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首页> 外文期刊>Genetics and Molecular Research >Molecular analysis and frequency of Staphylococcus aureus virulence genes isolated from bloodstream infections in a teaching hospital in Tianjin, China
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Molecular analysis and frequency of Staphylococcus aureus virulence genes isolated from bloodstream infections in a teaching hospital in Tianjin, China

机译:天津市一家教学医院从血流感染中分离出的金黄色葡萄球菌致病基因的分子分析和频率

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Staphylococcus aureus is an important cause of bloodstream infections worldwide. We examined the prevalence of genes that encode erythromycin ribosome methylase and bacterial toxins in S. aureus collected from bloodstream infections. Sixty different S. aureus isolates were obtained from blood cultures of patients who were admitted to a Teaching Hospital in Tianjin from January 2006 to August 2011. The susceptibility of the isolates to 16 antibiotics was tested. Methicillin-resistant S. aureus (MRSA) was identified using the disk diffusion method with cefoxitin. PCR was used to detect genes that encode the staphylococcal enterotoxins, Panton-Valentine leukocidin, toxic shock syndrome toxin 1 and erythromycin ribosome methylase. Molecular analysis of the MRSA strains was done using pulsed-field gel electrophoresis (PFGE) and staphylococcal cassette chromosome mec (SCCmec) typing. The positivity rates of mecA, ermA, ermB, and ermC in the isolates were 13/60, 10/60, 18/60, and 18/60, respectively. Among the 60 isolates, 30 harbored enterotoxin genes, with sea as the most frequent toxin gene (33%), followed by sec (15%), sed (12%), and seb (5%). The see and tst genes were not found in any of the isolates. The pvl gene was detected in four strains. Eleven MRSA isolates were of the SCCmec type III; two MRSA isolates could not be determined through SCCmec typing. PFGE analysis of the 13 MRSA isolates produced 8 distinct pulsotypes. Virulence genes and erythromycin ribosome methylase genes were highly prevalent in these isolates. The PFGE results demonstrated that the MRSA spread through cloning, mainly involving SCCmec type III.
机译:金黄色葡萄球菌是全世界血流感染的重要原因。我们检查了从血流感染中收集的金黄色葡萄球菌中编码红霉素核糖体甲基化酶和细菌毒素的基因的普遍性。从2006年1月至2011年8月在天津市教学医院住院的患者的血液培养物中获得了60种不同的金黄色葡萄球菌分离株。测试了分离株对16种抗生素的敏感性。使用头孢西丁的纸片扩散法鉴定了耐甲氧西林的金黄色葡萄球菌(MRSA)。 PCR用于检测编码葡萄球菌肠毒素,潘顿-华伦特白介素,中毒性休克综合征毒素1和红霉素核糖体甲基化酶的基因。使用脉冲场凝胶电泳(PFGE)和葡萄球菌盒式染色体mec(SCCmec)分型对MRSA菌株进行分子分析。分离物中mecA,ermA,ermB和ermC的阳性率分别为13 / 60、10 / 60、18 / 60和18/60。在这60种分离物中,有30种带有肠毒素基因,其中海洋是最常见的毒素基因(33%),其次是sec(15%),sed(12%)和seb(5%)。在任何分离物中均未发现see和tst基因。在四个菌株中检测到pvl基因。十一株MRSA分离株属于SCCmec III型。无法通过SCCmec分型确定两个MRSA分离株。对13个MRSA分离株的PFGE分析产生了8种不同的脉冲型。在这些分离物中,毒力基因和红霉素核糖体甲基化酶基因高度流行。 PFGE结果表明,MRSA通过克隆传播,主要涉及III型SCCmec。

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