Deletion of a 197-Amino-Acid Region in the N-Terminal Domain of Spike Protein Attenuates Porcine Epidemic Diarrhea Virus in Piglets

Public Deposited
Analytics

Downloadable Content

Download PDF
Request Version for Screen Reader
Creator
  • Hou, Yixuan
    • Other Affiliation: Department of Veterinary Preventive Medicine; The Ohio State University
  • Lin, Chun-Ming
    • Other Affiliation: Department of Veterinary Preventive Medicine; The Ohio State University
  • Yokoyama, Masaru
    • Other Affiliation: Pathogen Genomics Center; National Institute of Infectious Diseases
  • Yount, Boyd L.
    • Affiliation: University of North Carolina at Chapel Hill
  • Marthaler, Douglas
    • Other Affiliation: Department of Veterinary Population Medicine; College of Veterinary Medicine; University of Minnesota
  • Douglas, Arianna L.
    • Affiliation: University of North Carolina at Chapel Hill
  • Ghimire, Shristi
    • Other Affiliation: Department of Veterinary Preventive Medicine; The Ohio State University
  • Qin, Yibin
    • Other Affiliation: Department of Virology; Guangxi Veterinary Research Institute
  • Baric, Ralph S.
    • Affiliation: University of North Carolina at Chapel Hill
  • Saif, Linda J.
    • Other Affiliation: Department of Veterinary Preventive Medicine; The Ohio State University
  • Wang, Qiuhong
    • Other Affiliation: Department of Veterinary Preventive Medicine; The Ohio State University
Abstract
  • ABSTRACT We previously isolated a porcine epidemic diarrhea virus (PEDV) strain, PC177, by blind serial passaging of the intestinal contents of a diarrheic piglet in Vero cell culture. Compared with the highly virulent U.S. PEDV strain PC21A, the tissue culture-adapted PC177 (TC-PC177) contains a 197-amino-acid (aa) deletion in the N-terminal domain of the spike (S) protein. We orally inoculated neonatal, conventional suckling piglets with TC-PC177 or PC21A to compare their pathogenicities. Within 7 days postinoculation, TC-PC177 caused mild diarrhea and lower fecal viral RNA shedding, with no mortality, whereas PC21A caused severe clinical signs and 55% mortality. To investigate whether infection with TC-PC177 can induce cross-protection against challenge with a highly virulent PEDV strain, all the surviving piglets were challenged with PC21A at 3 weeks postinoculation. Compared with 100% protection in piglets initially inoculated with PC21A, 88% and 100% TC-PC177- and mock-inoculated piglets had diarrhea following challenge, respectively, indicating incomplete cross-protection. To investigate whether this 197-aa deletion was the determinant for the attenuation of TC-PC177, we generated a mutant (icPC22A-S1Δ197) bearing the 197-aa deletion from an infectious cDNA clone of the highly virulent PEDV PC22A strain (infectious clone PC22A, icPC22A). In neonatal gnotobiotic pigs, the icPC22A-S1Δ197 virus caused mild to moderate diarrhea, lower titers of viral shedding, and no mortality, whereas the icPC22A virus caused severe diarrhea and 100% mortality. Our data indicate that deletion of this 197-aa fragment in the spike protein can attenuate a highly virulent PEDV, but the virus may lose important epitopes for inducing robust protective immunity. IMPORTANCE The emerging, highly virulent PEDV strains have caused substantial economic losses worldwide. However, the virulence determinants are not established. In this study, we found that a 197-aa deletion in the N-terminal region of the S protein did not alter virus (TC-PC177) tissue tropism but reduced the virulence of the highly virulent PEDV strain PC22A in neonatal piglets. We also demonstrated that the primary infection with TC-PC177 failed to induce complete cross-protection against challenge by the highly virulent PEDV PC21A, suggesting that the 197-aa region may contain important epitopes for inducing protective immunity. Our results provide an insight into the role of this large deletion in virus propagation and pathogenicity. In addition, the reverse genetics platform of the PC22A strain was further optimized for the rescue of recombinant PEDV viruses in vitro . This breakthrough allows us to investigate other virulence determinants of PEDV strains and will provide knowledge leading to better control PEDV infections.
Date of publication
Keyword
DOI
Identifier
Resource type
  • Article
Rights statement
  • In Copyright
Journal title
  • Journal of Virology
Journal volume
  • 91
Journal issue
  • 14
Page start
  • e00227-17
Language
  • English
ISSN
  • 0022-538X
  • 1098-5514
  • 1070-6321

Relations

Parents:

This work has no parents.

Items

Thumbnail Title Date Uploaded Visibility Actions
file details PubMedCentral-PMC5487580.pdf 2017 Public Download