“…Because their sequences had higher intraspecific variation than the ribosomal RNA gene regions (Morgan et al, 1999b), it was suggested that other Cryptosporidium genes targets should be used for amplification including the Cryptosporidium oocyst wall protein (COWP), 16S rRNA, Hsp70, Actin, β-Tubulin, gp60, microsatellites, minisatellites and extrachromosomal double-stranded RNA (Xiao et al, 2004;Caccio et al, 2005;Coklin et al, 2007). As well as the Internal Transcribed Spacers (ITS) of ribosomal DNA were useful for the detection of genetic variability within species (Chalmers et al, 2005;Schindler et al, 2005). Synchronized analysis of the obtained morphological simultaneous with molecular criteria of Cryptosporidium buffalo's oocytes in the present study could prove that the isolates were C. parvum.…”