| Literature DB >> 33683665 |
Tong Chen1,2, Xiaoyan Duan1,2, Hengrui Hu1,2, Yu Shang1, Yangbo Hu1, Fei Deng1, Hualin Wang1, Manli Wang3, Zhihong Hu4.
Abstract
Baculoviruses have been widely used as a vector for expressing foreign genes. Among numerous baculoviruses, Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is the most frequently used and it encodes 155 open reading frames (ORFs). Here, we systematically investigated the impact of 42 genes of AcMNPV on the production of infectious budded viruses (BVs) by constructing gene-knockout bacmids and subsequently conducting transfection and infection assays. The results showed that among the 39 functionally unverified genes and 3 recently reported genes, 36 are dispensable for infectious BV production, as the one-step growth curves of the gene-knockout viruses were not significantly different from those of the parental virus. Three genes (ac62, ac82 and ac106/107) are essential for infectious BV production, as deletions thereof resulted in complete loss of infectivity while the repaired viruses showed no significant difference in comparison to the parental virus. In addition, three genes (ac13, ac51 and ac120) are important but not essential for infectious BV production, as gene-knockout viruses produced significantly lower BV levels than that of the parental virus or repaired viruses. We then grouped the 155 AcMNPV genes into three categories (Dispensable, Essential, or Important for infectious BV production). Based on our results and previous publications, we constructed a schematic diagram of a potential mini-genome of AcMNPV, which contains only essential and important genes. The results shed light on our understanding of functional genomics of baculoviruses and provide fundamental information for future engineering of baculovirus expression system.Entities:
Keywords: Autographa californica multiple nucleopolyhedrovirus (AcMNPV); BV production; Dispensable genes; Essential genes; Important genes
Mesh:
Year: 2021 PMID: 33683665 PMCID: PMC8379328 DOI: 10.1007/s12250-021-00355-1
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327