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Uncovering the first atypical ds-1-like g1p[8] rotavirus strains that circulated during pre-rotavirus vaccine introduction era in South Africa

  • Peter N. Mwangi
  • , Milton T. Mogotsi
  • , Sebotsana P. Rasebotsa
  • , Mapaseka L. Seheri
  • , M. Jeffrey Mphahlele
  • , Valantine N. Ndze
  • , Francis E. Dennis
  • , Khuzwayo C. Jere
  • , Martin M. Nyaga
  • University of the Free State
  • Med. University of Southern Africa
  • South African Medical Research Council
  • University of Buea
  • University of Ghana
  • University of Liverpool
  • Kamuzu University of Health Sciences

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)

Abstract

Emergence of DS-1-like G1P[8] group A rotavirus (RVA) strains during post-rotavirus vaccination period has recently been reported in several countries. This study demonstrates, for the first time, rare atypical DS-1-like G1P[8] RVA strains that circulated in 2008 during pre-vaccine era in South Africa. Rotavirus positive samples were subjected to whole-genome sequencing. Two G1P[8] strains (RVA/Human-wt/ZAF/UFS-NGS-MRC-DPRU1971/2008/G1P[8] and RVA/Human-wt/ZAF/UFS-NGS-MRC-DPRU1973/2008/G1P[8]) possessed a DS-1-like genome constellation background (I2-R2-C2-M2-A2-N2-T2-E2-H2). The outer VP4 and VP7 capsid genes of the two South African G1P[8] strains had the highest nucleotide (amino acid) nt (aa) identities of 99.6–99.9% (99.1–100%) with the VP4 and the VP7 genes of a locally circulating South African strain, RVA/Human-wt/ZAF/MRC-DPRU1039/2008/G1P[8]. All the internal backbone genes (VP1–VP3, VP6, and NSP1-NSP5) had the highest nt (aa) identities with cognate internal genes of another locally circulating South African strain, RVA/Human-wt/ZAF/MRC-DPRU2344/2008/G2P[6]. The two study strains emerged through reassortment mechanism involving locally circulating South African strains, as they were distinctly unrelated to other reported atypical G1P[8] strains. The identification of these G1P[8] double-gene reassortants during the pre-vaccination period strongly supports natural RVA evolutionary mechanisms of the RVA genome. There is a need to maintain long-term whole-genome surveillance to monitor such atypical strains.

Original languageEnglish
Article number391
JournalPathogens
Volume9
Issue number5
DOIs
Publication statusPublished - May 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Atypical strains
  • Genome constellation
  • Reassortment
  • Rotavirus
  • Whole-genome characterization

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