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Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence

Porcine reproductive and respiratory syndrome virus (PRRSV) causes huge economic loss to the global swine industry. Even though several control strategies have been applied, PRRS is still not effectively controlled due to the continuous emergence of new variants and limited cross-protection by curre...

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Autores principales: Chen, Nanhua, Ye, Mengxue, Huang, Yucheng, Li, Shuai, Xiao, Yanzhao, Li, Xinshuai, Li, Shubin, Li, Xiangdong, Yu, Xiuling, Tian, Kegong, Zhu, Jianzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783987/
https://www.ncbi.nlm.nih.gov/pubmed/31540541
http://dx.doi.org/10.3390/v11090875
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author Chen, Nanhua
Ye, Mengxue
Huang, Yucheng
Li, Shuai
Xiao, Yanzhao
Li, Xinshuai
Li, Shubin
Li, Xiangdong
Yu, Xiuling
Tian, Kegong
Zhu, Jianzhong
author_facet Chen, Nanhua
Ye, Mengxue
Huang, Yucheng
Li, Shuai
Xiao, Yanzhao
Li, Xinshuai
Li, Shubin
Li, Xiangdong
Yu, Xiuling
Tian, Kegong
Zhu, Jianzhong
author_sort Chen, Nanhua
collection PubMed
description Porcine reproductive and respiratory syndrome virus (PRRSV) causes huge economic loss to the global swine industry. Even though several control strategies have been applied, PRRS is still not effectively controlled due to the continuous emergence of new variants and limited cross-protection by current vaccines. During the routine epidemiological investigation in 2017, two PRRSV variants were identified from a severe abortion farm and a clinically healthy farm, respectively. The viruses were isolated and denominated as XJ17-5 and JSTZ1712-12. Genomic sequencing indicated that their genomes are both 14,960 bp in length sharing 99.45% nucleotide identity. Sequence alignments identified a discontinuous 30-amino-acid deletion and a continuous 120-amino-acid deletion in nsp2 of both isolates. Genome-based phylogenetic analysis confirmed that XJ17-5 and JSTZ1712-12 belong to the HP-PRRSV subtype but form a new branch with other isolates containing the same 150-amino-acid deletion in nsp2. Pathogenic analysis showed that XJ17-5 is highly virulent causing 60% mortality, while JSTZ1712-12 is avirulent for piglets. Furthermore, fragment comparisons identified 34-amino-acid differences between XJ17-5 and JSTZ1712-12 that might be associated with the distinct virulence. The identification of highly homologous HP-PRRSV variants with new genetic feature and distinct virulence contributes to further analyze the pathogenesis and evolution of PRRSV in the field.
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spelling pubmed-67839872019-10-16 Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence Chen, Nanhua Ye, Mengxue Huang, Yucheng Li, Shuai Xiao, Yanzhao Li, Xinshuai Li, Shubin Li, Xiangdong Yu, Xiuling Tian, Kegong Zhu, Jianzhong Viruses Article Porcine reproductive and respiratory syndrome virus (PRRSV) causes huge economic loss to the global swine industry. Even though several control strategies have been applied, PRRS is still not effectively controlled due to the continuous emergence of new variants and limited cross-protection by current vaccines. During the routine epidemiological investigation in 2017, two PRRSV variants were identified from a severe abortion farm and a clinically healthy farm, respectively. The viruses were isolated and denominated as XJ17-5 and JSTZ1712-12. Genomic sequencing indicated that their genomes are both 14,960 bp in length sharing 99.45% nucleotide identity. Sequence alignments identified a discontinuous 30-amino-acid deletion and a continuous 120-amino-acid deletion in nsp2 of both isolates. Genome-based phylogenetic analysis confirmed that XJ17-5 and JSTZ1712-12 belong to the HP-PRRSV subtype but form a new branch with other isolates containing the same 150-amino-acid deletion in nsp2. Pathogenic analysis showed that XJ17-5 is highly virulent causing 60% mortality, while JSTZ1712-12 is avirulent for piglets. Furthermore, fragment comparisons identified 34-amino-acid differences between XJ17-5 and JSTZ1712-12 that might be associated with the distinct virulence. The identification of highly homologous HP-PRRSV variants with new genetic feature and distinct virulence contributes to further analyze the pathogenesis and evolution of PRRSV in the field. MDPI 2019-09-18 /pmc/articles/PMC6783987/ /pubmed/31540541 http://dx.doi.org/10.3390/v11090875 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Nanhua
Ye, Mengxue
Huang, Yucheng
Li, Shuai
Xiao, Yanzhao
Li, Xinshuai
Li, Shubin
Li, Xiangdong
Yu, Xiuling
Tian, Kegong
Zhu, Jianzhong
Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence
title Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence
title_full Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence
title_fullStr Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence
title_full_unstemmed Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence
title_short Identification of Two Porcine Reproductive and Respiratory Syndrome Virus Variants Sharing High Genomic Homology but with Distinct Virulence
title_sort identification of two porcine reproductive and respiratory syndrome virus variants sharing high genomic homology but with distinct virulence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783987/
https://www.ncbi.nlm.nih.gov/pubmed/31540541
http://dx.doi.org/10.3390/v11090875
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