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Journal of Virology, March 2007, p. 2382-2390, Vol. 81, No. 5
0022-538X/07/$08.00+0 doi:10.1128/JVI.01622-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
Evolutionary History and Global Spread of the Emerging G12 Human Rotaviruses
,
Mustafizur Rahman,1,2
Jelle Matthijnssens,1
Xuelei Yang,1
Thomas Delbeke,1
Ingrid Arijs,1
Koki Taniguchi,3
Miren Iturriza-Gómara,4
Nadia Iftekharuddin,2
Tasnim Azim,2 and
Marc Van Ranst1*
Laboratory
of Clinical and Epidemiological Virology, Department of Microbiology
and Immunology, Rega Institute for Medical Research, University of
Leuven, Leuven, Belgium,1
Laboratory of
Virology, ICDDR,B, GPO Box 128, Dhaka 1000,
Bangladesh,2
Department of
Virology and Parasitology, Fujita Health University School of Medicine,
Toyoake, Aichi 470-1192, Japan,3
Enteric and Respiratory Virus
Laboratory, Virus Reference Division, Central Public Health Laboratory,
Colindale, London NW9 5HT, United
Kingdom4
Received 28 July 2006/
Accepted 1 December 2006
G12
rotaviruses were first detected in diarrheic children in the
Philippines in 1987, but no further cases were reported until 1998.
However, G12 rotaviruses have been detected all over the world in
recent years. Here, we report the worldwide variations of G12
rotaviruses to investigate the evolutionary mechanisms by which they
managed to spread globally in a short period of time. We sequenced the
complete genomes (11 segments) of nine G12 rotaviruses isolated in
Bangladesh, Belgium, Thailand, and the Philippines and compared them
with the genomes of other rotavirus strains. Our genetic analyses
revealed that after introduction of the VP7 gene of the rare G12
genotype into more common local strains through reassortment, a vast
genetic diversity was generated and several new variants with distinct
gene constellations emerged. These reassortment events most likely took
place in Southeast Asian countries and spread to other parts of the
world. The acquirement of gene segments from human-adapted rotaviruses
might allow G12 to better propagate in humans and hence to develop into
an important emerging human
pathogen.
* Corresponding author. Mailing address: Laboratory of Clinical and Epidemiological
Virology, Department of Microbiology and Immunology, Rega Institute for
Medical Research, Minderbroedersstraat 10, B-3000 Leuven, Belgium.
Phone: 32-16-347908. Fax: 32-16-332131. E-mail:
marc.vanranst{at}uz.kuleuven.ac.be.
Published
ahead of print on 13 December 2006.
Supplemental material for this article may be found at
http://jvi.asm.org/.
Journal of Virology, March 2007, p. 2382-2390, Vol. 81, No. 5
0022-538X/07/$08.00+0 doi:10.1128/JVI.01622-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.
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