Effect of protease class-specific inhibitors on in vitro development of the third- to fourth-stage larvae of Ascaris suum

Third-stage larvae (L3) of Ascaris suum develop and molt to fourth-stage larvae (L4) during in vitro cultivation; consistently greater than 80% of the larvae develop to L4 during 7 days in culture (DIC). To assess the role of proteases in this process, the effect of protease class-specific inhibitor...

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Published in:The Journal of parasitology Vol. 84; no. 4; pp. 686 - 690
Main Authors: Rhoads, M.L. (Parasite Biology and Epidemiology Laboratory, USDA, ARS, Beltsville, MD.), Fetterer, R.H, Urban, J.F. Jr
Format: Journal Article
Language:English
Published: Lawrence, KS American Society of Parasitologists 01-08-1998
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Summary:Third-stage larvae (L3) of Ascaris suum develop and molt to fourth-stage larvae (L4) during in vitro cultivation; consistently greater than 80% of the larvae develop to L4 during 7 days in culture (DIC). To assess the role of proteases in this process, the effect of protease class-specific inhibitors was studied. The presence of either a serine protease inhibitor (AEBSF, 100 µM) or an aspartic protease inhibitor (pepstatin A, 100 µM) had no effect on the percentage of L4 after 7 DIC. However, the presence of either a cysteine protease inhibitor (Z-Phe-Ala-FMK, 100 µM) or an aminopeptidase inhibitor (amastatin, 100 µM) resulted in 77% and 34% reductions, respectively, in the percentage of L4 compared to untreated cultures; viability of the larvae was not affected. The effect of Z-Phe-Ala-FMK on molting was time and dose dependent. In contrast to Z-Phe-Ala-FMK, E-64, another specific inhibitor of cysteine proteases, had no effect on molting. The data support a role for an aminopeptidase and suggest a role for a cysteine protease in the development of the L3 to L4 stage of A. suum.
Bibliography:L72
1999010532
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ISSN:0022-3395
1937-2345
DOI:10.2307/3284570