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10.1099/vir.0.063016-0

http://scihub22266oqcxt.onion/10.1099/vir.0.063016-0
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suck abstract from ncbi


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pmid24668525
      J+Gen+Virol 2014 ; 95 (Pt 6 ): 1307-1319
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  • Human pegivirus RNA is found in multiple blood mononuclear cells in vivo and serum-derived viral RNA-containing particles are infectious in vitro #MMPMID24668525
  • Chivero ET ; Bhattarai N ; Rydze RT ; Winters MA ; Holodniy M ; Stapleton JT
  • J Gen Virol 2014[Jun]; 95 (Pt 6 ): 1307-1319 PMID24668525 show ga
  • Human pegivirus (HPgV; previously called GB virus C/hepatitis G virus) has limited pathogenicity, despite causing persistent infection, and is associated with prolonged survival in human immunodeficiency virus-infected individuals. Although HPgV RNA is found in and produced by T- and B-lymphocytes, the primary permissive cell type(s) are unknown. We quantified HPgV RNA in highly purified CD4(+) and CD8(+) T-cells, including naïve, central memory and effector memory populations, and in B-cells (CD19(+)), NK cells (CD56(+)) and monocytes (CD14(+)) using real-time reverse transcription-PCR. Single-genome sequencing was performed on viruses within individual cell types to estimate genetic diversity among cell populations. HPgV RNA was present in CD4(+) and CD8(+) T-lymphocytes (nine of nine subjects), B-lymphocytes (seven of ten subjects), NK cells and monocytes (both four of five). HPgV RNA levels were higher in naïve (CD45RA(+)) CD4(+) cells than in central memory and effector memory cells (P<0.01). HPgV sequences were highly conserved among subjects (0.117±0.02 substitutions per site; range 0.58-0.14) and within subjects (0.006±0.003 substitutions per site; range 0.006-0.010). The non-synonymous/synonymous substitution ratio was 0.07, suggesting a low selective pressure. Carboxyfluorescein succinimidyl ester (CFSE)-labelled HPgV RNA-containing particles precipitated by a commercial exosome isolation reagent delivered CSFE to uninfected monocytes, NK cells and T- and B-lymphocytes, and HPgV RNA was transferred to PBMCs with evidence of subsequent virus replication. Thus, HPgV RNA-containing serum particles including microvesicles may contribute to delivery of HPgV to PBMCs in vivo, explaining the apparent broad tropism of this persistent human RNA virus.
  • |Adult [MESH]
  • |Amino Acid Sequence [MESH]
  • |B-Lymphocytes/virology [MESH]
  • |Base Sequence [MESH]
  • |CD4-Positive T-Lymphocytes/virology [MESH]
  • |CD8-Positive T-Lymphocytes/virology [MESH]
  • |Conserved Sequence [MESH]
  • |Female [MESH]
  • |Flaviviridae Infections/complications/virology [MESH]
  • |GB virus C/genetics/*isolation & purification/*pathogenicity [MESH]
  • |HIV Infections/complications [MESH]
  • |Hepatitis, Viral, Human/complications/virology [MESH]
  • |Humans [MESH]
  • |Killer Cells, Natural/virology [MESH]
  • |Leukocytes, Mononuclear/*virology [MESH]
  • |Male [MESH]
  • |Middle Aged [MESH]
  • |Molecular Sequence Data [MESH]
  • |Monocytes/virology [MESH]
  • |Phylogeny [MESH]
  • |RNA Helicases/genetics [MESH]
  • |RNA, Viral/*blood/genetics [MESH]
  • |Serine Endopeptidases/genetics [MESH]
  • |Viral Nonstructural Proteins/genetics [MESH]
  • |Virulence [MESH]


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