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Implementing a community vector collection strategy using xenomonitoring for the endgame of lymphatic filariasis elimination

Author:
Pi-Bansa, Sellase, Osei, Joseph Harold Nyarko, Joannides, Joannitta, Woode, Maame Esi, Agyemang, David, Elhassan, Elizabeth, Dadzie, Samuel Kweku, Appawu, Maxwell Alexander, Wilson, Michael David, Koudou, Benjamin Guibehi, de Souza, Dziedzom Komi, Utzinger, Jürg, Boakye, Daniel Adjei
Source:
Parasites & vectors 2018 v.11 no.1 pp. 672
ISSN:
1756-3305
Subject:
Bancroftian filariasis, Culicidae, Wuchereria bancrofti, blood, collectors, data analysis, drugs, humans, microfilariae, motivation, quality control, sampling, supervisors, traps
Abstract:
BACKGROUND: The global strategy for elimination of lymphatic filariasis is by annual mass drug administration (MDA). Effective implementation of this strategy in endemic areas reduces Wuchereria bancrofti in the blood of infected individuals to very low levels. This minimises the rate at which vectors successfully pick microfilariae from infected blood, hence requiring large mosquito numbers to detect infections. The aim of this study was to assess the feasibility of using trained community vector collectors (CVCs) to sample large mosquito numbers with minimal supervision at low cost for potential scale-up of this strategy. METHODS: CVCs and supervisors were trained in mosquito sampling methods, i.e. human landing collections, pyrethrum spray collections and window exit traps. Mosquito sampling was done over a 13-month period. Validation was conducted by a research team as quality control for mosquitoes sampled by CVCs. Data were analyzed for number of mosquitoes collected and cost incurred by the research team and CVCs during the validation phase of the study. RESULTS: A total of 31,064 and 8720 mosquitoes were sampled by CVCs and the research team, respectively. We found a significant difference (F₍₁,₁₃₎ = 27.1606, P = 0.0001) in the total number of mosquitoes collected from southern and northern communities. Validation revealed similar numbers of mosquitoes sampled by CVCs and the research team, both in the wet (F₍₁,₄₎ = 1.875, P = 0.309) and dry (F₍₁,₄₎ = 2.276, P = 0.258) seasons in the southern communities, but was significantly different for both wet (F₍₁,₄₎ = 0.022, P = 0.005) and dry (F₍₁,₄ ₎ = 0.079, P = 0.033) seasons in the north. The cost of sampling mosquitoes per season was considerably lower by CVCs compared to the research team (15.170 vs 53.739 USD). CONCLUSIONS: This study revealed the feasibility of using CVCs to sample large numbers of mosquitoes with minimal supervision from a research team at considerably lower cost than a research team for lymphatic filariasis xenomonitoring. However, evaluation of the selection and motivation of CVCs, acceptability of CVCs strategy and its epidemiological relevance for lymphatic filariasis xenomonitoring programmes need to be assessed in greater detail.
Agid:
6267825