Diversity and species composition of microbiota associated with dengue mosquito breeding habitats: A cross-sectional study from selected areas in Udapalatha MOH division, Sri Lanka

Yashoda Kumari , Deepika Amarasinghe , Koshila Ranasinghe

Asian Pacific Journal of Tropical Medicine ›› 2023, Vol. 16 ›› Issue (8) : 363 -370.

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Asian Pacific Journal of Tropical Medicine ›› 2023, Vol. 16 ›› Issue (8) :363 -370. DOI: 10.4103/1995-7645.380722
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Diversity and species composition of microbiota associated with dengue mosquito breeding habitats: A cross-sectional study from selected areas in Udapalatha MOH division, Sri Lanka
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Abstract

Objective: To determine the diversity of microbiota associated with different breeding habitats of dengue vector mosquitoes Aedes (Ae.) aegypti and Ae. albopictus and to identify any parasitic, epibiont, pathogenic, competitive or predatory species. Methods: Sampling was performed from a variety of breeding habitats using dipping, pipetting and siphoning techniques. Microbiota in water samples were preserved using Rose Bengal solution and Lugol’s iodine, and were identified. Live samples of microbiota were kept under laboratory conditions to observe any pathogenic or parasitic microbiota interacting with larvae. Results: A total of eleven microbiota species (Canthocamptus staphylinus, Canthocamptus microstaphylinus, Parastenocaris brevipes, Lepadella ovalis, Lepadella patella, Rotatoria rotatoria, Rotatoria macrura, Asplanchna brightwelli, Trichocerca rattus, Euglena variabilis, and Flagilaria capucina) belonging to four (4) phyla (Arthropoda, Rotifera, Euglenozoa, and Ochrophyta) and 8 microbiota species belonged to four phyla (Arthropoda, Rotifera, Euglenozoa, and Ochrophyta) were identified from Ae. aegypti and Ae. albopictus breeding habitats respectively. There was a higher percentage (54.54%) of larval habitats positive for the secondary vector Ae. albopictus than through the primary vector Ae. aegypti in the Gampola urban area indicating higher possibility of transmitting the dengue virus through the secondary vector. However, no pathogenic or parasitic ciliates on mosquito larvae were encountered in the present study. Those findings may be due to sampling maingly from temporary container-type breeding habitats. Conclusions: The relative distribution of microbiota associated with mosquito species differed significantly among Ae. aegypti and Ae. albopictus. The overall findings of this study could help in implementing novel eco-friendly vector-control strategies in the study area.

Keywords

Aedes / Biological / Mosquito-control / Vectors

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Yashoda Kumari, Deepika Amarasinghe, Koshila Ranasinghe. Diversity and species composition of microbiota associated with dengue mosquito breeding habitats: A cross-sectional study from selected areas in Udapalatha MOH division, Sri Lanka. Asian Pacific Journal of Tropical Medicine, 2023, 16 (8) : 363-370 DOI:10.4103/1995-7645.380722

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References

[1]

Becker N, Zgomba M, Petric D, Dahl C, Boase C, Lane J, et al. Mosquitoes and their control. Springer Science & Business Media; 2003, p. 453-485.

[2]

Simsek F. Seasonal larval and adult population dynamics and breeding habitat diversity of Culex theileri Theobald 1903 (Diptera: Culicidae) in the Golbasi district, Ankara. Turk J Zool 2004; 28:337-344.

[3]

Chaves L, Koenraadt CJM. Climate change and highland malaria: Fresh air for a hot debate. Q Rev Biol 2010; 85(1):27-55.

[4]

Day, J. Mosquito oviposition behavior and vector control. Insects 2016; 7(4):65.

[5]

Bentley MD, Day JF. Chemical ecology and behavioral aspects of mosquito oviposition. Annu Rev Entomol 1989; 34(1):401-421.

[6]

Barrera R, Amador M, Clark GG. Ecological factors influencing Aedes aegypti (Diptera: Culicidae) productivity in artificial containers in Salinas, Puerto Rico. J Med Entomol 2006; 43(3):484-492. doi: 10.1093/jmedent/43.3.484.

[7]

Amerasinghe F, Indrajith N, Ariyasena T. Physicochemical characteristics of mosquito breeding habitats in an irrigation development area in Sri Lanka. Ceylon J Sci 1995; 24(2):13-29.

[8]

Muturi EJ, Mwangangi J, Shililu J, Muriu S, Jacob B, Kabiru E, et al. Mosquito species succession and physicochemical factors affecting their abundance in rice fields in Mwea, Kenya. J Med Entomol 2007; 44(2):336-344.

[9]

Oyewole OI, Momol OO, Anyasor GN. Physicochemical characteristics of Anopheles breeding sites: Impact on fecundity and progeny development. Afr J Environ Sci & Technol 2009; 3(12):447-452.

[10]

Meyabeme Elono AL, Liess M, Duquesne S. Influence of competing and predatory invertebrate taxa on larval populations of mosquitoes in temporary ponds of wetland areas in Germany. J Vector Ecol 2010; 35(2):419-427.

[11]

Loria K. Freshwater zooplankton communities as indicators of habitat quality: Testing responses. Ph.D thesis submitted to University of Colorado at Boulder; 2017, p. 36.

[12]

Ranasinghe HAK, Amarasinghe LD. Naturally occurring microbiota associated with mosquito breeding habitats and potential parasitic species against mosquito larvae: A study from Gampaha District, Sri Lanka. BioMed Res Int 2020; 1-12. doi: 10.1155/2020/4602084.

[13]

Nilsson LKJ, de Oliveira MR, Marinotti O, Rocha EM, Håkansson S, Tadei WP, et al. Characterization of bacterial communities in breeding waters of Anopheles darlingi in Manaus in the Amazon basin malaria-endemic area. Microb Ecol 2019; 78(4):781-791.

[14]

Yee DA, Allgood D, Kneitel JM, Kuehn KA. Constitutive differences between natural and artificial container mosquito habitats: Vector communities, resources, microorganisms and habitat parameters. J Med Entomol 2012; 49(3):482-491.

[15]

Chelliah RV. Keys and illustrated key to the genera of mosquitoes of Sri Lanka (Diptera: Culicidae). Contrib Am Entomol Inst 1984; 7(4):1-84.

[16]

Rueda LM. Pictorial keys for the identification of mosquitoes (Diptera: Culicidae) associated with dengue virus transmission. Zootaxa 2004; 589(1):1-60.

[17]

Fernando CH, Weerawardhena SR. A guide to the freshwater fauna of Ceylon (Sri Lanka). Ceylon, Sri Lanka: Fisheries Research Station; 2002.

[18]

Abeywickrama BA, Abeywickrama L. The genera of the freshwater algae of Sri Lanka. Part 1. Colombo: National Science Council, Sri Lanka; 1979.

[19]

Corliss JO. The ciliated protozoa: Characterization, classification, and guide to the literature. 2nd ed. London, UK: Pergamon Press; 1979.

[20]

Gunathilaka N. Illustrated key to the adult female Anopheles (Diptera: Culicidae) mosquitoes of Sri Lanka. Appl Entomol Zool 2017; 52(1):69-77.

[21]

Gunathilaka N. Annotated checklist and review of the mosquito species (Diptera: Culicidae) in Sri Lanka. J Insect Biodivers 2018; 7(3):38-50.

[22]

Lobo E, Leighton G. Estructuras comunitarias de las fitocenosis planctonicas de los sistemas de desembocaduras de rios y esteros de la zona central de Chile. Rev Biol Mar Oceanogr 1986; 22:1-29.

[23]

Harrison S, Ross SJ, Lawton JH. Beta diversity on geographic gradients in Britain. J Anim Ecol 1992; 62:151-158.

[24]

Shannon CE, Weaver W. The mathematical theory of communication. Urbana: The University of Illinois Press; 1949.

[25]

Pielou EC. Ecological diversity. New York: John Wiley; 1975.

[26]

Wijegunawardana NDAD, Gunawardene YINS, Chandrasena TGAN, Dassanayake RS, Udayanga NWBAL, Abeyewickreme W. Evaluation of the effects of Aedes vector indices and climatic factors on dengue incidence in Gampaha District, Sri Lanka. BioMed Res Int 2019; 1-11. doi: 10.1155/2019/2950216.

[27]

Hawley W, Reiter P, Copeland R, Pumpuni C, Craig Jr. G. Aedes albopictus in North America: Probable introduction in used tires from Northern Asia. Science 1987; 236(4805):1114-1116.

[28]

Saleeza SNR, Rashid YN, Azirun MS. Mosquitoes larval breeding habitat in urban and suburban areas, Peninsular Malaysia. IJABE 2011; 5:599-603.

[29]

Philbert A, Ijumba JN. Preferred breeding habitats of Aedes aegypti (Diptera: Culicidae) mosquito and its public health implications in Dar es Salaam, Tanzania. J Environ Res Manage 2013; 4(10):344-351.

[30]

Wilson JJ, Sevarkodiyone SP. Spatial and temporal distribution of mosquitoes (Culicidae) in Virudhunagar district, Tamil Nadu, South India. Int J Mosq Res 2014; 1(3):4-9.

[31]

Sedaghat MM, Bozorg Omid F, Karimi M, Haghi S, Hanafi-Bojd AA. Modelling the probability of presence of Aedes aegypti and Aedes albopictus in Iran until 2070. Asian Pac J Trop Med 2023; 16(1):16-25.

[32]

Weeraratne TC, Perera BMD, Mansoor MACM, Karunaratne SHPP. Prevalence and breeding habitats of the dengue vectors Aedes aegypti and Aedes albopictus (Diptera: Culicidae) in the semi-urban areas of two different climatic zones in Sri Lanka. Int J Trop Insect Sci 2013; 33(4):216-226. doi: 10.1017/s174275841300026x.

[33]

Amarasinghe LD, Rathnayake ARLK. Prevalence of microfauna associated with different mosquito breeding habitats in a selected area of Sri Lanka. Int J Curr Microbiol Appl Sci 2014; 3(5):587-598.

[34]

Marten GG. Impact of the copepod Mesocyclops leukarti pilosa and green alga Kirchneriella irregularis upon larval Aedes albopictus (Diptera: Culicidae). Bull Soc Vector Ecol 1984; 9(1):1-5.

[35]

Marten GG. Mosquito control by plankton management: The potential of indigestible green algae. J Trop Med Hyg 1986; 89:213-222.

[36]

Ranasinghe HAK, Amarasinghe LD. Naturally occurring microbiota associated with mosquito breeding habitats and their effects on mosquito larvae. BioMed Re Int 2020; 1-11. doi: 10.1155/2020/4065315.

[37]

Thakur A, Kocher DK. Impact of antagonistic crustaceans on the population of Aedes aegypti L. larvae under laboratory conditions. J Vector Borne Dis 2020; 57(1):58-62. doi: 10.4103/0972-9062.308802.

[38]

Blaustein L, Chase JM. Interactions between mosquito larvae and species that share the same trophic level. Ann Rev Entomol 2007; 52(1):489-507. doi: 10.1146/annurev.ento.52.110405.091431.

[39]

Duquesne S, Kroeger I, Kutyniok M, Liess M. The potential of cladocerans as controphic competitors of the mosquito Culex pipiens. J Med Entomol 2011; 48(3):554-560. doi: 10.1603/me09282.

[40]

Duguma D, Kaufman MG, Simas Domingos AB. Aquatic microfauna alter larval food resources and affect development and biomass of West Nile and Saint Louis encephalitis vector Culex nigripalpus (Diptera: Culicidae). Ecol Evolut 2017; 7(10):3507-3519.

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