The application of drones for mosquito larval habitat identification in rural environments: a practical approach for malaria control?

Michelle C Stanton, Patrick Kalonde, Kennedy Zembere, Remy Hoek Spaans, Christopher M Jones, Michelle C Stanton, Patrick Kalonde, Kennedy Zembere, Remy Hoek Spaans, Christopher M Jones

Abstract

Background: Spatio-temporal trends in mosquito-borne diseases are driven by the locations and seasonality of larval habitat. One method of disease control is to decrease the mosquito population by modifying larval habitat, known as larval source management (LSM). In malaria control, LSM is currently considered impractical in rural areas due to perceived difficulties in identifying target areas. High resolution drone mapping is being considered as a practical solution to address this barrier. In this paper, the authors' experiences of drone-led larval habitat identification in Malawi were used to assess the feasibility of this approach.

Methods: Drone mapping and larval surveys were conducted in Kasungu district, Malawi between 2018 and 2020. Water bodies and aquatic vegetation were identified in the imagery using manual methods and geographical object-based image analysis (GeoOBIA) and the performances of the classifications were compared. Further, observations were documented on the practical aspects of capturing drone imagery for informing malaria control including cost, time, computing, and skills requirements. Larval sampling sites were characterized by biotic factors visible in drone imagery and generalized linear mixed models were used to determine their association with larval presence.

Results: Imagery covering an area of 8.9 km2 across eight sites was captured. Larval habitat characteristics were successfully identified using GeoOBIA on images captured by a standard camera (median accuracy = 98%) with no notable improvement observed after incorporating data from a near-infrared sensor. This approach however required greater processing time and technical skills compared to manual identification. Larval samples captured from 326 sites confirmed that drone-captured characteristics, including aquatic vegetation presence and type, were significantly associated with larval presence.

Conclusions: This study demonstrates the potential for drone-acquired imagery to support mosquito larval habitat identification in rural, malaria-endemic areas, although technical challenges were identified which may hinder the scale up of this approach. Potential solutions have however been identified, including strengthening linkages with the flourishing drone industry in countries such as Malawi. Further consultations are therefore needed between experts in the fields of drones, image analysis and vector control are needed to develop more detailed guidance on how this technology can be most effectively exploited in malaria control.

Keywords: Anopheles; Drones; Larval habitat; Machine-learning; Malaria; Mapping; Mosquito; Object-based image classification.

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Locations of sites surveyed within the ‘humanitarian drone testing corridor’, centred on Kasungu town, Central Malawi (inset). Coordinates can be found in Additional file 1
Fig. 2
Fig. 2
Processes undertaken to identify larval habitat from drone imagery
Fig. 3
Fig. 3
Image captured by the Phantom 4 Pro in Kasungu in February 2020 covering 800 m by 600 m, with each grid representing 200 m by 200 m. Grids 4, 5, 7 and 8 were used for training the classification algorithm, and an assessment of its accuracy was made using features both within this area (interpolation) and in the surrounding grids (extrapolation)
Fig. 4
Fig. 4
Examples of the segmentation process under different values for spatial radius s (0,10, 30), range radius r (25, 50) with a minimum segment size of 100. Time t corresponds to the time taken in seconds to segment a 100 m by 100 m image with a spatial resolution of 3 cm using the LargeScaleMeanShift algorithm in Orfeo Toolbox. This process includes calculating the mean and variance of the RGB and elevation values for each segment
Fig. 5
Fig. 5
Boxplots of class-level user and producer accuracy for the classifications undertaken without using NIR-derived variables
Fig. 6
Fig. 6
Example of a classification obtained for the entire study area using the random forests algorithm without including NIR-derived variables (left), with a more detailed view of a smaller area comparing the original image (top right) with the classified image (bottom right)
Fig. 7
Fig. 7
Examples of sampling sites where anopheline larvae were found. The top row indicates the precise GPS location captured using ODK (yellow circle), the expected sampling area based on these coordinates (1 m radius), and the expected accuracy of the coordinates (3 m radius), overlaid on top of the drone imagery. The middle row presents the classified imagery for these sites and the bottom row contains photographs of each site taken at the time of sampling
Fig. 8
Fig. 8
Comparisons of aerial images captured at different seasonal time points. Left images display a comparison between consecutive dry (Oct 2019) and wet (Feb 2020) seasons around the Malangano dam. Right images display comparisons between dry seasons over 2 consecutive years (June 2018, Oct 2019) around the Chitete dam

References

    1. Stresman G, Bousema T, Cook J. Malaria hotspots: is there epidemiological evidence for fine-scale spatial targeting of interventions? Trends Parasitol. 2019;35:822–34. doi: 10.1016/j.pt.2019.07.013.
    1. Bousema T, Stresman G, Baidjoe AY, et al. The impact of hotspot-targeted interventions on malaria transmission in Rachuonyo South District in the Western Kenyan Highlands: a cluster-randomized controlled trial. PLoS Med. 2016;13:e1001993. doi: 10.1371/journal.pmed.1001993.
    1. Hsiang MS, Ntuku H, Roberts KW, Dufour MSK, Whittemore B, Tambo M, et al. Effectiveness of reactive focal mass drug administration and reactive focal vector control to reduce malaria transmission in the low malaria-endemic setting of Namibia: a cluster-randomised controlled, open-label, two-by-two factorial design trial. Lancet. 2020;395:1361–73. doi: 10.1016/S0140-6736(20)30470-0.
    1. Sy O, Niang EHA, Diallo A, Ndiaye A, Konaté L, Ba EHCC, et al. Evaluation of the effectiveness of a targeted community-based IRS approach for malaria elimination in an area of low malaria transmission of the central-western Senegal. Parasite Epidemiol Control. 2019;6:e00109. doi: 10.1016/j.parepi.2019.e00109.
    1. Nambunga IH, Ngowo HS, Mapua SA, Hape EE, Msugupakulya BJ, Msaky DS, et al. Aquatic habitats of the malaria vector Anopheles funestus in rural south-eastern Tanzania. Malar J. 2020;19:219. doi: 10.1186/s12936-020-03295-5.
    1. Gowelo SA, Chirombo J, Koenraadt CJM, Mzilahowa T, Berg H, Takken W, et al. Characterisation of anopheline larval habitats in southern Malawi. Acta Trop. 2020;210:105558. doi: 10.1016/j.actatropica.2020.105558.
    1. Eneh LK, Fillinger U, Borg Karlson AK, Kuttuva Rajarao G, Lindh J. Anopheles arabiensis oviposition site selection in response to habitat persistence and associated physicochemical parameters, bacteria and volatile profiles. Med Vet Entomol. 2019;33:56–67. doi: 10.1111/mve.12336.
    1. Musiime AK, Smith DL, Kilama M, Geoffrey O, Kyagamba P, Rek J, et al. Identification and characterization of immature Anopheles and culicines (Diptera: Culicidae) at three sites of varying malaria transmission intensities in Uganda. Malar J. 2020;19:221. doi: 10.1186/s12936-020-03304-7.
    1. Beck-Johnson LM, Nelson WA, Paaijmans KP, Read AF, Thomas MB, Bjørnstad ON. The effect of temperature on Anopheles mosquito population dynamics and the potential for malaria transmission. PLoS ONE. 2013;8:79276. doi: 10.1371/journal.pone.0079276.
    1. Vantaux A, Ouattarra I, Lefèvre T, Dabiré KR. Effects of larvicidal and larval nutritional stresses on Anopheles gambiae development, survival and competence for Plasmodium falciparum. Parasit Vectors. 2016;9:226. doi: 10.1186/s13071-016-1514-5.
    1. WHO. Larval source management—a supplementary measure for malaria vector control. An operational manual. Geneva, World Health Organization. 2013. .
    1. Tusting LS, Thwing J, Sinclair D, Fillinger U, Gimnig J, Bonner KE, et al. Mosquito larval source management for controlling malaria. Cochrane Database Syst Rev. 2013;CD008923.
    1. Fillinger U, Lindsay SW. Larval source management for malaria control in Africa: myths and reality. Malar J. 2011;10:353. doi: 10.1186/1475-2875-10-353.
    1. Killeen GF. Characterizing, controlling and eliminating residual malaria transmission. Malar J. 2014;13:330. doi: 10.1186/1475-2875-13-330.
    1. Hardy A, Makame M, Cross D, Majambere S, Msellem M. Using low-cost drones to map malaria vector habitats. Parasit Vectors. 2017;10:29. doi: 10.1186/s13071-017-1973-3.
    1. Carrasco-Escobar G, Manrique E, Ruiz-Cabrejos J, Saavedra M, Alava F, Bickersmith S, et al. High-accuracy detection of malaria vector larval habitats using drone-based multispectral imagery. PLoS Negl Trop Dis. 2019;13:e0007105. doi: 10.1371/journal.pntd.0007105.
    1. Tokarz R, Novak RJ. Spatial–temporal distribution of Anopheles larval habitats in Uganda using GIS/remote sensing technologies. Malar J. 2018;17:420. doi: 10.1186/s12936-018-2567-z.
    1. Hardy A, Ettritch G, Cross D, Bunting P, Liywalii F, Sakala J, et al. Automatic detection of open and vegetated water bodies using sentinel 1 to map African malaria vector mosquito breeding habitats. Remote Sens. 2019;11:593. doi: 10.3390/rs11050593.
    1. Chipeta MG, Giorgi E, Mategula D, Macharia PM, Ligomba C, Munyenyembe A, et al. Geostatistical analysis of Malawi’s changing malaria transmission from 2010 to 2017. Wellcome Open Res. 2019;4:57. doi: 10.12688/wellcomeopenres.15193.2.
    1. Kibret S, Lautze J, McCartney M, Nhamo L, Wilson GG. Malaria and large dams in sub-Saharan Africa: future impacts in a changing climate. Malar J. 2016;15:448. doi: 10.1186/s12936-016-1498-9.
    1. Sentera. 2020. .
    1. Anderson K, Westoby MJ, James MR. Low-budget topographic surveying comes of age: structure from motion photogrammetry in geography and the geosciences. Prog Phys Geogr Earth Environ. 2019;43:163–73. doi: 10.1177/0309133319837454.
    1. Haralick RM, Dinstein I, Shanmugam K. Textural features for image classification. IEEE Trans Syst Man Cybern. 1973;SMC-3:610–21. doi: 10.1109/TSMC.1973.4309314.
    1. Kuhn M. Building predictive models in R using the caret package. J Stat Softw. 2008;28:1–26. doi: 10.18637/jss.v028.i05.
    1. De Luca G, Silva N, Cerasoli JM, Araújo S, Campos J, Di Fazio J, et al. Object-based land cover classification of cork oak woodlands using UAV imagery and Orfeo ToolBox. Remote Sens. 2019;11:1238. doi: 10.3390/rs11101238.
    1. Ma L, Fu T, Blaschke T, Li M, Tiede D, Zhou Z, et al. Evaluation of feature selection methods for object-based land cover mapping of unmanned aerial vehicle imagery using random forest and support vector machine classifiers. ISPRS Int J Geo-Inf. 2017;6:51. doi: 10.3390/ijgi6020051.
    1. Pontius RG, Millones M. Death to Kappa: Birth of quantity disagreement and allocation disagreement for accuracy assessment. Int J Remote Sens. 2011;32:4407–29. doi: 10.1080/01431161.2011.552923.
    1. Coetzee M. Key to the females of Afrotropical Anopheles mosquitoes (Diptera: Culicidae) Malar J. 2020;19:70. doi: 10.1186/s12936-020-3144-9.
    1. Stanton MC. Figshare dataset: larval sampling data, Kasungu. Figshare. 2020. .
    1. Standridge Z. Design and development of low-cost multi-function UAV suitable for production and operation in low resource environments. Thesis, MSc Aerospace Engineering, Virginia Polytechnic Institute and State University; 2018.
    1. UNICEF. African Drone and Data Academy. 2020. .
    1. Hossain MD, Chen D. Segmentation for Object-Based Image Analysis (OBIA): a review of algorithms and challenges from remote sensing perspective. J Photogramm Remote Sens. 2019;150:115–34. doi: 10.1016/j.isprsjprs.2019.02.009.
    1. Pande-Chhetri R, Abd-Elrahman A, Liu T, Morton J, Wilhelm VL. Object-based classification of wetland vegetation using very high-resolution unmanned air system imagery. Eur J Remote Sens. 2017;50:564–76. doi: 10.1080/22797254.2017.1373602.
    1. Khanh Ni TN, Tin HC, Thach VT, Jamet C, Saizen I. Mapping submerged aquatic vegetation along the central Vietnamese coast using multi-source remote sensing. Int J Geo-Inf. 2020;9:395. doi: 10.3390/ijgi9060395.
    1. DroneDeploy. Introducing map engine. 2018. .
    1. Mutanga O, Kumar L. Google earth engine applications. Remote Sens. 2019;11:591. doi: 10.3390/rs11050591.
    1. Hardy A, Oakes G, Ettritch G. Tropical wetland (TropWet) mapping tool: the automatic detection of open and vegetated waterbodies in Google Earth engine for tropical wetlands. Remote Sens. 2020;12:1182. doi: 10.3390/rs12071182.

Source: PubMed

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