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从阿格拉代尔巴格的一块田地里的绿豆中分离到一种新的印度绿豆黄花叶病毒。

A new isolate of mungbean yellow mosaic India virus in Vigna mungo L. reported from a Dayalbagh field, Agra.

机构信息

Department of Botany, Dayalbagh Educational Institute, Dayalbagh, Agra, 282005, India.

Division of Plant Pathology, Indian Agriculture Research Institute, Pusa, New Delhi, 110012, India.

出版信息

Virus Genes. 2024 Dec;60(6):747-751. doi: 10.1007/s11262-024-02099-y. Epub 2024 Aug 21.

Abstract

Black gram (Vigna mungo L.) plants showing yellow mosaic symptoms during 2019-2022 crop seasons were collected randomly from a Dayalbagh field, Agra Region of Uttar Pradesh, India. Total genomic DNA was isolated from the infected leaf samples by the Cetyltrimethylammonium bromide (CTAB) method and subjected to PCR. After viral confirmation, the viral genome was amplified by rolling circle amplification following the standard protocol. The DNA A and DNA B subgenomes were cloned individually as a PstI and BamHI fragment in the pUC18 vector. Positive clones were subjected to DNA sequencing. The results revealed that DNA A and DNA B show the closest nucleotide identity with "mungbean yellow mosaic India virus-[Mungbean], DNA-A, the complete sequence" (GeneBank Accession No AF416742.1) with 98.14% identity, and "mungbean yellow mosaic India virus isolate Mu1-Dholi segment DNA-B, the complete sequence" (GeneBank Accession No MW814723.1) with 97.94% identity, respectively. The new isolate of mungbean yellow mosaic India virus (MYMIV) shows sequence similarity with the coat protein gene of various strains of MYMIV. In the new isolate of MYMIV, a point mutation was observed at the 2036th nucleotide of DNA B, which disrupts the reading frame to introduce a stop codon and thus leading to a decrease in the size of the movement protein gene. In the present study we are reporting the whole genome sequence of the MYMIV Dayalbagh isolate for the first time.

摘要

2019-2022 作物季节期间,在印度北方邦阿格拉地区的代亚尔巴格田间,随机采集到表现黄色花叶症状的绿豆(Vigna mungo L.)植株。采用溴化十六烷基三甲铵 (CTAB) 法从感染叶片样本中提取总基因组 DNA,并进行 PCR。病毒确认后,按照标准方案通过滚环扩增扩增病毒基因组。将 DNA A 和 DNA B 亚基因组分别作为 PstI 和 BamHI 片段克隆到 pUC18 载体中。对阳性克隆进行 DNA 测序。结果表明,DNA A 和 DNA B 与“绿豆黄花叶印度病毒-[绿豆],DNA-A,全长序列”(GeneBank 登录号 AF416742.1)的核苷酸同一性最高,为 98.14%,与“绿豆黄花叶印度病毒分离株 Mu1-Dholi 段 DNA-B,全长序列”(GeneBank 登录号 MW814723.1)的核苷酸同一性最高,为 97.94%。绿豆黄花叶印度病毒(MYMIV)的新分离株与各种 MYMIV 株的外壳蛋白基因具有序列相似性。在新分离株的 MYMIV 中,在 DNA B 的第 2036 个核苷酸处观察到一个点突变,破坏了阅读框并引入一个终止密码子,从而导致运动蛋白基因大小减小。在本研究中,我们首次报道了 MYMIV 代亚尔巴格分离株的全基因组序列。

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