Evolutionary changes between pre- and post-vaccine South African group A G2P[4] rotavirus strains, 2003–2017

dc.contributor.authorMwangi, Peter N.
dc.contributor.authorPage, Nicola Anne
dc.contributor.authorSeheri, Mapaseka L.
dc.contributor.authorMphahlele, M.
dc.contributor.authorNadan, Sandrama
dc.contributor.authorEsona, Mathew D.
dc.contributor.authorKumwenda, Benjamin
dc.contributor.authorKamng’ona, Arox W.
dc.contributor.authorDonato, Celeste M.
dc.contributor.authorSteele, Duncan A.
dc.contributor.authorNdze, Valantine N.
dc.contributor.authorDennis, Francis E.
dc.contributor.authorJere, Khuzwayo C.
dc.contributor.authorNyaga, Martin M.
dc.date.accessioned2023-09-18T12:23:56Z
dc.date.available2023-09-18T12:23:56Z
dc.date.issued2022-04
dc.descriptionDATA STATEMENT : All supporting data, code and protocols have been provided within the article or through supplementary data files.en_US
dc.description.abstractThe transient upsurge of G2P[4] group A rotavirus (RVA) after Rotarix vaccine introduction in several countries has been a matter of concern. To gain insight into the diversity and evolution of G2P[4] strains in South Africa pre- and post-RVA vaccination introduction, whole-genome sequencing was performed for RVA positive faecal specimens collected between 2003 and 2017 and samples previously sequenced were obtained from GenBank (n=103; 56 pre- and 47 post-vaccine). Pre-vaccine G2 sequences predominantly clustered within sub-lineage IVa-1. In contrast, post-vaccine G2 sequences clustered mainly within sub-lineage IVa-3, whereby a radical amino acid (AA) substitution, S15F, was observed between the two sub-lineages. Pre-vaccine P[4] sequences predominantly segregated within sub-lineage IVa while post-vaccine sequences clustered mostly within sub-lineage IVb, with a radical AA substitution R162G. Both S15F and R162G occurred outside recognised antigenic sites. The AA residue at position 15 is found within the signal sequence domain of Viral Protein 7 (VP7) involved in translocation of VP7 into endoplasmic reticulum during infection process. The 162 AA residue lies within the hemagglutination domain of Viral Protein 4 (VP4) engaged in interaction with sialic acid-containing structure during attachment to the target cell. Free energy change analysis on VP7 indicated accumulation of stable point mutations in both antigenic and non-antigenic regions. The segregation of South African G2P[4] strains into pre- and post-vaccination sub-lineages is likely due to erstwhile hypothesized stepwise lineage/sub-lineage evolution of G2P[4] strains rather than RVA vaccine introduction. Our findings reinforce the need for continuous whole-genome RVA surveillance and investigation of contribution of AA substitutions in understanding the dynamic G2P[4] epidemiology.en_US
dc.description.departmentMedical Virologyen_US
dc.description.librarianam2023en_US
dc.description.sponsorshipThe Bill and Melinda Gates Foundation, the South African Medical Research Council (SAMRC) through the Self-Initiated Research grant (SIR), Poliomyelitis Research Foundation, the National Research Foundation, a Wellcome Training Fellowship and the PRF.en_US
dc.description.urihttps://www.microbiologyresearch.org/content/journal/mgenen_US
dc.identifier.citationMwangi, P.N., Page, N.A., Seheri, M.L. et al. 2022, 'Evolutionary changes between pre- and post-vaccine South African group A G2P[4] rotavirus strains, 2003–2017', Microbial Genomics, vol. 2022, no. 8, pp. 1-14. DOI 10.1099/mgen.0.000809.en_US
dc.identifier.issn2057-5858
dc.identifier.other10.1099/mgen.0.000809
dc.identifier.urihttp://hdl.handle.net/2263/92310
dc.language.isoenen_US
dc.publisherMicrobiology Societyen_US
dc.rights© 2022 The Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution License.en_US
dc.subjectG2P[4] Group A rotavirus strainsen_US
dc.subjectRotavirusen_US
dc.subjectSub-lineagesen_US
dc.subjectWhole-genome analysisen_US
dc.titleEvolutionary changes between pre- and post-vaccine South African group A G2P[4] rotavirus strains, 2003–2017en_US
dc.typeArticleen_US

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