Cargando…
Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission
BACKGROUND: Chagas disease, a vector-borne parasitic disease caused by Trypanosoma cruzi, affects millions in the Americas. Dogs are important reservoirs of the parasite. Under laboratory conditions, canine treatment with the systemic insecticide fluralaner demonstrated efficacy in killing Triatoma...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901065/ https://www.ncbi.nlm.nih.gov/pubmed/36747723 http://dx.doi.org/10.1101/2023.01.24.23284917 |
_version_ | 1784882966820814848 |
---|---|
author | Rokhsar, Jennifer L. Raynor, Brinkley Sheen, Justin Goldstein, Neal D. Levy, Michael Z. Castillo-Neyra, Ricardo |
author_facet | Rokhsar, Jennifer L. Raynor, Brinkley Sheen, Justin Goldstein, Neal D. Levy, Michael Z. Castillo-Neyra, Ricardo |
author_sort | Rokhsar, Jennifer L. |
collection | PubMed |
description | BACKGROUND: Chagas disease, a vector-borne parasitic disease caused by Trypanosoma cruzi, affects millions in the Americas. Dogs are important reservoirs of the parasite. Under laboratory conditions, canine treatment with the systemic insecticide fluralaner demonstrated efficacy in killing Triatoma infestans and T. brasiliensis, T. cruzi vectors, when they feed on dogs. This form of pest control is called xenointoxication. However, T. cruzi can also be transmitted orally when mammals ingest infected bugs, so there is potential for dogs to become infected upon consuming infected bugs killed by the treatment. Xenointoxication thereby has two contrasting effects on dogs: decreasing the number of insects feeding on the dogs but increasing opportunities for exposure to T. cruzi via oral transmission to dogs ingesting infected insects. OBJECTIVE: Examine the potential for increased infection rates of T. cruzi in dogs following xenointoxication. DESIGN/METHODS: We built a deterministic mathematical model, based on the Ross-MacDonald malaria model, to investigate the net effect of fluralaner treatment on the prevalence of T. cruzi infection in dogs in different epidemiologic scenarios. We drew upon published data on the change in percentage of bugs killed that fed on treated dogs over days post treatment. Parameters were adjusted to mimic three scenarios of T. cruzi transmission: high and low disease prevalence and domestic vectors, and low disease prevalence and sylvatic vectors. RESULTS: In regions with high endemic disease prevalence in dogs and domestic vectors, prevalence of infected dogs initially increases but subsequently declines before eventually rising back to the initial equilibrium following one fluralaner treatment. In regions of low prevalence and domestic or sylvatic vectors, however, treatment seems to be detrimental. In these regions our models suggest a potential for a rise in dog prevalence, due to oral transmission from dead infected bugs. CONCLUSION: Xenointoxication could be a beneficial and novel One Health intervention in regions with high prevalence of T. cruzi and domestic vectors. In regions with low prevalence and domestic or sylvatic vectors, there is potential harm. Field trials should be carefully designed to closely follow treated dogs and include early stopping rules if incidence among treated dogs exceeds that of controls. |
format | Online Article Text |
id | pubmed-9901065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-99010652023-02-07 Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission Rokhsar, Jennifer L. Raynor, Brinkley Sheen, Justin Goldstein, Neal D. Levy, Michael Z. Castillo-Neyra, Ricardo medRxiv Article BACKGROUND: Chagas disease, a vector-borne parasitic disease caused by Trypanosoma cruzi, affects millions in the Americas. Dogs are important reservoirs of the parasite. Under laboratory conditions, canine treatment with the systemic insecticide fluralaner demonstrated efficacy in killing Triatoma infestans and T. brasiliensis, T. cruzi vectors, when they feed on dogs. This form of pest control is called xenointoxication. However, T. cruzi can also be transmitted orally when mammals ingest infected bugs, so there is potential for dogs to become infected upon consuming infected bugs killed by the treatment. Xenointoxication thereby has two contrasting effects on dogs: decreasing the number of insects feeding on the dogs but increasing opportunities for exposure to T. cruzi via oral transmission to dogs ingesting infected insects. OBJECTIVE: Examine the potential for increased infection rates of T. cruzi in dogs following xenointoxication. DESIGN/METHODS: We built a deterministic mathematical model, based on the Ross-MacDonald malaria model, to investigate the net effect of fluralaner treatment on the prevalence of T. cruzi infection in dogs in different epidemiologic scenarios. We drew upon published data on the change in percentage of bugs killed that fed on treated dogs over days post treatment. Parameters were adjusted to mimic three scenarios of T. cruzi transmission: high and low disease prevalence and domestic vectors, and low disease prevalence and sylvatic vectors. RESULTS: In regions with high endemic disease prevalence in dogs and domestic vectors, prevalence of infected dogs initially increases but subsequently declines before eventually rising back to the initial equilibrium following one fluralaner treatment. In regions of low prevalence and domestic or sylvatic vectors, however, treatment seems to be detrimental. In these regions our models suggest a potential for a rise in dog prevalence, due to oral transmission from dead infected bugs. CONCLUSION: Xenointoxication could be a beneficial and novel One Health intervention in regions with high prevalence of T. cruzi and domestic vectors. In regions with low prevalence and domestic or sylvatic vectors, there is potential harm. Field trials should be carefully designed to closely follow treated dogs and include early stopping rules if incidence among treated dogs exceeds that of controls. Cold Spring Harbor Laboratory 2023-01-25 /pmc/articles/PMC9901065/ /pubmed/36747723 http://dx.doi.org/10.1101/2023.01.24.23284917 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Rokhsar, Jennifer L. Raynor, Brinkley Sheen, Justin Goldstein, Neal D. Levy, Michael Z. Castillo-Neyra, Ricardo Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission |
title | Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission |
title_full | Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission |
title_fullStr | Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission |
title_full_unstemmed | Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission |
title_short | Modeling the impact of xenointoxication in dogs to halt Trypanosoma cruzi transmission |
title_sort | modeling the impact of xenointoxication in dogs to halt trypanosoma cruzi transmission |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901065/ https://www.ncbi.nlm.nih.gov/pubmed/36747723 http://dx.doi.org/10.1101/2023.01.24.23284917 |
work_keys_str_mv | AT rokhsarjenniferl modelingtheimpactofxenointoxicationindogstohalttrypanosomacruzitransmission AT raynorbrinkley modelingtheimpactofxenointoxicationindogstohalttrypanosomacruzitransmission AT sheenjustin modelingtheimpactofxenointoxicationindogstohalttrypanosomacruzitransmission AT goldsteinneald modelingtheimpactofxenointoxicationindogstohalttrypanosomacruzitransmission AT levymichaelz modelingtheimpactofxenointoxicationindogstohalttrypanosomacruzitransmission AT castilloneyraricardo modelingtheimpactofxenointoxicationindogstohalttrypanosomacruzitransmission |