Prathyusha V Bindu, Swathi E, Divya D, Reddy B V Bhaskar, Bentur J S, Chalam V Celia, Wankhede D P, Singh Kuldeep, Anitha K
Agri Biotech Foundation, Rajendranagar, Hyderabad, TG 500 030 India.
ICAR-National Bureau of Plant Genetic Resources, Regional Station, Hyderabad, TG 500 030 India.
3 Biotech. 2023 Jun;13(6):194. doi: 10.1007/s13205-023-03610-2. Epub 2023 May 16.
Yellow mosaic disease (YMD) is a major problem in Urd bean ( L.) in India, which causes huge yield losses. Breeding for wide spectrum and durable (MYMV) resistance and cultivating resistant cultivars is the most appropriate and effective approach. However, the task has become challenging with the report of at least two species of the virus, viz., (MYMV) and (MYMIV) and their recombinants; the existence of various isolates of these species with varied virulence and rapid mutations noted in the virus as well as in the whitefly vector population. Thus the present study was carried out to identify and characterize novel and diverse sources of YMV resistance and develop linked molecular markers for breeding durable and broadspectrum resistant urdbean cultivars against YMV. Towards this goal, we have screened 998 accessions of urdbean national collection of germplasm against YMD Hyderabad isolate both in a field under the natural level of disease incidence and through agro inoculation in the laboratory using viruliferous clones of the same isolate. Ten highly resistant accessions identified through repeated testing have been characterized in terms of reported linked markers. We attempted to see diversity among the ten resistant accessions reported here using earlier reported resistance-linked SCAR marker YMV1 and SSR CEDG180 marker. SCAR marker YMV1 did not amplify with any of the 10 accessions. But with CEDG180, results suggested that 10 accessions shortlisted through field and laboratory tests do not carry PU31 allele and this shows that it may be likely to carry novel gene(s). Further studies are needed to genetically characterize these new sources.
黄花叶病(YMD)是印度黑绿豆(Vigna mungo (L.))面临的一个主要问题,它会导致巨大的产量损失。培育具有广谱和持久抗绿豆黄花叶病毒(MYMV)能力的品种并种植抗性品种是最合适、最有效的方法。然而,随着至少两种该病毒物种(即绿豆黄花叶病毒(MYMV)和绿豆黄花叶印度病毒(MYMIV))及其重组体的报道,这项任务变得具有挑战性;这些物种存在各种毒力不同的分离株,并且在病毒以及粉虱载体种群中都发现了快速突变。因此,开展本研究以鉴定和表征新型且多样的黄花叶病毒抗性来源,并开发与之连锁的分子标记,用于培育对黄花叶病毒具有持久和广谱抗性的黑绿豆品种。为实现这一目标,我们针对海得拉巴分离株的黄花叶病,在自然发病水平的田间对998份黑绿豆国家种质资源收集品进行了筛选,并在实验室中通过使用同一分离株的带毒克隆进行农艺接种筛选。通过反复测试鉴定出的10份高抗种质资源已根据报道的连锁标记进行了表征。我们尝试使用先前报道的抗性连锁SCAR标记YMV1和SSR CEDG180标记来观察这里报道的10份抗性种质资源之间的多样性。SCAR标记YMV1在这10份种质资源中均未扩增出产物。但对于CEDG180,结果表明通过田间和实验室测试筛选出的10份种质资源不携带PU31等位基因,这表明它们可能携带新基因。需要进一步研究对这些新来源进行遗传表征。