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      A Diverse Range of Novel RNA Viruses in Geographically Distinct Honey Bee Populations

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          ABSTRACT

          Understanding the diversity and consequences of viruses present in honey bees is critical for maintaining pollinator health and managing the spread of disease. The viral landscape of honey bees ( Apis mellifera) has changed dramatically since the emergence of the parasitic mite Varroa destructor, which increased the spread of virulent variants of viruses such as deformed wing virus. Previous genomic studies have focused on colonies suffering from infections by Varroa and virulent viruses, which could mask other viral species present in honey bees, resulting in a distorted view of viral diversity. To capture the viral diversity within colonies that are exposed to mites but do not suffer the ultimate consequences of the infestation, we examined populations of honey bees that have evolved naturally or have been selected for resistance to Varroa. This analysis revealed seven novel viruses isolated from honey bees sampled globally, including the first identification of negative-sense RNA viruses in honey bees. Notably, two rhabdoviruses were present in three geographically diverse locations and were also present in Varroa mites parasitizing the bees. To characterize the antiviral response, we performed deep sequencing of small RNA populations in honey bees and mites. This provided evidence of a Dicer-mediated immune response in honey bees, while the viral small RNA profile in Varroa mites was novel and distinct from the response observed in bees. Overall, we show that viral diversity in honey bee colonies is greater than previously thought, which encourages additional studies of the bee virome on a global scale and which may ultimately improve disease management.

          IMPORTANCE Honey bee populations have become increasingly susceptible to colony losses due to pathogenic viruses spread by parasitic Varroa mites. To date, 24 viruses have been described in honey bees, with most belonging to the order Picornavirales. Collapsing Varroa-infected colonies are often overwhelmed with high levels of picornaviruses. To examine the underlying viral diversity in honey bees, we employed viral metatranscriptomics analyses on three geographically diverse Varroa-resistant populations from Europe, Africa, and the Pacific. We describe seven novel viruses from a range of diverse viral families, including two viruses that are present in all three locations. In honey bees, small RNA sequences indicate that these viruses are processed by Dicer and the RNA interference pathway, whereas Varroa mites produce strikingly novel small RNA patterns. This work increases the number and diversity of known honey bee viruses and will ultimately contribute to improved disease management in our most important agricultural pollinator.

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          A slicer-mediated mechanism for repeat-associated siRNA 5' end formation in Drosophila.

          In Drosophila, repeat-associated small interfering RNAs (rasiRNAs) are produced in the germ line by a Dicer-independent pathway and function through the PIWI subfamily of Argonautes to ensure silencing of retrotransposons. We sequenced small RNAs associated with the PIWI subfamily member AGO3. Although other members of PIWI, Aubergine (Aub) and Piwi, associated with rasiRNAs derived mainly from the antisense strand of retrotransposons, AGO3-associated rasiRNAs arose mainly from the sense strand. Aub- and Piwi-associated rasiRNAs showed a strong preference for uracil at their 5' ends, and AGO3-associated rasiRNAs showed a strong preference for adenine at nucleotide 10. Comparisons between AGO3- and Aub-associated rasiRNAs revealed pairs of rasiRNAs showing complementarities in their first 10 nucleotides. Aub and AGO3 exhibited Slicer activity in vitro. These data support a model in which formation of a 5' terminus within rasiRNA precursors is guided by rasiRNAs originating from transcripts of the other strand in concert with the Slicer activity of PIWI.
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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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              Temporal Analysis of the Honey Bee Microbiome Reveals Four Novel Viruses and Seasonal Prevalence of Known Viruses, Nosema, and Crithidia

              Honey bees (Apis mellifera) play a critical role in global food production as pollinators of numerous crops. Recently, honey bee populations in the United States, Canada, and Europe have suffered an unexplained increase in annual losses due to a phenomenon known as Colony Collapse Disorder (CCD). Epidemiological analysis of CCD is confounded by a relative dearth of bee pathogen field studies. To identify what constitutes an abnormal pathophysiological condition in a honey bee colony, it is critical to have characterized the spectrum of exogenous infectious agents in healthy hives over time. We conducted a prospective study of a large scale migratory bee keeping operation using high-frequency sampling paired with comprehensive molecular detection methods, including a custom microarray, qPCR, and ultra deep sequencing. We established seasonal incidence and abundance of known viruses, Nosema sp., Crithidia mellificae, and bacteria. Ultra deep sequence analysis further identified four novel RNA viruses, two of which were the most abundant observed components of the honey bee microbiome (∼1011 viruses per honey bee). Our results demonstrate episodic viral incidence and distinct pathogen patterns between summer and winter time-points. Peak infection of common honey bee viruses and Nosema occurred in the summer, whereas levels of the trypanosomatid Crithidia mellificae and Lake Sinai virus 2, a novel virus, peaked in January.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                J Virol
                J. Virol
                jvi
                jvi
                JVI
                Journal of Virology
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                0022-538X
                1098-5514
                17 May 2017
                27 July 2017
                15 August 2017
                27 July 2017
                : 91
                : 16
                : e00158-17
                Affiliations
                [a ]Behaviour and Genetics of Social Insects Laboratory, School of Life and Environmental Sciences, The University of Sydney, Sydney, Australia
                [b ]Marie Bashir Institute for Infectious Diseases and Biosecurity, Sydney Medical School, The University of Sydney, Sydney, Australia
                [c ]Charles Perkins Centre, The University of Sydney, Sydney, Australia
                [d ]School of Life and Environmental Sciences, The University of Sydney, Sydney, Australia
                [e ]Wageningen University & Research, Wageningen, The Netherlands
                University of Illinois at Chicago
                Author notes
                Address correspondence to Emily J. Remnant, emily.remnant@ 123456sydney.edu.au .

                Citation Remnant EJ, Shi M, Buchmann G, Blacquière T, Holmes EC, Beekman M, Ashe A. 2017. A diverse range of novel RNA viruses in geographically distinct honey bee populations. J Virol 91:e00158-17. https://doi.org/10.1128/JVI.00158-17.

                Author information
                http://orcid.org/0000-0001-9596-3552
                Article
                00158-17
                10.1128/JVI.00158-17
                5533899
                28515299
                e029e815-3f2f-4ce9-b9e3-d51715b1fd3d
                Copyright © 2017 Remnant et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 27 January 2017
                : 26 April 2017
                Page count
                supplementary-material: 1, Figures: 6, Tables: 5, Equations: 1, References: 89, Pages: 19, Words: 11243
                Funding
                Funded by: Marie Bashir Institute for Infectious Diseases and Biosecurity
                Award Recipient : Emily J. Remnant Award Recipient : Edward C. Holmes Award Recipient : Madeleine Beekman
                Funded by: Department of Health | National Health and Medical Research Council (NHMRC) https://doi.org/10.13039/501100000925
                Award ID: GNT1037231
                Award Recipient : Edward C. Holmes
                Funded by: Australian Research Council (ARC) https://doi.org/10.13039/501100000923
                Award ID: DP170100844
                Award Recipient : Madeleine Beekman
                Funded by: Australian Research Council (ARC) https://doi.org/10.13039/501100000923
                Award ID: DE140100199
                Award Recipient : Alyson Ashe
                Funded by: Australia and Pacific Science Foundation (APSF) https://doi.org/10.13039/501100001037
                Award ID: APSF15-02
                Award Recipient : Emily J. Remnant Award Recipient : Madeleine Beekman
                Categories
                Genetic Diversity and Evolution
                Custom metadata
                August 2017

                Microbiology & Virology
                rna interference,arthropod vectors,insect viruses,metagenomics,negative-strand rna virus,phylogenetic analysis,plus-strand rna virus

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