4.5 Article

Development of a quadruple PCR-based gene microarray for detection of vaccine and wild-type classical swine fever virus, African swine fever virus and atypical porcine pestivirus

Journal

VIROLOGY JOURNAL
Volume 19, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12985-022-01933-9

Keywords

Classical swine fever; African swine fever; Atypical pestivirus; Polymerase chain reaction; Differential diagnosis; Gene chip

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Funding

  1. National Natural Science Foundation of China [31872484]
  2. IVDC Non-profit Key Program of Veterinary Drug Industry [GY202011]

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A quadruple PCR-based gene microarray assay was developed to simultaneously detect and differentiate wild-type and vaccine strains of CSFV, ASFV, and APPV with high specificity and sensitivity. It provides a practical and reliable method for rapid detection and accurate diagnosis of these three viral diseases in the Chinese pig industry.
Background Classical swine fever (CSF), African swine fever (ASF), and atypical porcine pestivirus (APPV) are acute, virulent, and contagious viral diseases currently hampering the pig industry in China, which result in mummification or stillbirths in piglets and mortality in pigs. Diagnostic assays for the differentiation of infection and vaccination of CSFV, in addition to the detection of ASFV and APPV, are urgently required for better prevention, control, and elimination of these viral diseases in China. Methods A quadruple PCR-based gene microarray assay was developed in this study to simultaneously detect wild-type and vaccine CSFV strains, ASFV and APPV according to their conserved regions. Forty-two laboratory-confirmed samples, including positive samples of 10 other swine viral diseases, were tested using this assay to confirm its high specificity. Results This assay's limit of detections (LODs) for the wild-type and vaccine CSFV were 6.98 and 6.92 copies/mu L. LODs for ASFV and APPV were 2.56 x 10 and 1.80 x 10 copies/mu L, respectively. When compared with standard RT-PCR or qPCR for CSFV (GB/T 26875-2018), ASFV (MARR issue No.172), or APPV (CN108611442A) using 219 clinical samples, the coincidence was 100%. The results showed that this assay with high sensitivity could specifically distinguish ASFV, APPV, and CSFV, including CSFV infection and immunization. Conclusion This assay provides a practical, simple, economic, and reliable test for the rapid detection and accurate diagnosis of the three viruses and may have good prospects for application in an epidemiological investigation, prevention, and control and elimination of these three diseases.

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