Srivastava A, Kumar S, Raj S K
Plant Molecular Virology Laboratory, CSIR-National Botanical Research Institute, Lucknow 226001, India.
Plant Dis. 2014 Sep;98(9):1285. doi: 10.1094/PDIS-04-14-0338-PDN.
During a survey in February 2011, severe symptoms of upward leaf curling, vein enation on lower side of the leaves, and shortening of internodes were observed on 20 out of 117 Amaranthus hypochondriacus plants (17% disease incidence) examined at breeding plots of CSIR-NBRI, Lucknow. These symptoms are typical of begomovirus infection. PCR with begomovirus-specific primers (3) produced the expected ~1.1-kb product from DNA extracts of 20 symptomatic plants but not from a non-symptomatic plant, suggesting the association of a begomovirus. The full-length begomoviral genome from a representative sample was amplified by rolling circle amplification using Ø-29 DNA polymerase and digested by BamHI, which resulted in a ~2.7 kb product when electrophoresed in 1.0% agarose gel. The product obtained was cloned, sequenced, and sequence data of 2,753 nucleotides was deposited in GenBank (Accession No. JF682242). BLASTn analysis revealed 97 to 98% nucleotide identity and forms a distinct clade with Ageratum enation virus (AEV) isolates. This shows the virus in A. hypochondriacus to be an isolate of AEV. The separate PCRs were also performed with betasatellite and alphasatellite specific primers (1,2) that resulted in ~1.3-kb amplicons from all samples, suggesting their association. The amplification products were cloned and sequenced. An analysis of betasatellite (JX512904) revealed highest 98% nucleotide identity and close phylogenetic relationship with Ageratum leaf curl betasatellite (ALCB, JQ710745). The alphasatellite (JX512905) showed highest 95% identity and close relationship with Hibiscus leaf curl alphasatellite (HLCA, FN794199). This shows the betasatellite and alphasatellite in A. hypochondriacus to be isolates of ALCB and HLCA, respectively. The partial direct repeat clones of the begomovirus (pCAM-AEV), betasatellite (pCAM-ALCB), alphasatellite (pCAM-HLCA) were generated and mobilized into Agrobacterium tumefaciens strain GV3101 and infiltrated in A. hypochondriacus seedlings. The plants inoculated with pCAM-AEV, pCAM-ALCB, and pCAM-HLCA; pCAM-AEV and pCAM-ALCB developed severe leaf curl and enation symptoms on 5/5 plant at 35 days post inoculation, which were similar to those of naturally infected plants, satisfying Koch's postulates. On the other hand, plants inoculated with pCAM-AEV alone or in combination with pCAM-HLCA developed mild symptoms. Plants inoculated with pCAM-ALCB and pCAM-HLCA did not develop symptoms. The results here show that leaf curl and enation disease of A. hypochondriacus in India is caused by AEV and ALCB and that an alphasatellite may be associated with symptomatic plants. References: (1) R. W. Briddon et al. Mol. Biotechnol. 20:315, 2002. (2) S. E. Bull et al. Mol. Biotechnol. 23:83, 2003. (3) M. R. Rojas et al. Plant Dis. 77:340, 1993.
在2011年2月的一项调查中,在勒克瑙CSIR-NBRI育种试验田检查的117株皱果苋植株中,有20株(发病率为17%)出现了严重的叶片向上卷曲、叶片下侧叶脉肿大和节间缩短症状。这些症状是双生病毒感染的典型症状。用双生病毒特异性引物进行PCR扩增(3),从20株有症状植株的DNA提取物中得到了预期的约1.1 kb产物,而无症状植株中未得到该产物,这表明存在双生病毒。使用φ-29 DNA聚合酶通过滚环扩增对代表性样品中的双生病毒全基因组进行扩增,并使用BamHI进行酶切,在1.0%琼脂糖凝胶中电泳时产生了约2.7 kb的产物。将得到的产物进行克隆、测序,并将2753个核苷酸的序列数据存入GenBank(登录号JF682242)。BLASTn分析显示其核苷酸同一性为97%至98%,并与藿香脉肿病毒(AEV)分离物形成一个独特的进化分支。这表明皱果苋中的病毒是AEV的一个分离物。还用卫星β和卫星α特异性引物分别进行了PCR扩增(1,2),所有样品均产生了约1.3 kb的扩增子,表明它们之间存在关联。对扩增产物进行克隆和测序。对卫星β(JX512904)的分析显示其核苷酸同一性最高为98%,与藿香叶卷曲卫星β(ALCB,JQ710745)有密切的系统发育关系。卫星α(JX512905)显示最高95%的同一性,与木槿叶卷曲卫星α(HLCA,FN794199)关系密切。这表明皱果苋中的卫星β和卫星α分别是ALCB和HLCA的分离物。构建了双生病毒(pCAM-AEV)、卫星β(pCAM-ALCB)、卫星α(pCAM-HLCA)的部分直接重复克隆,并将其导入根癌农杆菌菌株GV3101中,然后注射到皱果苋幼苗中。接种pCAM-AEV、pCAM-ALCB和pCAM-HLCA;pCAM-AEV和pCAM-ALCB的植株在接种后35天,5/5的植株出现了严重的叶片卷曲和肿大症状,与自然感染植株的症状相似,满足柯赫氏法则。另一方面,单独接种pCAM-AEV或与pCAM-HLCA联合接种的植株出现轻微症状。接种pCAM-ALCB和pCAM-HLCA的植株未出现症状。这里的结果表明,印度皱果苋的叶片卷曲和肿大病是由AEV和ALCB引起的,并且一个卫星α可能与有症状植株有关。参考文献:(1)R. W. Briddon等人,《分子生物技术》20:315,2002年。(2)S. E. Bull等人,《分子生物技术》23:83,2003年。(3)M. R. Rojas等人,《植物病害》77:340,1993年。