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Molecular evolutionary and epidemiological dynamics of genotypes 1G and 2B of rubella virus.

Abstract
Rubella Virus (RV), which causes measles-like rashes in children, puts millions of infants at risk of congenital defects across the globe. Employing phylogenetic approaches to the whole genome sequence data and E1 glycoprotein sequence data, the present study reports the substitution rates and dates of emergence of all thirteen previously described rubella genotypes, and gains important insights into the epidemiological dynamics of two geographically widely distributed genotypes 1G and 2B. The overall nucleotide substitution rate of this non-vector-borne RV is in the order of 10-3 substitutions/site/year, which is considerably higher than the substitution rates previously reported for the vector-borne alphaviruses within the same family. Currently circulating strains of RV share a common ancestor that existed within the last 150 years, with 95% Highest Posterior Density values ranging from 1868 to 1926 AD. Viral strains within the respective genotypes began diverging between the year 1930 s and 1980 s. Both genotype 1G and 2B have shown a decline in effective number of infections since 1990 s, a period during which mass immunization programs against RV were adapted across the globe. Although both genotypes showed some extent of spatial genetic structuring, the analyses also depicted an inter-continental viral dispersal. Such a viral dispersal pattern could be related to the migration of infected individuals across the regions coupled with a low coverage of MMR vaccination.
AuthorsAbinash Padhi, Li Ma
JournalPloS one (PLoS One) Vol. 9 Issue 10 Pg. e110082 ( 2014) ISSN: 1932-6203 [Electronic] United States
PMID25329480 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Membrane Glycoproteins
  • Viral Envelope Proteins
Topics
  • Evolution, Molecular
  • Genotype
  • Measles (epidemiology)
  • Membrane Glycoproteins (genetics)
  • Phylogeny
  • Rubella virus (genetics)
  • Viral Envelope Proteins (genetics)

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