首页> 外文期刊>The Southeast Asian journal of tropical medicine and public health >MULTIPLEX PCR FOR DETECTION OF SUPERANTIGENIC TOXIN GENES IN METHICILLIN-SENSITIVE AND METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS ISOLATED FROM PATIENTS AND CARRIERS OF A HOSPITAL IN NORTHEAST THAILAND
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MULTIPLEX PCR FOR DETECTION OF SUPERANTIGENIC TOXIN GENES IN METHICILLIN-SENSITIVE AND METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS ISOLATED FROM PATIENTS AND CARRIERS OF A HOSPITAL IN NORTHEAST THAILAND

机译:多重PCR检测泰国东北部医院患者和携带者的甲氧西林敏感和耐甲氧西林金黄色葡萄球菌中的高抗原性毒素基因

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The aims of this study were to develop multiplex PCR for simultaneous detection of five superantigenic toxin genes (sea, seb, sec, sed and tst-1) in Staphylococcus aureus isolated from 149 clinical samples and nasal swabs from 201 healthy subjects in Thailand, and to compare prevalence and expression of those genes between methicillin-resistant S. aureus (MRSA) and methicillin-sensitive S. aureus (MSSA). The sensitivity of multiplex PCR was 10~3 CFU/ml (60 CFU/PCR reaction) for DNA templates extracted by both boiling and extraction methods. S. aureus strains from patients (65%) harbored more superantigenic toxin genes than healthy subjects (54%). MRSA (80%) isolated from patients harbored more superantigenic toxin genes than MSSA (52%). Sea was the most frequently found gene in S. aureus strains from patients and carriers. MRSA isolates harbored sea and produced SEA more frequently than MSSA isolates (p < 0.05) and MRSA isolates (59%) from blood samples consisted of a higher number of superantigenic toxin producers than MSSA (9%) (p < 0.05). More S. aureus strains isolated from patients with severe septicemia contained superantigenic toxin genes (94%) and produced toxins (82%) than those from non-severe patients (64% and 57%, respectively). The multiplex PCR method described here offers a reliable tool for simultaneous detection of various staphylococcal toxin genes.
机译:这项研究的目的是开发多重PCR,同时检测泰国201例健康受试者的149份临床样本和鼻拭子分离的金黄色葡萄球菌中的五个超抗原毒素基因(海,皮脂,秒,sed和tst-1),以及比较那些耐甲氧西林的金黄色葡萄球菌(MRSA)和耐甲氧西林的金黄色葡萄球菌(MSSA)的这些基因的发生率和表达。对于通过煮沸和提取方法提取的DNA模板,多重PCR的灵敏度为10〜3 CFU / ml(60 CFU / PCR反应)。来自患者的金黄色葡萄球菌菌株(65%)比健康受试者(54%)具有更多的超抗原毒素基因。从患者中分离出的MRSA(80%)具有比MSSA(52%)更多的超抗原毒素基因。在来自患者和携带者的金黄色葡萄球菌菌株中,海是最常见的基因。 MRSA分离物比MSSA分离物(p <0.05)掩藏在海上并产生SEA的频率更高,血液样品中的MRSA分离物(59%)的数量超过MSSA(9%)(p <0.05),其中超级抗原毒素的生产者数量更多。从重度败血病患者中分离出的金黄色葡萄球菌菌株比非重症患者(分别为64%和57%)包含超抗原毒素基因(94%)和产生毒素(82%)。此处描述的多重PCR方法为同时检测各种葡萄球菌毒素基因提供了可靠的工具。

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