{"title":"从阿格拉的 Dayalbagh 农田中报告了绿豆黄镶嵌印度病毒的新分离株。","authors":"Ambika Chaturvedi, Dipinte Gupta, Bikash Mandal, Rajiv Ranjan","doi":"10.1007/s11262-024-02099-y","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":51212,"journal":{"name":"Virus Genes","volume":" ","pages":"747-751"},"PeriodicalIF":1.9000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A new isolate of mungbean yellow mosaic India virus in Vigna mungo L. reported from a Dayalbagh field, Agra.\",\"authors\":\"Ambika Chaturvedi, Dipinte Gupta, Bikash Mandal, Rajiv Ranjan\",\"doi\":\"10.1007/s11262-024-02099-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":51212,\"journal\":{\"name\":\"Virus Genes\",\"volume\":\" \",\"pages\":\"747-751\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virus Genes\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1007/s11262-024-02099-y\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virus Genes","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s11262-024-02099-y","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/21 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
摘要
从印度北方邦阿格拉地区的 Dayalbagh 田间随机采集了 2019-2022 年作物季节出现黄镶嵌症状的黑禾木(Vigna mungo L. )植株。用十六烷基三甲基溴化铵(CTAB)法从受感染的叶片样本中分离出总基因组 DNA,并进行 PCR 检测。病毒确认后,按照标准方案通过滚圆扩增法扩增病毒基因组。DNA A 和 DNA B 亚基因组分别以 PstI 和 BamHI 片段的形式克隆到 pUC18 载体中。对阳性克隆进行 DNA 测序。结果显示,DNA A 和 DNA B 分别与 "印度绿豆黄曲霉病毒-[Mungbean],DNA-A,完整序列"(GeneBank Accession No AF416742.1)和 "印度绿豆黄曲霉病毒分离株 Mu1-Dholi 片段 DNA-B,完整序列"(GeneBank Accession No MW814723.1)显示出最接近的核苷酸同一性,同一性为 98.14%;与 "印度绿豆黄曲霉病毒分离株 Mu1-Dholi 片段 DNA-B,完整序列"(GeneBank Accession No MW814723.1)的同一性为 97.94%。新分离的印度绿豆黄曲霉病毒(MYMIV)与多种印度绿豆黄曲霉病毒株系的衣壳蛋白基因序列相似。在 MYMIV 的新分离株中,DNA B 的第 2036 个核苷酸处出现了点突变,该突变破坏了阅读框,引入了终止密码子,从而导致运动蛋白基因的大小减小。在本研究中,我们首次报告了 MYMIV Dayalbagh 分离物的全基因组序列。
A new isolate of mungbean yellow mosaic India virus in Vigna mungo L. reported from a Dayalbagh field, Agra.
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.
期刊介绍:
Viruses are convenient models for the elucidation of life processes. The study of viruses is again on the cutting edge of biological sciences: systems biology, genomics, proteomics, metagenomics, using the newest most powerful tools.
Huge amounts of new details on virus interactions with the cell, other pathogens and the hosts – animal (including human), insect, fungal, plant, bacterial, and archaeal - and their role in infection and disease are forthcoming in perplexing details requiring analysis and comments.
Virus Genes is dedicated to the publication of studies on the structure and function of viruses and their genes, the molecular and systems interactions with the host and all applications derived thereof, providing a forum for the analysis of data and discussion of its implications, and the development of new hypotheses.