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用于识别小鼠模型中诺卡菌感染的血清学检测方法的开发。

Development of a serologic panel for the recognition of nocardial infections in a murine model.

作者信息

Kjelstrom J A, Beaman B L

机构信息

Department of Medical Microbiology/Immunology, School of Medicine, University of California, Davis 95616.

出版信息

Diagn Microbiol Infect Dis. 1993 May-Jun;16(4):291-301. doi: 10.1016/0732-8893(93)90079-m.

Abstract

A murine model was used to develop a sensitive and specific serologic test for clinical and subclinical infections caused by Nocardia. The following tests were used: (a) enzyme-linked immunosorbent assays (ELISAs) with culture filtrate and cytoplasmic extract antigens from Nocardia asteroides; (b) ELISA with N. asteroides trehalose dimycolate (cord factor); (c) indirect immunofluorescent antibody assay with whole cells of N. asteroides; and (d) Western-blot analysis for the 54 to 55-kD, 36-kD, and 62-kD proteins of N. asteroides. The sera from BALB/c mice, experimentally infected with nonlethal doses of three species of Nocardia, nine species of Mycobacterium, Rhodococcus equi, two species of Actinomadura, and two species of Streptomyces were tested using this panel. The serologic tests did, indeed, identify mice infected with nocardiae and could differentiate them from mice infected with the other actinomycetes, including mycobacteria.

摘要

使用鼠类模型开发了一种针对诺卡菌引起的临床和亚临床感染的灵敏且特异的血清学检测方法。采用了以下检测:(a) 用来自星形诺卡菌的培养滤液和细胞质提取物抗原进行酶联免疫吸附测定(ELISA);(b) 用星形诺卡菌海藻糖二甲酯(索状因子)进行ELISA;(c) 用星形诺卡菌全细胞进行间接免疫荧光抗体测定;以及(d) 对星形诺卡菌的54至55kD、36kD和62kD蛋白进行蛋白质印迹分析。使用该检测组对经非致死剂量的三种诺卡菌、九种分枝杆菌、马红球菌、两种马杜拉放线菌和两种链霉菌实验感染的BALB/c小鼠血清进行检测。血清学检测确实能够识别感染诺卡菌的小鼠,并能将它们与感染其他放线菌(包括分枝杆菌)的小鼠区分开来。

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