Ardisson-Araújo Daniel M P, Lima Rayane Nunes, Melo Fernando L, Clem Rollie J, Huang Ning, Báo Sônia Nair, Sosa-Gómez Daniel R, Ribeiro Bergmann M
Laboratory of Baculovirus, Cell Biology Department, University of Brasília, Brasília, DF, Brazil.
Division of Biology, Kansas State University, Manhattan, KS, USA.
Sci Rep. 2016 Jun 7;6:24612. doi: 10.1038/srep24612.
The genome of a novel group II alphabaculovirus, Perigonia lusca single nucleopolyhedrovirus (PeluSNPV), was sequenced and shown to contain 132,831 bp with 145 putative ORFs (open reading frames) of at least 50 amino acids. An interesting feature of this novel genome was the presence of a putative nucleotide metabolism enzyme-encoding gene (pelu112). The pelu112 gene was predicted to encode a fusion of thymidylate kinase (tmk) and dUTP diphosphatase (dut). Phylogenetic analysis indicated that baculoviruses have independently acquired tmk and dut several times during their evolution. Two homologs of the tmk-dut fusion gene were separately introduced into the Autographa californica multiple nucleopolyhedrovirus (AcMNPV) genome, which lacks tmk and dut. The recombinant baculoviruses produced viral DNA, virus progeny, and some viral proteins earlier during in vitro infection and the yields of viral occlusion bodies were increased 2.5-fold when compared to the parental virus. Interestingly, both enzymes appear to retain their active sites, based on separate modeling using previously solved crystal structures. We suggest that the retention of these tmk-dut fusion genes by certain baculoviruses could be related to accelerating virus replication and to protecting the virus genome from deleterious mutation.
对一种新型II组杆状病毒——甘薯天蛾单核多角体病毒(PeluSNPV)的基因组进行了测序,结果显示其基因组包含132,831个碱基对,有145个推定的开放阅读框(ORF),每个ORF至少含50个氨基酸。这个新基因组的一个有趣特征是存在一个推定的核苷酸代谢酶编码基因(pelu112)。预测pelu112基因编码胸苷酸激酶(tmk)和dUTP二磷酸酶(dut)的融合蛋白。系统发育分析表明,杆状病毒在进化过程中曾多次独立获得tmk和dut。将tmk-dut融合基因的两个同源基因分别导入缺乏tmk和dut的苜蓿银纹夜蛾多核多角体病毒(AcMNPV)基因组中。重组杆状病毒在体外感染早期产生病毒DNA、病毒后代和一些病毒蛋白,与亲本病毒相比,病毒包涵体产量提高了2.5倍。有趣的是,根据使用先前解析的晶体结构进行的单独建模,这两种酶似乎都保留了它们的活性位点。我们认为,某些杆状病毒保留这些tmk-dut融合基因可能与加速病毒复制以及保护病毒基因组免受有害突变有关。