热带城乡交错带本地和入侵小型哺乳动物的宿主-微生物组关联。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Alessandra Giacomini, Maklarin B. Lakim, Fred Y. Y. Tuh, Matthew Hitchings, Sofia Consuegra, Tamsyn Uren Webster, Konstans Wells
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引用次数: 0

摘要

全球变化和城市化深刻地改变了野生动物的栖息地,迫使本土动物进入新的栖息地,同时增加了本土物种和入侵物种的共存。宿主-微生物组的关联是由宿主特征和环境特征决定的,但对于它们在城乡梯度中共存的本地和入侵物种中的可塑性知之甚少。在这里,我们沿着婆罗洲的城乡交错区探索了四种同域小型哺乳动物的肠道微生物群,婆罗洲是地球上最古老的雨林地区之一,经历了最近的城市扩张。宿主物种身份是微生物组组成的最重要决定因素,而土地利用和空间邻近性决定了三种大鼠体内和之间微生物组的相似性。城市生活大鼠Rattus Rattus的微生物组成更接近于当地的城市适应大鼠Sundamys muelleri (Rattus最强的环境生态位重叠),而不是与城市生活大鼠褐家鼠相似。居住在城市的鼩鼱Suncus murinus表现出最独特的微生物组。褐家鼠的微生物群对土地利用强度最敏感,其组成和细菌丰度在不同的交错带上发生显著变化。我们的研究结果表明,本地和入侵物种之间的环境生态位重叠促进了相似的肠道微生物群。即使是像褐家鼠这样分布在世界各地的杂食性城市居民,肠道微生物群也可能在精细尺度的环境梯度中发生变化。未来的研究需要确认土地利用强度是否可以成为哺乳动物肠道微生物群的强大选择力,影响本地和入侵物种能够利用新环境的方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Host-Microbiome Associations of Native and Invasive Small Mammals Across a Tropical Urban–Rural Ecotone

Global change and urbanisation profoundly alter wildlife habitats, driving native animals into novel habitats while increasing the co-occurrence between native and invasive species. Host-microbiome associations are shaped by host traits and environmental features, but little is known about their plasticity in co-occurring native and invasive species across urban–rural gradients. Here, we explored gut microbiomes of four sympatric small mammal species along an urban–rural ecotone in Borneo, one of the planet's oldest rainforest regions experiencing recent urban expansion. Host species identity was the strongest determinant of microbiome composition, while land use and spatial proximity shaped microbiome similarity within and among the three rat species. The urban-dwelling rat Rattus rattus had a microbiome composition more similar to that of the native, urban-adapted rat Sundamys muelleri (R. rattus' strongest environmental niche overlap), than to the closely related urban-dwelling R. norvegicus. The urban-dwelling shrew Suncus murinus presented the most distinct microbiome. The microbiome of R. norvegicus was the most sensitive to land use intensity, exhibiting significant alterations in composition and bacterial abundance across the ecotone. Our findings suggest that environmental niche overlap among native and invasive species promotes similar gut microbiomes. Even for omnivorous urban-dwellers with a worldwide distribution like R. norvegicus, gut microbiomes may change across fine-scale environmental gradients. Future research needs to confirm whether land use intensity can be a strong selective force on mammalian gut microbiomes, influencing the way in which native and invasive species are able to exploit novel environments.

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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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