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首页> 外文期刊>BMC Infectious Diseases >Rapid screening for Chlamydia trachomatis infection by detecting α-mannosidase activity in urogenital tract specimens
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Rapid screening for Chlamydia trachomatis infection by detecting α-mannosidase activity in urogenital tract specimens

机译:通过检测泌尿生殖道标本中的α-甘露糖苷酶活性快速筛查沙眼衣原体感染

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Background Chlamydia trachomatis may cause multiple different urogenital tract disorders, but current non-culture assays for rapid screening of C. trachomatis typically use immunochromatography-based methods. We established another new rapid non-culture method for detection of C. trachomatis based on the measurement of α-mannosidase enzymatic activity in urogenital tract specimens. Method To evaluate the performance of this method, α-mannosidase activities of C. trachomatis serotype D strain 、 and 29 standard strains related to clinical urogenital pathogens were investigated. Furthermore, 553 urogenital tract specimens were used for clinical assays via cell culture method and ligase chain reaction method (LCR), adopting an expanded gold standard. Results Only C. trachomatis was positive for α-mannosidase activity among different types of microbes tested in the research. When prostate fluid specimens, which have some interfering activity, were excluded, the sensitivity and specificity of the enzymatic method were 91.8% (78/85) and 98.3% (409/416), respectively. There were no significant differences (P > 0.05). Conclusions These results showed that α-mannosidase activity could be utilised as a screening marker of C. trachomatis infection.
机译:背景沙眼衣原体可能会引起多种不同的泌尿生殖道疾病,但是当前用于快速筛查沙眼衣原体的非培养测定法通常使用基于免疫色谱的方法。我们基于对泌尿生殖道标本中α-甘露糖苷酶酶活性的测量,建立了另一种新的快速非培养方法来检测沙眼衣原体。方法评价沙眼衣原体D血清型和29种与临床泌尿生殖道病原体有关的标准菌株的α-甘露糖苷酶活性。此外,采用扩展的金标准,通过细胞培养方法和连接酶链反应方法(LCR)将553个泌尿生殖道标本用于临床测定。结果在研究中测试的不同类型微生物中,仅沙眼衣原体的α-甘露糖苷酶活性为阳性。当排除具有某些干扰活性的前列腺液标本时,酶法的敏感性和特异性分别为91.8%(78/85)和98.3%(409/416)。没有显着差异(P> 0.05)。结论这些结果表明,α-甘露糖苷酶活性可以用作沙眼衣原体感染的筛选标志。

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