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Development and application of a colloidal-gold dual immunochromatography strip for detecting African swine fever virus antibodies

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Abstract

African swine fever (ASF) is an acute and highly contagious infectious disease caused by the African swine fever virus (ASFV). Currently, there is no vaccine against ASF worldwide, and no effective treatment measures are available. For this reason, developing a simple, rapid, specific, and sensitive serological detection method for ASFV antibodies is crucial for the prevention and control of ASF. In this study, a 1:1 mixture of gold-labeled p30 and p72 probes was used as the gold-labeled antigen. The p30 and p72 proteins and their monoclonal antibodies were coated on a nitrocellulose membrane (NC) as a test (T) line and control (C) line, respectively. A colloidal-gold dual immunochromatography strip (ICS) for ASFV p30 and p72 protein antibodies was established. The results showed that the colloidal-gold dual ICS could specifically detect ASFV antibodies within 5–10 min. There was no cross-reaction after testing healthy pig serum; porcine reproductive and respiratory syndrome virus (PRRSV), foot-and-mouth disease type A virus (FMDV-A), foot-and-mouth disease type O virus (FMDV-O), porcine circovirus type 2 (PCV-2), and classical swine fever virus (CSFV) positive sera. A positive result was obtained only for the positive control P1. The sensitivity of the test strips was 1:256, which was equivalent to that of commercially ELISA kits. Their coincidence rate with the two commercial ASFV ELISA antibodies detection kits was higher than 98%. The test strips were stably stored at 18–25 °C and 4 °C for 4 and 6 months, respectively. The colloidal-gold dual ICS prepared in this study had high sensitivity and specificity and were characterized by rapid detection, simple operation, and easy interpretation of results. Therefore, they are of great significance to diagnose, prevent, and control African swine fever.

Key points

We establish an antibody detection that is quick and can monitor an ASF infection.

We observe changes in two protein antibodies to dynamically monitor ASF infection.

We use diversified detection on a single test strip to detect both antibodies.

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Data availability

The authors declare that the data supporting the findings of this study are available within the article.

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Funding

This work was supported by the National Key R&D Program of the Ministry of Science and Technology (2018YFC0840400).

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Contributions

YW performed the experiments, analyzed the data, and wrote the manuscript. ZS and GP participated in the data analysis and wrote the paper. LW, JL, YR, GZ, YM, RS, BY, and LC revised the manuscript. HT and HZ conceived and designed the study, participated in experimental work and wrote the paper. All authors read and approved the final version of the manuscript.

Corresponding authors

Correspondence to Hong Tian or Haixue Zheng.

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The authors confirm that the ethical policies of the journal, as noted on the journal’s author guidelines page, have been adhered to, and the appropriate ethical review committee approval has been received. All animal experimental procedures have been reviewed and approved by the Animal Care and Use Committee of Lanzhou Veterinary Research Institute of the Chinese Academy of Agricultural Sciences (approval ID: SYXK(Gan) 2015–0003).

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All authors listed on this manuscript have read and agreed to the publication of this research.

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The authors declare no competing interests.

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Wan, Y., Shi, Z., Peng, G. et al. Development and application of a colloidal-gold dual immunochromatography strip for detecting African swine fever virus antibodies. Appl Microbiol Biotechnol 106, 799–810 (2022). https://doi.org/10.1007/s00253-021-11706-z

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  • DOI: https://doi.org/10.1007/s00253-021-11706-z

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