ArticleScientific reports2024
Larvicidal and enzyme inhibition effects of Phoenix pusilla derived Methyl oleate and malathion on Aedes aegypti strains.
Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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2 citing papers in PubMed.
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Authors and funding
10 authors.
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Abstract
This study explores the larvicidal potential of methanolic flower extracts from Phoenix pusilla (Pp-Fe), its major compound, and malathion (MLT), against laboratory strain (LS) and field strain (FS) of Aedes aegypti, the dengue mosquito vector. We identified thirty-one derivatives, with methyl oleate (MO) comprising 28.5% of Pp-Fe. Comparative efficacy evaluations were performed using peak dosages of Pp-Fe (500 ppm), MO (5 ppm), and MLT (5 ppm) on LS and FS larvae. Both LS and FS second instars showed higher susceptibility to Pp-Fe (95% and 93%, respectively) and MO (85% and 83%, respectively). MLT resulted in significant mortality rates among LS larvae (98%) and notable reductions among FS larvae (71%). The expression levels of key biomarker enzymes (carboxylesterase, GST, and CYP450) exhibited a consistent decrease and subsequent upregulation in LS and FS larvae following exposure to Pp-Fe and MO, contrasting with the significant expression variations observed in LS and FS larvae exposed to MLT. LS larvae demonstrated heightened susceptibility and evident midgut cell damage following all treatments, suggesting potential disparities in susceptibility and adaptive responses between LS and FS strains towards MLT. These observations underscore the promising larvicidal attributes of Pp-Fe and MO, emphasizing the need for further exploration of their mechanisms of action in the development of environmentally sustainable mosquito control strategies and resistance management.
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