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首页> 外文期刊>British Journal of Pharmaceutical Research >Study of Bacterial Resistance in Clinical Isolates of Staphylococcus aureus by Comparison of Conventional in-vitro Methods with PCR & RFLP Based Genotypic Methods
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Study of Bacterial Resistance in Clinical Isolates of Staphylococcus aureus by Comparison of Conventional in-vitro Methods with PCR & RFLP Based Genotypic Methods

机译:通过将传统的体外方法与基于PCR和RFLP的基因型方法进行比较,研究金黄色葡萄球菌临床分离株中的细菌耐药性

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Methicillin Resistant S. aureus is an increasingly common cause of nosocomial infections, causing severe morbidity and mortality worldwide and accounting for more than 50% of all S. aureus diseases. S. aureus used in our study were procured isolates from the microbiology lab of a corporate hospital. Reference culture of S. aureus NCIM 5021 was obtained from NCIM, Pune. Clinical isolates were subjected to antimicrobial susceptibility testing by standard antibiotic disc (Cefoxitin 30 μg). The selected clinical strains were tested for sensitivity to different antibiotics by Kirby Bauer disc diffusion method. The MIC was determined by two fold serial dilution in broth individually against various antibacterial agents. That was followed by a study on a combination of Ciprofloxacin & Linezolid by two dimensional checkerboard method of synergism testing against the clinical isolates and reference S. aureus NCIM culture. FIC index of combination indicated synergism against MRSA. MRSA was used for PCR based study of the resistant gene namely mecA . PCR-RFLP method was used to study 16S rRNA by restriction digestion using Taq 1 . This is indicative of the possible serological differences among clinical isolates and was compared to NCIM culture based on restriction fragments.
机译:耐甲氧西林的金黄色葡萄球菌是医院感染的越来越普遍的原因,在全世界引起严重的发病率和死亡率,占所有金黄色葡萄球菌疾病的50%以上。在我们的研究中使用的金黄色葡萄球菌是从公司医院的微生物实验室采购的分离株。金黄色葡萄球菌NCIM 5021的参考培养物获自Pune的NCIM。临床分离株通过标准抗生素椎间盘(Cefoxitin 30μg)进行了药敏试验。通过Kirby Bauer纸片扩散法测试了所选临床菌株对不同抗生素的敏感性。通过在肉汤中分别对各种抗菌剂进行两次连续稀释来确定MIC。随后通过二维棋盘法对环丙沙星和利奈唑胺进行组合研究,针对临床分离株和参比金黄色葡萄球菌NCIM培养物进行协同测试。组合的FIC指数表明对MRSA有协同作用。 MRSA用于基于PCR的抗性基因mecA的研究。 PCR-RFLP方法用于Taq 1限制性酶切研究16S rRNA。这表明临床分离株之间可能存在血清学差异,并与基于限制性片段的NCIM培养进行了比较。

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