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具有耐甲氧西林表型的金黄色葡萄球菌菌株的基因型

[Genotypes of Staphylococcus aureus strains with methicillin resistant phenotype].

作者信息

Wilson Myra S, Otth Carola L, Medina Gustavo S, Otth Laura R, Fernández Heriberto J, Arce María, Zaror Angela C, Lizama Víctor, Gil Mónica D, von Chrismar Ana María

机构信息

Instituto de Microbiología Clínica, Universidad Austral de Chile, Valdivia, Chile.

出版信息

Rev Med Chil. 2007 May;135(5):596-601. doi: 10.4067/s0034-98872007000500007. Epub 2007 Jul 9.

Abstract

BACKGROUND

Methicillin resistant strains of Staphylococcus aureus (MRSA) are an important cause of nosocomial infections.

AIM

To determine the genotypes of MRSA strains.

MATERIAL AND METHODS

Fifty five strains of MRSA, isolated from patients hospitalized in Hospital Base Valdivia, were studied. The phenotype was determined through MicroScan in all strains and by minimum inhibitory concentration (MIC) in 41. The genotype of the strains was analyzed by a duplex polymerase chain reaction (PCR) of the mecA gene, amplifying eight hypervariable DNA regions associated to such gene.

RESULTS

According to MIC, 88% of strains had a pattern of resistance against multiple antimicrobial (penicillin, ampicillin, cephradine, gentamycin, ciprofloxacin, lincomycin and erythromycin). Vancomicin resistan strains were not detected. Only 53 strains (96%) had at least one of the eight hypervariable regions and were classified as MRSA. Genotypic patterns types 15 were the most commonly detected in 38% and 34% of strains, respectively. MicroScan erroneously classified five strains in an incorrect phenotype, according to results obtained with duplex PCR. MIC results did not differ from those of duplex PCR.

CONCLUSIONS

Duplex- PCR is a useful tool to detect hyper variable regions associated to mecA gene.

摘要

背景

耐甲氧西林金黄色葡萄球菌(MRSA)是医院感染的重要原因。

目的

确定MRSA菌株的基因型。

材料与方法

对从瓦尔迪维亚基地医院住院患者中分离出的55株MRSA菌株进行了研究。所有菌株均通过MicroScan确定表型,41株通过最低抑菌浓度(MIC)确定表型。通过对mecA基因进行双重聚合酶链反应(PCR)分析菌株的基因型,扩增与此基因相关的八个高变DNA区域。

结果

根据MIC,88%的菌株对多种抗菌药物(青霉素、氨苄西林、头孢拉定、庆大霉素、环丙沙星、林可霉素和红霉素)具有耐药模式。未检测到耐万古霉素菌株。只有53株(96%)具有八个高变区域中的至少一个,并被归类为MRSA。基因型模式类型15分别在38%和34%的菌株中最常被检测到。根据双重PCR获得的结果,MicroScan错误地将五株菌株分类为错误的表型。MIC结果与双重PCR结果无差异。

结论

双重PCR是检测与mecA基因相关的高变区域的有用工具。

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