Alessandra Giacomini, Maklarin B. Lakim, Fred Y. Y. Tuh, Matthew Hitchings, Sofia Consuegra, Tamsyn Uren Webster, Konstans Wells
{"title":"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。","authors":"Alessandra Giacomini, Maklarin B. Lakim, Fred Y. Y. Tuh, Matthew Hitchings, Sofia Consuegra, Tamsyn Uren Webster, Konstans Wells","doi":"10.1111/mec.17782","DOIUrl":null,"url":null,"abstract":"<p>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 <i>Rattus rattus</i> had a microbiome composition more similar to that of the native, urban-adapted rat <i>Sundamys muelleri</i> (<i>R. rattus</i>' strongest environmental niche overlap), than to the closely related urban-dwelling <i>R. norvegicus</i>. The urban-dwelling shrew <i>Suncus murinus</i> presented the most distinct microbiome. The microbiome of <i>R. norvegicus</i> 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 <i>R. norvegicus</i>, 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.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":"34 11","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/mec.17782","citationCount":"0","resultStr":"{\"title\":\"Host-Microbiome Associations of Native and Invasive Small Mammals Across a Tropical Urban–Rural Ecotone\",\"authors\":\"Alessandra Giacomini, Maklarin B. Lakim, Fred Y. Y. Tuh, Matthew Hitchings, Sofia Consuegra, Tamsyn Uren Webster, Konstans Wells\",\"doi\":\"10.1111/mec.17782\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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 <i>Rattus rattus</i> had a microbiome composition more similar to that of the native, urban-adapted rat <i>Sundamys muelleri</i> (<i>R. rattus</i>' strongest environmental niche overlap), than to the closely related urban-dwelling <i>R. norvegicus</i>. The urban-dwelling shrew <i>Suncus murinus</i> presented the most distinct microbiome. The microbiome of <i>R. norvegicus</i> 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 <i>R. norvegicus</i>, gut microbiomes may change across fine-scale environmental gradients. 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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.
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