Sex-Dependent Influence of Major Histocompatibility Complex Diversity on Fitness in a Social Mammal.

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nadine Schubert, Hazel J Nichols, Francis Mwanguhya, Robert Businge, Solomon Kyambulima, Kenneth Mwesige, Joseph I Hoffman, Michael A Cant, Jamie C Winternitz
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Abstract

Parasite infections affect males and females differently across a wide range of species, often due to differences in immune responses. Generally, females tend to have stronger immune defences and lower parasite loads than males. The major histocompatibility complex (MHC) plays a crucial role in the adaptive immune response, and extensive research has explored how variation in this region influences infection and fitness outcomes. However, studies of sex-specific relationships between MHC variation and infection are scarce, perhaps because MHC genes are located on the autosomes, which are shared by both sexes. Here, we provide evidence of sexually antagonistic selection in a wild, group-living mammal-the banded mongoose. Using genetic and life history data collected from over 300 individuals across 25 years, we found that both MHC class I (MHC-I) and MHC class II (MHC-II) diversity influence lifetime reproductive success differently in males and females. Specifically, higher MHC diversity is linked to increased fitness in males but decreased fitness in females. Furthermore, MHC diversity did not differ between the sexes, indicating an unresolved genetic sexual conflict. Our findings demonstrate that sexually antagonistic selection acts on the MHC and may operate across both MHC classes but differently. This study contributes to the growing body of evidence that sex is a significant factor in shaping host immunity and fitness.

社会性哺乳动物主要组织相容性复合体多样性对适应性的性别依赖性影响。
寄生虫感染对许多物种的雄性和雌性的影响不同,这通常是由于免疫反应的差异。一般来说,雌性往往比雄性有更强的免疫防御和更低的寄生虫负荷。主要组织相容性复合体(MHC)在适应性免疫反应中起着至关重要的作用,广泛的研究已经探索了该区域的变化如何影响感染和适应性结果。然而,MHC变异与感染之间的性别特异性关系的研究很少,这可能是因为MHC基因位于常染色体上,这是两性共享的。在这里,我们提供了一种野生群居哺乳动物——带状猫鼬的性对抗选择的证据。利用25年来收集的300多个个体的遗传和生活史数据,我们发现MHC I类(MHC-I)和MHC II类(MHC-II)多样性对男性和女性终生生殖成功率的影响是不同的。具体来说,更高的MHC多样性与男性的适应性增加有关,而与女性的适应性降低有关。此外,MHC多样性在两性之间没有差异,这表明尚未解决的遗传性别冲突。我们的研究结果表明,性拮抗选择作用于MHC,并且可能在两类MHC中都起作用,但不同。这项研究提供了越来越多的证据,证明性别是塑造宿主免疫力和健康的重要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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