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A Vaccine Targeting Ovine Herpesvirus 2 Glycoprotein B Protects against Sheep-Associated Malignant Catarrhal Fever.
Cunha, Cristina W; Baker, Katherine N; O'Toole, Donal; Cole, Emily; Shringi, Smriti; Dewals, Benjamin G; Vanderplasschen, Alain; Li, Hong.
Afiliação
  • Cunha CW; Animal Disease Research Unit, Agricultural Research Service, USDA, Pullman, WA 99164, USA.
  • Baker KN; Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164, USA.
  • O'Toole D; Animal Disease Research Unit, Agricultural Research Service, USDA, Pullman, WA 99164, USA.
  • Cole E; Department of Veterinary Sciences, University of Wyoming, Laramie, WY 82070, USA.
  • Shringi S; Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164, USA.
  • Dewals BG; Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164, USA.
  • Vanderplasschen A; Fundamental and Applied Research in Animals and Health (FARAH), Immunology-Vaccinology, Faculty of Veterinary Medicine, University of Liège, 4000 Liège, Belgium.
  • Li H; Fundamental and Applied Research in Animals and Health (FARAH), Immunology-Vaccinology, Faculty of Veterinary Medicine, University of Liège, 4000 Liège, Belgium.
Vaccines (Basel) ; 10(12)2022 Dec 15.
Article em En | MEDLINE | ID: mdl-36560568
Malignant catarrhal fever (MCF) is a complex and often fatal disease of ungulates. Effective vaccines are needed to avoid MCF outbreaks and mitigate losses. This study aimed to evaluate a sheep-associated MCF (SA-MCF) vaccine candidate targeting ovine herpesvirus 2 (OvHV-2) glycoprotein B (gB). Rabbits were used as a laboratory animal model to test the safety, immunogenicity, and protective efficacy of a chimeric virus consisting of a recombinant, non-pathogenic strain of alcelaphine herpesvirus-1 encoding OvHV-2 ORF8 to express gB (AlHV-1∆ORF73/OvHV-2-ORF8). Viral-vectored immunizations were performed by using the AlHV-1∆ORF73/OvHV-2-ORF8 chimera alone or as a DNA prime (OvHV-2-ORF8)-virus boost regimen. The viral vector was inoculated by intravenous or intramuscular routes and the DNA was delivered by intradermal shots using a gene gun. The vaccine candidates were deemed safe as no clinical signs were observed following any of the immunizations. Anti-OvHV-2 gB antibodies with neutralizing activity were induced by all immunogens. At three weeks post-final immunization, all animals were challenged intranasally with a lethal dose of OvHV-2. MCF protection rates ranging from 66.7% to 71.4% were observed in vaccinated rabbits, while all mock-vaccinated animals developed the disease. The significant protective efficacy obtained with the vaccine platforms tested in this study encourages further trials in relevant livestock species, such as cattle and bison.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article