两栖动物皮肤微生物组和MHC II类多样性之间的关系。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
M. Cortazar-Chinarro, A. Richter-Boix, P. Rödin-Mörch, P. Halvarsson, J. B. Logue, A. Laurila, J. Höglund
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引用次数: 0

摘要

微生物群在决定宿主的生态和行为方面发挥着重要作用。然而,宿主遗传学如何塑造微生物组,以及微生物组组成如何影响宿主适应性,仍然存在问题。我们探讨了地理、进化史和宿主遗传学对广泛分布的两栖动物皮肤微生物组多样性和结构的影响。更具体地说,我们在属于两个地理集群的12只沼蛙(Rana arvalis)种群中检测了细菌多样性和组成与主要组织相容性复合体II类外显子2多样性之间的关系,这两个集群显示了过去和正在进行的差异选择的特征。我们发现,虽然两个集群之间的细菌α多样性没有差异,但MHC等位基因/超型和遗传多样性因地理和进化史的不同而有很大差异。细菌α多样性与预期的MHC杂合性呈正相关,与MHC核苷酸多样性呈负相关。此外,细菌群落组成在两个地理集群之间以及特定MHC等位基因/超型之间表现出显著差异。我们的发现强调了历史人口统计学事件对全基因组变异的重要性,并为免疫遗传宿主变异性和微生物多样性如何共同影响宿主适应性以及对疾病易感性和种群持久性的影响提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association between the skin microbiome and MHC class II diversity in an amphibian

Association between the skin microbiome and MHC class II diversity in an amphibian

Microbiomes play an important role in determining the ecology and behaviour of their hosts. However, questions remain pertaining to how host genetics shape microbiomes, and how microbiome composition influences host fitness. We explored the effects of geography, evolutionary history and host genetics on the skin microbiome diversity and structure in a widespread amphibian. More specifically, we examined the association between bacterial diversity and composition and the major histocompatibility complex class II exon 2 diversity in 12 moor frog (Rana arvalis) populations belonging to two geographical clusters that show signatures of past and ongoing differential selection. We found that while bacterial alpha diversity did not differ between the two clusters, MHC alleles/supertypes and genetic diversity varied considerably depending on geography and evolutionary history. Bacterial alpha diversity was positively correlated with expected MHC heterozygosity and negatively with MHC nucleotide diversity. Furthermore, bacterial community composition showed significant variation between the two geographical clusters and between specific MHC alleles/supertypes. Our findings emphasize the importance of historical demographic events on hologenomic variation and provide new insights into how immunogenetic host variability and microbial diversity may jointly influence host fitness with consequences for disease susceptibility and population persistence.

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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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