|
Basic Characteristics of Mutations
|
|
Mutation Site
|
A226V |
|
Mutation Site Sentence
|
Chikungunya viruses containing the A226V mutation detected retrospectively in Cameroon form a new geographical subclade. |
|
Mutation Level
|
Amino acid level |
|
Mutation Type
|
Nonsynonymous substitution |
|
Gene/Protein/Region
|
E1 |
|
Standardized Encoding Gene
|
E1
|
|
Genotype/Subtype
|
ECSA |
|
Viral Reference
|
AF079456.1
|
|
Functional Impact and Mechanisms
|
|
Disease
|
Chikungunya Fever
|
|
Immune
|
- |
|
Target Gene
|
-
|
|
Clinical and Epidemiological Correlations
|
|
Clinical Information
|
- |
|
Treatment
|
- |
|
Location
|
Cameroon |
|
Literature Information
|
|
PMID
|
34592442
|
|
Title
|
Chikungunya viruses containing the A226V mutation detected retrospectively in Cameroon form a new geographical subclade
|
|
Author
|
Agbodzi B,Yousseu FBS,Simo FBN,Kumordjie S,Yeboah C,Mosore MT,Bentil RE,Prieto K,Colston SM,Attram N,Nimo-Paintsil S,Fox AT,Bonney JHK,Ampofo W,Coatsworth HG,Dinglasan RR,Wolfe DM,Wiley MR,Demanou M,Letizia AG
|
|
Journal
|
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
|
|
Journal Info
|
2021 Dec;113:65-73
|
|
Abstract
|
BACKGROUND: Chikungunya virus (CHIKV) is a re-emerging arbovirus associated with sporadic outbreaks in Cameroon since 2006. Viral whole genomes were generated to analyze the origins of evolutionary lineages, the potential of emergence/re-emergence, and to infer transmission dynamics of recent Cameroon CHIKV outbreak strains. METHODS: Samples collected between 2016 and 2019 during CHIKV outbreaks in Cameroon were screened for CHIKV using reverse transcription PCR (RT-PCR), followed by whole genome sequencing of positive samples. RESULTS: Three coding-complete CHIKV genomes were obtained from samples, which belong to an emerging sub-lineage of the East/Central/South African genotype and formed a monophyletic taxon with previous Central African strains. This clade, which we have named the new Central African clade, appears to be evolving at 3.0 x 10(-4) nucleotide substitutions per site per year (95% highest posterior density (HPD) interval of 1.94 x 10(-4) to 4.1 x 10(-4)). Notably, mutations in the envelope proteins (E1-A226V, E2-L210Q, and E2-I211T), which are known to enhance CHIKV adaptability and infectious potential in Aedes albopictus, were present in all strains and mapped to established high-density Ae. albopictus populations. CONCLUSIONS: These new CHIKV strains constitute a conserved genomic pool of an emerging sub-lineage, reflecting a putative vector host adaptation to Ae. albopictus, which has practically displaced Aedes aegypti from select regions of Cameroon.
|
|
Sequence Data
|
MT666071-MT666073
|
|
|