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Journal of Clinical Microbiology, November 2009, p. 3735-3738, Vol. 47, No. 11
0095-1137/09/$08.00+0 doi:10.1128/JCM.01201-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Institute of Immunology, Laboratoire National de Santé/Centre de Recherche Public-Santé, Luxembourg, Luxembourg,1 National Center of Infectious & Parasitic Diseases, Department of Virology, Measles/Rubella Laboratory, Sofia, Bulgaria,2 Laboratory of Medical Microbiology, Institut Pasteur Hellenique, Athens, Greece,3 Division of Microbiology, Laboratoire National de Santé, Luxembourg, Luxembourg,4 Central Virology Laboratory, Sheba Medical Center, Ramat Gan, Israel,5 National Virological Laboratory, Department of the State Sanitary and Epidemiological Surveillance, Ministry of Health of Kyrgyz Republic, Bishkek, Kyrgyzstan,6 Central Laboratory of Communicable Diseases, Health Protection Inspectorate, Tallinn, Estonia,7 Respiratory Department, TORLAK Institute of Immunology and Virology, Belgrade, Serbia,8 Institut de Recherche en Sciences de la Santé, Bobo-Dioulasso, Burkina Faso,9 Gabrichevsky G.N. Research Institute of Epidemiology and Microbiology, Moscow, Russian Federation,10 Measles/Rubella Group, National Center for Disease Control and Public Health, Tbilisi, Georgia,11 Virology Laboratory, Innovative Biotech-Keffi No. 1, Keffi, Nasarawa State, Nigeria,12 Department of Virology, College of Medicine, University of Ibadan, Ibadan, Oyo State, Nigeria,13 Department of Medicine, University College Hospital & University of Ibadan, Ibadan, Nigeria,14
Received 19 June 2009/ Returned for modification 19 August 2009/ Accepted 1 September 2009
Phylogenetic analysis of 166 human parvovirus B19 sequences from 11 different countries attributed 91.57% to genotype 1, 5.42% to genotype 3b, and 3.01% to genotype 3a. Very similar viruses of genotype 1 circulated widely in Europe and Israel. Genotype 3b seems to show an increasing spread outside of Africa.
Published ahead of print on 9 September 2009.
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