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首页> 外文期刊>British Biotechnology Journal >Molecular Diversity Analysis of Coat Protein Gene Encoded by Legume Begomoviruses and PCR Assay to Detect Yellow Mosaic Viruses Infecting Soybean in India
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Molecular Diversity Analysis of Coat Protein Gene Encoded by Legume Begomoviruses and PCR Assay to Detect Yellow Mosaic Viruses Infecting Soybean in India

机译:印度豆科植物豆科病毒编码的外壳蛋白基因的分子多样性分析和PCR分析方法检测印度感染大豆的黄色花叶病毒

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Aim: Coat protein (CP) genes encoded by Legume yellow mosaic viruses (LYMVs) were analysed to study molecular diversity and to devise effective PCR based assay to distinguish major Begomovirus species ( Mungbean yellow mosaic India virus and Mungbean yellow mosaic virus ) infecting soybean Design of the Study: All the known coat protein gene sequences encoded by begomoviruses causing yellow mosaic disease (YMD) in legumes were obtained from GenBank. YMD infected soybean leaf samples were collected from different parts of India during Kharif 2012 and species of virus infections identified using CP gene based primers in a PCR assay. Methodology: DNA polymorphism, phylogeny, and test of theory of neutral evolution were studied to decode variability and molecular evolutionary lineage of LYMVs encoded CP gene. CP based primers have been designed and employed to differentiate MYMIV and MYMV using infected soybean samples collected across India. Results: Nucleotide diversity and DNA polymorphism studies revealed relatively low levels of diversity in CP genes encoded by LYMV isolates. Test of neutral evolution and codon substitution analysis also reiterated the operation of purifying selection indicating deleterious mutations in CP gene are not tolerated in the LYMV population. Geographical confinement of species of yellow mosaic viruses infecting soybean is further validated as diseased soybean samples collected from Northern and Central India showed infection due to MYMIV and samples obtained from Southern and Western India were infected with MYMV. Conclusion: Evolutionary genomic analysis revealed conserved nature of LYMV encoded CP gene however a variable region has been identified.PCR assay for differentiation of two major begomoviruses viz .,) MYMV and MYMIV infecting soybean in India has been standardised. This is the first report of population genetics in LYMVs and it’s implications for yellow mosaic disease (YMD) resistance breeding in soybean are also discussed.
机译:目的:分析豆科植物黄花叶病毒(LYMVs)编码的外壳蛋白(CP)基因,以研究分子多样性,并设计出基于PCR的有效方法,以区分感染大豆的主要介形虫病毒(绿豆黄花叶印度病毒和绿豆黄花叶病毒)研究的结果:由豆科病毒引起的豆科植物黄花叶病(YMD)编码的所有已知外壳蛋白基因序列均来自GenBank。在2012年Kharif期间从印度不同地区收集了受YMD感染的大豆叶片样品,并在PCR分析中使用基于CP基因的引物鉴定了病毒感染的种类。方法:研究了DNA多态性,系统发育和中性进化理论的检验,以解码LYMV编码CP基因的变异性和分子进化谱系。已经设计并使用了基于CP的引物,以利用从印度各地收集的受感染大豆样品区分MYMIV和MYMV。结果:核苷酸多样性和DNA多态性研究表明,LYMV分离物编码的CP基因的多样性相对较低。中性进化和密码子替代分析的测试也重申了纯化选择的操作,表明在LYMV群体中不容许CP基因中的有害突变。进一步验证了感染大豆的黄色花叶病毒种类的地理范围,因为从印度北部和中部收集的患病大豆样品显示出由于MYMIV感染,而从印度南部和西部获得的样品也受到MYMV感染。结论:进化基因组分析揭示了LYMV编码CP基因的保守性质,但已鉴定出一个可变区。已标准化了印度两种感染大豆的主要Begomovirus病毒(MYMV和MYMIV)的PCR检测方法。这是LYMV种群遗传学的第一份报告,还讨论了其对大豆黄花叶病(YMD)抗性育种的意义。

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