基于小RNA测序和PCR检测的肯尼亚芋病毒和类病毒多样性

David K Muruu, J. Kinyua, M. Kepue, Linnet Kerubo,  Isaac Njaci, Bernard Mware
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摘要

目的:病毒性疾病在世界范围内造成严重的作物产量损失和品质下降。尽管具有重要的经济意义,但感染芋头的主要病毒和类病毒在肯尼亚的发生和分布情况仍然很差,这限制了制定强有力的疾病管理战略以减轻其传播。因此,本研究旨在确定感染肯尼亚芋头的病毒和类病毒,作为制定有效管理战略的基础,以支持预防和控制芋头病毒。方法:在肯尼亚农业生态条件不同的9个芋头种植县进行了病毒调查和抽样,以确定影响芋头的病毒的发病率和分布。采集有症状食用芋头和野生芋头的叶片和整株样品,采用PCR、RT-PCR和小RNA测序方法测定芋头感染病毒和类病毒的多样性。结果:观察到发育迟缓、卷叶、收缩、叶形变形、花叶黄脉、矮化等病样症状。所有调查地点的总体平均发病率为32-60%。小RNA测序揭示了DNA和RNA病毒的存在。检测到的DNA病毒包括芋头杆状病毒(TaBV)和芋头杆状CH病毒(TaBCHV)、芋头特有的坏病毒、甘薯坏病毒B、甘蔗杆状病毒和甘薯卷曲叶病毒。RNA病毒包括甘薯羽毛斑驳病毒和菜豆甲内啡肽病毒。柑橘外皮类病毒也被检测到。有趣的是,芋头的野生近缘种显示出很少的病毒序列匹配。本研究报道了在肯尼亚流行的芋头病毒和类病毒,并首次描述了肯尼亚TaBV的发病率、分布和序列变异性。建议:未来的研究应侧重于开发有效的管理策略,以支持芋头病毒的预防和控制,包括病毒与芋头相互作用的遗传资源、去除受感染的作物、控制昆虫媒介和开发无病毒种植材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diversity of Viruses and Viroids Infecting Taro in Kenya Based on Small RNA Sequencing and PCR Detection
Purpose: Viral diseases cause severe yield losses and quality decline in crops worldwide. Despite their economic significance, the occurrence and distribution of the major viruses and viroids infecting Taro in Kenya remain poor, limiting the development of robust disease management strategies to mitigate their spread. This study thus aimed to identify the viruses and viroids infecting Taro in Kenya as a basis for developing effective management strategies to support the prevention and control of Taro viruses. Methodology: Viral surveys and sampling were conducted across nine Taro-growing counties with diverse agroecological conditions in Kenya to determine the incidence and distribution of viruses affecting Taro. Leaf and whole plant samples of symptomatic edible and wild Taro were collected for PCR, RT-PCR, and small RNA sequencing assays to determine the diversity of viruses and viroids infecting Taro. Results: Disease-like symptoms, including stunting, leaf rolling, shrinkage, deformed leaves with mosaic and yellow veins, and dwarfism, were observed. An overall mean disease incidence of 32-60% was recorded in all sites surveyed. Small RNA sequencing revealed the presence of both DNA and RNA viruses. Detected DNA viruses included the Taro Bacilliform Virus (TaBV) and Taro Bacilliform CH Virus (TaBCHV), badnaviruses specific to Taro, the sweet potato Badnavirus B, sugarcane bacilliform virus, and sweet potato leaf curl virus. The RNA viruses included the sweet potato feathery mottle and Phaseolus vulgaris alphaendornavirus. A Citrus exocortis viroid was also detected. Interestingly, the wild relatives of Taro displayed very few viral sequence hits. This study reports the Taro viruses and viroids circulating in Kenya and is the first to describe the incidence, distribution, and sequence variability of TaBV in Kenya. Recommendations: Future studies should focus on developing effective management strategies to support the prevention and control of Taro viruses, including genetic resources for virus-Taro interactions, removing infected crops, controlling insect vectors, and developing virus-free planting materials.
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