Abstract

A mosquito species has its own favourable requirements of abiotic and biotic characteristics including microbiota, in a breeding habitat. Some of the microbiota may cause parasitic or pathogenic effects to mosquito larvae such as species of viruses, parasitic bacteria, fungi, protists, entomopathogenic nematodes, and filamentous fungi. In Sri Lanka, there is a scarcity of information on microbiota associated with mosquito breeding habitats and their effect on mosquito larvae. Hence, the present study was conducted to determine microbiota species/taxa associated with a variety of mosquito breeding habitats in selected areas of the Gampaha District in Sri Lanka and the relationship, if any, the microbiota has with mosquito larva survival and breeding. Forty-five microbiota species belonging to 11 phyla were found from different mosquito breeding habitats with the highest percentage belonging to phylum Euglenozoa (27.89%). Species that belonged to the phylum Amoebozoa (1.22%) and Sarcodina (1.17%) had the lowest abundance, and each of its species richness was recorded as one. Philodina citrina followed by Monostyla bulla comprised 30.8% and 16.59%, respectively, of the total rotifer population. From the total microbiota, 25-50% existed as accidental while less than 25% rare, in the habitat type according to their abundance. Paddy fields had the highest species richness (17), evenness (23.52), Shannon-Weiner (66.64), and beta diversity (0.65) over 50% indicating high heterogeneity in microbiota composition among the habitats. Ciliated protists, namely, Vorticella microstoma, Zoothamnium spp., and Chilodinella sp., were identified as naturally occurring microbiota associated with Culex mosquito larvae that inhabited in paddy fields and associated irrigation canals. Only Vorticella microstoma caused a significant lethal effect on mosquito larvae. This study revealed that species of Cx. gelidus, Cx. pseudovishnui, Cx. tritaeniorhynchus, Cx. quinquefasciatus, and Cx. whitmorei served as hosts for V. microstoma where infectivity rate in Cx. tritaeniorhynchus reached 73.22. Chilodinella sp. selectively served as endoparasitic to Cx. gelidus larvae causing only 4.58% mortality, and invasive cysts of the pathogen were observed in the subcuticular layer of the host body. Even though Zoothamnium spp. were found on Cx. tritaeniorhynchus larvae, there was no lethal effect due to the attachment of the parasitic agent. The potential of these microbiotas in integrated vector controlling approaches in future perspectives is recommended.

Highlights

  • Distribution, abundance, and individual fitness of mosquito immatures in a particular breeding habitat are known to be dependent on mainly three factors: biotic [1, 2], abiotic [3,4,5], and their interaction between each other and with other associated taxa [6, 7]

  • Ostracods act as both food competitors and predators of mosquito larvae while copepods act as omnivorous filter feeders which consume mostly large-sized food particles [17]

  • The present study was conducted to identify naturally occurring microbiota species associated with a variety of vector mosquito breeding habitats and to identify potential parasitic or pathogenic microbiota on mosquito larvae under the natural environment

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Summary

Introduction

Distribution, abundance, and individual fitness of mosquito immatures in a particular breeding habitat are known to be dependent on mainly three factors: biotic [1, 2], abiotic [3,4,5], and their interaction between each other and with other associated taxa [6, 7]. There is an interspecific resource competition under food-limiting environments when multiple mosquito species present simultaneously within the same mosquito breeding habitats [10]. The major controphic competitors such as cladocerans and ostracods exhibit polyphagous activities with larvae and an effect on their abundance in breeding habitats. There is a need to develop biopesticides against vector mosquito larvae as a useful substitute to chemical insecticides In this contest, information on microbiota species association with vector mosquito breeding habitats as potential parasitic or pathogenic species against mosquito immature stages in Sri Lanka should be further studied. The present study was conducted to identify naturally occurring microbiota species associated with a variety of vector mosquito breeding habitats and to identify potential parasitic or pathogenic microbiota on mosquito larvae under the natural environment

Results
Discussion
Conclusion

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