College of Marine Science, University of South Florida, Tampa, Florida, United States of America.
PLoS One. 2011 Apr 22;6(4):e19050. doi: 10.1371/journal.pone.0019050.
Current knowledge of plant virus diversity is biased towards agents of visible and economically important diseases. Less is known about viruses that have not caused major diseases in crops, or viruses from native vegetation, which are a reservoir of biodiversity that can contribute to viral emergence. Discovery of these plant viruses is hindered by the traditional approach of sampling individual symptomatic plants. Since many damaging plant viruses are transmitted by insect vectors, we have developed "vector-enabled metagenomics" (VEM) to investigate the diversity of plant viruses. VEM involves sampling of insect vectors (in this case, whiteflies) from plants, followed by purification of viral particles and metagenomic sequencing. The VEM approach exploits the natural ability of highly mobile adult whiteflies to integrate viruses from many plants over time and space, and leverages the capability of metagenomics for discovering novel viruses. This study utilized VEM to describe the DNA viral community from whiteflies (Bemisia tabaci) collected from two important agricultural regions in Florida, USA. VEM successfully characterized the active and abundant viruses that produce disease symptoms in crops, as well as the less abundant viruses infecting adjacent native vegetation. PCR assays designed from the metagenomic sequences enabled the complete sequencing of four novel begomovirus genome components, as well as the first discovery of plant virus satellites in North America. One of the novel begomoviruses was subsequently identified in symptomatic Chenopodium ambrosiodes from the same field site, validating VEM as an effective method for proactive monitoring of plant viruses without a priori knowledge of the pathogens. This study demonstrates the power of VEM for describing the circulating viral community in a given region, which will enhance our understanding of plant viral diversity, and facilitate emerging plant virus surveillance and management of viral diseases.
目前对植物病毒多样性的了解偏向于可见的和具有经济重要性的疾病的病原体。对于那些尚未在作物中引起重大疾病的病毒,或者来自原生植被的病毒,我们的了解较少,这些病毒是生物多样性的储备库,可能有助于病毒的出现。这些植物病毒的发现受到传统的逐个采样有症状植物的方法的阻碍。由于许多有害的植物病毒是通过昆虫媒介传播的,我们开发了“媒介增强宏基因组学”(VEM)来调查植物病毒的多样性。VEM 涉及从植物中采样昆虫媒介(在这种情况下是粉虱),然后纯化病毒颗粒并进行宏基因组测序。VEM 方法利用了高度移动的成年粉虱随着时间和空间从许多植物中整合病毒的自然能力,并利用宏基因组学发现新病毒的能力。本研究利用 VEM 描述了从美国佛罗里达州两个重要农业区采集的粉虱(Bemisia tabaci)中的 DNA 病毒群。VEM 成功地描述了在作物中产生疾病症状的活跃且丰富的病毒,以及感染相邻原生植被的较少丰富的病毒。从宏基因组序列设计的 PCR 检测方法能够完成四个新的烟粉虱病毒基因组组件的测序,以及在北美首次发现植物病毒卫星。随后在同一田间地点的有症状的 Chenopodium ambrosiodes 中鉴定出了一种新的烟粉虱病毒,验证了 VEM 作为一种在没有病原体先验知识的情况下主动监测植物病毒的有效方法。本研究证明了 VEM 用于描述特定区域内循环病毒群的能力,这将增强我们对植物病毒多样性的理解,并有助于新兴植物病毒的监测和病毒病的管理。