MosAIC: An annotated collection of mosquito-associated bacteria with high-quality genome assemblies.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences PLoS Biology Pub Date : 2024-11-15 DOI:10.1371/journal.pbio.3002897
Aidan Foo, Laura E Brettell, Holly L Nichols, Miguel Medina Muñoz, Jessica A Lysne, Vishaal Dhokiya, Ananya F Hoque, Doug E Brackney, Eric P Caragata, Michael L Hutchinson, Marcelo Jacobs-Lorena, David J Lampe, Edwige Martin, Claire Valiente Moro, Michael Povelones, Sarah M Short, Blaire Steven, Jiannong Xu, Timothy D Paustian, Michelle R Rondon, Grant L Hughes, Kerri L Coon, Eva Heinz
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Abstract

Mosquitoes transmit medically important human pathogens, including viruses like dengue virus and parasites such as Plasmodium spp., the causative agent of malaria. Mosquito microbiomes are critically important for the ability of mosquitoes to transmit disease-causing agents. However, while large collections of bacterial isolates and genomic data exist for vertebrate microbiomes, the vast majority of work in mosquitoes to date is based on 16S rRNA gene amplicon data that provides limited taxonomic resolution and no functional information. To address this gap and facilitate future studies using experimental microbiome manipulations, we generated a bacterial Mosquito-Associated Isolate Collection (MosAIC) consisting of 392 bacterial isolates with extensive metadata and high-quality draft genome assemblies that are publicly available, both isolates and sequence data, for use by the scientific community. MosAIC encompasses 142 species spanning 29 bacterial families, with members of the Enterobacteriaceae comprising 40% of the collection. Phylogenomic analysis of 3 genera, Enterobacter, Serratia, and Elizabethkingia, reveal lineages of mosquito-associated bacteria isolated from different mosquito species in multiple laboratories. Investigation into species' pangenomes further reveals clusters of genes specific to these lineages, which are of interest for future work to test for functions connected to mosquito host association. Altogether, we describe the generation of a physical collection of mosquito-associated bacterial isolates, their genomic data, and analyses of selected groups in context of genome data from closely related isolates, providing a unique, highly valuable resource for research on bacterial colonisation and adaptation within mosquito hosts. Future efforts will expand the collection to include broader geographic and host species representation, especially from individuals collected from field populations, as well as other mosquito-associated microbes, including fungi, archaea, and protozoa.

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MosAIC:具有高质量基因组组装的蚊子相关细菌注释集。
蚊子传播医学上重要的人类病原体,包括登革热病毒等病毒和疟疾病原体疟原虫等寄生虫。蚊子微生物组对蚊子传播致病因子的能力至关重要。然而,虽然脊椎动物微生物组存在大量细菌分离物和基因组数据,但迄今为止绝大多数蚊子微生物组的研究工作都是基于 16S rRNA 基因扩增片段数据,这些数据只能提供有限的分类分辨率,而且没有功能信息。为了填补这一空白,并促进未来利用微生物组实验操作进行研究,我们建立了一个细菌蚊虫相关分离物收集(MosAIC),其中包括392个细菌分离物,这些分离物具有广泛的元数据和高质量的基因组组装草案,分离物和序列数据都是公开的,可供科学界使用。MosAIC 包含 142 个物种,横跨 29 个细菌科,其中肠杆菌科成员占 40%。对 3 个属,即肠杆菌属、沙雷氏菌属和伊丽莎白金格菌属进行的系统发生组分析揭示了多个实验室从不同蚊子物种中分离出的蚊子相关细菌的系谱。对物种庞基因组的研究进一步揭示了这些菌系的特异基因簇,这对今后测试与蚊子宿主相关功能的工作很有意义。总之,我们描述了蚊子相关细菌分离物的物理收集、其基因组数据,以及结合密切相关分离物的基因组数据对所选组别进行的分析,为研究细菌在蚊子宿主内的定殖和适应提供了独特、极具价值的资源。未来的工作将扩大收集范围,以包括更广泛的地理和宿主物种代表性,特别是从野外种群中收集的个体,以及其他与蚊子相关的微生物,包括真菌、古生菌和原生动物。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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