革兰氏阴性群体感应信号增强革兰氏阳性病原体粪肠球菌的生物膜形成和毒力特性。

IF 3.7 2区 医学 Q2 MICROBIOLOGY
Ana Parga, Daniel Manoil, Malin Brundin, Ana Otero, Georgios N Belibasakis
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引用次数: 2

摘要

酰基高丝氨酸内酯(ahl)是革兰氏阴性菌典型的群体感应分子。最近的证据表明ahl也可能影响革兰氏阳性,尽管对这些相互作用的了解仍然很少。在这里,我们评估了AHLs对革兰氏阳性粪肠球菌生物膜形成和转录调控的影响。本文对5株粪肠球菌进行了研究。结晶紫被用来量化形成的生物量,共聚焦显微镜结合SYTO9/PI可以可视化生物膜的结构。利用反转录- qpcr技术评估了参与群体感应、生物膜形成和胁迫反应的10个基因的差异表达。暴露于AHL显著增加菌株ATCC 29212和感染牙根的两个分离株UmID4和UmID5的生物膜产量。在菌株ATCC 29212和UmID7中,AHLs上调群体感应基因(fsrC、cylA)、粘附素ace、efaA和asa1以及糖基转移酶epaQ。在菌株UmID7中,AHL暴露还上调了与抗逆性和毒力增加相关的两个膜胁迫响应基因(σV, groEL)。总之,我们的研究结果表明,ahl促进了几种粪肠球菌菌株的生物膜形成,并上调了与毒力和应激耐受性有关的转录网络。这些数据为粪肠杆菌对ahl的生物膜反应提供了尚未报道的见解,ahl是一个长期被认为是革兰氏阴性信号单极子的分子家族。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gram-negative quorum sensing signalling enhances biofilm formation and virulence traits in gram-positive pathogen <i>Enterococcus faecalis</i>.

Gram-negative quorum sensing signalling enhances biofilm formation and virulence traits in gram-positive pathogen <i>Enterococcus faecalis</i>.

Gram-negative quorum sensing signalling enhances biofilm formation and virulence traits in gram-positive pathogen <i>Enterococcus faecalis</i>.

Gram-negative quorum sensing signalling enhances biofilm formation and virulence traits in gram-positive pathogen Enterococcus faecalis.

Acyl-homoserine lactones (AHLs) are typical quorum-sensing molecules of gram-negative bacteria. Recent evidence suggests that AHLs may also affect gram-positives, although knowledge of these interactions remains scarce. Here, we assessed the effect of AHLs on biofilm formation and transcriptional regulations in the gram-positive Enterococcus faecalis. Five E. faecalis strains were investigated herein. Crystal violet was employed to quantify the biomass formed, and confocal microscopy in combination with SYTO9/PI allowed the visualisation of biofilms' structure. The differential expression of 10 genes involved in quorum-sensing, biofilm formation and stress responses was evaluated using reverse-transcription-qPCR. The AHL exposure significantly increased biofilm production in strain ATCC 29212 and two isolates from infected dental roots, UmID4 and UmID5. In strains ATCC 29212 and UmID7, AHLs up-regulated the quorum-sensing genes (fsrC, cylA), the adhesins ace, efaA and asa1, together with the glycosyltransferase epaQ. In strain UmID7, AHL exposure additionally up-regulated two membrane-stress response genes (σV, groEL) associated with increased stress-tolerance and virulence. Altogether, our results demonstrate that AHLs promote biofilm formation and up-regulate a transcriptional network involved in virulence and stress tolerance in several E. faecalis strains. These data provide yet-unreported insights into E. faecalis biofilm responses to AHLs, a family of molecules long-considered the monopole of gram-negative signalling.

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来源期刊
CiteScore
8.00
自引率
4.40%
发文量
52
审稿时长
12 weeks
期刊介绍: As the first Open Access journal in its field, the Journal of Oral Microbiology aims to be an influential source of knowledge on the aetiological agents behind oral infectious diseases. The journal is an international forum for original research on all aspects of ''oral health''. Articles which seek to understand ''oral health'' through exploration of the pathogenesis, virulence, host-parasite interactions, and immunology of oral infections are of particular interest. However, the journal also welcomes work that addresses the global agenda of oral infectious diseases and articles that present new strategies for treatment and prevention or improvements to existing strategies. Topics: ''oral health'', microbiome, genomics, host-pathogen interactions, oral infections, aetiologic agents, pathogenesis, molecular microbiology systemic diseases, ecology/environmental microbiology, treatment, diagnostics, epidemiology, basic oral microbiology, and taxonomy/systematics. Article types: original articles, notes, review articles, mini-reviews and commentaries
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