Genetic Diversity of Human Enterovirus 68 Strains Isolated in Kenya Using the Hypervariable 3′- End of VP1 Gene
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Date
2014Author
Opanda, SM
Wamunyokoli, F
Khamadi, S
Coldren, R
Bulimo, WD
Language
enMetadata
Show full item recordAbstract
Reports of increasing worldwide circulation of human enterovirus-68 (EV68) are well documented. Despite health concerns
posed by resurgence of these viruses, little is known about EV68 strains circulating in Kenya. In this study, we characterized
13 EV68 strains isolated in Kenya between 2008 and 2011 based on the Hypervariable 39- end of the VP1 gene. Viral RNA
was extracted from the isolates and partial VP1 gene amplified by RT-PCR, followed by nucleotide sequencing. Alignment of
deduced amino acid sequences revealed substitutions in Kenyan EV68 isolates absent in the prototype reference strain
(Fermon). The majority of these changes were present in the BC and DE-loop regions, which are associated with viral
antigenicity and virulence. The Kenyan strains exhibited high sequence homology with respect to those from other
countries. Natural selection analysis based on the VP1 region showed that the Kenyan EV68 isolates were under purifying
selection. Phylogenetic analysis revealed that majority (84.6%) of the Kenyan strains belonged to clade A, while a minority
belonged to clades B and C. Overall, our results illustrate that although EV68 strains isolated in Kenya were genetically and
antigenically divergent from the prototype strain (Fermon), they were closely related to those circulating in other countries,
suggesting worldwide transmissibility. Further, the presence of shared mutations by Kenyan EV68 strains and those isolated
in other countries, indicates evolution in the VP1 region may be contributing to increased worldwide detection of the
viruses. This is the first study to document circulation of EV68 in Kenya
Citation
Opanda SM, Wamunyokoli F, Khamadi S, Coldren R, Bulimo WD. "Genetic Diversity of Human Enterovirus 68 Strains Isolated in Kenya Using the Hypervariable 3′- End of VP1 Gene." PLoS ONE. 2014;9(7):e102866-.Publisher
University of Nairobi
Collections
- Faculty of Health Sciences (FHS) [10385]