Crop Improvement Division, ICAR-Indian Institute of Pulses Research, Kalyanpur, Kanpur, Uttar Pradesh, 208024, India.
Krishi Vigyan KendraRama Krishna Mission Ashram, Ranchi, Jharkhand, 834008, India.
Mol Genet Genomics. 2017 Dec;292(6):1237-1245. doi: 10.1007/s00438-017-1343-z. Epub 2017 Jul 1.
Fusarium wilt caused by F. oxysporum f. sp. ciceris causes extensive damage to chickpea (Cicer arietinum L.) in many parts of the world. In the central part of India, pathogen race 2 (Foc 2) causes severe yield losses. We initiated molecular marker-assisted backcrossing (MABC) using desi cultivar, Vijay, as a donor to introgress resistance to this race (Foc2) in Pusa 256, another elite desi cultivar of chickpea. To confirm introgression of resistance for this race, foreground selection was undertaken using two SSR markers (TA 37 and TA110), with background selection to observe the recovery of recurrent parent genome using 45 SSRs accommodated in 8 multiplexes. F plants were confirmed with molecular markers and backcrossed with Pusa 256, followed by cycles of foreground and background selection at each stage to generate 161 plants in BCF during the period 2009-2013. Similarly, 46 BCF plants were also generated in another set during the same period. On the basis of foreground selection, 46 plants were found homozygotes in BCF. Among them, 17 plants recorded >91% background recovery with the highest recovery percentage of 96%. In BCF also, 14 hybrid plants recorded a background recovery of >85% with the highest background recovery percentage of >94%. The identified plants were selfed to obtain 1341 BCF and 2198 BCF seeds which were screened phenotypically for resistance to fusarium wilt (race 2) besides doing marker analysis. Finally, 17 BCF and 11 BCF lines were obtained which led to identification of 5 highly resistant lines of Pusa 256 with Foc 2 gene introgressed in them. Development of these lines will help in horizontal as well as vertical expansion of chickpea in central part of India.
尖镰孢菌枯萎病(Fusarium wilt caused by F. oxysporum f. sp. ciceris)在世界许多地区对鹰嘴豆(Cicer arietinum L.)造成广泛破坏。在印度中部,病原菌 2 号(Foc 2)导致严重的产量损失。我们利用本土品种 Vijay 启动了分子标记辅助回交 (MABC),将其作为供体,将对这种病原菌 (Foc2)的抗性导入到另一个鹰嘴豆的本土品种 Pusa 256 中。为了确认对该病原菌的抗性导入,使用两个 SSR 标记 (TA 37 和 TA110)进行了前景选择,同时观察了 8 个多重 PCR 中包含的 45 个 SSR 对轮回亲本基因组的恢复情况。利用分子标记对 F1 植株进行了确认,并与 Pusa 256 回交,随后在每个阶段进行前景和背景选择,在 2009 年至 2013 年期间共产生了 161 株 BCF 植株。同期也产生了另外 46 株 BCF 植株。根据前景选择,在 BCF 中发现 46 株为纯合子。其中,有 17 株记录的背景恢复率超过 91%,最高恢复率为 96%。在 BCF 中,有 14 株杂种植物的背景恢复率超过 85%,最高背景恢复率超过 94%。鉴定出的植株自交获得了 1341 株和 2198 株 BCF 种子,除了进行标记分析外,还对这些种子进行了对尖镰孢枯萎病(2 号病原菌)的抗性表型筛选。最终获得了 17 株和 11 株 BCF 系,从而鉴定出 5 株携带 Foc 2 基因的高抗 Pusa 256 系。这些系的开发将有助于印度中部地区鹰嘴豆的水平和垂直扩展。