Widespread distribution of Aedes aegypti larvae, a potential risk of arbovirus transmission in the Grand Lomé health region, Togo, West Africa
Author:
Akagankou Kossivi I.1, Ahadji-Dabla Koffi M.1, Romero-Alvarez Daniel2, Ortega-López Leonardo2, Villanueva-Sarmiento Manuel2, N’Tsoukpoe Komlan G. J., Koffi Edoh1, Kondo Yovo1, Amekudi Adjo A.1, Apetogbo Yawo1, Lenhart Audrey3, Ketoh Guillaume Koffivi1
Affiliation:
1. Université de Lomé 2. Universidad Internacional SEK (UISEK) 3. Centers for Disease Control and Prevention (CDC)
Abstract
Abstract
Background
Understanding the population dynamics and geographic range of Aedes aegypti is of high importance for arbovirus vector surveillance and control. Little is known about the current distribution and seasonality of Ae. aegypti in Grand Lomé, Togo.
Methods
Mosquito oviposition traps (n = 70) were deployed in houses in the thirteen communes in Grand Lomé health region and examined weekly between May 2022 and April 2023. Generalized linear mixed models (GLMM) were applied to investigate the relationship between larval collections and seasonality. The European Space Agency (ESA) World cover 10m 2020 product was used to represent different land cover classes and determine whether sites with higher larval numbers differed from sites with lower numbers.
Results
A total of 52,768 Ae. aegypti larvae were collected in Grand Lomé. The highest incidence of Ae. aegypti larvae was observed in the commune of Bè-Ouest (= 122.74 per 1,000 population). Agoè-Nyivé was the commune with the lowest incidence over the entire study period. Eight land-use classes were represented by the ESA 10 m product in Grand Lomé. The chi-square test to determine whether larval abundance categories and land cover classes were associated revealed a significant relationship (X2 = 2883.5, df = 14, p < 0.005).
Conclusion
This study provided information on the seasonal distribution of Ae. aegypti larvae in the health region of Grand Lomé. The results of this study could be useful in guiding disease vector surveillance and control efforts.
Publisher
Springer Science and Business Media LLC
Reference45 articles.
1. Mousson L, Dauga C, Garrigues T. « Phylogeography of Aedes (Stegomyia) aegypti (L.) and Aedes (Stegomyia) albopictus (Skuse, Diptera: Culicidae) based on mitochondrial DNA variations ». Genet. Res.2005, vol. 86, no 1, p. 1–11 (PMID 16181519, DOI 10.1017/S0016672305007627). 2. Womack M. « The yellow fever mosquito, Aedes aegypti », Wing Beats. 1993, vol. 5, no 4, 1993, p. 4. 3. Transtadial passage of St. Louis Encephalitis virus in Aedes aegypti mosquitoes;Collins WE;Am. J. Trop. Med. Hyg,1962 4. Christophers SR, Rickard S. Aedes aegypti (L.), The Yellow Fever Mosquito. Its Life History,Bionomics and Structure, London: The Syndics of the Cambridge University Press, Bentley House, 200, Euston Road. 1960, N.W.I. 739. 5. Human impacts have shaped Historical and recent evolution in Aedes aegypti, the Dengue and Yellow fever mosquito. Evolution;;Brown JE;International Journal of Organic Evolution,2014
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