In vitro effect on Cryptosporidium parvum of short-term exposure to cathelicidin peptides
Author(s) -
Maria Carla Re
Publication year - 2003
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkg149
Subject(s) - cathelicidin , cryptosporidium parvum , microbiology and biotechnology , biology , population , cryptosporidium , staining , in vitro , parasite hosting , apicomplexa , chemistry , immunology , biochemistry , antimicrobial , antimicrobial peptides , plasmodium falciparum , medicine , feces , genetics , environmental health , world wide web , computer science , malaria
Two laboratory methods, a cell culture system and double fluorogenic staining, were used to study the viability and infective ability of Cryptosporidium parvum sporozoites and oocysts after short-term exposure to four cathelicidin peptides. The compounds, SMAP-29, BMAP-28, PG-1 and Bac7(1-35), exerted a strong cytotoxic effect on sporozoites, but did not affect the viability and function of oocysts consistently. Overall, in the sporozoite series, a percentage of the viable population decreased rapidly to less than detectable levels after 15 and 60 min exposure to the peptides at concentrations of 100 and 10 micro g/mL, respectively. In the oocyst series, no compound produced complete inhibition of parasite growth: 60-85% of the oocyst population was viable after 180 min exposure at 100 micro g/mL. SMAP-29 exerted the highest activity against both sporozoites and oocysts.
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