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评估间接法和抗生物素蛋白-生物素酶联免疫吸附测定法检测牛乳样品中抗李斯特菌溶血素O抗体的效果。

Evaluation of indirect and avidin-biotin enzyme linked immunosorbent assays for detection of anti-listeriolysin O antibodies in bovine milk samples.

作者信息

Kalorey D R, Kurkure N V, Warke S R, Barbuddhe S B

机构信息

Department of Veterinary Microbiology, Nagpur Veterinary College, Maharashtra Animal and Fishery Sciences University, Nagpur 440 006, India.

出版信息

Zoonoses Public Health. 2007;54(8):301-6. doi: 10.1111/j.1863-2378.2007.01066.x.

Abstract

Listeria monocytogenes is a foodborne pathogen that causes a wide spectrum of diseases in humans and animals. Enzyme linked immunosorbent assays (ELISA) [indirect and avidin-biotin (A-B)] for detecting L. monocytogenes antibodies in bovine milk samples (n = 2060) were standardized and evaluated by comparison with bacteriological examination. The tests were standardized by checker board titration. Highly purified listeriolysin O (LLO) was used as an antigen. Receiver operating characteristic (ROC) analysis was performed to decide the cut-off values. The ROC analysis revealed the sensitivities of indirect and A-B ELISA as 100% and specificities as 97.1 and 99.9% respectively. Listeria monocytogenes was isolated from 105 (5.1%) milk samples collected from 52 farms. Anti-LLO IgG antibodies were detected from 137 and 112 milk samples when tested by indirect and A-B ELISA respectively. Of the 52 farms screened, 28 (53.8%) yielded one or more isolates of L. monocytogenes and 33 (63.5%) of the farms had one or more animals simultaneously positive by one or both the assays for anti-LLO antibodies.

摘要

单核细胞增生李斯特菌是一种食源性病原体,可在人和动物中引发多种疾病。通过与细菌学检查进行比较,对用于检测牛奶样本(n = 2060)中单核细胞增生李斯特菌抗体的酶联免疫吸附测定(ELISA)[间接法和抗生物素蛋白-生物素(A-B)法]进行了标准化和评估。通过棋盘滴定法对试验进行标准化。使用高度纯化的李斯特菌溶血素O(LLO)作为抗原。进行受试者工作特征(ROC)分析以确定临界值。ROC分析显示间接ELISA和A-B ELISA的灵敏度分别为100%,特异性分别为97.1%和99.9%。从52个农场采集的105份(5.1%)牛奶样本中分离出单核细胞增生李斯特菌。分别通过间接ELISA和A-B ELISA检测时,在137份和112份牛奶样本中检测到抗LLO IgG抗体。在筛查的52个农场中,28个(53.8%)分离出一种或多种单核细胞增生李斯特菌,33个(63.5%)农场中有一只或多只动物通过一种或两种抗LLO抗体检测同时呈阳性。

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