Atovaquone-proguanil remains effective against multidrug-resistant in Southeast Asia, but resistance is mediated by a single point mutation in cytochrome () that can arise during treatment. Among 14 atovaquone-proguanil treatment failures in a clinical trial in Cambodia, only one recrudescence harbored the mutation Y268C. Deep sequencing did not detect the mutation at baseline or in the first 3 days of treatment, suggesting that it arose Further sequencing across similarly found no low-frequency mutations that were up-selected from baseline to recrudescence. Copy number amplification in dihydroorotate dehydrogenase (DHODH) and cytb as markers of atovaquone tolerance was also absent. mutation played a minor role in atovaquone-proguanil treatment failures in an active comparator clinical trial.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092515 | PMC |
http://dx.doi.org/10.1128/AAC.01249-20 | DOI Listing |
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