Wood-Charlson Elisha M, Weynberg Karen D, Suttle Curtis A, Roux Simon, van Oppen Madeleine J H
Australian Institute of Marine Science, PMB 3 Townsville MC, Townsville, Qld, 4810, Australia.
Departments of Earth, Ocean and Atmospheric Sciences, Microbiology and Immunology, Botany and the Canadian Institute for Advanced Research, University of British Columbia, Vancouver, BC, Canada.
Environ Microbiol. 2015 Oct;17(10):3440-9. doi: 10.1111/1462-2920.12803. Epub 2015 Mar 27.
Reef-building corals form close associations with organisms from all three domains of life and therefore have many potential viral hosts. Yet knowledge of viral communities associated with corals is barely explored. This complexity presents a number of challenges in terms of the metagenomic assessments of coral viral communities and requires specialized methods for purification and amplification of viral nucleic acids, as well as virome annotation. In this minireview, we conduct a meta-analysis of the limited number of existing coral virome studies, as well as available coral transcriptome and metagenome data, to identify trends and potential complications inherent in different methods. The analysis shows that the method used for viral nucleic acid isolation drastically affects the observed viral assemblage and interpretation of the results. Further, the small number of viral reference genomes available, coupled with short sequence read lengths might cause errors in virus identification. Despite these limitations and potential biases, the data show that viral communities associated with corals are diverse, with double- and single-stranded DNA and RNA viruses. The identified viruses are dominated by double-stranded DNA-tailed bacteriophages, but there are also viruses that infect eukaryote hosts, likely the endosymbiotic dinoflagellates, Symbiodinium spp., host coral and other eukaryotes in close association.
造礁珊瑚与生命的所有三个域中的生物形成紧密联系,因此有许多潜在的病毒宿主。然而,与珊瑚相关的病毒群落的知识几乎未被探索。这种复杂性在珊瑚病毒群落的宏基因组评估方面带来了许多挑战,需要专门的方法来纯化和扩增病毒核酸,以及进行病毒组注释。在这篇小型综述中,我们对现有数量有限的珊瑚病毒组研究以及可用的珊瑚转录组和宏基因组数据进行了荟萃分析,以确定不同方法中固有的趋势和潜在问题。分析表明,用于分离病毒核酸的方法会极大地影响观察到的病毒组合以及结果的解释。此外,可用的病毒参考基因组数量较少,再加上短序列读取长度,可能会导致病毒鉴定出现错误。尽管存在这些限制和潜在偏差,但数据表明与珊瑚相关的病毒群落是多样的,包括双链和单链DNA及RNA病毒。鉴定出的病毒以双链DNA尾噬菌体为主,但也有感染真核宿主的病毒,可能是共生双鞭毛虫、共生藻属、宿主珊瑚以及其他紧密相关的真核生物。