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Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis

SIMPLE SUMMARY: Canine leishmaniosis (CanL), the most severe, visceralizing form of disease caused by Leishmania infantum transmitted by phlebotomine sand flies. CanL is frequently diagnosed in the Mediterranean basin and South America, although it is also found in other regions, including the Unite...

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Autores principales: Beasley, Erin A., Pessôa-Pereira, Danielle, Scorza, Breanna M., Petersen, Christine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614518/
https://www.ncbi.nlm.nih.gov/pubmed/34827938
http://dx.doi.org/10.3390/ani11113206
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author Beasley, Erin A.
Pessôa-Pereira, Danielle
Scorza, Breanna M.
Petersen, Christine A.
author_facet Beasley, Erin A.
Pessôa-Pereira, Danielle
Scorza, Breanna M.
Petersen, Christine A.
author_sort Beasley, Erin A.
collection PubMed
description SIMPLE SUMMARY: Canine leishmaniosis (CanL), the most severe, visceralizing form of disease caused by Leishmania infantum transmitted by phlebotomine sand flies. CanL is frequently diagnosed in the Mediterranean basin and South America, although it is also found in other regions, including the United States (U.S.). Dogs in these regions are at risk for co-infections, prominently tick-borne diseases. Our review examines epidemiologic, clinical, and immunologic mechanisms found during the most common eight CanL co-infections reported in published literature. Co-infections alter immunologic processes and disease progression impacting CanL diagnosis, therapeutic responses, and prognosis. ABSTRACT: Canine leishmaniosis (CanL) is a vector-borne, parasitic disease. CanL is endemic in the Mediterranean basin and South America but also found in Northern Africa, Asia, and the U.S. Regions with both competent sand fly vectors and L. infantum parasites are also endemic for additional infectious diseases that could cause co-infections in dogs. Growing evidence indicates that co-infections can impact immunologic responses and thus the clinical course of both CanL and the comorbid disease(s). The aim for this review is to summarize epidemiologic, clinical, and immunologic factors contributing to eight primary co-infections reported with CanL: Ehrlichia spp., Anaplasma spp., Borrelia spp., Babesia spp., Trypanosoma cruzi, Toxoplasma gondii, Dirofilaria immitis, Paracoccidioides braziliensis. Co-infection causes mechanistic differences in immunity which can alter diagnostics, therapeutic management, and prognosis of dogs with CanL. More research is needed to further explore immunomodulation during CanL co-infection(s) and their clinical impact.
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spelling pubmed-86145182021-11-26 Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis Beasley, Erin A. Pessôa-Pereira, Danielle Scorza, Breanna M. Petersen, Christine A. Animals (Basel) Review SIMPLE SUMMARY: Canine leishmaniosis (CanL), the most severe, visceralizing form of disease caused by Leishmania infantum transmitted by phlebotomine sand flies. CanL is frequently diagnosed in the Mediterranean basin and South America, although it is also found in other regions, including the United States (U.S.). Dogs in these regions are at risk for co-infections, prominently tick-borne diseases. Our review examines epidemiologic, clinical, and immunologic mechanisms found during the most common eight CanL co-infections reported in published literature. Co-infections alter immunologic processes and disease progression impacting CanL diagnosis, therapeutic responses, and prognosis. ABSTRACT: Canine leishmaniosis (CanL) is a vector-borne, parasitic disease. CanL is endemic in the Mediterranean basin and South America but also found in Northern Africa, Asia, and the U.S. Regions with both competent sand fly vectors and L. infantum parasites are also endemic for additional infectious diseases that could cause co-infections in dogs. Growing evidence indicates that co-infections can impact immunologic responses and thus the clinical course of both CanL and the comorbid disease(s). The aim for this review is to summarize epidemiologic, clinical, and immunologic factors contributing to eight primary co-infections reported with CanL: Ehrlichia spp., Anaplasma spp., Borrelia spp., Babesia spp., Trypanosoma cruzi, Toxoplasma gondii, Dirofilaria immitis, Paracoccidioides braziliensis. Co-infection causes mechanistic differences in immunity which can alter diagnostics, therapeutic management, and prognosis of dogs with CanL. More research is needed to further explore immunomodulation during CanL co-infection(s) and their clinical impact. MDPI 2021-11-10 /pmc/articles/PMC8614518/ /pubmed/34827938 http://dx.doi.org/10.3390/ani11113206 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Beasley, Erin A.
Pessôa-Pereira, Danielle
Scorza, Breanna M.
Petersen, Christine A.
Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis
title Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis
title_full Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis
title_fullStr Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis
title_full_unstemmed Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis
title_short Epidemiologic, Clinical and Immunological Consequences of Co-Infections during Canine Leishmaniosis
title_sort epidemiologic, clinical and immunological consequences of co-infections during canine leishmaniosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614518/
https://www.ncbi.nlm.nih.gov/pubmed/34827938
http://dx.doi.org/10.3390/ani11113206
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