AI Article Synopsis

  • The study investigated the immune response of the snails Biomphalaria alexandrina and Bulinus truncatus to Schistosoma mansoni and S. haematobium using the indirect immunoperoxidase technique.
  • A new method called Agarose cell block was utilized for collecting haemolymph, yielding more well-formed cells compared to traditional cytospin methods.
  • Results showed positive peroxidase reactions in the haemolymph and tissues of infected snails, indicating effective detection of schistosome antigens, particularly in specific cell types within the snails.

Article Abstract

The reaction of the haemolymph and the tissue of infected intermediate hosts, Biomphalaria alexandrina and Bulinus truncatus to Schistosoma mansoni and S. haematobium antigens were investigated using the indirect immunoperoxidase technique. A new technique, Agarose cell block was used in collection of haemolymph which helped in collecting plenty of well formed cells in comparison to the ordinary one using the cytospin. Collected haemolymph and prepared tissues of uninfected and infected B. alexandria and B. truncatus were fixed and then reacted with anti-S. mansoni and anti-S. haematobium IgG polyclonal antibodies. The haemolymph and tissue of infected B. alexandrina and B. truncatus gave a positive peroxidase reaction represented by a brown colour. In haemolymph, the positive peroxidase reaction was detected mainly in the cytoplasm of the amoebocytes. In the tissue, it was detected in epithelial cells lining the tubules, male cells in the lumen of the tubules and in female oogonia cells along the periphery of the tubules. The similarity in the strength and distribution of positive reaction in B. alexandrina and B. truncates was observed as compared to control. Thus, the immunoperoxidase technique proved to be an effective indicator for the schistosome-antigen in the snails.

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