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PARV4 prevalence, phylogeny, immunology and coinfection with HIV, HBV and HCV in a multicentre African cohort.
Sharp, Colin P; Gregory, William F; Hattingh, Louise; Malik, Amna; Adland, Emily; Daniels, Samantha; van Zyl, Anriette; Carlson, Jonathan M; Wareing, Susan; Ogwu, Anthony; Shapiro, Roger; Riddell, Lynn; Chen, Fabian; Ndung'u, Thumbi; Goulder, Philip J R; Klenerman, Paul; Simmonds, Peter; Jooste, Pieter; Matthews, Philippa C.
Affiliation
  • Sharp CP; Roslin Institute, University of Edinburgh, Edinburgh, EH25 9RG, UK.
  • Gregory WF; Edinburgh Genomics, University of Edinburgh, Edinburgh, EH9 3FL, UK.
  • Hattingh L; Roslin Institute, University of Edinburgh, Edinburgh, EH25 9RG, UK.
  • Malik A; Kimberley Hospital, Kimberley, Northern Cape, 8301, South Africa.
  • Adland E; Department of Paediatrics, University of Oxford, Oxford, OX1 3SY, UK.
  • Daniels S; Department of Paediatrics, University of Oxford, Oxford, OX1 3SY, UK.
  • van Zyl A; Kimberley Hospital, Kimberley, Northern Cape, 8301, South Africa.
  • Carlson JM; Kimberley Hospital, Kimberley, Northern Cape, 8301, South Africa.
  • Wareing S; Microsoft Research, Redmond, WA, 98052, USA.
  • Ogwu A; Department of Microbiology and Infectious Diseases, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
  • Shapiro R; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Riddell L; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
  • Chen F; Northampton General Hospital NHS Trust, Northampton, NN1 5BD, UK.
  • Ndung'u T; Royal Berkshire Hospital, Reading, RG1 5AN, UK.
  • Goulder PJR; HIV Pathogenesis Program, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, KwaZulu-Natal, 4041, South Africa.
  • Klenerman P; Department of Paediatrics, University of Oxford, Oxford, OX1 3SY, UK.
  • Simmonds P; Department of Microbiology and Infectious Diseases, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
  • Jooste P; Nuffield Department of Medicine, University of Oxford, Oxford, OX1 3SY, UK.
  • Matthews PC; NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
Wellcome Open Res ; 2: 26, 2017 Apr 07.
Article in En | MEDLINE | ID: mdl-28497124
Background: The seroprevalence of human parvovirus-4 (PARV4) varies considerably by region. In sub-Saharan Africa, seroprevalence is high in the general population, but little is known about the transmission routes or the prevalence of coinfection with blood-borne viruses, HBV, HCV and HIV.  Methods: To further explore the characteristics of PARV4 in this setting, with a particular focus on the prevalence and significance of coinfection, we screened a cohort of 695 individuals recruited from Durban and Kimberley (South Africa) and Gaborone (Botswana) for PARV4 IgG and DNA, as well as documenting HIV, HBV and HCV status.  Results: Within these cohorts, 69% of subjects were HIV-positive. We identified no cases of HCV by PCR, but 7.4% were positive for HBsAg. PARV4 IgG was positive in 42%; seroprevalence was higher in adults (69%) compared to children (21%) (p<0.0001) and in HIV-positive (52%) compared to HIV-negative individuals (24%) (p<0.0001), but there was no association with HBsAg status. We developed an on-line tool to allow visualization of coinfection data (https://purl.oclc.org/coinfection-viz). We identified five subjects who were PCR-positive for PARV4 genotype-3. Ex vivo CD8+ T cell responses spanned the entire PARV4 proteome and we propose a novel HLA-B*57:03-restricted epitope within the NS protein.  Conclusions: This characterisation of PARV4 infection provides enhanced insights into the epidemiology of infection and co-infection in African cohorts, and provides the foundations for planning further focused studies to elucidate transmission pathways, immune responses, and the clinical significance of this organism.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prevalence_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Wellcome Open Res Year: 2017 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prevalence_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Wellcome Open Res Year: 2017 Type: Article