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Multiple DNA Markers Differentiate Sarcocystis neurona and Sarcocystis falcatula

1999; American Society of Parasitologists; Volume: 85; Issue: 2 Linguagem: Inglês

10.2307/3285623

1937-2345

Susan M. Tanhauser, Charles A. Yowell, Tim J. Cutler, Ellis C. Greiner, R. J. MacKay, John B. Dame,

Yersinia bacterium, plague, ectoparasites research

Studies designed to investigate the causative agent of equine protozoal myeloencephalitis and its life cycle have been hampered by the marked similarity of Sarcocystis neurona to other Sarcocystis spp. present in the same definitive host. Random-amplified polymorphic DNA techniques were used to amplify DNA from isolates of S. neurona and Sarcocystis falcatula. DNA sequence analysis of polymerase chain reaction (PCR) products was then used to design PCR primers to amplify specific Sarcocystis spp. DNA products. The ribosomal RNA internal transcribed spacer was also amplified and compared between S. neurona and S. falcatula. Useful sequence heterogeneity between the 2 organisms was identified, creating potential markers to distinguish these Sarcocystis spp. These markers were used to characterize Sarcocystis isolates from opossum (Didelphis virginiana) feces. Our data suggest that S. neurona and S. falcatula can be differentiated with these markers and that multiple Sarcocystis spp., including S. neurona and S. falcatula, are shed by opossums.