Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Jan;67(1):284-297.
doi: 10.1111/tbed.13350. Epub 2019 Oct 8.

Development of a novel quantitative real-time PCR assay with lyophilized powder reagent to detect African swine fever virus in blood samples of domestic pigs in China

Affiliations

Development of a novel quantitative real-time PCR assay with lyophilized powder reagent to detect African swine fever virus in blood samples of domestic pigs in China

Aiping Wang et al. Transbound Emerg Dis. 2020 Jan.

Abstract

African swine fever (ASF) is a devastating disease, which is causing huge economic losses in China. Therefore, it is urgent to provide a rapid, highly specific and sensitive diagnostic method for the detection of African swine fever virus (ASFV), the ASF infectious agent. In this study, a novel quantitative real-time polymerase chain reaction (qPCR) assay with lyophilized powder reagents (LPR), targeting the major structural protein p72 gene, was established for the detection of ASFV. This assay had many advantages, such as saving time and money, good sensitivity and repeatability. The sensitivity of this assay was 100 copies/μl of ASFV plasmid templates, and the assay showed 10-fold greater sensitivity than a qPCR assay recommended by OIE. Furthermore, specificity analysis showed that qPCR with LPR for ASFV had no cross-reactivity with other important swine pathogens. In clinical diagnoses of 218 blood samples of domestic pigs in China, the positive rate of the diagnosis of ASFV by qPCR with the LPR and commercial kit reached 80.73% (176/218) and 76.61% (167/218) respectively. The coincidence rate between the two assays is 92.20% (201/218), and kappa value is 0.768 (p < .0001) by SPSS analysis. The overall agreement between the two assays was 95.87% (209/218). Further Pearson correlation and linear regression analysis showed a significant correlation between the two assays with an R2 value of 0.9438. The entire procedure, from specimen processing to result reporting, can be completed within 2 hr. Our results demonstrated that the qPCR-LPR assay is a good laboratory diagnostic tool for sensitive and efficient detection of ASFV.

Keywords: African swine fever virus; laboratory diagnosis; lyophilized powder reagent; real-time PCR.

PubMed Disclaimer

Similar articles

Cited by

References

REFERENCES

    1. Agüero, M., Fernández, J., Romero, L. C., Mascaraque, S., Arias, M., & SánchezVizcaíno, J. M. (2003). Highly sensitive PCR assay for routine diagnosis of African swine fever virus in clinical samples. Journal of Clinical Microbiology, 41(9), 4431-4434. https://doi.org/10.1128/JCM.41.9.4431-4434.2003
    1. Bao, J., Wang, Q., Lin, P., Liu, C., Li, L., Wu, X., … Wang, Z. (2019). Genome comparison of African swine fever virus China/2018/AnhuiXCGQ strain and related European p72 Genotype II strains. Transboundary and Emerging Diseases. 66(3), 1167-1176. https://doi.org/10.1111/tbed.13124.
    1. Dixon, L. K., Sun, H., & Roberts, H. (2019). African swine fever. Antiviral Research, 165, 34-41. https://doi.org/10.1016/j.antiviral.2019.02.018
    1. Fernández-Pinero, J., Gallardo, C., Elizalde, M., Robles, A., Gómez, C., Bishop, R., … Arias, M. (2012). Molecular diagnosis of African swine fever by a new real-time PCR using universal probe library. Transboundary and Emerging Diseases, 60(1), https://doi.org/10.1111/j.1865-1682.2012.01317.x
    1. Galindo, I., & Alonso, C. (2017). African swine fever virus: A review. Viruses, 9(5), 103 https://doi.org/10.3390/v9050103

Associated data

LinkOut - more resources