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免疫荧光聚集法检测环境水样中的霍乱弧菌 O1 和 O139。

Detection of Vibrio cholerae O1 and O139 in environmental water samples by an immunofluorescent-aggregation assay.

机构信息

State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Changping, Beijing, China.

出版信息

Appl Environ Microbiol. 2010 Aug;76(16):5520-5. doi: 10.1128/AEM.02559-09. Epub 2010 Jun 25.

Abstract

Environmental waters are an important reservoir for Vibrio cholerae, and effective surveillance of the pathogen can help to warn of and prevent infection with this potentially fatal pathogen. An immunofluorescent-aggregation (IFAG) assay to detect V. cholerae O1 and O139 was established and evaluated with estuarine water samples. The practical application of this assay was compared with the conventional culture method and real-time PCR. The IFAG method had a sensitivity of 10(3) CFU/ml for detection of V. cholerae O1 and O139 strains in a suspension containing 10 different species of enterobacterial strains (total, 10(5) CFU/ml). Ten fluorescent bacterial aggregate colonies were randomly picked and tested positive in serum agglutination tests for the V. cholerae O1 and O139 strains, showing a high specificity. The enrichment broths of 146 samples of estuarine water were tested, and the percentage positive by the IFAG assay was 19.9% (29/146), which was significantly higher than that of the conventional culture method (10.3%, 15/146; P < 0.01) but lower than that of real-time PCR (29.5%, 43/146; P < 0.01). The coincidence rates of real-time PCR and IFAG detection were decreased with the reduction of the V. cholerae concentration. The IFAG method, with a high specificity and a relatively high sensitivity, may be used for detection and isolation of V. cholerae in environmental water samples.

摘要

环境水是霍乱弧菌的重要储存库,有效监测该病原体有助于预警和预防这种潜在致命病原体的感染。建立了一种用于检测霍乱弧菌 O1 和 O139 的免疫荧光聚集(IFAG)检测方法,并对河口水样进行了评估。将该检测方法与常规培养方法和实时 PCR 进行了比较。IFAG 方法对包含 10 种不同肠杆菌属菌株(总浓度为 105 CFU/ml)的悬液中霍乱弧菌 O1 和 O139 菌株的检测灵敏度为 103 CFU/ml。随机挑取 10 个荧光细菌聚集菌落,进行血清凝集试验均对 O1 和 O139 菌株呈阳性,特异性高。对 146 份河口水样的富集培养液进行了检测,IFAG 检测的阳性率为 19.9%(29/146),明显高于常规培养方法(10.3%,15/146;P < 0.01),但低于实时 PCR(29.5%,43/146;P < 0.01)。随着霍乱弧菌浓度的降低,实时 PCR 和 IFAG 检测的符合率降低。IFAG 方法具有较高的特异性和相对较高的灵敏度,可用于检测和分离环境水样中的霍乱弧菌。

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