AUTHOR=Jiang Hongbo , Liu Jinghui , Bao Jie , Xing Yuenan , Feng Chengcheng , Hu Qingbiao , Li Xiaodong , Chen Qijun TITLE=Rapid detection of Enterocytospora artemiae in Chinese grass shrimp (Palaemonetes sinensis) through isothermal recombinase polymerase amplification JOURNAL=Frontiers in Marine Science VOLUME=9 YEAR=2022 URL=https://www.frontiersin.org/journals/marine-science/articles/10.3389/fmars.2022.945809 DOI=10.3389/fmars.2022.945809 ISSN=2296-7745 ABSTRACT=

Enterospora artemiae, an obligate intracellular parasitic microsporidium, severely affects the development of Chinese grass shrimp (Palaemonetes sinensis) aquaculture. Currently, no effective drugs or vaccines are available for treatment. To improve the diagnosis and prevention of microsporidia infection in P. sinensis, two recombinase polymerase amplification (RPA) detection methods (visualized by electrophoresis [RPA-AGE] and a colloidal gold lateral flow dip-strip [RPA-LFD], respectively) were established based on the E. artemiae S8 serine protease gene. RPA-AGE showed optimal amplification at 37°C for 30 min, and amplification by RPA-LFD was completed in 10 min at 37°C and produced detection results within 5 min. Regarding specificity, both methods showed specific amplification of E. artemiae but not of other pathogens. Regarding sensitivity, the minimum detection limit for both RPA-AGE and RPA-LFD was 4.7 copies/μL. Using 30 clinical samples, the 70%-positive rate was lower than that of fluorescence quantitation, but accuracy was improved compared with conventional polymerase chain reaction-based amplification (56.7%). Our RPA-AGE and RPA-LFD methods showed high specificity and sensitivity, with short detection time. In particular, the RPA-LFD method can be used for simple on-site detection of E. artemiae in P. sinensis farms without the requirement of experimental equipment, which can facilitate the prevention and control of this microsporidial disease.