Molecular identification of ascochyta blight of Cicer montbretii Jaub. & Spach

Fevzi Bulat, Duygu Sari, H. Sari, Tuba Eker, Hilal Özay, C. Toker
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引用次数: 1

Abstract

Molecular detection of ascochyta blight caused by Ascochyta rabiei (Pass.) Labr. is important for effective control of the ascochyta blight and efficient chickpea (Cicer arietinum L.) breeding program. The present research was therefore aimed to diagnose ascochyta blight of C. montbretii Jaub. & Spach via molecular techniques. Infected plant samples were collected and placed on potato dextrose agar (PDA) medium for 1 week at 20-24℃, and colonies with typical ascochyta blight symptoms were transferred to new PDA medium and incubated for 1 week at 25℃. DNA was isolated from small parts of fungus isolates via the CTAB method. Internal transcribed spacer (ITS) regions (ITS-1, 5.8S rDNA subunit, ITS-2) were amplified with ITS 5 and ITS 4 primers for molecular characterization. Based on the BLAST analysis, the sequence had 99 and 100% nucleotide identity with the corresponding sequence of A. rabiei in GeneBank. To our knowledge, this is the first report of ascochyta blight of C. montbretii in Turkiye. The pathogen is considered to be co-evolved with C. montbretii. Molecular techniques, as in the present study, can be diagnosed with great accuracy, in a short time, and with relatively little effort and expense.
孟氏白僵菌的分子鉴定。和软轴
狂犬病阿斯科塔(ascochyta rabiei)致阿斯科塔疫病的分子检测Labr。对有效防治鹰嘴豆疫病和鹰嘴豆高效育种具有重要意义。因此,本研究旨在诊断白僵菌。通过分子技术和Spach。采集侵染植株样品,置于马铃薯葡萄糖琼脂(PDA)培养基上,20 ~ 24℃培养1周,将具有典型穗轴疫病症状的菌落转移到新的PDA培养基上,25℃培养1周。用CTAB法从真菌分离物的一小部分分离出DNA。利用ITS 5和ITS 4引物扩增内部转录间隔区(ITS-1、5.8S rDNA亚基、ITS-2)进行分子鉴定。经BLAST分析,该序列与GeneBank中rabiei A.对应序列的核苷酸同源性分别为99%和100%。据我们所知,这是土耳其首次报道的蒙氏梭菌阿斯柯氏枯萎病。该病原体被认为是与蒙氏梭菌共同进化的。在目前的研究中,分子技术可以在很短的时间内,以相对较少的努力和费用,非常准确地进行诊断。
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