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Evolutionary changes between pre- and post-vaccine South African group A G2P[4] rotavirus strains, 2003-2017.
Mwangi, Peter N; Page, Nicola A; Seheri, Mapaseka L; Mphahlele, M Jeffrey; Nadan, Sandrama; Esona, Mathew D; Kumwenda, Benjamin; Kamng'ona, Arox W; Donato, Celeste M; Steele, Duncan A; Ndze, Valantine N; Dennis, Francis E; Jere, Khuzwayo C; Nyaga, Martin M.
Afiliación
  • Mwangi PN; Next Generation Sequencing Unit and Division of Virology, Faculty of Health Sciences, University of the Free State, Bloemfontein 9300, South Africa.
  • Page NA; Centre for Enteric Disease, National Institute for Communicable Diseases, Private Bag X4, Sandringham, 2131, Johannesburg, South Africa.
  • Seheri ML; Department of Medical Virology, Faculty of Health Sciences, University of Pretoria, Private Bag X323, Arcadia, 0007, Pretoria, South Africa.
  • Mphahlele MJ; Diarrheal Pathogens Research Unit, Sefako Makgatho Health Sciences University, Medunsa 0204, Pretoria, South Africa.
  • Nadan S; Diarrheal Pathogens Research Unit, Sefako Makgatho Health Sciences University, Medunsa 0204, Pretoria, South Africa.
  • Esona MD; Office of the Deputy Vice Chancellor for Research and Innovation, North-West University, Potchefstroom 2351, South Africa.
  • Kumwenda B; South African Medical Research Council, Pretoria 0001, South Africa.
  • Kamng'ona AW; Centre for Enteric Disease, National Institute for Communicable Diseases, Private Bag X4, Sandringham, 2131, Johannesburg, South Africa.
  • Donato CM; Diarrheal Pathogens Research Unit, Sefako Makgatho Health Sciences University, Medunsa 0204, Pretoria, South Africa.
  • Steele DA; Department of Biomedical Sciences, School of Life Sciences and Applied Health Professions, Kamuzu University of Health Sciences, Private Bag 360, Chichiri, Blantyre 3, Malawi.
  • Ndze VN; Department of Biomedical Sciences, School of Life Sciences and Applied Health Professions, Kamuzu University of Health Sciences, Private Bag 360, Chichiri, Blantyre 3, Malawi.
  • Dennis FE; Department of Medical Laboratory Sciences, School of Life Sciences and Applied Health Professions, Kamuzu University of Health Sciences, Private Bag 360, Chichiri, Blantyre3, Malawi.
  • Jere KC; Enteric Diseases Group, Murdoch Children's Research Institute, 50 Flemington Road, Parkville, Melboune 3052, Australia.
  • Nyaga MM; Department of Paediatrics, the University of Melbourne, Parkville 3010, Australia.
Microb Genom ; 8(4)2022 04.
Article en En | MEDLINE | ID: mdl-35446251
ABSTRACT
The 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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Infecciones por Rotavirus / Rotavirus Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Microb Genom Año: 2022 Tipo del documento: Article País de afiliación: Sudáfrica

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Infecciones por Rotavirus / Rotavirus Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Microb Genom Año: 2022 Tipo del documento: Article País de afiliación: Sudáfrica