Metabolic resistance mechanism in Aedes aegypti from Lagos State, Nigeria

Abstract

Background

Aedes aegypti transmits several arboviral diseases of global public health threat such as dengue, zika, and yellow fever. Recently, a series of yellow fever outbreaks have been reported in different parts of the country. Globally, the control of mosquito-borne diseases has relied heavily on insecticides based vector control efforts. Therefore, we assessed the susceptibility status to three different classes of WHO approved insecticides and evaluated the importance of detoxifying enzymes on insecticides resistance in Aedes aegypti collected from Lagos State, Nigeria. Aedes aegypti immature stages were collected from suitable habitats in peri-domestic areas of Alimosho, Kosofe, Badagry, and Ibeju-Lekki Local Government Areas (LGAs) of Lagos State, 2–5 days old glucose-fed adult female mosquitoes were exposed to discriminating doses of DDT, permethrin, bendiocarb, and PBO synergist using WHO standard procedure and kits. Identification was through morphological means only.

Results

Resistance to DDT and permethrin was recorded in all the LGAs, suspected resistance to bendiocarb was recorded in Aedes aegypti from Alimosho while full susceptibility was recorded in other LGAs. PBO synergist significantly increases the 24 h mortality of DDT and permethrin-resistant Aedes aegypti in all the LGAs. The activities of both GSTs and cytochrome P450s increase with decreasing mortality for Aedes aegypti, regression value (R²) ranges from 0.8889 to 0.6224 for GSTs and 0.4379 to 0.616 for cytochrome P450s.

Conclusions

Aedes aegypti population from Lagos State, Nigeria, have developed resistance to DDT and permethrin, the activities of P450s and GST were implicated in DDT and permethrin resistance in this study. Therefore, a need for regular insecticides monitoring and PBO should be incorporated into Aedes aegypti insecticides control strategies to forestall development of resistance to DDT and pyrethriods.

Background

Aedes aegypti is the main vector of Yellow fever virus, dengue virus (DENV), chikungunya virus (CHIKV), and zika virus (ZIKV); this mosquito has been a source of global public health concern with the increasing prevalence and incessant outbreaks of yellow fever virus, dengue, and zika virus (WHO, 2017). Aedes aegypti is found in close proximity with humans, and lays its eggs in mainly artificial containers commonly found in domestic and peri-domestic areas, such as water-storage containers, flower pots, discarded plastics, and automobile tyres. The risk of Aedes aegypti borne infection is particularly high in several parts of Nigeria especially Lagos State, where there is a proliferation of urban slums due to increasing population and lack of adequate planning and amenities. In 2019, there were several reported cases of yellow fever outbreak in some states in Nigeria and at least a suspected case of the infection in all the states, 48 yellow fever-related death cases were recorded in four states between the months January and July in Nigeria (NCDC, 2019). Insecticides-based vector control measures have been vital in the management and reduction of mosquito borne diseases globally, though the development and spread of insecticides resistance in different mosquito species of public and veterinary health importance has had significantly negative impact on this progress (Hemingway & Ranson, 2000; WHO, 2017). Resistance to different classes of insecticides has been reported in Aedes aegypti from different parts of the world (Moyes et al., 2017; Weetman et al., 2018). Resistance mechanisms in mosquitoes can be mediated by the combination of mutation in the target site, increased activities of metabolic enzymes, physiological adaptation, and behavioral changes (Liu, 2015; Moyes et al., 2017; Smith, Kasai, & Scott, 2016). Pyrethroids and DDT metabolic insecticides resistance mechanism in Aedes aegypti has often been associated with elevated activities/overexpression of cytochrome P450 monooxygenases (P450s), carboxylesterases (ESTs), and glutathione-S-transferases (GSTs) (Brengues et al., 2003; Harris, Rajatileka, & Ranson, 2010; Smith et al., 2016). The importance of detoxifying enzymes in Aedes resistance to different classes of insecticides has been emphasized in several previous studies in various parts of the world (Bingham, Strode, Tran, Khoa, & Jamet, 2011; Ishak, Riveron, Ibrahim, & Stott, 2016; Kamgang, Yougang, Tchoupo, Riveron, & Wondji, 2017; Li et al., 2018). Piperonyl butoxide (PBO) insecticide synergist is a non-toxic compound that interferes with the ability of P450s in insects to metabolize insecticides (Bingham et al., 2011). Studies in Africa and other parts of the world have shown higher mortality in insecticides resistant Aedes pre-exposed to PBO synergist (Bingham et al., 2011; Kamgang et al., 2017; Kumar et al., 2002; Smith, Kasai, & Scott, 2018). In Nigeria, there is paucity of information on the susceptibility status of Aedes aegypti to the different classes of neurotoxic insecticides used in public health, as most of mosquito insecticides studies are focused on the malaria vectors. This study is therefore aimed at determining the current insecticides resistance status of Aedes aegypti to three insecticides of different classes and also evaluating the activities of P450s and GST in insecticides resistant Aedes aegypti.

Materials and methods

Study area

The study was carried out in four Local Government Areas (LGAs) of Lagos State, southwestern Nigeria. Comprising of two densely populated LGAs: Alimosho LGA, and Kosofe LGA; and two less densely populated LGAs: Ibeju-Lekki LGA situated within the southern area of Lagos State, just below the Lagos lagoon and Badagry LGA, a coastal town located between Metropolitan Lagos and the border with Republic of Benin.

Study design

Aedes aegypti immature stages were located from water pots, tyre holes, abandoned wells, and suitable larval habitats in peri-domestic areas of the four surveyed LGAs. They were collected separately in well labelled containers and transferred to the insectary of the University of Lagos and allowed to develop to adult stage under suitable insectary conditions (27 °C ± 2 °C and relative humidity 80% ± 10%). Insecticides susceptibility assay, PBO assay, and morphological identification was carried out at the Zoology laboratory of the University of Lagos. Biochemical assays were carried out at the vector research unit of the Nigeria Institute of Medical Research (NIMR), Yaba, Lagos, Nigeria.

Insecticide and PBO synergist bioassay

The tests were performed using WHO test filter paper impregnated with the selected insecticides and piperonyl butoxide (PBO) impregnated papers obtained from the Vector Control Research Unit (VCRU), University Sains Malaysia (http:/www.inreskit.usm.my). Non-blood fed, 2–3 days old laboratory emerged adult female mosquitoes were exposed to DDT (4%) and permethrin (0.75%) WHO insecticide-treated paper.

A total of 25 female mosquitoes were pre-exposed to 4% piperonyl butoxide (PBO) for 1 h using four replicates. Thereafter, PBO-treated mosquitoes were exposed to either DDT (4%) or Permethrin (0.75%) for another 1 h. Each experiment consisted of four replicates. Knockdown rates of mosquitoes were recorded at intervals for one hour, mosquitoes were later transferred into holding tubes with untreated papers, allowed a 24-h recovery period and were supplied with a 10% sugar meal during this period after which mortality was recorded. All the bioassays were accompanied by negative control.

Microplate metabolic enzyme activity assay

Eight (8) adult female mosquitoes that were pre-exposed to a WHO insecticide test paper were homogenized singly in 200 μL of cold distilled water in a 1.5 mL centrifuge tube. The homogenate was centrifuged at 14,000 rpm for 20 s. The supernatant was stored at – 20 °C (Hemingway 1998). Two metabolic enzymes; Cytochrome P450 monooxygenase (P450s) and Glutathione S-transferase (GSTs) were analyzed on individual insecticide-resistant females mosquitoes, and on the laboratory susceptible strain according to WHO protocols (Hemingway 1998). Mean absorbance values for each tested mosquito and enzyme were converted into enzyme activity and standardized based on the total protein amount.

Glutathione S-transferase assay

This test was carried out in two replicates, 10 μl of mosquito homogenate were placed in separate wells of the microtitre plate, 200 μl of the GSH/CDNB working solution was then added. Three plate blanks containing 10 μl distilled water and 200 μl of the GSH/CDNB working solution were used per microtitre plate. The test was then left at room temperature for 20 min, and the absorbance value was read at 340 nm.

Cytochrome P450 monooxygenase assay

Two microliters of mosquito homogenate was placed in separate wells of a microplate, 80 μl of 0.625 M potassium phosphate (pH 7.2) was added to each replicate, 200 μl of the mixture of 5 ml methanol solution of tetramethyl benzidine with 15 ml of 0.25 M sodium acetate buffer (pH 5.0) was added to each well, 25 μl of 3% hydrogen peroxide was also added to each replicate, the preparation was left for 2 h at room temperature before reading of absorbance at 650 nm. Control was run at 20 μl of distilled water instead of mosquito homogenate and the assay was carried out in two replicates.

Protein assay

Total protein was measured for each mosquito using Biuret test. All measurements were done in duplicate. Protein concentration in sample was calculated as: absorbance of sample/absorbance of standard multiplied by concentration of standard (60 g/dl). Enzyme activities were calculated as nmol/g/dl protein.

Data analysis

Insecticides susceptibility was classified based on the criteria that 98–100% mortality of mosquitoes implies susceptibility, 80–97% mortality indicates possible resistance that needs to be further confirmed via biochemical or molecular assays and < 80% mortality implies resistance (WHO, 2016). Regression probit was used to compute the KDT₅₀ and KDT₉₅. Chi-square was used to compare percentage mortality between insecticide only and PBO plus insecticide. Regression analysis was used to compute the association between percentage mortality of mosquitoes and the activities of detoxifying enzymes. All data analyses were computed using Microsoft Excel version 2016 and IBM SPSS Statistics 23. P was considered significant at P < 0.05.

Results

Aedes aegypti from the four surveyed LGAs showed high level of resistance to DDT and permethrin with 24 h percentage mortality ranging from 20 to 46% and 29 to 70%, respectively. The estimated knockdown time (KDT) for 50% Aedes aegypti to exposed DDT was lowest in Alimosho LGA (91.8 min) and highest in Ibeju-Lekki LGA (150.1 min), similarly KDT₉₅ was lowest in Alimosho LGA (444min) and highest in Ibeju-Lekki LGA (965.1 min). KDT₅₀ and KDT₉₅ for permethrin was reduced as compared to DDT, ranging from 45 to 113.6 min for KDT₅₀ and 145.5–599.3 min for KDT₉₅ (Table 1). In this study, full susceptibility to bendiocarb was recorded in Kosofe, Ibeju-Lekki, and Badagry LGAs while possible resistance to bendiocarb was reported in Alimosho LGA (Table 2). PBO synergist significantly (P < 0.05) reduces the level of resistance of Aedes aegypti to DDT and permethrin in all surveyed locations, likewise the KDT₅₀ and KDT₉₅ for PBO synergized bioassays were lower compared to that of non-synergized bioassays (Table 1). The mean progressive knockdown of both PBO synergized and non-synergized of Aedes aegypti are shown in Fig. 1a–d with the PBO synergized assay showing faster knockdown compared to non-synergized assay. Figure 2 shows the relationship between 24 h percentage mortality of DDT-resistant Ae. aegypti from Lagos State and the activities of detoxifying enzymes. Figure 3 also shows the association between the percentage mortality of permethrin-resistant Aedes aegypti and the mean level of detoxifying enzymes activities in the four studied LGAs. The activities of both GSTs and cytochrome P450s increases with decreasing mortality for Ae. aegypti, regression value (R²) ranges from 0.8889 to 0.6224 for GSTs and 0.4379 to 0.616 for cytochrome P450s.

Table 1 The probit knockdown time (KDT₅₀ and KDT₉₅) values and percentage mortality of Aedes aegypti to DDT, permethrin, and PBO synergist in Lagos State

Table 2 The probit knockdown time (KDT₅₀ and KDT₉₅) values and percentage mortality of mosquito exposed to bendiocarb (0.1%) in Lagos State, Nigeria

Fig. 1

a–d Percentage knockdown time comparison of Aedes aegypti between PBO synergized and non-synergized assay in Kosofe, Ibeju-Lekki, Alimosho, Badagry LGAs

Fig. 2

Regression of mortality rate of Aedes aegypti exposed to DDT and mean level enzymes activity in four LGAs from Lagos state, Nigeria

Fig. 3

Regression of mortality rate of Aedes aegypti exposed to permethrin and mean level enzymes activity in four LGAs from Lagos state, Nigeria

Discussion

This study provides information on the susceptibility status of dengue and yellow fever vector to three different classes of insecticides and also provides insight into the biochemical resistance mechanisms of this mosquito in Lagos State.

In this study, resistance to DDT was recorded in all the four surveyed LGAs similar to a previous report from three LGAs in Lagos State between 2011 and 2012 (Ayorinde, Oboh, Oduola, Otubanjo, & Zhu, 2015), Aedes aegypti resistance to DDT has also been recently reported in Umudike, southeastern Nigeria (Ukpai & Ekedo, 2018) and Cameroon (Kamgang et al., 2011; Kamgang et al., 2017). Though the level of 24 h percentage resistance and knockdown time recorded in this study was higher than that of previous studies in different areas of Lagos State and Cameroon (Ayorinde et al., 2015; Kamgang et al., 2011). Pyrethroid resistance was recorded in all the study areas in this study, similar to previous studies in Lagos and Kwara States, Nigeria, reported susceptibility of Aedes aegypti to permethrin (Ayorinde et al., 2015; Oduola, Obembe, Adelaja, & Ande, 2016), though suspected resistance to deltamethrin has been reported in Lagos (Ayorinde et al., 2015) and Umudike, (Ukpai & Ekedo, 2018) both in the southern part of Nigeria. Pyrethroids resistance in Aedes aegypti has also been previously reported in Cameroon (Kamgang et al., 2011; 2017), Burkina Faso (Badolo et al., 2019), Malaysia (Ishak et al., 2017), and several other parts of the world. Selection pressure as a result of indiscriminate usage of insecticides for agricultural, domestic, and public health purposes has been associated with DDT and pyrethroids resistance in mosquitoes (Awolola et al., 2007; Fagbohun, Oyeniyi, Idowu, Otubanjo, & Awolola, 2019; Kamgang et al., 2011). The increased level of insecticides resistance recorded in this study may be a result of increase in the deployment of insecticide based measures in the control measures for the control of malaria vectors in the study locations.

In this study, susceptibility to bendiocarb was recorded in three of the four surveyed LGAs namely; Kosofe, Badgry and Ibeju-Lekki while suspected resistance was reported in Alimosho LGA. Similar studies have reported Aedes aegypti susceptibility to carbamates in Umudike, southeastern Nigeria (Ukpai & Ekedo, 2018) and Cameroon (Kamgang et al., 2011) while carbamates resistance has been previously reported in Kwara State, Nigeria (Oduola et al., 2016), Burkina Faso (Badolo et al., 2019), Indonesia (Hamid et al., 2018), and Sri Lanka (Leong, Vythilingam, Wee, Liew, & Wong, 2019).

PBO synergist was able to significantly increase the 24-h percentage and also reduce the knockdown time of Aedes aegypti to DDT and permethrin in this study; previous studies in different parts of the world have demonstrated the efficacy of PBO synergists in the management of insecticides resistant vectors. PBO is well known for its ability to inhibit the activities of P450s in insects and has been used in combination with insecticides for several mosquito control tools (Fagbohun et al., 2019). Similar previous studies in some parts of Africa have confirmed the efficacy of PBO synergists in controlling DDT and pyrethroids resistant Aedes mosquitoes (Badolo et al., 2019; Kamgang et al., 2017).

The mean enzymes activities of GST and P450s were inversely correlated to the 24-h percentage mortality of Aedes aegypti to DDT and permethrin, indicating lower mortality rate with increasing activities of GST and P450s in this study. As recorded in this study, previous studies have linked the activities of GST and P450s to DDT and pyrethriods resistance in Aedes (Brengues et al., 2003; Ishak et al., 2016; Leong et al., 2019; Li et al., 2018).

Conclusion

Findings from this study is very timely, considering the recent outbreaks of Aedes-borne diseases in several parts of Nigeria, the study has been able to provide the current resistance profile of Aedes aegypti in Lagos State, Nigeria, and also highlighted the importance of GSTs and P450s resistance mechanisms in the areas. We recommend regular insecticides monitoring and the use of PBO-based insecticides control tools in Aedes aegypti control in Lagos State, Nigeria.