多重PCR检测德黑兰糖果店奶油泡芙金黄色葡萄球菌pton - valentine Leukocidin PVL毒力基因和甲氧西林耐药基因mecA的存在及耐药性研究

Mahya Mozaffarzogh, Hadis Khaleghnezhad
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引用次数: 0

摘要

金黄色葡萄球菌是世界上因食用受污染的食物而导致食物中毒的主要原因。对各种常见和特殊抗生素的耐药性正在增加。包括PVL和基因mecA在内的金黄色葡萄球菌对高温巴氏杀菌和许多蛋白水解酶都是稳定的,并能在食品样品中长时间保持活性。本研究目的是利用多重PCR技术分离金黄色葡萄球菌,并鉴定面包糕点奶油中的毒力基因PVL和耐甲氧西林基因。本研究共采集50份面包糕点奶油样品,检出金黄色葡萄球菌23例(49%)。按照CLSI指南采用纸片扩散法进行抗生素药敏试验。采用多重PCR法鉴定和确认金黄色葡萄球菌的毒力和耐药基因。抗菌谱结果显示,抗生素对万古霉素、四环素和盐酸多西环素的敏感性分别为100%、100%和100%。对青霉素、头孢克肟的耐药率分别为65/3%、56/5%。甲氧西林耐药基因mecA阳性率为0%,未检出PVL基因。在所有样本中鉴定出16个rRNA基因属和种并确认。本研究中耐甲氧西林基因的不同分布与其他研究显示耐甲氧西林金黄色葡萄球菌在世界范围内的潜在风险。因此,及早发现并及时发现耐药菌株,以防止耐药性的蔓延显得十分必要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determining the Presence of Panton-Valentine Leukocidin PVL Virulence Geneand Methicillin-Resistant Gene mecA in Staphylococcus aureus Strains Isolatedfrom Cream Puffs Sold by Confectionaries in Tehran by Multiplex PCR andStudying their Antibiotic Resistance
Staphylococcus aureus is a major cause of food poisoning in the world that is created by consumption of contaminated food. Resistance to a variety of common and specific antibiotics is increasing. Staphylococcus aureus including PVL and gene mecA to heat pasteurization and many proteolytic enzymes are stable and can remain active for a long time in food samples. The purpose of this study was to isolate Staphylococcus aureus and identify virulence gene PVL and gene of methicillin resistance in bread pastry cream by multiplex PCR technique has been used. The study included 50 samples of bread pastry cream collected 23 cases (49%) Staphylococcus aureus isolates were detected. Antibiotic susceptibility testing by disk diffusion method according to CLSI guidelines was conducted. To identify and confirm Staphylococcus aureus virulence and resistance genes from multiple PCR assay was used. Antibiogram results showed that antibiotics are among the most sensitive to the antibiotic vancomycin, Tetracyclin, and doxycyclin hydrochloride respectively 100%, 100%, and 100%. Resistance to penicillin, cefixime, 65/3%, 56/5% more than other antibiotics was tested. Prevalence of methicillin resistance gene mecA in total 0% and PVL gene was not detected. Also, 16 rRNA genes in all samples were identified genus and species and confirmed. Different distribution of methicillin resistance gene in this study with other studies showing the potential risk of methicillin-resistant Staphylococcus aureus in the world. Therefore, early detection and timely resistant strains, in order to prevent the spread of resistance appears to be necessary.
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