Impact of feacal coliforms and interspecific cohabitation on the productivity of culicidae breeding sites, littoral-Cameroon

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DOI:

https://doi.org/10.51867/ajernet.7.2.38

Keywords:

Breeding Sites, Culicidae, Faecal Coliforms, Inter-Specific Cohabitation, Larval Productivity

Abstract

The demographic structure and emergence dynamics of Culicidae depend on biotic and abiotic interactions in the environment. The objective of this study is to determine the influence of bacteriological parameters, abundance, and interspecific cohabitation on the development of the pre-imaginal stages of Culicidae. Larvae were sampled using the “dipping” method and identified using dichotomous keys after rearing to adulthood; species of the Anopheles gambiae complex were distinguished using molecular techniques. The standard method for isolating and quantifying bacteria in water was used to quantify coliforms in water samples. The effect of density and interspecific cohabitation on the aquatic development of Culicidae was studied. The larvae were reared at different densities in a monospecific situation or in interspecific cohabitation. The number of individuals at each stage of development, the number of dead larvae, and the number of emergences were counted every 24 hours. The culicid fauna in Youpwé during the study period consisted of Culex quinquefasciatus (42.6%, n = 415), Anopheles coluzzii (39.8%, n = 388), and Aedes aegypti (17.6%, n = 171). Fecal coliforms were found at all breeding sites; the species identified were Enterobacter aerogenes (51.8%), Escherichia coli (6.5%), and Salmonella typhimurium (9.4%). A positive and significant correlation was observed between E. coli density and larval productivity of the genus Aedes (P-value = 0.002). In the laboratory, significantly slower pre-imaginal development was observed in a high-density interspecific cohabitation environment than in a monospecific environment. This was the case, for example, for the interspecific combination Anopheles gambiae/Culex quinquefasciatus, which had a significantly longer development time than Anopheles gambiae reared in a monospecific environment (P-value < 0.05). The same observation was made for the interspecific combination Anopheles culuzzii/Culex quinquefasciatus and Anopheles culuzzii in a monospecific environment (P-value ˂ 0.05). In addition, a bias in favor of females in interspecific cohabitation was noted. It would therefore be appropriate, based on the results of more specific work on the mechanisms influencing fecal coliforms, to move towards integrated vector management. This requires the integration of sex ratio and cohabitation into entomological surveillance programs.

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References

Agnew, P., Hide, M., Sidobre, C., & Michalakis, Y. (2002). A minimalist approach to the effects of density-dependent competition on insect life-history traits. Ecological Entomology, 27(3), 396-402. https://doi.org/10.1046/j.1365-2311.2002.00430.x

Akono, N. P., Mbongue, R. S., Foko, D. G. A., Tsila, H. G., Offono, E. M. L., Nopowo, T. F., Ekoko, W. E., & Mbida, M. J. A. (2022). Habitats larvaires d'Anopheles gambiae s.l. et mécanismes de résistance à Kribi (Cameroun). MTSI-Revue, 2(4). https://doi.org/10.48327/mtsi.v2i4.2022.284

Antonio, C., Ndo, C., Costantini, C., Awono, A. P., Fontenille, D., & Simard, F. (2009). Distribution and larval habitat characterization of Anopheles moucheti, Anopheles nili, and other malaria vectors in river networks of southern Cameroon. Acta Tropica, 112(3), 270-276. https://doi.org/10.1016/j.actatropica.2009.08.009

Bornert, G. (2000). Importance of psychrotrophic bacteria in food hygiene. Veterinary Medical Journal, 15(11), 1003-1010.

Carnevale, P., Robert, V., Manguin, S., Corbel, V., Fontenille, D., Garros, C., & Rogier, C. (2009). Anopheles Biology, Plasmodium Transmission and Vector Control. Didactique Marseille Collection, IRD Editions. https://doi.org/10.4000/books.irdeditions.10374

Coon, K. L., Brown, M. R., & Strand, M. R. (2016). Mosquitoes host communities of bacteria that are essential for development but vary greatly between local habitats. Molecular Ecology, 25(22), 5806-5826. https://doi.org/10.1111/mec.13877

Darriet, F., Robert, V., & Carnevale, P. (1986). New perspectives in the fight against Culex quinquefasciatus in the city of Bobo-Dioulasso (Burkina Faso). In "Water, the City and Development" Congress (p. 205). I.S.T.E.D., Marseille.

Delatte, H., Dehecq, J. S., Thiria, J., Domerg, C., Paupy, C., & Fontenille, D. (2007). Geographic distribution and developmental sites of Ae. albopictus (Diptera: Culicidae) during a Chikungunya epidemic event. Vector Borne and Zoonotic Diseases, 7(1), 1-11.

https://doi.org/10.1089/vbz.2007.0649

Desfontaine, M., Tchikangwa, I., Le Goff, G., Robert, V., & Carnevale, P. (1991). Influence of the feeding of the larvae of Anopheles gambiae (Diptera, Culicidae) on preimaginal development in an insectarium. Liaison and Documentation Bulletin - OCEAC, 98, 12-14.

Djeunang, D., Venturi, G., Fortuna, C., Paganotti, G. M., Severini, C., L'Episcopia, L., Tiotsia, T. A., Benedetti, E., Marsili, G., Amendola, A., Rezza, G., Sanou, S. M., & Russo, G. (2022). Dengue and chikungunya virus circulation in Cameroon and Gabon: Molecular evidence among symptomatic individuals. Access Microbiology, 4(4), 000340. https://doi.org/10.1099/acmi.0.000340

Duvalet, G. (2006). Parasites, vectors of pathogens and climate change. Applied Hydroecology, 15, 87-96. https://doi.org/10.1051/hydro:2006008

Etang, J., Mbida, M. J. A., Ntonga, A. P., & Mimpgoundi, R. (2016). Anopheles coluzzii larval habitat and insecticide resistance in the island area of Manoka, Cameroon. BMC Infectious Diseases, 16, 217. https://doi.org/10.1186/s12879-016-1542-y

European Centre for Disease Prevention and Control. (2026). Dengue worldwide overview. https://www.ecdc.europa.eu/en/dengue-monthly

Gillies, M., & Coetzee, M. (1987). A supplement to the Anophelinae of Africa south of the Sahara (Publication No. 55, pp. 1-143). South African Institute for Medical Research.

Gillies, M., & De Meillon, B. (1968). The Anophelinae of Africa south of the Sahara (Publication No. 54, 343 p.). South African Institute for Medical Research.

Gimnig, J. E., Ombok, M., Otieno, S., Kaufman, M. G., Vulule, J. M., & Walker, E. D. (2002). Density-dependent development of Anopheles gambiae (Diptera: Culicidae) larvae in artificial habitats. Journal of Medical Entomology, 39(1), 162-172. https://doi.org/10.1603/0022-2585-39.1.162

Gimonneau, G., Brossette, L., Mamai, W., Dabire, K., & Simard, F. (2014). Larval competition between An. coluzzii and An. gambiae in insectary and semi-field conditions in Burkina Faso. Acta Tropica, 130, 155-161. https://doi.org/10.1016/j.actatropica.2013.11.007

Gimonneau, G., Pombi, M., Dabiré, K., Diabaté, A., Morand, S., & Simard, F. (2012). Behavioral responses of Anopheles gambiae sensu stricto M and S molecular form larvae to an aquatic predator in Burkina Faso. Parasites & Vectors, 5, 65. https://doi.org/10.1186/1756-3305-5-65

Guerin-Faublée, V., Karray, S., Tilly, B., & Richard, Y. (1992). Actinomyces pyogenes: Conventional bacteriological study and on API galleries of 103 strains isolated from ruminants. Annals of Veterinary Research, 23(2), 151-160.

Hadji, M., Belghyti, D., EL Assal, M., Elomari, F., & Rahmoun, H. (2013). Entomological, physico-chemical study of mosquito breeding places (Anopheles, Culex). Science Lib, 5(130206).

Harrison, R. E., Yang, X., Eum, J. H., Martinson, V. G., Dou, X., Valzania, L., Wang, Y., Boyd, B. M., Brown, M. R., & Strand, M. R. (2023). The mosquito Aedes aegypti requires a gut microbiota for normal fecundity, longevity and vector competence. Communications Biology, 6, 1154. https://doi.org/10.1038/s42003-023-05545-z

Holstein, M. (1949). A practical guide to Anophelism in A.O.F. General Directorate of Public Health, General Mobile Hygiene and Prophylaxis Service, Dakar.

Hoyochi, I., Padonou, G. G., Tokponnon, T. F., Konkon, A. K., Zoungbédji, D. M., Salako, A. S., Dangnon, B., Akowanou, A. V. O., Sintondji, L. O., Sossoukpe, E., Baba-Moussa, L., & Akogbéto, M. C. (2025). Influence of the physicochemical characteristics of mosquito breeding sites in domestic environments on the distributions of Anopheles, Aedes and Culex mosquitoes in Benin. Tropical Medicine and Health, 53(1), 100. https://doi.org/10.1186/s41182-025-00786-6

Jupp, G. (1996). Mosquitoes of southern Africa: Culicinae and Toxorhynchitinae. Ekolgilde Publishers, Hartebeespoort, South Africa.

Kbibch, A., Elkharim, K., Elkhokh, K., Chentoufi, M., & Belghyti, D. (2009). Study of the impact of wastewater on the proliferation of mosquitoes (Culex pipiens). Science Lib, 5, 96.

Khandaker, J., & Roitberg, B. D. (2013). Effects of larval density and feeding rates on larval life history traits in Anopheles gambiae s.s. (Diptera: Culicidae). Journal of Vector Ecology, 38, 120-126. https://doi.org/10.1111/j.1948-7134.2013.12017.x

Koffi, A. A., Camara, S., Ahoua Alou, L. P. A., Oumbouke, W. A., Wolie, R. Z., Tia, I. Z., Sternberg, E. D., Yapo, F. H. A., Koffi, F. M., Assi, S. B., Cook, J., Thomas, M. B., & N'Guessan, R. (2023). Anopheles vector distribution and malaria transmission dynamics in Gbêkê region, central Côte d'Ivoire. Malaria Journal, 22, 192. https://doi.org/10.1186/s12936-023-04623-1

Kweka, E. J., Zhou, G., Beilhe, B., Dixit, A., Afrane, Y., Gilbreath, T. M., Munga, S., Nyindo, M., Githeko, A., & Yan, G. (2012). Effects of co-habitation between Anopheles gambiae s.s. and Culex quinquefasciatus aquatic stages on life history traits. Parasites & Vectors, 5(1), 1-9. https://doi.org/10.1186/1756-3305-5-33

Letouzey, R. (1985). Notice of the phytogeographic map of Cameroon at 1/50000. Herbier National Cameroun / Institute of the International Vegetation Map, Toulouse, France.

Mbakop, L. R., Awono-Ambene, P. H., Ekoko, W. E., Mandeng, S. E., Nwane, P., Fesuh, B. N., Toto, J. C., Alenou, L. D., Onguina, H. G., Piameu, M., Fomena, A., & Etang, J. (2022). Malaria transmission and vector resistance to insecticides in a changing environment: Case of Simbock in Yaoundé-City, Cameroon. Frontiers in Tropical Diseases, 3, 902211. https://doi.org/10.3389/fitd.2022.902211

Mbida, J. A., Etang, J., Akono, N. P., Eboumbou, M. C., Awono-Ambene, P., Talipouo, A., Ekoko, A. W., Binyang, G., Tchoffo, R., Lehman, G., & Minpfoundi, R. (2017). New insight into the larval ecology of Anopheles coluzzii Coetzee and Wilkerson, 2013 in the Wouri estuary, Littoral-Cameroon. Bulletin of the Society of Exotic Pathology, 110, 92-101. https://doi.org/10.1007/s13149-016-0519-9

Merritt, R. W., Dadd, R. H., & Walker, E. D. (1992). Feeding behavior, natural diet and nutritional relationships of larval mosquitoes. Annual Review of Entomology, 37, 349-376. https://doi.org/10.1146/annurev.en.37.010192.002025

Moore, C. G., & Fisher, B. R. (1969). Competition in mosquitoes. Density and species ratio effects on growth, mortality, fecundity and production growth retardant. Annals of the Entomological Society of America, 62, 1325-1331. https://doi.org/10.1093/aesa/62.6.1325

Moore, C. G., & Whitacre, D. M. (1972). Competition in mosquitoes. Production of Aedes aegypti larval growth retardant on various densities and nutrition levels. Annals of the Entomological Society of America, 65, 915-918. https://doi.org/10.1093/aesa/65.4.773

MR4 (Malaria Research and Reference Reagent Resource Center). (2010). Methods in Anopheles Research (2nd ed., 343 p.). CDC: Atlanta, GA, USA.

Muturi, E. J., Chang, H. R., Jacob, B. G., Murphy, S., & Novak, R. J. (2010). Interspecies predation between Anopheles gambiae s.s. and Culex quinquefasciatus larvae. Journal of Medical Entomology, 47, 287-290. https://doi.org/10.1603/me09085

Nekrasova, L. (2003). Experimental study on the effects of population density of bloodsucking mosquito (Aedes communis Deg.) larvae

Rejmankova, E., Grieco, J., Achee, N., & Robert, R. (2013). Ecology of larval habitats. In Chapter 13, Collection (pp. 1-51). https://doi.org/10.5772/55229

Roubaud, E., & Toumanoff, C. (1930). Congestion poisoning in Culex larvae living in non-renewed medium. Bulletin of the Society of Exotic Pathology, 23, 978-986.

Sutcliffe, A. C., & Benedict, M. Q. (2012). Effective larval foraging in large low diet environments by Anopheles gambiae. Journal of Entomology, 2012(1), 1-8. https://doi.org/10.1155/2012/480483

Tawidian, P., Coon, K. L., Jumpponen, A., Cohnstaedt, L. W., & Michel, K. (2021). Host environment interplay shapes fungal diversity in mosquitoes. MSphere, 6(10), e00646-21. https://doi.org/10.1128/mSphere.00646-21

World Health Organization. (2024). Global situation, surveillance and progress. Weekly Epidemiological Record, N 52, 26 December 2025.

World Health Organization. (2025). World Malaria Report: Executive summary (21 pp.).

World Meteorological Organization. (2012). Douala 2012 historical weather database. https://weatherspark.com/h/y/61814/2012/Historical-Weather-during-2012-in-Douala-Cameroon

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Published

2026-04-23

How to Cite

Offono Enama, M. L., Laclong Lontchi, R. A., Mbongue, R. S., Mache Nkouandou, P., Foutchou, A., Eyebe, S. B., … Mbida Mbida, J. A. (2026). Impact of feacal coliforms and interspecific cohabitation on the productivity of culicidae breeding sites, littoral-Cameroon. African Journal of Empirical Research, 7(2), 420–428. https://doi.org/10.51867/ajernet.7.2.38

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