Development of a GeXP-multiplex PCR assay for the simultaneous detection and differentiation of six cattle viruses

被引:8
作者
Fan, Qing [1 ]
Xie, Zhixun [1 ]
Xie, Zhiqin [1 ]
Deng, Xianwen [1 ]
Xie, Liji [1 ]
Huang, Li [1 ]
Luo, Sisi [1 ]
Huang, Jiaoling [1 ]
Zhang, Yanfang [1 ]
Zeng, Tingting [1 ]
Wang, Sheng [1 ]
Liu, Jiabo [1 ]
Pang, Yaoshan [1 ]
机构
[1] Guangxi Vet Res Inst, Guangxi Key Lab Vet Biotechnol, Nanning, Guangxi Provinc, Peoples R China
关键词
VIRAL DIARRHEA VIRUS; MOUTH-DISEASE; VESICULAR-STOMATITIS; ANALYZER; FOOT; SWINE; DIAGNOSIS; ANTIBODIES; DESIGN; HERDS;
D O I
10.1371/journal.pone.0171287
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Foot-and-mouth disease virus ( FMDV), Bluetongue virus (BTV), Vesicular stomatitis Virus (VSV), Bovine viral diarrheal (BVDV), Bovine rotavirus (BRV), and Bovine herpesvirus 1 (IBRV) are common cattle infectious viruses that cause a great economic loss every year in many parts of the world. A rapid and high-throughput GenomeLab Gene Expression Profiler (GeXP) analyzer-based multiplex PCR assay was developed for the simultaneous detection and differentiation of these six cattle viruses. Six pairs of chimeric primers consisting of both the gene-specific primer and a universal primer were designed and used for amplification. Then capillary electrophoresis was used to separate the fluorescent labeled PCR products according to the amplicons size. The specificity of GeXP-multiplex PCR assay was examined with samples of the single template and mixed template of six viruses. The sensitivity was evaluated using the GeXP-multiplex PCR assay on serial 10-fold dilutions of ssRNAs obtained via in vitro transcription. To further evaluate the reliability, 305 clinical samples were tested by the GeXP-multiplex PCR assay. The results showed that the corresponding virus specific fragments of genes were amplified. The detection limit of the GeXP-multiplex PCR assay was 100 copies/mu L in a mixed sample of ssRNAs containing target genes of six different cattle viruses, whereas the detection limit for the Gexp-mono PCR assay for a single target gene was 10 copies/mu L. In detection of viruses in 305 clinical samples, the results of GeXP were consistent with simplex real-time PCR. Analysis of positive samples by sequencing demonstrated that the GeXP-multiplex PCR assay had no false positive samples of nonspecific amplification. In conclusion, this GeXP-multiplex PCR assay is a high throughput, specific, sensitive, rapid and simple method for the detection and differentiation of six cattle viruses. It is an effective tool that can be applied for the rapid differential diagnosis of clinical samples and for epidemiological investigation.
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页数:14
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共 34 条
[1]  
Brito B.P., 2015, Transbound. Emerg. Dis
[2]   Evaluation of economic and performance outcomes associated with the number of treatments after an initial diagnosis of bovine respiratory disease in commercial feeder cattle [J].
Cernicchiaro, Natalia ;
White, Brad J. ;
Renter, David G. ;
Babcock, Abram H. .
AMERICAN JOURNAL OF VETERINARY RESEARCH, 2013, 74 (02) :300-309
[3]   Custom Design of a GeXP Multiplexed Assay Used to Assess Expression Profiles of Inflammatory Gene Targets in Normal Colon, Polyp, and Tumor Tissue [J].
Drew, Janice E. ;
Mayer, Claus-Dieter ;
Farquharson, Andrew J. ;
Young, Pauline ;
Barrera, Lawrence N. .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2011, 13 (02) :233-242
[4]   Rapid and differential diagnosis of foot-and-mouth disease, swine vesicular disease, and vesicular stomatitis by a new multiplex RT-PCR assay [J].
Fernandez, Jovita ;
Agueero, Montserrat ;
Romero, Luis ;
Sanchez, Carmen ;
Belak, Sandor ;
Arias, Marisa ;
Sanchez-Vizcaino, Jos Manuel .
JOURNAL OF VIROLOGICAL METHODS, 2008, 147 (02) :301-311
[5]   A Multiepitope Fusion Antigen Elicits Neutralizing Antibodies against Enterotoxigenic Escherichia coli and Homologous Bovine Viral Diarrhea Virus In Vitro [J].
Hashish, Emad A. ;
Zhang, Chengxian ;
Ruan, Xiaosai ;
Knudsen, David E. ;
Chase, Christopher C. ;
Isaacson, Richard E. ;
Zhou, Guoqiang ;
Zhang, Weiping .
CLINICAL AND VACCINE IMMUNOLOGY, 2013, 20 (07) :1076-1083
[6]   A universal heterologous internal control system for duplex real-time RT-PCR assays used in a detection system for pestiviruses [J].
Hoffmann, B. ;
Depner, K. ;
Schirrmeier, H. ;
Beer, M. .
JOURNAL OF VIROLOGICAL METHODS, 2006, 136 (1-2) :200-209
[7]   Bluetongue disease teaches Switzerland [J].
Hofmann, M. ;
Griot, C. ;
Chaignat, V. ;
Perler, L. ;
Thuer, B. .
SCHWEIZER ARCHIV FUR TIERHEILKUNDE, 2008, 150 (02) :49-56
[8]   Simultaneously Typing Nine Serotypes of Enteroviruses Associated with Hand, Foot, and Mouth Disease by a GeXP Analyzer-Based Multiplex Reverse Transcription-PCR Assay [J].
Hu, Xiumei ;
Zhang, Yong ;
Zhou, Xiaomian ;
Xu, Banglao ;
Yang, Mengjie ;
Wang, Miao ;
Zhang, Chen ;
Li, Jin ;
Bai, Ruyin ;
Xu, Wenbo ;
Ma, Xuejun .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (02) :288-293
[9]  
Karreman Hubert J., 2009, Animal Health Research Reviews, V10, P121, DOI 10.1017/S1466252309990156
[10]   The development of a GeXP-based multiplex reverse transcription-PCR assay for simultaneous detection of sixteen human respiratory virus types/subtypes [J].
Li, Jin ;
Mao, Nai-Ying ;
Zhang, Chen ;
Yang, Meng-Jie ;
Wang, Miao ;
Xu, Wen-Bo ;
Ma, Xue-Jun .
BMC INFECTIOUS DISEASES, 2012, 12