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Comorbid infections induce progression of visceral leishmaniasis

BACKGROUND: Visceral leishmaniasis (VL) is a vector borne zoonotic disease endemic in humans and dogs in Brazil. Due to the increased risk of human infection secondary to the presence of infected dogs, public health measures in Brazil mandate testing and culling of infected dogs. Despite this import...

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Autores principales: Toepp, Angela J., Monteiro, Glória R. G., Coutinho, José F. V., Lima, Adam Leal, Larson, Mandy, Wilson, Geneva, Grinnage-Pulley, Tara, Bennett, Carolyne, Mahachi, Kurayi, Anderson, Bryan, Ozanne, Marie V., Anderson, Michael, Fowler, Hailie, Parrish, Molly, Willardson, Kelsey, Saucier, Jill, Tyrell, Phyllis, Palmer, Zachary, Buch, Jesse, Chandrashekar, Ramaswamy, Brown, Grant D., Oleson, Jacob J., Jeronimo, Selma M. B., Petersen, Christine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345068/
https://www.ncbi.nlm.nih.gov/pubmed/30674329
http://dx.doi.org/10.1186/s13071-019-3312-3
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author Toepp, Angela J.
Monteiro, Glória R. G.
Coutinho, José F. V.
Lima, Adam Leal
Larson, Mandy
Wilson, Geneva
Grinnage-Pulley, Tara
Bennett, Carolyne
Mahachi, Kurayi
Anderson, Bryan
Ozanne, Marie V.
Anderson, Michael
Fowler, Hailie
Parrish, Molly
Willardson, Kelsey
Saucier, Jill
Tyrell, Phyllis
Palmer, Zachary
Buch, Jesse
Chandrashekar, Ramaswamy
Brown, Grant D.
Oleson, Jacob J.
Jeronimo, Selma M. B.
Petersen, Christine A.
author_facet Toepp, Angela J.
Monteiro, Glória R. G.
Coutinho, José F. V.
Lima, Adam Leal
Larson, Mandy
Wilson, Geneva
Grinnage-Pulley, Tara
Bennett, Carolyne
Mahachi, Kurayi
Anderson, Bryan
Ozanne, Marie V.
Anderson, Michael
Fowler, Hailie
Parrish, Molly
Willardson, Kelsey
Saucier, Jill
Tyrell, Phyllis
Palmer, Zachary
Buch, Jesse
Chandrashekar, Ramaswamy
Brown, Grant D.
Oleson, Jacob J.
Jeronimo, Selma M. B.
Petersen, Christine A.
author_sort Toepp, Angela J.
collection PubMed
description BACKGROUND: Visceral leishmaniasis (VL) is a vector borne zoonotic disease endemic in humans and dogs in Brazil. Due to the increased risk of human infection secondary to the presence of infected dogs, public health measures in Brazil mandate testing and culling of infected dogs. Despite this important relationship between human and canine infection, little is known about what makes the dog reservoir progress to clinical illness, significantly tied to infectiousness to sand flies. Dogs in endemic areas of Brazil are exposed to many tick-borne pathogens, which are likely to alter the immune environment and thus control of L. infantum. RESULTS: A cross-sectional study of 223 dogs from an area of Natal, in the Rio Grande do Norte, Brazil, were studied to determine the association between comorbid tick-borne disease and Leishmania infection in this endemic area. The risk of Leishmania seropositivity was 1.68× greater in dogs with tick-borne disease seropositivity compared to those without (Adjusted RR: 1.68, 95% CI: 1.09–2.61, P = 0.019). A longitudinal study of 214 hunting dogs in the USA was conducted to determine the causal relationship between infection with tick-borne diseases and progression of VL. Hunting dogs were evaluated three times across a full tick season to detect incident infection with tick-borne diseases. A logistic regression model with generalized estimating equations to estimate the parameters was used to determine how exposure to tick-borne disease altered VL progression over these three time points when controlling for other variables. Dogs infected with three or more tick-borne diseases were 11× more likely to be associated with progression to clinical VL than dogs with no tick-borne disease (Adjusted RR: 11.64, 95% CI: 1.22–110.99, P = 0.03). Dogs with exposure to both Leishmania spp. and tick-borne diseases were five times more likely to die during the study period (RR: 4.85, 95% CI: 1.65–14.24, P = 0.0051). CONCLUSIONS: Comorbid tick-borne diseases dramatically increased the likelihood that a dog had clinical L. infantum infection, making them more likely to transmit infection to sand flies and people. As an important consequence, reduction of tick-borne disease exposure through topical or oral insecticides may be an important way to reduce progression and transmissibility of Leishmania infection from the canine reservoir to people. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3312-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-63450682019-01-29 Comorbid infections induce progression of visceral leishmaniasis Toepp, Angela J. Monteiro, Glória R. G. Coutinho, José F. V. Lima, Adam Leal Larson, Mandy Wilson, Geneva Grinnage-Pulley, Tara Bennett, Carolyne Mahachi, Kurayi Anderson, Bryan Ozanne, Marie V. Anderson, Michael Fowler, Hailie Parrish, Molly Willardson, Kelsey Saucier, Jill Tyrell, Phyllis Palmer, Zachary Buch, Jesse Chandrashekar, Ramaswamy Brown, Grant D. Oleson, Jacob J. Jeronimo, Selma M. B. Petersen, Christine A. Parasit Vectors Research BACKGROUND: Visceral leishmaniasis (VL) is a vector borne zoonotic disease endemic in humans and dogs in Brazil. Due to the increased risk of human infection secondary to the presence of infected dogs, public health measures in Brazil mandate testing and culling of infected dogs. Despite this important relationship between human and canine infection, little is known about what makes the dog reservoir progress to clinical illness, significantly tied to infectiousness to sand flies. Dogs in endemic areas of Brazil are exposed to many tick-borne pathogens, which are likely to alter the immune environment and thus control of L. infantum. RESULTS: A cross-sectional study of 223 dogs from an area of Natal, in the Rio Grande do Norte, Brazil, were studied to determine the association between comorbid tick-borne disease and Leishmania infection in this endemic area. The risk of Leishmania seropositivity was 1.68× greater in dogs with tick-borne disease seropositivity compared to those without (Adjusted RR: 1.68, 95% CI: 1.09–2.61, P = 0.019). A longitudinal study of 214 hunting dogs in the USA was conducted to determine the causal relationship between infection with tick-borne diseases and progression of VL. Hunting dogs were evaluated three times across a full tick season to detect incident infection with tick-borne diseases. A logistic regression model with generalized estimating equations to estimate the parameters was used to determine how exposure to tick-borne disease altered VL progression over these three time points when controlling for other variables. Dogs infected with three or more tick-borne diseases were 11× more likely to be associated with progression to clinical VL than dogs with no tick-borne disease (Adjusted RR: 11.64, 95% CI: 1.22–110.99, P = 0.03). Dogs with exposure to both Leishmania spp. and tick-borne diseases were five times more likely to die during the study period (RR: 4.85, 95% CI: 1.65–14.24, P = 0.0051). CONCLUSIONS: Comorbid tick-borne diseases dramatically increased the likelihood that a dog had clinical L. infantum infection, making them more likely to transmit infection to sand flies and people. As an important consequence, reduction of tick-borne disease exposure through topical or oral insecticides may be an important way to reduce progression and transmissibility of Leishmania infection from the canine reservoir to people. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3312-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-23 /pmc/articles/PMC6345068/ /pubmed/30674329 http://dx.doi.org/10.1186/s13071-019-3312-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Toepp, Angela J.
Monteiro, Glória R. G.
Coutinho, José F. V.
Lima, Adam Leal
Larson, Mandy
Wilson, Geneva
Grinnage-Pulley, Tara
Bennett, Carolyne
Mahachi, Kurayi
Anderson, Bryan
Ozanne, Marie V.
Anderson, Michael
Fowler, Hailie
Parrish, Molly
Willardson, Kelsey
Saucier, Jill
Tyrell, Phyllis
Palmer, Zachary
Buch, Jesse
Chandrashekar, Ramaswamy
Brown, Grant D.
Oleson, Jacob J.
Jeronimo, Selma M. B.
Petersen, Christine A.
Comorbid infections induce progression of visceral leishmaniasis
title Comorbid infections induce progression of visceral leishmaniasis
title_full Comorbid infections induce progression of visceral leishmaniasis
title_fullStr Comorbid infections induce progression of visceral leishmaniasis
title_full_unstemmed Comorbid infections induce progression of visceral leishmaniasis
title_short Comorbid infections induce progression of visceral leishmaniasis
title_sort comorbid infections induce progression of visceral leishmaniasis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345068/
https://www.ncbi.nlm.nih.gov/pubmed/30674329
http://dx.doi.org/10.1186/s13071-019-3312-3
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