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January 23, 2026Microorganisms0 citationsOpen Access

A Recombinant Porcine Epidemic Diarrhea Virus with Multiple S2 Subunit Mutations from China: Isolation, Genetic Characterization, and Pathogenicity Analysis

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NYNana YanJXJingru XuYLYuqi Li

Key Points

  • The aim is to understand the genetic evolution and pathogenicity of a novel PEDV strain from China.
  • Isolated a new PEDV strain from intestinal samples of a diarrheal piglet.
  • Sequenced the complete genome of the PEDV strain.
  • Conducted phylogenetic and recombination analyses to assess genetic relationships.
  • Identified PEDV/FJLY202201 as a recombinant strain from G2a and G2b.
  • Found multiple mutations in the S2 subunit; their occurrence is rarely reported.
  • Piglets challenged with the strain showed 30.35% weight loss and 100% mortality, indicating high virulence.

Abstract

Porcine epidemic diarrhea virus (PEDV) is a major cause of fatal diarrhea in piglets. The continuous emergence of new variants, driven by recombination and mutation, poses a persistent global threat to the swine industry, resulting in significant economic losses. Therefore, ongoing surveillance of PEDV evolution is critical. In this study, we isolated a novel PEDV strain, designated PEDV/FJLY202201, from experimental intestinal samples collected from a diarrheal piglet in Fujian, China, and sequenced its complete genome. Complete genome analysis, phylogenetic analysis, and recombination analysis were conducted. Results showed that PEDV/FJLY202201 was a recombinant strain derived from two recombination events between G2a and G2b strains, with three breakpoints located in the ORF1b, Domain 0 (D0) and S2 subunit, respectively. Notably, multiple mutations were identified in the S2 subunit, a finding that has been rarely reported before. Furthermore, following challenge with the PEDV/FJLY202201 strain, 3-day-old piglets exhibited severe diarrhea, sustained a 30.35% weight loss, and reached 100% mortality, collectively demonstrating its high virulence. These data reveal the complex evolution of PEDV/FJLY202201 and provide a foundation for a better understanding of the genetic evolution and molecular pathogenesis of PEDV.

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Cite This Study

Yan et al. (2026) studied this question.

synapsesocial.com/papers/69730f59c8125b09b0d1f295https://doi.org/10.3390/microorganisms14010242
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