Detection and phylogenetic analysis of porcine circovirus type 3 in central China

• Published in: Transboundary and emerging diseases Vol. 65; no. 5; pp. 1163 - 1169
• Main Authors: Xu, Peng‐Li, Zhang, Yu, Zhao, Yu, Zheng, Hui‐Hua, Han, Hao‐Ying, Zhang, Hong‐Xin, Chen, Hong‐Ying, Yang, Ming‐Fan, Zheng, Lan‐Lan
• Format: Journal Article
• Language: English
• Published: Germany Hindawi Limited 01.10.2018
• Subjects: Animals; Base Sequence; Capsid Proteins - genetics; China - epidemiology; Circoviridae Infections - virology; Circovirus - genetics; Epidemics; Epidemiology; Farms; Genes; Genetic diversity; Genetic Variation; Genomes; Infectious diseases; Molecular Epidemiology; phylogenetic analysis; Phylogenetics; Phylogeny; porcine circovirus type 3; Real-Time Polymerase Chain Reaction; Republic of Korea; Strains (organisms); Swine; Swine Diseases - epidemiology; Swine Diseases - virology; Viruses; China; molecular epidemiology; phylogenetic analysis; porcine circovirus type 3; real-time polymerase chain reaction
• ISSN: 1865-1674; 1865-1682
• DOI: 10.1111/tbed.12920

Porcine circovirus type 3 (PCV3) is the pathogen responsible for a new infectious disease that was first reported in 2016 in the United States. To further investigate the epidemic profile and genetic diversity of the virus, one hundred and seventy clinical samples (110 tissue samples and 60 serum samples) were collected from 41 different pig farms in 14 cities in central China, and a SYBR Green I‐based quantitative real‐time PCR method was developed to detect PCV3. The partial cap genes of four field strains from four different farms were sequenced and analysed. The results showed the detection limit was 2.19 × 101 genome copies/μl. Fifty‐three of 170 samples were detected as positive for PCV3, giving a PCV3‐positive rate of 31.18%, with 48.78% (20/41) of pig farms harbouring PCV3, which varied from 20% to 42.86% between 2013 and 2017. PCV3 could be detected in samples from pigs with different clinical presentations, and the PCV3‐positive rates varied for these different clinical presentations. The partial capsid genes of four PCV3 strains (designated YZ, LY‐03, NY and SP) shared 96.3%–99.4% nucleotide identity with those available in GenBank. Phylogenetic analysis based on the capsid gene of 32 PCV3 strains showed that the four PCV3 strains in this study were clustered with the China/GD2016 and South Korea Ku‐1606 strains. The results of this study will aid our understanding of the molecular epidemiology of PCV3.