| Literature DB >> 27212681 |
Leyuan Zhu1, Shan Zhang1, Zihao Deng1, Zhihong Huang1, Meijin Yuan1, Wenbi Wu2, Kai Yang3.
Abstract
The Autographa californica multiple nucleopolyhedrovirus (AcMNPV) ac110 gene is especially conserved in lepidopteran-specific baculoviruses and is uncharacterized. To investigate the role of ac110 in the baculovirus life cycle, an ac110-knockout (vAc110KO) and a repair (vAc110:HA) viruses were constructed in this study. Budded virion production and occlusion body formation were unaffected in vAc110KO-transfected or infected Sf9 cells. Intrahemocoelic injection of budded virions of vAc110KO killed Trichoplusia ni larvae as efficiently as the repair or the wild-type viruses. However, per os inoculation of occlusion bodies of vAc110KO failed to establish infection in T. ni larvae, while the repair virus was as efficient as the wild-type virus. Treatment with calcofluor white, a reagent that damages the peritrophic membrane, did not rescue the oral infectivity of vAc110KO. These results suggested that Ac110 is a new per os infectivity factor that may play a role after occlusion-derived virions pass through the peritrophic membrane during oral infection.Entities:
Keywords: AcMNPV; Baculovirus; Peritrophic membrane; ac110; per os infectivity factor
Mesh:
Year: 2016 PMID: 27212681 DOI: 10.1016/j.virusres.2016.05.017
Source DB: PubMed Journal: Virus Res ISSN: 0168-1702 Impact factor: 3.303