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Applied and Environmental Microbiology, April 1999, p. 1578-1583, Vol. 65, No. 4
0099-2240/99/$04.00+0
Phylogenetic Analysis of Cryptosporidium
Parasites Based on the Small-Subunit rRNA Gene Locus
Lihua
Xiao,1
Lillian
Escalante,1
Chunfu
Yang,1
Irshad
Sulaiman,1
Anannias A.
Escalante,1,2
Richard J.
Montali,3
Ronald
Fayer,4 and
Altaf A.
Lal1,*
Division of Parasitic Diseases, National
Center for Infectious Diseases, Centers for Disease Control and
Prevention, U.S. Department of Health and Human Services, Atlanta,
Georgia 303411; Instituto Venezolano de
Investigaciones Cientificas, Caracas,
Venezuela2; Department of Pathology,
National Zoological Park, Smithsonian Institution, Washington, D.C.
200083; and Parasite Immunobiology
Laboratory, Agricultural Research Service, U.S. Department of
Agriculture, Beltsville, Maryland 207054
Received 23 September 1998/Accepted 8 January 1999
Biological data support the hypothesis that there are multiple
species in the genus Cryptosporidium, but a recent analysis of the available genetic data suggested that there is insufficient evidence for species differentiation. In order to resolve the controversy in the taxonomy of this parasite genus, we characterized the small-subunit rRNA genes of Cryptosporidium parvum,
Cryptosporidium baileyi, Cryptosporidium muris,
and Cryptosporidium serpentis and performed a phylogenetic
analysis of the genus Cryptosporidium. Our study revealed
that the genus Cryptosporidium contains the phylogenetically distinct species C. parvum, C. muris, C. baileyi, and C. serpentis,
which is consistent with the biological characteristics and host
specificity data. The Cryptosporidium species formed two
clades, with C. parvum and C. baileyi belonging
to one clade and C. muris and C. serpentis
belonging to the other clade. Within C. parvum, human
genotype isolates and guinea pig isolates (known as
Cryptosporidium wrairi) each differed from bovine genotype isolates by the nucleotide sequence in four regions. A C. muris isolate from cattle was also different from parasites
isolated from a rock hyrax and a Bactrian camel. Minor differences were also detected between C. serpentis isolates from snakes and
lizards. Based on the genetic information, a species- and
strain-specific PCR-restriction fragment length polymorphism diagnostic
tool was developed.
*
Corresponding author. Mailing address: Division of
Parasitic Diseases, Mail Stop F-12, 4770 Buford Hwy., Chamblee, GA
30341. Phone: (770) 488-4047. Fax: (770) 488-4454. E-mail:
aal1{at}cdc.gov.
Applied and Environmental Microbiology, April 1999, p. 1578-1583, Vol. 65, No. 4
0099-2240/99/$04.00+0
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