Abstract
Knowledge on the factors associated with the development of Aedes aegypti (Linnaeus) can provide a better understanding of vector surveillance and encourage prevention practices for Aedes control strategy. The purpose of this research was to study the effect of different plant materials contained in the water in artificial container towards the development of Ae. aegypti. This is an experimental research that involve triplication of artificial containers each filled with a total of 30 eggs exposed to different plant materials (twig, dry grasses and dry leaves) at different concentration (i.e., 1.7 g/l, 2.5 g/l and 3.3 g/l) respectively. Observation on the development day, number or larvae at each fourth instar, and pupation period were monitored daily until adult emergence under controlled environment in insectarium. The experiment indicated that the time period required for the development of larvae was positively influenced by the presence of plant materials found in water for a conducive larval growth environment. This study revealed that the presence of plant materials contained in the water of breeding habitat support the development of Ae. aegypti larvae until its adult emergence. In conclusion, organic matters present in plant materials were identified as responsible factors in response to the development time of Ae. aegypti larvae during their aquatic stage.
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42690-022-00909-0/MediaObjects/42690_2022_909_Fig1_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42690-022-00909-0/MediaObjects/42690_2022_909_Fig2_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42690-022-00909-0/MediaObjects/42690_2022_909_Fig3_HTML.png)
Similar content being viewed by others
Data availability
Not applicable.
References
Arunachalam N, Tyagi BK, Samuel M, Krishnamoorthi R, Manavalan R, Tewari SC, Petzold M (2012) Community-based control of Aedes aegypti by adoption of eco-health methods in Chennai City, India. Pathog Glob Health 106:488–496
Aznar VR, Otero M, De Majo MS, Fischer S, Solari HG (2013) Modeling the complex hatching and development of Aedes aegypti in temperate climates. Ecol Model 24(253):44–55
Barrera R, Mackay AJ, Amador M (2013) An improved trap to capture adult container-inhabiting mosquitoes. J Am Mosq Control Assoc 29:358
Bond JG, Ramírez-Osorio A, Marina CF, Fernández-Salas I, Liedo P, Dor A, Williams T (2017) Efficiency of two larval diets for mass-rearing of the mosquito Aedes aegypti. PLoS ONE 12(33):37
Bowatte G, Perera P, Senevirathne G, Meegaskumbura S, Meegaskumbura M (2013) Tadpoles as dengue mosquito (Aedes aegypti) egg predators. Biol Control 67:469–474
Brady OJ, Johansson MA, Guerra CA, Bhatt S, Golding N, Pigott DM, Styer LM (2013) Modelling adult Aedes aegypti and Aedes albopictus survival at different temperatures in laboratory and field settings. Parasite Vector 6:351
Burkot TR, Handzel T, Schmaedick MA, Tufa J, Roberts JM, Graves PM (2007) Productivity of natural and artificial containers for Aedes polynesiensis and Aedes aegypti in four American Samoan villages. Med Vet Entomol 21(1):22–29
Clark TM, Flis BJ, Remold SK (2004) pH tolerances and regulatory abilities of freshwater and euryhaline Aedine mosquito larvae. J Exp Biol 207:2297–2304
Clemon A, Mori A, Haugen M, Severson D, Duman-Scheel M (2010) Aedes aegypti culturing and eggs collection. Cold Spring Harbor Protocol 29:2010
Couret J, Dotson E, Benedict MQ (2014) Temperature, larval diet, and density effects on development rate and survival of Aedes aegypti (Diptera: Culicidae). PLoS One 9:274
Darriet F, Zumbo B, Corbel V, Chandre F (2010) Influence of plant matter and NPK fertilizer on the biology of Aedes aegypti (Diptera: Culicidae). Parasite (Paris, France) 17:149–154
Darriet F (2016) Development of Aedes aegypti and Aedes albopictus (Diptera: Culicidae) Larvae Feeding on the Plant Material Contained in the Water. Annal Commun Med Pract 2:117–119
Daugherty MP, Alto BW, Juliano SA (2000) Invertebrate carcasses as a resource for competing Aedes albopictus and Aedes aegypti (Diptera: Culicidae). J Med Entomol 37:364–372
Dom NC, Ahmad AH, Ismail R (2013) Habitat characterization of Aedes sp. breeding in urban hotspot area. Procedia Soc Behav Sci 85:100–109
Dom NC, Madzlan MF, Nur S, Hasnan A, Misran N (2016) Water quality characteristics of dengue vectors breeding containers. Int J Mosq Res 3:25–29
Elora S, Sarkar M (2018) Larval diet influences development, growth, and survival of mosquitoes in artificial rearing condition. J Med Entomol 12:12–21
Fouque F, Vazeille M, Mousson L, Gaborit P, Carinci R, Issaly J, Failloux AB (2001) Aedes aegypti in French Guiana: susceptibility to a dengue virus. Trop Med Int Health 6(1):76–82
Flaibani N, Pérez AA, Barbero IM, Burroni NE (2020) Different approaches to characterize artificial breeding sites of Aedes aegypti using generalized linear mixed models. Infect Dis Poverty 9(04):97–107
Joy TK, Arik AJ, Corby-Harris V, Johnson AA, Riehle MA (2010) The impact of larval and adult dietary restriction on lifespan, reproduction and growth in the mosquito Aedes aegypti. Exp Gerontol 45:685–690
Juliano SA, Philip Lounibos L (2005) Ecology of invasive mosquitoes: effects on resident species and on human health. Ecol Lett 8:558–574
Juliano SA (2009) Species interactions among larval mosquitoes: context dependence across habitat gradients. Annu Rev Entomol 54:37–56
Kenawy MA, Ammar SE, Abdel-Rahman HA (2013) Physico-chemical characteristics of the mosquito breeding water in two urban areas of Cairo Governorate. Egypt. J Entomol Acarol Res 45:e17
Khormi HM, Kumar L (2014) Climate change and the potential global distribution of Aedes aegypti: spatial modelling using geographical information system and CLIMEX. Geospat Health 31:405–415
Kraemer MU, Sinka ME, Duda KA, Mylne AQ, Shearer FM, Barker CM, Hendrickx G (2015) The global distribution of the arbovirus vectors Aedes aegypti and Aedes albopictus. Elife 4(1):e08347
Lambrechts L, Paaijmans KP, Fansiri T, Carrington LB, Kramer LD, Thomas MB, Scott TW (2011) Impact of daily temperature fluctuations on dengue virus transmission by Aedes aegypti. Proc Natl Acad Sci 108:7460–7465
Leite NR, Krogh R, Xu W, Ishida Y, Iulek J, Leal WS, Oliva G (2009) Structure of an odorant-binding protein from the mosquito Aedes aegypti suggests a binding pocket covered by a pH-sensitive “Lid.” PLoS ONE 4:12
Linenberg I, Christophides GK, Gendrin M (2016) Larval diet affects mosquito development and permissiveness to Plasmodium infection. Sci Rep 6:38230
Lounibos LP, Suárez S, Menéndez Z, Nishimura N, Escher RL, O Connell SM, Rey JR (2002) Does temperature affect the outcome of larval competition between Aedes aegypti and Aedes albopictus? J Vector Ecol 27:86–95
Manawadu UD, Deepananda KHMA, Wegiriya HCE (2005) Comparative study on the diversity and abundance of mosquito fauna in relation to anthropogenic activities and environmental factors in selected sites of Matara area. Univ Ruhuna 31:22–29
Murrell S, Wu SC, Butler M (2011a) Review of dengue virus and the development of a vaccine. Biotechnol Adv 29:239–247
Murrell EG, Damal K, Lounibos LP, Juliano SA (2011b) Distributions of competing container mosquitoes depend on detritus types, nutrient ratios, and food availability. Ann Entomol Soc Am 104:688–698
Ooi EE, Gubler DJ (2009) Dengue in Southeast Asia: epidemiological characteristics and strategic challenges in disease prevention. Cad Saude Publica 25:S115–S124
Padmanabha H, Lord CC, Lounibos LP (2011) Temperature induces trade-offs between development and starvation resistance in Aedes aegypti (L.) larvae. Med Vet Entomol 25:445–453
Pompon J, Morales-Vargas R, Manuel M, Tan CH, Vial T, Tan JH, Missé DA (2017) Zika virus from America is more efficiently transmitted than an Asian virus by Aedes aegypti mosquitoes from Asia. Sci Rep 7:1–8
Powell JR (2018) Mosquito-borne human viral diseases: why Aedes aegypti? Am J Trop Med Hyg 98:1563–1565
Ramasamy R, Surendran SN, Jude PJ, Dharshini S, Vinobaba M (2011) Larval development of Aedes aegypti and Aedes albopictus in peri-urban brackish water and its implications for transmission of arboviral diseases. PLoS Negl Trop Dis 5:112–117
Ramasamy R, Jude PJ, Veluppillai T, Eswaramohan T, Surendran SN (2014) Biological differences between brackish and fresh water-derived Aedes aegypti from two locations in the Jaffna Peninsula of Sri Lanka and the implications for arboviral disease transmission. PLoS ONE 9:227–232
Rohani A, Azahary AA, Malinda M, Zurainee MN, Rozilawati H, Najdah WW, Lee HL (2014) Eco-virological survey of Aedes mosquito larvae in selected dengue outbreak areas in Malaysia. J Vector Borne Dis 51:327
Stewart Ibarra AM, Ryan SJ, Beltrán E, Mejía R, Silva M, Muñoz ÁG (2013) Dengue vector dynamics (Aedes aegypti) influenced by climate and social factors in Ecuador: implications for targeted control. PLoS ONE 32:18
Tomé HV, Pascini TV, Dângelo RA, Guedes RN, Martins GF (2014) Survival and swimming behavior of insecticide-exposed larvae and pupae of the yellow fever mosquito Aedes aegypti. Parasit Vectors 7:195
Tun-Lin W, Burkot TR, Kay BH (2000) Effects of temperature and larval diet on development rates and survival of the dengue vector Aedes aegypti in north Queensland, Australia. Med Vet Entomol 14:31–44
Yoshioka M, Couret J, Kim F, McMillan J, Burkot TR, Dotson EM, Vazquez Prokopec GM (2012) Diet and density dependent competition affect larval performance and oviposition site selection in the mosquito species Aedes albopictus (Diptera: Culicidae). Parasit Vectors 5(1):225
Zettel H, Phauk S, Kheam S, Freitag H (2017) Checklist of the aquatic Hemiptera (Heteroptera: Gerromorpha and Nepomorpha) of Cambodia, with descriptions of new species of Microvelia Westwood, 1834 and Ranatra Fabricius, 1790. Aquat Insects 38(1-2):21–48
Funding
This research work was funded by the Fundamental Research Grant (FRGS), Ministry of Higher Education (600-RMC/FRGS 5/3 (141/2021).
Author information
Authors and Affiliations
Contributions
This study was contributed by all the authors; Nurlyana Mahmud Syah and Nazri Che-Dom wrote the manuscript, Rahmat Dapari and Samsuri Abdullah collected the data and did the analysis; Nopadol Precha proofred and edited the manuscript.
Corresponding author
Ethics declarations
Ethics approval
Not applicable.
Consent to participate
Not applicable.
Consent for publication
Not Applicable.
Conflict of interest
The author declare that they have no conflict of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Shah, N.l.M., Dom, N.C., Abdullah, S. et al. Evaluation on the effects of different plant matter in water on Aedes aegypti development (Diptera: Culicidae). Int J Trop Insect Sci 42, 3831–3838 (2022). https://doi.org/10.1007/s42690-022-00909-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s42690-022-00909-0