Mosquito Surveillance in the Seaport of Cotonou, Benin: Monitoring of Species Diversity and Assessment of Susceptibility of Mosquitoes to Insecticides
Abstract
Background: Seaports are one of the most important gateways forcoastal countries and deserve permanent surveillance of invasive species.
Objectives: This study aims to monitor the species diversity of mosquitoes in the seaport of Cotonou and determine the phenotypic resistance profile to multiple insecticides.
Methods: The study was conducted at the Port Autonome de Cotonou (PAC) from May to August 2022. BG sentinel traps were used to capture adults which were then identified morphologically. Additionally, larvae
of Aedes and Culex mosquitoes were collected and reared until adult emergence. Four batches of 25 adult female mosquitoes, aged 3 to 5 days, were exposed to four insecticides (bendiocarb 0.1%, pirimiphosmethyl 0.25%, permethrin 0.75% and deltamethrin 0.05%) for 60 minutes using the WHO tube test protocol. Mosquito susceptibility was determined after 24 hours.
Results: The captured adults yielded 455 adult mosquitoes, divided into six species: Anopheles gambiae, Anopheles pharoensis, Culex quinquefasciatus, Mansonia africana, Mansonia uniformism and Aedes aegypti, with Culex quinquefasciatus predominating (54.15%) and Aedes aegypti (30.66%) being the second most abundant. The females of Culex quinquefasciatus and Aedes aegypti were exposed to insecticides. Aedes aegypti showed resistance to pyrethroids but were susceptible to bendiocarb and pirimiphosmethyl, whereas Culex quinquefasciatus was resistant to pyrethroids and bendiocarb but susceptible to pirimiphos-methyl.
Conclusion: Mosquito surveillance in the seaport of Cotonou is essential for detection and vector control in the event of invasion by new vectors carried by boats and cargo ships.
How to cite this article:
Lokossou AS, Aïkpon R, Razaki O, Tchabi A, Houémenou G. Mosquito Surveillance in the Seaport of Cotonou, Benin: Monitoring of Species Diversity and Assessment of Susceptibility of Mosquitoes to Insecticides. J Commun Dis. 2023;55(4):80-85.
DOI: https://doi.org/10.24321/0019.5138.202359
References
Schaffner F, Medlock JM, Bortel WV. Public health significance of invasive mosquitoes in Europe. Clin MicrobiolInfect. 2013;19(8):685-92. [PubMed] [Google Scholar]
Wilke AB, Beier JC, Benelli G. Complexity of the relationship between global warming and urbanization–an
obscure future for predicting increases in vector-borne infectious diseases. Curr Opin Insect Sci. 2019;35:1-9.
[PubMed] [Google Scholar]
Monaghan AJ, Eisen RJ, Eisen L, McAllister J, Savage HM, Mutebi JP, Johansson MA. Consensus and uncertainty in the geographic range of Aedes aegypti and Aedes albopictus in the contiguous United States: multi-model assessment and synthesis. PLoS Comput Biol. 2019;15(10):e1007369. [PubMed] [Google Scholar]
Wilke AB, Vasquez C, Carvajal A, Moreno M, Petrie WD, Beier JC. Evaluation of the effectiveness of BG-Sentinel
and CDC light traps in assessing the abundance, richness, and community composition of mosquitoes in rural and natural areas. Parasit Vectors. 2022;15(1):51. [PubMed] [Google Scholar]
Reiter P. Aedes albopictus and the world trade in used tires, 1988-1995: the shape of things to come? J Am
Mosq Control Assoc. 1998;14(1):83-94. [PubMed] [Google Scholar]
Tatem AJ, Hay SI, Rogers DJ. Global traffic and disease vector dispersal. Proc Natl Acad Sci U S A. 2006;103(16):6242-7. [PubMed] [Google Scholar]
Ammar SE, McIntyre M, Swan T, Kasper J, Derraik JG, Baker MG, Hales S. Intercepted mosquitoes at New Zealand’s ports of entry, 2001 to 2018: current status and future concerns. Trop Med Infect Dis. 2019;4(3):101.
[PubMed] [Google Scholar]
Ibañez-Justicia A, Gloria-Soria A, den Hartog W, Dik M, Jacobs F, Stroo A. The first detected airline introductions
of yellow fever mosquitoes (Aedes aegypti) to Europe, at Schiphol International airport, the Netherlands.
Parasit Vectors. 2017;10(1):603. [PubMed] [Google Scholar]
Osório HC, Ze-Ze L, Neto M, Silva S, Marques F, Silva AS, Alves MJ. Detection of the invasive mosquito
species Aedes (Stegomyia) albopictus (Diptera: Culicidae) in Portugal. Int J Environ Res Public Health. 2018;15(4):820. [PubMed] [Google Scholar]
10. Wilke AB, Benelli G, Beier JC. Beyond frontiers: on invasive alien mosquito species in America and Europe.
PLoS Negl Trop Dis. 2020;14(1):e0007864. [PubMed] [Google Scholar]
Schmidt TL, Rooyen AR, Chung J, Endersby-Harshman NM, Griffin PC, Sly A, Hoffman AA, Weeks AR. Tracking
genetic invasions: genome-wide single nucleotide polymorphisms reveal the source of pyrethroid-resistant
Aedes aegypti (yellow fever mosquito) incursions at international ports. Evol Appl. 2019;12(6):1136-46.
[PubMed] [Google Scholar]
Wilke AB, Carvajal A, Medina J, Anderson M, Nieves VJ, Ramirez M, Vasquez C, Petrie W, Cardenas G, Beier JC.
Assessment of the effectiveness of BG-Sentinel traps baited with CO2
and BG-Lure for the surveillance of vector mosquitoes in Miami-Dade County, Florida. PLoS
One. 2019;14(2):e0212688. [PubMed] [Google Scholar]
Azari-Hamidian S, Harbach RE. Keys to the adult females and fourth-instar larvae of the mosquitoes of Iran (Diptera: Culicidae). Zootaxa. 2009;2078:1-33. [Google Scholar]
World Health Organization [Internet]. Guidelines for Testing Mosquito Adulticides Intended for Indoor Residual Spraying (IRS) and Insecticide Treated Nets (ITNs). Geneva: WHO/CDS/NTD/ WHOPES/
GCDDP/2006.3; 2006. Available from: https:// www.google.com/search?q=13.+WHO%3A+Guidelines+for+Testing+Mosquito+Adulticides+Intended+for+Indoor+Residual+Spraying+(IRS)+and+Insecticide+Treated+Nets(ITNs).+Geneva%3A+WHO%2FCDS%2FNTD%2F+WHOPES%2FGCDDP%2F2006.3%3B+2006%3A2&oq=13.%09WHO%3A+Guidelines+for+Testing+Mosquito+Adulticides+Intended+for+Indoor+Residual+Spraying(IRS)+and+Insecticide+Treated+Nets(ITNs).+Geneva%3A+WHO%2FCDS%2FNTD%2F+WHOPES%2FGCDDP%2F2006.3%3B+2006%3A2&aqs=chrome..69i57 j69i60.1008j0j7&sourceid=chrome&ie=UTF-8
Padonou GG, Sezonlin M, Gbedjissi GL, Ayi I, Azondekon R, Djenontin A, Bio-Bangana S, Oussou O, Yadouleton A, Boakye D, Akogbeto M. Biology of Anopheles gambiae and insecticide resistance: entomological study for a large scale of indoor residual spraying in south east Benin. J Parasitol Vector Biol. 2011;3(4):59-68.
[Google Scholar]
Agbanrin R, Padonou GG, Anges Y, Attolou R, Badirou K, Govoetchan R, Gnanaguenon V, Sovi A, Anagonou
R, Akogbeto M. Abundance and diversity of culicidae fauna at Cotonou in Southern Benin. Int J Curr Res
[Internet]. 2015;7(3):14085-91. Available from: https:// www.researchgate.net/publication/274953677_ABUNDANCE_AND_DIVERSITY_OF_CULICIDAE_FAUNA_AT_
COTONOU_IN_SOUTHERN_BENIN
Kamgang B, Happi JY, Boisier P, Njiokou F, Herve JP, Simard F, Paupy C. Geographic and ecological distribution
of the dengue and chikungunya virus vectors Aedes aegypti and Aedes albopictus in three major Cameroonian towns. Med Vet Entomol. 2010;24(2):132-41. [PubMed] [Google Scholar]
Kamgang B, Ngoagounj C, Manirakiza A, Nakoune E,Paupy C, Kazanji M. Temporal patterns of abundance of Aedes aeg ypti and Aedes albopictus (Diptera: Culicidae) and mitochondrial DNA analysis of Ae. albopictus
in the Central African Republic. PLoS Negl Trop Dis. 2013;7(12):e2590. [PubMed] [Google Scholar]
Sagbohan HW, Kpanou CD, Osse R, Dagnon F, PadonouGG, Sominahouin AA, Salako AS, Sidick A, Sewade W, Akinro B, Ahmed S, Impoinvil D, Agbangla C, Akogbeto M. Intensity and mechanisms of deltamethrin and permethrin resistance in Anopheles gambiae s.l. populations in southern Benin. Parasit Vectors. 2021;14(1):202.
[PubMed] [Google Scholar]
Badirou K, Osse R, Yadouleton A, Attolou R, Youssouf RA, Gnaguenon V, Akinrou B, Govoetchan R, Akogbeto
M. Redistribution of kdr L1014F and ACE-1 mutations involved in the resistance of vectors to insecticides
in Benin. Asian J Pharm Sci Technol. 2016;6(1):48-57. [Google Scholar]
Djègbè I, Boussari O, Sidick A, Martin T, Ranson H, Chandre F, Akogbeto M, Corbel V. Dynamics of insecticide
resistance in malaria vectors in Benin: first evidence of the presence of L1014S kdr mutation in Anopheles
gambiae from West Africa. Malar J. 2011;10:261. [PubMed] [Google Scholar]
Padonou GG, Gbedjissi G, Yadouleton A, Azondekon R, Razack O, Oussou O, Gnanguenon V, Rock A, Sezonlin M, Akogbeto M. Decreased proportions of indoor feeding and endophily in Anopheles gambiae s.l. populations
following the indoor residual spraying and insecticide-treated net interventions in Benin (West Africa).
Parasit Vectors. 2012;5:262. [PubMed] [Google Scholar]
Yadouleton AW, Padonou G, Asidi A, Moiroux N, Bio-Banganna S, Corbel V, N’guessan R, Gbenou D,
Yacoubou I, Gazard K, Akogbeto MC. Insecticide resistance status in Anopheles gambiae in southern Benin.
Malar J. 2010;9:83. [PubMed] [Google Scholar]
Salako AS, Ahogni I, Kpanou C, Sovi A, Azondekon R, Sominahounin AA, Tokponnon F, Gnanguenon V,
Dagnon F, Iyikirenga L, Akogbeto MC. Baseline entomologic data on malaria transmission in prelude to an indoor residual spraying intervention in the regions of Alibori and Donga, Northern Benin, West Africa. Malar
J. 2018;17(1):392. [PubMed] [Google Scholar]
Sovi A, Djegbe I, Soumanou L, Tokponnon F, Gnanguenon V, Azondekon R, Oke-Agbo F, Oke M, Adechoubou
A, Massougbodji A, Corbel V, Akogbeto M. Microdistribution of the resistance of malaria vectors to deltamethrin in the region of Plateau (southeastern Benin) in preparation for an assessment of the impact
of resistance on the effectiveness of Long Lasting Insecticidal Nets (LLINs). BMC Infect Dis. 2014;14:103.
[PubMed] [Google Scholar]
Copyright (c) 2024 Journal of Communicable Diseases (E-ISSN: 2581-351X & P-ISSN: 0019-5138)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.