AI Article Synopsis

  • The study identifies a new strain of porcine epidemic diarrhea virus (PEDV) from an outbreak in Chongqing, China, highlighting the rise in multiviral infections and mutations.
  • The optimal trypsin concentration for virus adaptation in Vero cells was determined to be 7.5 µg/mL, but the virus required passage in IPEC-J2 cells for successful adaptation, with a different concentration of 5 µg/mL.
  • Genetic analysis revealed that the S gene of this new strain is a recombinant from two parent strains, with significant implications for understanding PEDV evolution and vaccine development.

Article Abstract

Background: In recent years, the prevalence and incidence of porcine epidemic diarrhea virus (PEDV) infection have been on the rise. The occurrence of multiviral infections and recombination mutations has led to accelerated viral evolution and reduced vaccine efficacy. In the present study, a PEDV strain was isolated from a pig farm (Chongqing Province, China) with an outbreak of porcine diarrhea, and its S gene was found to be recombinant.

Results: The optimal trypsin concentration for blind passage of PEDV in Vero cells was determined to be 7.5 µg/mL. Following two blind passages of the virus in Vero cells, the virus was unable to adapt to the cells. Therefore, PEDV was blindly passaged in IPEC-J2 cells using the optimal concentration of trypsin (5 µg/mL). Next, a series of characterization experiments were performed. Recombination analyses of the isolates using software revealed that the S gene of strain CHCQ-2023 was derived from the primary parent strain PEDV-1 C and secondary parent strain SQ2014, with recombination occurring at a 3152 bp breakpoint. Furthermore, a specific B-cell antigenic epitope was predicted on the S2 subunit of the S protein.

Conclusion: A PEDV strain was isolated and characterized, and its S gene was characterized. The findings provide a bioinformatic basis for the study of PEDV strain variation due to genetic recombination.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11657806PMC
http://dx.doi.org/10.1186/s12917-024-04390-4DOI Listing

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