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生物膜形成的耐甲氧苄啶/磺胺甲恶唑的小菌落变异体对各种抗菌药物的耐受性。

Tolerability of Biofilm-Forming Trimethoprim-/Sulfamethoxazole-Resistant Small Colony Variants of Against Various Antimicrobial Agents.

机构信息

Division of Clinical Infectious Diseases and Chemotherapy, Tohoku Medical and Pharmaceutical University, Sendai, Japan.

出版信息

Microb Drug Resist. 2021 Sep;27(9):1282-1289. doi: 10.1089/mdr.2020.0379. Epub 2021 Mar 9.

Abstract

Trimethoprim-/sulfamethoxazole-resistant small colony variants (SCVs) of , which are selected by use of trimethoprim/sulfamethoxazole, are involved in intractable biofilm-forming infection. This study aimed to determine the biofilm formation ability in trimethoprim-/sulfamethoxazole-resistant SCVs of and investigate the bactericidal activity of differential antimicrobial agents to its biofilm-forming . Between 32 wild type (WT) and 32 SCVs selected from its WT, the amount of formed biofilm was compared. Vancomycin, daptomycin, rifampicin, and minocycline were exposed to biofilm-forming to determine viable bacterial counts and its susceptibility. The biofilm-producing quantify of SCVs was approximately twice that formed by its WT. Vancomycin and daptomycin reduce 4 logs the bacterial counts of biofilm-forming WT at 24 hours, but did not affect SCVs. Rifampicin and minocycline considerably decreased both WT and SCVs; however, both bacterial counts recovered to an initial number 48 hours later. These survival strains showed resistance to each drug, and mutation or mRNA overexpression was confirmed.

摘要

对 中由甲氧苄啶/磺胺甲恶唑选择的耐甲氧苄啶/磺胺甲恶唑小菌落变异体 (SCVs) 与难以治疗的生物膜形成感染有关。本研究旨在确定 中耐甲氧苄啶/磺胺甲恶唑的 SCVs 的生物膜形成能力,并研究不同抗菌药物对其生物膜形成 的杀菌活性。在 32 株野生型 (WT) 和 32 株从 WT 中选择的 SCVs 之间,比较了形成的生物膜的量。将万古霉素、达托霉素、利福平、米诺环素暴露于生物膜形成 中,以确定活菌数及其敏感性。SCVs 形成的生物膜产生量约为 WT 的两倍。万古霉素和达托霉素在 24 小时内将形成生物膜的 WT 的细菌计数减少了 4 个对数级,但对 SCVs 没有影响。利福平和米诺环素大大减少了 WT 和 SCVs 的数量;然而,48 小时后,细菌计数恢复到初始数量。这些存活株对每种药物均表现出耐药性,并且证实了 突变或 mRNA 过表达。

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