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Review of two decades of cholera diagnostics--how far have we really come?回顾二十年来的霍乱诊断——我们真的取得了多大进展?
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Cholera.霍乱。
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Binary toxin and death after Clostridium difficile infection.艰难梭菌感染后的二元毒素和死亡。
Emerg Infect Dis. 2011 Jun;17(6):976-82. doi: 10.3201/eid/1706.101483.
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The use of real-time cell analyzer technology in drug discovery: defining optimal cell culture conditions and assay reproducibility with different adherent cellular models.实时细胞分析仪技术在药物研发中的应用:利用不同贴壁细胞模型确定最佳细胞培养条件及检测重现性
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Binding assay for cholera toxin based on sequestration electrochemistry using lactose labeled with an electroactive compound.基于与电化学活性化合物标记乳糖结合的霍乱毒素封闭电化学测定法。
Analyst. 2011 Jun 7;136(11):2373-8. doi: 10.1039/c1an15100b. Epub 2011 Apr 14.
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EIS microfluidic chips for flow immunoassay and ultrasensitive cholera toxin detection.EIS 微流控芯片用于流动免疫分析和超灵敏霍乱毒素检测。
Lab Chip. 2011 Feb 21;11(4):658-63. doi: 10.1039/c0lc00409j. Epub 2010 Dec 3.
7
The liposome PCR assay is more sensitive than the Vibrio cholerae enterotoxin and Escherichia coli heat-labile enterotoxin reversed passive latex agglutination test at detecting cholera toxin in feces and water.脂质体 PCR 检测法在检测粪便和水中霍乱毒素时比霍乱弧菌肠毒素和大肠杆菌不耐热肠毒素反向被动乳胶凝集试验更灵敏。
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Assessment of Clostridium difficile infections by quantitative detection of tcdB toxin by use of a real-time cell analysis system.应用实时细胞分析系统定量检测 tcdB 毒素评估艰难梭菌感染。
J Clin Microbiol. 2010 Nov;48(11):4129-34. doi: 10.1128/JCM.01104-10. Epub 2010 Aug 18.
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Treatment of surfaces with poly-L-lysine for Drosophila cell cultivation.
Cold Spring Harb Protoc. 2010 Jun;2010(6):pdb.prot5001. doi: 10.1101/pdb.prot5001.
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Sensitive detection of multiplex toxins using antibody microarray.利用抗体微阵列进行多重毒素的灵敏检测。
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通过实时动态细胞毒性监测对霍乱弧菌毒素进行定量检测。

Quantitative detection of Vibrio cholera toxin by real-time and dynamic cytotoxicity monitoring.

作者信息

Jin Dazhi, Luo Yun, Zheng Min, Li Haijing, Zhang Jing, Stampfl Melinda, Xu Xiao, Ding Gangqiang, Zhang Yanjun, Tang Yi-Wei

机构信息

Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, China.

出版信息

J Clin Microbiol. 2013 Dec;51(12):3968-74. doi: 10.1128/JCM.01959-13. Epub 2013 Sep 18.

DOI:10.1128/JCM.01959-13
PMID:24048535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3838090/
Abstract

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 (ρ = -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.

摘要

我们在此报告,通过在实时细胞分析(RTCA)系统中动态监测霍乱毒素(CT)介导的细胞毒性全过程,对分离株和粪便标本中的霍乱弧菌毒素进行定量检测。评估了四种细胞系,包括Y-1小鼠肾上腺肿瘤细胞、中国仓鼠卵巢(CHO)细胞、小肠上皮(FHs74Int)细胞和小鼠肾上腺(PC12-Adh)细胞,以确定它们对CT诱导的细胞毒性测试的适用性。其中,Y-1细胞系被证明对CT介导的细胞毒性最敏感,纯化CT的检测限为7.0 pg/ml,在合并的阴性粪便标本中加标CT的检测限为0.11 ng/ml。对于非产毒霍乱弧菌、非霍乱弧菌属或非霍乱弧菌肠毒素,未观察到CT介导的细胞毒性。与使用三种检测方法的参考方法相比,CT-RTCA检测法进一步用从腹泻患者连续收集的100份粪便标本以及从患者和环境中分离出的200株霍乱弧菌进行了验证。CT-RTCA检测法对霍乱弧菌分离株的敏感性和特异性分别为97.5%和100.0%,对粪便标本的敏感性和特异性分别为90.0%和97.2%。对于加标CT浓度范围为3.5 pg/ml至1.8 ng/ml的粪便标本,接种至检测时间为1.12±0.38小时,且该值与CT浓度呈负相关(ρ=-1;P=0.01)。结果表明,使用Y-1细胞系的CT-RTCA检测法为临床标本中CT活性的定量检测提供了一种快速且灵敏的工具。