Larvicidal effects of various Euro-Asiatic plants against Culex quinquefasciatus Say larvae (Diptera: Culicidae)

Extracts from 56 species of plants in the Euro-Asiatic region were tested for larvicidal activity against the fourth larval instar of the mosquito Culex quinquefasciatus Say (Diptera: Culicidae). All plant extracts showed larvicidal activity after 24 h of exposure to the plant extracts in a maximal dose of 500 ppm. The extracts of the plants Otanthus maritimus and Ammi visnaga displayed the highest larvicidal effect (LD₅₀ 7 and 9 ppm, respectively) followed by Acer pseudoplatanus, Humulus japonicus, Acer platanoides, Satureja hortensis, Ocimum basilicum and Thymus vulgaris (LD₅₀ 23, 25, 28, 28, 32 and 48 ppm respectively). For eight species, the appraisal value of LD₅₀ was between 51 and 100 ppm, another eight species from 101 to 200 ppm, 15 species from 201 to 500 ppm and for 17 species, low mortality showed no lethal dose (LD₅₀ > 500 ppm).     

Larvicidal activity of pectolinaringenin from Clerodendrum phlomidis L. against Culex quinquefasciatus Say and Aedes aegypti L. (Diptera: Culicidae)

Larvicidal activity of 12 fractions and a compound of chloroform extract of Clerodendrum phlomidis L. (Lamiaceae) was assayed for their toxicity against the early fourth-instar larvae of the filarial vector Culex quinquefasciatus Say and dengue vector Aedes aegypti L. The fractions were tested at 100-, 50-, 25- and 12.5-ppm concentrations. The compound pectolinaringenin was tested at 5-, 2.5-, 1.0- and 0.5-ppm concentrations. Among the different fractions, fraction 5 recorded the lowest LC(50) and LC(90) values of 5.02, 61.63?ppm and 32.86, 73.62?ppm against C. quinquefasciatus and A. aegypti, respectively. The compound pectolinaringenin showed the lowest LC(50) and LC(90) values of 0.62, 2.87?ppm and 0.79, 5.31?ppm against C. quinquefasciatus and A. aegypti, respectively. This is the first report on the mosquito larvicidal activity of the isolated compound pectolinaringenin from C. phlomidis. The results of this study show that the chloroform extract of C. phlomidis can be used as a potent source and pectolinaringenin as a new natural mosquito larvicidal agent.     

Larvicidal activity of saponin from Achyranthes aspera against Aedes aegypti and Culex quinquefasciatus (Diptera: Culicidae)

The acetone, chloroform, ethyl acetate, hexane and methanol leaf extracts of Acalypha indica, Achyranthes aspera, Leucas aspera, Morinda tinctoria and Ocimum sanctum were studied against the early fourth-instar larvae of Aedes aegypti L and Culex quinquefasciatus Say. The larval mortality was observed after 24 h exposure. All extracts showed moderate larvicidal effects; however, the highest larval mortality was found in the ethyl acetate extract of A. aspera. In the present study, bioassay-guided fractionation of A. aspera led to the separation and identification of a saponin as a potential mosquito larvicidal compound, with LC₅₀ value of 18.20 and 27.24 ppm against A. aegypti and C. quinquefasciatus, respectively. ¹H NMR, ¹³C NMR and mass spectral data confirmed the identification of the active compound. This is the first report on the mosquito larvicidal activity of the saponin from the ethyl acetate extract of A. aspera. This study investigates the potential of crude extracts from commonly used medical herbs in India as an environmentally safe measure to control the vector of dengue and lymphatic filariasis.     

Larvicidal and pupicidal activity of extracts and fractionates of Eichhornia crassipes (Mart.) Solms against the filarial vector Culex quinquefasciatus Say

Petroleum ether, acetone, ethyl acetate, aqueous extract, methanol and ethanol fractionate of Eichhornia crassipes (Mart.) Solms was tested for their larvicidal efficacy against the different instars (I, II, III and IV) and pupae of Culex quinquefasciatus Say. The larval mortality was observed after 24?h of the treatment. The extracts showed a dose-dependent toxicity to larvae. The toxicity of the extracts decreased with increase in larval stage. Ethanol fractionate of E. crassipes showed the highest larvicidal and pupicidal activity against C. quinquefasciatus compared to other solvent extracts and fractionates with LC₅₀ 71.43, 94.68,120.42, 152.15 and 173.35?ppm for I, II, III, IV and pupae, respectively. Presence of metabolites like flavonoids, alkaloids, anthroquinones and anthocyanins in the tested extracts might be the reason for the larvicidal and pupicidal activity of the plant extracts and fractionates of waterhyacinth. Mosquito-repellent activity was not exhibited by these extracts at the tested concentrations. The results demonstrated the potential of the aquatic plant E. crassipes in the successful control of the filarial vector C. quinquefasciatus.     

Larvicidal activity of some Euphorbiaceae plant extracts against Aedes aegypti and Culex quinquefasciatus (Diptera: Culicidae)

Larvicidal activity of ethyl acetate, butanol, and petroleum ether extracts of five species of Euphorbiaceae plants, Jatropha curcas, Pedilanthus tithymaloides, Phyllanthus amarus, Euphorbia hirta, and Euphorbia tirucalli, were tested against the early fourth instar larvae of Aedes aegypti L. and Culex quinquefasciatus (Say). The larval mortality was observed after 24 h of exposure. All extracts showed low larvicidal effects; however, the highest larval mortality was found in petroleum ether extract. The LC₅₀ value of petroleum ether extracts of J. curcas, P. tithymaloides, P. amarus, E. hirta, and E. tirucalli were 8.79, 55.26, 90.92, 272.36, and 4.25 ppm, respectively, against A. aegypti and 11.34, 76.61, 113.40, 424.94, and 5.52 ppm, respectively, against C quinquefasciatus. Of the various ratios tested, the petroleum ether extracts of J. curcas and E. tirucalli were observed to be more efficient than the other plant extracts. It is, therefore, suggested that E. tirucalli can be applied as an ideal potential larvicide against A. aegypti and C. quinquefasciatus. This is an ideal ecofriendly approach for the control of the dengue vector, A. aegypti, and the lymphatic filariasis vector, C. quinquefasciatus.     

Larvicidal efficacy of Sphaeranthus indicus, Cleistanthus collinus and Murraya koenigii leaf extracts against filarial vector, Culex quinquefasciatus Say (Diptera: Culicidae)

Sphaeranthus indicus, Cleistanthus collinus and Murraya koenigii leaf extracts were tested against the third instar larvae of Culex quinquefasciatus. The plant material was shade dried at room temperature and powdered coarsely. From each plant, 500?g powder was macerated with 1.5?L of hexane, chloroform and ethyl acetate sequentially for a period of 72?h each and filtered. The yield of the S. indicus, C. collinus and M. koenigii crude extracts by hexane, chloroform and ethyl acetate was 9.16, 11.71 and 10.83?g for S. indicus; 8.17, 10.69 and 9.85?g for C. collinus; and 10.11, 11.92 and 9.87?g for M. koenigii, respectively. The extracts were concentrated at reduced temperature on a rotary vacuum evaporator and stored at a temperature of 4°C. The S. indicus, C. collinus and M. koenigii leaf extracts at 250, 500, 750 and 1,000?ppm caused a significant mortality of C. quinquefasciatus. The LC(50) and LC(90) values of S. indicus, C. collinus and M. koenigii against third instar larvae at 24, 48 and 72?h (hexane, chloroform and ethyl acetate) were the following: S. indicus LC(50) values were 544.93, 377.86 and 274.79?ppm and LC(90) values were 1,325.32, 1,572.55 and 1,081.29?ppm at 24?h; C. collinus LC(50) values were 375.34, 318.29 and 226.10?ppm and LC(90) values were 699.65, 1,577.62 and 1,024.92?ppm at 24?h; and M. koenigii LC(50) values were 963.53, 924.85 and 857.62?ppm and LC(90) values were 1,665.12, 1,624.68 and 1,564.37?ppm at 24?h, respectively. However, the highest larval mortality was observed in C. collinus followed by S. indicus and M. koenigii of various concentrations at 24, 48 and 72?h. The study proved that S. indicus, C. collinus and M. koenigii leaf extracts had larvicidal property against species of C. quinquefasciatus. This is an ideal ecofriendly approach for the control of vector control programmes.     

Larvicidal, pupicidal, repellent and adulticidal activity of Citrus sinensis orange peel extract against Anopheles stephensi, Aedes aegypti and Culex quinquefasciatus (Diptera: Culicidae)

Mosquitoes are the carriers of severe and well-known illnesses such as malaria, arboviral encephalitis, dengue fever, chikunguniya fever, West Nile virus and yellow fever. These diseases produce significant morbidity and mortality in humans and livestock around the world. The present study explored the effects of orange peel ethanol extract of Citrus sinensis on larvicidal, pupicidal, repellent and adulticidal activity against Anopheles stephensi, Aedes aegypti and Culex quinquefasciatus. The orange peel material was shade dried at room temperature and powdered coarsely. From orange peel, 300?g powdered was macerated with 1?L of ethanol sequentially for a period of 72?h each and filtered. The yields of the orange peel ethanol crude extract of C. sinensis 13.86?g, respectively. The extracts were concentrated at reduced temperature on a rotary vacuum evaporator and stored at a temperature of 4?°C. The larvicidal, pupicidal and adult mortality was observed after 24?h of exposure; no mortality was observed in the control group. For C. sinensis, the median lethal concentration values (LC(50)) observed for the larvicidal and pupicidal activities against mosquito vector species A. stephensi first to fourth larval instars and pupae were 182.24, 227.93, 291.69, 398.00 and 490.84?ppm; A. aegypti values were 92.27, 106.60, 204.87, 264.26, 342.45, 436.93 and 497.41?ppm; and C. quinquefasciatus values were 244.70, 324.04, 385.32, 452.78 and 530.97?ppm, respectively. The results of maximum repellent activity were observed at 450?ppm in ethanol extracts of C. sinensis and the mean complete protection time ranged from 150 to 180?min was tested. The ethanol extract of C. sinensis showed 100?% repellency in 150?min and showed complete protection in 90?min at 350?ppm against A. stephensi, A. aegypti and C. quinquefasciatus, respectively. The adult mortality was found in ethanol extract of C. sinensis with the LC(50) and LC(90) values of 272.19 and 457.14?ppm, A. stephensi; 289.62 and 494.88?ppm, A. aegypti; and 320.38 and 524.57?ppm, respectively. These results suggest that the orange peel extracts of C. sinensis have the potential to be used as an ideal eco-friendly approach for the control of the vector control programmes.     

Mosquito larvicidal and pupicidal efficacy of Solanum xanthocarpum (Family: Solanaceae) leaf extract and bacterial insecticide, Bacillus thuringiensis, against Culex quinquefasciatus Say (Diptera: Culicidae)

The bio-efficacy of Solanum xanthocarpum leaf extract and bacterial insecticide, Bacillus thuringiensis, were assessed against the first to fourth instar larvae and pupae of Culex quinquefasciatus, under the laboratory conditions. The medicinal plants were collected from the outskirt Bharathiar University, Coimbatore, Tamil Nadu, India. The shade dried plant materials were extracted by employing the Soxhlet apparatus with ethanol (organic solvent) for 8 h and filtered. The extracts were concentrated at reduced temperature on a rotary evaporator and stored at a temperature of 4°C. Both S. xanthocarpum and B. thuringiensis show varied degree of larvicidal and pupicidal activity against various stages of C. quinquefasciatus. The LC(50) and LC(90) of S. xanthocarpum against the first to fourth instar larvae and pupae were 155.29, 198.32, 271.12, 377.44, and 448.41 ppm and 687.14, 913.10, 1,011.89, 1,058.85, and 1,141.65 ppm, respectively. On the other hand, the LC(50) values of B. thuringiensis against the first to fourth instar larvae and pupae were 133.88, 157.14, 179.44, 206.80, and 240.74 ppm; the LC(90) values were 321.04, 346.89, 388.86, 430.95, and 492.70 ppm, respectively. However, the combined treatment of S. xanthocarpum?+?B. thuringiensis (1:2) material shows highest larvicidal and pupicidal activity of the LC(50) values 126.81, 137.62, 169.14, 238.27, and 316.02 ppm and the LC(90) values 476.36, 613.49, 705.29, 887.85, and 1,041.73 ppm against C. quinquefasciatus in all the tested concentrations than the individuals and clearly established that there is a substantial amount of synergist act. Therefore, the present investigation clearly exhibit that both S. xanthocarpum and B. thuringiensis materials could serve as a potential of highest mortality rate against the mosquito larvae laboratory as well as the field conditions. Since C. quinquefasciatus is a ditch breeder vector mosquito, this is a user and eco-friendly biopesticide for the control of mosquito vector management program.     

Persistence of hepatitis B antigen in Culex quinquefasciatus (Diptera: Culicidae)

Groups of wild-caught Culex quinquefaciatus Say, previously tested for the presence of hepatitis B surface antigen (HBsAg), were tested for the presence of hepatitis B e antigen (HBeAg). This antigen was detected at low levels in blood-fed, half-gravid, and gravid groups. A colony of Cx. quinquefasciatus was established in the laboratory and tested for the persistence of HBsAg and HBeAg. Five days after feeding on blood infected with HBsAg and HBeAg, 9 of 20 (45%) pools of Cx. quinquefasciatus were HBeAg-positive and 5 of 20 (25%) pools were HBeAg-positive; low levels of HBsAg and HBeAg were still detectable 28 d after the infective meal in 2 of 20 (10%) and 1 of 20 (5%) pools, respectively. A crude protease extract was prepared from colony mosquitoes, and the effect of this extract on HBsAg and HBeAg present in human serum was tested in vitro. After 20 h, tests for both antigens were still strongly positive. Low levels of HBsAg were detected in ovaries 7 d after infection. Salivary glands were HBsAg- and HBeAg-negative.     

Laboratory and field evaluation of medicinal plant extracts against filarial vector, Culex quinquefasciatus Say (Diptera: Culicidae)

The present study explored the effects of Jatropha curcas, Hyptis suaveolens, Abutilon indicum, and Leucas aspera tested against third instar larvae of filarial vector, Culex quinquefasciatus. The dried plant materials were powdered by an electrical blender. From each sample, 500 g powder was macerated with 1.5 L of hexane, chloroform, ethyl acetate, and methanol 8h, using Soxhlet apparatus, and filtered. The extracts were concentrated at reduced temperature on a rotary evaporator and stored at a temperature of 4°C. The yield of crude extract was 11.4, 12.2, 10.6, and 13.5 g in hexane, chloroform, ethyl acetate, and methanol, respectively. The hexane, chloroform, ethyl acetate, and methanol extract of J. curcas with LC(50) values of 230.32, 212.85, 192.07, and 113.23 ppm; H. suaveolens with LC(50) values of 213.09, 217.64, 167.59, and 86.93 ppm; A. indicum with LC(50) values of 204.18, 155.53, 166.32, and 111.58 ppm; and L. aspera with LC(50) values of 152.18, 118.29, 111.43, and 107.73 ppm, respectively, against third instar larvae of C. quinquefasciatus. The larval mortality was observed after 24 h of exposure. Maximum larvicidal activity was observed in the methanolic extract followed by ethyl acetate, chloroform, and hexane extract. No mortality was observed in the control. The observed mortality were statistically significant at P?相似文献   

Larvicidal activity of Ocimum sanctum Linn. (Labiatae) against Aedes aegypti (L.) and Culex quinquefasciatus (Say)

The acetone, chloroform, ethyl acetate, hexane, and methanol leaf and flower extracts of Ocimum sanctum were studied against fourth instar larvae of Aedes aegypti and Culex quinquefasciatus. The highest larval mortality was found in leaf extract of O. sanctum against the larvae of A. aegypti and C. quinquefasciatus. The LC₅₀ values of O. sanctum against the larvae of A. aegypti were 425.94, 150.40, 350.78, 575.26, and 175.67 and against the larvae of C. quinquefasciatus were 592.60, 93.92, 212.36, 76.61, and 82.12 ppm, respectively.     

Overproduced esterases in Culex pipiens quinquefasciatus (Diptera: Culicidae) from Vietnam

The electrophoretic polymorphism of loci encoding for 10 enzymes was studied in Culex p. quinquefasciatus Say from six localities of Vietnam. The analysis of 11 "neutral genes" showed that differentiation among samples was low, but significant (Fst = 0.06), and significantly related to geographic distance between sample sites. These results are similar to those observed in other countries (Europe and west Africa). A single type of overproduced esterases (A2-B2) was observed, and its frequency was high (60-100%) in all samples. This situation is in sharp contrast with that observed in other countries of South East Asia (China, South Korea and Japan), where two or more types of overproduced esterases have been reported. A map summarizing the geographic distribution of Asian Cr. p. quinquefasciatus with overproduced esterases is provided.     

Stable, germ-line transformation of Culex quinquefasciatus (Diptera: Culicidae)

A Hermes-based transposable element transformation system incorporating an enhanced green fluorescent protein (EGFP) marker was used to produce two transgenic lines of Culex quinquefasciatus (Say). The transformation frequency was approximately 12% and transformation of Culex was shown to be dependent on the presence of Hermes transposase. Injected Culex embryos were treated with four different heat shock regimes, two of which produced transformed individuals. These individuals were mated with wild-type mosquitoes and produced offspring which expressed the dominant EGFP gene in Mendelian ratios predicted for the stable integration of a gene at a single locus. The two transformed lines displayed distinct patterns of phenotypic expression, the expression of which has remained stable after fifteen generations. In these transgenic lines both the Hermes element and flanking plasmid DNA integrated into the Culex genome, as has been previously seen in Hermes-mediated transgenic strains of Aedes aegypti (L.). The high frequency of Culex transformation together with the dependence on the presence of Hermes transposase suggests that, as for Ae. aegypti, this mode of transposition into the germ-line genome occurs by an alternate mechanisms to the cut and paste type of transposition seen for this element in other insect species and in the somatic nuclei of mosquitoes. This is the first report of the genetic transformation of a species in the genus Culex and demonstrates that this medically important mosquito species can now, along with several other Culicine and Anopheline mosquito species, be genetically manipulated.     

Cyt1A from Bacillus thuringiensis restores toxicity of Bacillus sphaericus against resistant Culex quinquefasciatus (Diptera: Culicidae)

The 2362 strain of Bacillus sphaericus, which produces a binary toxin highly active against Culex mosquitoes, has been developed recently as a commercial larvicide. It is being used currently in operational mosquito control programs in several countries including Brazil, France, India, and the United States. Laboratory studies have shown that mosquitoes can develop resistance to B. sphaericus, and low levels of resistance have already been reported in field populations in Brazil, France, and India. To develop tools for resistance management, the Cyt1A protein of Bacillus thuringiensis subsp. israelensis De Barjac was evaluated for its ability to suppress resistance to B. sphaericus in a highly resistant population of Culex quinquefasciatus Say. A combination of B. sphaericus 2362 in a 10:1 ratio with a strain of B. thuringiensis subsp. israelensis that only produces Cyt1A reduced resistance by >30,000-fold. Resistance was suppressed completely when B. sphaericus was combined with purified Cyt1A crystals in a 10:1 ratio. Synergism was observed between the Cyt1A toxin and B. sphaericus against the resistant mosquito population and accounted for the marked reduction in resistance. However, no synergism was observed between the toxins against a nonresistant mosquito population. These results indicate that Cyt1A could be useful for managing resistance to B. sphaericus 2362 in Culex populations, and also provide additional evidence that Cyt1A may synergize toxicity by enhancing the binding to and insertion of toxins into the mosquito microvillar membrane.     

Larvicidal,ovicidal, and adulticidal efficacy of Erythrina indica (Lam.) (Family: Fabaceae) against Anopheles stephensi,Aedes aegypti,and Culex quinquefasciatus (Diptera: Culicidae)

Mosquitoes are the major vector for the transmission of malaria, dengue fever, yellow fever, filariasis, schistosomiasis, and Japanese encephalitis. Mosquito control is facing a threat because of the emergence of resistance to synthetic insecticides. Insecticides of botanical origin may serve as suitable alternative biocontrol techniques in the future. In view of the recently increased interest in developing plant origin insecticides as an alternative to chemical insecticide, this study was undertaken to assess the larvicidal, ovicidal, and adulticidal potential of the crude hexane, benzene, chloroform, ethyl acetate, and methanol solvent extracts from the medicinal plant Erythrina indica against the medically important mosquito vectors, Anopheles stephensi, Aedes aegypti, and Culex quinquefasciatus (Diptera: Culicidae). The larval mortality was observed after 24 h of exposure. All extracts showed moderate larvicidal effects; however, the highest larval mortality was found in methanol extract of leaf of E. indica against the larvae of A. stephensi, A. aegypti, and C. quinquefasciatus with the LC₅₀ and LC₉₀ values of 69.43, 75.13, and 91.41 ppm and 125.49, 134.31, and 167.14 ppm, respectively. The mean percent hatchability of the eggs was observed after 48 h post treatment. The percent hatchability was inversely proportional to the concentration of extract and directly proportional to the eggs. All the five solvent extracts showed moderate ovicidal activity; however, the methanol extract showed the highest ovicidal activity. The methanol extract of E. indica against A. stephensi, A. aegypti, and C. quinquefasciatus exerted 100 % mortality (zero hatchability) at 150, 200, and 250 ppm, respectively. Control eggs showed above 99.3–100 % hatchability. The adult mortality was observed after 24 h recovery period. The plant crude extracts showed dose-dependent mortality. At higher concentrations, the adult showed restless movement for some times with abnormal wagging and then died. Among the extracts tested, the highest adulticidal activity was observed in methanol extract against A. stephensi followed by A. aegypti and C. quinquefasciatus with the LD₅₀ and LD₉₀ values of 88.76, 94.09, and 119.64 ppm and 160.83, 169.01, and 219.77 ppm, respectively. No mortality was recorded in the control. Our data suggest that the crude hexane, benzene, chloroform, ethyl acetate, and methanol solvent extracts of E. indica have the potential to be used as an eco-friendly approach for the control of the A. stephensi, A. aegypti, and C. quinquefasciatus.     

Larvicidal effects of some Euro-Asiatic plants against Culex quinquefasciatus Say larvae (Diptera: Culicidae)

Methanol extracts of the aerial parts from 62 Euro-Asiatic plant species were tested for larvicidal activity against the mosquito Culex quinquefasciatus Say (Diptera: Culicidae) under laboratory conditions. The fourth larval instar was tested. The extracts of the plants Seseli pallasii and Schisandra chinencis displayed the highest larvicidal activities with LD₅₀ 6 and 15 ppm, respectively, followed by Arthemisia campestris, Verbena officinalis, and Imperatoria osthruthium with LD₅₀ 23, 38, and 49 ppm, respectively. The appraised value of LD₅₀ for two species was between 51–100 ppm; eight species had lethal doses from 101 to 500 ppm, 13 species showed lethal doses from 501 to 1,000 ppm, and 34 species did not show lethal doses for low mortality (LD₅₀ > 1,000 ppm).     

Temporal and geographic genetic variation in Culex pipiens quinquefasciatus (Diptera: Culicidae) from Florida

Culex (Culex) pipiens quinquefasciatus Say field population from Vero Beach, FL, sampled monthly over a period of 8 mo, a colony sample, and six geographic samples were analyzed for genetic variation at 12 enzymes (10 "neutral" gene enzymes with 11 putative loci and two "complex" gene enzymes) by using polyacrylamide gel electrophoresis. The analysis of the 11 putative loci in both temporal and geographic samples showed that the four loci (Gpi, Hk, Mdhp-2, and Pgm) diagnostic of Cx. p. quinquefasciatus in the southern United States are present in similar frequencies in Florida samples. The Cx. p. quinquefasciatus colony sample showed significantly lower genetic variation than the temporal field samples, measured by mean number of alleles per locus (colony 1.2 +/- 0.1 versus field 1.44 +/- 0.03), percentage of polymorphic loci (colony 18.2% versus field 28.4%), mean observed heterozygosity (H(o) = colony 0.027 +/- 0.02 versus field 0.09 +/- 0.01), and mean Hardy-Weinberg expected heterozygosity (H(e) = colony 0.025 +/- 0.02 versus field 0.085 +/- 0.01). Three of the 11 loci (Acoh, Pgd, and Pgm) from the Vero Beach field samples showed bimodal patterns in their frequencies of the most common allele during peak density of the population. The low value of F(st) of 0.058 indicated minimum population substructuring among the temporal samples. Genetic variability values between geographic samples from the Florida panhandle and south Florida were not significant. Gene flow estimates based on F(ST), = 0.05, indicating low levels of gene flow among the geographic samples of Cx. p. quinquefasciatus. The average Nei's and modified Rogers' genetic distances among the six populations were 0.005 +/- 0.001 and 0.077 +/- 0.007, respectively. The cluster analysis did not suggest geographic clustering. The analysis of the "complex" gene enzymes in both temporal and geographic samples of Cx. p. quinquefasciatus from Florida showed the presence of two highly amplified esterases (Estbeta1 and Estalpha2\Estbeta2), indicating resistance to organophosphate insecticides and highly amplified Aldox enzyme (an enzyme that indicates resistance to at least one insecticide and a herbicide). Comparison of our results with previous studies on Cx. p. quinquefasciatus populations in the United States indicates that the genetic characteristics of the Florida populations of Cx. p. quinquefasciatus are very similar to populations from areas where ecological conditions are very different.