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淋病奈瑟菌中孔蛋白IB介导对青霉素和四环素中度耐药的氨基酸突变的鉴定与分析。

Identification and analysis of amino acid mutations in porin IB that mediate intermediate-level resistance to penicillin and tetracycline in Neisseria gonorrhoeae.

作者信息

Olesky Melanie, Hobbs Marcia, Nicholas Robert A

机构信息

Department of Pharmacology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7365, USA.

出版信息

Antimicrob Agents Chemother. 2002 Sep;46(9):2811-20. doi: 10.1128/AAC.46.9.2811-2820.2002.

Abstract

PenB is the third resistance determinant in the stepwise acquisition of multiple resistance genes in chromosomally mediated resistant Neisseria gonorrhoeae (CMRNG). Alterations in por(IB), one of two alleles at the por locus that encodes the outer membrane protein porin IB (PIB), were recently reported to be responsible for the increased resistance to penicillin and tetracycline conferred by penB, but the specific mutations conferring antibiotic resistance were not identified experimentally. To determine which amino acids in PIB confer increased resistance, we transformed a recipient strain with chimeras of the por(IB) genes from strains FA1090 and FA140 (penB2). These studies revealed that two amino acid changes, G120D and A121D, were both necessary and sufficient to confer increased resistance to penicillin and tetracycline. Site-saturation and site-directed mutagenesis of Gly-120 and Ala-121 revealed that both a single mutation, G120K, and the double mutations G120R A121H and G120P A121P also conferred antibiotic resistance to the recipient strain. The identical mutations in PIA increased penicillin and tetracycline resistance either moderately or not at all. Analysis of por(IB) genes present in the GenBank database from 51 clinical isolates demonstrated that lysine and aspartate mutations at positions 120 and/or 121 also occur in nature. These studies demonstrate that charged amino acids at positions 120 and 121 in PIB are highly preferential for conferring resistance to penicillin and tetracycline in N. gonorrhoeae.

摘要

PenB是染色体介导的耐淋病奈瑟菌(CMRNG)逐步获得多个耐药基因过程中的第三个耐药决定因素。最近有报道称,编码外膜蛋白孔蛋白IB(PIB)的por基因座上两个等位基因之一的por(IB)发生改变,是导致penB赋予对青霉素和四环素耐药性增加的原因,但实验中尚未确定赋予抗生素耐药性的具体突变。为了确定PIB中的哪些氨基酸赋予了更高的耐药性,我们用来自菌株FA1090和FA140(penB2)的por(IB)基因嵌合体转化了一个受体菌株。这些研究表明,两个氨基酸变化,G120D和A121D,对于赋予对青霉素和四环素的耐药性增加既是必要的也是充分的。对Gly-120和Ala-121进行位点饱和诱变和定点诱变表明,单个突变G120K以及双突变G120R A121H和G120P A121P也赋予了受体菌株抗生素耐药性。PIA中的相同突变对青霉素和四环素耐药性的增加要么适度,要么根本没有作用。对GenBank数据库中51株临床分离株中存在的por(IB)基因进行分析表明,120和/或121位的赖氨酸和天冬氨酸突变在自然界中也会出现。这些研究表明,PIB中120和121位的带电荷氨基酸对于淋病奈瑟菌对青霉素和四环素的耐药性赋予具有高度优先性。

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