...
首页> 外文期刊>Japanese Journal of Ophthalmology >Detection of methicillin-resistant Staphylococcus aureus in donor eye preservation media by polymerase chain reaction.
【24h】

Detection of methicillin-resistant Staphylococcus aureus in donor eye preservation media by polymerase chain reaction.

机译:通过聚合酶链反应检测供体眼保存介质中耐甲氧西林的金黄色葡萄球菌。

获取原文
获取原文并翻译 | 示例
           

摘要

To examine contamination of donor eye preservation media with methicillin-resistant Staphylococcus aureus (MRSA), we studied the media to detect specific genes for MRSA by use of the polymerase chain reaction (PCR) method. The materials were 36 samples of donor eye preservation media (EP-II) in which donor eyes had been stored for keratoplasty. Polymerase chain reaction procedures were carried out to simultaneously detect the spa gene, which codes protein A of S. aureus, and the mecA gene, which codes penicillin-binding protein-2' contributing resistance to methicillin. Along with PCR analyses, the preservation media was examined by conventional culture methods to determine bacteriologic contamination. The PCR analyses of the 36 samples revealed that both the spa and the mecA genes were positive in five samples, only the spa gene was positive in two, and only the mecA gene was positive in two. The conventional culture of the media showed positive for MRSA in 5 samples, methicillin-susceptible S. aureus (MSSA) in 2, methicillin-susceptible coagulase-negative staphylococci (MS-CNS) in 4, and methicillin-resistant coagulase-negative staphylococci (MR-CNS) in 2 of the 36 samples. The results of PCR coincided well with those of conventional bacteriologic culture. Polymerase chain reaction analysis for spa and mecA genes is useful in detecting contamination of donor eye preservation media by MRSA, MSSA, MR-CNS, or MS-CNS in a shorter time than by conventional culture.
机译:为了检查耐甲氧西林金黄色葡萄球菌(MRSA)对供体眼保存介质的污染,我们研究了使用聚合酶链反应(PCR)方法检测该介质以检测MRSA特定基因的方法。这些材料是36个供体眼睛保存介质(EP-II)的样品,其中已保存了供体眼睛用于角膜移植术。进行聚合酶链反应程序以同时检测编码金黄色葡萄球菌蛋白A的spa基因和编码对青霉素有抗性的青霉素结合蛋白2'的mecA基因。与PCR分析一起,通过常规培养方法检查保存培养基,以确定细菌污染。对36个样品的PCR分析显示,spa和mecA基因在5个样品中均为阳性,只有spa基因在2个样品中为阳性,只有mecA基因在2个样品中为阳性。常规培养基在5个样本中显示MRSA阳性,在2个样本中对甲氧西林敏感的金黄色葡萄球菌(MSSA),在4个样本中对甲氧西林敏感的凝固酶阴性葡萄球菌(MS-CNS),对耐甲氧西林的凝固酶阴性葡萄球菌( MR-CNS),共36个样本中的2个。 PCR的结果与常规细菌培养的结果非常吻合。 spa和mecA基因的聚合酶链反应分析可用于检测MRSA,MSSA,MR-CNS或MS-CNS在比传统培养更短的时间内检测供体眼保存介质的污染。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号