| Literature DB >> 33845333 |
Changhoon Park1, Myung-Shin Lee1, Jong Hyuk Baek2, Sun Hee Cho2, Bang-Hun Hyun3, Su-Hwa You3, Sang-Ho Cha4.
Abstract
The objective of this study was to assess protective efficacy of vaccination using CPD-attenuated chimeric PRRSV and Toll like receptor (TLR) agonists (HSP70 c-terminal domain and HSPX) as adjuvants through different inoculation routes. In this study, a chimeric PRRSV composed of two field isolates was synthesized and attenuated by CPD in NSP1 as described in the previous study. The infection of the CPD-attenuated chimeric PRRSV to pigs of 3 weeks-old showed no clinical signs without pathological lesions in necropsy, while it induced improved cross immunity between its parent strains. The TLR agonists were expressed in E. coli and purified to be used. In challenge experiment, pigs of 3 weeks-old were vaccinated using the CPD-attenuated chimeric virus with the prepared TLR agonists through intramuscular or intradermal route, following heterologous challenge after 4 weeks of vaccination. In results, intramuscular or intradermal inoculation of the CPD-attenuated chimeric virus demonstrated excellent protective efficacy against heterologous challenges. Importantly, intradermal inoculation with the TLR agonists enhanced protective effects as shown in the significantly increased level of PRRSV-specific IFN-γ-SCs and cytokines in sera, and the significant reduction of pathological lesion and viral load in lung. This study suggested that the intradermal inoculation of CPD-attenuated chimeric PRRSV plus TLR agonists should be more effective for protection of pigs against diverse PRRS field viruses.Entities:
Keywords: Chimera; Codon-pair deoptimization; Porcine reproductive and respiratory syndrome virus; Toll like receptor (TLR) agonists; Vaccine
Year: 2021 PMID: 33845333 DOI: 10.1016/j.vetmic.2021.109048
Source DB: PubMed Journal: Vet Microbiol ISSN: 0378-1135 Impact factor: 3.293