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Correlation between the Resistance Genotype Determined by Multiplex PCR Assays and the Antibiotic Susceptibility Patterns of Staphylococcus aureus and Staphylococcus epidermidis

机译:多重PCR测定抗药性基因型与金黄色葡萄球菌和表皮葡萄球菌的抗生素敏感性模式之间的相关性

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摘要

Clinical isolates of Staphylococcus aureus (a total of 206) and S. epidermidis (a total of 188) from various countries were tested with multiplex PCR assays to detect clinically relevant antibiotic resistance genes associated with staphylococci. The targeted genes are implicated in resistance to oxacillin (mecA), gentamicin [aac(6′)-aph(2")], and erythromycin (ermA, ermB, ermC, and msrA). We found a nearly perfect correlation between genotypic and phenotypic analysis for most of these 394 strains, showing the following correlations: 98% for oxacillin resistance, 100% for gentamicin resistance, and 98.5% for erythromycin resistance. The discrepant results were (i) eight strains found to be positive by PCR for mecA or ermC but susceptible to the corresponding antibiotic based on disk diffusion and (ii) six strains of S. aureus found to be negative by PCR for mecA or for the four erythromycin resistance genes targeted but resistant to the corresponding antibiotic. In order to demonstrate in vitro that the eight susceptible strains harboring the resistance gene may become resistant, we subcultured the susceptible strains on media with increasing gradients of the antibiotic. We were able to select cells demonstrating a resistant phenotype for all of these eight strains carrying the resistance gene based on disk diffusion and MIC determinations. The four oxacillin-resistant strains negative for mecA were PCR positive for blaZ and had the phenotype of β-lactamase hyperproducers, which could explain their borderline oxacillin resistance phenotype. The erythromycin resistance for the two strains found to be negative by PCR is probably associated with a novel mechanism. This study reiterates the usefulness of DNA-based assays for the detection of antibiotic resistance genes associated with staphylococcal infections.
机译:使用多重PCR分析法检测了来自多个国家的金黄色葡萄球菌(共206个)和表皮葡萄球菌(共188个)的临床分离株,以检测与葡萄球菌相关的临床相关抗生素耐药基因。靶向的基因与奥沙西林(mecA),庆大霉素[aac(6')-aph(2“)]和红霉素(ermA,ermB,ermC和msrA)具有抗性。我们发现基因型与对这394个菌株中的大多数进行表型分析,结果显示出以下相关性:奥沙西林抗药性为98%,庆大霉素抗药性为100%,红霉素抗药性为98.5%。差异的结果是(i)经PCR检测,mecA阳性的8个菌株或ermC或ermC,但容易因盘扩散而对相应的抗生素敏感;(ii)通过PCR发现六株金黄色葡萄球菌对mecA或四个针对但对相应抗生素具有耐药性的红霉素抗性基因均为阴性。在体外,八种带有抗性基因的易感菌株可能会产生抗性,我们在抗生素梯度逐渐增加的培养基上对易感菌株进行了亚培养,从而能够筛选出具有抗性的细胞。根据圆盘扩散和MIC测定,这八个带有抗性基因的菌株的所有表型。四个对mecA阴性的奥沙西林抗性菌株PCR blaZ阳性,并具有β-内酰胺酶高产表型,这可以解释其临界的奥西西林抗性表型。通过PCR发现为阴性的两个菌株的红霉素抗性可能与新机制有关。这项研究重申了基于DNA的检测方法在检测与葡萄球菌感染相关的抗生素抗性基因方面的有用性。

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