Quantitative Detection of Vibrio cholera Toxin by Real-Time and Dynamic Cytotoxicity Monitoring

被引:13
作者
Jin, Dazhi [1 ,2 ]
Luo, Yun [1 ]
Zheng, Min [3 ]
Li, Haijing [4 ]
Zhang, Jing [5 ]
Stampfl, Melinda [5 ]
Xu, Xiao [5 ]
Ding, Gangqiang [1 ]
Zhang, Yanjun [1 ]
Tang, Yi-Wei [2 ,4 ]
机构
[1] Zhejiang Prov Ctr Dis Control & Prevent, Hangzhou, Zhejiang, Peoples R China
[2] Mem Sloan Kettering Canc Ctr, Dept Lab Med, New York, NY 10021 USA
[3] Zhejiang Univ, Sch Med, State Key Lab Diag & Treatment Infect Dis, Hangzhou 310003, Zhejiang, Peoples R China
[4] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA
[5] ACEA Biosci Inc, San Diego, CA USA
关键词
PASSIVE LATEX AGGLUTINATION; POLYMERASE-CHAIN-REACTION; HEAT-LABILE ENTEROTOXIN; BACTERIAL TOXINS; PCR ASSAY; IMMUNOASSAY; INFECTIONS; LIPOSOMES; BIOSENSOR; CULTURE;
D O I
10.1128/JCM.01959-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report here the quantitative detection of Vibrio cholerae toxin (CT) in isolates and stool specimens by dynamic monitoring of the full course of CT-mediated cytotoxicity in a real-time cell analysis (RTCA) system. Four cell lines, including Y-1 mouse adrenal tumor cells, Chinese hamster ovary (CHO) cells, small intestine epithelial (FHs74Int) cells, and mouse adrenal gland (PC12-Adh) cells, were evaluated for their suitability for CT-induced cytotoxicity testing. Among them, the Y-1 line was demonstrated to be the most sensitive for CT-mediated cytotoxicity, with limits of detection of 7.0 pg/ml for purified CT and 0.11 ng/ml for spiked CT in pooled negative stool specimens. No CT-mediated cytotoxicity was observed for nontoxigenic V. cholerae, non-V. cholerae species, or non-V. cholerae enterotoxins. The CT-RTCA assay was further validated with 100 stool specimens consecutively collected from patients with diarrhea and 200 V. cholerae isolates recovered from patients and the environment, in comparison to a reference using three detection methods. The CT-RTCA assay had sensitivities and specificities of 97.5% and 100.0%, respectively, for V. cholerae isolates and 90.0% and 97.2% for stool specimens. For stool specimens spiked with CT concentrations ranging from 3.5 pg/ml to 1.8 ng/ml, the inoculation-to-detection time was 1.12 +/- 0.38 h, and the values were inversely correlated with CT concentrations (rho = -1; P = 0.01). The results indicate that the CT-RTCA assay with the Y-1 cell line provides a rapid and sensitive tool for the quantitative detection of CT activities in clinical specimens.
引用
收藏
页码:3968 / 3974
页数:7
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