LAMP assay to detect Vibrio parahaemolyticus causing acute hepatopancreatic necrosis disease in shrimp

Verfasser / Beitragende:
[Jetnaphang Kongrueng, Natta Tansila, Pimonsri Mitraparp-arthorn, Mitsuaki Nishibuchi, Gary Vora, Varaporn Vuddhakul]
Ort, Verlag, Jahr:
2015
Enthalten in:
Aquaculture International, 23/5(2015-10-01), 1179-1188
Format:
Artikel (online)
ID: 605464855
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024 7 0 |a 10.1007/s10499-014-9874-3  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s10499-014-9874-3 
245 0 0 |a LAMP assay to detect Vibrio parahaemolyticus causing acute hepatopancreatic necrosis disease in shrimp  |h [Elektronische Daten]  |c [Jetnaphang Kongrueng, Natta Tansila, Pimonsri Mitraparp-arthorn, Mitsuaki Nishibuchi, Gary Vora, Varaporn Vuddhakul] 
520 3 |a Acute hepatopancreatic necrosis disease (AHPND) is a serious disease in shrimp and results in considerable losses for the shrimp aquaculture industry. The etiologic agent of AHPND has recently been identified as a unique strain of Vibrio parahaemolyticus: One that is different from human pathogenic V. parahaemolyticus strains. In this study, two sets of primers (LAMP-A2 and LAMP-A3) were developed and validated for use in a LAMP assay to specifically identify V. parahaemolyticus causing AHPND (V. parahaemolyticus AHPND). LAMP-A2 and LAMP-A3 detected all 33 V. parahaemolyticus AHPND isolates except the non-V. parahaemolyticus AHPND isolates and 19 other closely related bacterial species. In pure culture and in spiked shrimp experiments, the LAMP assay was superior to PCR for the detection of V. parahaemolyticus AHPND. In pure cultures, the detection limit of LAMP-A3 was 53CFU/ml or 0.1CFU per reaction (10× lower than LAMP-A2), whereas in spiked shrimp experiments, the detection limit was 4.4×105CFU/ml or 8.8×102 CFU per reaction. Further testing of 24 post-larvae, shrimp, sediment and water samples collected from a shrimp farm revealed that V. parahaemolyticus AHPND was detected mostly in the sediment samples. Taken together, the results suggested that the LAMP-A3-based LAMP assay, but not LAMP-A2 or PCR, was suitable for the identification of V. parahaemolyticus AHPND in shrimp aquaculture. 
540 |a Springer International Publishing Switzerland, 2015 
690 7 |a Vibrio parahaemolyticus  |2 nationallicence 
690 7 |a AHPND  |2 nationallicence 
690 7 |a Shrimp  |2 nationallicence 
690 7 |a LAMP  |2 nationallicence 
690 7 |a Vibriosis  |2 nationallicence 
700 1 |a Kongrueng  |D Jetnaphang  |u Food safety and health research unit, Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, Thailand  |4 aut 
700 1 |a Tansila  |D Natta  |u Faculty of Medical Technology, Prince of Songkla University, Songkhla, Thailand  |4 aut 
700 1 |a Mitraparp-arthorn  |D Pimonsri  |u Food safety and health research unit, Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, Thailand  |4 aut 
700 1 |a Nishibuchi  |D Mitsuaki  |u Center for Southeast Asian Studies, Kyoto University, Kyoto, Japan  |4 aut 
700 1 |a Vora  |D Gary  |u Center for Bio/Molecular Science and Engineering, Naval Research Laboratory, Washington, DC, USA  |4 aut 
700 1 |a Vuddhakul  |D Varaporn  |u Food safety and health research unit, Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, Thailand  |4 aut 
773 0 |t Aquaculture International  |d Springer International Publishing  |g 23/5(2015-10-01), 1179-1188  |x 0967-6120  |q 23:5<1179  |1 2015  |2 23  |o 10499 
856 4 0 |u https://doi.org/10.1007/s10499-014-9874-3  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s10499-014-9874-3  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kongrueng  |D Jetnaphang  |u Food safety and health research unit, Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, Thailand  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Tansila  |D Natta  |u Faculty of Medical Technology, Prince of Songkla University, Songkhla, Thailand  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Mitraparp-arthorn  |D Pimonsri  |u Food safety and health research unit, Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, Thailand  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Nishibuchi  |D Mitsuaki  |u Center for Southeast Asian Studies, Kyoto University, Kyoto, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Vora  |D Gary  |u Center for Bio/Molecular Science and Engineering, Naval Research Laboratory, Washington, DC, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Vuddhakul  |D Varaporn  |u Food safety and health research unit, Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, Thailand  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Aquaculture International  |d Springer International Publishing  |g 23/5(2015-10-01), 1179-1188  |x 0967-6120  |q 23:5<1179  |1 2015  |2 23  |o 10499