Key result
The PCV2 VLP-based indirect ELISA demonstrated a diagnostic sensitivity of 98.33% and a diagnostic specificity of 93.33% compared to the immunofluorescence assay.
Why the study?
Porcine circovirus type 2 is a persistent threat to the swine industry, making serological detection methods necessary for clinical diagnosis and epidemiological investigations.
Does a VLP-based indirect ELISA accurately detect anti-PCV2 antibodies in pig serum compared to immunofluorescence assay?
Does a VLP-based indirect ELISA accurately detect anti-PCV2 antibodies in pig serum compared to immunofluorescence assay?
The developed VLP-based indirect ELISA provides a rapid, specific, and reproducible method for large-scale serological detection of PCV2 antibodies in pigs.
May enable large-scale PCV2 serosurveillance in swine; leaves open routine adoption pending independent validation.
Backgroud Porcine circovirus type 2 (PCV-2) infection is a growing and persistent threat to the swine industry, and thus the development of serological detection methods for PCV2 is of great necessity for clinical diagnosis, as well as epidemiological investigations. The study aimed to build an indirect enzyme-linked immunosorbent assay (ELISA) to examine antibodies against PCV2 based on virus-like particle (VLP). Results Through transmission electron microscopy (TEM), the VLPs were morphologically similar to authentic PCV-2 viruses. Purified VLPs can be detected in immunoblots with PCV-2 antisera, and a predominant protein of approximately 30 kDa was determined by Western blot. The VLPs were shown to have good immunogenicity in mice and stimulated a high level of PCV2-specific antibody titers. The indirect ELISA can detect PCV2 antibody responses in animals had a diagnostic sensitivity and specificity of 98.33% and 93.33% compared to immunofluorescence assay (IFA), respectively. The intra-assay and inter-assay coefficient variations (CVs) within a plate was <10%, and the CV of different ELISA plates was <15%, indicating good repeatability. There was no cross-reaction of this ELISA with antisera against other porcine viruses. A total of 170 serum samples collected from different pig farms in China were tested for anti-PCV2 antibodies, and 151 (88.9%) of the 170 samples were PCV2 antibody positive. Conclusion Our findings suggest that this ELISA assay was rapid, specific, and reproducible and can be used for large-scale serological investigations of PCV2 antibodies in pigs.
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Li et al. (2022) studied Porcine circovirus type 2 (PCV2) infection (n=150). PCV2 VLP-based indirect ELISA vs. Indirect immunofluorescence assay (IFA) was evaluated on Diagnostic sensitivity and specificity for detecting PCV2 antibodies. The PCV2 VLP-based indirect ELISA demonstrated a diagnostic sensitivity of 98.33% and a diagnostic specificity of 93.33% compared to the immunofluorescence assay.
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