Research Article

Toxicity of Different Insecticides against Dengue Vector Aedes aegypti Larvae under Laboratory Conditions

Ghulam Murtaza1,6*, Muhammad Irfan Fareed2, Noshaba Munawar3, Muhammad Nadeem Khan4, Gul-E- Zahra5, Taskeen Ahmad6, Muhammad Daud6 and Taqi Raza6

1Department of Entomology, College of Plant Protection, China Agricultural University, Beijing, China; 2School of Sciences, Department of Life Sciences, University of Management and Technology, Johar Town Lahore; 3Department of Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad, Pakistan; 4Pest warning and Quality Control of Pesticides Punjab Lahore, Pakistan; 5Institute of Botany, University of Punjab, Lahore, Pakistan; 6Department of Entomology, University of Agriculture, Faisalabad, Pakistan.

Received | July 03, 2021; Accepted | August 23, 2021; Published | June 20, 2022

*Correspondence | Ghulam Murtaza, Department of Entomology, College of Plant Protection, China Agricultural University, Beijing, China; Email: [email protected]

Citation | Murtaza, G., Fareed, M.I., Munawar, N., Khan, M.N., Zahra, G., Ahmad, T., Daud, M. and Raza, T., 2022. Toxicity of different insecticides against dengue vector Aedes aegypti larvae under laboratory conditions. Journal of Innovative Sciences, 8(1): 08-12.

DOI | https://dx.doi.org/10.17582/journal.jis/2022/8.1.08.12

Keywords | Aedes aegypti, Vector control, Insecticides, Spinosad, Pyriproxyfen

Copyright: 2022 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

1. Introduction

Mosquitoes are a vector for a variety of human diseases such as dengue fever, lymphatic filariasis, yellow fever, and malaria (Damapong et al., 2016). These diseases wreaked havoc on people’s health in regions with hot and humid climates all across the world (Ayudhaya and Wassanasompong, 2017). Female mosquitos have an important role in the transmission of illness viruses to humans during blood feeding (Sharma et al., 2010). Dengue fever (DF) is a viral infection spread by mosquito bites of the Aedes aegypti and Aedes albopictus species (Eggar et al., 2008). Around two-thirds of the world’s population lives in places plagued with Aedes aegypti, the disease’s main vector (Claro et al., 2004).

In tropical and subtropical locations of the world, DF is a major cause of illness (Endy et al., 2002). Globally, 50–100 million incidence of DF and 250,000–500,000 cases of DHF are anticipated to occur each year (Guzman and Kouri, 2003). Dengue fever outbreaks were recorded in Pakistan in 2006 and 2007 in Karachi, Islamabad, Mirpur-Khas, Haripur, Hyderabad, Lahore, and Rawalpindi, with 2700 confirmed cases and 24 deaths. In 2008, 1800 instances were reported in Lahore, Punjab province (WHO, 2012; Jahan and Sarwar, 2013).

Mosquitoes have acquired resistance to chemical insecticides as a result of decades of widespread usage of these pesticides to control mosquito populations (Hemingway and Ranson, 2000). Furthermore, public health concerns have prompted research into alternate insecticides for mosquito vector control (Uragayala et al., 2015). Low mammalian toxicity, low environmental impact, a broad spectrum of activity against all target mosquito species, and a long duration of effect that reduces application frequency are the primary characteristics for an efficient mosquito larvicide. Researchers began looking for new insecticides with novel mechanisms of action in order to prevent or mitigate the effects of pesticide resistance in the previous generation of insecticides (Darriet and Corbel, 2006; Perez et al., 2007; WHO, 2012). Because of their low mammalian toxicity, biological specificity, and environmental safety, insect growth regulators (IGRs) have been advocated as an alternative to synthetic pesticides (Thavara et al., 2004; Silva et al., 2009; Ramzan et al., 2019; Murtaza et al., 2021).

The acceptability of insecticidal compounds used in insect vector control programmes is determined by a number of factors, including their environmental persistence and the behavioral tendencies of insect vectors exposed to the compound. So, the present experiment was conducted to evaluate toxicity of five different insecticides against A. aegypti larval mortality under laboratory conditions.

2. Materials and Methods

2.1 Mosquito rearing

Aedes aegypti was chosen as the investigational insect in this study because it is a key vector for the propagation of dengue fever and one of the most important and irritating. Mosquitoes larvae were gathered using a normal dipper from mosquito breeding places such as pots, tyres, stagnant water reservoirs, and various locations around the University. Mosquito larvae and pupa were collected and identified in the lab based on their larval stage. Adult Aedes aegypti specimens were housed in screened cages until they emerged as adults. Adults were gathered using a mouth aspirator after emergence and placed in rearing cages. Male mosquitoes were fed honey and water solution for raising, whereas female mosquitoes were fed white rat blood. The female lays her eggs on filter paper that is wrapped around the water-filled beaker. Tetraamine, a larval meal comprising 5.0 percent crude fat, 1.3 percent phosphorus, 45.0 percent crude protein, 183 mg vitamin C per kg, and 2.0 percent crude fiber were dissolved in water. The pupae were separated and transferred into the cages for adult emergence after pupation.

2.2 Study layout

The experiment was set up in the form of a Complete Randomized Design (CRD) under laboratory conditions. Five different insecticides (spinosad 100% EC, chlorfenapyr 36% SC, pyriproxyfen 10% EC, matrine 0.5 AS and imidacloprid 70% WDG) were tested for toxicity against Aedes aegypti larvae. All insecticides were used at a normal dose and replicated three times with a control group.

2.3 Bioassay for larvae of mosquito

The bioassays were carried out in accordance with the World Health Organization’s criteria (1981). In the bioassay, Aedes aegypti third and early emerging forth instar larvae were used. Insecticides were sprayed into plastic cups with a capacity of 150 ml. To determine toxicity, cups were filled to the top with water and pesticide stock solution, and 25 larvae were released into the cups. Only distilled water was used as a control, and larvae were released. The mortality rates were measured after 12, 24, and 48 hours of pesticide exposure. Larvae that did not move in response to repeated prodding were assumed to be dead. Daily mortalities of larvae and pupae were recorded, and alive pupae were transferred to untreated water in fresh beakers and allowed until the final mosquito emerged. Dead adults were reported for both partially emerged mosquitoes and those found fully emerged but unable to escape the water surface.

2.4 Statistically analysis

Bioassay data was collected and analyzed using standard Probit analysis (Finney, 1971), with bioassay results corrected using Abbot’s algorithm (Abbott, 1925). The LC50 results were statistically significant (P≤0.05).

3. Results and Discussion

Result indicated that Spinosad (77.32% mortality) and pyriproxyfen (66.28% mortality) are more toxic to A. aegypti larvae as compared to matrine, chlorfenapyr and imidacloprid after 72-h exposure. While minimum mortality was recorded after 24-h exposure of insecticides in all treatments shown in Figure 1.

 

 

The comparative analysis of the spinosad 100EC, chlorfenapyr, pyriproxyfen, matrine, and imidacloprid on larval mortality after 24-h shown in Figure 1. Our result revealed that non-significant reduction in larval mortality after 24-h in all insecticides except spinosad somehow have more toxic to kill A. aegypti larvae after 24-h of application. While after 48-h larval exposure to insecticides indicated that more larval mortality was found in case of spinosad and pyriproxyfen as compared to Matrine, Chlorfenapyr and imidacloprid shown in Figure 2.

After 72-h larval exposure to insecticides shows that spinosad and pyriproxyfen were more toxic to cause 77.32% and 66.28 % mortality (Figure 3). Meanwhile pyriproxyfen is harmful to mosquito larvae after spinosad and can be found in their environments for several months (Yapabandara and Curtis, 2004; Sihuincha et al., 2005). The high efficacy of pyriproxyfen against vulnerable mosquito larvae of A. aegypti has been established in our recent investigation. pyriproxyfen, on the other hand, inhibits adult emergence but does not kill larvae, unlike other chemical larvicides. Even though pyriproxyfen appears to have no cross-resistance with conventional insecticides (Ishaaya et al., 2005), its mechanism of action may offer some practical problems, since the prolonged presence of larvae may be perceived as a treatment failure by homeowners.

 

 

In contrast, after 72 hours of pesticide treatment, spinosad demonstrated significant toxicity against mosquito larvae (Al-Azab and Shaalan, 2018) shown in Figures 3 and 4. Spinosad have a strong insecticidal action against target pests and minimal danger to people and nontarget animals, it considered as a potential bioinsecticide for public health (Williams et al., 2003). It kills a wide spectrum of mosquito species quickly and has no cross-resistance to other insecticides like organophosphates, carbamates, or pyrethroids (Darriet and Corbel, 2005).

Conclusions and Recommendations

Generally, it can be concluded that our present findings suggest that spinosad is comparatively a safe alternative to the insecticides in use for the control of A. aegypti larvae. Spinosad was most toxic among the tested insecticides followed by pyriproxyfen, matrine, chlorfenapyr and imidacloprid against A. aegypti larvae.

Novelty Statement

Mosquito Aedes aegypti is a serious public health concern since it is the principal vector of several arboviruses. Mostly different insecticides are used to control mosquito. So, this study will be help to researcher and scientists to select most suitable insecticides for the control of mosquito.

Author’s Contribution

GM conducted the study and wrote the manuscript, MIF critically reviewed the manuscript and help in data analyzing, NM, MNK, TR helped in data collection and manuscript writing, GEZ, TA MD and helped in data analyzing and critically reviewed the manuscript.

Conflict of interest

The authors have declared no conflict of interest.

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