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Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels

BACKGROUND: Respiratory diseases are among the most common and expensive to treat diseases in camels with a great economic impact on camel health, welfare, and production. Bronchoalveolar lavage fluid (BALF) has been proven as a valuable sample for investigating the leukocyte populations in the resp...

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Autores principales: Shawaf, Turke, Schuberth, Hans-Joachim, Hussen, Jamal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490690/
https://www.ncbi.nlm.nih.gov/pubmed/36131278
http://dx.doi.org/10.1186/s12917-022-03446-7
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author Shawaf, Turke
Schuberth, Hans-Joachim
Hussen, Jamal
author_facet Shawaf, Turke
Schuberth, Hans-Joachim
Hussen, Jamal
author_sort Shawaf, Turke
collection PubMed
description BACKGROUND: Respiratory diseases are among the most common and expensive to treat diseases in camels with a great economic impact on camel health, welfare, and production. Bronchoalveolar lavage fluid (BALF) has been proven as a valuable sample for investigating the leukocyte populations in the respiratory tract of several species. In the present study, fluorescent antibody labeling and flow cytometry were used to study the immune cell composition of BALF in dromedary camels. Animals with clinical respiratory diseases (n = seven) were compared with apparently healthy animals (n = 10). In addition, blood leukocytes from the same animals were stained in parallel with the same antibodies and analyzed by flow cytometry. RESULTS: Camel BALF macrophages, granulocytes, monocytes, and lymphocytes were identified based on their forward and side scatter properties. The expression pattern of the cell markers CD172a, CD14, CD163, and MHCII molecules on BALF cells indicates a similar phenotype for camel, bovine, and porcine BALF myeloid cells. The comparison between camels with respiratory disease and healthy camels regarding cellular composition in their BALF revealed a higher total cell count, a higher fraction of granulocytes, and a lower fraction of macrophages in diseased than healthy camels. Within the lymphocyte population, the percentages of helper T cells and B cells were also higher in diseased than healthy camels. The elevated expression of the activation marker CD11a on helper T cells of diseased camels is an indication of the expansion of helper T cells population due to infection and exposure to respiratory pathogens. The higher abundance of MHCII molecules on BALF macrophages from diseased camels indicates a polarization toward an inflammatory macrophage phenotype (M1) in respiratory diseased camels. No significant differences were observed in the systemic leukogram between healthy and diseased animals. CONCLUSIONS: Collectively, the current study represents the first report on flow cytometric analysis of immune cell composition of bronchoalveolar lavage fluid (BALF) in dromedary camels.
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spelling pubmed-94906902022-09-21 Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels Shawaf, Turke Schuberth, Hans-Joachim Hussen, Jamal BMC Vet Res Research BACKGROUND: Respiratory diseases are among the most common and expensive to treat diseases in camels with a great economic impact on camel health, welfare, and production. Bronchoalveolar lavage fluid (BALF) has been proven as a valuable sample for investigating the leukocyte populations in the respiratory tract of several species. In the present study, fluorescent antibody labeling and flow cytometry were used to study the immune cell composition of BALF in dromedary camels. Animals with clinical respiratory diseases (n = seven) were compared with apparently healthy animals (n = 10). In addition, blood leukocytes from the same animals were stained in parallel with the same antibodies and analyzed by flow cytometry. RESULTS: Camel BALF macrophages, granulocytes, monocytes, and lymphocytes were identified based on their forward and side scatter properties. The expression pattern of the cell markers CD172a, CD14, CD163, and MHCII molecules on BALF cells indicates a similar phenotype for camel, bovine, and porcine BALF myeloid cells. The comparison between camels with respiratory disease and healthy camels regarding cellular composition in their BALF revealed a higher total cell count, a higher fraction of granulocytes, and a lower fraction of macrophages in diseased than healthy camels. Within the lymphocyte population, the percentages of helper T cells and B cells were also higher in diseased than healthy camels. The elevated expression of the activation marker CD11a on helper T cells of diseased camels is an indication of the expansion of helper T cells population due to infection and exposure to respiratory pathogens. The higher abundance of MHCII molecules on BALF macrophages from diseased camels indicates a polarization toward an inflammatory macrophage phenotype (M1) in respiratory diseased camels. No significant differences were observed in the systemic leukogram between healthy and diseased animals. CONCLUSIONS: Collectively, the current study represents the first report on flow cytometric analysis of immune cell composition of bronchoalveolar lavage fluid (BALF) in dromedary camels. BioMed Central 2022-09-21 /pmc/articles/PMC9490690/ /pubmed/36131278 http://dx.doi.org/10.1186/s12917-022-03446-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Shawaf, Turke
Schuberth, Hans-Joachim
Hussen, Jamal
Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
title Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
title_full Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
title_fullStr Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
title_full_unstemmed Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
title_short Immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
title_sort immune cell composition of the bronchoalveolar lavage fluid in healthy and respiratory diseased dromedary camels
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490690/
https://www.ncbi.nlm.nih.gov/pubmed/36131278
http://dx.doi.org/10.1186/s12917-022-03446-7
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