Bloom M E, Alexandersen S, Perryman S, Lechner D, Wolfinbarger J B
J Virol. 1988 Aug;62(8):2903-15. doi: 10.1128/JVI.62.8.2903-2915.1988.
A DNA sequence of 4,592 nucleotides (nt) was derived for the nonpathogenic ADV-G strain of Aleutian mink disease parvovirus (ADV). The 3'(left) end of the virion strand contained a 117-nt palindrome that could assume a Y-shaped configuration similar to, but less stable than, that of other parvoviruses. The sequence obtained for the 5' end was incomplete and did not contain the 5' (right) hairpin structure but ended just after a 25-nt A + T-rich direct repeat. Features of ADV genomic organization are (i) major left (622 amino acids) and right (702 amino acids) open reading frames (ORFs) in different translational frames of the plus-sense strand, (ii) two short mid-ORFs, (iii) eight potential promoter motifs (TATA boxes), including ones at 3 and 36 map units, and (iv) six potential polyadenylation sites, including three clustered near the termination of the right ORF. Although the overall homology to other parvoviruses is less than 50%, there are short conserved amino acid regions in both major ORFs. However, two regions in the right ORF allegedly conserved among the parvoviruses were not present in ADV. At the DNA level, ADV-G is 97.5% related to the pathogenic ADV-Utah 1. A total of 22 amino acid changes were found in the right ORF; changes were found in both hydrophilic and hydrophobic regions and generally did not affect the theoretical hydropathy. However, there is a short heterogeneous region at 64 to 65 map units in which 8 out of 11 residues have diverged; this hypervariable segment may be analogous to short amino acid regions in other parvoviruses that determine host range and pathogenicity. These findings suggested that this region may harbor some of the determinants responsible for the differences in pathogenicity of ADV-G and ADV-Utah 1.
推导得到了阿留申水貂病细小病毒(ADV)非致病性ADV - G株的一段4592个核苷酸(nt)的DNA序列。病毒链的3'(左)端包含一个117 nt的回文序列,该序列可形成一种Y形结构,与其他细小病毒的类似,但稳定性较差。所获得的5'端序列不完整,不包含5'(右)发夹结构,而是在一个25 nt富含A + T的直接重复序列之后结束。ADV基因组组织的特征包括:(i)正义链不同翻译框架中的主要左(622个氨基酸)和右(702个氨基酸)开放阅读框(ORF);(ii)两个短的中间ORF;(iii)八个潜在的启动子基序(TATA框),包括位于3和36个图位处的基序;(iv)六个潜在的聚腺苷酸化位点,包括三个聚集在右ORF终止附近的位点。尽管与其他细小病毒的总体同源性低于50%,但在两个主要ORF中都有短的保守氨基酸区域。然而,在ADV中不存在据称在细小病毒中保守的右ORF中的两个区域。在DNA水平上,ADV - G与致病性ADV - Utah 1的相关性为97.5%。在右ORF中总共发现了22个氨基酸变化;在亲水和疏水区域均有变化,且一般不影响理论亲水性。然而,在64至65个图位处有一个短的异质区域,其中11个残基中有8个发生了分歧;这个高变区段可能类似于其他细小病毒中决定宿主范围和致病性的短氨基酸区域。这些发现表明,该区域可能包含一些负责ADV - G和ADV - Utah 1致病性差异的决定因素。