Aedes albopictus microbiome derives from environmental sources and partitions across distinct host tissues

IF 3.9 3区 生物学 Q2 MICROBIOLOGY MicrobiologyOpen Pub Date : 2023-06-12 DOI:10.1002/mbo3.1364
Priscilla S. Seabourn, Danya E. Weber, Helen Spafford, Matthew C. I. Medeiros
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Abstract

The mosquito microbiome consists of a consortium of interacting microorganisms that reside on and within culicid hosts. Mosquitoes acquire most of their microbial diversity from the environment over their life cycle. Once present within the mosquito host, the microbes colonize distinct tissues, and these symbiotic relationships are maintained by immune-related mechanisms, environmental filtering, and trait selection. The processes that govern how environmental microbes assemble across the tissues within mosquitoes remain poorly resolved. We use ecological network analyses to examine how environmental bacteria assemble to form bacteriomes among Aedes albopictus host tissues. Mosquitoes, water, soil, and plant nectar were collected from 20 sites in the Mānoa Valley, Oahu. DNA was extracted and associated bacteriomes were inventoried using Earth Microbiome Project protocols. We find that the bacteriomes of A. albopictus tissues were compositional taxonomic subsets of environmental bacteriomes and suggest that the environmental microbiome serves as a source pool that supports mosquito microbiome diversity. Within the mosquito, the microbiomes of the crop, midgut, Malpighian tubules, and ovaries differed in composition. This microbial diversity partitioned among host tissues formed two specialized modules: one in the crop and midgut, and another in the Malpighian tubules and ovaries. The specialized modules may form based on microbe niche preferences and/or selection of mosquito tissues for specific microbes that aid unique biological functions of the tissue types. A strong niche-driven assembly of tissue-specific microbiotas from the environmental species pool suggests that each tissue has specialized associations with microbes, which derive from host-mediated microbe selection.

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白纹伊蚊微生物群来自环境来源,并在不同的宿主组织中划分
蚊子微生物群由寄生在杀虫宿主上和宿主内的相互作用的微生物组成。蚊子在整个生命周期中从环境中获得大部分微生物多样性。一旦存在于蚊子宿主体内,这些微生物就会在不同的组织中定植,这些共生关系通过免疫相关机制、环境过滤和性状选择来维持。控制环境微生物如何在蚊子的组织中聚集的过程仍然没有得到很好的解决。我们使用生态网络分析来研究环境细菌如何在白纹伊蚊宿主组织中组装形成细菌组。在瓦胡岛Mānoa山谷的20个地点采集了蚊子、水、土壤和植物花蜜。根据地球微生物组计划方案提取DNA并清点相关细菌组。研究发现,白纹伊蚊组织的菌群是环境菌群的组成亚群,提示环境菌群是支持蚊子菌群多样性的源库。在蚊子体内,作物、中肠、马尔比氏小管和卵巢的微生物组成不同。这种微生物多样性在宿主组织中形成了两个专门的模块:一个在作物和中肠,另一个在马氏小管和子房。专门化模块可以基于微生物生态位偏好和/或特定微生物的蚊子组织选择而形成,这有助于该组织类型的独特生物学功能。来自环境物种库的组织特异性微生物群的强大生态位驱动组装表明,每个组织都与微生物有专门的关联,这源于宿主介导的微生物选择。
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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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