Rapid detection of infectious hypodermal and hematopoietic necrosis virus (IHHNV) by real-time, isothermal recombinase polymerase amplification assay

被引:37
作者
Xia, Xiaoming [1 ,2 ,3 ]
Yu, Yongxin [1 ,2 ,3 ]
Hu, Linghao [1 ,3 ]
Weidmann, Manfred [4 ]
Pan, Yingjie [1 ,2 ,3 ]
Yan, Shuling [3 ,5 ]
Wang, Yongjie [1 ,2 ,3 ]
机构
[1] Minist Agr, Lab Qual & Safety Risk Assessment Aquat Prod Stor, Shanghai, Peoples R China
[2] Shanghai Engn Res Ctr Aquat Prod Proc & Preservat, Shanghai, Peoples R China
[3] Shanghai Ocean Univ, Coll Food Sci & Technol, Shanghai, Peoples R China
[4] Univ Stirling, Inst Aquaculture, Stirling FK9 4LA, Scotland
[5] Univ Gottingen, Inst Biochem & Mol Cell Biol, D-37073 Gottingen, Germany
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
PRAWN PENAEUS-MONODON; HISTORIC EMERGENCE; SHRIMP PATHOGENS; PCR ASSAY; QUANTIFICATION; STYLIROSTRIS; VANNAMEI; DISEASES; AMERICA; GENOME;
D O I
10.1007/s00705-015-2357-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Infectious hypodermal and hematopoietic necrosis virus (IHHNV) causes mortality or runt deformity syndrome in penaeid shrimps and is responsible for significant economic losses in the shrimp aquaculture industry. Here, we describe a novel real-time isothermal recombinase polymerase amplification (RPA) assay developed for IHHNV detection. Using IHHNV plasmid standards and DNA samples from a variety of organisms, we evaluated the ability of the IHHNV-RPA assay to detect IHHNV based on analysis of its sensitivity, specificity, rapidity, and reproducibility. Probit analysis of eight independent experimental replicates indicated satisfactory performance of the RPA assay, which is sufficiently sensitive to detect as few as 4 copies of the IHHNV genome within 7 min at 39 degrees C with 95 % reliability. Therefore, this rapid RPA method has great potential for applications, either in field use or as a point of care diagnostic technique.
引用
收藏
页码:987 / 994
页数:8
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