Evaluation of indigenous plant extracts against larvae of <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> Say (Diptera: Culicidae)

This study investigates the larvicidal potential of indigenous plant extracts from commonly used medicinal herbs as an environmentally safe measure to control the filarial vector, Culex quinquefasciatus Say (Diptera: Culicidae). The early fourth-instar larvae of C. quinquefasciatus, reared in the laboratory, were used for larvicidal assay with water, hot water, acetone, chloroform, and methanol leaf, stem-bark, and flower extracts of Acacia arabica Willd. Sans, Cedrus deodara Roxb, Hibiscus rosa-sinensis L., Mangifera indica L., Nerium indicum Mill., Nicotiana tabacum Linn., Pongamia pinnata (L.) Pierre, and Solanum nigrum Linn. All plant extracts showed moderate larvicidal effects after 24 h of exposure at 1,000 ppm; however, the highest larval mortality was found in stem-bark hot water, acetone, and methanol extracts of C. deodara (LC₅₀ = 133.85, 141.60, and 95.19 ppm, LC₉₀ = 583.14, 624.19, and 639.99 ppm) and leaf hot water, acetone, methanol, and chloroform extracts of N. tabacum (LC₅₀ = 76.27, 163.81, 83.38, and 105.85 ppm, LC₉₀ = 334.72, 627.38, 709.51, and 524.39 ppm) against the larvae of C. quinquefasciatus, respectively. This is an ideal ecofriendly approach for the control of lymphatic filariasis vector, C. quinquefasciatus.     

Larvicidal activity of micronized aqueous suspension of calcium hydroxide against <Emphasis Type="Italic">Aedes aegypti</Emphasis> and <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> (Diptera: Culicidae)

In the search of alternatives for the control of mosquitoes of medical importance, we evaluated the larvicidal activity of micronized suspensions of calcium hydroxide [Ca(OH)₂] against Aedes aegypti and Culex quinquefasciatus. Tests conducted under laboratory conditions determined a LC50 = 0.027% (LC90 = 0.096%) for A. aegypti and a LC50 = 0.092% (LC90 = 0.2%) for C. quinquefasciatus, at 24 h post-treatment. Considering that the LC50 for the less susceptible species killed 100% of larvae for both species at 48 h post-treatment, we decided to use the diagnostic concentration of 0.1% which eliminated 100% of larvae at 48 h under a simulated field trial. There was a residual effect for up to 84 and 70 days for A. aegypti and C. quinquefasciatus, respectively. Evaluation of Ca(OH)₂ on breeding sites showed a larvicidal activity of 100% for up to 56 days. When the micronized Ca(OH)₂ was incorporated at concentrations from 0.02% (w/v), a superficial film was formed which killed 100% of the larvae of both species after 24 h of contact, and the activity remains until the film broke apart due to stirring. The fact that Ca(OH)₂ is cheap and the people in rural areas of Mexico and other countries know the handling procedures for this compound led us to consider that 0.1% suspensions of Ca(OH)₂ could be used for mosquito control in deposits of water placed in human premises both in urban and rural areas.     

Efficacy of larvicidal botanical extracts against <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> Say (Diptera: Culicidae)

The present study explored the effects of crude leaf acetone, chloroform, hot water, methanol, petroleum ether (60–80°C), and water extracts of Calotropis procera (Ait) R. Br., Canna indica L., Hibiscus rosa-sinensis Linn., Ipomoea carnea Jacq. spp. fistulosa Choisy, and Sarcostemma brevistigma Wight that were selected for investigating larvicidal potential against second and fourth instar larvae of the laboratory-reared mosquito species, Culex quinquefasciatus Say, in which the major lymphatic filariasis was used. All plant extracts showed moderate larvicidal effects after 24 h of exposure at 1,000 ppm; however, the highest larval mortality was found in leaf acetone, chloroform, methanol, and petroleum ether of C. indica (LC₅₀ = 29.62, 59.18, 40.77, and 44.38 ppm; LC₉₀ = 148.55, 267.87, 165.00, and 171.91 ppm) against second instar larvae (LC₅₀ = 121.88, 118.25, 69.76, and 56.31 ppm; LC₉₀ = 624.35, 573.93, 304.27, and 248.24 ppm) and against fourth instar larvae and acetone, hot water, methanol, and petroleum ether extracts of I. carnea (LC₅₀ = 61.17, 41.07, 41.82, and 39.32 ppm; LC₉₀ = 252.91, 142.67, 423.76, and 176.39 ppm) against second instar larvae (LC₅₀ = 145.37, 58.00, 163.81, and 41.75 ppm; LC₉₀ = 573.30, 181.10, 627.38, and 162.63 ppm) and against fourth instar larvae of C. quinquefasciatus, respectively. These results suggest that the acetone, methanol extracts of C. indica and hot water, petroleum ether extracts of I. carnea have the potential to be used as an ideal eco-friendly approach for the control of the major lymphatic filariasis vector, C. quinquefasciatus.     

Insecticidal properties of essential oils from <Emphasis Type="Italic">Lippia turbinata</Emphasis> and <Emphasis Type="Italic">Lippia polystachya</Emphasis> (Verbenaceae) against <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> (Diptera: Culicidae)

Mosquitoes are important vectors of diseases to humans and domestic animals. Chemical control of vectors remains a main resource for the prevention and control of vector-borne diseases. Due to the development of insecticide resistance and risks to human health and the environment of synthetic compounds, the search for alternative pesticides is encouraged. This work assessed the insecticidal activity of essential oils (EOs) from Lippia turbinata and L. polystachya from Argentina on Culex quinquefasciatus mosquitoes. EOs were extracted by hydro-distillation and analyzed with gas–liquid chromatography and mass spectrometry. The insecticidal activity against mosquito larvae, pupae, and adults were evaluated according to World Health Organization protocols. Concentrations ranking from 10 to 160 ppm were assessed at 1, 2, 3, and 24 h posttreatment. The composition of the EO of L. polystachya and L. turbinata were qualitatively similar, with α-thujone and carvone as main constituent; differences were mostly due to the proportion of each component. β-caryophyllene was also an important constituent of the EO of L. turbinata. Both EO were larvicidal at concentrations of 80 ppm or higher, but only L. turbinata was adulticidal. No pupal mortality was detected. The potential of these EOs for vector control is discussed.     

Oviposition-deterrent,ovicidal, and repellent activities of indigenous plant extracts against <Emphasis Type="Italic">Anopheles subpictus</Emphasis> Grassi (Diptera: Culicidae)

Insecticides of botanical origin may serve as suitable alternative biocontrol techniques in the future. The leaf acetone, ethyl acetate, and methanol extracts of Aegle marmelos (Linn.) Correa ex Roxb, Andrographis lineata Wallich ex Nees, and Cocculus hirsutus (L.) Diels were tested for oviposition-deterrent, ovicidal, and repellent activities against Anopheles subpictus Grassi (Diptera: Culicidae). The percentage of effective oviposition repellency of 92.60 , 93.04, 95.20, 88.26, 92.80, 94.01, 95.77, 96.93, and 92.54 at 500 ppm and the lowest repellency of 47.14, 58.00, 56.52, 64.93, 71.09, 66.42, 50.62, 57.62, and 65.73 at 31.25 ppm in acetone, ethyl acetate, and methanol extracts of Aegle marmelos, Andrographis lineata, and Cocculus hirsutus, respectively. The oviposition activity index (OAI) value of acetone, ethyl acetate, and methanol extracts of Aegle marmelos, Andrographis lineata, and Cocculus hirsutus at 500 ppm were −0.86, −0.87, −0.90, −0.78, −0.87, −0.86, −0.91, −0.94, and −0.86 respectively. The OAI values revealed that the solvent plant extracts have deterrent effect, and they caused a remarkable negative response resulting in oviposition of very few eggs. Mean percent hatchability of the ovicidal activity was observed 24 h after treatment. The percent hatchability was inversely proportional to the concentration of extract and directly proportional to the eggs. Mortality of 100% with ethyl acetate extract of Aegle marmelos, methanol extracts Aegle marmelos, Andrographis lineata, and Cocculus hirsutus were exerted at 1,000 ppm. The maximum repellent activity was observed at 500 ppm in methanol extracts of Aegle marmelos, Andrographis lineata, and ethyl acetate extract of Cocculus hirsutus, and the mean complete protection time ranged from 90 to 120 min with the different extracts tested. These results suggest that the leaf extracts of Aegle marmelos, Andrographis lineata, and Cocculus hirsutus have the potential to be used as an ideal ecofriendly approach for the control of the Anopheles subpictus. Therefore, this study provides first report on the oviposition, ovicidal, and repellent activities against malaria vector, Anopheles subpictus of plant extracts from Southern India.     

Larvicidal efficacy of <Emphasis Type="Italic">Jatropha curcas</Emphasis> and bacterial insecticide, <Emphasis Type="Italic">Bacillus thuringiensis</Emphasis>, against lymphatic filarial vector<Emphasis Type="Italic">, Culex quinquefasciatus</Emphasis> Say (Diptera: Culicidae)

The present study explored the effects of Jatropha curcas leaf extract and Bacillus thuringiensis israelensis larvicidal activity against the lymphatic filarial vector, Culex quinquefasciatus. Wights were selected for investigating the larvicidal potential against the first to fourth instar larvae of the laboratory-reared mosquito species, C. quinquefasciatus Say, in which the major lymphatic filariasis was used. The medicinal plants were collected from the area around Bharathiar University, Coimbatore. The dried plant materials were powdered by an electric blender. From the powder, 100 g of the plant materials was extracted with 300 ml of organic solvents of methanol for 8 h, using a Soxhlet apparatus, and filtered. The crude plant extracts were evaporated to dryness in a rotary vacuum evaporator. The plant extract showed larvicidal effects after 24 h of exposure; however, the highest larval mortality was found in the leaf extract of methanol J. curcas against the first to fourth instar larvae of values LC₅₀ = 1.200%, 1.290%, 1.358%, and 1.448% and LC₉₀ = 2.094%, 2.323%, 2.444%, and 2.544% and B. thuringiensis israelensis against the first to fourth instar larvae of values LC₅₀ = 9.332%, 9.832%, 10.212%, 10.622% and LC₉₀ = 15.225%, 15.508%, 15.887%, and 15.986% larvae of C. quinquefasciatus, respectively. No mortality was observed in the control. These results suggest methanol extracts of J. curcas and B. thuringiensis israelensis have potential to be used as an ideal eco-friendly approach for the control of the major lymphatic filarial vector, C. quinquefasciatus.     

Laboratory study on larvicidal activity of indigenous plant extracts against <Emphasis Type="Italic">Anopheles subpictus</Emphasis> and <Emphasis Type="Italic">Culex tritaeniorhynchus</Emphasis>

Anopheles subpictus and Culex tritaeniorhynchus have developed resistance to various synthetic insecticides, making its control increasingly difficult. Insecticides of botanical origin may serve as suitable alternative biocontrol techniques in the future. The leaf acetone, chloroform, ethyl acetate, hexane, and methanol extracts of Aegle marmelos (Linn.) Correa ex Roxb, Andrographis lineata Wallich ex Nees., Andrographis paniculata (Burm.f.) Wall. ex Nees., Cocculus hirsutus (L.) Diels, Eclipta prostrata L., and Tagetes erecta L. were tested against fourth-instar larvae of malaria vector, A. subpictus Grassi and Japanese encephalitis vector, C. tritaeniorhynchus Giles (Diptera: Culicidae). All plant extracts showed moderate larvicidal effects after 24 h of exposure at 1,000 ppm; however, the highest larval mortality was found in leaf ethyl acetate of A. marmelos, E. prostrata, hexane, methanol of A. paniculata and C. hirsutus against the larvae of A. subpictus (LC₅₀ = 167.00, 78.28, 67.24, 142.83 ppm; LC₉₀ = 588.31, 360.75, 371.91, and 830.01 ppm) and against the larvae of C. tritaeniorhynchus (LC₅₀ = 99.03, 119.89, 88.50, 105.19 ppm; LC₉₀ = 479.23, 564.85, 416.39, and 507.86 ppm), respectively. These results suggest that the leaf hexane extract of A. paniculata and ethyl acetate extract of E. prostrata have the potential to be used as an ideal eco-friendly approach for the control of the A. subpictus and C. tritaeniorhynchus. Therefore, this study provides first report on the mosquito larvicidal activity of plant extracts against vectors from Southern India.     

The essential oil of <Emphasis Type="Italic">Zingiber officinalis</Emphasis> Linn (Zingiberaceae) as a mosquito larvicidal and repellent agent against the filarial vector <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> Say (Diptera: Culicidae)

Essential oils extracted by steam distillation from Zingiber officinalis was evaluated for larvicidal and repellent activity against the filarial mosquito Culex quinquefasciatus. The larval mortality was observed after 24 h treated for late third instar. The LC₅₀ value was 50.78 ppm. Skin repellent test at 1.0, 2.0, 3.0, and 4.0 mg/cm² concentration of Z. officinalis gave 100% protection up to 15, 30, 60, and 120 min. These results clearly reveal that the essential oil of Z. officinalis served as a potential larvicidal and repellent agent against filarial vector C. quinquefasciatus.     

A novel herbal formulation against dengue vector mosquitoes <Emphasis Type="Italic">Aedes aegypti</Emphasis> and <Emphasis Type="Italic">Aedes albopictus</Emphasis>

The objective of this study was to develop a herbal formulation to control dengue vector mosquitoes. PONNEEM, a novel herbal formulation prepared using the oils of neem (Azadirachta indica), karanj (Pongamia glabra) and their extracts, was tested for larvicidal, ovicidal and oviposition deterrent activities against Aedes aegypti and Aedes albopictus at 1, 0.5, 0.3 and 0.1 ppm concentrations. Cent percent larvicidal and ovicidal activities were observed at 0.1 ppm in the two mosquito species under laboratory and sunlight-exposed conditions up to 12 months from the date of manufacture. Oviposition deterrent activity of 69.97% and 71.05% was observed at 1 ppm concentration of PONNEEM against A. aegypti and A. albopictus, respectively. Reduction in enzyme levels for α-esterase was 0.089 ± 0.008 and 0.099 ± 0.140 μg napthol produced/min/mg larval protein; for β-esterase, it was 0.004 ± 0.009 and 0.001 ± 0.028 μg napthol produced/min/mg larval protein; for glutathione S-transferase, it was 10.4814 ± 0.23 and 11.4811 ± 0.21 μmol/min/mg larval protein and for total protein, it was 0.177 ± 0.010 and 0.008 ± 0.005 mg/individual larva in treated groups of A. aegypti and A. albopictus, respectively. The nontarget organisms such as Gambusia affinis and Diplonychus indicus were not affected. No mortality was observed in control. PONNEEM can be used effectively for the management of human vector mosquitoes.     

Larvicidal activity of silver nanoparticles synthesized using <Emphasis Type="Italic">Plumeria rubra</Emphasis> plant latex against <Emphasis Type="Italic">Aedes aegypti</Emphasis> and <Emphasis Type="Italic">Anopheles stephensi</Emphasis>

In the present study activity of silver nanoparticles (AgNPs) synthesized using Plumeria rubra plant latex against second and fourth larval instar of Aedes aegypti and Anopheles stephensi was determined. Range of concentrations of synthesized AgNps (10, 5, 2.5, 1.25, 0.625, 0.3125 ppm) and aqueous crude latex (1,000, 500, 250, 125, 62.50, 31.25 ppm) were tested against larvae of A. aegypti and A. Stephensi. The synthesized AgNps from P. rubra latex were highly toxic than crude latex extract in both mosquito species. The LC₅₀ values for second and fourth larval instars after 24 h of crude latex exposure were 1.49, 1.82 ppm against A. aegypti and 1.10, 1.74 ppm against A. stephensi respectively. These figures were 181.67, 287.49 ppm against A. aegypti and 143.69, 170.58 ppm against A. stephensi respectively for crude latex extract. The mortality rates were positively correlated with the concentration of AgNPs. The characterization studies of synthesized AgNPs by UV–Vis spectrophotometry, transmission electron microscopy (TEM), Particle size analysis (PSA) and zeta potential confirmed the spherical shape and size (32–200 nm) of silver nanoparticles alongwith stability. Toxicity studies carried out against non-target fish species Poecilia reticulata, the most common organism in the habitats of A. aegypti and A. stephensi showed no toxicity at LC₅₀ and LC₉₀ doses of the AgNPs. This is the first report on mosquito larvicidal activity of latex synthesized nanoparticles.     

First report on susceptibility of wild <Emphasis Type="Italic">Aedes aegypti</Emphasis> (Diptera: Culicidae) using <Emphasis Type="Italic">Carapa guianensis</Emphasis> (Meliaceae) and <Emphasis Type="Italic">Copaifera</Emphasis> sp. (Leguminosae)

Oils of Carapa guianensis and Copaifera spp. are well known in the Amazonian region as natural insect repellent, and studies have reported their efficiency as larvicide against some laboratory mosquito species. However, in wild populations of mosquitoes, these oils have not yet been evaluated. Thus, the objective of this study was to investigate their efficiency as larvicide in wild populations of Aedes aegypti with a history of exposure to organophosphate. The susceptibility of larvae was determined under three different temperatures, 15°C, 20°C, and 30°C. For each test, 1,000 larvae were used (late third instar and early fourth instar—four replicates of 25 larvae per concentration). Statistical tests were used to identify significant differences. The results demonstrated that as the laboratory A. aegypti, the wild populations of A. aegypti were also susceptible to C. guianensis and Copaifera sp. oils. The lethal concentrations for Copaifera sp. ranged from LC₅₀ 47 to LC₉₀ 91 (milligrams per liter), and for C. guianensis, they were LC₅₀ 136 to LC₉₀ 551 (milligrams per liter). In relation to different temperature, the effectiveness of the oils on larvae mortality was directly related to the increase of temperature, and better results were observed for temperature at 25°C. The results presented here indicate the potential larvicidal activity of C. guianensis and species of Copaifera, in populations of A. aegypti from the wild. Therefore, the results presented here are very important since such populations are primarily responsible for transmitting the dengue virus in the environment.     

Differential larvicidal efficacy of four species of <Emphasis Type="Italic">Vitex</Emphasis> against <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> larvae

The early fourth instar larvae of Culex quinquefasciatus, reared in the laboratory were used for larvicidal assay with leaf extracts of Vitex negundo, Vitex trifolia, Vitex peduncularis and Vitex altissima. The methanol extracts of the four species possessed varying levels of larvicidal nature. The highest larvicidal activity was found with the extract of V. trifolia (LC₅₀ = 41.41 ppm) followed by V. peduncularis (LC₅₀ = 76.28 ppm), V. altissima (LC₅₀ = 128.04 ppm) and V. negundo (LC₅₀ = 212.57 ppm).     

Efficacy of female <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis> with entomopathogenic fungus <Emphasis Type="Italic">Fusarium pallidoroseum</Emphasis>

This study was conducted to isolate and identify natural entomopathogenic fungi from female Culex quinquefasciatus and to test their adulticidal activity. Field-collected female C. quinquefasciatus died early and were placed on a Saboraud’s dextrose agar plates for growth and isolation of natural entomopathogenic fungi. The plates were maintained in an incubator at 24 ± 2°C for 3 days. Four fungal species were isolated in two genera namely, Aspergillus and Fusarium. The identified fungal species were A. niger, A. flavus, A. nidulans var acristatus (ITCC-6327.04), and F. pallidoroseum (ITCC-6324.06). Adult bioassays were carried out using spore-impregnated paper in WHO-holding tubes. F. pallidoroseum was found to be more effective than the others. Exposure of C. quinquefasciatus to spores of A. flavus and A. niger for 4 h caused 5.53% and 5.51% mortality in the mosquitoes within a week, respectively. All the female C. quinquefasciatus were killed within 4 days of exposure to F. pallidoroseum at a concentration of 1.11 × 10¹⁰ conidia per m². Significant difference of longevity was observed between the F. pallidoroseum-treated C. quinquefasciatus and control mosquitoes. The LT₅₀ of F. pallidoroseum was 2.08 days for 4 h exposure to C. quinquefasciatus. Results of the present study confirm that F. pallidoroseum is one of the alternative biological control agents of adult mosquitoes.     

Larvicidal activity of fatty acid methyl esters of <Emphasis Type="Italic">Vitex</Emphasis> species against <Emphasis Type="Italic">Culex quinquefasciatus</Emphasis>

The larvicidal activity of fatty acid methyl ester (FAME) extracts of Vitex altissima, Vitex negundo and Vitex trifolia was studied against early fourth-instar larvae of Culex quinquefasciatus. The fatty composition was analysed by gas chromatography. The highest percentage of lauric acid, palmitic acid, stearic acid, oleic acid and linolenic acid were recorded in V. negundo. The highest percentage of linolenic acid was recorded in V. trifolia. The FAME extract of V. trifolia showed the highest larvicidal activity with an LC50 value of 9.25 ppm followed by V. altissima (14.82 ppm) and V. negundo (18.64 ppm).     

Effect of bioactive fractions of <Emphasis Type="Italic">Citrullus vulgaris</Emphasis> Schrad. leaf extract against <Emphasis Type="Italic">Anopheles stephensi</Emphasis> and <Emphasis Type="Italic">Aedes aegypti</Emphasis>

The benzene extract of Citrullus vulgaris was tested against Anopheles stephensi and Aedes aegypti for the larvicidal activity and ovicidal properties. The crude benzene extract was found to be more effective against A. stephensi than A. aegypti. The LC₅₀ values were 18.56 and 42.76 ppm respectively. The LC₅₀ values for silica gel fractions (bioactive fractions I, II, III and IV) were 11.32, 14.12, 14.53 and 16.02 ppm respectively. The mean per cent hatchability of the egg rafts were observed after 48 h post treatment. The crude extract of benzene exerted 100% mortality at 250 ppm against A. stephensi and at 300 ppm against A. aegypti. The silica gel fractions I and II afforded 100% mortality at 100 ppm and III and IV exerted the hatchability rate of 4.9 and 5.3% at the same concentration against A. stephensi.     

<Emphasis Type="Italic">Aedes aegypti</Emphasis> (Diptera: Culicidae): monitoring of populations to improve control strategies in Argentina

To study the seasonal fluctuations of populations of Aedes aegypti (L.), to improve control strategies, or to monitor chemical control interventions, a lightweight, inexpensive ovitrap made of black plastic, pail-shaped, stackable, and provided with a wood tongue depressor was used. Field assays were performed in the northeast and northwest part of Argentina. In a 1-year trial performed in Tartagal (Salta), almost 100% of the ovitraps were highly positive, collecting a total of 1,000/2,000 eggs during March and the first part of April. A focal treatment in the corresponding neighborhood, performed at this time, immediately began to reduce positive ovitraps in spite of the high temperatures registered, rising again in November after winter season. Another field trial was performed in the whole urban area of Iguazú (Misiones). Mosquito populations were evaluated after three weekly ultra low volume (ULV) applications with an EC formulation of permethrin in water. The number of positive ovitraps diminished from 49% to 10% after the treatments. The last one performed in Wanda (Misiones) showed that positive ovitraps inside the dwellings aided in determining reinfestation rates after an intervention with a smoke-generating formulation containing beta-cypermethrin. The work performed in three different situations in urban areas at high risk of dengue can be considered a preliminary assay to establish the effective performance of simple ovitraps, allowing the Vector Control Service of the Argentinian Ministry of Health its use to improve surveillance and control strategies.     

Evaluation of larvicidal and nymphicidal potential of plant extracts against <Emphasis Type="Italic">Anopheles subpictus</Emphasis> Grassi, <Emphasis Type="Italic">Culex tritaeniorhynchus</Emphasis> Giles and <Emphasis Type="Italic">Aphis gossypii</Emphasis> Glover

The acetone, chloroform, ethyl acetate, hexane and methanol extracts of peel and leaf extracts of Citrus sinensis, Ocimum canum, Ocimum sanctum and Rhinacanthus nasutus were tested against fourth instar larvae of malaria vector, Anopheles subpictus Grassi, Japanese encephalitis vector, Culex tritaeniorhynchus Giles (Diptera: Culicidae) and feeding deterrence to nymphs of cotton pest, Aphis gossypii Glover (Homoptera: Aphididae). The larval and nymph mortality were observed after 24 h of exposure. All extracts showed moderate larvicidal and nymphicidal effects; however, the highest mortality was found in peel chloroform extract of C. sinensis, leaf ethyl acetate extracts of O. canum and O. sanctum and leaf chloroform extract of R. nasutus against the larvae of A. subpictus (LC₅₀ = 58.25, 88.15, 21.67 and 40.46 ppm; LC₉₀ = 298.31, 528.70, 98.34 and 267.20 ppm), peel methanol extract of C. sinensis, leaf methanol extract of O. canum, ethyl acetate extracts of O. sanctum and R. nasutus against the larvae of C. tritaeniorhynchus (LC₅₀ = 38.15, 72.40, 109.12 and 39.32 ppm; LC₉₀ = 184.67, 268.93, 646.62 and 176.39 ppm), peel hexane extract of C. sinensis, leaf methanol extracts of O. canum and R. nasutus and leaf ethyl acetate extract of O. sanctum against the nymph of A. gossypii (LC₅₀ = 162.89, 80.99, 73.27 and 130.19 ppm; LC₉₀ = 595.40, 293.33, 338.74 and 450.90 ppm), respectively. These results suggest that the peel methanol extracts of C. sinensis and O. canum, ethyl acetate leaf extract of O. sanctum and leaf chloroform and ethyl acetate extract of R. nasutus have the potential to be used as an ideal eco-friendly approach for the control of the A. subpictus, C. tritaeniorhynchus and A. gossypii.     

Bioactivity of flavonoid compounds from <Emphasis Type="Italic">Poncirus trifoliata</Emphasis> L. (Family: Rutaceae) against the dengue vector, <Emphasis Type="Italic">Aedes aegypti</Emphasis> L. (Diptera: Culicidae)

The bioactivity of four flavonoid compounds, namely poncirin, rhoifolin, naringin and marmesin, from Poncirus trifoliata was studied against the Aedes aegypti. Larvicidal assays were conducted to evaluate the 24 h LC(50) and LC(90) values of the flavonoid compounds. The lethal concentration (LC(50) and LC(90)) values ranged from 0.082 to 0.122 mg/l and 0.152 to 0.223 mg/l, respectively. The result of ovicidal test suggests that the ovicidal activity of the flavonoid compounds was influenced by the concentration of flavonoid compounds and age of the eggs. The result of oviposition test showed that the four flavonoid compounds exhibited oviposition-deterrent activity against gravid female mosquitoes. Oviposition decreased with an increase in concentration of flavonoid compounds. A laboratory test was carried out to evaluate protection period and percentage of repellency of four compounds diluted in ethanol (10 mg/l). The compound rhoifolin provided maximum 365.0 +/- 12.0 min protection and also 100.0% +/- 0.0 repellency against mosquito bite followed by poncirin, marmesin and naringin. None of the 25 volunteers of either sex exposed to 10% (w/v) flavonoid compounds (4-h patch test) showed a positive skin irritant reaction. All of the tested compounds proved to have various activities against different life stages of A. aegypti. Therefore, flavonoid compounds from P. trifoliata can be a potential candidate for use in the development of commercial mosquitocidal products that may be an alternative to conventional synthetic chemicals, particularly in integrated vector control applications.     

Efficacy of fungus mediated silver and gold nanoparticles against <Emphasis Type="Italic">Aedes aegypti</Emphasis> larvae

Chrysosporium tropicum is a pathogenic fungus. It is known to be an effective mosquito control agent. In the present study, we have synthesized the silver and gold nanoparticles using C. tropicum. These nanoparticles have been characterized through Microscan reader, X-ray diffractometer, transmission electron microscopy, and further confirmed by scanning electron microscopy. The characterization study confirmed the spherical shape and size (2–15 and 20–50 nm) of gold and silver nanoparticles. These silver and gold nanoparticles have been tested as a larvicide against the Aedes aegypti larvae. The larvicidal efficacy was noted when performed against all instars of A. aegypti at six different log concentrations, and significant results could be observed. The gold nanoparticles used as an efficacy enhancer have shown mortality at three times higher concentration than the silver nanoparticles. The larval mortality was observed after different time of exposures. The mortality values were obtained using the probit analysis. The larvae of A. aegypti were found to be highly susceptible for the silver nanoparticles. The second instar larvae have shown 100% mortality against the silver nanoparticles after 1 h, whereas the first, third, and fourth instars have shown efficacy (LC₅₀ = 3.47, 4, and 2; LC₉₀ = 12.30, 8.91, and 4; LC₉₉ = 13.18, 13.18, and 7.58, respectively) after 1 h. The results could suggest that the use of fungus C. tropicum, silver, and gold nanoparticles is a rapid, environmentally safer, and greener approach for mosquito control. This could lead us to a new possibility in vector control strategy.     

Effect of <Emphasis Type="Italic">Myracrodruon urundeuva</Emphasis> leaf lectin on survival and digestive enzymes of <Emphasis Type="Italic">Aedes aegypti</Emphasis> larvae

Aedes aegypti transmits the viruses that cause yellow and dengue fevers. Vector control is essential, since a vaccine for dengue has not as yet been made available. This work reports on the larvicidal activity of Myracrodruon urundeuva leaf lectin (MuLL) against A. aegypti fourth-stage larvae (L₄). Also, the resistance of MuLL to digestion by L₄ gut proteases and the effects of MuLL on protease, trypsin-like and α-amylase activities from L₄ gut were evaluated to determine if lectin remains active in A. aegypti gut and if insect enzyme activities can be modulated by MuLL. MuLL promoted mortality of L₄ with LC₅₀ of 0.202 mg/ml. Haemagglutinating activity of MuLL was detected even after incubation for 96 h with L₄ gut preparation containing protease activity. MuLL affected the activity of gut enzymes, inhibiting protease and trypsin activities and stimulating α-amylase activity. The results suggest that MuLL may become a new biodegradable larvicidal agent for dengue control. Larvicidal activity of MuLL may be linked to its resistance to proteolysis by larval enzymes and interference in the activity of digestive larval enzymes.