Visual and equipment-free reverse transcription recombinase polymerase amplification method for rapid detection of foot-and-mouth disease virus

被引:31
作者
Liu, Libing [1 ]
Wang, Jinfeng [1 ]
Zhang, Ruoxi [3 ]
Lin, Mi [5 ]
Shi, Ruihan [1 ,4 ]
Han, Qingan [3 ]
Wang, Jianchang [1 ,4 ]
Yuan, Wanzhe [2 ]
机构
[1] Hebei Entry Exit Inspect & Quarantine Bur, Ctr Inspect & Quarantine, Shijiazhuang 050051, Hebei, Peoples R China
[2] Agr Univ Hebei, Coll Vet Med, 38 Lingyusi St, Baoding 071001, Hebei, Peoples R China
[3] Hebei Anim Dis Control Ctr, Shijiazhuang 050050, Hebei, Peoples R China
[4] Hebei Acad Sci & Technol Inspect & Quarantine, Shijiazhuang 050051, Hebei, Peoples R China
[5] Chinese Acad Agr Sci, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, Lanzhou 730046, Peoples R China
关键词
FMDV; 3D gene; RPA; LF probe; Lateral flow strip; CHAIN-REACTION ASSAY; REAL-TIME; ISOTHERMAL AMPLIFICATION; PCR; PATHOGENESIS; SEROTYPES; DIAGNOSIS; STRIP;
D O I
10.1186/s12917-018-1594-x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: Foot-and-mouth disease (FMD), which is caused by foot-and-mouth disease virus (FMDV), is a highly contagious tansboundary disease of cloven-hoofed animals and causes devastating economic damages. Accurate, rapid and simple detection of FMDV is critical to containing an FMD outbreak. Recombinase polymerase amplification (RPA) has been explored for detection of diverse pathogens because of its accuracy, rapidness and simplicity. A visible and equipment-free reverse-transcription recombinase polymerase amplification assay combined with lateral flow strip (LFS RT-RPA) was developed to detect the FMDV using primers and LF probe specific for the 3D gene. Results: The FMDV LFS RT-RPA assay was performed successfully in a closed fist using body heat for 15 min, and the products were visible on the LFS inspected by the naked eyes within 2 min. The assay could detect FMDV serotypes O, A and Asia1, and there were no cross-reactions with vesicular stomatitis virus (VSV), encephalomyocarditis virus (EMCV), classical swine fever virus (CSFV), porcine reproductive and respiratory syndrome virus (PRRSV), porcine circovirus 2 (PCV2) and pseudorabies virus (PRV). The analytical sensitivity was 1.0 x 10(2) copies in vitro transcribed FMDV RNA per reaction, which was the same as a real-time RT-PCR. For the 55 samples, FMDV RNA positive rate was 45.5% (25/55) by LFS RT-RPA and 52.7% (29/55) by real-time RT-PCR. For the LFS RT-RPA assay, the positive and negative predicative values were 100% and 80%, respectively. Conclusions: The performance of the LFS RT-RPA assay was comparable to real-time RT-PCR, while the LFS RT-RPA assay was much faster and easier to be performed. The developed FMDV LFS RT-RPA assay provides an attractive and promising tool for rapid and reliable detection of FMDV in under-equipped laboratory and at point-of-need facility, which is of great significance in FMD control in low resource settings.
引用
收藏
页数:8
相关论文
共 33 条
[1]  
Abd El Wahed A, 2013, PLOS ONE, V8, DOI [10.1371/journal.pone.0071642, 10.1371/currents.outbreaks.62df1c7c75ffc96cd59034531e2e8364]
[2]   Rapid Genome Detection of Schmallenberg Virus and Bovine Viral Diarrhea Virus by Use of Isothermal Amplification Methods and High-Speed Real-Time Reverse Transcriptase PCR [J].
Aebischer, Andrea ;
Wernike, Kerstin ;
Hoffmann, Bernd ;
Beer, Martin .
JOURNAL OF CLINICAL MICROBIOLOGY, 2014, 52 (06) :1883-1892
[3]  
Alexandersen S, 2005, CURR TOP MICROBIOL, V288, P9
[4]   The pathogenesis and diagnosis of foot-and-mouth disease [J].
Alexandersen, S ;
Zhang, Z ;
Donaldson, AI ;
Garland, AJM .
JOURNAL OF COMPARATIVE PATHOLOGY, 2003, 129 (01) :1-36
[5]   Field-Deployable Reverse Transcription-Insulated Isothermal PCR (RT-iiPCR) Assay for Rapid and Sensitive Detection of Foot-and-Mouth Disease Virus [J].
Ambagala, A. ;
Fisher, M. ;
Goolia, M. ;
Nfon, C. ;
Furukawa-Stoffer, T. ;
Polo, R. Ortega ;
Lung, O. .
TRANSBOUNDARY AND EMERGING DISEASES, 2017, 64 (05) :1610-1623
[6]  
[Anonymous], MOL CELL PROBES
[7]   Use of a portable real-time reverse transcriptase-polymerase chain reaction assay for rapid detection of foot-and-mouth disease virus [J].
Callahan, JD ;
Brown, F ;
Csorio, FA ;
Sur, JH ;
Kramer, E ;
Long, GW ;
Lubroth, J ;
Ellis, SJ ;
Shoulars, KS ;
Gaffney, KL ;
Rock, DL ;
Nelson, WM .
JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 2002, 220 (11) :1636-1642
[8]   A method to detect major serotypes of foot-and-mouth disease virus [J].
Collins, RA ;
Ko, LS ;
Fung, KY ;
Lau, LT ;
Xing, J ;
Yu, ACH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 297 (02) :267-274
[9]   Equipment-Free Incubation of Recombinase Polymerase Amplification Reactions Using Body Heat [J].
Crannell, Zachary Austin ;
Rohrman, Brittany ;
Richards-Kortum, Rebecca .
PLOS ONE, 2014, 9 (11)
[10]   Recombinase Polymerase Amplification for Diagnostic Applications [J].
Daher, Rana K. ;
Stewart, Gale ;
Boissinot, Maurice ;
Bergeron, Michel G. .
CLINICAL CHEMISTRY, 2016, 62 (07) :947-958