» Articles » PMID: 30290799

Shady Business: Understanding the Spatial Ecology of Exophilic Anopheles Mosquitoes

Overview
Journal Malar J
Publisher Biomed Central
Specialty Tropical Medicine
Date 2018 Oct 7
PMID 30290799
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Understanding the ecology of exophilic anophelines is a key step toward developing outdoor control strategies to complement existing indoor control tools against malaria vectors. This study was conducted to assess the movement pattern of exophilic Anopheles mosquitoes between blood meal sources and resting habitats, and the landscape factors dictating their resting habitat choice.

Results: Resting clay pots were placed at 5 m, 25 m, 50 m, 75 m and 100 m away from isolated focal houses, radiating from them in four directions. The locations of the clay pots represent heterogeneous land cover types at a relatively fine spatial scale in the landscape. The effect of the landscape characters on the number of both female and male anophelines caught was modelled using zero-inflated negative binomial regression with a log link function. A total of 420 Anopheles mosquitoes (353 females and 67 males) belonging to three species; Anopheles arabiensis, Anopheles pharoensis, and Anopheles tenebrosus were caught in the resting clay pots, with An. arabiensis being the dominant species. Canopy cover, distance from the house, and land cover type were the significant landscape characters influencing the aggregation of resting mosquitoes. Both the count and binary models showed that canopy cover was the strongest predictor variable on the counts and the presence of Anopheles mosquitoes in the clay pots. Female Anopheles were most frequently found resting in the pots placed in banana plantations, and at sampling points that were at the greater distances (75 m and 100 m) from the focal house.

Conclusions: This study showed that exophilic Anopheles mosquitoes tend to rest in shaded areas some distance away from human habitation. These findings are important when targeting mosquitoes outdoors, complementing the existing effort being made to control malaria vectors indoors.

Citing Articles

Transmission of transgenic mosquito-killing fungi during copulation.

Bilgo E, Lovett B, Millogo A, Sare I, Gnambani E, Leger R Sci Rep. 2025; 15(1):2181.

PMID: 39819965 PMC: 11739586. DOI: 10.1038/s41598-024-83242-5.


Mosquito odour-baited mass trapping reduced malaria transmission intensity: a result from a controlled before-and-after intervention study.

Debebe Y, Tekie H, Dugassa S, Hopkins R, Hill S, Ignell R BMC Med. 2024; 22(1):41.

PMID: 38281908 PMC: 10823605. DOI: 10.1186/s12916-024-03255-9.


Fine-scale mapping of urban malaria exposure under data scarcity: an approach centred on vector ecology.

Vanhuysse S, Diedhiou S, Grippa T, Georganos S, Konate L, Niang E Malar J. 2023; 22(1):113.

PMID: 37009873 PMC: 10069057. DOI: 10.1186/s12936-023-04527-0.


Outdoor and early hour human biting activities of malaria mosquitoes and the suitability of clay pot for outdoor resting mosquito collection in malaria endemic villages of southern Rift Valley, Ethiopia.

Tomas T, Eligo N, Tamiru G, Massebo F Parasite Epidemiol Control. 2022; 19:e00278.

PMID: 36345433 PMC: 9636569. DOI: 10.1016/j.parepi.2022.e00278.


Impact of cattle on the abundance of indoor and outdoor resting malaria vectors in southern Malawi.

Mburu M, Zembere K, Mzilahowa T, Terlouw A, Malenga T, van den Berg H Malar J. 2021; 20(1):353.

PMID: 34446033 PMC: 8390081. DOI: 10.1186/s12936-021-03885-x.


References
1.
Zhu L, Muller G, Marshall J, Arheart K, Qualls W, Hlaing W . Is outdoor vector control needed for malaria elimination? An individual-based modelling study. Malar J. 2017; 16(1):266. PMC: 5496196. DOI: 10.1186/s12936-017-1920-y. View

2.
Sougoufara S, Doucoure S, Backe Sembene P, Harry M, Sokhna C . Challenges for malaria vector control in sub-Saharan Africa: Resistance and behavioral adaptations in populations. J Vector Borne Dis. 2017; 54(1):4-15. View

3.
Githeko A, Service M, Mbogo C, Atieli F . Resting behaviour, ecology and genetics of malaria vectors in large scale agricultural areas of Western Kenya. Parassitologia. 1996; 38(3):481-9. View

4.
Diuk-Wasser M, Brown H, Andreadis T, Fish D . Modeling the spatial distribution of mosquito vectors for West Nile virus in Connecticut, USA. Vector Borne Zoonotic Dis. 2006; 6(3):283-95. DOI: 10.1089/vbz.2006.6.283. View

5.
Ranson H, NGuessan R, Lines J, Moiroux N, Nkuni Z, Corbel V . Pyrethroid resistance in African anopheline mosquitoes: what are the implications for malaria control?. Trends Parasitol. 2010; 27(2):91-8. DOI: 10.1016/j.pt.2010.08.004. View