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Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis

Gut microbiota seems to interact with immune system. Canine leishmaniasis pathogenesis and severity of disease lean on the host immunity, but there is no information in literature about gut microbiota in infected animals. Thus, this study aims to compare the microbiota composition and leukocyte subs...

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Autores principales: Meazzi, Sara, Lauzi, Stefania, Martini, Valeria, Ferriani, Riccardo, Peri, Margherita, Zanzani, Sergio Aurelio, Giordano, Alessia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326463/
https://www.ncbi.nlm.nih.gov/pubmed/35909678
http://dx.doi.org/10.3389/fvets.2022.868967
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author Meazzi, Sara
Lauzi, Stefania
Martini, Valeria
Ferriani, Riccardo
Peri, Margherita
Zanzani, Sergio Aurelio
Giordano, Alessia
author_facet Meazzi, Sara
Lauzi, Stefania
Martini, Valeria
Ferriani, Riccardo
Peri, Margherita
Zanzani, Sergio Aurelio
Giordano, Alessia
author_sort Meazzi, Sara
collection PubMed
description Gut microbiota seems to interact with immune system. Canine leishmaniasis pathogenesis and severity of disease lean on the host immunity, but there is no information in literature about gut microbiota in infected animals. Thus, this study aims to compare the microbiota composition and leukocyte subset of healthy dogs with those of asymptomatic dogs exposed to Leishmania spp. and dogs with clinical leishmaniasis. Thirty-nine dogs were enrolled and grouped into three groups: healthy, exposed asymptomatic and infected symptomatic for Leishmania spp. Flow cytometry on whole blood evaluated the prevalence of CD4, CD5, CD8, CD11b, CD14, and CD21 positive cells. Gut microbiota was investigated using a next generation sequencing (NGS) technique. Firmicutes resulted significantly more abundant in the healthy dogs compared with the other two groups. Conversely, Proteobacteria were more abundant in symptomatic dogs. Even in rarest phyla comparison some significant differences were found, as well as in comparison at classes, order, family and genus levels. The symptomatic group had lower concentration of all the lymphocyte classes (CD5, CD21, CD4, CD8) compared to the other groups. A lower abundance of Firmicutes is reported in literature in diseased animals compared to the healthy ones and this is in agreement with the results of this study. Increased Proteobacteria in sick animals could suggest a dysbiosis status, even without distinct gastrointestinal signs. The leukocyte classes results indicate a decreased Th1 response in symptomatic dogs. Studies also investigating the cytokine response could deepen the knowledge on the pathogenesis of canine leishmaniasis.
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spelling pubmed-93264632022-07-28 Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis Meazzi, Sara Lauzi, Stefania Martini, Valeria Ferriani, Riccardo Peri, Margherita Zanzani, Sergio Aurelio Giordano, Alessia Front Vet Sci Veterinary Science Gut microbiota seems to interact with immune system. Canine leishmaniasis pathogenesis and severity of disease lean on the host immunity, but there is no information in literature about gut microbiota in infected animals. Thus, this study aims to compare the microbiota composition and leukocyte subset of healthy dogs with those of asymptomatic dogs exposed to Leishmania spp. and dogs with clinical leishmaniasis. Thirty-nine dogs were enrolled and grouped into three groups: healthy, exposed asymptomatic and infected symptomatic for Leishmania spp. Flow cytometry on whole blood evaluated the prevalence of CD4, CD5, CD8, CD11b, CD14, and CD21 positive cells. Gut microbiota was investigated using a next generation sequencing (NGS) technique. Firmicutes resulted significantly more abundant in the healthy dogs compared with the other two groups. Conversely, Proteobacteria were more abundant in symptomatic dogs. Even in rarest phyla comparison some significant differences were found, as well as in comparison at classes, order, family and genus levels. The symptomatic group had lower concentration of all the lymphocyte classes (CD5, CD21, CD4, CD8) compared to the other groups. A lower abundance of Firmicutes is reported in literature in diseased animals compared to the healthy ones and this is in agreement with the results of this study. Increased Proteobacteria in sick animals could suggest a dysbiosis status, even without distinct gastrointestinal signs. The leukocyte classes results indicate a decreased Th1 response in symptomatic dogs. Studies also investigating the cytokine response could deepen the knowledge on the pathogenesis of canine leishmaniasis. Frontiers Media S.A. 2022-07-13 /pmc/articles/PMC9326463/ /pubmed/35909678 http://dx.doi.org/10.3389/fvets.2022.868967 Text en Copyright © 2022 Meazzi, Lauzi, Martini, Ferriani, Peri, Zanzani and Giordano. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Meazzi, Sara
Lauzi, Stefania
Martini, Valeria
Ferriani, Riccardo
Peri, Margherita
Zanzani, Sergio Aurelio
Giordano, Alessia
Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis
title Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis
title_full Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis
title_fullStr Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis
title_full_unstemmed Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis
title_short Gut Microbiota and Lymphocyte Subsets in Canine Leishmaniasis
title_sort gut microbiota and lymphocyte subsets in canine leishmaniasis
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326463/
https://www.ncbi.nlm.nih.gov/pubmed/35909678
http://dx.doi.org/10.3389/fvets.2022.868967
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