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J Gen Virol 86 (2005), 2661-2672; DOI 10.1099/vir.0.81215-0

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© 2005 Society for General Microbiology

A tale of two clades: monkeypox viruses

Anna M. Likos1,{dagger}, Scott A. Sammons1,{dagger}, Victoria A. Olson1, A. Michael Frace1, Yu Li1, Melissa Olsen-Rasmussen1, Whitni Davidson1, Renee Galloway1, Marina L. Khristova1, Mary G. Reynolds1, Hui Zhao1, Darin S. Carroll1, Aaron Curns1, Pierre Formenty2, Joseph J. Esposito1, Russell L. Regnery1 and Inger K. Damon1

1 National Center for Infectious Disease, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop G43, Atlanta, GA 30333, USA
2 World Health Organization, Geneva, Switzerland

Correspondence
Inger K. Damon
iad7{at}cdc.gov

Human monkeypox was first recognized outside Africa in 2003 during an outbreak in the USA that was traced to imported monkeypox virus (MPXV)-infected West African rodents. Unlike the smallpox-like disease described in the Democratic Republic of the Congo (DRC; a Congo Basin country), disease in the USA appeared milder. Here, analyses compared clinical, laboratory and epidemiological features of confirmed human monkeypox case-patients, using data from outbreaks in the USA and the Congo Basin, and the results suggested that human disease pathogenicity was associated with the viral strain. Genomic sequencing of USA, Western and Central African MPXV isolates confirmed the existence of two MPXV clades. A comparison of open reading frames between MPXV clades permitted prediction of viral proteins that could cause the observed differences in human pathogenicity between these two clades. Understanding the molecular pathogenesis and clinical and epidemiological properties of MPXV can improve monkeypox prevention and control.

Published online ahead of print on 25 July 2005 as DOI 10.1099/vir.0.81215-0.

The GenBank/EMBL/DDBJ accession numbers for the sequences reported in this paper are DQ011153–DQ011157.

Supplementary material is available in JGV Online.

{dagger}These authors contributed equally to this work.




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