Johnson K N, Zeddam J L, Ball L A
Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
J Virol. 2000 Jun;74(11):5123-32. doi: 10.1128/jvi.74.11.5123-5132.2000.
Pariacoto virus (PaV) was recently isolated in Peru from the Southern armyworm (Spodoptera eridania). PaV particles are isometric, nonenveloped, and about 30 nm in diameter. The virus has a bipartite RNA genome and a single major capsid protein with a molecular mass of 39.0 kDa, features that support its classification as a Nodavirus. As such, PaV is the first Alphanodavirus to have been isolated from outside Australasia. Here we report that PaV replicates in wax moth larvae and that PaV genomic RNAs replicate when transfected into cultured baby hamster kidney cells. The complete nucleotide sequences of both segments of the bipartite RNA genome were determined. The larger genome segment, RNA1, is 3,011 nucleotides long and contains a 973-amino-acid open reading frame (ORF) encoding protein A, the viral contribution to the RNA replicase. During replication, a 414-nucleotide long subgenomic RNA (RNA3) is synthesized which is coterminal with the 3' end of RNA1. RNA3 contains a small ORF which could encode a protein of 90 amino acids similar to the B2 protein of other alphanodaviruses. RNA2 contains 1,311 nucleotides and encodes the 401 amino acids of the capsid protein precursor alpha. The amino acid sequences of the PaV capsid protein and the replicase subunit share 41 and 26% identity with homologous proteins of Flock house virus, the best characterized of the alphanodaviruses. These and other sequence comparisons indicate that PaV is evolutionarily the most distant of the alphanodaviruses described to date, consistent with its novel geographic origin. Although the PaV capsid precursor is cleaved into the two mature capsid proteins beta and gamma, the amino acid sequence at the cleavage site, which is Asn/Ala in all other alphanodaviruses, is Asn/Ser in PaV. To facilitate the investigation of PaV replication in cultured cells, we constructed plasmids that transcribed full-length PaV RNAs with authentic 5' and 3' termini. Transcription of these plasmids in cells recreated the replication of PaV RNA1 and RNA2, synthesis of subgenomic RNA3, and translation of viral proteins A and alpha.
帕里亚科托病毒(PaV)最近在秘鲁从南方黏虫(草地贪夜蛾)中分离得到。PaV病毒粒子呈等轴对称,无包膜,直径约30纳米。该病毒具有双分体RNA基因组和一种分子量为39.0 kDa的主要衣壳蛋白,这些特征支持将其归类为诺达病毒。因此,PaV是首个从澳大拉西亚以外地区分离得到的α-诺达病毒。在此我们报告,PaV可在蜡螟幼虫中复制,并且当转染到培养的幼仓鼠肾细胞中时,PaV基因组RNA也能复制。我们测定了双分体RNA基因组两个片段的完整核苷酸序列。较大的基因组片段RNA1长度为3011个核苷酸,包含一个973个氨基酸的开放阅读框(ORF),编码蛋白A,这是病毒对RNA复制酶的贡献。在复制过程中,会合成一个414个核苷酸长的亚基因组RNA(RNA3),它与RNA1的3'末端共末端。RNA3包含一个小的ORF,可编码一个90个氨基酸的蛋白质,类似于其他α-诺达病毒的B2蛋白。RNA2包含1311个核苷酸,编码衣壳蛋白前体α的401个氨基酸。PaV衣壳蛋白和复制酶亚基的氨基酸序列与禽舍病毒同源蛋白的同一性分别为41%和26%,禽舍病毒是α-诺达病毒中特征最明确的。这些以及其他序列比较表明,PaV在进化上是迄今为止所描述的α-诺达病毒中距离最远的,这与其新的地理起源一致。尽管PaV衣壳前体被切割成两种成熟的衣壳蛋白β和γ,但切割位点的氨基酸序列在所有其他α-诺达病毒中是Asn/Ala,而在PaV中是Asn/Ser。为便于研究PaV在培养细胞中的复制,我们构建了能转录具有真实末端5'和3'的全长PaV RNA的质粒。这些质粒在细胞中的转录重现了PaV RNA1和RNA2的复制、亚基因组RNA3的合成以及病毒蛋白A和α的翻译。