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结核分枝杆菌中利福平耐药性及rpoB基因突变

Rifampicin resistance and mutation of the rpoB gene in Mycobacterium tuberculosis.

作者信息

Taniguchi H, Aramaki H, Nikaido Y, Mizuguchi Y, Nakamura M, Koga T, Yoshida S

机构信息

Department of Microbiology, University of Occupational and Environmental Health, Fukuoka, Japan.

出版信息

FEMS Microbiol Lett. 1996 Oct 15;144(1):103-8. doi: 10.1111/j.1574-6968.1996.tb08515.x.

Abstract

Using 39 clinical isolates of Mycobacterium strains with a broad range of susceptibility to rifampicin, we examined the relationship between the degree of resistance to rifampicin and mutational sites of the rpoB gene. All rifampicin-resistant strains had missense mutations. Twenty strains (95%) had a mutation in the cluster I region, which has also been reported in Escherichia coli [Jin and Gross (1988) J. Mol. Biol. 202, 45-58], and the remaining one strain had a mutation at codon 381 [Ala-->Val] in the N-terminal region, which has not been reported in E. coli. Among 18 rifampicin-susceptible strains, two had a mutation in the cluster I region and the other three strains had a mutation in the cluster III region. The mutations at codons 513 (5%), 526 (33%) or 531 (43%) in the cluster I region led to high level resistance to rifampicin (50 micrograms ml-1 < or = MIC). The mutations at the other sites, in the cluster III region (codons 679 or 687) and even in the cluster I region (codon 514, 521, or 533), showed low level (MIC = 12.5 micrograms ml-1) or no (MIC < 0.39 microgram ml-1) resistance to rifampicin. These results suggest that mutations in the rpoB gene are, mostly, but not necessarily, associated with rifampicin resistance of M. tuberculosis, and the sites of mutations on the rpoB gene will affect the level of resistance to rifampicin.

摘要

我们使用了39株对利福平敏感性范围广泛的分枝杆菌临床分离株,研究了对利福平的耐药程度与rpoB基因突变位点之间的关系。所有耐利福平菌株均有错义突变。20株(95%)在簇I区域发生了突变,大肠杆菌中也有该区域突变的报道[Jin和Gross(1988年)《分子生物学杂志》202卷,45 - 58页],其余1株在N端区域的密码子381处发生了[Ala→Val]突变,大肠杆菌中未见此突变报道。在18株利福平敏感菌株中,2株在簇I区域有突变,另外3株在簇III区域有突变。簇I区域密码子513(5%)、526(33%)或531(43%)处的突变导致对利福平的高水平耐药(50微克/毫升≤MIC)。簇III区域(密码子679或687)以及簇I区域(密码子514、521或533)其他位点的突变显示对利福平低水平耐药(MIC = 12.5微克/毫升)或无耐药(MIC < 0.39微克/毫升)。这些结果表明,rpoB基因突变大多但不一定与结核分枝杆菌对利福平的耐药性相关,rpoB基因上的突变位点会影响对利福平的耐药水平。

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