Discussion
The World Health
Organization (WHO) has identified
Cryptosporidium
spp. as globally the most common diarrhea-causing protozoan. The protozoan
is the second most important cause of moderate-to-severe childhood diarrhea in
developing countries whereas, in high-income countries it is an
under-recognized pathogen in sporadic gastroenteritis. Humans can acquire
Cryptosporidiuminfections through
person-to-person transmission, zoonotic transmission, and waterborne/foodborne
transmission. The potential for foodborne
transmission of the protozoan parasite
Cryptosporidium spp. is widely acknowledged. In this
case, the role of food handlers is very important because they can make unsafe
and hazardous foods for consumption. Indeed,
outbreaks of Cryptosporidiosis Linked to a Foodhandler have been already observed
in schools and in university campus. Since unhygienic preparation, storage and
handling of food by infected individuals are a major cause for food-borne
diseases, food handlers need to be screened before they are allowed to work in
food establishments such as restaurants, hotels, food stores, factories or as
helpers and cooks in private houses. Moreover, changes
in nutritional habits have resulted in increased consumption of undercooked or
raw foods, exposing consumers to parasites that proper food processing would
otherwise reduce or eliminate. The aim of this study was to assess the
prevalence of
Cryptosporidium
infection and its molecular characterization among foodhandlers in Qatar to
check the relative
importance of this transmission route in the epidemiology of cryptosporidiosis.
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.