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农业生物技术学报  2024, Vol. 32 Issue (4): 961-973    DOI: 10.3969/j.issn.1674-7968.2024.04.020
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Detection of Acute Hepatopancreatic Necrosis Disease in Pacific White Shrimp (Penaeus vannamei) by Recombinase Polymerase Amplification
JIN Dong-Sheng1,2, LOU Yi-Rong2, WANG Yao-Hua3, DUAN Li-Jun2, LI Qi-Ang2, CHEN Chen3, YAN Mao-Cang3, CHEN Jiong1,2, ZHOU Qian-Jin1,2,*
1 State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Ningbo University, Ningbo 315211, China;
2 School of Marine Science, Ningbo University, Ningbo 315832, China;
3 Zhejiang Key Laboratory of Exploitation and Preservation of Coastal Bio-resource, Zhejiang Mariculture Research Institute, Wenzhou 325005, China
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Abstract  Acute hepatopancreatic necrosis disease (AHPND) is a newly emerged bacterial disease in shrimps (Penaeidae), causing significant economic losses in the global shrimp farming industry. AHPND is primarily caused by Vibrio spp. carrying virulent pirA and pirB. In this study, specific primers and probes were designed and screened for pirA and pirB, and a recombinase polymerase amplification (RPA) method was developed. This RPA reaction ran in 39 ℃ for 20 min. The results revealed successful screening of primer/probe combinations for both pirA and pirB genes. Through a series of tests using the RPA method, these primer/probe combinations demonstrated specific detection of the target virulence genes, without amplification of genomic DNA from 13 microorganisms, such as Vibrio alginolyticus, V. parahaemolyticus, and Enterocytozoon hepatomegaly. The detection limit of the RPA method was 0.01 and 0.1 fg/μL of recombinant plasmid pirAB-pMD19, when the primers and probes targeting pirA or pirB were used. The primer concentrations were optimized at 0.4 µmol/L each, while the optimal concentration for the probe was 0.16 µmol/L. The RPA method was used to detect suspicious tissues of Penaeus vannamei using optimized sets of primers and probe. The results showed that the RPA method could accurately detect pirA and pirB from shrimp tissues, which was consistent with the PCR method recommended by the World Organization for Animal Health (WOAH). In summary, this PRA methods targeting pirA and pirB respectively could rapid and accurately detect ANPND-causing bacteria with easy operation and short time-consumption, making it a promising supplementary tool for routine monitoring and rapid detection of AHPND.
Key wordsRecombinase polymerase amplification (RPA)      Acute hepatopancreatic necrosis disease (AHPND)      pirA      pirB      Detection     
Received: 08 May 2023     
ZTFLH:  S945.1  
Corresponding Authors: *zhouqianjin@nbu.edu.cn   
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Articles by authors
JIN Dong-Sheng
LOU Yi-Rong
WANG Yao-Hua
DUAN Li-Jun
LI Qi-Ang
CHEN Chen
YAN Mao-Cang
CHEN Jiong
ZHOU Qian-Jin
Cite this article:   
JIN Dong-Sheng,LOU Yi-Rong,WANG Yao-Hua, et al. Detection of Acute Hepatopancreatic Necrosis Disease in Pacific White Shrimp (Penaeus vannamei) by Recombinase Polymerase Amplification[J]. 农业生物技术学报, 2024, 32(4): 961-973.
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https://journal05.magtech.org.cn/Jwk_ny/EN/10.3969/j.issn.1674-7968.2024.04.020     OR     https://journal05.magtech.org.cn/Jwk_ny/EN/Y2024/V32/I4/961
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