,5'-tetramethylbenzidine (TMB) was used as the substrate for the HRP, and the color change reaction was stopped using 0.2 M H2SO4. Absorbance was read at 450 nm on a standard plate reader. Relative serum concentrations were calculated using the “calibFit” package in R .
Quantification of natural antibodies against keyhole limpet hemocyanin (KLH)
We used naturally-occurring anti-KLH antibodies as our measure of nAbs . KLH is a standard immunogen in laboratory studies; it is unlikely that either captive or wild hyenas could ever have been exposed to KLH, which is derived from marine gastropods . Natural anti-KLH is detectable in pre-immune human serum, and concentrations are relatively stable over time [49, 50]. nAbs were quantified using the same protocol as above, but with the following changes. Instead of coating capture antibodies to the plates, we coated KLH (EMD Millipore # 374805) at 10 μg/ml. The pooled sera again underwent 12 doubling dilutions, with starting dilutions of 1:50 and 1:12.5 for IgG and IgM, respectively. Serum samples were diluted 1:250 for IgG and 1:100 for IgM, and 100 μl were aliquoted into each well and incubated for 60 minutes. The horseradish peroxidase (HRP)-conjugated anti-IgG or anti–IgM detection antibodies were added to the plates at concentrations of 0.2 μg/ml and 0.25 μg/ml, respectively.
Quantification of anti-nuclear antibodies (ANA)
We used commercially available in vitro diagnostic ANA kits (Hemagen # 6659 96, Columbia, MD, USA) to assess aIgG and aIgM concentrations . Sera were diluted 1:1,600 and 1:400 for IgG and IgM, respectively. We again used HRP-conjugated anti-IgG or anti-IgM detection antibodies added to the plates at concentrations of 0.2 μg/ml and 0.25 μg/ml, respectively. See the manufacturer’s product data sheet for a full description of the test kit.
Quantification of serum bacterial killing capacity (BKC)
Two strains of bacteria were tested: Escherichia coli (ATCC# 8739) was chosen because it has been used as a standard bacterial strain in several other studies of bactericidal capacity ; Proteus mirabilis (ATCC# 35659) was chosen because, like E. coli, it is a gram negative bacterium that is commonly found in the gastrointestinal tract of many animals and was more susceptible to complement-mediated killing than most other strains in preliminary testing. All bacterial killing assays were conducted in 96-well round bottom plates. All serum samples from both wild and captive hyenas were passed through a 0.22 μm filter prior to adding to the 96-well plate to remove residual red blood cells and other cellular debris. Sera were then diluted in phosphate buffered saline (PBS), added to row 1 and serially diluted in PBS. 50 μl of bacteria in cation-adjusted Mueller-Hinton broth II (MHBII) was then added to each well [53, 54] to reach a total volume of 100 μl, with the final serum dilutions ranging from 1:8 to 1:1,024 for E. coli 1:4 to 1:512 for P. mirabilis Control wells were loaded with bacteria, but no serum, and blank wells were loaded with PBS and MHBII without bacteria.
One day prior to beginning the bacterial killing assay, E. coli or P. mirabilis were inoculated into MHBII and incubated overnight at 37°C while shaking at 120 rpm. After overnight incubation, bacterial cell concentration was adjusted to approximately 108 CFU/ml by diluting bacteria in sterile PBS until optical density at 600 nm matched the corresponding turbidity of the McFarland turbidity standard (BD Biosciences # 287298). Bacteria were then serially diluted in PBS to a concentration of 104 CFU/ml. Control wells, serum wells and antibiotic wells were next quickly loaded with 50 μl stock bacteria-containing broth, resulting in a final concentration of 500 CFU/well and a total volume of 100 μl/well. 50 μl of sterile MHB were added to blank wells to bring the total volume of each well to 100 μl. Plates were then placed in an incubator at 37°C and turbidity was measured after 24 hours on a Bio-Tek plate reader at 600 nm. Percent inhibition was calculated by dividing the optical density of each sample well by the mean optical density of the control bacteria wells. Because the assay allows the bacteria to grow to saturation, there was a clear distinction among wells exhibiting bacterial growth and those without growth. The minimum inhibitory concentration (MIC) was defined as the negative log2 of the lowest dilution that exhibited over 90 percent inhibition compared to the mean of the control wells [55, 56]. For example, if 1:40 was the lowest dilution exhibiting complete growth inhibition, the response variable value would be:-log2 (1/40) = 5.32. Additionally, the plates were visually inspected to ensure that there was no bacterial growth at the calculated MIC. The mean of triplicates for each sample was used as the final MIC, and we used the combined mean MIC for both E. coli and P. mirabilis as a general measure of serum BKC.
We used version 3.0.3 of the software package R  to create linear regression models to assess the effects of captivity on immune function in spotted hyenas. Age and sex are known to affect aspects of immune function in some species, so we included age in months and sex as covariates in all of the models. Because no single model is a perfect representation of nature , we used an information theoretic multimodel inference approach rather than choosing a single best model . The full models included captivity status, sex, and age as input variables, as well as all two-way interactions between input variables. We explored all possible subsets of the full model, which yielded 18 candidate models for each dependent variable . All subset models were ranked according to Akaike’s information criteria corrected for small sample size (AICc) . Models with a difference in AICc of less than two (Δ AICc < 2) are considered to be equally good . The top models, those with Δ AICc < 2, were then averaged using the 'MuMIn' package in R to produce weighted averages of regression parameter coefficients, 95% confidence intervals, and p-values for each input variable in the top models . In cases where only a single model had Δ AICc < 2, we report the results directly from the linear model, rather than weighted averages.
The response variables total IgG, total IgM, anti-ANA IgG, anti-ANA IgM, anti-KLH IgG anti-KLH IgM, and BKC were normalized by log transformation; the input variable age was normalized using a square root transformation. All continuous response and predictor variables were then centered and standardized by subtracting the mean and dividing by the standard deviation; standardization allows for more interpretable comparisons of effect sizes by measuring all effects on a common scale, and centering makes the main effects more biologically interpretable when interactions are present [60, 61]. Prior to the beginning of data analysis, we excluded four captive hyenas from the analysis of anti-KLH natural antibodies because they were immunized with KLH one year prior to the collection of the serum samples used in this study; anti-KLH IgG and IgM levels in these individuals had already returned to pre-immunization levels , but, nevertheless, we excluded these animals because their anti-KLH antibodies no longer satisfied the criteria for natural antibodies. One wild hyena was excluded from the study prior to beginning data analysis because its serum contained a large lipid globule and could not be filtered in a manner consistent with the other serum samples. Additionally, we ran out of sera from two wild hyenas prior to performing the anti-ANA IgM assay so their values are not represented in that assay.
We also performed univariate non-parametric tests of the effects of captivity on immune function and the results were similar to the AICc model selection approach. Correlations among total IgG, total IgM, anti-ANA IgG, anti-ANA IgM, anti-KLH IgG, anti-KLH IgM, and BKC were assessed using Pearson product-moment correlation tests. Differences in variability between immune measures in captive and wild hyenas were assessed using Levene’s test for homogeneity of variance.
Total IgG and IgM
We assessed the relative concentrations of total IgG and IgM in 15 captive and 14 wild hyenas. For total IgG, only a single model had Δ AICc < 2; captivity status was the only input variable in this model, indicating the wild hyenas had significantly higher serum concentrations of total IgG than did captive hyenas (p < 0.001) (Fig 2A). Wild hyenas also had significantly more total IgM than captive hyenas (p < 0.001) (Fig 2B); here age was non-significant (p = 0.100), but was included in the top model set (Δ AICc < 2). (See S1 Table for full list of effect sizes, confidence intervals, and p-values for the analysis of total IgG and IgM).
Natural IgG and IgM against KLH
We measured natural antibodies to KLH in sera from 11 captive hyenas and 14 wild hyenas. As with total IgG, there was again only a single model with Δ AICc < 2, however, this time the model included captivity status, sex, and an interaction between captivity status and sex. Wild hyenas had significantly higher concentrations of anti-KLH nIgG than captive hyenas (p < 0.001) (Fig 3A). There was also a significant interaction between captivity status and sex (p = 0.003), with all wild female hyenas having higher concentrations of anti-KLH nIgG than wild male hyenas (Fig 3A). The weighted averages from the four anti-KLH nIgM models with Δ AICc < 2 suggest that there was no statistically significant difference (p = 0.116) between anti-KLH nIgM concentrations in wild hyenas than captive hyenas (Fig 3B). a marginally non-significant interaction between sex and age (p = 0.051), with anti-KLH nIgM decreasing with age in females. (See S2 Table for full list of effect sizes, confidence intervals, and p-values for the analysis of natural anti-KLH nIgG and nIgM)
Anti-KLH natural IgG (A) is significantly higher in wild hyenas (n = 14) than in captive hyenas (n = 11), but there is no difference in anti-KLH natural IgM (B) between wild (n = 14) captive (n = 11) hyenas. Females are indicated by open circles and males by filled circles. *** p < 0.001.
Autoreactive IgG and IgM
We assessed the relative concentrations of aIgG in 15 captive and 14 wild hyenas, and aIgM in 15 captive and 12 wild hyenas. Wild hyenas had significantly higher levels of both aIgG (p < 0.001) and aIgM (p < 0.001) (Fig 4). aIgM decreased with age (p = 0.039), particularly in females. (See S3 Table for full list of effect sizes, confidence intervals, and p-values for the analysis of aIgG and aIgM)
Anti-nuclear IgG (A) and anti-nuclear IgM (B) are significantly higher in wild hyenas (n = 14 for IgG; n = 12 for IgM) than in captive hyenas (n = 15 for IgG and IgM). Females are indicated by open circles and males by filled circles. *** p < 0.001.
Bacterial killing capacity (BKC)
We assessed BKC for 15 captive and 14 wild hyenas and found that none of the input variables or interactions significantly affected the BKC in the hyenas we tested. Captivity status and sex were included in the best fitting model set (Δ AICc < 2), but neither captivity status (p = 0.336) nor sex (p = 0.433) significantly affected BKC (Fig 5). The null model, which included only the intercept, had the lowest AICc value. (See S4 Table for full list of effect sizes, confidence intervals, and p-values for the analysis of BKC)
Homogeneity of variance and correlations among immune measures
Levene’s tests revealed no difference with respect to homogeneity of variance between captive and wild hyenas for any immune measure (p > 0.45 in all cases), indicating that variance in immune measurements was homogenous across all samples. Additionally, see Table 1 for a full list of correlations among immune measures.
Here we show that wild hyenas inhabiting a pathogen-rich environment have higher levels of induced immune defenses than captive hyenas, whereas we observed no significant difference between wild and captive hyenas with respect to the constitutive immune defenses we tested. Our study is one of the first to use a non-rodent species to make comparisons of antibody concentrations using wild and wild-derived animals that are genetically similar. Importantly, our captive population was derived directly from the wild population, and has been maintained in captivity for less than four generations.
Previous research that compared immunoglobulin levels among human populations reported that total IgM concentrations were greater in populations where infectious disease prevalence was higher [63, 64], suggesting the environmental factors can influence total IgM concentrations. However, several studies comparing laboratory mice inhabiting antigen-free, germ-free, or specific pathogen-free environments detected no difference in total IgM concentrations in the three different environments, suggesting that in mice IgM is primarily a constitutive defense that is not affected by environment [65–67]. Similarly, Devalapalli, Lesher, et al.  found no difference in total IgM levels between laboratory mice and wild mice. However, Devalapalli, Lesher, et al.  reported significantly greater concentrations of total IgM in wild-caught rats than in laboratory rat strains, and these studies have recently been extended to demonstrate that biome enrichment are important for the development of the humoral immune system . Here we found that total IgM concentrations are significantly greater in wild hyenas than in a captive population. Collectively, these studies indicate that total IgM concentrations in some species may be affected by their environment, and highlight the importance of using multiple model systems, including some natural models, when attempting to understand the role of the immune system in health and disease.
Here we observed significantly greater nIgG against KLH in wild than in captive hyenas. Previous research in mice showed that approximately 20% of the expanded nAb-producing B-1 cell population showed an activation-induced cytidine deaminase IgM to IgG isotype switch . Repeated stimulation of B-1 cells could lead to a higher proportion of nIgG-producing B-1 cells compared to nIgM-producing B-1 cells, and competition for antigen could further augment production of nIgG and decrease production of nIgM. This might account for the lack of a significant difference in nIgM against KLH in the captive and wild hyenas, and suggests that over the long-term nIgM is the least inducible antibody type described in Fig 1. However, quantification of nAbs against targets other than KLH and a larger sample size would provide greater statistical power to detect differences in nIgM and would help to further clarify this issue.
Interestingly, wild females had higher concentrations of nIgG against KLH than did the wild males, but this difference was not apparent in captive hyenas. Previous work has shown that nAbs, particularly natural autoantibodies, are important for the establishment of self-tolerance [34, 69, 70]. Very little is known about self-tolerance and autoimmunity in wild animals, but in humans, autoimmune diseases are more common in women than men, and are often associated with hormonal changes associated with pregnancy and tolerance to fetal antigens .
Despite the positive correlation between autoantibody levels and some autoimmune diseases such as systemic lupus erythematosus, high levels of aIgG are associated with a reduced risk of Alzheimer’s disease, Parkinson’s disease, and multiple sclerosis . In a well-studied wild population of Soay sheep (Ovis aries) females had higher levels of aIgG than did males, and aIgG-positive females were more likely to survive harsh winters, had higher offspring survival, but reduced fecundity than did autoantibody-negative females , again demonstrating a context-dependent positive role for aIgG. Interestingly, in the study of wild of the Soay sheep the concentration of serum ANAs was positively correlated with the concentration of antibodies that bind antigens derived from an important parasitic trematode . No parasitic helminths have been detected in the captive hyena colony in nearly 30 years by either fecal flotation or during postmortem assessment of the GI tract, whereas every fecal sample ever tested from wild hyenas harbored at least one genus of parasitic helminth egg, and many samples contained thousands of eggs .
Here we show that both aIgG and aIgM levels are significantly higher in wild hyenas than in captive hyenas. Low-affinity aAbs, which may be derived from B-1 or marginal zone B cells, might be critically important for maintenance of physiological homeostasis in wild hyenas that are faced with a relentless assault of viral pathogens, because aAbs are critical for efficient clearance of virally-infected apoptotic and necrotic cells. Further research is needed to differentiate between high- and low-affinity ANAs in hyenas, and this could provide much needed insight into the relationship between autoimmunity and pregnancy in female mammals.
Surprisingly, nIgM and aIgM were negatively correlated with age in females, and there was no association between any measure of IgG and age. Several studies have found that nIgG and aIgG increase with age [48, 73, 74]. It is possible that isotype switching from IgM to IgG may account for the decreased nIgM and aIgM observed in older hyenas.
An alternative to the hypothesis that differences in pathogen exposure lead to the observed differences in induced immune function observed in wild and captive hyenas is that resource availability varies between the two populations and could drive the observed differences. The captive hyenas used in this study were fed a standard diet of 0.5–1 kg of carnivore chow and approximately 0.5 kg of meat and bone daily, which is adequate for maintaining stable body mass. Several days may pass between meals for wild hyenas, and their body masses are highly variable, depending on the size and timing of the last meal. If resources are the primary mediator of the immune defenses tested here, then we would expect to see more variable immune defense levels in wild hyenas. However, our results indicate that variance in immune defenses was similar among captive and wild hyenas. Nevertheless we would need serum samples collected at multiple time points from the same individuals to rule out this hypothesis altogether.
Currently there is a dearth of data in regard to allergy and autoimmunity in animals other than humans and rodents, but collaborative studies between wildlife biologists, immunologists, and managers of captive animals could greatly expand the range of comparative work in this area. Importantly, the groundwork for this type of comparative research is already in place in the form of zoos and wildlife research studies that routinely collect tissue samples from captive animals and keep accurate records of the medical history for each animal. The feasibility and impact of comparative immunology research should be augmented by the rapidly increasing availability of published genomes and decreasing costs of monoclonal antibody production, which should allow reagents, such as isotype subclass specific antibodies, to be developed in a cost-effective manner for non-traditional study species. The recent discovery of the important role of TLR10, which is expressed in human and hyenas but not in mice , in the innate immune response to influenza virus in humans  suggests that some infectious disease research might progress more rapidly by incorporating comparative studies of non-traditional species. However, in future studies, we do caution that the genetic distance between the captive and wild populations should be minimal, and meticulous monitoring and record keeping are needed to establish unambiguous differences between the captive and wild populations.
This work shows that wild hyenas from the Masai Mara in Kenya had significantly higher serum antibody concentrations than hyenas born and raised in a captive facility. Importantly, the captive hyena population was derived directly from the wild population and has been in captivity for less than four generations. The striking differences observed here suggest that environmental and ecological factors are important modulators of the immune response, and that comparative analysis of captive and wild animals may help to uncover patterns that are not apparent in traditional laboratory studies of immune defenses.
S1 Dataset. Spreadsheet containing the data used in this study.
S1 Table. Results of AICc based multimodel weighted-averages for total IgG and IgM.
S2 Table. Results of AICc based multimodel weighted-averages for natural anti-KLH IgG and IgM.
S3 Table. Results of AICc based multimodel weighted-averages for anti-ANA IgG and IgM.
This study was possible only with the help of Dr. Stephen E. Glickman and the staff of the Field Station for Behavioral Research at UC Berkeley. We would like to thank the Kenya Wildlife Service and Narok County Council for allowing us to perform the field research in Masai Mara. We also thank Dr. Julia Bell for her advice on laboratory procedures, Emily Johnston Flies for her help with the research and writing, and Dr. John Hayball and Dr. Dallas Flies for their comments on the manuscript.
Conceived and designed the experiments: ASF LSM CKG KEH. Performed the experiments: ASF MLW. Analyzed the data: ASF LSM KEH. Contributed reagents/materials/analysis tools: ASF LSM CKG KEH MLW. Wrote the paper: ASF LSM CKG KEH. Submitted the manuscript: ASF.
- 1. Viney ME, Riley EM, Buchanan KL. Optimal immune responses: immunocompetence revisited. Trends Ecol Evol. 2005;20(12):665–9. pmid:16701455
- 2. Horrocks NP, Matson KD, Tieleman BI. Pathogen pressure puts immune defense into perspective. Integr Comp Biol. 2011;51(4):563–76. Epub 2011/06/22. pmid:21690107.
- 3. Hamilton W, Zuk M. Heritable true fitness and bright birds: a role for parasites? Science. 1982;218(4570):384–7. pmid:7123238
- 4. Folstad I, Karter AJ. Parasites, bright males, and the immunocompetence handicap. Am Nat. 1992;139(3):603–22.
- 5. Schmid-Hempel P. Variation in immune defence as a question of evolutionary ecology. Proc Biol Sci. 2003;270(1513):357–66. Epub 2003/03/18. pmid:12639314; PubMed Central PMCID: PMC1691258.
- 6. Joop G, Rolff J. Plasticity of immune function and condition under the risk of predation and parasitism. Evolutionary Ecology Research. 2004;6(7):1051–62.
- 7. Thomas AM, Rudolf VHW. Challenges of metamorphosis in invertebrate hosts: maintaining parasite resistance across life-history stages. Ecological Entomology. 2010;35(2):200–5.
- 8. Maizels RM, McSorley HJ, Smyth DJ. Helminths in the hygiene hypothesis: sooner or later? Clinical & Experimental Immunology. 2014;177(1):38–46.
- 9. Strachan DP. Hay fever, hygiene, and household size. BMJ. 1989;299(6710):1259–60. pmid:2513902
- 10. Wander K, O'Connor K, Shell-Duncan B. Expanding the hygiene hypothesis: Early exposure to infectious agents predicts delayed-type hypersensitivity to Candida among children in Kilimanjaro. PLoS One. 2012;7(5):e37406. pmid:22616000
- 11. Yazdanbakhsh M, Kremsner PG, van Ree R. Allergy, parasites, and the hygiene hypothesis. Science. 2002;296(5567):490–4. pmid:11964470
- 12. Pi C, Allott EH, Ren D, Poulton S, Lee SYR, Perkins S, et al. Increased Biodiversity in the Environment Improves the Humoral Response of Rats. PLoS One. 2015;10(4):e0120255. pmid:25853852
- 13. Buehler DM, Piersma T, Irene Tieleman B. Captive and free-living red knots Calidris canutus exhibit differences in non-induced immunity that suggest different immune strategies in different environments. Journal of Avian Biology. 2008;39(5):560–6.
- 14. Abolins SR, Pocock MJ, Hafalla JC, Riley EM, Viney ME. Measures of immune function of wild mice, Mus musculus. Mol Ecol. 2011;20(5):881–92. Epub 2010/11/16. pmid:21073587.
- 15. Devalapalli AP, Lesher A, Shieh K, Solow JS, Everett ML, Edala AS, et al. Increased levels of IgE and autoreactive, polyreactive IgG in wild rodents: implications for the hygiene hypothesis. Scand J Immunol. 2006;64(2):125–36. Epub 2006/07/27. pmid:16867157.
- 16. Boysen P, Eide DM, Storset AK. Natural killer cells in free-living Mus musculus have a primed phenotype. Mol Ecol. 2011;20(23):5103–10. pmid:21895821
- 17. Viney M, Lazarou L, Abolins S. The laboratory mouse and wild immunology. Parasite Immunology. 2014:n/a-n/a.
- 18. Buehler D, Piersma T, Irene Tieleman B. Captive and free-living red knots Calidris canutus exhibit differences in non-induced immunity that suggest different immune strategies in different environments. Journal of Avian Biology. 2008;39(5):560–6.
- 19. Friend M, Franson J. Field Manual of Wildlife Diseases. General Field Procedures and Diseasesof Birds. Storming Media; 1999.
- 20. Harrison TM, Harrison SH, Rumbeiha WK, Sikarskie J, McClean M. Surveillane for selected bacterial and toxicologic contaminants in donated carcass meat fed to carnivores. Journal of Zoo and Wildlife Medicine. 2006;37(2):102–7. pmid:17312786
- 21. Miko A, Pries K, Haby S, Steege K, Albrecht N, Krause G, et al. Assessment of Shiga toxin-producing Escherichia coli isolates from wildlife meat as potential pathogens for humans. Appl Environ Microbiol. 2009;75(20):6462–70. Epub 2009/08/25. pmid:19700552; PubMed Central PMCID: PMC2765146.
- 22. Lembo T, Hampson K, Auty H, Beesley CA, Bessell P, Packer C, et al. Serologic surveillance of anthrax in the Serengeti ecosystem, Tanzania, 1996–2009. Emerg Infect Dis. 2011;17(3):387–94. Epub 2011/03/12. pmid:21392428; PubMed Central PMCID: PMC3166018.
- 23. Engh AL, Nelson KG, Peebles R, Hernandez AD, Hubbard KK, Holekamp KE. Coprologic survey of parasites of spotted hyenas (Crocuta crocuta) in the Masai Mara National Reserve, Kenya. Journal of Wildlife Diseases. 2003;39(1):224–7. pmid:12685088
- 24. Harrison TM, Mazet JK, Holekamp KE, Dubovi E, Engh AL, Nelson K, et al. Antibodies to canine and feline viruses in spotted hyenas (Crocuta crocuta) in the Masai, Mara National Reserve. Journal of Wildlife Diseases. 2004;40(1):1–10. pmid:15137483
- 25. East ML, Hofer H, Cox JH, Wulle U, Wiik H, Pitra C. Regular exposure to rabies virus and lack of symptomatic disease in Serengeti spotted hyenas. Proc Natl Acad Sci U S A. 2001;98(26):15026–31. Epub 2001/12/14. pmid:11742089; PubMed Central PMCID: PMC64977.
- 26. Alexander RD. The evolution of social behavior. Annual review of ecology and systematics. 1974:325–83.
- 27. Boots M, Bowers RG. The evolution of resistance through costly acquired immunity. Proceedings of the Royal Society of London Series B: Biological Sciences. 2004;271(1540):715–23. pmid:15209105
- 28. Schmid-Hempel P, Ebert D. On the evolutionary ecology of specific immune defence. Trends Ecol Evol. 2003;18(1):27–32.
- 29. Choi YS, Baumgarth N. Dual role for B-1a cells in immunity to influenza virus infection. J Exp Med. 2008;205(13):3053–64. pmid:19075288
- 30. Baumgarth N. The double life of a B-1 cell: self-reactivity selects for protective effector functions. Nat Rev Immunol. 2011;11(1):34–46. Epub 2010/12/15. pmid:21151033.
- 31. Baumgarth N, Tung JW, Herzenberg LA. Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion. Springer Seminars in Immunopathology. 2005;26(4):347–62. pmid:15633017
- 32. Dishaw LJ, Cannon JP, Litman GW, Parker W. Immune-directed support of rich microbial communities in the gut has ancient roots. Developmental & Comparative Immunology. 2014;47(1):36–51.
- 33. Avrameas S. Natural autoantibodies: from ‘horror autotoxicus’ to ‘gnothi seauton’. Immunology Today. 1991;12(5):154–9. pmid:1715166
- 34. Lacroix-Desmazes S, Mouthon L, Coutinho A, Kazatchkine MD. Analysis of the natural human IgG antibody repertoire: life-long stability of reactivities towards self antigens contrasts with age-dependent diversification of reactivities against bacterial antigens. Eur J Immunol. 1995;25(9):2598–604. pmid:7589132
- 35. Reeves WH, Satoh M, Richards H, editors. Origins of antinuclear antibodies2004.
- 36. Ricklin D, Hajishengallis G, Yang K, Lambris JD. Complement: a key system for immune surveillance and homeostasis. Nat Immunol. 2010;11(9):785–97. Epub 2010/08/20. pmid:20720586; PubMed Central PMCID: PMC2924908.
- 37. Carroll MC. The role of complement and complement receptors in induction and regulation of immunity. Annu Rev Immunol. 1998;16(1):545–68.
- 38. Carroll MC. The complement system in regulation of adaptive immunity. Nat Immunol. 2004;5(10):981–6. pmid:15454921
- 39. Glickman SE, Frank LG, Licht P, Yalcinkaya T, Siiteri PK, Davidson J. Sexual differentiation of the female spotted hyena. Ann N Y Acad Sci. 1992;662(1):135–59.
- 40. Alexander KA, Kat PW, Frank LG, Holekamp KE, Smale L, House C, et al. Evidence of canine distemper virus infection among free-ranging spotted hyenas (Crocuta crocuta) in the Masai Mara, Kenya. Journal of Zoo and Wildlife Medicine. 1995;26(2):201–6.
- 41. East ML, Moestl K, Benetka V, Pitra C, Honer OP, Wachter B, et al. Coronavirus infection of spotted hyenas in the Serengeti ecosystem. Vet Microbiol. 2004;102(1–2):1–9. Epub 2004/08/04. pmid:15288921.
- 42. East ML, Wibbelt G, Lieckfeldt D, Ludwig A, Goller K, Wilhelm K, et al. A Hepatozoon species genetically distinct from H. canis infecting spotted hyenas in the Serengeti Ecosystem, Tanzania. Journal of Wildlife Diseases. 2008;44(1):45–52. pmid:18263820
- 43. Cooper SM, Holekamp KE, Smale L. A seasonal feast: long-term analysis of feeding behaviour in the spotted hyaena (Crocuta crocuta). African Journal of Ecology. 1999;37(2):149–60.
- 44. Rifkin JL, Nunn CL, Garamszegi LZ. Do animals living in larger groups experience greater parasitism? A meta-analysis. Am Nat. 2012;180(1):70–82. pmid:22673652
- 45. Holekamp KE, Dantzer B, Stricker G, Shaw Yoshida KC, Benson-Amram S. Brains, brawn and sociality: a hyaena's tale. Animal Behaviour. 2015;(0).
- 46. Holekamp KE, Sisk CL. Effects of dispersal status on pituitary and gonadal function in the male spotted hyena. Horm Behav. 2003;44(5):385–94. pmid:14644632
- 47. R Development Core Team. R: A language and environment for statistical computing. 3.0.3 ed: R Foundation for Statistical Computing; 2014.
- 48. Parmentier HK, Lammers A, Hoekman JJ, Reilingh GDV, Zaanen ITA, Savelkoul HFJ. Different levels of natural antibodies in chickens divergently selected for specific antibody responses. Developmental & Comparative Immunology. 2004;28(1):39–49.
- 49. Korver K, Zeijlemaker WP, Schellekens PTA, Vossen JM. Measurement of primary in vivo IgM- and IgG-antibody response to KLH in humans: Implications of pre-immune IgM binding in antigen-specific ELISA. J Immunol Methods. 1984;74(2):241–51. pmid:6501888
- 50. Thornton BP, Vĕtvicka V, Ross GD. Natural antibody and complement-mediated antigen processing and presentation by B lymphocytes. The Journal of Immunology. 1994;152(4):1727–37. pmid:8120381
- 51. Graham AL, Hayward AD, Watt KA, Pilkington JG, Pemberton JM, Nussey DH. Fitness correlates of heritable variation in antibody responsiveness in a wild mammal. Science. 2010;330(6004):662–5. pmid:21030656
- 52. Liebl AL, Martin LB. Simple quantification of blood and plasma antimicrobial capacity using spectrophotometry. Functional Ecology. 2009;23(6):1091–6.
- 53. Reller LB, Stratton CW. Serum dilution test for bactericidal activity. II. Standardization and correlation with antimicrobial assays and susceptibility tests. Journal of Infectious Diseases. 1977;136(2):196. pmid:408424
- 54. CLSI. Methods for dilution antimicrobial susceptibility tests for bacterial that grow aerobically; approved standard. 8th ed: Clinical and Laboratory Standards Institute; 2009.
- 55. Tennessen JA, Woodhams DC, Chaurand P, Reinert LK, Billheimer D, Shyr Y, et al. Variations in the expressed antimicrobial peptide repertoire of northern leopard frog (Rana pipiens) populations suggest intraspecies differences in resistance to pathogens. Dev Comp Immunol. 2009;33(12):1247–57. Epub 2009/07/23. pmid:19622371; PubMed Central PMCID: PMC2927990.
- 56. Waitz JA. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically: National Committee for Clinical Laboratory Standards; 1990.
- 57. Burnham KP, Anderson DR. Multimodel Inference. Sociological Methods & Research. 2004;33(2):261–304.
- 58. Moore SM, Borer ET. The influence of host diversity and composition on epidemiological patterns at multiple spatial scales. Ecology. 2012;93(5):1095–105. pmid:22764495
- 59. Burnham KP, Anderson DR. Model selection and multimodel inference: a practical information-theoretic approach: Springer Verlag; 2002.
- 60. Gelman A. Scaling regression inputs by dividing by two standard deviations. Statistics in Medicine. 2008;27(15):2865–73. pmid:17960576
- 61. Schielzeth H. Simple means to improve the interpretability of regression coefficients. Methods in Ecology and Evolution. 2010;1(2):103–13.
- 62. Flies AS, Grant CK, Mansfield LS, Smith EJ, Weldele ML, Holekamp KE. Development of a hyena immunology toolbox. Vet Immunol Immunopathol. 2012;145(1–2):110–9. pmid:22173276
- 63. Rowe D, McGregor I, Smith SJ, Hall P, Williams K. Plasma immunoglobulin concentrations in a West African (Gambian) community and in a group of healthy British adults. Clinical and Experimental Immunology. 1968;3(1):63. pmid:4171047
- 64. Turner MW, Voller A. Studies on immunoglobulins of Nigerians. I. The immunoglobulin levels of a Nigerian population. The Journal of Tropical Medicine and Hygiene. 1966;69(5):99. pmid:4161313
- 65. Haury M, Sundblad A, Grandien A, Barreau C, Coutinho A, Nobrega A. The repertoire of serum IgM in normal mice is largely independent of external antigenic contact. Eur J Immunol. 1997;27(6):1557–63. pmid:9209510
- 66. Bos NA, Kimura H, Meeuwsen CG, De Visser H, Hazenberg MP, Wostmann BS, et al. Serum immunoglobulin levels and naturally occurring antibodies against carbohydrate antigens in germ-free BALB/c mice fed chemically defined ultrafiltered diet. Eur J Immunol. 1989;19(12):2335–9. pmid:2606142.
- 67. Hooijkaas H, Benner R, Pleasants JR, Wostmann BS. Isotypes and specificities of immunoglobulins produced by germ-free mice fed chemically defined ultrafiltered “antigen-free” diet. Eur J Immunol. 1984;14(12):1127–30. pmid:6083871
- 68. Yang Y, Ghosn EEB, Cole LE, Obukhanych TV, Sadate-Ngatchou P, Vogel SN, et al. Antigen-specific antibody responses in B-1a and their relationship to natural immunity. Proceedings of the National Academy of Sciences. 2012;109(14):5382–7.
- 69. Coutinho A. Beyond Clonal Selection and Network. Immunological Reviews. 1989;110(1):63–88.
- 70. Lleo A, Invernizzi P, Gao B, Podda M, Gershwin ME. Definition of human autoimmunity—autoantibodies versus autoimmune disease. Autoimmunity Reviews. 2010;9(5):A259–A66. pmid:19963079
- 71. Whitacre CC. Sex differences in autoimmune disease. Nat Immunol. 2001;2(9):777–80. pmid:11526384
- 72. Nagele EP, Han M, Acharya NK, DeMarshall C, Kosciuk MC, Nagele RG. Natural IgG Autoantibodies Are Abundant and Ubiquitous in Human Sera, and Their Number Is Influenced By Age, Gender, and Disease. PLoS One. 2013;8(4):e60726. pmid:23589757
- 73. Attanasio R, Brasky K, Robbins S, Jayashankar L, Nash R, Butler T. Age‐related autoantibody production in a nonhuman primate model. Clinical & Experimental Immunology. 2001;123(3):361–5.
- 74. Ujvari B, Madsen T. Do natural antibodies compensate for humoral immunosenescence in tropical pythons? Functional Ecology. 2011;25(4):813–7.
- 75. Flies AS, Maksimoski MT, Mansfield LS, Weldele ML, Holekamp KE. Characterization of toll-like receptors 1–10 in spotted hyenas. Vet Res Commun. 2014:1–6.
- 76. Lee SMY, Kok K-H, Jaume M, Cheung TKW, Yip T-F, Lai JCC, et al. Toll-like receptor 10 is involved in induction of innate immune responses to influenza virus infection. Proceedings of the National Academy of Sciences. 2014.