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Applied and Environmental Microbiology, August 1999, p. 3386-3391, Vol. 65, No. 8
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Genetic Diversity within Cryptosporidium parvum and Related Cryptosporidium Species

Lihua Xiao,1,* Una M. Morgan,2 Josef Limor,1 Ananias Escalante,3 Michael Arrowood,1 William Shulaw,4 R. C. A. Thompson,2 Ronald Fayer,5 and Altaf A. Lal1

Division of Parasitic Diseases, Centers for Disease Control and Prevention, Public Health Service, U.S. Department of Health and Human Services, Atlanta, Georgia 303411; State Agricultural Biotechnology Centre, Murdoch University, Murdoch, WA 6150, Australia2; Centro de Ecologia, Instituto Venezolano de Investigaciones Cientificas, IVIC, KM11 Carretera, Panamericana, Caracas, Venezuela3; Department of Veterinary Preventive Medicine, The Ohio State University College of Veterinary Medicine, Columbus, Ohio 432194; and Immunology and Disease Resistance Laboratory, Agriculture Research Service, U.S. Department of Agriculture, Beltsville, Maryland 207055

Received 20 January 1999/Accepted 25 May 1999

To assess the genetic diversity in Cryptosporidium parvum, we have sequenced the small subunit (SSU) rRNA gene of seven Cryptosporidium spp., various isolates of C. parvum from eight hosts, and a Cryptosporidium isolate from a desert monitor. Phylogenetic analysis of the SSU rRNA sequences confirmed the multispecies nature of the genus Cryptosporidium, with at least four distinct species (C. parvum, C. baileyi, C. muris, and C. serpentis). Other species previously defined by biologic characteristics, including C. wrairi, C. meleagridis, and C. felis, and the desert monitor isolate, clustered together or within C. parvum. Extensive genetic diversities were present among C. parvum isolates from humans, calves, pigs, dogs, mice, ferrets, marsupials, and a monkey. In general, specific genotypes were associated with specific host species. A PCR-restriction fragment length polymorphism technique previously developed by us could differentiate most Cryptosporidium spp. and C. parvum genotypes, but sequence analysis of the PCR product was needed to differentiate C. wrairi and C. meleagridis from some of the C. parvum genotypes. These results indicate a need for revision in the taxonomy and assessment of the zoonotic potential of some animal C. parvum isolates.


* Corresponding author. Mailing address: Division of Parasitic Diseases, Mail Stop F-12, Centers for Disease Control and Prevention, 4770 Buford Highway, Atlanta, GA 30341. Phone: (770) 488-4840. Fax: (770) 488-4454. E-mail: lax0{at}cdc.gov.


Applied and Environmental Microbiology, August 1999, p. 3386-3391, Vol. 65, No. 8
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



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