Laidlaw Stephen M, Skinner Michael A
Institute for Animal Health, Division of Molecular Biology, Compton, Newbury, Berks RG20 7NN, UK.
J Gen Virol. 2004 Feb;85(Pt 2):305-322. doi: 10.1099/vir.0.19568-0.
The 266 kbp genome sequence of plaque-purified, tissue culture-adapted, attenuated European Fowlpox virus FP9 has been determined and compared with the 288 kbp sequence of a pathogenic US strain (FPVUS). FP9 carries 244 of the 260 reported FPVUS ORFs (both viruses also have an unreported orthologue of conserved poxvirus gene A14.5L). Relative to FPVUS, FP9 differed by 118 mutations (26 deletions, 15 insertions and 77 base substitutions), affecting FP9 equivalents of 71 FPVUS ORFs. To help to identify mutations involved in adaptation and attenuation, the virulent parent of FP9, HP1, was sequenced at positions where FP9 differed from FPVUS. At 68 positions, FP9 and HP1 sequences were identical, reflecting differences between American and European lineages. Mutations at the remaining 50 positions in FP9 relative to FPVUS and HP1, involving 46 ORFs, therefore accounted for adaptation and attenuation. ORFs deleted during passage included those encoding members of multigene families: 12 ankyrin repeat proteins, three C-type lectin-like proteins, two C4L/C10L-like proteins, one G-protein coupled receptor protein, one V-type Ig domain protein, two N1R/p28 proteins and one EFc family protein. Tandem ORFs encoding Variola virus B22R orthologues were fused by a 5.8 kbp deletion. Single-copy genes disrupted or deleted during passage included those encoding a homologue of murine T10, a conserved DNA/pantothenate metabolism flavoprotein, photolyase, the A-type inclusion protein and an orthologue of vaccinia A47L. Gene assignments have been updated for DNase II/DLAD, binding proteins for IL-18 and interferon-gamma, phospholipid hydroperoxide glutathione peroxidase (PHGPX/GPX-4) and for a highly conserved homologue of ELOVL4.
已测定经蚀斑纯化、适应组织培养且减毒的欧洲鸡痘病毒FP9的266kbp基因组序列,并与致病性美国毒株(FPVUS)的288kbp序列进行了比较。FP9携带了260个已报道的FPVUS开放阅读框(ORF)中的244个(两种病毒还都有一个未报道的痘病毒保守基因A14.5L的直系同源物)。相对于FPVUS,FP9有118个突变(26个缺失、15个插入和77个碱基替换),影响了71个FPVUS ORF的FP9对应物。为了帮助鉴定参与适应和减毒的突变,对FP9的强毒株亲本HP1在FP9与FPVUS不同的位置进行了测序。在68个位置,FP9和HP1序列相同,反映了美国和欧洲谱系之间的差异。因此,相对于FPVUS和HP1,FP9中其余50个位置的突变(涉及46个ORF)导致了适应和减毒。传代过程中缺失的ORF包括那些编码多基因家族成员的:12个锚蛋白重复蛋白、3个C型凝集素样蛋白、2个C4L/C10L样蛋白、1个G蛋白偶联受体蛋白、1个V型免疫球蛋白结构域蛋白、2个N1R/p28蛋白和1个EFc家族蛋白。编码天花病毒B22R直系同源物的串联ORF通过一个5.8kbp的缺失而融合。传代过程中被破坏或缺失的单拷贝基因包括那些编码小鼠T10同源物、一种保守的DNA/泛酸盐代谢黄素蛋白、光裂合酶、A型包涵体蛋白和痘苗病毒A47L直系同源物的基因。已更新了对脱氧核糖核酸酶II/DLAD、白细胞介素-18和干扰素-γ结合蛋白、磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPX/GPX-4)以及ELOVL4高度保守同源物的基因注释。