Biology subjects

Pedersen, A. B.

Publications and source records attributed to Pedersen, A. B..

At least 19 recordsLinked to original sources

bioRxiv2026

Wild wood mouse gut microbiota are influenced by captivity and cross-fostering

Background Wild and laboratory animals harbour profoundly different gut microbiota, but how microbiomes shift between these states, and the relative roles of captivity, microbial history, and host identity in shaping that shift, remain unclear. Here, we developed a unique wood mouse (Apodemus sylvaticus) system comprising free-living mice (Wild:As), a wild-derived colony maintained in captivity for over a decade (Wild-like:As), and a second colony that we generated from the Wild-like:As mice by caesarean rederivation and cross-fostering to laboratory Mus musculus (Lab-like:As). We compared these three Apodemus cohorts with conventional laboratory Mus musculus (Lab:Mm) to ask how microbial diversity, community composition, and functional potential vary across a spectrum of wild-to-laboratory conditions. Results We found that alpha diversity varied substantially among cohorts but showed no consistent wild-to-laboratory trend: Shannon diversity was higher in Lab:Mm and Lab-like:As than in Wild:As and Wild-like:As mice, whereas phylogenetic diversity was similarly high in both the Wild:As and Lab:Mm groups. Community composition more closely reflected cohort histories. Despite over a decade in captivity, Wild-like:As mice remained most similar to Wild:As conspecifics, whereas Lab-like:As mice shifted strongly away from Wild-like:As and toward, but remained distinct from, Lab:Mm mice. The clearest wild-to-laboratory pattern emerged in microbiome consistency: core ASVs (present in [≥]90% of individuals) increased from 9 in Wild:As to 46 in Wild-like:As, 72 in Lab-like:As, and 138 in Lab:Mm mice. Predicted functional potential revealed a further distinction between taxonomic and functional patterns: Wild:As and Wild-like:As microbiomes did not differ significantly, whereas Lab-like:As shifted toward the Lab:Mm state despite remaining taxonomically distinct. Conclusions Together, these results show that laboratory-associated microbiomes do not emerge through simple loss of wild microbial diversity, but through broader reorganisation of community composition, consistency, and predicted functional potential reflecting microbial history and host context. The persistent Wild-like and Lab-like microbiome states within Apodemus provide a powerful experimental system for future timely work testing how microbiome history influences host physiology, resilience, and responses to environmental challenges.

microbiology↗

bioRxiv2026

Evolutionary adaptation of helminth immunomodulators to their hosts

Background: Parasitic nematodes have evolved secreted effector proteins which interact with host molecules to modulate the host immune response. These interactions can be highly specific and are under strong selective pressure. Here, we investigate the host-pathogen interaction between Heligmosomoides bakeri and its natural host Mus musculus, and between H. polygyrus and its natural host Apodemus sylvaticus. We focus on the Alarmin Release Inhibitor family (previously called HpARI) produced by heligmosomid parasites, which interact with IL-33 and heparan sulphate. Results: Using comparative genomics, we identified duplications and diversifications of the ARI family including multiple copies of ARI1 and conserved ARI3 homologues in both H. bakeri and H. polygyrus. We identify a new family member, HpolARI4, encoded by H. polygyrus, as well as a more distant homologue, HmixARI, encoded by Heligmosomum mixtum, a parasite of the bank vole (Myodes glareolus). Our functional assays identify that HpolARI4 preferentially blocks A. sylvaticus IL-33 but has little activity against M. musculus IL-33, whereas HbakARI2 is highly specific for M. musculus IL-33. We furthermore show differential interaction with host heparan sulphate, with HbakARI2 and HpolARI4 showing high affinity binding, whereas HbakARI3 shows no binding. We further test this family against non-host human IL-33 and show that functional suppression can be achieved by HbakARI3 in vitro and in vivo. Conclusion: By integrating genomic data, structural insights, and functional assays, we reveal how the expansion and diversification of the ARI family drive host-specific IL-33 modulation, providing a molecular model for nematode-host co-evolution.

immunology↗

bioRxiv2026

Helminth coinfection facilitates gammaherpesvirus infection in the wood mouse Apodemus sylvaticus

Helminths are widespread parasites that can modulate host immunity, potentially increasing susceptibility to viral infections. However, evidence for these effects varies across systems and environments, and links between laboratory and wild populations remain unclear. We developed a tractable system using wood mice, Heligmosomoides spp. nematodes, and wood mouse herpes virus (WMHV) to bridge this gap. Combining laboratory and field experiments with population modelling, we examined how helminth infection, anthelmintic treatment and diet affect viral dynamics. Across lab and field data, helminth infection consistently increased WMHV risk, with stronger effects at higher worm burdens. Field results showed that anthelmintic treatment reduced viral infection, and laboratory experiments showed that improved nutrition mitigates helminth-induced increases in viral susceptibility. Our population-level modelling suggested that helminth burden-dependent facilitation can generate nonlinear effects on viral spread, dependent on helminth virulence. Our findings highlight the potential importance of helminths as facilitators of viral infections, and suggest that anthelmintic treatment may provide indirect benefits for viral control. We also show the value of integrating lab and field approaches on the same (or closely related) species, in particular the potential offered by the wood mouse - Heligmosomoides - WMHV system, to understand the drivers and consequences of host-helminth-viral interactions.

ecology↗

bioRxiv2025

Resource supplementation alters host exposure, susceptibility, and infection dynamics across a diverse parasite community

Resource availability is crucial in shaping exposure and resistance to parasites. Although effects are expected to vary across parasite species, most of our knowledge comes from single-host, single-parasite studies. In a wild wood mouse population (Apodemus sylvaticus), we supplemented dietary resources over 3 years and quantified effects on a diverse parasite community alongside host behaviour and physiology. Resource supplementation had diverse impacts on 12 parasite taxa including positive (3/12), negative (6/12), and null (3/12) results. Supplementation also influenced host biology, with supplemented mice moving less, experiencing higher conspecific densities, improved conditions, and increased reproduction. These findings experimentally demonstrate that resource availability can multifacetedly affect disease dynamics. The complexity likely arises due to combined effects on exposure and susceptibility processes. Our study advances understanding of disease drivers at the human-wild interface and underscores the importance of assessing whole parasite communities to predict responses to changing resource landscapes in the wild.

ecology↗

bioRxiv2025

Environmental drivers of low vaccine responsiveness in a lab-to-wild rodent model

Vaccination is the most effective way to prevent infectious diseases and safeguard public health. Yet, most new vaccines fail in late clinical trials, and even estab-lished ones often underperform in populations apart from those in which they were initially tested. This can lead to reduced vaccine responsiveness, breakthrough infections, and prevent or delay herd immunity. While the causes of vaccine hypore-sponsiveness remain difficult to identify, quantify, and therefore address, numerous reports indicate a predominant role of environmental factors. This has notably been demonstrated by a reduction in the immunogenicity and efficacy of various vaccines when transitioning from urban to rural human populations. Here, we tested whether and, if so, how the environment can cause vaccine hyporesponsive-ness. We hypothesised that if the leading causes of vaccine hyporesponsiveness were environmental, then the reduced efficacy would be exacerbated when indi-viduals are under nutritional stress; specifically predicting that high quality diet supplementation would increase vaccine responsiveness. Finally, we predicted that parasitic helminth infection, which are more common in rural populations, would degrade vaccine responsiveness, e.g. due to their ability to suppress host immunity, and that anthelmintic treatment could rescue vaccine responsiveness in infected individuals. To test these hypotheses, we coupled lab and field experiments with structural causal modelling, and measured antibody responses of paired conspecific cohorts of laboratory-reared and wild wood mice (Apodemus sylvaticus) to a single or two doses of diphtheria toxoid vaccine formulated with alum; with and without diet supplementation. We found that vaccine-specific IgG1 antibodies were [~]47% lower in the wild wood mice compared to the laboratory reared population. We also demonstrate that, across both habitats (wild and lab), substantial variation in vaccine responsiveness was caused by diet. However, contrary to our predictions, this high quality dietary supplementation resulted in lower vaccine responsiveness. Further, once the effects of habitat, diet, and sex were adjusted for, increasing hel-minth infection burdens negatively affected vaccine-specific antibody production. Using counterfactual modelling, we show that targeting anthelmintic treatment at heavily infected individuals would have improved their vaccine responsiveness by 2 to 4-fold. Our results indicate that the wild environment and access to a high-quality diet play a dramatic role in shaping the immune systems response to immunisation. Further, we show that laboratory settings, even when using a genetic diverse, non-traditional model, may systematically overestimate vaccine performance by failing to capture natural environmental variability. Our study provides a robust, causally explicit modelling approach to disentangle and quantify the complex factors that drive vaccine responsiveness in focal populations. This framework offers a path-way for predicting vaccine performance across diverse populations and identifying targeted interventions to enhance immunisation outcomes in real-world settings.

systems biology↗

bioRxiv2025

Comparative transcriptomics reveals an extracellular worm argonaute as an ancestral regulator of LTR retrotransposons.

Safeguarding the genome from non-self elements is essential for reproduction, development, and ageing. One of the major threats to genome integrity is Transposable Elements (TEs), which can be post-transcriptionally silenced through small RNAs (sRNAs) and argonaute proteins. Recent work suggests TE-derived sRNAs may also act as virulence factors in host-pathogen interactions. During infection, the intestinal parasite Heligmosomoides bakeri secretes a single argonaute protein (exWAGO) and a wide variety of TE-derived sRNAs. Although exWAGO is highly expressed, conserved, and secreted by parasitic nematodes, its function and sRNA guide preference remain unclear. Using comparative transcriptomics of the sRNAs bound to exWAGO within parasites of rodents, livestock and humans, and its orthologs in C. elegans, we found that exWAGO is capable of loading sRNAs produced from all classes of TEs in addition to some protein-coding and non-coding transcripts. However, our results suggest that the ancestral endogenous function of exWAGO was likely linked to LTR retrotransposon regulation. To understand how this relates to potential extracellular functions of exWAGO we also examined the sRNAs bound to exWAGO secreted by H. bakeri in both vesicular and non-vesicular forms. Extracellular exWAGO preferentially loads sRNA guides derived from non-autonomous and fragmented LTRs, suggesting the existence of adaptable reservoirs of regulatory sRNAs with potential roles in cross-species RNA communication. Together, our results show that exWAGO is part of an evolutionarily conserved pathway for LTR retrotransposon regulation, while preferentially utilising degenerated elements as sources of secreted sRNAs.

genomics↗

bioRxiv2025

Reducing food stress and parasitism may have unexpected consequences on faecal corticosterone in a wild rodent

In wild animals, glucocorticoid hormones play a key role in responses to environmental stressors and the maintenance of homeostasis, allocating energy between energy-demanding processes. Although acute rises in glucocorticoids are beneficial for short-term survival, prolonged exposure can be detrimental to reproduction and survival. Thus, understanding the factors driving glucocorticoid concentrations is crucial for understanding key processes in ecology and evolution. Here, we examined how manipulation of two environmental stressors - food availability and parasite burden, influence levels of faecal corticosterone in a wild population of wood mice (Apodemus sylvaticus). To do so, we experimentally altered nutrition via food supplementation and reduced gastrointestinal nematode infection by anthelmintic treatment, using Heligmosomoides polygyrus as an indicator of treatment efficacy. Faecal corticosterone was not found to be impacted by food supplementation or anthelminthic treatment. However, our results may be mediated by variation in resource availability or masked by other factors that affect corticosterone. For example, corticosterone declined seasonally and was higher in adult, female mice. While we expected higher food availability and lower worm burden to decrease stress, putatively higher rates of reproduction in food supplemented areas could neutralise any decreases in corticosterone associated with alleviation of food and parasite stress. Thus, alleviating stress in the wild may have unintended consequences on fitness.

evolutionary biology↗

bioRxiv2025

A DNA methylation-based clock for age estimates in the wood mouse (Apodemus sylvaticus)

Environmental stressors are expected to accelerate senescence but demonstrating this requires both a measure of senescence and knowledge of chronological age - data rarely available for most wild animals. Here, we constructed a DNA methylation-based epigenetic clock for the wood mouse (Apodemus sylvaticus) using known-aged laboratory individuals and applied it to a wild population of unknown ages. This represents one of the first demonstrations that a laboratory-trained epigenetic clock can be used to infer age structure in free-living animals. Multiple lines of evidence validated use of the clock in wild individuals: age estimates fell within expected ranges, recapitulated population demographic structure, and recovered predicted signatures of senescence, including an increase in infection probability with age. Moreover, wild mice given experimental food supplementation and parasite-removal drugs exhibited slower epigenetic ageing rates. Together, our findings demonstrate that epigenetic clocks can infer both chronological age and ageing rates in the wild, providing a powerful framework to identify the ecological and individual determinants of ageing.

genomics↗

bioRxiv2024

Mast cells are not essential for pubertal mammary gland branching.

Mast cells are long-lived, tissue-resident immune cells of the myeloid lineage with cardinal functions in allergy and atopic disease. They are now increasingly recognized also for protective roles e.g. against infections and venoms. Other functions originally assigned to mast cells in development and physiology, however, have been refuted, and for yet others, their true contribution remains uncertain. Mast cells have been implicated in promoting ductal branching in the pubertal mammary gland, the organ that produces and secretes milk in mammals, but these findings are based on mouse models that are not mast cell-specific. In this study, we therefore re-addressed the impact of mast cells on mammary gland branching using several complementary genetic models, including a new transgenic line. We report that neither constitutive deficiency of mast cells, nor their conditional ablation induced at puberty affected mammary gland branching. Our results thus dispute that mast cells promote this process in mice, at least in a unique and non-redundant manner. This study adds to a growing body of work clarifying the biological roles of mast cells, and further expands the toolbox available to the field of mast cell research.

developmental biology↗

bioRxiv2023

The impact of within-host coinfection interactions on between-host parasite transmission dynamics varies with spatial scale

Within-host interactions among coinfecting parasites can have major consequences for individual infection risk and disease severity. However, the impact of these within-host interactions on between-host parasite transmission, and the spatial scales over which they occur, remain unknown. We developed and apply a novel spatially-explicit analysis to parasite infection data from a wild wood mouse (Apodemus sylvaticus) population. We previously demonstrated a strong negative interaction within individual hosts gastrointestinal parasites, the nematode Heligmosomoides polygyrus and the coccidia Eimeria hungaryensis, using drug-treatment experiments. Here, we find that this negative within-host interaction can significantly alter the between-host transmission dynamics of E. hungaryensis, but only within spatially-restricted neighbourhoods around each host. However, for the closely-related species E. apionodes, which experiments show does not interact strongly with H. polygyrus, we did not find any effect on transmission over any spatial scale. Our results demonstrate that the effects of within-host coinfection interactions can ripple out beyond each host to alter the transmission dynamics of the parasites, but only over local scales that likely reflect the spatial dimension of transmission. Hence there may be knock-on consequences of drug treatments impacting the transmission of non-target parasites, altering infection risks even for non-treated individuals in the wider neighbourhood.

ecology↗

bioRxiv2023

Ancient diversity in host-parasite interaction genes in a model parasitic nematode

Host-parasite interactions exert strong selection pressures on the genomes of both host and parasite. These interactions can lead to increased fitness of rare alleles, resulting in negative frequency-dependent selection, a form of balancing selection that is hypothesised to explain the high levels of polymorphism seen in many host immune and parasite antigen loci. Despite their economic and ecological importance, there is limited evidence for balancing selection in parasitism-relevant genes in parasitic nematodes. Here, we sequenced the genomes of several individuals of Heligmosomoides bakeri, a parasite of house mice that is a well-established model parasitic nematode, and Heligmosomoides polygyrus, a closely related parasite of wood mice. We combined our single nematode genome assemblies with chromatin conformation capture (Hi-C) libraries derived from pools of individuals to generate chromosome-level reference genomes for both species. Although H. bakeri is commonly referred to as H. polygyrus in the literature, their genomes show levels of divergence that are consistent with millions of years of independent evolution. We found that the H. bakeri genome, which we expected to be highly homozygous through inbreeding, contained hundreds of hyper-divergent haplotypes, similar to those recently reported in free-living nematodes. Within these haplotypes, we found an enrichment of protein families that interact with the host immune response, including protease inhibitors and transthyretin-related proteins. We also found that many of these haplotypes originated prior to the divergence between H. bakeri and H. polygyrus, suggesting that they have been maintained since the last common ancestor of the two species by long-term balancing selection. Together, our results suggest that selection pressures exerted on parasites by their hosts have led to unexpected modes and levels of genetic diversity in the genomes of these economically and ecologically important species.

evolutionary biology↗

bioRxiv2022

Long-term temporal trends in gastrointestinal parasite infection in wild Soay sheep

Monitoring the prevalence and abundance of parasites over time is important for addressing their potential impact on host life-histories, immunological profiles, and their influence as a selective force. Only long-term ecological studies have the potential to shed light on both the temporal trends in infection prevalence and abundance and the drivers of such trends, because of their ability to dissect drivers that may be confounded over shorter time scales. Despite this, only a relatively small number of such studies exist. Here, we analysed changes in the prevalence and abundance of gastrointestinal parasites in the wild Soay sheep population of St Kilda across 31 years. The host population density has increased across the study, and population density is known to increase parasite transmission, but we found that density and year explained temporal variation in parasite prevalence and abundance independently. Prevalence of both strongyle nematodes and coccidian microparasites increased during the study, and this effect varied between lambs, yearlings and adults. Meanwhile, abundance of strongyles was more strongly linked to host density than to temporal (yearly) dynamics, while abundance of coccidia showed a strong temporal trend without any influence of density. Strikingly, coccidian abundance increased threefold across the course of the study in lambs, while increases in yearlings and adults were negligible. Our decades-long, intensive, individual-based study will enable the role of environmental change and selection pressures in driving these dynamics to be determined, potentially providing unparalleled insight into the drivers of temporal variation in parasite dynamics in the wild. Key findingsO_LIWe studied temporal trends in gastrointestinal parasites of wild sheep over 31 years C_LIO_LIYear and host population density explained temporal variation in parasites independently C_LIO_LIPrevalence of both strongyle nematodes and coccidia varied across the study period C_LIO_LIAbundance of strongyles was more closely linked to host density than year C_LIO_LIAbundance of coccidia increased threefold over time in lambs, but did not vary in adults C_LI

ecology↗

bioRxiv2021

The impact of resource provisioning on the epidemiological responses of different parasites

O_LIEvents such as anthropogenic activities and periodic tree masting can alter resource provisioning in the environment, directly affecting animals, and potentially impacting the spread of infectious diseases in wildlife. The effect of these supplemental resources on infectious diseases can manifest through different pathways, affecting host susceptibility, transmission and host demography. C_LIO_LITo date however, empirical research has tended to examine these different pathways in isolation, for example by quantifying the effects of provisioning on host behaviour in the wild or changes in immune responses in controlled laboratory studies. Further, while theory has investigated the interactions between these pathways, thus far this work has focussed on a narrow subset of pathogen types, typically directly-transmitted microparasites. Given the diverse ways that provisioning can affect host susceptibility, contact patterns or host demography, we may expect the epidemiological consequences of provisioning to depend on key aspects of parasite life-history, such as the duration of infection and transmission mode. C_LIO_LIWe developed a suite of generic epidemiological models to compare how resource provisioning alters responses for different parasites that vary in their biology (micro- and macro-parasite), transmission mode (direct, environmental, and vector transmitted) and duration of infection (acute, latent, and chronic). Next, we parameterised these different parasite types using data from the diverse parasite community of wild wood mice as a case study. C_LIO_LIWe show there are common epidemiological responses to host resource provisioning across all parasite types examined. In particular, the response to provisioning could be driven in opposite directions, depending on which host pathways (contact rate, susceptibility or host demography) are most altered by the addition of resources to the environment. Broadly, these responses were qualitatively consistent across all parasite types, emphasising the importance of identifying general trade-offs between provisioning-altered parameters. C_LIO_LIDespite the qualitative consistency in responses to provisioning across parasite types, we found notable quantitative differences between parasites, suggesting specific epidemiological outcomes could strongly depend on parasite type, infection duration and permanency of recovery, and whether the parasite is directly, environmentally, or vector transmitted. These analyses therefore highlight the importance of knowing key specific aspects of host-parasite biology, such as host contact behaviours, parasite interactions with the host immune system, and how resource availability shapes host demographics, in order to understand and predict epidemiological responses to provisioning for any specific host-parasite system. C_LI

ecology↗

bioRxiv2020

Who acquires infection from whom? Estimating herpesvirus transmission rates between wild rodent host groups

To date, few studies of parasite epidemiology have investigated who acquires infection from whom in wildlife populations. Nonetheless, identifying routes of disease transmission within a population, and determining the key groups of individuals that drive parasite transmission and maintenance, are fundamental to understanding disease dynamics. Gammaherpesviruses are a widespread group of DNA viruses that infect many vertebrate species, and murine gammaherpesviruses (i.e. MuHV-4) are a standard lab model for studying human herpesviruses, for which much about the pathology and immune response elicited to infection is well understood. However, despite this extensive research effort, primarily in the lab, the transmission route of murine gammaherpesviruses within their natural host populations is not well understood. Here, we aimed to understand wood mouse herpesvirus (WMHV) transmission, by fitting a series of population dynamic models to field data on wood mice naturally infected with WMHV and then estimating transmission parameters within and between demographic groups of the host population. Different models accounted for different combinations of host sex (male/female), age (subadult/adult) and transmission functions (density/frequency-dependent). We found that a density-dependent transmission model incorporating explicit sex groups fitted the data better than all other proposed models. Male-to-male transmission was the highest among all demographic groups, suggesting that male behaviour is a key factor driving WMHV transmission. Our models also suggest that transmission between sexes, although important, wasnt symmetrical, with infected males playing a significant role in infecting naive females but not vice versa. Overall this work shows the power of coupling population dynamic models with long-term field data to elucidate otherwise unobservable transmission processes in wild disease systems.

ecology↗

bioRxiv2020

Experimental parasite community perturbation reveals associations between Sin Nombre virus and gastrointestinal nematodes in a rodent reservoir host

Individuals are often co-infected with several parasite species, yet measuring within-host interactions remains difficult in the wild. Consequently, such interactions impacts on host fitness and epidemiology are often unknown. We used anthelmintic drugs to experimentally reduce nematode infection and measured the effects on both nematodes and the important zoonosis Sin Nombre virus (SNV) in its primary wild reservoir (Peromyscus spp.). Treatment significantly reduced nematode infection, but increased SNV seroprevalence. Furthermore, mice that were co-infected with both nematodes and SNV were in better condition and survived as much as four times longer than mice infected with either parasite alone. These results highlight the importance of investigating multiple parasites for understanding interindividual variation and epidemiological dynamics in reservoir populations with zoonotic transmission potential.

ecology↗

bioRxiv2020

Methylation-Based Age Estimation in a Wild Mouse

The age structure of populations, or the ageing rate of individuals, impacts aspects of ecology, epidemiology and conservation. Yet for many wild organisms, age is an inaccessible trait. In many cases measuring age or ageing rates in the wild requires molecular biomarkers of age. Epigenetic clocks based on DNA methylation have been shown to accurately estimate the age of humans and laboratory mice, but they also show variable ticking rates that are associated with mortality risk above and beyond that predicted by chronological age. Thus, epigenetic clocks are proving to be useful markers of both chronological and biological age, and they are beginning to be applied to wild mammals and birds. We have acquired strong evidence that an accurate clock is possible for the wood mouse Apodemus sylvaticus by adapting epigenetic information from the laboratory mouse (Mus musculus). Apodemus sylvaticus is a well-studied, common small mammal in the UK and Europe, which is amenable to large-scale experimental perturbations and longitudinal sampling of individuals across their lives. These features of the wood mouse system offer opportunities to disentangle causal relationships between ageing rates and environmental stress. Our wood mouse epigenetic clock is PCR-based, and so requires only tiny amounts of tissue accessible through non-destructive sampling. We quantified methylation using Oxford Nanopore sequencing technology and present a new bioinformatics pipeline for data analysis. We thus describe a new and generalizable system that should enable ecologists and other field biologists to go from small tissue samples to an epigenetic clock for their study animal, which will enable investigations of ageing in the wild which where previously inaccessible.

genetics↗

bioRxiv2020

Spatiotemporal variation in drivers of parasitism in a wild wood mouse population

O_LIHost-parasite interactions in nature are driven by a range of factors across several ecological scales, so observed relationships are often context-dependent. Importantly, if these factors vary across space and time, practical sampling limitations can limit or bias inferences, and the relative importance of different drivers can be hard to discern. C_LIO_LIWe collected a replicated, longitudinal dataset of >1000 individual wood mice (Apodemus sylvaticus) encompassing 6 years of sampling across 5 different woodland sites to investigate how environmental, host and within-host factors determine infection intensity of a highly prevalent gastrointestinal nematode, Heligmosomoides polygyrus. C_LIO_LIWe used a Bayesian modelling approach to further quantify if and how each factor varied in space and time. Finally, we examined the extent to which a lack of spatially or temporally replication (i.e., within single years or single sites) and single (cross-sectional) versus repeated (longitudinal) sampling of individuals would affect which drivers were found to predict H. polygyrus infection. C_LIO_LISeason, host body condition, and sex were the three most important determinants of infection intensity; however, the strength and even direction of these effects varied in time, but not in space. Additionally, longitudinal datasets, in which we can control for within-individual variation through repeat observations, provided more robust estimates of the drivers of parasite intensity compared to cross-sectional data. C_LIO_LIThese results highlight the importance of accounting for spatiotemporal variation in drivers of disease dynamics and the need to incorporate spatiotemporal replication when designing sampling regimes. Furthermore, they suggest that embracing rather than simply controlling for spatiotemporal variation can reveal important insight into host-parasite relationships in the wild. C_LI

ecology↗

bioRxiv2019

Supplemented nutrition increases immunity and drug efficacy in a natural host-helminth system

Gastrointestinal helminths are common parasites of humans, wildlife, and livestock, leading to chronic infections in large parts of the world. In humans, there is also an overlap in the incidence of malnutrition and helminth infections which can predispose individuals to higher infection burdens and reduced anthelmintic efficacy due to compromised immunity. This relationship has been well-studied in laboratory models by testing for the impact of dramatic reductions of specific nutrients on infection outcomes. However, much less is known about the benefits of whole-diet supplementation in natural host-helminth systems. We experimentally supplemented the diet of wood mice (Apodemus sylvaticus) and measured resistance to the gastrointestinal nematode Heligmosomoides polygyrus and anthelmintic treatment efficacy in both natural and captive populations. Supplemented wood mice were more resistant to H. polygyrus infection, cleared worms more efficiently after treatment, produced stronger general and parasite-specific antibody responses, and maintained better body condition. In addition, supplemented nutrition in conjunction with anthelminthic treatment significantly reduced H. polygyrus transmission potential. These large-scale improvements in condition and immunity of supplemented nutrition found in controlled and wild environments show the rapid and extensive benefits of a well-balanced diet and have important implications for using diet interventions to improve disease control programmes. Author SummaryGastrointestinal helminths are ubiquitous parasites which cause chronic infections and debilitating symptoms worldwide for human and animal populations alike. Efforts to control helminth infections rely primarily on deworming drugs. However, despite high availability and low cost of these drugs, reinfection is common and helminths remain a substantial problem in many areas of the world. One factor which contributes to the persistence of helminth infections is co-occurrence of malnutrition. Extensive work in model laboratory systems has shown that deficiencies in both macro- and micronutrients can impair host immune responses to helminth infections, but how this relationship translates to natural host-helminth systems and drug efficacy is still poorly understood. Here, we used a combination of experimental nutrition supplementation and deworming treatment in paired wood mouse populations in both wild and captive environments to determine the role of a well-balanced diet for infection control in a natural host-helminth system. We found that mice on a supplemented diet had lower burden of infection and increased drug efficacy, body condition, and immune responses. We also found that supplementation lowered transmission potential of hosts. These broad and rapid effects of increased nutrition quality have important implications for the benefits of diet interventions alongside deworming drugs.

ecology↗