Viability of developmental stages of Schistosoma mansoni quantified with xCELLigence worm real-time motility assay (xWORM). Issue 3 (December 2015)

• Record Type: Journal Article
• Authors: Rinaldi, Gabriel; Loukas, Alex; Brindley, Paul J.; Irelan, Jeff T.; Smout, Michael J.
• Is Part Of: International journal for parasitology. Volume 5:Issue 3(2015)
• Page Start: 141
• Page End: 148
• Publication Date: 2015-12
• Subjects: Helminths -- Viability -- xCELLigence -- Schistosome -- Strictly standardized mean difference (SSMD) -- High-throughput; Parasitic diseases -- Chemotherapy -- Periodicals; Drug resistance -- Periodicals; 616.96061
• DOI: 10.1016/j.ijpddr.2015.07.002
• Languages: English
• ISSNs: 2211-3207

Abstract

Abstract: Infection with helminth parasites causes morbidity and mortality in billions of people and livestock worldwide. Where anthelmintic drugs are available, drug resistance is a major problem in livestock parasites, and a looming threat to public health. Monitoring the efficacy of these medicines and screening for new drugs has been hindered by the lack of objective, high-throughput approaches. Several cell monitoring technologies have been adapted for parasitic worms, including video-, fluorescence-, metabolism enzyme- and impedance-based tools that minimize the screening bottleneck. Using the xCELLigence impedance-based system we previously developed a motility-viability assay that is applicable for a range of helminth parasites. Here we have improved substantially the assay by using diverse frequency settings, and have named it the x CELLigence wo rm r eal-time m otility assay (xWORM). By utilizing strictly standardized mean difference analysis we compared the xWORM output measured with 10, 25 and 50 kHz frequencies to quantify the motility of schistosome adults (human blood flukes) and hatching of schistosome eggs. Furthermore, we have described a novel application of xWORM to monitor movement of schistosome cercariae, the developmental stage that is infectious to humans. For all three stages, 25 kHz was either optimal or near-optimal for monitoring and quantifying schistosome motility. These improvements in methodology sensitivity should enhance the capacity to screen small compound libraries for new drugs both for schistosomes and other helminth pathogens at large. Graphical abstract: Highlights: 25 kHz on the xCELLigence system dramatically improves the schistosome xWORM assay. xWORM assay can efficiently determine viability of Schistome adults or eggs. First time cercariae have been incorporated into an automated viability assay. Other helminth monitoring may benefit from alternate xCELLigence frequency options.