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      Enteric virome of Ethiopian children participating in a clean water intervention trial

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          Abstract

          Background

          The enteric viruses shed by different populations can be influenced by multiple factors including access to clean drinking water. We describe here the eukaryotic viral genomes in the feces of Ethiopian children participating in a clean water intervention trial.

          Methodology/principal findings

          Fecal samples from 269 children with a mean age of 2.7 years were collected from 14 villages in the Amhara region of Ethiopia, half of which received a new hand-dug water well. Feces from these villages were then analyzed in 29 sample pools using viral metagenomics. A total of 127 different viruses belonging to 3 RNA and 3 DNA viral families were detected. Picornaviridae family sequence reads were the most commonly found, originating from 14 enterovirus and 6 parechovirus genotypes plus multiple members of four other picornavirus genera (cosaviruses, saliviruses, kobuviruses, and hepatoviruses). Picornaviruses with nearly identical capsid VP1 were detected in different pools reflecting recent spread of these viral strains. Next in read frequencies and positive pools were sequences from the Caliciviridae family including noroviruses GI and GII and sapoviruses. DNA viruses from multiple genera of the Parvoviridae family were detected (bocaviruses 1–4, bufavirus 3, and dependoparvoviruses), together with four species of adenoviruses and common anelloviruses shedding. RNA in the order Picornavirales and CRESS-DNA viral genomes, possibly originating from intestinal parasites or dietary sources, were also characterized. No significant difference was observed between the number of mammalian viruses shed from children from villages with and without a new water well.

          Conclusions

          We describe an approach to estimate the efficacy of potentially virus transmission-reducing interventions and the first complete (DNA and RNA viruses) description of the enteric viromes of East African children. A wide diversity of human enteric viruses was found in both intervention and control groups. Mammalian enteric virome diversity was not reduced in children from villages with a new water well. This population-based sampling also provides a baseline of the enteric viruses present in Northern Ethiopia against which to compare future viromes.

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          Most cited references26

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          BLAST: improvements for better sequence analysis

          Basic local alignment search tool (BLAST) is a sequence similarity search program. The National Center for Biotechnology Information (NCBI) maintains a BLAST server with a home page at . We report here on recent enhancements to the results produced by the BLAST server at the NCBI. These include features to highlight mismatches between similar sequences, show where the query was masked for low-complexity sequence, and integrate information about the database sequences from the NCBI Entrez system into the BLAST display. Changes to how the database sequences are fetched have also improved the speed of the report generator.
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            Altered Virome and Bacterial Microbiome in Human Immunodeficiency Virus-Associated Acquired Immunodeficiency Syndrome.

            Human immunodeficiency virus (HIV) infection is associated with increased intestinal translocation of microbial products and enteropathy as well as alterations in gut bacterial communities. However, whether the enteric virome contributes to this infection and resulting immunodeficiency remains unknown. We characterized the enteric virome and bacterial microbiome in a cohort of Ugandan patients, including HIV-uninfected or HIV-infected subjects and those either treated with anti-retroviral therapy (ART) or untreated. Low peripheral CD4 T cell counts were associated with an expansion of enteric adenovirus sequences and this increase was independent of ART treatment. Additionally, the enteric bacterial microbiome of patients with lower CD4 T counts exhibited reduced phylogenetic diversity and richness with specific bacteria showing differential abundance, including increases in Enterobacteriaceae, which have been associated with inflammation. Thus, immunodeficiency in progressive HIV infection is associated with alterations in the enteric virome and bacterial microbiome, which may contribute to AIDS-associated enteropathy and disease progression.
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              A geminivirus-related DNA mycovirus that confers hypovirulence to a plant pathogenic fungus.

              Mycoviruses are viruses that infect fungi and have the potential to control fungal diseases of crops when associated with hypovirulence. Typically, mycoviruses have double-stranded (ds) or single-stranded (ss) RNA genomes. No mycoviruses with DNA genomes have previously been reported. Here, we describe a hypovirulence-associated circular ssDNA mycovirus from the plant pathogenic fungus Sclerotinia sclerotiorum. The genome of this ssDNA virus, named Sclerotinia sclerotiorum hypovirulence-associated DNA virus 1 (SsHADV-1), is 2166 nt, coding for a replication initiation protein (Rep) and a coat protein (CP). Although phylogenetic analysis of Rep showed that SsHADV-1 is related to geminiviruses, it is notably distinct from geminiviruses both in genome organization and particle morphology. Polyethylene glycol-mediated transfection of fungal protoplasts was successful with either purified SsHADV-1 particles or viral DNA isolated directly from infected mycelium. The discovery of an ssDNA mycovirus enhances the potential of exploring fungal viruses as valuable tools for molecular manipulation of fungi and for plant disease control and expands our knowledge of global virus ecology and evolution.
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                Author and article information

                Contributors
                Role: MethodologyRole: ResourcesRole: Writing – original draft
                Role: Data curationRole: MethodologyRole: Resources
                Role: Methodology
                Role: Formal analysisRole: Methodology
                Role: Data curation
                Role: Data curation
                Role: Data curation
                Role: Funding acquisitionRole: ResourcesRole: Writing – review & editing
                Role: InvestigationRole: Project administrationRole: SupervisionRole: Writing – original draftRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                16 August 2018
                2018
                : 13
                : 8
                : e0202054
                Affiliations
                [1 ] Blood Systems Research Institute, San Francisco, California, United States of America
                [2 ] University of California San Francisco, Department of Laboratory Medicine, San Francisco, California, United States of America
                [3 ] Francis I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America
                [4 ] Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, United States of America
                [5 ] The Carter Center Ethiopia, Addis Ababa, Ethiopia
                [6 ] The Carter Center, Atlanta, Georgia, United States of America
                Oklahoma State University, UNITED STATES
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0001-7903-6986
                http://orcid.org/0000-0002-6296-4484
                Article
                PONE-D-18-13041
                10.1371/journal.pone.0202054
                6095524
                30114205
                f0d2401c-8ecf-456f-8814-7d37837f3f46
                © 2018 Altan et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 1 May 2018
                : 26 July 2018
                Page count
                Figures: 6, Tables: 1, Pages: 20
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100008495, Blood Systems Research Institute;
                Funded by: funder-id http://dx.doi.org/10.13039/100000009, Foundation for the National Institutes of Health;
                Award ID: NEI U10 EY016214
                Funded by: funder-id http://dx.doi.org/10.13039/100000009, Foundation for the National Institutes of Health;
                Award ID: NEI K23EY019071
                Funded by: funder-id http://dx.doi.org/10.13039/100000009, Foundation for the National Institutes of Health;
                Award ID: NICHD F31HD088070-01A1
                Funded by: The Sara & Evan Williams Foundation
                Funded by: The Bernard Osher Foundation
                Funded by: That Man May See
                Funded by: The Harper Inglis Trust
                Funded by: The Bodri Foundation
                Funded by: The South Asia Research Fund, and Research to Prevent Blindness
                The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This work was entirely supported by funds from the Blood Systems Research Institute, the National Institutes of Health (NEI U10 EY016214, NEI K23EY019071, and NICHD F31 HD088070-01A1), the Sara & Evan Williams Foundation, the Bernard Osher Foundation, That Man May See, the Harper Inglis Trust, the Bodri Foundation, the South Asia Research Fund, Research to Prevent Blindness, and the Carter Center Ethiopia. There was no additional external funding received for this study.
                Categories
                Research Article
                Biology and life sciences
                Organisms
                Viruses
                RNA viruses
                Picornaviruses
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                Organisms
                Viruses
                RNA viruses
                Enteroviruses
                Coxsackieviruses
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                Microbiology
                Medical Microbiology
                Microbial Pathogens
                Viral Pathogens
                Enteroviruses
                Coxsackieviruses
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                Enteroviruses
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                Custom metadata
                The genomes of viruses are available on the NCBI website; the accession numbers are given in Tables 1 and S1. The raw sequence data is available at NCBI’s Short Reads Archive under GenBank accession number SRP120619.

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