Insights into the evolutionary history and epidemiological characteristics of the emerging lineage 1 porcine reproductive and respiratory syndrome viruses in China. Issue 6 (5th June 2020)

• Record Type: Journal Article
• Authors: Sun, Yan‐Kuo; Chen, Yong‐Jie; Cai, Yu; Li, Qi; Xie, Jie‐Xiong; Liang, Guan; Gao, Qi; Yu, Zhi‐Qing; Lu, Gang; Huang, Liang‐Zong; Ma, Chun‐Quan; Gong, Lang; Wang, Heng; Shi, Mang; Zhang, Gui‐Hong
• Is Part Of: Transboundary and emerging diseases. Volume 67:Issue 6(2020)
• Page Start: 2630
• Page End: 2641
• Publication Date: 2020-06-05
• Subjects: China -- genome recombination -- lineage 1 -- molecular characterization -- phylogenetic -- porcine reproductive and respiratory syndrome virus; Veterinary medicine -- Periodicals; 636.089
• DOI: 10.1111/tbed.13613
• Languages: English
• ISSNs: 1865-1674

Abstract

Abstract: The newly emerged lineage 1 porcine reproductive and respiratory syndrome viruses (PRRSVs) (especially the NADC30‐like and NADC34‐like viruses) have posed a direct threat to the Chinese pig industry since 2013. The phylogenetic, epidemic, and recombinant properties of these viruses have not yet systematically analysed in China. This report presents regular surveillance and field epidemiological studies for PRRSV across China from 2007 to 2019. From over 4, 000 detected clinical samples, 70 open reading frame five sequences and four complete genomes of lineage 1 viruses were successfully obtained. Combined with global data, we conducted an extensive and systematic molecular phylogeny analysis using a maximum likelihood tree. The Chinese lineage 1 viruses were clustered, and their temporal and spatial distribution was further explored. Multiple viral introductions of lineage 1 virus from the United States to China were detected, and some became endemic in China. There are three sub‐lineage 1 clusters: lineage 1.5 (NADC34‐like), lineage 1.6 and New Intro cluster (NADC30‐like). These viruses show high genetic diversity and a wide distribution in China, with Henan Province showing the highest diversity. Moreover, Chinese lineage 1 viruses have developed an endemic NADC30‐like cluster. The demographic feature of this cluster showed a more or less constant population expansion history with a recent decreasing trend. Moreover, the genome recombination of Chinese lineage 1 with two dominant clusters (Chinese HP‐PRRSVs: lineage 8.7 and VR2332‐like: lineage 5.1) was frequently detected, both of which have commercial vaccine strains available. Furthermore, recombination hotspots were discovered near NSP9 and ORF2‐4 regions of the genome. Overall, these findings provide important insights into the evolution and geographical diversity of Chinese lineage 1 PRRSV. These results will facilitate the development of programmes for the control and prevention of the emerging lineage 1 viruses in China.