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Journal of Virology, December 1999, p. 9969-9975, Vol. 73, No. 12
0022-538X/99/$04.00+0
Molecular Epidemiology and Evolution of Enterovirus
71 Strains Isolated from 1970 to 1998
Betty A.
Brown,1,*
M. Steven
Oberste,1
James P.
Alexander Jr.,1
Margery L.
Kennett,2 and
Mark A.
Pallansch1
Division of Viral and Rickettsial Diseases,
National Center for Infectious Diseases, Centers for Disease Control
and Prevention, Public Health Service, U.S. Department of Health and
Human Services, Atlanta, Georgia 30333,1 and
Victorian Infectious Diseases Reference Laboratory, North
Melbourne 3051, Victoria, Australia2
Received 14 June 1999/Accepted 2 September 1999
Enterovirus 71 (EV71) (genus Enterovirus, family
Picornaviridae), a common cause of hand, foot, and mouth
disease (HFMD), may also cause severe neurological diseases, such as
encephalitis and poliomyelitis-like paralysis. To examine the genetic
diversity and rate of evolution of EV71, we have determined and
analyzed complete VP1 sequences (891 nucleotides) for 113 EV71 strains isolated in the United States and five other countries from 1970 to
1998. Nucleotide sequence comparisons demonstrated three distinct EV71
genotypes, designated A, B, and C. The genetic variation within
genotypes (12% or fewer nucleotide differences) was less than the
variation between genotypes (16.5 to 19.7%). Strains of all three
genotypes were at least 94% identical to one another in deduced amino
acid sequence. The EV71 prototype strain, BrCr-CA-70, isolated in
California in 1970, is the sole member of genotype A. Strains isolated
in the United States and Australia during the period from 1972 to 1988, a 1994 Colombian isolate, and isolates from a large HFMD outbreak in
Malaysia in 1997 are all members of genotype B. Although strains of
genotype B continue to circulate in other parts of the world, none have
been isolated in the United States since 1988. Genotype C contains
strains isolated in 1985 or later in the United States, Canada,
Australia, and the Republic of China. The annual rate of evolution
within both the B and C genotypes was estimated to be approximately
1.35 × 10
2 substitutions per nucleotide and is
similar to the rate observed for poliovirus. The results indicate that
EV71 is a genetically diverse, rapidly evolving virus. Its worldwide
circulation and potential to cause severe disease underscore the need
for additional surveillance and improved methods to identify EV71 in
human disease.
*
Corresponding author. Mailing address: Respiratory and
Enteric Viruses Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Rd. NE, Mailstop G-17, Atlanta, GA 30333. Phone: (404) 639-2751. Fax: (404) 639-4011. E-mail:
bzb2{at}cdc.gov.
Journal of Virology, December 1999, p. 9969-9975, Vol. 73, No. 12
0022-538X/99/$04.00+0
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