首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Exfoliative toxin detection using reversed passive latex agglutination: clinical and epidemiologic applications.
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Exfoliative toxin detection using reversed passive latex agglutination: clinical and epidemiologic applications.

机译:使用反向被动乳胶凝集的剥脱毒素检测:临床和流行病学应用。

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摘要

A rapid and simple method for detecting exfoliative toxin serotypes A and B from clinical isolates has been developed as a test kit (EXT-RPLA; Denka Seiken Co. Ltd., Niigata, Japan). This method is based on reversed passive latex agglutination. The detection limit of the EXT-RPLA observed for purified exfoliative toxin serotypes A and B was 1 ng/ml. We evaluated the clinical and epidemiologic uses of the EXT-RPLA. A total of 381 isolates of Staphylococcus aureus, 292 from various clinical specimens and 89 from the skin of dermatologic patients, were studied. The EXT-RPLA detected 19 exfoliative toxin producers, including 16 serotype A producers and 3 serotype B producers, but no double producers. The sensitivity and specificity of the EXT-RPLA were confirmed by the newborn mouse bioassay and a PCR assay for the structural genes for exfoliative toxin serotypes A and B (eta and etb, respectively). The overall positivity rate of exfoliative toxin producers was 5.0% (19 of 381), including 16 serotype A isolates and 3 serotype B isolates. Of the 89 isolates from the skin of dermatologic patients, 12 (13.5%) were positive for exfoliative toxin production. Only 2 (1.3%) of the 153 methicillin-resistant S. aureus isolates produced exfoliative toxin, while 17 (7.5%) of the 228 methicillin-sensitive isolates produced exfoliative toxin. The EXT-RPLA assay is a simple and reliable method for detecting exfoliative toxin, and we recommend its use for the rapid diagnosis of staphylococcal scalded skin syndrome. We also recommend its use for detection of this syndrome so that effective control measures can be taken against the spread of this syndrome.
机译:作为检测试剂盒(EXT-RPLA;日本新泻市Denka Seiken Co. Ltd.),已开发出一种快速,简单的方法,可从临床分离物中检测脱落性毒素血清型A和B。该方法基于反向被动胶乳凝集。纯化的剥脱性毒素血清型A和B观察到的EXT-RPLA的检出限为1 ng / ml。我们评估了EXT-RPLA的临床和流行病学用途。共研究了381株金黄色葡萄球菌,来自各种临床标本的292株和皮肤病患者皮肤的89株。 EXT-RPLA检测到19个剥脱性毒素生产者,包括16个A型血清型生产者和3个B型血清型生产者,但没有双重生产者。 EXT-RPLA的敏感性和特异性已通过新生小鼠的生物测定和针对脱落性毒素血清型A和B(分别为eta和etb)的结构基因的PCR测定得以证实。剥脱性毒素产生者的总体阳性率为5.0%(381个中的19个),包括16个A型血清型分离物和3个B型血清型分离物。在皮肤病患者皮肤的89种分离物中,有12种(13.5%)的剥脱性毒素阳性。 153个耐甲氧西林的金黄色葡萄球菌菌株中只有2个(1.3%)产生了脱落毒素,而228个对甲氧西林敏感的菌株中有17个(7.5%)产生了脱落毒素。 EXT-RPLA测定法是检测剥脱性毒素的简单可靠的方法,我们建议将其用于快速诊断葡萄球菌烫伤性皮肤综合症。我们还建议将其用于检测该综合征,以便可以采取有效的控制措施来防止该综合征的传播。

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