dc.contributor.author |
Esona, Mathew Dioh
|
|
dc.contributor.author |
Kerin, Tara
|
|
dc.contributor.author |
Peenze, Ina
|
|
dc.contributor.author |
Nicola Page, James Nyangao
|
|
dc.contributor.author |
Akran Agbaya, Veronigue
|
|
dc.contributor.author |
Aminu, Maryam
|
|
dc.contributor.author |
Sebunya,Theresia
|
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dc.contributor.author |
Glass, Roger
|
|
dc.contributor.author |
Steele, Duncan
|
|
dc.contributor.author |
Armah, George
|
|
dc.contributor.author |
Page, Nicola
|
|
dc.contributor.author |
Nyangao, James
|
|
dc.contributor.author |
Trabelsi, Abdelhalim
|
|
dc.contributor.author |
Gentsch, Jon
|
|
dc.date.accessioned |
2011-01-18T10:35:36Z |
|
dc.date.available |
2011-01-18T10:35:36Z |
|
dc.date.issued |
2010-09 |
|
dc.identifier.citation |
DOI: 10.1086/653552 |
en |
dc.identifier.uri |
http://hdl.handle.net/10500/3933 |
|
dc.description |
Acknowledgments:
The postdoctoral fellowship of Dr Esona was provided through the Rotavirus Vaccine Program, a collaboration between the Program for Appropriate Technology in Health, the World Health Organization, and the Centers
for Disease Control and Prevention. Our sincere thanks also go to all the staff of the Medical Research Council Diarrhoeal Pathogens Research Unit, University of Limpopo, and the Gastroenteritis and Respiratory Viruses Laboratory Branch at the Centers for Disease Control and revention,Atlanta, for their immense assistance. |
en |
dc.description.abstract |
A total of 215 nontypeable rotavirus samples collected from children 5 years of age by members of the African Rotavirus Network were characterized using reverse-transcription polymerase chain reaction analysis and sequencing. The most predominant strain identified was P[8]G1 (46.9%). Genotypes P[8]G10, P[8]G8, P[6]G8, and P[7]G5 were also detected at frequencies varying from 0.5% to 2.3%. This study suggests that reassortment of unusual G types into a background of globally common genotype P[8] strains may be a major mechanism of generating rotavirus diversity. Nucleotide substitutions at the P[8], P[6], and G1 primer binding sites accounted for the failure to type these strains initially. Hence, these findings highlight the need for regular evaluation of rotavirus genotyping methods. |
en |
dc.description.sponsorship |
Financial support:
World Health Organization (grant V27/181/113), Norwegian
Programme for Development, Research and Higher Education (research grant PRO
48/2002), and Rotavirus Vaccine Program, PATH (grant GAV.1142–01-07211-SPS).
Supplement sponsorship: This article is part of a supplement entitled “Rotavirus
Infection In Africa: Epidemiology, Burden of Disease, and Strain Diversity,” which
was prepared as a project of the Rotavirus Vaccine Program, a partnership among
PATH, the World Health Organization, and the US Centers for Disease Control and
Prevention, and was funded in full or in part by the GAVI Alliance. |
en |
dc.language.iso |
en_US |
en |
dc.publisher |
The University of Chicago Press |
en |
dc.subject |
Rotavirus |
en |
dc.subject |
Rotavirus genotyping methods |
en |
dc.subject |
African Rotavirus Network |
en |
dc.subject |
Genotypes P[8]G10 |
en |
dc.subject |
Genotypes P[8]G1 |
en |
dc.subject |
Genotypes P[6]G8 |
en |
dc.subject |
Genotypes P[8]G8 |
en |
dc.subject |
Genotypes P[7]G5 |
en |
dc.title |
Determination of the G and P types of previously nontypeable rotavirus strains from the African notavirus network, 1996–2004 : identification of unusual G types |
en |
dc.type |
Article |
en |