Evidence map›Paper›PMID 30832687›Full record

ArticleVirology journal2019

Characterization of a hepatitis C virus genotype 1 divergent isolate from an HIV-1 coinfected individual in Germany assigned to a new subtype 1o.

Bo Wang, Luise Krüger, Patrycja Machnowska, Amare Eshetu, Barbara Gunsenheimer-Bartmeyer, Viviane Bremer, Andrea Hauser, Norbert Bannert, C-Thomas Bock

Abstract read
In one paragraph

Article in Virology journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Bo WangDivision of Viral Gastroenteritis, Hepatitis Pathogens and Enteroviruses, Department of Infectious Diseases, Robert Koch Institute, 13353, Berlin, Germany.
Luise KrügerDivision of Viral Gastroenteritis, Hepatitis Pathogens and Enteroviruses, Department of Infectious Diseases, Robert Koch Institute, 13353, Berlin, Germany.
Patrycja MachnowskaDivision of HIV and other Retroviruses, Department of Infectious Diseases, Robert Koch Institute, 13353, Berlin, Germany.
Amare EshetuDivision of HIV and other Retroviruses, Department of Infectious Diseases, Robert Koch Institute, 13353, Berlin, Germany.
Barbara Gunsenheimer-BartmeyerDivision of HIV/AIDS, STI and Blood-borne Infections, Department of Infectious Diseases Epidemiology, Robert Koch Institute, 13353, Berlin, Germany.
Viviane BremerDivision of HIV/AIDS, STI and Blood-borne Infections, Department of Infectious Diseases Epidemiology, Robert Koch Institute, 13353, Berlin, Germany.
Andrea HauserDivision of HIV and other Retroviruses, Department of Infectious Diseases, Robert Koch Institute, 13353, Berlin, Germany.
Norbert BannertDivision of HIV and other Retroviruses, Department of Infectious Diseases, Robert Koch Institute, 13353, Berlin, Germany.
C-Thomas BockDivision of Viral Gastroenteritis, Hepatitis Pathogens and Enteroviruses, Department of Infectious Diseases, Robert Koch Institute, 13353, Berlin, Germany. bockc@rki.de.ORCID 0000-0002-2773-486X

Funding

Bundesministerium für Gesundheit ZMVI1-2516-AUK-701 / BMG: 321-4471-02/157
6 · The paper itself

Abstract

backgroundHCV exhibits a high genetic diversity and is classified into 7 genotypes which are further divided into 86 confirmed subtypes. However, there are multiple isolates with unassigned subtypes. We aimed to amplify and characterize the full-length genome sequence of an HCV genotype 1 (HCV-1) divergent isolate (DE/17-0414) in Germany.

methodsThe HCV infection was detected in an HIV-1-positive German female within an HCV/HIV-coinfection study using a commercially available antigen-antibody HCV ELISA kit and confirmed by an in-house quantitative real-time RT-PCR assay. Preliminary genotyping was done by sequencing and phylogenetic analysis on partial NS5B region. The full-length genome sequence was determined by consensus RT-PCR assays. Resistance-associated substitutions (RASs) were analyzed using the web-based tool Geno2pheno

resultsPartial NS5B region of the isolate DE/17-0414 showed more than 95% identity to 73-08460349-1 l and HCV_Fr_003 from France and QC316 from Canada. Full-length genome analysis of the DE/17-0414 strain showed 91.8% identity to QC316 but less than 79.6% to other HCV-1 strains. Phylogenetic analyses demonstrated that DE/17-0414, 73-08460349-1 l, HCV_Fr_003, and QC316 formed a separate subcluster within HCV-1. DE/17-0414 had a distinct 3 amino acids insertion at the N-terminal of hypervariable region 1 (HVR1) within viral envelope glycoprotein 2 (E2) and several potential antiviral RASs among the NS3 and NS5A genes.

conclusionsWe identified and analyzed an HCV-1 divergent isolate derived from an HIV-1 coinfected individual in Germany, which will be assigned to a new HCV-subtype 1o. Our understanding of the origin and transmission dynamics of this new subtype 1o requires further assessments from patients worldwide.

Indexed as

Genetic VariationGenotypeFemaleGenome, ViralGermanyHepacivirusHIV-1HIV InfectionsHumansMiddle AgedPhylogenyRNA-Dependent RNA PolymeraseSequence Analysis, DNAViral Envelope ProteinsViral Nonstructural Proteinsglycoprotein E2, Hepatitis C virusNS-5 protein, hepatitis C virusRNA-Dependent RNA PolymeraseViral Envelope ProteinsViral Nonstructural ProteinsFull-length genomeHCV genotype 1 subtypesHepatitis C virusHIV-1HVR1RASs

Identifiers

PMID30832687
PMCPMC6399946

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.