群落环境影响大肠埃希菌的连接效率。

FEMS microbes Pub Date : 2024-07-27 eCollection Date: 2024-01-01 DOI:10.1093/femsmc/xtae023
Misshelle Bustamante, Floor Koopman, Jesper Martens, Jolanda K Brons, Javier DelaFuente, Thomas Hackl, Oscar P Kuipers, G Sander van Doorn, Marjon G J de Vos
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引用次数: 0

摘要

在尿路感染(UTI)中,不同的细菌可能生活在由不同物种组成的多微生物群落中。目前还不清楚群落成员如何影响尿路致病性大肠杆菌的共轭效率。我们研究了经常从泌尿感染(UTI)中共分离出的个别物种对人工尿液培养基中分离出的大肠杆菌的共轭效率的影响。我们在含有和不含有多微生物UTI中常见的五种不同菌种的情况下,在含有pOXA-48质粒的供体大肠杆菌菌株和六株尿路致病性大肠杆菌分离株之间进行了配对共轭率实验,以阐明它们对大肠杆菌共轭效率的影响。我们发现,在没有其他物种存在的情况下,pOXA-48 的基础共轭率取决于细菌宿主的遗传背景。此外,我们还发现细菌间的相互作用对 pOXA-48 的共轭率总体上有积极影响。特别是,我们发现革兰氏阳性肠球菌能提高对尿路致病性大肠杆菌分离物的共轭率。我们推测,在人工尿液培养基环境中,共培养的性质和物理相互作用对共轭率的提高非常重要。
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Community context influences the conjugation efficiency of Escherichia coli.

In urinary tract infections (UTIs), different bacteria can live in a polymicrobial community consisting of different species. It is unknown how community members affect the conjugation efficiency of uropathogenic Escherichia coli. We investigated the influence of individual species often coisolated from urinary infections (UTI) on the conjugation efficiency of E. coli isolates in artificial urine medium. Pairwise conjugation rate experiments were conducted between a donor E. coli strain containing the pOXA-48 plasmid and six uropathogenic E. coli isolates, in the presence and absence of five different species commonly coisolated in polymicrobial UTIs to elucidate their effect on the conjugation efficiency of E. coli. We found that the basal conjugation rates of pOXA-48, in the absence of other species, are dependent on the bacterial host genetic background. Additionally, we found that bacterial interactions have an overall positive effect on the conjugation rate of pOXA-48. Particularly, Gram-positive enterococcal species were found to enhance the conjugation rates towards uropathogenic E. coli isolates. We hypothesize that the nature of the coculture and physical interactions are important for these increased conjugation rates in an artificial urine medium environment.

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CiteScore
3.30
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审稿时长
15 weeks
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