Abstracts

INTRODUCTION

The prevention of dengue depends primarily on the decrease of vector populations in urban and periurban regions.⁸8 . Corrêa PRL, França E, Bogutchi TF. Infestação pelo Aedes aegypti e ocorrência da dengue em Belo Horizonte, Minas Gerais. Rev Saude Publica. 2005;39(1):33-40. DOI:10.1590/S0034-89102005000100005 However, Aedes aegypti’s high degree of adaptation to urban environments hinders the control of its population density, increasing the prevalence of dengue throughout Brazil.¹²12 . Kubota RL, Brito M, Voltolini JC. Método de varredura para exame de criadouros de vetores de dengue e febre amarela urbana. Rev Saude Publica. 2003;37(2):263-5. DOI:10.1590/S0034-89102003000200017

In Brazil, control programs for Ae. aegypti primarily use chemical insecticides, with an emphasis on organophosphates and pyrethroids, which require constant monitoring.¹⁴14 . Luna JED, Martins MF, Anjos AF, Kuwabara EF, Navarro-Silva MA. Susceptibility of Aedes aegypti to temephos and cypermethrin insecticides, Brazil. Rev Saude Publica. 2004;38(6):833-4. DOI:10.1590/S0034-89102004000600013 This control strategy faces numerous difficulties, the most important of which is mosquito resistance to the insecticides used (Tauil,²¹21 . Tauil PL. Aspectos críticos do controle do dengue no Brasil. Cad Saude Publica. 2002;18(3):867-71. DOI:10.1590/S0102-311X2002000300035 2002).

The resistance of Ae. aegypti to insecticides has been reported by numerous researchers in Brazil.²2 . Beserra EB, Fernandes CRM, Queiroga MFC, Castro Jr FP. Resistência de Aedes aegypti (L.) (Diptera: Culicidae) ao organofosforado temefós na Paraíba. Neotrop Entomol. 2007;36(2):303-7. DOI:10.1590/S1519-566X2007000200019^,55 . Campos J, Andrade CFS. Susceptibilidade larval de duas populações de Aedes aegypti a inseticidas químicos. Rev Saude Publica. 2001;35(3):232-6. DOI:10.1590/S0034-89102001000300003^,1010 . Gambarra WPT, Martins WFS, Lucena Filho MLL, Albuquerque IMC, Apolinário OKS, Beserra EB. Spatial distribution and sterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos. Rev Soc Bra Med Trop. 2013;46(2):178-84. DOI:10.1590/0037-8682-1727-2013^,1313 . Lima EP, Oliveira Filho AM, Lima JWO, Ramos Jr AN, Cavalcanti LPG, Pontes RJS. Resistência do Aedes aegypti ao temefós em Municípios do Estado do Ceará. Rev Soc Bras Med Trop. 2006;39(3):259-63. DOI:10.1590/S0037-86822006000300006^,1414 . Luna JED, Martins MF, Anjos AF, Kuwabara EF, Navarro-Silva MA. Susceptibility of Aedes aegypti to temephos and cypermethrin insecticides, Brazil. Rev Saude Publica. 2004;38(6):833-4. DOI:10.1590/S0034-89102004000600013^,1717 . Prophiro JS, Silva OS, Luna JED, Piccoli CF, Kanis LA, Silva MAN. Aedes aegypti and Aedes albopictus (Diptera: Culicidae): coexistence and susceptibility to temephos, in municipalites with occurrence of dengue and differentiated characteristics of urbanization. Rev Bras Med Tropical. 2011;44(3):300-5. DOI:10.1590/S0037-86822011005000025 In the state of Ceará, Northeastern Brazil, resistant populations have been detected in the municipalities of Juazeiro do Norte, Crato, and Barbalha, as well as in neighborhoods in the capital Fortaleza (Lima et al,¹³13 . Lima EP, Oliveira Filho AM, Lima JWO, Ramos Jr AN, Cavalcanti LPG, Pontes RJS. Resistência do Aedes aegypti ao temefós em Municípios do Estado do Ceará. Rev Soc Bras Med Trop. 2006;39(3):259-63. DOI:10.1590/S0037-86822006000300006 2006). In Paraíba, Northeastern Brazil, resistance was diagnosed in insects collected in the municipalities of Boqueirão, Brejo dos Santos, Campina Grande, Itaporanga, Remígio,²2 . Beserra EB, Fernandes CRM, Queiroga MFC, Castro Jr FP. Resistência de Aedes aegypti (L.) (Diptera: Culicidae) ao organofosforado temefós na Paraíba. Neotrop Entomol. 2007;36(2):303-7. DOI:10.1590/S1519-566X2007000200019 Alagoa Nova, Alagoa Grande, Serra Redonda, and Lagoa Seca.¹⁰10 . Gambarra WPT, Martins WFS, Lucena Filho MLL, Albuquerque IMC, Apolinário OKS, Beserra EB. Spatial distribution and sterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos. Rev Soc Bra Med Trop. 2013;46(2):178-84. DOI:10.1590/0037-8682-1727-2013

The detection of resistance and knowledge of the underlying resistance mechanisms can help to elucidate basic aspects of insecticide resistance and allow resistance management.⁴4 . Braga IA, Valle D. Aedes aegypti: histórico de controle no Brasil. Epidemiol Serv Saude. 2007;16(2):113-8.^,1919 . Scott JA. The molecular genetics of resistance: resistance as a response to stress. Flor Entomol. 1995;78(3):399-414. DOI:10.2307/3495526 In populations with a fitness cost resulting from insecticide resistance, instability can be exploited in resistance-management programs (Konno & Omoto,¹¹11 . Konno RH, Omoto C. Custo adaptativo associado à resistência de Aphis gossypi Glover (Hemiptera: Aphididae) ao inseticida carbosulfam. Neotrop Entomol. 2006;35(2):246-50. DOI:10.1590/S1519-566X2006000200014 2006) because some of their main characteristics include adaptive disadvantage and loss of the biotic potential of resistant strains. Resistant populations are less fit than susceptible ones in the absence of selection pressure. This lower adaptive response of resistant populations may be associated with decreased overall viability and fertility, extended development time, decreased competitiveness for mating, and increased susceptibility to natural enemies.¹⁸18 . Roush RT, Mackenzie JA. Ecological genetics of insecticide and acaricide resistance. Ann Rev Entomol. 1987;32:361-80. DOI:10.1146/annurev.en.32.010187.002045

Considering that the evaluation of competition and fitness cost in resistant populations of Ae. aegypti can help guide resistance-management programs, the present study aimed to evaluate the resistance of Ae. aegypti to temephos Fersol 1G (temephos 1% w/w) associated with the adaptive disadvantage of these populations in the absence of selection pressure.

METHODS

The study was conducted between August 2007 and July 2008. The laboratory bioassays and the rearing of Ae. aegypti were performed in the Laboratory of Entomology in the Center for Insect Bioecology and Systematics (Núcleo de Bioecologia e Sistemática) of the Universidade Estadual da Paraíba. Insects were maintained at 27.0ºC [SE (standard error): 2.0], in a 12:12-h light-dark cycle, and the F1 generation of newly hatched eggs was collected in the neighborhoods of Catolé, Monte Santo, Nova Brasília, Liberdade, and Estação Velha, in the city of Campina Grande, PB, Northeastern Brazil. In these neighborhoods, traps for egg collection (ovitraps) were randomly distributed in 100 households and collected four days after installation. In the laboratory, this material was used to identify the species and establish the insect strains, following the methodology described by Beserra et al²2 . Beserra EB, Fernandes CRM, Queiroga MFC, Castro Jr FP. Resistência de Aedes aegypti (L.) (Diptera: Culicidae) ao organofosforado temefós na Paraíba. Neotrop Entomol. 2007;36(2):303-7. DOI:10.1590/S1519-566X2007000200019 (2007) and Beserra & Castro Jr³3 . Beserra EB, Castro Jr FP. Biologia Comparada de Populações de Aedes (Stegomyia) aegypti (L.) (Diptera: Culicidae) da Paraíba. Neotrop Entomol. 2008;37(1):81-5. DOI:10.1590/S1519-566X2008000100012 (2008).

Resistance was assessed using the larvicide temephos Fersol 1G (temephos 1% w/w). This product was initially diluted in water to obtain a stock solution of 100 mg a.i./L and then diluted into the working concentrations. The diagnostic dose was determined using a multiple-concentration test and the diagnostic dose was considered to be twice the LC₉₀ value for the susceptible population (S). Temephos resistance in field populations of Ae. aegypti was evaluated starting with the diagnostic dose measured in tests involving susceptible populations (S) and in the multiple-concentration test, where the dose varied between 0.28 mg a.i./L and 1.4 mg a.i./L.

For each test, 25 late-third-stage larvae (L3) and/or early fourth instar larvae (L4) were transferred to polyethylene beakers (500 mL) containing 250 mL of each insecticide solution diluted in distilled water, and this procedure was repeated four times. After larval exposure to the larvicide for 24h, the mortality rate was evaluated. Populations with a mortality rate of 98.0% were considered susceptible, those with a mortality rate between 80.0% and 98.0% were considered as requiring verification of resistance, and those with a mortality of ≤ 80.0% were considered resistant. Each bioassay was repeated three times on successive weeks.

Using a susceptible laboratory population (Rockefeller) and a temephos-resistant population from Catolé established in a previous bioassay, populations with 20.0%, 40.0%, 60.0%, and 80.0% resistant insects were produced. For each established population, 100 larvae of Ae. aegypti were transferred to plastic trays using different ratios of susceptible and resistant larvae and reared until the pupal stage. The adults were maintained in screened cages (20 cm³) for mating to produce eggs for the susceptibility bioassays.

The susceptibility to temephos Fersol 1G was monitored for two months, starting with the diagnostic dose determined in tests involving the susceptible population, and in a multiple-concentration test where the dose varied between 0.14 mg a.i./L and 1.96 mg a.i./L. Mortality data for each population were subjected to Probit analysis using POLO-PC software for calculating the LC₅₀ and LC₉₀ values.

The life cycles of the susceptible and resistant populations were compared in 100 newly hatched larvae, which were maintained in groups of five per 250 mL polyethylene beaker in distilled water. The following parameters were measured daily: temperature and pH of the water used for larval and pupal development using a chemical thermometer with an upper temperature limit of 60°C and a digital pH meter, and humidity using a digital thermo-hygrometer model HT-210. The pupae were classified by sex and adults were maintained in wooden screened cages (20 cm³) using five cages per population, each cage containing 10 male and 10 female insects. Larvae and adults were fed according to a method used for rearing Ae. aegypti. The embryo phase was assessed on the eggs resulting from the first 10 ovipositions, which were transferred to Petri dishes (9.0 cm diameter × 1.5 cm deep) containing enough distilled water to cover the eggs. The embryo phase was evaluated daily and involved the recording of the development period and mortality rates of the egg, larval, and pupal phases as well as the sex ratio, longevity, and fecundity of the adult stage. The biological variables evaluated were subjected to variance analysis and the means were compared using the Tukey test (p < 0.05) following a completely randomized design.

The biological variables analyzed allowed the construction of fertility life tables (Silveira-Neto et al,²⁰20 . Silveira Neto S, Nakano O, Bardin D, Villa Nova NA. Manual de ecologia dos insetos. São Paulo: Agronômica Ceres; 1976. 1976). The age intervals (x), specific fecundity (m_x), and survival probability (l_x) were also evaluated. The net reproductive rate (R₀), mean generation time (T), intrinsic rate of natural increase (r_m), finite rate of increase (λ), and population-doubling time (DT) were calculated, where: R₀ = Σ (l_x.m_x); T = Σ (l_x.m_x.x) / Σ (l_x.m_x); r_m = ln(R₀) / T; λ = ^erm; TD = ln (2) / r_m

RESULTS

The tests conducted using the susceptible laboratory strain (Rockefeller) to determine the diagnostic dose to be applied to field populations yielded a LC₉₀ of 0.14 mg a.i./L. On the basis of this result, a diagnostic dose of 0.28 mg a.i./L was obtained, which is twice the LC₉₀ value for the susceptible strain.

All the populations collected in the districts of Catolé, Monte Santo, Nova Brasília, Liberdade, and Estação Velha showed no mortality when subjected to multiple insecticide concentrations varying between 0.28 mg a.i./L and 1.4 mg a.i./L. The absence of mortality in these populations hindered the calculation of LC₅₀ and LC₉₀, and consequently their resistance ratios. Considering that all populations were resistant, the Catolé population was randomly selected to investigate competition in the absence of selection pressure between Ae. aegypti populations that were susceptible and resistant to temephos.

Ae. aegypti populations with distinct ratios of resistant individuals in the absence of selection pressure showed different mortality rates when subjected to the diagnostic dose of 0.28 mg a.i./L. Higher mortality rates were observed for the populations containing 20.0% and 40.0% resistant individuals, and mortality rates decreased from June (91.0% and 59.0%, respectively) to July (78.0% and 31.0%, respectively) in these populations. Populations with 60.0% and 80.0% resistant individuals had the lowest mortality rates in June (12.0% and 42.0%, respectively) and July (6.0% and 0%, respectively).

The LC₅₀ and LC₉₀ values followed the increase in the number of resistant individuals in each population. These values increased from 0.073 mg a.i./L and 0.225 mg a.i./L, respectively, in the group with 20.0% resistant insects, to 1.627 mg a.i./L and 2.227 mg a.i./L, respectively, in the group with 80.0% resistant individuals (Table 1).

The mean temperature of the water where larval development occurred was 26.4°C for the susceptible Rockefeller and Catolé populations; 26.5°C for the populations collected in Monte Santo, Nova Brasília, and Estação Velha; and 26.7°C for the population collected in Liberdade (Table 2). The mean room temperature was 27.0°C (SE: 2.0°C) and the pH ranged from 5.8 to 6.1.

No significant differences were observed with respect to embryonic development period among the populations evaluated; this period ranged between 2.1 and 2.9 days (Table 3). However, significant differences were observed in egg viability: viability was lower (33.5%) in the susceptible population and higher (91.3%) in the Monte Santo population (Table 3). Significant differences were observed in the duration of larval development and larval viability, but not in the sex ratio (Table 3). The longest development period (9.0 days) and lowest larval viability (36.0%) were found in the population collected in Estação Velha. These variables were not significantly different in the remaining resistant populations (Table 3). The number of eggs per female did not significantly differ among the populations evaluated, and no significant variation was seen in adult longevity, which ranged between 26.5 and 37.7 days for male adults and between 23.8 and 37.9 days for female adults (Table 4).

The net reproductive rate (R₀), mean generation time (T), innate capacity for increase in numbers (r_m), finite rate of increase (λ), and DT for the susceptible population were 130.78, 4.11, 1.12, 3.06, and 0.61, respectively. The Ae. aegypti population from Estação Velha showed the highest R₀ (152.58) and r_m (1.14), the population from Liberdade showed the highest λ (3.18), and the population from Monte Santo had the largest T (5.12) and DT (0.83) (Table 5).

DISCUSSION

The occurrence of temephos resistance in all Ae. aegypti populations evaluated corroborates what has been observed in other Brazilian cities⁵5 . Campos J, Andrade CFS. Susceptibilidade larval de duas populações de Aedes aegypti a inseticidas químicos. Rev Saude Publica. 2001;35(3):232-6. DOI:10.1590/S0034-89102001000300003^,1313 . Lima EP, Oliveira Filho AM, Lima JWO, Ramos Jr AN, Cavalcanti LPG, Pontes RJS. Resistência do Aedes aegypti ao temefós em Municípios do Estado do Ceará. Rev Soc Bras Med Trop. 2006;39(3):259-63. DOI:10.1590/S0037-86822006000300006^,1414 . Luna JED, Martins MF, Anjos AF, Kuwabara EF, Navarro-Silva MA. Susceptibility of Aedes aegypti to temephos and cypermethrin insecticides, Brazil. Rev Saude Publica. 2004;38(6):833-4. DOI:10.1590/S0034-89102004000600013^,1717 . Prophiro JS, Silva OS, Luna JED, Piccoli CF, Kanis LA, Silva MAN. Aedes aegypti and Aedes albopictus (Diptera: Culicidae): coexistence and susceptibility to temephos, in municipalites with occurrence of dengue and differentiated characteristics of urbanization. Rev Bras Med Tropical. 2011;44(3):300-5. DOI:10.1590/S0037-86822011005000025 and in Paraíba,²2 . Beserra EB, Fernandes CRM, Queiroga MFC, Castro Jr FP. Resistência de Aedes aegypti (L.) (Diptera: Culicidae) ao organofosforado temefós na Paraíba. Neotrop Entomol. 2007;36(2):303-7. DOI:10.1590/S1519-566X2007000200019^,1010 . Gambarra WPT, Martins WFS, Lucena Filho MLL, Albuquerque IMC, Apolinário OKS, Beserra EB. Spatial distribution and sterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos. Rev Soc Bra Med Trop. 2013;46(2):178-84. DOI:10.1590/0037-8682-1727-2013 where resistance to this insecticide evolved rapidly in most studied populations. For example, of seven Ae. aegypti populations collected in Brasília (DF), Midwest Brazil, and evaluated by Carvalho et al⁷7 . Carvalho MSL, Caldas ED, Degallier N, Vilarinhos PTR, Souza LCKR, Yoshizawa MAC, et al. Suscetibilidade de larvas de Aedes aegypti ao inseticida temefós no Distrito Federal. Rev Saude Publica. 2004;38(5):623-9. DOI:10.1590/S0034-89102004000500002 (2004), three showed insecticide resistance, with mortality rates varying between 54.1% and 63.4% in the first year, and all population groups were resistant in the second year, with mortality rates between 44.4% and 66.4%. In Foz do Iguaçu, in the state of Paraná, Southern Brazil, low levels of temephos resistance were observed for both Ae. aegypti and Ae. albopictus populations.¹⁰10 . Gambarra WPT, Martins WFS, Lucena Filho MLL, Albuquerque IMC, Apolinário OKS, Beserra EB. Spatial distribution and sterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos. Rev Soc Bra Med Trop. 2013;46(2):178-84. DOI:10.1590/0037-8682-1727-2013

In this study, it was not possible to determine resistance ratios for the samples evaluated. However, considering the absence of mortality among individuals exposed to multiple temephos concentrations, it can be inferred that the resistance levels were high, and similar results were observed in Ae. aegypti populations in other cities in Paraíba.²2 . Beserra EB, Fernandes CRM, Queiroga MFC, Castro Jr FP. Resistência de Aedes aegypti (L.) (Diptera: Culicidae) ao organofosforado temefós na Paraíba. Neotrop Entomol. 2007;36(2):303-7. DOI:10.1590/S1519-566X2007000200019^,1010 . Gambarra WPT, Martins WFS, Lucena Filho MLL, Albuquerque IMC, Apolinário OKS, Beserra EB. Spatial distribution and sterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos. Rev Soc Bra Med Trop. 2013;46(2):178-84. DOI:10.1590/0037-8682-1727-2013 Beserra et al²2 . Beserra EB, Fernandes CRM, Queiroga MFC, Castro Jr FP. Resistência de Aedes aegypti (L.) (Diptera: Culicidae) ao organofosforado temefós na Paraíba. Neotrop Entomol. 2007;36(2):303-7. DOI:10.1590/S1519-566X2007000200019 (2007) showed that the levels of temephos resistance ranged from low to high in populations from Campina Grande, Brejo dos Santos, Boqueirão, Itaporanga, and Remígio. Gambarra et al¹⁰10 . Gambarra WPT, Martins WFS, Lucena Filho MLL, Albuquerque IMC, Apolinário OKS, Beserra EB. Spatial distribution and sterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos. Rev Soc Bra Med Trop. 2013;46(2):178-84. DOI:10.1590/0037-8682-1727-2013 (2013) showed that Ae. aegypti populations in Alagoa Nova, Alagoa Grande, Lagoa Seca, and Serra Redonda had high levels of resistance, supporting the hypothesis that temephos resistance is prevalent in several regions of the state.

The high levels of resistance of Ae. aegypti populations in Paraíba may be associated with the use of temephos at different intensities and frequencies of application, subjecting these groups to different selection pressures and resistance mechanisms, with a consequent increase in resistance.¹⁰10 . Gambarra WPT, Martins WFS, Lucena Filho MLL, Albuquerque IMC, Apolinário OKS, Beserra EB. Spatial distribution and sterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos. Rev Soc Bra Med Trop. 2013;46(2):178-84. DOI:10.1590/0037-8682-1727-2013

It is essential to elucidate the basic aspects of insect resistance to insecticides because this information can guide resistance-management programs for target species.¹⁹19 . Scott JA. The molecular genetics of resistance: resistance as a response to stress. Flor Entomol. 1995;78(3):399-414. DOI:10.2307/3495526 In competition tests in the absence of selection pressure, mortality rates decreased with increasing frequencies of resistant individuals, and this result was similar to that observed for Sitophilus zeamais after exposure to deltamethrin.¹⁶16 . Oliveira EE, Guedes RNC, Corrêa AS, Damasceno BL, Santos CT. Resistência vs susceptibilidade a piretróides em Sitophilus zeamais Motschulsky (Coleoptera: Curculionidae): há vencedor? Neotrop Entomol. 2005;34(6):981-90. DOI:10.1590/S1519-566X2005000600015

In general, the decreased survival rate among populations with different resistance ratios indicates that insecticide resistance is unstable in the absence of selection pressure.¹¹11 . Konno RH, Omoto C. Custo adaptativo associado à resistência de Aphis gossypi Glover (Hemiptera: Aphididae) ao inseticida carbosulfam. Neotrop Entomol. 2006;35(2):246-50. DOI:10.1590/S1519-566X2006000200014 However, although a high mortality rate (91.0%) was observed in the population with 20.0% resistant individuals, this rate tended to decrease in the subsequent month, and this was also observed in populations with 40.0%, 60.0%, and 80.0% resistant individuals. Therefore, it can be inferred that, for the Ae. aegypti population collected in Catolé, resistance remains stable in the absence of selection pressure. This is an important aspect from the standpoint of resistance management because the maintenance of stable resistance prevents its reversal and consequently the restoration of susceptibility over time.

These results differ from those observed in populations of Chrysoperla externa resistant to Karate¹⁵15 . Oliveira JEM, Bartoli AS, Ferreira RJ, Mirandea JE. Suscetibilidade de Chrysoperla externa (Hagen) (Neuroptera: Chrysopidae) a Karate® (Lambda-cialotrina) em condições de laboratório. Bol Sanid Veg. 2002;28(4):577-84. and Aphis gossypii resistant to carbosulfan,¹¹11 . Konno RH, Omoto C. Custo adaptativo associado à resistência de Aphis gossypi Glover (Hemiptera: Aphididae) ao inseticida carbosulfam. Neotrop Entomol. 2006;35(2):246-50. DOI:10.1590/S1519-566X2006000200014 in which the survival rate significantly decreased in the absence of selection pressure,¹¹11 . Konno RH, Omoto C. Custo adaptativo associado à resistência de Aphis gossypi Glover (Hemiptera: Aphididae) ao inseticida carbosulfam. Neotrop Entomol. 2006;35(2):246-50. DOI:10.1590/S1519-566X2006000200014 indicating the tendency for resistance to those insecticides to reverse.

The results of probit regression analysis indicated that the response to temephos differed between populations with different resistance ratios, i.e., the intensity and quality of the responses associated with insecticide resistance different in these groups. This is seen in the similarity tests and parallelism of the regression lines that rejected the hypothesis that the differences between the slopes and intercepts are the same for these populations. This result is corroborated when the nonoverlapping confidence intervals of the LC₅₀ and LC₉₀ values are compared (Table 1).

Certain factors can restore insecticide susceptibility in resistant populations during resistance management. One of these factors is the fitness cost, since the evolution of resistance is usually associated with loss of biotic potential in the population.¹⁶16 . Oliveira EE, Guedes RNC, Corrêa AS, Damasceno BL, Santos CT. Resistência vs susceptibilidade a piretróides em Sitophilus zeamais Motschulsky (Coleoptera: Curculionidae): há vencedor? Neotrop Entomol. 2005;34(6):981-90. DOI:10.1590/S1519-566X2005000600015^,1818 . Roush RT, Mackenzie JA. Ecological genetics of insecticide and acaricide resistance. Ann Rev Entomol. 1987;32:361-80. DOI:10.1146/annurev.en.32.010187.002045 The period of embryonic development (Table 3) was considered short (ranging between 2.1 and 2.9 days on average) compared with the average development period observed by other authors in Ae. aegypti populations from Paraíba¹1 . Beserra EB, Castro Jr FP, Santos JW, Santos TS, Fernandes CRM. Biologia e exigências térmicas de Aedes aegypti (L.) (Diptera: Culicidae) provenientes de quatro regiões bioclimáticas da Paraíba. Neotrop Entomol. 2006;35(6):853-60. DOI:10.1590/S1519-566X2006000600021^,33 . Beserra EB, Castro Jr FP. Biologia Comparada de Populações de Aedes (Stegomyia) aegypti (L.) (Diptera: Culicidae) da Paraíba. Neotrop Entomol. 2008;37(1):81-5. DOI:10.1590/S1519-566X2008000100012 (between 3.8 to 6.1 days).

The longer development period and decreased larval viability found in the population collected in Estação Velha indicate a higher fitness cost in this population resulting from the development of resistance when compared with the fitness cost in the susceptible strain and the other resistant populations. In this case, at least for this population, it can be inferred that the fitness cost associated with resistance can be related to the parameters of larval development, and confers adaptive disadvantage for this vector population. However, regardless of population susceptibility or resistance, the results shown herein differ with those obtained by other authors. Beserra et al¹1 . Beserra EB, Castro Jr FP, Santos JW, Santos TS, Fernandes CRM. Biologia e exigências térmicas de Aedes aegypti (L.) (Diptera: Culicidae) provenientes de quatro regiões bioclimáticas da Paraíba. Neotrop Entomol. 2006;35(6):853-60. DOI:10.1590/S1519-566X2006000600021 (2006) investigated a population of Ae. aegypti from Campina Grande and observed that the average period of larval development and larval viability were 6.6 days and 92.5%, respectively. Similarly, the study by Beserra & Castro Jr²2 . Beserra EB, Fernandes CRM, Queiroga MFC, Castro Jr FP. Resistência de Aedes aegypti (L.) (Diptera: Culicidae) ao organofosforado temefós na Paraíba. Neotrop Entomol. 2007;36(2):303-7. DOI:10.1590/S1519-566X2007000200019 (2007) with Ae. aegypti in Boqueirão, Brejo dos Santos, Itaporanga, and Remígio showed an average larval development between 6.3 and 8.3 days and larval viability of 92.0%.

Despite the disadvantage in the development parameters of the population from Estação Velha compared with the susceptible strain, these variables were not significantly different in the other resistant populations, corroborating the results of previous studies involving carbosulfam-resistant populations of Aphis gossypii.¹¹11 . Konno RH, Omoto C. Custo adaptativo associado à resistência de Aphis gossypi Glover (Hemiptera: Aphididae) ao inseticida carbosulfam. Neotrop Entomol. 2006;35(2):246-50. DOI:10.1590/S1519-566X2006000200014 The duration of nymph development and nymph viability did not significantly differ from those of the susceptible strain.¹¹11 . Konno RH, Omoto C. Custo adaptativo associado à resistência de Aphis gossypi Glover (Hemiptera: Aphididae) ao inseticida carbosulfam. Neotrop Entomol. 2006;35(2):246-50. DOI:10.1590/S1519-566X2006000200014 Similarly, no significant differences were observed in the duration of developmental stages in resistant and susceptible populations of Brevipalpus phoenicis.⁹9 . Franco CR, Casarin NFB, Domingues FA, Omoto C. Resistência de Brevipalpus phoenicis (Geijskes) (Acari: Tenuipalpidae) a acaricidas inibidores da respiração celular em citros: resistência cruzada e custo adaptativo. Neotrop Entomol. 2007;36(4):565-76. DOI:10.1590/S1519-566X2007000400015

Adult longevity and the number of eggs per female did not differ between these populations. However, in all cases evaluated, the longevity of male adults (26.5-37.7 days) and female adults (23.8-37.9 days) (Table 4) was lower than that reported by Beserra & Castro Jr³3 . Beserra EB, Castro Jr FP. Biologia Comparada de Populações de Aedes (Stegomyia) aegypti (L.) (Diptera: Culicidae) da Paraíba. Neotrop Entomol. 2008;37(1):81-5. DOI:10.1590/S1519-566X2008000100012 (2008), who observed a mean variation between 42.1 and 46.1 days for female adults and between 42.8 and 44.5 days for male adults of Ae. aegypti collected in Brejo dos Santos, Boqueirão, Itaporanga, and Remígio. Although no significant differences were observed between the resistant and susceptible populations with regard to the number of eggs per female, lower average values were found for the populations in Catolé (113.9 eggs/female) and Nova Brasília (88.5 eggs/female) than for those obtained in the Rockefeller population (233.6 eggs/female). This may indicate that the resistance in these populations can confer reproductive disadvantages compared with the susceptible population in the absence of selection pressure. However, these results differ from those reported for resistant and susceptible populations of Brevipalpus phoenicis, which showed no significant differences in the fecundity and longevity of female adults.⁶6 . Campos FJ, Omoto C. Estabilidade da resistência de Brevipalpus phoenicis (Geijskes) (Acari: Tenuipalpidae) a hexythiazox em pomares de citros. Neotrop Entomol. 2006;35(6):840-8. DOI: 10.1590/S1519-566X2006000600019^,99 . Franco CR, Casarin NFB, Domingues FA, Omoto C. Resistência de Brevipalpus phoenicis (Geijskes) (Acari: Tenuipalpidae) a acaricidas inibidores da respiração celular em citros: resistência cruzada e custo adaptativo. Neotrop Entomol. 2007;36(4):565-76. DOI:10.1590/S1519-566X2007000400015

According to Table 2, water temperatures and pH during vector development showed little variation and these variables did not vary significantly to account for the biological differences observed between the samples evaluated. According to Beserra & Castro Jr³3 . Beserra EB, Castro Jr FP. Biologia Comparada de Populações de Aedes (Stegomyia) aegypti (L.) (Diptera: Culicidae) da Paraíba. Neotrop Entomol. 2008;37(1):81-5. DOI:10.1590/S1519-566X2008000100012 (2008), under these conditions, the observed biological differences result from the innate characteristics of each population.

The fertility life tables confirmed that the Ae. aegypti populations collected in Catolé, Monte Santo, and Nova Brasília, unlike the population from Estação Velha, showed a reproductive disadvantage compared with the susceptible strain in the absence of selection pressure (Table 5). In addition, the net reproductive rate (R₀) was 130.78 for the susceptible population, in contrast with 44.22, 71.69, and 35.53 for the resistant populations of Catolé, Monte Santo, and Nova Brasília, respectively. This demonstrates the increased reproductive potential of the susceptible population compared with the resistant groups. Although increased R₀ was observed in the susceptible population compared with that obtained in the Liberdade population (R₀ = 101.43), this difference can be compensated when considering T, r_m, λ, and DT, which corresponded to 3.97, 1.16, 3.18, and 0.59 respectively, and were superior to those observed in the Rockefeller strain (Table 5).

The r_m parameter, which corresponds to the optimal range of insect development, the number of times that a population multiplies per time unit, and the time required for the population to double in number, indicates that the development potential of resistant populations is lower than that of the susceptible population. Therefore, a fitness cost resulting from the resistance to temephos is harmful to the biotic potential of these populations.

ACKNOWLEDGMENTS

We are grateful to the 3^rd Regional Health Center of the Department of Health of Paraíba for their support and provision of material for performing the endurance test.

REFERENCES

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