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A survey of bacterial, fungal and plant metabolites against Aedes aegypti (Diptera: Culicidae), the vector of yellow and dengue fevers and Zika virus

机译:埃及伊蚊(双翅目:蚊科)的细菌,真菌和植物代谢物调查,黄色和登革热和寨卡病毒载体

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摘要

Aedes aegypti L. is the major vector of the arboviruses responsible for dengue fever, one of the most devastating human diseases. Some bacterial, fungal and plant metabolites belonging to different chemical subgroups, including Amaryllidaceae alkaloids, anthracenes, azoxymethoxytetrahydropyrans, cytochalasans, 2,5-diketopiperazines, isochromanones, naphthoquinones, organic small acids and their methyl esters, sterols and terpenes including sesquiterpenes and diterpenes, were tested for their larvicidal and adulticidal activity against Ae. aegypti. Out of 23 compounds tested, gliotoxin exhibited mosquitocidal activity in both bioassays with an LC50 value of 0.0257 ± 0.001 μg/μL against 1st instar Ae. aegypti and LD50 value of 2.79 ± 0.1197 μg/mosquito against adult female Ae. aegypti. 2-Methoxy-1,4-naphthoquinone and cytochalasin A showed LC50 values of 0.0851 ± 0.0012 μg/μL and 0.0854 ± 0.0019 μg/μL, respectively, against Ae. aegypti larvae. In adult bioassays, fusaric acid (LD50= 0.8349 ± 0.0118 μg/mosquito), 3-nitropropionic acid (LD50 = 1.6641 ± 0.0494 μg/mosquito) and α-costic acid (LD50 = 2.547 ± 0.0835 μg/mosquito) exhibited adulticidal activity. Results from the current study confirm that compounds belonging to cytochalsin, diketopiperazine, naphthoquinone and low molecular weight organic acid groups are active and may stimulate further SAR investigations.
机译:埃及伊蚊是导致登革热(人类最具破坏力的疾病之一)的虫媒病毒的主要载体。属于不同化学亚组的一些细菌,真菌和植物代谢物,包括金石科生物碱,蒽,甲氧基甲氧基四氢吡喃,细胞松弛素,2,5-二酮哌嗪,异色酮,萘醌,有机小酸及其甲基酯,固醇和萜烯,包括倍半萜和测试其对Ae的杀幼虫和杀螨活性。埃及。在这23种化合物中,葡聚糖毒素在两种生物测定中均表现出灭蚊活性,针对第一龄Ae的LC50值为0.0257±0.001μg/μL。对成年雌性Ae的埃及伊蚊和LD50值为2.79±0.1197μg/蚊。埃及。 2-甲氧基-1,4-萘醌和细胞松弛素A对Ae的LC50值分别为0.0851±0.0012μg/μL和0.0854±0.0019μg/μL。埃及象幼虫。在成人生物检测中,富马酸(LD50 = 0.8349±0.0118μg/蚊),3-硝基丙酸(LD50 = 1.6641±0.0494μg/蚊)和α-椰油酸(LD50 = 2.547±0.0835μg/蚊)具有杀灭活性。当前研究的结果证实,属于细胞钙素,二酮哌嗪,萘醌和低分子量有机酸基团的化合物具有活性,可能会刺激SAR研究的开展。

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