The Assessment of Morphometric Variation of Aedes aegypti Larvae with the Seasonal Environment Temperature Inversion in Selected Areas of Lahore, Pakistan
The Assessment of Morphometric Variation of Aedes aegypti Larvae with the Seasonal Environment Temperature Inversion in Selected Areas of Lahore, Pakistan
Muhammad Ahsan Riaz1, Ayesha Riaz2, Muhammad Asif Mahmood3, Muhammad Uzair Mukhtar3*, Zaib Un Nisa1, Beenish Ijaz4 and Muhammad Shahid Rasool5
1Department of Environmental Sciences and Engineering, Government College University Faisalabad, Pakistan.
2Department of Zoology, Government College Women University Faisalabad, Pakistan.
3Department of Medical Entomology and Parasitology, Institute of Public Health, Lahore, Pakistan.
4Sustainable Development Study Centre, Government College University Lahore, Pakistan.
5Department of Environment Sciences, National College of Business Administration and Economics, Lahore, Pakistan.
Abstract | Temperature is one of the critical abiotic environmental factors that can influence biological and physiological processes, including mobility, development, and reproduction in poikilotherms. Due to the medical importance of Aedes aegypti as a vector of several medically important pathogens, evaluating the body length variation of Aedes aegypti larvae with the changing seasonal temperature is important. The study was conducted to observe the difference in body size and different body structures of Ae. aegypti larvae in two seasons, i.e., southwest monsoon (June through September) and retreating monsoon (October and November). The fourth instar larvae were collected from areas of district Lahore. The collected larvae were preserved in formalin and transported to the laboratory of the Department of Environmental Science and Engineering at the Government College University Faisalabad for further analysis. The larval morphological measurements were carried out using a stereomicroscope, which included changes in head length and width, thoracic length and width, abdominal length and width, and total length of the larva. Every month, the fourth instar larvae (n=36) were investigated for body size measurement. The results showed that low temperatures of breeding water significantly increase (P≤0.05) the body size, head, thorax and abdomen of larvae. The results convinced that temperature inversion affects the immature development stages of Ae. aegypti. This study concluded that, Ae. aegypti larvae’s body size depends upon seasonal temperature inversion in the breeding water. These findings can help in predicting the variation in the development rate of Ae. aegypti larvae under different seasonal temperatures.
Novelty Statement | The determines the body length variation of Aedes aegypti larvae with the changing seasonal temperature and evaluates how breeding water temperature affects its development.
Article History
Received: December 22, 2022
Revised: January 11, 2023
Accepted: February 28, 2023
Published: April 03, 2023
Authors’ Contributions
Study conception and design: MSRData curation and Investigation: MAR. Formal analysis: AR. Methodology: MAM. Writing original draft: MAR and ZN. Writing review and editing: MUM and BI.
Keywords
Aedes aegypti, Dengue vector, Fourth-instar larvae, Larval body length, Seasonal temperature
Copyright 2023 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/).
Corresponding author: Muhammad Uzair Mukhtar
To cite this article: Riaz, M.A., Riaz, A., Mahmood, M.A., Mukhtar, M.U., Nisa, Z., Ijaz, B., and Rasool, M.S., 2023. The assessment of morphometric variation of Aedes aegypti larvae with the seasonal environment temperature inversion in selected areas of Lahore, Pakistan. Punjab Univ. J. Zool., 38(1): 37-41. https://dx.doi.org/10.17582/journal.pujz/2023/38.1.37.41
Introduction
Mosquitoes are an important group of insects because they spread pathogens that cause disease in human and animal (Giesen et al., 2020). The primary vector of various human arboviral diseases, including dengue, Zika, and chikungunya fever, is a mosquito of the genus Aedes, namely Aedes aegypti (Rocklov and Dubrow, 2020).
As a poikilotherm, the internal temperature of insects, including mosquitoes, fluctuates and rely on the temperature of the nearby environment (Reinhold et al. 2018). Temperature changes affect physiology, behaviour, ecology, and insect survival (Wimalasiri-Yapa et al. 2021). Because of seasonal thermal fluctuations, insect development faces the risks, such as desiccation, metabolic changes, and loss of mobility (Caminade et al., 2019).
The development of insects primarily depends on temperature and can be delayed or accelerated by altering the temperature (Beck-Johnson et al., 2013). The Aedes mosquitoes have 4 life stages: egg, larva, pupa and adult. The entire life cycle, from an egg to an adult, takes approximately 8-10 days. In Ae. aegypti, there is a direct association between the mosquito’s immature development stage and the temperature (Farjana et al., 2012). The development rate improved linearly with temperatures (22°C to 28°C) (Farjana et al., 2012; Barreaux et al., 2018; Sasmita et al., 2019). It is critical to follow on for about ten days the advancement from the egg to the adult stages (Bayoh and Lindsay, 2003) and Christiansen (2015) described that no adults appeared at temperatures below 18°C or above 34°C after pupation, but at 35°C, all larvae died before emergence (Christiansen-Jucht et al., 2015).
Since mosquitoes are also poikilotherms, almost all biological activity is affected by ambient environmental conditions, such as humidity and temperature (Wimalasiri-Yapa et al., 2021). Given the increasing phenomenon of climate change, it is important to understand how mosquitoes respond to changes in body characteristics and critical environmental parameters needed to predict survival rates. The present study assessed the changes in body sizes of Ae. aegypti larvae in two different seasons of the year, i.e., Southwest Monsoon (June through September) and Retreating Monsoon (October and November), to better understand the fluctuation in the development rate of Ae. Aegypti larvae in different environmental temperatures.
Materials and Methods
Larval collection, selection and identification
A total of 216 (n= 36/month) Ae. aegypti larvae were collected during the southwest monsoon (June through September) and retreating monsoon (October and November). The larvae were collected from selected areas of Wahga town and Allama Iqbal town of the district Lahore. The collected samples were then transported to the Department of Environmental Science and Engineering at the Government College University Faisalabad for further investigations. The larval samples were preserved in 70% formalin according to (Khan et al., 2018) method. The collected larvae were identified to species level with the aid of a microscope by (Rueda, 2004) identification key. For the control, larvae were reared at laboratory maintained optimum temperature and relative humidity i.e., 28±1°C and 80%±5, respectively.
Morphometric characterization of larvae
After mounting with Hoyer’s medium for morphometric parameters assessment, the dead larvae were scrutinized. The head length, head width, thoracic length, thoracic width, abdominal length, abdominal width, and total length of larvae were determined with the aid of a stereomicroscope (BOECO BST-606, Germany) and method described by (Gunathilaka et al., 2019; Sutiningsih et al., 2019).
Statistical analysis
The statistical determination of the length and width of variations in body segments of the larva was analyzed with Student’s t-test using Prism v.7 (GraphPad Software, San Diego, CA, USA). The P-value (p<0.05) was considered significant.
Results
The results showed that seasonal thermal fluctuations affected the total body size, head length and width, abdominal length and width, and thoracic length and width of Ae. aegypti larvae (Figure 1). It was found that the average head length (0.51±0.01mm) during southwest monsoon significantly increased (P ≤ 0.01) (0.62 ±0.02mm) during the retreating monsoon season (Figure 1a). Similarly, the average head width in southwest monsoon was 0.54±0.01mm, which significantly increased (P ≤ 0.05) in retreating monsoon (0.63±0.02mm) (Figure 1b). The abdominal length in southwest monsoon (3.57 ±0.07mm) got significantly increased (P ≤ 0.05) in retreating monsoon (3.91±0.09mm) (Figure 1c). At the same time the abdominal width in southwest monsoon (0.68±0.02mm) was also significantly increased (P ≤ 0.05) in retreating monsoon (0.74 ±0.02mm) (Figure 1d). Furthermore, the thoracic length significantly increased (P ≤ 0.05) during retreating monsoon from 0.83±0.01mm in southwest monsoon to 0.90±0.03mm (Figure 1e). The average thoracic width during southwest monsoon was recorded at 0.95±0.02mm which also significantly increased (P ≤ 0.05) in retreating monsoon (1.07±0.04mm) (Figure 1f). The overall size of Ae. aegypti larvae in Southwest Monsoon was recorded at 4.91±0.05mm that increased highly significantly (P≤0.001) in retreating monsoon (5.43±0.20mm) (Figure 1g). While the average overall size of the larvae under laboratory temperature were recorded as 4.343±0.40 mm. The temperature variation during Southwest Monsoon and Retreating Monsoon are shown in (Figure 2).
Discussion
Changing environmental temperatures affect the development stages of mosquitoes and have a significant impact on their population dynamics (Couret and Benedict, 2014). The temperatures between 16°C-34°C are suitable for Aedes aegypti development, and at water temperatures below 8°C, the larvae become immobile and die within a few weeks (Cristophers, 1960). In Pakistan, dengue control field staff identify Aedes mosquitoes, on the bases of larval and siphon tube size. So, the information about the size is important to minimize the chances of wrong identification of the dengue vectors at the initial stage. Therefore, we conducted this study to observe the difference in body size and different body structures of Ae. aegypti larvae in two seasons, i.e., southwest monsoon (June through September) and retreating monsoon (October and November). To our knowledge, this is the first study to assess the morphometric variation of Aedes aegypti larvae with the seasonal environment temperature inversion in selected areas of Lahore, Pakistan.
Recent studies also showed that at lower temperatures, the survival of larvae is correlated with food availability in water and intraspecific density (Couret and Benedict, 2014; Couret et al., 2014). Aedes aegypti larvae with sufficient nutrient supply at cool ambient temperatures (15°C) can remain at a particular age for several months (Andrew and Bar, 2013; Brady et al., 2014; Foster and Walker, 2019).
It has been established that a temperature between 31°C-32°C is optimal for larvae to complete their development, and mortality threshold temperature ranges between 14°C and 38°C (Bar-Zeev, 1957, 1958). The survival of mosquitoes during the development stages depends on the regional temperature and their tolerance to cold and heat (Teng and Apperson, 2000).
Previously the pattern of the development time and size of the A. aegypti and A. albopictus mosquito is affected by changes in the temperature of the surrounding environment when it exceeds the lower critical development threshold (Yang et al., 2009). The findings of (Couret et al., 2014) showed that changes in the temperature could alter the stage and size of development starting from the larval stage. In a study conducted by (Farjana et al., 2012) the rate of development slowed and size increased as temperature decreased.
Conclusion
The study concluded that changes in meteorological conditions during the development of Aedes aegypti have a significant effect on the larval size and low temperatures of breeding water significantly increase (P≤0.05) the body size, head, thorax and abdomen of larvae. Climate change affects the immature stages of larval development. The findings might help in improving Aedes aegypti control measures and monitoring strategies by better understanding variation in larval development rates under different environmental temperatures. However, the study is limited in scope due to the smaller sample sizes and was carried out in two towns of one district only i.e., district Lahore. We suggest further studies with larger sample size and different settings across the dengue-endemic areas of the country.
Acknowledgments
The authors thank the Department of Health, Government of Punjab for the permission for and support for this worthy study.
Conflict of interest
The authors have declared no conflict of interest.
References
Andrew, J., and Bar, A., 2013. Morphology and morphometry of Aedes aegypti adult mosquito. Annu. Res. Rev. Biol., 3: 52-69.
Barreaux, A.M., Stone, C.M., Barreaux, P., and Koella, J.C., 2018. The relationship between size and longevity of the malaria vector Anopheles gambiae (ss) depends on the larval environment. Parasit. Vectors, 11: 1-9. https://doi.org/10.1186/s13071-018-3058-3
Bar-Zeev, M., 1957. The effect of extreme temperatures on different stages of Aedes aegypti (L.). Bull. Entomol. Res., 48: 593-599. https://doi.org/10.1017/S0007485300002765
Bar-Zeev, M., 1958. The effect of temperature on the growth rate and survival of the immature stages of Aedes aegypti (L.). Bull. Entomol. Res., 49: 157-163. https://doi.org/10.1017/S0007485300053499
Bayoh, M.N., and Lindsay, S.W., 2003. Effect of temperature on the development of the aquatic stages of Anopheles gambiae sensu stricto (Diptera: Culicidae). Bull. Entomol. Res., 93: 375-381. https://doi.org/10.1079/BER2003259
Beck-Johnson, L.M., Nelson, W.A., Paaijmans, K.P., Read, A.F., Thomas, M.B., and Bjornstad, O.N., 2013. The effect of temperature on Anopheles mosquito population dynamics and the potential for malaria transmission. PLoS One, 8: e79276. https://doi.org/10.1371/journal.pone.0079276
Brady, O.J., Golding, N., Pigott, D.M., Kraemer, M.U., Messina, J.P., Reiner, R.C., Jr., Scott, T.W., Smith, D.L., Gething, P.W., and Hay, S.I., 2014. Global temperature constraints on Aedes aegypti and Ae. albopictus persistence and competence for dengue virus transmission. Parasit. Vectors, 7: 338. https://doi.org/10.1186/1756-3305-7-338
Caminade, C., Mcintyre, K.M., and Jones, A.E., 2019. Impact of recent and future climate change on vector-borne diseases. Ann. N. Y. Acad. Sci., 1436: 157-173. https://doi.org/10.1111/nyas.13950
Christiansen-Jucht, C.D., Parham, P.E., Saddler, A., Koella, J.C., and Basanez, M.G., 2015. Larval and adult environmental temperatures influence the adult reproductive traits of Anopheles gambiae s.s. Parasit. Vectors, 8: 456. https://doi.org/10.1186/s13071-015-1053-5
Couret, J., and Benedict, M.Q., 2014. A meta-analysis of the factors influencing development rate variation in Aedes aegypti (Diptera: Culicidae). BMC Ecol., 14: 3. https://doi.org/10.1186/1472-6785-14-3
Couret, J., Dotson, E., and Benedict, M.Q., 2014. Temperature, larval diet, and density effects on development rate and survival of Aedes aegypti (Diptera: Culicidae). PLoS One, 9: e87468. https://doi.org/10.1371/journal.pone.0087468
Cristophers, S., 1960. Aedes aegypti (L). The yellow fever mosquito. Its life history, bionomics and structure, Cambridge university press.
Farjana, T., Tuno, N., and Higa, Y., 2012. Effects of temperature and diet on development and interspecies competition in Aedes aegypti and Aedes albopictus. Med. Vet. Entomol., 26: 210-217. https://doi.org/10.1111/j.1365-2915.2011.00971.x
Foster, W.A., and Walker, E.D., 2019. Mosquitoes (Culicidae), Medical and veterinary entomology. Elsevier. https://doi.org/10.1016/B978-0-12-814043-7.00015-7
Giesen, C., J. Roche, L. Redondo-Bravo, C. Ruiz-Huerta, D. Gomez-Barroso, A. Benito, And Z. Herrador., 2020. The impact of climate change on mosquito-borne diseases in Africa. Pathog. Glob. Hlth., 114: 287-301. https://doi.org/10.1080/20477724.2020.1783865
Gunathilaka, N., Upulika, H., Udayanga, L., and Amarasinghe, D., 2019. Effect of larval nutritional regimes on morphometry and vectorial capacity of Aedes aegypti for dengue transmission. Biomed. Res. Int., 3607342. https://doi.org/10.1155/2019/3607342
Khan, J., Ghaffar, A., and Khan, S.A., 2018. The changing epidemiological pattern of Dengue in Swat, Khyber Pakhtunkhwa. PLoS One, 13: e0195706. https://doi.org/10.1371/journal.pone.0195706
Reinhold, J.M., Lazzari, C.R., and Lahondere, C., 2018. Effects of the Environmental Temperature on Aedes aegypti and Aedes albopictus Mosquitoes: A review. Insects, 9: 158. https://doi.org/10.3390/insects9040158
Rocklov, J., and Dubrow, R., 2020. Climate change: An enduring challenge for vector-borne disease prevention and control. Nat. Immunol., 21: 479-483. https://doi.org/10.1038/s41590-020-0648-y
Rueda, L.M., 2004. Pictorial keys for the identification of mosquitoes (Diptera: Culicidae) associated with dengue virus transmission. Walter reed army inst of research Washington Dc Department Of Entomology. https://doi.org/10.11646/zootaxa.589.1.1
Sasmita, H.I., Tu, W.C., Bong, L.J., and Neoh, K.B., 2019. Effects of larval diets and temperature regimes on life history traits, energy reserves and temperature tolerance of male Aedes aegypti (Diptera: Culicidae): optimizing rearing techniques for the sterile insect programmes. Parasit. Vectors, 12: 578. https://doi.org/10.1186/s13071-019-3830-z
Sutiningsih, D., Nurjazuli, N., Nugroho, D., and Satoto, T.B.T., 2019. Larvicidal activity of brusatol isolated from Brucea javanica (L) Merr on Culex quinquefasciatus. Iran. J. Publ. Hlth., 48: 688-696. https://doi.org/10.18502/ijph.v48i4.1002
Teng, H.J., and Apperson, C.S., 2000. Development and survival of immature Aedes albopictus and Aedes triseriatus (Diptera: Culicidae) in the laboratory: effects of density, food, and competition on response to temperature. J. Med. Entomol., 37: 40-52. https://doi.org/10.1603/0022-2585-37.1.40
Wimalasiri-Yapa, B., Barrero, R.A., Stassen, L., Hafner, L.M., Mcgraw, E.A., Pyke, A.T., Jansen, C.C., Suhrbier, A., Yakob, L., Hu, W., Devine, G.J., and Frentiu, F.D., 2021. Temperature modulates immune gene expression in mosquitoes during arbovirus infection. Open Biol., 11: 200246. https://doi.org/10.1098/rsob.200246
Yang, H.M., Macoris, M.L., Galvani, K.C., Andrighetti, M.T., and Wanderley, D.M., 2009. Assessing the effects of temperature on the population of Aedes aegypti, the vector of dengue. Epidemiol. Infect., 137: 1188-1202. https://doi.org/10.1017/S0950268809002040
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