{"title":"从本地物种到入侵物种的微生物组转移可能会增加入侵风险。","authors":"Maria M Martignoni, Oren Kolodny","doi":"10.1098/rspb.2024.1318","DOIUrl":null,"url":null,"abstract":"<p><p>In a fast-changing world, understanding how organisms adapt to their environment is a pressing necessity. Research has focused on genetic adaptation, while our understanding of non-genetic modes is still in its infancy. The host-associated microbiome can be considered a non-genetic mode of adaptation, which can strongly influence an organism's ability to cope with its environment. However, the role of the microbiome in host ecological dynamics is largely unexplored, particularly in animal communities. Here, we discuss the following hypothesis: invasive species may rapidly adapt to local conditions by adopting beneficial microbes from similar co-occurring native species. This occurs when the invader's fitness is influenced by adaptation to local conditions that is facilitated by microbes acquired from native microbiomes. We present a minimal mathematical model to explore this hypothesis and show that a delayed acquisition of native microbes may explain the occurrence of an invasion lag. Overall, our results contribute to broadening the conceptualization of rapid adaptation via microbiome transfer and offer insights towards designing early intervention strategies for invasive species management.</p>","PeriodicalId":20589,"journal":{"name":"Proceedings of the Royal Society B: Biological Sciences","volume":"291 2034","pages":"20241318"},"PeriodicalIF":3.8000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537765/pdf/","citationCount":"0","resultStr":"{\"title\":\"Microbiome transfer from native to invasive species may increase invasion risk.\",\"authors\":\"Maria M Martignoni, Oren Kolodny\",\"doi\":\"10.1098/rspb.2024.1318\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In a fast-changing world, understanding how organisms adapt to their environment is a pressing necessity. Research has focused on genetic adaptation, while our understanding of non-genetic modes is still in its infancy. The host-associated microbiome can be considered a non-genetic mode of adaptation, which can strongly influence an organism's ability to cope with its environment. However, the role of the microbiome in host ecological dynamics is largely unexplored, particularly in animal communities. Here, we discuss the following hypothesis: invasive species may rapidly adapt to local conditions by adopting beneficial microbes from similar co-occurring native species. This occurs when the invader's fitness is influenced by adaptation to local conditions that is facilitated by microbes acquired from native microbiomes. We present a minimal mathematical model to explore this hypothesis and show that a delayed acquisition of native microbes may explain the occurrence of an invasion lag. Overall, our results contribute to broadening the conceptualization of rapid adaptation via microbiome transfer and offer insights towards designing early intervention strategies for invasive species management.</p>\",\"PeriodicalId\":20589,\"journal\":{\"name\":\"Proceedings of the Royal Society B: Biological Sciences\",\"volume\":\"291 2034\",\"pages\":\"20241318\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2024-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537765/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the Royal Society B: Biological Sciences\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1098/rspb.2024.1318\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Royal Society B: Biological Sciences","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1098/rspb.2024.1318","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/6 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
Microbiome transfer from native to invasive species may increase invasion risk.
In a fast-changing world, understanding how organisms adapt to their environment is a pressing necessity. Research has focused on genetic adaptation, while our understanding of non-genetic modes is still in its infancy. The host-associated microbiome can be considered a non-genetic mode of adaptation, which can strongly influence an organism's ability to cope with its environment. However, the role of the microbiome in host ecological dynamics is largely unexplored, particularly in animal communities. Here, we discuss the following hypothesis: invasive species may rapidly adapt to local conditions by adopting beneficial microbes from similar co-occurring native species. This occurs when the invader's fitness is influenced by adaptation to local conditions that is facilitated by microbes acquired from native microbiomes. We present a minimal mathematical model to explore this hypothesis and show that a delayed acquisition of native microbes may explain the occurrence of an invasion lag. Overall, our results contribute to broadening the conceptualization of rapid adaptation via microbiome transfer and offer insights towards designing early intervention strategies for invasive species management.
期刊介绍:
Proceedings B is the Royal Society’s flagship biological research journal, accepting original articles and reviews of outstanding scientific importance and broad general interest. The main criteria for acceptance are that a study is novel, and has general significance to biologists. Articles published cover a wide range of areas within the biological sciences, many have relevance to organisms and the environments in which they live. The scope includes, but is not limited to, ecology, evolution, behavior, health and disease epidemiology, neuroscience and cognition, behavioral genetics, development, biomechanics, paleontology, comparative biology, molecular ecology and evolution, and global change biology.