与军团菌定植相关的饮用水生物膜形成动态。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Céline Margot, William Rhoads, Marco Gabrielli, Margot Olive, Frederik Hammes
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引用次数: 0

摘要

了解军团菌如何在多菌种生物膜中增殖,对于制定控制其在建筑冷热水管道中存在的策略至关重要。在这里,我们分析了生物膜的形成和军团菌属在新管道材料上的定殖情况。生物膜形成的特点是最初完整细胞浓度增加到 9.5 × 105 cells/cm2,随后稳步下降。我们发现 Comamonas、Caulobacter、Schlegella、Blastomonas 和 Methyloversatilis 是生物膜形成过程中的先驱菌属。重要的是,嗜肺军团菌是最主要的军团菌属,并迅速在生物膜上定植,4 周后可培养细胞浓度达到 3.1 × 104 MPN/cm2。此外,还有几种军团菌同时出现,并且在生物膜定殖过程中具有不同的动态变化。通过 18S rRNA 基因扩增片段测序发现,蛭形目蛭吸虫(V. vermiformis)是最主要的原生动物。我们的研究结果突出表明,引入新的建筑管道材料后形成的生物膜是一个动态过程,致病性军团菌可能是最早的定殖者之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamics of drinking water biofilm formation associated with Legionella spp. colonization.

Understanding how Legionella spp. proliferate in multispecies biofilms is essential to develop strategies to control their presence in building plumbing. Here, we analyzed biofilm formation and Legionella spp. colonization on new plumbing material during 8 weeks. Biofilm formation was characterized by an initial increase in intact cell concentrations up to 9.5 × 105 cells/cm2, followed by a steady decrease. We identified Comamonas, Caulobacter, Schlegella, Blastomonas and Methyloversatilis as pioneer genera in the biofilm formation process. Importantly, L. pneumophila was the dominant Legionella spp. and rapidly colonized the biofilms, with culturable cell concentrations peaking at 3.1 × 104 MPN/cm2 after 4 weeks already. Moreover, several Legionella species co-occurred and had distinct dynamics of biofilm colonization. Vermamoeba vermiformis (V. vermiformis) was the dominant protist identified with 18S rRNA gene amplicon sequencing. Together our results highlight that biofilm formation upon introduction of new building plumbing material is a dynamic process where pathogenic Legionella species can be part of the earliest colonizers.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
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.
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