Modelling livestock test-and-treat: A novel One Health strategy to control schistosomiasis and mitigate drug resistance
2022
Díaz, Adriana, V. | Lambert, Sébastien | Neves, M. Inês | Borlase, Anna | Léger, Elsa | Diouf, Nicolas, D. | Sène, Mariama | Webster, Joanne, P. | Walker, Martin | Department of Pathobiology and Population Sciences ; Royal Veterinary College | Department of Infectious Disease Epidemiology [London] (DIDE) ; Imperial College London | Interactions hôtes-agents pathogènes [Toulouse] (IHAP) ; Ecole Nationale Vétérinaire de Toulouse (ENVT) ; Institut National Polytechnique (Toulouse) (Toulouse INP) ; Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National Polytechnique (Toulouse) (Toulouse INP) ; Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE) | Big Data Institute ; University of Oxford | Université Gaston Berger - UFR Sciences Agronomiques, de l'Aquaculture et des Technologies Alimentaires [Sénégal] (UFR S2ATA) ; Université Gaston Berger de Saint-Louis Sénégal (UGB) | AD was funded by a Biotechnology and Biological Sciences Research Council (BBSRC) (London Interdisciplinary Doctoral Training Program funding studentship, grant number BB/M009513/1) under the supervision of JW and MW. The larger project that this work was embedded within was funded by the BBSRC, the Department for International Development, the Economic & Social Research Council, the Medical Research Council, the Natural Environment Research Council and the Defence Science & Technology Laboratory, under the Zoonoses and Emerging Livestock Systems (ZELS : SR) program (grant number BB/S013822/1: ‘CATTLES - Control And Targeted Treatment for Livestock Emerging Schistosomiasis’); PI: JW, co-I MW, co-Is within Senegal: MS and ND), and a Research England grant: The Bloomsbury SET - Connecting Capability to Combat Infectious Disease and Antimicrobial Resistance project (grant number CCF-17-7779; PI: JW, co-Is MW and EL).
Data availability statement: The original contributions presented in the study are publicly available. Code for dynamic transmission model and associated data available at https://github.com/martwalker/schistoTnT and for the statistical model at https://github.com/martwalker/trueprev. Further inquiries can be directed to the corresponding authors.Ethics statement: The animal study was reviewed and approved by: (i) Imperial College London (London, UK) application 03.36; (ii) the CRERB at the Royal Veterinary College (London, UK) application URN20151327; and (iii) the Comité National d’Ethique pour la Recherche en Santé (Dakar, Senegal) application SEN15/68. Written informed consent was obtained from the owners for the participation of their animals in this study.
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Show more [+] Less [-]English. Schistosomiasis, a neglected tropical disease, is a widespread chronic helminthiasis reported in 78 countries, predominantly those within sub-Saharan Africa, as well as Latin America, Asia, and most recently, even Europe. Species of the causative blood fluke infect not only humans but also animals, and hybrids between previously assumed human-specific and animal-specific schistosomes are being increasingly reported. Existing control programs across Africa focus on humans and rely heavily on mass drug administration of praziquantel, the sole drug available against schistosomiasis. Praziquantel is safe and highly efficacious but could become ineffective if resistance emerges. To reach the revised World Health Organization goal of elimination of schistosomiasis as a public health problem, and interruption of transmission within selected regions, by 2030, new consideration of the role of animal reservoirs in human transmission in general, and whether to also treat livestock with praziquantel in particular, has been raised. However, whilst there are no dedicated control programs targeting animals outside of Asia, there are emerging reports of the use and misuse of praziquantel in livestock across Africa. Therefore, to effectively treat livestock in Africa and to help mitigate against the potential evolution of praziquantel resistance, structured control strategies are required. Here, using a transmission modelling approach, we evaluate the potential effectiveness of a theoretical test-and-treat (TnT) strategy to control bovine schistosomiasis using a currently available point-of-care diagnostic test (developed for human use) to detect circulating cathodic antigen (POC-CCA). We show that implementing TnT at herd-level from 2022 to 2030 could be highly effective in suppressing infection in cattle and even, in lower prevalence settings, reaching nominal ‘elimination’ targets. We highlight the importance of enhancing the specificity of POC-CCA for use in livestock to avoid unnecessary treatments and discuss the outstanding challenges associated with implementing TnT as part of a holistic One Health approach to tackling human and animal schistosomiasis.
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