Variable infection mechanisms of mungbean yellow mosaic India virus in diverse Vigna species: New insights from differential gene expression.

IF 3.4 3区 生物学 Q1 PLANT SCIENCES
Kuppuraj Jagadeesan, Nagendran Krishnan, Asmita Sirari, Bharathi Mohindru, Manmohan Dhkal
{"title":"Variable infection mechanisms of mungbean yellow mosaic India virus in diverse <i>Vigna</i> species: New insights from differential gene expression.","authors":"Kuppuraj Jagadeesan, Nagendran Krishnan, Asmita Sirari, Bharathi Mohindru, Manmohan Dhkal","doi":"10.1007/s12298-025-01547-9","DOIUrl":null,"url":null,"abstract":"<p><p>The extent of viral infection significantly shapes disease susceptibility. Yellow mosaic disease induced by the begomovirus pathogen mungbean yellow mosaic India virus (MYMIV), revealed varying infection levels in both compatible and incompatible interactions across three distinct <i>Vigna</i> species such black gram, green gram, and rice bean. Differential gene expression analysis focused on MYMIV coat protein (<i>AV1</i>) and replication protein (<i>AC1</i>) highlighted elevated <i>AV1</i> expression in the susceptible green gram genotype SML1082 compared to the black gram genotype KUG253. Conversely, <i>AC1</i> showed higher expression in black gram than green gram, illustrating complex infection mechanisms among compatible MYMIV-<i>Vigna</i> interactions. A novel infection pathway, termed \"Lack of Efficient Assembly (LEA),\" has been hypothesized in MYMIV-<i>Vigna</i> interactions. Additionally, a whitefly-mediated artificial transmission model for begomoviruses, named Transparent Airflow Stress-free Container (TASC), has been designed and demonstrated for the efficient transmission of MYMIV. This study enhances the understanding of begomovirus infection dynamics in diverse <i>Vigna</i> species, offering insights into disease management strategies.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s12298-025-01547-9.</p>","PeriodicalId":20148,"journal":{"name":"Physiology and Molecular Biology of Plants","volume":"31 1","pages":"153-162"},"PeriodicalIF":3.4000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11787106/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiology and Molecular Biology of Plants","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s12298-025-01547-9","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/15 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

The extent of viral infection significantly shapes disease susceptibility. Yellow mosaic disease induced by the begomovirus pathogen mungbean yellow mosaic India virus (MYMIV), revealed varying infection levels in both compatible and incompatible interactions across three distinct Vigna species such black gram, green gram, and rice bean. Differential gene expression analysis focused on MYMIV coat protein (AV1) and replication protein (AC1) highlighted elevated AV1 expression in the susceptible green gram genotype SML1082 compared to the black gram genotype KUG253. Conversely, AC1 showed higher expression in black gram than green gram, illustrating complex infection mechanisms among compatible MYMIV-Vigna interactions. A novel infection pathway, termed "Lack of Efficient Assembly (LEA)," has been hypothesized in MYMIV-Vigna interactions. Additionally, a whitefly-mediated artificial transmission model for begomoviruses, named Transparent Airflow Stress-free Container (TASC), has been designed and demonstrated for the efficient transmission of MYMIV. This study enhances the understanding of begomovirus infection dynamics in diverse Vigna species, offering insights into disease management strategies.

Supplementary information: The online version contains supplementary material available at 10.1007/s12298-025-01547-9.

求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.10
自引率
0.00%
发文量
126
期刊介绍: Founded in 1995, Physiology and Molecular Biology of Plants (PMBP) is a peer reviewed monthly journal co-published by Springer Nature. It contains research and review articles, short communications, commentaries, book reviews etc., in all areas of functional plant biology including, but not limited to plant physiology, biochemistry, molecular genetics, molecular pathology, biophysics, cell and molecular biology, genetics, genomics and bioinformatics. Its integrated and interdisciplinary approach reflects the global growth trajectories in functional plant biology, attracting authors/editors/reviewers from over 98 countries.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信