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凝固酶阴性葡萄球菌中甲氧苄啶耐药性的分子流行病学

Molecular epidemiology of trimethoprim resistance among coagulase-negative staphylococci.

作者信息

Galetto D W, Johnston J L, Archer G L

机构信息

Department of Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0049.

出版信息

Antimicrob Agents Chemother. 1987 Nov;31(11):1683-8. doi: 10.1128/AAC.31.11.1683.

DOI:10.1128/AAC.31.11.1683
PMID:3435115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC175020/
Abstract

A 42% (70 of 167 isolates) incidence of resistance to 20 micrograms of trimethoprim per ml was found among clinical isolates of coagulase-negative staphylococci from two hospitals. A specific trimethoprim resistance gene probe from a conjugative Staphylococcus aereus plasmid was used to investigate the location of the trimethoprim resistance gene among 29 isolates. In 14 trimethoprim-resistant isolates, the probe hybridized with only chromosomal DNA, in 9 it hybridized with only plasmid DNA, and in 1 isolate both plasmid and chromosomal sequences showed hybridization. In five isolates there was no hybridization of the probe with either chromosomal or plasmid DNA. Four of these five nonhybridizing isolates were Staphylococcus haemolyticus. In contrast, all 22 Staphylococcus epidermidis isolates tested hybridized with the probe. The presence of the trimethoprim resistance gene in a chromosomal location was correlated with a lower MIC (median, 80 micrograms/ml) than when it was plasmid encoded (median, 1,250 micrograms/ml). Restriction endonuclease mapping as well as DNA hybridization of cloned plasmid and chromosomal DNA showed that there were 2.7 kilobases of common DNA in the two loci. This included the 500 base pairs of DNA mediating trimethoprim resistance and a total of 2.2 kilobases of 3'- and 5'-flanking sequences. The presence of the same gene and flanking sequences in chromosomal and plasmid locations suggests that the trimethoprim resistance determinant is translocated among different genetic loci.

摘要

在来自两家医院的凝固酶阴性葡萄球菌临床分离株中,发现对每毫升20微克甲氧苄啶耐药的发生率为42%(167株分离株中有70株)。使用来自接合性金黄色葡萄球菌质粒的特异性甲氧苄啶耐药基因探针,对29株分离株中的甲氧苄啶耐药基因位置进行研究。在14株甲氧苄啶耐药分离株中,探针仅与染色体DNA杂交;在9株中,仅与质粒DNA杂交;在1株中,质粒和染色体序列均显示杂交。在5株分离株中,探针与染色体或质粒DNA均未杂交。这5株未杂交的分离株中有4株是溶血葡萄球菌。相比之下,所有检测的22株表皮葡萄球菌分离株均与探针杂交。与质粒编码时(中位数为1250微克/毫升)相比,染色体位置存在甲氧苄啶耐药基因时的最低抑菌浓度较低(中位数为80微克/毫升)。克隆质粒和染色体DNA的限制性内切酶图谱以及DNA杂交显示,两个位点存在2.7千碱基的共同DNA。这包括介导甲氧苄啶耐药的500个碱基对的DNA以及总共2.2千碱基的3'和5'侧翼序列。染色体和质粒位置存在相同的基因和侧翼序列,表明甲氧苄啶耐药决定簇在不同遗传位点之间易位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/175020/ed53bef60994/aac00101-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/175020/65d645e95916/aac00101-0043-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/175020/ed53bef60994/aac00101-0044-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/175020/65d645e95916/aac00101-0043-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d020/175020/ed53bef60994/aac00101-0044-a.jpg

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