Zhu Shan-Ying, Yi Jian-Ping, Shen Wei-De, Wang Li-Qun, He Hua-Gang, Wang Yong, Li Bing, Wang Wen-Bing
Institute of Life Sciences, Jiangsu University, Zhenjiang 212013, PR China.
BMC Genomics. 2009 Feb 25;10:91. doi: 10.1186/1471-2164-10-91.
Baculoviruses are well known for their potential as biological agents for controlling agricultural and forest pests. They are also widely used as expression vectors in molecular cloning studies. The genome sequences of 48 baculoviruses are currently available in NCBI databases. As the number of sequenced viral genomes increases, it is important for the authors to present sufficiently detailed analyses and annotations to advance understanding of them. In this study, the complete genome of Clanis bilineata nucleopolyhedrovirus (ClbiNPV) has been sequenced and analyzed in order to understand this virus better.
The genome of ClbiNPV contains 135,454 base pairs (bp) with a G+C content of 37%, and 139 putative open reading frames (ORFs) of at least 150 nucleotides. One hundred and twenty-six of these ORFs have homologues with other baculovirus genes while the other 13 are unique to ClbiNPV. The 30 baculovirus core genes are all present in ClbiNPV. Phylogenetic analysis based on the combined pif-2 and lef-8 sequences places ClbiNPV in the Group II Alphabaculoviruses. This result is consistent with the absence of gp64 from the ClbiNPV genome and the presence instead of a fusion protein gene, characteristic of Group II. Blast searches revealed that ClbiNPV encodes a photolyase-like gene sequence, which has a 1-bp deletion when compared with photolyases of other baculoviruses. This deletion disrupts the sequence into two small photolyase ORFs, designated Clbiphr-1 and Clbiphr-2, which correspond to the CPD-DNA photolyase and FAD-binding domains of photolyases, respectively.
ClbiNPV belongs to the Group II Alphabaculoviruses and is most closely related to OrleNPV, LdMNPV, TnSNPV, EcobNPV and ChchNPV. It contains a variant DNA photolyase gene, which only exists in ChchNPV, TnSNPV and SpltGV among the baculoviruses.
杆状病毒以其作为控制农业和森林害虫的生物制剂的潜力而闻名。它们也被广泛用作分子克隆研究中的表达载体。目前NCBI数据库中已有48种杆状病毒的基因组序列。随着测序病毒基因组数量的增加,作者进行充分详细的分析和注释以促进对它们的理解变得很重要。在本研究中,为了更好地了解双线盗毒蛾核多角体病毒(ClbiNPV),对其全基因组进行了测序和分析。
ClbiNPV的基因组包含135,454个碱基对(bp),G+C含量为37%,有139个推定的开放阅读框(ORF),长度至少为150个核苷酸。其中126个ORF与其他杆状病毒基因有同源性,另外13个是ClbiNPV特有的。30个杆状病毒核心基因在ClbiNPV中均有存在。基于pif-2和lef-8序列组合的系统发育分析将ClbiNPV置于Ⅱ组甲型杆状病毒中。这一结果与ClbiNPV基因组中不存在gp64而是存在融合蛋白基因(Ⅱ组的特征)一致。Blast搜索显示ClbiNPV编码一个类似光裂合酶的基因序列,与其他杆状病毒的光裂合酶相比,该序列有一个1-bp的缺失。这个缺失将序列分成两个小的光裂合酶ORF,分别命名为Clbiphr-1和Clbiphr-2,它们分别对应于光裂合酶的CPD-DNA光裂合酶和FAD结合结构域。
ClbiNPV属于Ⅱ组甲型杆状病毒,与OrleNPV、LdMNPV、TnSNPV、EcobNPV和ChchNPV关系最为密切。它包含一个变异的DNA光裂合酶基因,该基因在杆状病毒中仅存在于ChchNPV、TnSNPV和SpltGV中。