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Kloch, A.

Publications and source records attributed to Kloch, A..

4 recordsLinked to original sources

Genome-wide associations of host susceptibility to helminth and blood pathogens in spatially structured rodent populations

Parasites are ubiquitous drivers of host evolution by exerting strong selective pressure on natural populations. Understanding the genetic basis of host susceptibility to infection is important to know how host-pathogen interactions shape patterns of resistance and diversity in natural populations. We conducted a genome-wide association study (GWAS) to identify host genetic variants associated with infection by helminth and blood pathogens in spatially structured populations of Bank voles (Myodes glareolus; (Schreber, 1780). We genotyped 182 individuals sampled from ten sites in central Europe using quaddRAD sequencing, retaining 30,206 high-quality single-nucleotide polymorphisms (SNPs). Associations between SNP genotypes and parasite infection status were tested using mixed models controlling for relatedness, with host body mass included as a covariate. Across parasite taxa, we identified twelve SNPs exceeding genome-wide significance with the strongest signals detected for the intestinal nematode Heligmosomum mixtum. The variants identified are all intergenic, intronic, upstream or downstream of genes, with none predicted to alter coding sequences. These genes are not classical immunity genes but some are implicated in cytokine production, PI3K/AKT signalling and p38 MAPK pathway, suggesting that selective pressure from pathogens does not only act on known immunity genes, but on broader regulatory and metabolic networks. This finding suggests that variation in gene expression may be important for the differences in host susceptibility or resistance to parasitic infections.

evolutionary biology↗

Species-specific responses of helminths to temperature and moisture: long-term and multi-scale analyses in a free-living rodent

Parasite infections in wildlife vary across time and space due to interactions among host biology, ecological processes, and climatic variability. Under ongoing climate change, understanding how temperature, precipitation, or humidity influences parasite dynamics is important for predicting shifts in infection patterns and host-parasite interactions. Here, we examine how variation in climatic conditions is associated with helminth infections in a free-living rodent, the bank vole (Myodes glareolus), across 17 years and multiple spatial scales. Using zero-inflated generalised linear models, we quantified the effects of climatic variables on individual parasite burden. Climatic conditions (temperature and humidity or precipitation) affected helminth infections across all analysed scales, though the strength and direction of these effects differed among parasite species and between temporal and spatial scales. In the temporal dataset, parasite load was associated with seasonal variation in weather conditions, whereas in the spatial datasets, infection levels were linked to yearly average climatic variables. The differences reflect species-specific parasites life histories and transmission strategies. Our findings highlight the importance of analysing individual parasite species rather than overall parasite load or aggregated infection indices when assessing the impacts of climatic variation on host-parasite dynamics.

ecology↗

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↗

Cytokine gene polymorphism and parasite susceptibility in free-living rodents: importance of non-coding variants

Associations between genetic variants and susceptibility to infections have long been studied in free-living hosts to infer contemporary evolutionary forces shaping genetic polymorphisms of the immunity genes. Despite extensive studies of receptors, such as MHC or TLR, little is known about efferent arm of the immune system. Cytokines are signalling molecules that trigger and modulate the immune response, acting as a crucial link between innate and adaptive immunity. In the present study we investigated how genetic variation in cytokines affects susceptibility to parasitic diseases in bank voles. We focused on three cytokines: tumour necrosis factor (TNF), lymphotoxin alpha (LT), and interferon beta (IFN{beta}1). Two SNPs in LT and two in IFN{beta}1 significantly affected susceptibility to nematodes, and was of them was also associated with susceptibility to microbial pathogen Bartonella. All these variants displayed signatures of selection. One of the variants was synonymous, and one was located in an intron. Our study shows that cytokines are prone to parasite-driven selection, and non-coding variants may play an important role in susceptibility to infections in wild systems.

evolutionary biology↗