Development of a Real-Time Recombinase Polymerase Amplification Assay for the Rapid Detection of African Swine Fever Virus Genotype I and II

被引:12
作者
Ilya, Titov [1 ,2 ]
Monoldorova, Sezim [1 ]
Kang, Shin-Seok [1 ]
Yun, Seungri [1 ]
Byeon, Hyeon-Seop [3 ]
Mariia, Nefedeva [2 ]
Jeon, Bo-Young [1 ,4 ]
机构
[1] Yonsei Univ, Coll Software & Digital Healthcare Convergence, Dept Biomed Lab Sci, Wonju 26493, South Korea
[2] Fed Res Ctr Virol & Microbiol, Lab Mol Genet Res, Volginskii 601125, Russia
[3] Chungbuk Vet Serv & Res, Cheongju 28153, South Korea
[4] One Hlth Frontier Inc, Wonju 26493, South Korea
基金
芬兰科学院;
关键词
African swine fever virus (ASFV); recombinase polymerase amplification (RPA); CP204; gene; genotype I; genotype II; EPIDEMIC; CHINA; PIGS;
D O I
10.3390/pathogens11040439
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
African swine fever (ASF) is a contagious viral disease in pigs and wild boars which poses a major threat to the pig industry. Rapid and accurate diagnosis is necessary to control ASF. Hence, we developed a rapid diagnostic method using a recombinase polymerase amplification (RPA) assay targeting the conserved sequences of CP204L (p30) thatcan rapidly detect ASF virus (ASFV) genotype strains I and II. The lower detection limit of the real-time RPA assay was 5 x 10(1) copies per reaction. The real-time RPA assay effectively detected ASFV isolates and clinical specimens belonging to ASFV genotypes I and II. The sensitivity and specificity of the assay were 96.8% (95% confidence interval (CI): 83.3-99.9) and 100% (95% CI: 88.4-100.0), respectively. The agreement between the real-time RPA assay and a reference commercial real-time quantitative polymerase chain reaction (qPCR) was 100%. The real-time RPA assay had a detection time of 6.0 min (95% CI: 5.7-6.2), which was significantly shorter than that of qPCR (49 min; 95% CI: 47.4-50.6; p < 0.001). Thus, the developed real-time RPA assay is a rapid and accurate diagnostic tool for detecting ASFV genotypes I and II.
引用
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页数:10
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