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候选基因和中性遗传多样性均与雌性地中海摩弗伦羊的寄生虫抗性相关。

Both candidate gene and neutral genetic diversity correlate with parasite resistance in female Mediterranean mouflon.

机构信息

Univ Lyon, Université Claude Bernard Lyon 1, CNRS, Laboratoire de Biométrie et Biologie Évolutive, 69100, Villeurbanne, France.

Office National de la Chasse et de la Faune Sauvage, Unité Ongulés Sauvages, 5 allée de Bethléem, Z.I. Mayencin, 38610, Gières, France.

出版信息

BMC Ecol. 2019 Mar 5;19(1):12. doi: 10.1186/s12898-019-0228-x.

DOI:10.1186/s12898-019-0228-x
PMID:30836982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6402107/
Abstract

BACKGROUND

Parasite infections can have substantial impacts on population dynamics and are accordingly a key challenge for wild population management. Here we studied genetic mechanisms driving parasite resistance in a large herbivore through a comprehensive approach combining measurements of neutral (16 microsatellites) and adaptive (MHC DRB1 exon 2) genetic diversity and two types of gastrointestinal parasites (nematodes and coccidia).

RESULTS

While accounting for other extrinsic and intrinsic predictors known to impact parasite load, we show that both neutral genetic diversity and DRB1 are associated with resistance to gastrointestinal nematodes. Intermediate levels of multi-locus heterozygosity maximized nematodes resistance, suggesting that both in- and outbreeding depression might occur in the population. DRB1 heterozygosity and specific alleles effects were detected, suggesting the occurrence of heterozygote advantage, rare-allele effects and/or fluctuating selection. On the contrary, no association was detected between genetic diversity and resistance to coccidia, indicating that different parasite classes are impacted by different genetic drivers.

CONCLUSIONS

This study provides important insights for large herbivores and wild sheep pathogen management, and in particular suggests that factors likely to impact genetic diversity and allelic frequencies, including global changes, are also expected to impact parasite resistance.

摘要

背景

寄生虫感染会对种群动态产生重大影响,因此是野生动物种群管理的一个关键挑战。在这里,我们通过结合测量中性(16 个微卫星)和适应性(MHC DRB1 外显子 2)遗传多样性以及两种类型的胃肠道寄生虫(线虫和球虫)的综合方法,研究了驱动大型食草动物寄生虫抗性的遗传机制。

结果

在考虑了已知会影响寄生虫负荷的其他外在和内在预测因子的情况下,我们表明中性遗传多样性和 DRB1 都与抵抗胃肠道线虫有关。多基因座杂合度的中间水平最大限度地提高了线虫的抗性,表明种群中可能存在近交和远交衰退。检测到了 DRB1 杂合性和特定等位基因的影响,表明存在杂合优势、稀有等位基因效应和/或波动选择。相反,遗传多样性与球虫抗性之间没有关联,表明不同的寄生虫类群受到不同的遗传驱动因素的影响。

结论

本研究为大型食草动物和野生绵羊病原体管理提供了重要的见解,特别是表明可能影响遗传多样性和等位基因频率的因素,包括全球变化,也可能影响寄生虫抗性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd18/6402107/c4c5f553c7db/12898_2019_228_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd18/6402107/342dac0ebba1/12898_2019_228_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd18/6402107/c4c5f553c7db/12898_2019_228_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd18/6402107/342dac0ebba1/12898_2019_228_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd18/6402107/c4c5f553c7db/12898_2019_228_Fig2_HTML.jpg

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