Peer-reviewed veterinary case report
Safety and immunogenicity of an attenuated Chinese pseudorabies variant by dual deletion of TK&gE genes.
- Journal:
- BMC veterinary research
- Year:
- 2018
- Authors:
- Wang, Jichun et al.
- Affiliation:
- National Research Center of Engineering and Technology for Veterinary Biologicals/Institute of Veterinary Immunology & Engineering · China
- Species:
- rodent
Abstract
BACKGROUND: Since the outbreak of a new emerging virulent pseudorabies virus mutant in Chinese pig herds, intensive research has been focused on the construction of novel gene deletion vaccine based on the variant virulent viruses. An ideal vaccine candidate is expected to have a balanced safety and immunogenicity. RESULTS: From the infectious clone of PRV AH02LA strain, a TK deletion mutant was generated through two-step Red mutagenesis. After homologous recombination with a transfer vector, a TK&gE dual deficient mutant PRV (PRV) was generated, and its structure verified by PCR, RFLP and sequencing. Growth kinetics test showed that PRVreached a titer of 10TCID/mL on ST cells. The PRVat a dose of 10TCID/animal was not virulent in mice or 1-day-old piglets with maternal PRV antibodies. No clinical signs or virus shedding were detected in 28~ 35-day-old piglets without maternal PRV antibodies after nasal or intramuscular administration with a dose of 10TCID, although it caused one death of four 1-day-old piglets without maternal PRV antibodies. In the efficiency test of PRV, all four 28~ 35-day-old piglets without PRV antibody in the challenge control showed typical clinical symptoms and virus shedding, and two died at 4~ 5 days post challenge. All piglets in 10, 10and 10TCID/dose PRVgroups provided complete protection against challenge at only 7 days post intramuscular vaccination. More importantly, PRVstopped virus shedding in these piglets. In contrast, all four piglets in PRV Bartha K61 vaccine group developed high body temperature (≥40.5 °C) and viral shedding, despite they had mild or even no clinical symptoms. CONCLUSIONS: The constructed TK&gE dual deletion mutant PRVcan reach high titers on ST cells. The live vaccine of PRVis highly safe, and can not only provide clinical protection but also stops virus shedding. This study suggests that PRVmight work as a promising vaccine candidate to combat the PRV variant emerging in Chinese herds since 2011.
Find similar cases for your pet
PetCaseFinder finds other peer-reviewed reports of pets with the same symptoms, plus a plain-English summary of what was tried across them.
Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/30241529/