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肺炎链球菌青霉素结合蛋白1A保守氨基酸基序中的苏氨酸-371替代与青霉素耐药性的关联

Association of a thr-371 substitution in a conserved amino acid motif of penicillin-binding protein 1A with penicillin resistance of Streptococcus pneumoniae.

作者信息

Asahi Y, Ubukata K

机构信息

Department of Clinical Pathology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.

出版信息

Antimicrob Agents Chemother. 1998 Sep;42(9):2267-73. doi: 10.1128/AAC.42.9.2267.

Abstract

We determined the nucleotide sequence between 1,903 and 3,097 bp of pbp1a, which encodes the transpeptidase domain of PBP 1A, from clinical isolates of penicillin-resistant Streptococcus pneumoniae (PRSP) serotypes 19 (n = 8), 6 (n = 9), 23 (n = 6), and 14 (n = 2) and two penicillin-susceptible S. pneumoniae (PSSP) isolates. These serotyped PRSP strains were isolated predominantly in Japan from 1993 through 1997. The 25 resistant strains were classified into five groups on the basis of the extent of sequence differences. Strains in groups I (n = 5; serotype 6), II (n = 3; serotype 19), and III (n = 12; different serotypes) had sequences highly homologous to the sequence of pbp1a of PRSP strains from South Africa, Spain, and the United States. The group IV strain (n = 1; serotype 14) had unique deletions from or insertions in the sequences. The sequences of group V strains (n = 4; serotypes 6 and 23) had relatively few differences from the sequences of the PSSP strains. For strains (n = 18) for which the threonine at codon 371 (Thr-371) in a conserved STMK motif of PBP 1A was substituted with an alanine or a serine (in addition to having altered pbp2x and pbp2b genes), penicillin MICs were >/= 1.0 microgram/ml. The PBPs 1A of these strains showed decreased affinities for [3H]benzylpenicillin and slightly faster mobilities on sodium dodecyl sulfate-polyacrylamide gels. In contrast, for strains (n = 4) without a substitution at Thr-371 in PBP 1A but with mutations in both pbp2x and pbp2b, penicillin MICs were 0.125 to 0.25 microgram/ml, and the affinities of their PBPs 1A were similar to that of PSSP PBPs 1A. Furthermore, for the Thr-371-substituted strains (n = 3) with altered pbp2x genes but native pbp2b genes, penicillin MICs were 0.125 to 0.25 microgram/ml. These results suggest that amino acid substitution of Thr-371 contributes to the development of penicillin resistance in PRSP strains with altered pbp2x and pbp2b genes.

摘要

我们测定了肺炎链球菌青霉素耐药株(PRSP)19型(n = 8)、6型(n = 9)、23型(n = 6)和14型(n = 2)以及两株青霉素敏感肺炎链球菌(PSSP)分离株中,编码PBP 1A转肽酶结构域的pbp1a基因1903至3097 bp之间的核苷酸序列。这些分型的PRSP菌株主要于1993年至1997年在日本分离得到。根据序列差异程度,将25株耐药菌株分为五组。I组(n = 5;6型)、II组(n = 3;19型)和III组(n = 12;不同血清型)菌株的序列与来自南非、西班牙和美国的PRSP菌株pbp1a序列高度同源。IV组菌株(n = 1;14型)在序列中有独特的缺失或插入。V组菌株(n = 4;6型和23型)的序列与PSSP菌株的序列差异相对较少。对于PBP 1A保守STMK基序中第371位密码子的苏氨酸(Thr-371)被丙氨酸或丝氨酸取代的菌株(n = 18)(此外pbp2x和pbp2b基因也发生了改变),青霉素最低抑菌浓度(MIC)≥1.0微克/毫升。这些菌株的PBP 1A对[3H]苄青霉素的亲和力降低,在十二烷基硫酸钠-聚丙烯酰胺凝胶上的迁移速度略快。相比之下,对于PBP 1A中Thr-371未被取代但pbp2x和pbp2b均发生突变的菌株(n = 4),青霉素MIC为0.125至0.25微克/毫升,其PBP 1A的亲和力与PSSP的PBP 1A相似。此外,对于pbp2x基因发生改变但pbp2b基因为天然型的Thr-371取代菌株(n = 3),青霉素MIC为0.125至0.25微克/毫升。这些结果表明,Thr-371的氨基酸取代在pbp2x和pbp2b基因发生改变的PRSP菌株青霉素耐药性的产生中起作用。

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