Aggarwal Rashmi, Agarwal Shweta, Sharma Sapna, Gurjar Malkhan Singh, Bashyal Bishnu Maya, Rao Atmakuri Ramakrishna, Sahu Sarika, Jain Prachi, Saharan Mahender Singh
Fungal Molecular Biology Laboratory, Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110 012 India.
Indian Council of Agricultural Research, New Delhi, 110 012 India.
3 Biotech. 2022 Jul;12(7):151. doi: 10.1007/s13205-022-03213-3. Epub 2022 Jun 20.
Spot blotch disease of wheat caused by Boerma (Sacc.) is an emerging problem in South Asian countries. Whole genome of a highly virulent isolate of BS112 (BHU, Uttar Pradesh; Accession no. GCA_004329375.1) was sequenced using a hybrid assembly approach. Secreted proteins, virulence gene(s), pathogenicity-related gene(s) were identified and the role of gene present in this genome, in the development of disease was recognized. gene (535 bp) was analyzed and identified in the genome of (BS112) which revealed 100% homology with the gene of (Accession no. MH017419) Furthermore, gene was amplified, sequenced and validated in 39 isolates of which confirmed the presence of gene in all the isolates taken for this study. All sequences were submitted in NCBI database (MN601358-MN601396). As gene interacts with gene of host, 13 wheat genotypes were evaluated out of which 5 genotypes (38.4%) were found to be positive with more severe necrotic lesions compared to -negative wheat genotypes. In vitro expression analysis of gene in the pathogen using qPCR revealed maximum upregulation (14.67 fold) at 1st day after inoculation (DAI) in the medium. Furthermore, expression analysis of gene in -positive and negative genotypes, revealed maximum expression (7.89-fold) in positive genotype, Agra local at 5th DAI compared to negative genotype Chiriya 7 showing minimum expression (0.048-fold) at 5th DAI. - interaction studies suggested that spot blotch disease is more severe in positive genotypes, which will be helpful in better understanding and management of spot blotch disease of wheat.
The online version contains supplementary material available at 10.1007/s13205-022-03213-3.
由博尔马氏菌(Sacc.)引起的小麦叶斑病在南亚国家正成为一个新问题。使用混合组装方法对高毒力分离株BS112(印度北方邦贝拿勒斯印度教大学;登录号GCA_004329375.1)的全基因组进行了测序。鉴定了分泌蛋白、毒力基因、致病相关基因,并认识到该基因组中存在的基因在疾病发展中的作用。对基因(535 bp)进行了分析并在BS112的基因组中鉴定出来,该基因与博尔马氏菌的基因(登录号MH017419)显示出100%的同源性。此外,在39株博尔马氏菌分离株中对该基因进行了扩增、测序和验证,证实了本研究中所取的所有分离株中都存在该基因。所有序列都提交到了NCBI数据库(MN601358 - MN601396)。由于该基因与宿主的基因相互作用,对13个小麦基因型进行了评估,其中5个基因型(38.4%)被发现为阳性,与阴性小麦基因型相比,坏死病斑更严重。使用qPCR对病原体中的该基因进行体外表达分析,发现在接种后第1天(DAI)在培养基中上调最大(14.67倍)。此外,对阳性和阴性基因型中的该基因进行表达分析,发现在第5天DAI时,阳性基因型阿格拉本地的表达最大(7.89倍),而阴性基因型奇里亚7在第5天DAI时表达最小(0.048倍)。基因相互作用研究表明,阳性基因型中的叶斑病更严重,这将有助于更好地理解和管理小麦叶斑病。
在线版本包含可在10.1007/s13205 - 022 - 03213 - 3获取的补充材料。