Browsing by Author "Pillai, Dylan R."
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- ItemOpen AccessComparative Genomic Analyses of Streptococcus pseudopneumoniae Provide Insight into Virulence and Commensalism Dynamics(PLoS, 2013-06-19) Shahinas, Dea; Thornton, Christina S.; Tamber, Gurdip Singh; Arya, Gitanjali; Wong, Andrew; Jamieson, Frances B.; Ma, Jennifer H.; Alexander, David C.; Low, Donald E.; Pillai, Dylan R.
- ItemOpen AccessDevelopment and application of ultra-sensitive tools for the detection of malaria(2020-01) Mohon, Md Abu Naser; Pillai, Dylan R.; Wasmuth, James D.; Parkins, Michael D.The goal to eliminate malaria has been challenged by the lack of accurate diagnostic tools to identify symptomatic, asymptomatic, and drug-resistant malaria carriers. In this dissertation, we have shown the potential of the Loop-mediated Isothermal Amplification (LAMP)-based diagnostic approaches to be a powerful tool available for malaria elimination. We have validated the combination of the Non-instrumented Nucleic Acid (NINA) platform heater (PATH, Seattle) with a commercial LAMP kit (LoopAmp malaria Pan/Pf detection kit), with a view to deploying it in extremely resource-limited settings in the future. An ultrasensitive (US)-LAMP assay was also developed and validated to identify asymptomatic malaria reservoirs. Moreover, a novel strategy for detecting single nucleotide polymorphisms (SNPs) by the LAMP method was designed and deployed for spotting artemisinin resistance in P. falciparum. We conclude that the NINA-LAMP assay can be a convenient test for detecting symptomatic malaria cases with a sensitivity of 100% and specificity of 98.6% compared to the gold standard nested PCR. Additionally, the US-LAMP assay was able to achieve a limit of detection (LOD) between 25 to 100 parasites/mL from dried blood spots. We have also found that the overall prevalence of asymptomatic malaria was 22.1% in the Gambella region of Ethiopia, detected by the US-LAMP assay. The sensitivity and the specificity of the US-LAMP assay were 92.6% and 97.1%, respectively compared to an ultrasensitive quantitative reverse transcriptase PCR. Additionally, the SNP-LAMP assay was 100% sensitive and 97.3% specific to identify the C580Y mutation in the kelch 13 propeller gene, which is known as the major genetic determinant of artemisinin resistance in Southeast Asia. Furthermore, we conclude that artemisinin resistance-linked kelch 13 propeller mutations are absent in the Bangladeshi P. falciparum isolates. However, two cases of the A578S SNP in the kelch 13 propeller gene were found in those P. falciparum isolates, although this SNP was not associated with artemisinin resistance. In conclusion, as the LAMP-based diagnostic approaches are simple, low-cost, and accurate compared to currently available nucleic acid tests, they can be used at different aspects to diagnose malaria and expedite elimination.
- ItemOpen AccessFalse positive malaria rapid diagnostic test in returning traveler with typhoid fever(BioMed Central, 2014-06-09) Meatherall, Bonnie; Preston, Keith; Pillai, Dylan R.
- ItemOpen AccessPopulation-Based Laboratory Surveillance of Imported Malaria in Metropolitan Calgary, 2000–2011(PLoS ONE, 2013-04-15) Lee, Clara S.; Gregson, Daniel B.; Church, Deirdre; Laupland, Kevin B.; Eckhardt, Rose; Ross, Terry; Chan, Wilson; Pillai, Dylan R.
- ItemOpen AccessA Purine Analog Synergizes with Chloroquine (CQ) by Targeting Plasmodium falciparum Hsp90 (PfHsp90)(Public Library of Science (PLoS), 2013-09-30) Shahinas, Dea; Folefoc, Asongna; Taldone, Tony; Chiosis, Gabriela; Crandall, Ian; Pillai, Dylan R.