4.6 Article

Prevalence of porcine parvovirus 1 through 7 (PPV1-PPV7) and co-factor association with PCV2 and PRRSV in Korea

Journal

BMC VETERINARY RESEARCH
Volume 18, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12917-022-03236-1

Keywords

Pig; Porcine parvoviruses; Porcine circovirus type 2; Porcine reproductive and respiratory syndrome virus; Coinfections; Porcine respiratory disease complex

Funding

  1. Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry (IPET) through the Animal Disease Management Technology Development Programs - Ministry of Agriculture, Food and Rural Affairs (MAFRA) in the Republic of Korea [118093-03, 320060-02]

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This study investigated the prevalence rates of PPV1-PPV7 in Korea and found that these viruses are widespread. The highest detection rates were found in lung samples, and fattening pigs had higher detection rates, indicating the chronic nature of PPV infections. There were associations between PPV infections and PCV2 and PRRSV, with different viruses having different prevalence rates.
Background Classical porcine parvovirus (PPV1) and novel porcine parvoviruses designated porcine parvovirus 2 through 7 (PPV2-PPV7) are widespread in pig populations. The objective of this study was to investigate the prevalence rates of PPV1-PPV7 in Korea by detecting PPVs in serum, lung and fecal samples and to elucidate the association of PPVs with porcine circovirus type 2 (PCV2) and porcine reproductive and respiratory virus (PRRSV), major pathogens involved in porcine respiratory disease complex (PRDC). A total of 286 serum, 481 lung, and 281 fecal samples collected from 2018 to 2020 were analyzed. Results The results showed that PPVs are widespread in Korea; the highest detection rates were found in lung samples and ranged from 7.9% (PPV1) to 32.6% (PPV2). Regarding age groups, fattening pigs had the highest detection rates of PPVs, ranging from 6.4% (PPV1) to 36.5% (PPV6); this finding suggests the chronic nature of PPV infections and the continual circulation of these viruses. When compared with PCV2- and PRRSV-negative lung samples, PCV2-positive samples with or without PRRSV positivity had significantly higher detection levels of PPV1 and PPV6. In contrast, the prevalence of PPV2 and PPV7 was significantly higher in PRRSV-infected lung samples regardless of PCV2 detection. PPV5 was detected significantly more frequently in samples with both PCV2 and PRRSV positivity. Conclusions This study could offer a better understanding of the role of PPVs in PCV2 and/or PRRSV infection though further studies are needed to experimentally assess the impact of PPVs in coinfections.

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