{"title":"吸食植物的昆虫从环境中选择组合肠道微生物群,以提高宿主的繁殖能力。","authors":"Hong-Wei Shan, Xie-Jiang Xia, Yi-Lu Feng, Wei Wu, Hong-Jie Li, Zong-Tao Sun, Jun-Min Li, Jian-Ping Chen","doi":"10.1038/s41522-024-00539-z","DOIUrl":null,"url":null,"abstract":"<p><p>Plant-sucking insects have intricate associations with a diverse array of microorganisms to facilitate their adaptation to specific ecological niches. The midgut of phytophagous true bugs is generally structured into four distinct compartments to accommodate their microbiota. Nevertheless, there is limited understanding regarding the origins of these gut microbiomes, the mechanisms behind microbial community assembly, and the interactions between gut microbiomes and their insect hosts. In this study, we conducted a comprehensive survey of microbial communities within the midgut compartments of a bean bug Riptortus pedestris, soybean plant, and bulk soil across 12 distinct geographical fields in China, utilizing high-throughput sequencing of the 16 S rRNA gene. Our findings illuminated that gut microbiota of the plant-sucking insects predominantly originated from the surrounding soil environment, and plants also play a subordinate role in mediating microbial acquisition for the insects. Furthermore, our investigation suggested that the composition of the insect gut microbiome was probably shaped by host selection and/or microbe-microbe interactions at the gut compartment level, with marginal influence from soil and geographical factors. Additionally, we had unveiled a noteworthy dynamic in the acquisition of core bacterial taxa, particularly Burkholderia, which were initially sourced from the environment and subsequently enriched within the insect midgut compartments. This bacterial enrichment played a significant role in enhancing insect host reproduction. These findings contribute to our evolving understanding of microbiomes within the insect-plant-soil ecosystem, shedding additional light on the intricate interactions between insects and their microbiomes that underpin the ecological significance of microbial partnerships in host adaptation.</p>","PeriodicalId":19370,"journal":{"name":"npj Biofilms and Microbiomes","volume":"10 1","pages":"64"},"PeriodicalIF":7.8000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11289440/pdf/","citationCount":"0","resultStr":"{\"title\":\"The plant-sucking insect selects assembly of the gut microbiota from environment to enhance host reproduction.\",\"authors\":\"Hong-Wei Shan, Xie-Jiang Xia, Yi-Lu Feng, Wei Wu, Hong-Jie Li, Zong-Tao Sun, Jun-Min Li, Jian-Ping Chen\",\"doi\":\"10.1038/s41522-024-00539-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Plant-sucking insects have intricate associations with a diverse array of microorganisms to facilitate their adaptation to specific ecological niches. The midgut of phytophagous true bugs is generally structured into four distinct compartments to accommodate their microbiota. Nevertheless, there is limited understanding regarding the origins of these gut microbiomes, the mechanisms behind microbial community assembly, and the interactions between gut microbiomes and their insect hosts. In this study, we conducted a comprehensive survey of microbial communities within the midgut compartments of a bean bug Riptortus pedestris, soybean plant, and bulk soil across 12 distinct geographical fields in China, utilizing high-throughput sequencing of the 16 S rRNA gene. Our findings illuminated that gut microbiota of the plant-sucking insects predominantly originated from the surrounding soil environment, and plants also play a subordinate role in mediating microbial acquisition for the insects. Furthermore, our investigation suggested that the composition of the insect gut microbiome was probably shaped by host selection and/or microbe-microbe interactions at the gut compartment level, with marginal influence from soil and geographical factors. Additionally, we had unveiled a noteworthy dynamic in the acquisition of core bacterial taxa, particularly Burkholderia, which were initially sourced from the environment and subsequently enriched within the insect midgut compartments. This bacterial enrichment played a significant role in enhancing insect host reproduction. 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引用次数: 0
摘要
吸食植物的昆虫与各种微生物有着复杂的联系,以帮助它们适应特定的生态位。植食性真虫的中肠一般分为四个不同的区域,以容纳它们的微生物群。然而,人们对这些肠道微生物群的起源、微生物群落组装背后的机制以及肠道微生物群与其昆虫宿主之间的相互作用了解有限。在这项研究中,我们利用 16 S rRNA 基因的高通量测序,对中国 12 个不同地理区域的豆角蝇、大豆植株和大块土壤的中肠内的微生物群落进行了全面调查。我们的研究结果表明,植物吸食昆虫的肠道微生物群主要来源于周围的土壤环境,植物在昆虫获取微生物方面也起着辅助作用。此外,我们的调查还表明,昆虫肠道微生物组的组成可能是由宿主选择和/或肠道分区水平上微生物与微生物之间的相互作用形成的,土壤和地理因素的影响微乎其微。此外,我们还揭示了获得核心细菌类群(尤其是伯克霍尔德氏菌)的一个值得注意的动态过程。这种细菌富集在提高昆虫宿主繁殖能力方面发挥了重要作用。这些发现加深了我们对昆虫-植物-土壤生态系统中微生物组的理解,进一步揭示了昆虫与其微生物组之间错综复杂的互动关系,而这种互动关系正是微生物伙伴关系在宿主适应过程中的生态意义所在。
The plant-sucking insect selects assembly of the gut microbiota from environment to enhance host reproduction.
Plant-sucking insects have intricate associations with a diverse array of microorganisms to facilitate their adaptation to specific ecological niches. The midgut of phytophagous true bugs is generally structured into four distinct compartments to accommodate their microbiota. Nevertheless, there is limited understanding regarding the origins of these gut microbiomes, the mechanisms behind microbial community assembly, and the interactions between gut microbiomes and their insect hosts. In this study, we conducted a comprehensive survey of microbial communities within the midgut compartments of a bean bug Riptortus pedestris, soybean plant, and bulk soil across 12 distinct geographical fields in China, utilizing high-throughput sequencing of the 16 S rRNA gene. Our findings illuminated that gut microbiota of the plant-sucking insects predominantly originated from the surrounding soil environment, and plants also play a subordinate role in mediating microbial acquisition for the insects. Furthermore, our investigation suggested that the composition of the insect gut microbiome was probably shaped by host selection and/or microbe-microbe interactions at the gut compartment level, with marginal influence from soil and geographical factors. Additionally, we had unveiled a noteworthy dynamic in the acquisition of core bacterial taxa, particularly Burkholderia, which were initially sourced from the environment and subsequently enriched within the insect midgut compartments. This bacterial enrichment played a significant role in enhancing insect host reproduction. These findings contribute to our evolving understanding of microbiomes within the insect-plant-soil ecosystem, shedding additional light on the intricate interactions between insects and their microbiomes that underpin the ecological significance of microbial partnerships in host adaptation.
期刊介绍:
npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.