Development of a real-time PCR assay with an internal amplification control for detection of Gram-negative histamine-producing bacteria in fish

被引:35
|
作者
Bjornsdottir-Butler, Kristin [1 ]
Jones, Jessica L. [1 ]
Benner, Ronald [1 ]
Burkhardt, William, III [1 ]
机构
[1] US FDA, Gulf Coast Seafood Lab, Dauphin Isl, AL 36528 USA
关键词
Histamine; Biogenic amines; Histidine decarboxylase; Real-time PCR; Bacteria; Fish; LACTIC-ACID BACTERIA; HISTIDINE-DECARBOXYLASE; BIOGENIC-AMINES; QUANTITATIVE DETECTION; FORMING BACTERIA; SUBSP DAMSELAE; TUNA; IDENTIFICATION; PURIFICATION; OYSTERS;
D O I
10.1016/j.fm.2010.06.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Prompt detection of bacteria that contribute to scombrotoxin (histamine) fish poisoning can aid in the detection of potentially toxic fish products and prevent the occurrence of illness. We report development of the first real-time PCR method for rapid detection of Gram-negative histamine-producing bacteria (HPB) in fish. The real-time PCR assay was 100% inclusive for detecting high-histamine producing isolates and did not detect any of the low- or non-histamine producing isolates. The efficiency of the assay with/without internal amplification control ranged from 96-104% and in the presence of background flora and inhibitory matrices was 92/100% and 73-96%, respectively. This assay was used to detect HPB from naturally contaminated yellowfin tuna, bluefish, and false albacore samples. Photobacterium damselae (8), Plesiomonas shigelloides (2), Shewanella sp. (1), and Morganella morganii (1) were subsequently isolated from the real-time PCR positive fish samples. These results indicate that the real-time PCR assay developed in this study is a rapid and sensitive method for detecting high-HPB. The assay may be adapted for quantification of HPB, either directly or with an MPN-PCR method. (C) 2010 Published by Elsevier Ltd.
引用
收藏
页码:356 / 363
页数:8
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