Noa-Carrazana J C, Silva-Rosales L
Centro de Investigacion y de Estudios Avanzados del IPN, Unidad Irapuato, Apdo Postal 629, Irapuato, Gto. 36500 Mexico.
Plant Dis. 2001 May;85(5):558. doi: 10.1094/PDIS.2001.85.5.558A.
Papaya mosaic virus (PMV) is a member of the Potexvirus group and has filamentous particles of 530 nm with a positive sense single-stranded RNA of 6.6Kb. PMV was detected in Mexico in diseased papaya plants growing alone and in mixed plantations with pumpkin. Reverse transcription polymerase chain reactions (RT-PCR) and standard double-antibody sandwich enzyme linked immunosorbent assay (DAS-ELISA) procedures were used on 45 leaf samples from single plants in seven locations in southeast Mexico (States of Yucatan, Campeche, and Quintana Roo). PCR primer design was based on a GenBank sequence with accession number D13957 (1). Amplified PCR products were cloned using a TOPO TA Cloning Kit and sequenced by the dideoxy chain termination method. Twenty-six samples tested positive for PMV using one or both detection techniques: 23 of 41 from papaya and three of four from pumpkin. The two sequences reported here, YY-15 and YY-22 (from papaya and pumpkin respectively, with accession numbers AYO17186 and AYO17187), were 1180 nucleotides long and contained a fragment of ORF3, the complete ORF4 and the putative CP gene, including the 3' end untranslatable region. Within the CP gene sequence, the amino acid sequence derived had a similarity of 88% with that of D13957 from the GenBank. The similarity of the CP between the two Mexican isolates (from papaya and pumpkin) was 94% and would therefore represent two variants of PMV. A healthy papaya plant in the greenhouse, inoculated with tissue from an infected papaya plant from the field, tested positive for PMV in DAS-ELISA. (PVX was used as a negative control). These results confirmed the identity of the isolate as PMV. Reference: (1) T. L. Sit, M. G. AbouHaidar, and S. Holi. J. Gen. Virol. 70:2335-2331, 1989.
番木瓜花叶病毒(PMV)是马铃薯X病毒组的成员,具有530纳米的丝状颗粒,其正义单链RNA为6.6千碱基。在墨西哥,单独种植的患病番木瓜植株以及与南瓜混种的种植园中均检测到了PMV。对来自墨西哥东南部七个地点(尤卡坦州、坎佩切州和金塔纳罗奥州)单株植物的45片叶片样本进行了逆转录聚合酶链反应(RT-PCR)和标准双抗体夹心酶联免疫吸附测定(DAS-ELISA)。PCR引物设计基于GenBank登录号为D13957的序列(1)。使用TOPO TA克隆试剂盒对扩增的PCR产物进行克隆,并通过双脱氧链终止法进行测序。使用一种或两种检测技术,26个样本检测出PMV呈阳性:41个番木瓜样本中的23个以及4个南瓜样本中的3个。这里报道的两个序列,YY-15和YY-22(分别来自番木瓜和南瓜,登录号为AYO17186和AYO17187),长度为1180个核苷酸,包含ORF3的一个片段、完整的ORF4和假定的CP基因,包括3'端非翻译区。在CP基因序列中,推导的氨基酸序列与GenBank中D13957的氨基酸序列相似度为88%。两个墨西哥分离株(来自番木瓜和南瓜)之间CP的相似度为94%,因此代表PMV的两个变体。温室中的一株健康番木瓜植株,接种了来自田间受感染番木瓜植株组织,在DAS-ELISA中检测出PMV呈阳性。(PVX用作阴性对照)。这些结果证实了该分离株为PMV。参考文献:(1)T. L. Sit、M. G. AbouHaidar和S. Holi。《普通病毒学杂志》70:2335 - 2331,1989年。