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BackgroundKenya introduced the monovalent G1P [8] Rotarix® vaccine into the infant immunization schedule in July 2014. We examined trends in rotavirus group A (RVA) genotype distribution pre- (January 2010-June 2014) and post- (July 2014-December 2018) RVA vaccine introduction.MethodsStool samples were collected from children aged ResultsWe genotyped 614 samples in pre-vaccine and 261 in post-vaccine introduction periods. During the pre-vaccine introduction period, the most frequent RVA genotypes were G1P [8] (45.8%), G8P [4] (15.8%), G9P [8] (13.2%), G2P [4] (7.0%) and G3P [6] (3.1%). In the post-vaccine introduction period, the most frequent genotypes were G1P [8] (52.1%), G2P [4] (20.7%) and G3P [8] (16.1%). Predominant genotypes varied by year and site in both pre and post-vaccine periods. Temporal genotype patterns showed an increase in prevalence of vaccine heterotypic genotypes, such as the commonly DS-1-like G2P [4] (7.0 to 20.7%, P ConclusionGenotype prevalence varied from before to after vaccine introduction. Such observations emphasize the need for long-term surveillance to monitor vaccine impact. These changes may represent natural secular variation or possible immuno-epidemiological changes arising from the introduction of the vaccine. Full genome sequencing could provide insights into post-vaccine evolutionary pressures and antigenic diversity.

Original publication

DOI

10.1186/s12879-020-05230-0

Type

Journal

BMC infectious diseases

Publication Date

07/2020

Volume

20

Addresses

Wellcome Trust Research Programme, Kenya Medical Research Institute, Kilifi, Kenya. mikemwanga6@gmail.com.

Keywords

Feces, Humans, Rotavirus, Rotavirus Infections, Gastroenteritis, Vaccines, Attenuated, Rotavirus Vaccines, Enzyme-Linked Immunosorbent Assay, Immunization Schedule, Vaccination, Prevalence, Phylogeny, Genotype, Child, Child, Preschool, Infant, Kenya, Female, Male