A novel assay for the detection of anthelmintic activity mediated by cuticular damage to nematodes: validation on Caenorhabditis elegans exposed to cysteine proteinases

• Published in: Parasitology Vol. 144; no. 5; p. 583
• Main Authors: Phiri, A M, DE Pomerai, D I, Buttle, D J, Behnke, J M
• Format: Journal Article
• Language: English
• Published: England 01-04-2017
• Subjects: Animals; Anthelmintics - isolation & purification; Anthelmintics - pharmacology; Caenorhabditis elegans - drug effects; Caenorhabditis elegans - genetics; Caenorhabditis elegans - ultrastructure; Carica - enzymology; Cystatins - genetics; Cysteine Proteases - isolation & purification; Cysteine Proteases - pharmacology; Cysteine Proteinase Inhibitors; Indicators and Reagents; Mutation; Neutral Red; Plant Proteins - pharmacology; Protozoan Proteins - genetics; cuticular damage; Caenorhabditis elegans; Neutral red; cysteine proteinases
• ISSN: 1469-8161
• DOI: 10.1017/S0031182016002353

Plant cysteine proteinases (CPs) from Carica papaya kill parasitic and free-living nematodes in vitro by hydrolysis of the worm cuticle, a mechanism that is different to all commercially available synthetic anthelmintics. We have developed a cheap and effective, rapid-throughput Caenorhabditis elegans-based assay for screening plant CP extracts for anthelmintic activity targeting cuticular integrity. The assay exploits colorimetric methodology for assessment of cuticular damage, and is based on the ability of viable cells to incorporate and bind Neutral red dye within lysosomes and to release the dye when damaged. Living worms are pre-stained with the dye, exposed to CPs and then leakage of the dye through the damaged cuticle is quantified by spectrophotometry. In contrast to motility assays and semi-subjective interpretation of microscopical images, this colorimetric assay is independent of observer bias. Our assay was applied to a series of C. elegans bus mutant strains with leaky cuticles and to cystatin knockout mutants. At ambient temperature and over 0.5-24 h, both bus mutants and the cystatin knockouts were highly susceptible to CPs, whereas wild-type Bristol N2 worms were essentially unstained by Neutral red and unaffected by CPs, providing validation for the utility of this assay.