当考虑空间自相关时,宿主混合物对野生家鼠肠道微生物群的影响较弱。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Dagmar Čížková, Lucie Schmiedová, Martin Kváč, Bohumil Sak, Miloš Macholán, Jaroslav Piálek, Jakub Kreisinger
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引用次数: 0

摘要

肠道微生物组和脊椎动物宿主之间的相互作用如何促进宿主适应和物种形成是当前进化研究的主要问题之一。使用细菌组和真菌生物群落代谢编码,我们研究了肠道微生物群的这两个组成部分如何随着两个家鼠亚种(Mus musculus和M.M.domesticus)二次接触中宿主混合程度的变化而变化。我们使用了在混合区的两个重复处收集的大型数据集和基于模型的统计分析,以确保我们的结果的稳健性。假设野生宿主的微生物群存在空间自相关,我们直接比较了空间天真的统计模型与考虑空间自相关的统计模型的结果。我们发现,忽视空间自相关会强烈影响结果,并导致误导性结论。空间分析显示,亚种之间在微生物组组成和单个细菌谱系方面几乎没有差异。同样,混合程度对肠道菌群和真菌生物群落的影响最小,是由与自由生活的家鼠常见共生体相对应的少数微生物谱系的变化引起的。与之前的研究相比,这些数据不支持微生物群在该特定模型系统中宿主繁殖隔离中发挥重要作用的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The effect of host admixture on wild house mouse gut microbiota is weak when accounting for spatial autocorrelation

The effect of host admixture on wild house mouse gut microbiota is weak when accounting for spatial autocorrelation

The question of how interactions between the gut microbiome and vertebrate hosts contribute to host adaptation and speciation is one of the major problems in current evolutionary research. Using bacteriome and mycobiome metabarcoding, we examined how these two components of the gut microbiota vary with the degree of host admixture in secondary contact between two house mouse subspecies (Mus musculus musculus and M. m. domesticus). We used a large data set collected at two replicates of the hybrid zone and model-based statistical analyses to ensure the robustness of our results. Assuming that the microbiota of wild hosts suffers from spatial autocorrelation, we directly compared the results of statistical models that were spatially naive with those that accounted for spatial autocorrelation. We showed that neglecting spatial autocorrelation can strongly affect the results and lead to misleading conclusions. The spatial analyses showed little difference between subspecies, both in microbiome composition and in individual bacterial lineages. Similarly, the degree of admixture had minimal effects on the gut bacteriome and mycobiome and was caused by changes in a few microbial lineages that correspond to the common symbionts of free-living house mice. In contrast to previous studies, these data do not support the hypothesis that the microbiota plays an important role in host reproductive isolation in this particular model system.

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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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