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Immobilization of Schistosoma mansoni miracidia by activation of the alternate complement pathway at unusually high serum dilution
Author(s) -
KNOPF PAUL M.,
PETZKE MARY M.,
McLAREN DIANE J.
Publication year - 1993
Publication title -
parasite immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.795
H-Index - 75
eISSN - 1365-3024
pISSN - 0141-9838
DOI - 10.1111/j.1365-3024.1993.tb00617.x
Subject(s) - serial dilution , schistosoma mansoni , biology , antibody , complement system , schistosomiasis , immunology , guinea pig , schistosoma , microbiology and biotechnology , andrology , helminths , endocrinology , pathology , medicine , alternative medicine
Summary Free‐swimming Schistosoma mansoni miracidia were immobilized by adding normal mammalian serum to the water. Miracidial immobilizing activity (MIA) was shown to result from activating the alternate pathway of complement (APC). MIA in normal sera was heat‐sensitive and anibody independent; it was greatly reduced in factor B‐depleted or C6‐depleted, but not in C1‐depleted, human serum. Addition of purified factor B to B‐depleted serum totally restored MIA. Half‐maximal MIA in normal human, rabbit, and guinea pig sera was detectable at final dilutions exceeding 1/100, 1/200, and 1/500, respectively, and normal rat serum was particularly potent, with MIA at dilutions exceeding 1/2000. Detection of APC activity at such high dilutions is quite extraordinary and attributed to the hypotonic conditions. We confirmed and extended previous findings that heat‐inactivated infection sera also display MIA. Immobilizing activity in irradiated‐cercarial vaccine rat serum cofractionated with rat IgG and anti‐SWAP antibody activity. Antibody‐dependent MIA titres were much lower than for APC‐dependent MIA. Based upon light microscope and transmission EM studies, immobilization of miracidia by APC activation was attributed to severe tegumental damage. Miracidia within egg shells were insensitive to MIA.