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Applied and Environmental Microbiology, April 2002, p. 2071-2076, Vol. 68, No. 4
0099-2240/02/$04.00+0 DOI: 10.1128/AEM.68.4.2071-2076.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Ecologie du Parasitisme, IFR 17, Institut Pasteur de Lille, 59019 Lille,1 Laboratoire Environnement et Santé, Université Catholique de Lille, 59046 Lille,2 Parasitologie-Mycologie, Faculté de Médecine et Centre Hospitalier Régional et Universitaire de Lille, 59045 Lille, France3
Received 30 July 2001/ Accepted 15 January 2002
Genomic DNAs from human Cryptosporidium isolates previously typed by analysis of the 18S ribosomal DNA locus (Cryptosporidium parvum bovine genotype, C. parvum human genotype, Cryptosporidium meleagridis, and Cryptosporidium felis) were used to amplify the diagnostic fragment described by Laxer et al. (M. A. Laxer, B. K. Timblin, and R. J. Patel, Am. J. Trop. Med. Hyg., 45:688-694, 1991). The obtained 452-bp amplified fragments were sequenced and aligned with the homologous Cryptosporidium wrairi sequence. Polymorphism was exploited to develop a restriction fragment length polymorphism method able to discriminate Cryptosporidium species and C. parvum genotypes.
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