Abstract

Outbreaks of highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV) have led to large economic losses in China. The attenuated vaccine (HP-PRRSV JXA1-R) was used to control HP-PRRSV. However, in recent years, co-infection with classical PRRSV (C-PRRSV), HP-PRRSV, and/or HP-PRRSV JXA1-R has been increasing in China, resulting in a significant impact on PRRSV diagnostics and management. To facilitate rapid discrimination of HP-PRRSV JXA1-R from HP-PRRSV and C-PRRSV, a multiplex RT-PCR assay for the visual detection of HP-PRRSV JXA1-R, HP-PRRSV, and C-PRRSV was established and evaluated with reference PRRSV strains and clinical samples. Primer specificities were evaluated with RNA/DNA extracted from 10 viral strains, and our results revealed that the primers had a high specificity for PRRSV. The assay sensitivity was 24 copies/μL for PRRSVs. A total of 516 serum samples were identified, of which 12.21% (63/516) were HP-PRRSV-positive, 2.33% (12/516) were HP-PRRSV JXA1-R-positive, and 1.16% (6/516) were C-PRRSV-positive, respectively, which was completely consistent with the sequencing method. The high specificity, sensitivity, and reliability of the multiplex RT-PCR assay described in this study indicate that it is useful for the rapid and differential diagnosis of HP-PRRSV JXA1-R, HP-PRRSV, and C-PRRSV.

Highlights

  • Porcine reproductive and respiratory syndrome (PRRS) is one of the most economically important swine diseases worldwide

  • The etiological agent of PRRS is the porcine reproductive and respiratory syndrome virus (PRRSV) which belongs to the order Nidovirales, family Arteriviridae [1]

  • classical PRRSV (C-PRRSV) strain CH-1a (GenBank ID: AY032626) is the first wild-type strain isolated from China, and was kindly provided by Hanzhong Wang (Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China)

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Summary

Introduction

Porcine reproductive and respiratory syndrome (PRRS) is one of the most economically important swine diseases worldwide. Classical PRRSV (C-PRRSV) is the prototypical strain of North American (type 2). American (type 2) genotype, and the PRRSV strains circulating in China are almost all of the North. Molecular typing methods have been developed, and are currently used for rapid detection and identification of PRRSV [10]. C-PRRSV [11]; and a one-step RT-PCR assay has been developed for the detection and differentiation of HP-PRRSV and C-PRRSV [12] These assays are not suitable for the differentiation of. A rapid, convenient, sensitive, and specific diagnostic method to discriminate between C-PRRSV, HP-PRRSV, and HP-PRRSV JXA1-R strains would be extremely useful for the diagnosis and control of PRRSV in China. A multiplex RT-PCR assay was developed for the detection and discrimination of C-PRRSV, HP-PRRSV, and HP-PRRSV JXA1-R strains. The proposed method was shown to be a convenient, sensitive, reliable, and suitable tool to aid the prevention and control of PRRS

Materials and Methods
Clinical Specimen Collection
Primers Design
Nucleic Acid Extractions
Single PCR and Plasmid Template Construction
Optimization of the MultiplexRT-PCR Assay
Specificity of the Proposed Multiplex RT-PCR Assay
Sensitivity of the Proposed Multiplex RT-PCR Assay
2.10. Detection of PRRSV in Clinical Specimens by the Multiplex PCR
MultiplexRT-PCR Assay Conditions
Specificity of the Proposed
Specificity
Sensitivity of Multiplex
Detection
Sequencing Method
Full Text
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