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通过抗H凝集反应快速血清学鉴定创伤弧菌。

Rapid serological identification of Vibrio vulnificus by anti-H coagglutination.

作者信息

Simonson J, Siebeling R J

出版信息

Appl Environ Microbiol. 1986 Dec;52(6):1299-304. doi: 10.1128/aem.52.6.1299-1304.1986.

Abstract

Staphylococcus aureus Cowan 1 cells were armed with anti-flagellar (anti-H) antibody produced in rabbits immunized with flagellar core protein prepared from Vibrio vulnificus. This reagent was assessed by coagglutination for its capacity to agglutinate and identify V. vulnificus. A species-specific H antigen is expressed in the core proteins of the polar flagella of V. vulnificus. Of 435 V. vulnificus isolates identified bacteriologically, 432 (99.3%) were agglutinated in the slide test within 2 min after the addition of the anti-V. vulnificus H coagglutination reagent. Other than Vibrio pelagius, the reagent did not agglutinate 19 heterologous Vibrio spp. tested, including 290 V. cholerae, 22 V. mimicus, 395 V. parahaemolyticus, and 16 V. fluvialis isolates recovered from seafood and the marine environment. The serological resolution of the coagglutination reaction was enhanced if the organism under test was suspended in 0.1 M Tris buffer-0.1 mM EDTA-1.0% Triton X-100 (TET) for 24 h before serological examination. The TET buffer also increased the sensitivity of the coagglutination reaction 100-fold over that for isolates suspended in 0.3% formalinized phosphate-buffered saline before testing. The anti-H coagglutination test is a rapid, serologically specific, and inexpensive procedure for identifying V. vulnificus one step beyond primary isolation.

摘要

用创伤弧菌鞭毛核心蛋白免疫兔子所产生的抗鞭毛(抗-H)抗体武装金黄色葡萄球菌科恩1型细胞。通过协同凝集评估该试剂凝集和鉴定创伤弧菌的能力。创伤弧菌极鞭毛的核心蛋白中表达一种种特异性H抗原。在435株经细菌学鉴定的创伤弧菌分离株中,加入抗创伤弧菌H协同凝集试剂后,432株(99.3%)在玻片试验中于2分钟内发生凝集。除了嗜盐弧菌外,该试剂对所检测的19种异源弧菌属不发生凝集,包括从海鲜和海洋环境中分离出的290株霍乱弧菌、22株模仿弧菌、395株副溶血性弧菌和16株河流弧菌。如果在血清学检查前将受试菌在0.1 M Tris缓冲液-0.1 mM EDTA-1.0% Triton X-100(TET)中悬浮24小时,协同凝集反应的血清学分辨率会提高。与在0.3%甲醛化磷酸盐缓冲盐水中悬浮的分离株相比,TET缓冲液还使协同凝集反应的灵敏度提高了100倍。抗-H协同凝集试验是一种快速、血清学特异且廉价的方法,用于在初步分离后进一步鉴定创伤弧菌。

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