Barinder Singh
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Barinder Singh has a total of 3 co-authors. Here are the top co-authors by number of shared publications:
- Faryal Dar
Vaccinology & Immunotherapeutics Program, School of Public Health, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada
2 shared publications - Shermila Kulanayake
Vaccinology & Immunotherapeutics Program, School of Public Health, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada
2 shared publications - Suresh Kumar Tikoo
Vaccinology & Immunotherapeutics Program, School of Public Health, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada
2 shared publications
Latest Publications
- Open Access
RETRACTED: Kulanayake et al. Role of Protein VII in the Production of Infectious Bovine Adenovirus-3 Virion. Viruses 2024, 16, 1323
The journal retracts the article “Role of Protein VII in the Production of Infectious Bovine Adenovirus-3 Virion”
Open AccessRETRACTED: Kulanayake et al. Role of Protein VII in the Production of Infectious Bovine Adenovirus-3 Virion. Viruses 2024, 16, 1323
The journal retracts the article “Role of Protein VII in the Production of Infectious Bovine Adenovirus-3 Virion”
- Open Access
RETRACTED: Role of Protein VII in the Production of Infectious Bovine Adenovirus-3 Virion
Bovine adenovirus (BAdV)-3 genome encodes a 26 kDa core protein designated as protein VII, which localizes to the nucleus/nucleolus. The requirement of a protein VII-complementing cell line for the replication of VII-deleted BAdV-3 suggests that protein VII is required for the production of infectious progeny virions. An analysis of the BAV.VIId+ virus (only phenotypically positive for protein VII) detected no noticeable differences in the expression and incorporation of viral proteins in the virions. Moreover, protein VII does not appear to be essential for the formation of mature BAV.VIId+. However, protein VII appeared to be required for the efficient assembly of mature BAV.VIId- virions. An analysis of the BAV.VIId- virus (genotypically and phenotypically negative for protein VII) in non-complementing cells detected the inefficient release of virions from endosomes, which affected the expression of viral proteins or DNA replication. Moreover, the absence of protein VII altered the proteolytic cleavage of protein VI of BAV.VIId-. Our results suggest that BAdV-3 protein VII appears to be required for efficient production of mature virions. Moreover, the absence of protein VII produces non-infectious BAdV-3 by altering the release of BAdV-3 from endosomes/vesicles.
Open AccessRETRACTED: Role of Protein VII in the Production of Infectious Bovine Adenovirus-3 Virion
Bovine adenovirus (BAdV)-3 genome encodes a 26 kDa core protein designated as protein VII, which localizes to the nucleus/nucleolus. The requirement of a protein VII-complementing cell line for the replication of VII-deleted BAdV-3 suggests that protein VII is required for the production of infectious progeny virions. An analysis of the BAV.VIId+ virus (only phenotypically positive for protein VII) detected no noticeable differences in the expression and incorporation of viral proteins in the virions. Moreover, protein VII does not appear to be essential for the formation of mature BAV.VIId+. However, protein VII appeared to be required for the efficient assembly of mature BAV.VIId- virions. An analysis of the BAV.VIId- virus (genotypically and phenotypically negative for protein VII) in non-complementing cells detected the inefficient release of virions from endosomes, which affected the expression of viral proteins or DNA replication. Moreover, the absence of protein VII altered the proteolytic cleavage of protein VI of BAV.VIId-. Our results suggest that BAdV-3 protein VII appears to be required for efficient production of mature virions. Moreover, the absence of protein VII produces non-infectious BAdV-3 by altering the release of BAdV-3 from endosomes/vesicles.