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Validation of multiplex PCR strategy for simultaneous detection and identification of methicillin resistant Staphylococcus aureus
被引:0
|作者:
Rallapalli, S.
[1
]
Verghese, S.
[2
]
Verma, R. S.
[1
]
机构:
[1] Indian Inst Technol, Dept Biotechnol, Madras 600036, Tamil Nadu, India
[2] Frontier Lifeline Pvt Ltd, Int Ctr Cardio Thorac & Vasc Dis, Dept Microbiol, Madras 600101, Tamil Nadu, India
关键词:
Methicillin resistance;
methicillin resistant Staphylococcus aureus;
polymerase chain reaction;
coag gene;
mecA gene;
D O I:
暂无
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Multiplex polymerase chain reaction (PCR) strategy is described for rapid identification of clinically relevant methicillin resistant Staphylococcus aureus (MRSA) that targets mecA and coag ulase genes. In this study, 150 staphylococcal clinical isolates were used that included 40 isolates of MRSA, 55 isolates of methicillin susceptible S. aureus (MSSA), 44 isolates of methicillin susceptible coag ulase negative Staphylococcus spp. (MS-CoNS) and 11 isolates of methicillin resistant coag ulase negative Staphylococcus spp. (MR-CoNS). Out of 55 S. aureus strains, three strains demonstrated mecA gene, which appeared to be oxacillin sensitive by disc diffusion. When (MS-CoNS) were evaluated, 10 isolates classified as oxacillin sensitive phenotypically, yielded positive results in PCR method. The results for mecA detection by PCR were more consistent with disk susceptibility tests in case of MRSA (100) and MSSA (95) isolates. In contrast to above results with MRSA and MSSA, mecAdetection by PCR in MS-CoNS showed less correlation with disk susceptibility tests (77). The results for coagdetection by PCR were consistent with phenotypic tests in all isolates.
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页码:361 / 364
页数:4
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