Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/9246
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dc.contributor.authorMbogori, Elius-
dc.contributor.authorThiongo, Kelvin-
dc.contributor.authorDeng, Harrison Yunying-
dc.contributor.authorGikunyu, Caroline-
dc.contributor.authorCheriro, Winfrida-
dc.contributor.authorMusyoki, Stanslaus-
dc.contributor.authorBiegon, Richard-
dc.contributor.authorMatoke-Muhia, Damaris-
dc.contributor.authorPatel, Kirtika-
dc.contributor.authorLiang, Binhua-
dc.contributor.authorSongok, Elijah-
dc.date.accessioned2024-06-10T13:01:58Z-
dc.date.available2024-06-10T13:01:58Z-
dc.date.issued2024-05-10-
dc.identifier.urihttps://doi.org/10.20944/preprints202405.0647.v1-
dc.identifier.urihttp://ir.mu.ac.ke:8080/jspui/handle/123456789/9246-
dc.description.abstractThe rise of new SARS-CoV-2 mutations brought challenges and progress in the global fight against COVID-19. Mutations in spike and accessory genes affect transmission, vaccine efficacy, treatments, testing, and public health strategies. Monitoring emerging variants is crucial to halt virus spread. Methods: 44 nasopharyngeal/oropharyngeal swabs from Kenyan patients were sequenced with the Illumina platform. Galaxy's bioinformatic tools were used for genomic analysis. SARS-CoV-2 genome classification was done using PANGOLIN and mutation annotation with the COVID-19 Annotator tool. Results: The study showed 5 clades to be circulating in the region. 38(86%) were BA.1.1; 2(5%) were BA.1.1.1; 1(2%) was BA.1; 1(2%) was BA.1.14 and 2(5%) were AY.46. These clades had a cumulative of 173 mutations among them with 50 novel mutations. Forty-eight of these novel mutations occurred in a low frequency of 2.3% of the sequences tested while the other two, S:R214R, and NSP2:A555A, were for 43.2% and 18.2% of the cases respectively. Conclusions: The high-frequency novel mutations were synonymous mutations, a phenomenon that was previously viewed as phenotypically silent but recent studies indicate they can affect viral fitness with potential functional associations. These findings add to the understanding of the SARS-CoV-2 virus future evolutionary and immunological dynamics in the regionen_US
dc.language.isoenen_US
dc.publisherPreprints.orgen_US
dc.subjectSARS-CoV-2en_US
dc.subjectCOVID-19en_US
dc.subjectSpike proteinen_US
dc.subjectEpistasisen_US
dc.subjectReverse transcriptionen_US
dc.subjectPathogenesisen_US
dc.subjectVaccine efficacyen_US
dc.subjectComplementary DNA;en_US
dc.subjectReverse transcription-polymerase chain reactionen_US
dc.titleEmerging Mutations of SARS-COV-2 in Kenyaen_US
dc.typeArticleen_US
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