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
相关论文
共 50 条
  • [41] Quantitative real-time PCR method with internal amplification control to quantify cyclopiazonic acid producing molds in foods
    Rodriguez, Alicia
    Werning, Maria L.
    Rodriguez, Mar
    Bermudez, Elena
    Cordoba, Juan J.
    FOOD MICROBIOLOGY, 2012, 32 (02) : 397 - 405
  • [42] Development of Real-Time PCR Assay for Detection of Vibrio cholerae
    Bielawska-Drozd, Agata
    Mirski, Tomasz
    Bartoszcze, Michal
    Cieslik, Piotr
    Roszkowiak, Anna
    Michalski, Aleksander
    POLISH JOURNAL OF ENVIRONMENTAL STUDIES, 2012, 21 (02): : 279 - 288
  • [43] Development, validation, and application of PCR primers for detection of tetracycline efflux genes of gram-negative bacteria
    Aminov, RI
    Chee-Sanford, JC
    Garrigues, N
    Teferedegne, B
    Krapac, IJ
    White, BA
    Mackie, RI
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (04) : 1786 - 1793
  • [44] A TaqMan-MGB real-time RT-PCR assay with an internal amplification control for rapid detection of Muscovy duck reovirus
    Zheng, Min
    Chen, Xiuqin
    Wang, Shao
    Wang, Jingxiang
    Huang, Meiqing
    Xiao, Shifeng
    Cheng, Xiaoxia
    Chen, Shilong
    Chen, Xiaoli
    Lin, Fengqianq
    Chen, Shaoying
    MOLECULAR AND CELLULAR PROBES, 2020, 52
  • [45] Adapting a conventional PCR assay for Toxoplasma gondii detection to real-time quantitative PCR including a competitive internal control
    Brenier-Pinchart, M. P.
    Morand-Bui, V
    Fricker-Hidalgo, H.
    Equy, V
    Marlu, R.
    Pelloux, H.
    PARASITE, 2007, 14 (02) : 149 - 154
  • [46] Development of two multiplex PCR assays for rapid detection of eleven Gram-negative bacteria in children with septicemia
    Miringu, Gabriel
    Musyoki, Abednego
    Muriithi, Betty
    Wandera, Ernest
    Waithiru, Dan
    Odoyo, Erick
    Shoji, Hisashi
    Menza, Nelson
    Ichinose, Yoshio
    TROPICAL MEDICINE AND HEALTH, 2024, 52 (01)
  • [47] Development of a Multiplex Real-Time PCR Assay for the Detection of Ruminant DNA
    Ekins, Jason
    Peters, Sharla M.
    Jones, Yolanda L.
    Swaim, Heidi
    Ha, Tai
    La Neve, Fabio
    Civera, Tiziana
    Blackstone, George
    Vickery, Michael C. L.
    Marion, Bill
    Myers, Michael J.
    Yancy, Haile F.
    JOURNAL OF FOOD PROTECTION, 2012, 75 (06) : 1107 - 1112
  • [48] Development of a Real-Time PCR Based Assay for Detection of Babesia microti
    Bloch, E. M.
    Lee, T.
    Krause, P. J.
    Telford, S. R.
    Montalvo, L.
    Chafets, D. M.
    Busch, M. P.
    TRANSFUSION, 2011, 51 : 27A - 27A
  • [49] Development of real-time PCR assay for specific detection of cowpox virus
    Gavrilova, Elena V.
    Shcherbakov, Dmitrii N.
    Maksyutov, Rinat A.
    Shchelkunov, Sergei N.
    JOURNAL OF CLINICAL VIROLOGY, 2010, 49 (01) : 37 - 40
  • [50] Development of a real-time PCR assay for the detection of Trichinella spiralis in situ
    Atterby, H.
    Learmount, J.
    Conyers, C.
    Zimmer, I.
    Boonham, N.
    Taylor, M.
    VETERINARY PARASITOLOGY, 2009, 161 (1-2) : 92 - 98