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      Virome of Camellia japonica: Discovery of and Molecular Characterization of New Viruses of Different Taxa in Camellias

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          Abstract

          Many species of the genus Camellia are native to China, and several species such as C. japonica have been cultivated as garden plants for over 1,000 years. Virus-like symptoms have been recorded for years. In this study, C. japonica plants with various leaf symptoms were observed in Jiangxi and Chongqing provinces. The species composition of potential viruses in the symptomatic plants was analyzed by next-generation sequencing of six libraries prepared from total RNAs of specimens from 10 trees. Five new viruses were discovered, and their genome sequences were determined. These viruses were tentatively named Camellia chlorotic ringspot viruses (CaCRSVs), Camellia yellow ringspot virus (CaYRSV), Camellia-associated badnavirus (CaBaV), and Camellia-associated marafivirus (CaMaV) based on comprehensive analyses. Among these viruses, CaYRSV, CaBaV, and CaMaV share similar genome organizations and clear sequence homology with known viruses in databases and could potentially be classified as new species of the genera Badnavirus, Idaeovirus, and Marafivirus, respectively. CaCRSVs comprise two distinct viruses, and each likely contains five genomic RNA segments that were found to be distantly related to viral RNAs of members in the genus Emaravirus (family Fimoviridae). The RNAs of CaCRSVs show conserved terminal sequences that differ markedly from those of emaraviral RNAs. These data, together with the phylogenetic analysis, suggest that the evolutionary status of CaCRSVs may represent a novel genus in the family Fimoviridae. In addition, two known viruses (geminivirus and blunervirus) and a mass of betaflexiviruses existing as heterogeneous mixtures were detected, and their roles in symptom formation were studied. Collectively, the information of the viral species and detection protocols that were developed can serve as a basis for better management of these viruses. Distinguishing the virus-related symptoms from genetic characteristics of C. japonica is also significant for breeding efforts.

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          Draft genome sequence of Camellia sinensis var. sinensis provides insights into the evolution of the tea genome and tea quality

          Significance A high-quality genome assembly of Camellia sinensis var. sinensis facilitates genomic, transcriptomic, and metabolomic analyses of the quality traits that make tea one of the world’s most-consumed beverages. The specific gene family members critical for biosynthesis of key tea metabolites, monomeric galloylated catechins and theanine, are indicated and found to have evolved specifically for these functions in the tea plant lineage. Two whole-genome duplications, critical to gene family evolution for these two metabolites, are identified and dated, but are shown to account for less amplification than subsequent paralogous duplications. These studies lay the foundation for future research to understand and utilize the genes that determine tea quality and its diversity within tea germplasm.
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            RNA-based antiviral immunity.

            In eukaryotic RNA-based antiviral immunity, viral double-stranded RNA is recognized as a pathogen-associated molecular pattern and processed into small interfering RNAs (siRNAs) by the host ribonuclease Dicer. After amplification by host RNA-dependent RNA polymerases in some cases, these virus-derived siRNAs guide specific antiviral immunity through RNA interference and related RNA silencing effector mechanisms. Here, I review recent studies on the features of viral siRNAs and other virus-derived small RNAs from virus-infected fungi, plants, insects, nematodes and vertebrates and discuss the innate and adaptive properties of RNA-based antiviral immunity.
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              Complete viral genome sequence and discovery of novel viruses by deep sequencing of small RNAs: a generic method for diagnosis, discovery and sequencing of viruses.

              We report the first identification of novel viruses, and sequence of an entire viral genome, by a single step of high-throughput parallel sequencing of small RNAs from diseased, as well as symptomless plants. Contigs were assembled from sequenced total siRNA from plants using small sequence assembly software and could positively identify RNA, ssDNA and dsDNA reverse transcribing viruses and in one case spanned the entire genome. The results present a novel approach which cannot only identify known viral pathogens, occurring at extremely low titers, but also novel viruses, without the necessity of any prior knowledge.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                15 May 2020
                2020
                : 11
                : 945
                Affiliations
                [1] 1National Citrus Engineering and Technology Research Center, Citrus Research Institute, Southwest University , Chongqing, China
                [2] 2State Cultivation Base of Crop Stress Biology for Southern Mountainous Land, Academy of Agricultural Sciences, Southwest University , Chongqing, China
                [3] 3USDA-ARS, National Germplasm Resources Laboratory , Beltsville, MD, United States
                Author notes

                Edited by: Ahmed Hadidi, Agricultural Research Service (USDA), United States

                Reviewed by: Donato Gallitelli, University of Bari Aldo Moro, Italy; Pasquale Saldarelli, Institute for Sustainable Plant Protection (CNR), Italy

                *Correspondence: Mengji Cao caomengji@ 123456cric.cn

                This article was submitted to Virology, a section of the journal Frontiers in Microbiology

                †ORCID: Mengji Cao orcid.org/0000-0003-0396-262X

                Article
                10.3389/fmicb.2020.00945
                7243478
                32499772
                b1777cd3-1a27-4fdb-88a8-0afed6020eab
                Copyright © 2020 Zhang, Yang, Ma, Tian, Li, Zhou and Cao.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 15 February 2020
                : 20 April 2020
                Page count
                Figures: 6, Tables: 1, Equations: 0, References: 78, Pages: 14, Words: 9351
                Funding
                Funded by: Fundamental Research Funds for the Central Universities 10.13039/501100012226
                Funded by: Chongqing Research Program of Basic Research and Frontier Technology 10.13039/501100013223
                Funded by: Venture and Innovation Support Program for Chongqing Overseas Returnees 10.13039/501100013160
                Funded by: Higher Education Discipline Innovation Project 10.13039/501100013314
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                camellia japonica,next-generation sequencing,virome,new viruses,rt-pcr detection,phylogenetic analysis

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