Molecular detection of Schistosoma haematobium in infected Bulinus truncatus snails associated with immune response.

Schistosomiasis is one of the most common waterborne parasite illnesses, it is a major public health issue in developing countries. The polymerase chain reaction (PCR) technique is used to find Schistosoma haematobium DNA in Bulinus truncatus, which could speed up the discovery of infections before cercariae are shed. DraI-PCR detected S.

Differentiation between Bulinus truncatus and Bulinus hexaploidus by morphological characters, chromosomal study and compatibility with Schistosoma haematobium.

Schistosomiasis is a snail-born, neglected tropical disease (NTD) caused by blood flukes (trematode worms) of the genusSchistosoma. It is the second most socioeconomically devastating parasitic disease after malaria. Urogenital schistosomiasis is caused by Schistosoma haematobium which is transmitted by snail intermediate host of the genus Bulinus.

DIVERSITY AND COMPARATIVE STUDIES ON BULINUS SNAILS COLLECTED FROM TWO LOCALITIES IN EGYPT.

A comparative study of the shell structure, seasonal temperature and Calcium content of Bulinus snails from two areas (Damietta and Giza) in Egypt was done and compared with laboratory snails from Schistosome Biological Supply Center (SBSC). The shells of collected snails identified as Bulinus truncatus, showed a wide variation in shape. The results showed a significant differences were detected between the populations from SBSC and Damietta (p<0.

Cytokines and mother sporocysts in susceptible and resistant Bulinus truncatus snails infected with Schistosoma haematobium.

The presence of immunoreactive interleukin (IL-2), interferon gamma (IFN-γ) and tumor necrosis factor alpha (TNF-α) in addition to the citation of mother sporscytes in cephalopodal musculature in the susceptible and resistance Bulinus truncatus the specific intermediate host for the trematode Schistosoma haematobium were investigated,. Using ELISA tests, Results indicated that the concentration of IL-2-like activity in the susceptible and resistant snails decreased significantly after infection then persisted at low levels until the 4th week post exposure (WPE) in susceptible snails, while in resistant snails elevated during the second WPE, and returned to initial level at 3 and 4 WPE. Susceptible snails had low detectable levels of TNF-α and INF-γ like-activity after infection.