流行性金黄色葡萄球菌青霉酶质粒大环内酯耐药基因的定位。

L Jánosi, E Bán
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摘要

研究了5株多重耐药流行金黄色葡萄球菌噬菌体复合体52,52a, 80,81对红霉素和夹竹桃霉素耐药基因的遗传定位。红霉素、夹竹桃霉素、两株临床分离株对青霉素(产青霉酶)和一定重金属离子的耐药性,两株临床分离株对这些耐药标记的共转导率均为100%,以及临床野生型消除后和转导后受体部分纯化的染色体外DNA谱的变化表明,红霉素和夹心桃霉素耐药决定基因位于青霉酶-重金属离子耐药质粒上在每个分离株中。4株大环内酯-青霉素酶-重金属离子抗性质粒(MacPc质粒)的电泳迁移率基本一致,其中1株的迁移率更高。这些MacPc质粒对螺旋霉素和林可霉素(即使在诱导后)或卡那霉素没有任何耐药性,这与之前在日本金黄色葡萄球菌中发现的MacPc质粒pI 258和pTU 512不同。
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Localization of genes coding for macrolide resistance on the penicillinase plasmid of isolates of an epidemic Staphylococcus aureus.

Genetic localization of gene(s) coding for erythromycin and oleandomycin resistance in five isolates of phage complex 52, 52A, 80, 81, multiple antibiotic resistant epidemic Staphylococcus aureus was studied. The 100% coelimination rate of erythromycin, oleandomycin, penicillin (penicillinase production) and certain heavy metal ion resistances from each of the clinical isolates and the 100% cotransduction rate of these resistance markers from two clinical isolates as well as changes in the partially purified extrachromosomal DNA patterns of the clinical wild types after elimination and the recipients after transduction indicated that erythromycin and oleandomycin resistance determining gene(s) resided on the penicillinase-heavy metal ion resistance plasmid in each of the isolates. The electrophoretic mobility of these macrolide-penicillinase-heavy metal ion resistance plasmids (MacPc plasmids) was the same in four strains and higher in one strain. These MacPc plasmids did not confer any resistance to spiramycin and lincomycin (even after induction) or to kanamycin, which features differentiate them from MacPc plasmids pI 258 and pTU 512 formerly identified in Staphylococcus aureus in Japan.

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