Distinct microbial communities of drain flies (Clogmia albipunctata) across sites with differing human influence.

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Hyun Seo Park, Xavier Chavarria, Arwa Shatta, Dongjun Kang, Singeun Oh, Du-Yeol Choi, Jun Ho Choi, Myungjun Kim, Yoon Hee Cho, Myung-Hee Yi, Ju Yeong Kim
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引用次数: 0

Abstract

Drain flies (Clogmia albipunctata) are insects that thrive in humid urban environments such as bathrooms drains and sewage systems. While their role in pathogen transmission has been suggested, little is known about their microbiome or ecology in non-clinical contexts. Using 16S rRNA gene metabarcoding, we characterized the bacterial communities of drain flies from three locations in South Korea, public bathrooms from a college in Seoul, a rural port in Ulleungdo island, and a highly frequented public park in Yeouido. In total, we obtained 221 families and 1 474 features. We found significant differences in microbiome composition and diversity as well as a small core microbiome shared among locations, with environmental bacteria such as Pseudomonas and Ralstonia being the dominant taxa across samples. The majority of the detected amplicon sequence variants (ASV) were not shared among locations. These findings suggest drain fly transport a location-specific environmental bacteria. Notably, we also identified ASVs of potential clinical relevance, including Mycobacterium, Acinetobacter baumanii, Providencia, and Nocardia. This is the first metagenomic insight into the microbiome of this species and adds to a renewed interest in the role that non-hematophagous insects play in urban microbial ecology and the spread of microbes.

不同地点的排水蝇(Clogmia albipunctata)不同的微生物群落与不同的人类影响。
排水蝇(Clogmia albipunctata)是一种在潮湿的城市环境中茁壮成长的昆虫,比如浴室的排水管和污水系统。虽然它们在病原体传播中的作用已被提出,但在非临床背景下对它们的微生物组或生态学知之甚少。利用16S rRNA基因元条形码,我们对韩国三个地点的下水道苍蝇的细菌群落进行了表征,分别是首尔一所大学的公共厕所、郁陵岛的一个农村港口和汝矣岛一个经常光顾的公园。我们总共获得221个家族和1474个特征。我们发现微生物组的组成和多样性存在显著差异,并且在不同地点之间共享一个小的核心微生物组,环境细菌如假单胞菌和Ralstonia是整个样本的优势分类群。大多数检测到的扩增子序列变异(ASV)在不同位点之间不共享。这些发现表明,排水沟蝇运输一种特定地点的环境细菌。值得注意的是,我们还发现了具有潜在临床相关性的asv,包括分枝杆菌、鲍曼不动杆菌、普罗维登西亚菌和诺卡菌。这是对该物种微生物组的第一次宏基因组研究,并增加了对非吸血昆虫在城市微生物生态和微生物传播中所起作用的新兴趣。
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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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