Poster
101 |
Molecular identification and characterizations of Cryptosporidium spp. among food-handlers in Qatar |
Stool samples were collected from workers related to food services. Samples were then subjected to DNA extraction and Real Time PCR detection. The positive RT-PCR products for Cryptosporidium spp. were analyzed by RFLP to identify the Cryptosporidium species. Specimens that contained Cryptosporidium parvum or Cryptosporidium hominis were further subtyped by DNA sequencing of the PCR product of the gp60 gene. The parasite was identified in 2.9% of the samples by RT-PCR targeting the 18S rRNA. PCR-RFLP analysis revealed distinctive banding patterns. The majority of isolates (45.45%) were identified as C. parvum. 9% were positives for C. hominis, 27.27% were C. parvum + C. hominis, and 18.18% were C. parvum + C. meleagridis. All C. parvum isolates were classified as allele IId and were assigned as IIdA20G1. The identified C. hominis subtype was the less common IeA12G3T3 subtype. The predominance of the zoonotic subtype families of C. parvum IId in the Middle Eastern regions suggests that animal-to human transmission may be a common transmission route of Cryptosporidium. However, this postulation may be premature in view of findings of studies conducted in Kuwait. The very limited molecular heterogeneity among the isolates reported in the present study may be due to a common origin of the infection and/or the infection was due to epidemic clone. Having anthroponotic Cryptosporidium strain predominance with no association between Cryptosporidium prevalence and animal contact in our study population reveals that population dynamics influence the transmission pattern of the parasite in Qatar. The role of foreign workers from Asia and Africa as a source of Cryptosporidium spp. infection in Arab countries has been suggested. Regarding the complications of cryptosporidiosis, the importance of its eradication / control becomes more evident.