4.5 Article

Two novel porcine epidemic diarrhea virus (PEDV) recombinants from a natural recombinant and distinct subtypes of PEDV variants

Journal

VIRUS RESEARCH
Volume 242, Issue -, Pages 90-95

Publisher

ELSEVIER
DOI: 10.1016/j.virusres.2017.09.013

Keywords

Porcine epidemic diarrhea virus (PEDV); Genomic sequencing; Phylogenetic analysis; Recombination; Vaccination failure

Categories

Funding

  1. National Natural Science Foundation of China [31672523]
  2. Natural Science Foundation of Jiangsu Province [BK20170492]
  3. China Postdoctoral Science Foundation [2016M590510]
  4. University Science Research Project of Jiangsu Province [16KJD230001]
  5. Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  7. Scientific Research Foundation of Yangzhou University [137010925]
  8. LvYangJinfeng Program of Yangzhou City [yzlyjfjh2015YB120]

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Porcine epidemic diarrhea virus (PEDV) causes devastating impact on global pig-breeding industry and current vaccines have become not effective against the circulating PEDV variants since 2011. During the up-to-date investigation of PEDV prevalence in Fujian China 2016, PEDV was identified in vaccinated pig farms suffering severe diarrhea while other common diarrhea-associated pathogens were not detected. Complete genomes of two PEDV representatives (XM1-2 and XM2-4) were determined. Genomic comparison showed that these two viruses share the highest nucleotide identities (99.10% and 98.79%) with the 2011 ZMDZY strain, but only 96.65% and 96.50% nucleotide identities with the attenuated CV777 strain. Amino acid alignment of spike (S) proteins indicated that they have the similar mutation, insertion and deletion pattern as other Chinese PEDV variants but also contain several unique substitutions. Phylogenetic analysis showed that 2016 PEDV variants belong to the cluster of recombination strains but form a new branch. Recombination detection suggested that both XM1-2 and XM2-4 are inter-subgroup recombinants with breakpoints within ORF1b. Remarkably, the natural recombinant HNQX-3 isolate serves as a parental virus for both natural recombinants identified in this study. This up-to-date investigation provides the direct evidence that natural recombinants may serve as parental viruses to generate recombined PEDV progenies that are probably associated with the vaccination failure.

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