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1.
PLoS One ; 10(12): e0144586, 2015.
Article in English | MEDLINE | ID: mdl-26650757

ABSTRACT

Aedes aegypti is responsible for the transmission of dengue, a disease that infects millions of people each year. Although essential oils are well recognized as sources of compounds with repellent and larvicidal activities against the dengue mosquito, much less is known about their oviposition deterrent effects. Commiphora leptophloeos, a tree native to South America, has important pharmacological properties, but the chemical profile and applicability of its essential oil in controlling the spread of the dengue mosquito have not been investigated. The aim of this study was to determine the composition of C. leptophloeos leaf oil and to evaluate its larvicidal and oviposition deterrent effects against A. aegypti. Fifty-five components of the essential oil were detected by gas chromatography (GC)-mass spectrometry, with α-phellandrene (26.3%), (E)-caryophyllene (18.0%) and ß-phellandrene (12.9%) identified as the major constituents. Bioassays showed that the oil exhibited strong oviposition deterrent effects against A. aegypti at concentrations between 25 and 100 ppm, and possessed good larvicidal activity (LC50 = 99.4 ppm). Analysis of the oil by GC coupled with electroantennographic detection established that seven constituents could trigger antennal depolarization in A. aegypti gravid females. Two of these components, namely (E)-caryophyllene and α-humulene, were present in substantial proportions in the oil, and oviposition deterrence assays confirmed that both were significantly active at concentrations equivalent to those present in the oil. It is concluded that these sesquiterpenes are responsible, at least in part, for the deterrent effect of the oil. The oviposition deterrent activity of the leaf oil of C. leptophloeos is one of the most potent reported so far, suggesting that it could represent an interesting alternative to synthetic insecticides. The results of this study highlight the importance of integrating chemical and electrophysiological methods for screening natural compounds for their potential in combating vectors of insect-borne diseases.


Subject(s)
Aedes/drug effects , Commiphora/chemistry , Oils, Volatile/pharmacology , Oviposition/drug effects , Plant Leaves/chemistry , Sesquiterpenes/pharmacology , Aedes/physiology , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Electrophysiology/methods , Female , Gas Chromatography-Mass Spectrometry/methods , Monocyclic Sesquiterpenes , Oils, Volatile/chemistry , Polycyclic Sesquiterpenes
2.
Exp Parasitol ; 156: 37-41, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26044355

ABSTRACT

Lactones are organic cyclic esters that have been described as larvicides against Aedes aegypti and as components of oviposition pheromone of Culex quinquefasciatus. This work describes the effect of six α,ß-unsaturated lactones (5a-5f) on survival of A. aegypti fourth instar larvae (L4). It is also reported the effects of the lactones on L4 gut trypsin activity and oviposition behavior of A. aegypti females. Five lactones were able to kill L4 being the lactones 5a (LC50 of 39.05 ppm), 5e (LC50 of 36.30 ppm) and 5f (LC50 of 40.46 ppm) the most promising larvicides. Only the lactone 5a inhibited L4 gut trypsin activity, with an IC50 of 115.15 µg/mL. Lactones 5a, 5c, 5d and 5e did not exert deterrent or stimulatory effects on oviposition, whereas lactone 5b exhibited a strong deterrent oviposition activity. In conclusion, this work introduces new α,ß-unsaturated lactones as promising alternatives to control A. aegypti dissemination. The larvicidal mechanism of the lactone 5a can involve the disruption of proteolysis at larval gut.


Subject(s)
Aedes/drug effects , Insect Vectors/drug effects , Insecticides/pharmacology , Lactones/pharmacology , Oviposition/drug effects , Trypsin/drug effects , Aedes/physiology , Animals , Female , Inhibitory Concentration 50 , Insect Vectors/physiology , Insecticides/chemistry , Lactones/chemistry , Larva/drug effects , Trypsin/metabolism , Trypsin Inhibitors/pharmacology
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