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A质粒促进生物膜形成以及[具体对象]中的1类整合子基因盒重排。 (你提供的原文中“in.”后面缺少具体内容)

A -Plasmid Promotes Biofilm Formation and Class 1 Integron Gene Cassette Rearrangements in .

作者信息

Babosan Anamaria, Gaschet Margaux, Muggeo Anaëlle, Jové Thomas, Skurnik David, Ploy Marie-Cécile, de Champs Christophe, Reffuveille Fany, Guillard Thomas

机构信息

Inserm UMR-S 1250 P3Cell, SFR CAP-Santé, Université de Reims-Champagne-Ardenne, 51100 Reims, France.

Université de Limoges, Inserm, CHU Limoges, UMR-S 1092, 87032 Limoges, France.

出版信息

Antibiotics (Basel). 2022 May 26;11(6):715. doi: 10.3390/antibiotics11060715.

Abstract

Bacteria within biofilms may be exposed to sub-minimum inhibitory concentrations (sub-MICs) of antibiotics. Cell-to-cell contact within biofilms facilitates horizontal gene transfers and favors induction of the SOS response. Altogether, it participates in the emergence of antibiotic resistance. Aminoglycosides at sub-MICs can induce the SOS response through NO accumulation in carrying the small plasmid with the quinolone resistance gene (pDIJ09-518a). In this study, we show that in pDIJ09-518a, the SOS response triggered by sub-MICs of aminoglycosides has important consequences, promoting genetic rearrangement in class 1 integrons and biofilm formation. We found that the integrase expression was increased in carrying pDIJ09-518a in the presence of tobramycin, which was not observed for the WT isogenic strain that did not carry the -plasmid. Moreover, we showed that biofilm production was significantly increased in WT/pDIJ09-518a compared to the WT strain. However, such a higher production was decreased when the Hmp-NO detoxification pathway was fully functional by overexpressing Hmp. Our results showing that a -plasmid can promote biofilm formation in and potentiate the acquisition and spread of resistance determinants for other antibiotics complicate the attempts to counteract antibiotic resistance and prevention of biofilm development even further. We anticipate that our findings emphasize the complex challenges that will impact the decisions about antibiotic stewardship, and other decisions related to retaining antibiotics as effective drugs and the development of new drugs.

摘要

生物膜内的细菌可能会接触到低于最低抑菌浓度(sub-MICs)的抗生素。生物膜内的细胞间接触促进水平基因转移,并有利于SOS反应的诱导。总之,它参与了抗生素耐药性的出现。低于最低抑菌浓度的氨基糖苷类药物可通过携带喹诺酮耐药基因(pDIJ09-518a)的小质粒中一氧化氮(NO)的积累来诱导SOS反应。在本研究中,我们表明,在携带pDIJ09-518a的菌株中,由低于最低抑菌浓度的氨基糖苷类药物引发的SOS反应具有重要影响,促进了1类整合子中的基因重排和生物膜形成。我们发现,在妥布霉素存在的情况下,携带pDIJ09-518a的菌株中整合酶表达增加,而未携带该质粒的野生型同基因菌株未观察到这种情况。此外,我们表明,与野生型菌株相比,WT/pDIJ09-518a中的生物膜产生显著增加。然而,当通过过表达Hmp使Hmp-NO解毒途径完全发挥功能时,这种较高的生物膜产生量会降低。我们的结果表明,一个质粒可以促进菌株中的生物膜形成,并增强其他抗生素耐药决定因素的获得和传播,这使得对抗抗生素耐药性和预防生物膜形成的努力更加复杂。我们预计,我们的发现强调了将影响抗生素管理决策以及与保留抗生素作为有效药物和新药开发相关的其他决策的复杂挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c3c/9220102/8706ffa50bb3/antibiotics-11-00715-g001.jpg

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