Bacterial aggregation triggered by low-level antibiotic-mediated lysis.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-09-26 DOI:10.1038/s41522-024-00553-1
Sharareh Tavaddod, Angela Dawson, Rosalind J Allen
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Abstract

Suspended bacterial aggregates play a central role in ocean biogeochemistry, industrial processes and probably many clinical infections - yet the factors that trigger aggregation remain poorly understood, as does the relationship between suspended aggregates and surface-attached biofilms. Here we show that very low doses of cell-wall targeting antibiotic, far below the minimal inhibitory concentration, can trigger aggregation of Escherichia coli cells. This occurs when a few cells lyse, releasing extracellular DNA - thus, cell-to-cell variability in antibiotic response leads to population-level aggregation. Although lysis-triggered aggregation echoes known trigger mechanisms for surface-attached biofilms, these aggregates may have different ecological implications since they do not show increased biofilm-forming potential or increased antibiotic resistance. Our work contributes to understanding the nature of bacterial aggregates and the factors that trigger their formation, and the possible consequences of widespread low-dose antibiotic exposure in the environment and in the body.

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抗生素介导的低水平裂解引发细菌聚集。
悬浮细菌聚集体在海洋生物地球化学、工业生产过程以及许多临床感染中发挥着核心作用,但人们对引发聚集的因素以及悬浮聚集体与表面附着的生物膜之间的关系仍然知之甚少。在这里,我们发现远低于最小抑制浓度的极低剂量细胞壁靶向抗生素就能引发大肠杆菌细胞聚集。当少数细胞裂解,释放出细胞外 DNA 时,就会发生这种情况--因此,细胞与细胞之间对抗生素反应的差异会导致群体聚集。虽然裂解触发的聚集与已知的表面附着生物膜触发机制相呼应,但这些聚集体可能具有不同的生态影响,因为它们并没有显示出更强的生物膜形成潜力或更强的抗生素耐药性。我们的工作有助于了解细菌聚集体的性质、引发其形成的因素,以及在环境和人体中广泛接触低剂量抗生素可能造成的后果。
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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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