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Differential Regulation of ponA and pilMNOPQ Expression by the MtrR Transcriptional Regulatory Protein in Neisseria gonorrhoeae▿

机译:MtrR转录调节蛋白在淋病奈瑟氏球菌中对ponA和pilMNOPQ表达的差异调节

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摘要

Neisseria gonorrhoeae utilizes the mtrCDE-encoded efflux pump system to resist not only host-derived, hydrophobic antimicrobials that bathe mucosal surfaces, which likely aids in its ability to colonize and infect numerous sites within the human host, but also antibiotics that have been used clinically to treat infections. Recently, overexpression of the MtrC-MtrD-MtrE efflux pump was shown to be critically involved in the capacity of gonococci to develop chromosomally mediated resistance to penicillin G, which for over 40 years was used to treat gonococcal infections. Mutations in either the promoter or the coding sequence of the mtrR gene, which encodes a repressor of the efflux pump operon, decrease gonococcal susceptibility to penicillin. We now describe the capacity of MtrR to directly or indirectly influence the expression of two other loci that are involved in gonococcal susceptibility to penicillin: ponA, which encodes penicillin-binding protein 1 (PBP 1), and the pilMNOPQ operon, which encodes components of the type IV pilus secretion system, with PilQ acting as a channel for entry for penicillin. We determined that MtrR increases the expression of ponA directly or indirectly, resulting in increased levels of PBP 1, while repressing the expression of the divergently transcribed pilM gene, the first gene in the pilMNOPQ operon. Taken together with other studies, the results presented herein indicate that transcriptional regulation of gonococcal genes by MtrR is centrally involved in determining levels of gonococcal susceptibility to penicillin and provides a framework for understanding how resistance developed over the years.
机译:淋病奈瑟氏球菌利用mtrCDE编码的外排泵系统不仅可以抵抗宿主的,浸润粘膜表面的疏水性抗菌剂,这可能有助于其在人类宿主内定居和感染许多部位的能力,还可以抵抗已经在临床上使用的抗生素治疗感染。最近,MtrC-MtrD-MtrE外排泵的过表达被证明与淋球菌发展出对青霉素G的染色体介导的耐药性有关,该能力已被用于治疗淋球菌感染长达40多年。编码外排泵操纵子阻遏物的mtrR基因的启动子或编码序列中的突变降低了淋球菌对青霉素的敏感性。现在,我们描述MtrR直接或间接影响淋球菌对青霉素敏感性的其他两个基因座的表达的能力:ponA编码青霉素结合蛋白1(PBP 1)和pilMNOPQ操纵子,编码青霉素结合蛋白IV型菌毛分泌系统,其中PilQ充当青霉素进入的通道。我们确定MtrR直接或间接增加ponA的表达,导致PBP 1水平增加,同时抑制发散转录的pilM基因(pilMNOPQ操纵子中的第一个基因)的表达。与其他研究一起,本文呈现的结果表明,MtrR对淋球菌基因的转录调控主要参与确定淋球菌对青霉素的敏感性水平,并为理解多年来的耐药性提供了框架。

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