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通过群体淬灭细菌菌株靶向酰基高丝氨酸内酯(AHLs)以控制生物膜形成 。 (你提供的原文句子不完整,翻译可能会有些突兀,建议补充完整原文再进行准确翻译)

Targeting Acyl Homoserine Lactones (AHLs) by the quorum quenching bacterial strains to control biofilm formation in .

作者信息

Khalid Syeda Javariya, Ain Quratul, Khan Sher Jamal, Jalil Amna, Siddiqui Muhammad Faisal, Ahmad Tahir, Badshah Malik, Adnan Fazal

机构信息

Atta ur Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad, Pakistan.

Institute of Environmental Sciences and Engineering (IESE), National University of Sciences and Technology (NUST), Islamabad, Pakistan.

出版信息

Saudi J Biol Sci. 2022 Mar;29(3):1673-1682. doi: 10.1016/j.sjbs.2021.10.064. Epub 2021 Oct 30.

Abstract

Navigating novel biological strategies to mitigate bacterial biofilms have great worth to combat bacterial infections. Bacterial infections caused by the biofilm forming bacteria are 1000 times more resistant to antibiotics than the planktonic bacteria. Among the known bacterial infections, more than 70% involve biofilms which severely complicates treatment options. Biofilm formation is mainly regulated by the Quorum sensing (QS) mechanism. Interference with the QS system by the quorum quenching (QQ) enzyme is a potent strategy to mitigate biofilm. In this study, bacterial strains with QQ activity were identified and their anti-biofilm potential was investigated against the Multidrug Resistant (MDR) . A CV026 and A136-based bioassays were used to confirm the degradation of different Acyl Homoserine Lactones (AHLs) by QQ isolates. The gene sequencing of the isolated strains identified them as strain QSP03, strain QSP10, strain QQ3 and strain QSP01. Biofilm mitigation potential of QQ isolates was tested against MDR and the results suggested that 50% biofilm reduction was observed by QQ3 and QSP01 strains, and around 60% reduction by QSP10 and QSP03 bacterial isolates. The presence of AHL degrading enzymes, lactonases and acylases, was confirmed by PCR based screening and sequencing of the already annotated genes , and Altogether, these results exhibit that QQ bacterial strains or their products could be useful to control biofilm formation in

摘要

探索新的生物学策略以减轻细菌生物膜对于对抗细菌感染具有重要价值。由形成生物膜的细菌引起的细菌感染对抗生素的耐药性比浮游细菌高1000倍。在已知的细菌感染中,超过70%涉及生物膜,这使得治疗选择严重复杂化。生物膜的形成主要由群体感应(QS)机制调控。通过群体淬灭(QQ)酶干扰QS系统是减轻生物膜的有效策略。在本研究中,鉴定了具有QQ活性的细菌菌株,并研究了它们对多重耐药(MDR)菌的抗生物膜潜力。基于CV026和A136的生物测定用于确认QQ分离株对不同酰基高丝氨酸内酯(AHLs)的降解。对分离菌株的基因测序确定它们为菌株QSP03、菌株QSP10、菌株QQ3和菌株QSP01。测试了QQ分离株对MDR菌的生物膜减轻潜力,结果表明QQ3和QSP01菌株使生物膜减少了50%,QSP10和QSP03细菌分离株使生物膜减少了约60%。通过基于PCR的筛选和对已注释基因的测序确认了AHL降解酶、内酯酶和酰基酶的存在。总之,这些结果表明QQ细菌菌株或其产物可能有助于控制生物膜的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14d7/8913397/013576ee9b0b/gr1.jpg

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