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Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis

OBJECTIVES: While feline chronic bronchitis (CB) is known as neutrophilic bronchial inflammation (NI), feline asthma (FA) is defined as an eosinophilic airway inflammation (EI). Feline chronic bronchial disease refers to both syndromes, with similar clinical presentations and applied treatment strat...

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Autores principales: Werner, Melanie, Weeger, Jasmin, Hörner-Schmid, Lina, Weber, Karin, Palić, Jelena, Shih, Jonathan, Suchodolski, Jan S., Pilla, Rachel, Schulz, Bianka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083293/
https://www.ncbi.nlm.nih.gov/pubmed/37051512
http://dx.doi.org/10.3389/fvets.2023.1148849
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author Werner, Melanie
Weeger, Jasmin
Hörner-Schmid, Lina
Weber, Karin
Palić, Jelena
Shih, Jonathan
Suchodolski, Jan S.
Pilla, Rachel
Schulz, Bianka
author_facet Werner, Melanie
Weeger, Jasmin
Hörner-Schmid, Lina
Weber, Karin
Palić, Jelena
Shih, Jonathan
Suchodolski, Jan S.
Pilla, Rachel
Schulz, Bianka
author_sort Werner, Melanie
collection PubMed
description OBJECTIVES: While feline chronic bronchitis (CB) is known as neutrophilic bronchial inflammation (NI), feline asthma (FA) is defined as an eosinophilic airway inflammation (EI). Feline chronic bronchial disease refers to both syndromes, with similar clinical presentations and applied treatment strategies. Recent studies described alterations of the microbiota composition in cats with FA, but little is known about the comparison of the lung microbiota between different types of feline bronchial disease. The study aimed to describe the bacterial microbiota of the lower respiratory tracts of cats with FA and CB and to identify potential differences. METHODS: Twenty-two client-owned cats with FA (n = 15) or CB (n = 7) confirmed via bronchoalveolar-lavage (BALF)-cytology were included. Next-generation sequencing analysis of 16S rRNA genes was performed on bacterial DNA derived from BALF samples. QIIME was used to compare microbial composition and diversity between groups. RESULTS: Evenness and alpha-diversity-indices did not significantly differ between cats with FA and CB (Shannon p = 0.084, Chao 1 p = 0.698, observed ASVs p = 0.944). Based on a PERMANOVA analysis, no significant differences were observed in microbial composition between animals of both groups (Bray-Curtis metric, R-value 0.086, p = 0.785; unweighted UniFrac metric, R-value −0.089, p = 0.799; weighted Unifrac metric, R-value −0.072, p = 0.823). Regarding taxonomic composition, significant differences were detected for Actinobacteria on the phylum level (p = 0.026), Mycoplasma spp. (p = 0.048), and Acinetobacteria (p = 0.049) on the genus level between cats with FA and CB, with generally strong interindividual differences seen. There was a significant difference in the duration of clinical signs before diagnosis in animals dominated by Bacteriodetes (median 12 months, range 2–58 months) compared to animals dominated by Proteobacteria (median 1 month, range 1 day to 18 months; p = 0.003). CONCLUSIONS AND RELEVANCE: Lung microbiota composition is very similar in cat populations with spontaneous FA and CB besides small differences in some bacterial groups. However, with disease progression, the lung microbiome of cats with both diseases appears to shift away from dominantly Proteobacteria to a pattern more dominated by Bacteriodetes. A substantial proportion of cats tested positive for Mycoplasma spp. via sequencing, while none of them tested positive using classical PCR.
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spelling pubmed-100832932023-04-11 Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis Werner, Melanie Weeger, Jasmin Hörner-Schmid, Lina Weber, Karin Palić, Jelena Shih, Jonathan Suchodolski, Jan S. Pilla, Rachel Schulz, Bianka Front Vet Sci Veterinary Science OBJECTIVES: While feline chronic bronchitis (CB) is known as neutrophilic bronchial inflammation (NI), feline asthma (FA) is defined as an eosinophilic airway inflammation (EI). Feline chronic bronchial disease refers to both syndromes, with similar clinical presentations and applied treatment strategies. Recent studies described alterations of the microbiota composition in cats with FA, but little is known about the comparison of the lung microbiota between different types of feline bronchial disease. The study aimed to describe the bacterial microbiota of the lower respiratory tracts of cats with FA and CB and to identify potential differences. METHODS: Twenty-two client-owned cats with FA (n = 15) or CB (n = 7) confirmed via bronchoalveolar-lavage (BALF)-cytology were included. Next-generation sequencing analysis of 16S rRNA genes was performed on bacterial DNA derived from BALF samples. QIIME was used to compare microbial composition and diversity between groups. RESULTS: Evenness and alpha-diversity-indices did not significantly differ between cats with FA and CB (Shannon p = 0.084, Chao 1 p = 0.698, observed ASVs p = 0.944). Based on a PERMANOVA analysis, no significant differences were observed in microbial composition between animals of both groups (Bray-Curtis metric, R-value 0.086, p = 0.785; unweighted UniFrac metric, R-value −0.089, p = 0.799; weighted Unifrac metric, R-value −0.072, p = 0.823). Regarding taxonomic composition, significant differences were detected for Actinobacteria on the phylum level (p = 0.026), Mycoplasma spp. (p = 0.048), and Acinetobacteria (p = 0.049) on the genus level between cats with FA and CB, with generally strong interindividual differences seen. There was a significant difference in the duration of clinical signs before diagnosis in animals dominated by Bacteriodetes (median 12 months, range 2–58 months) compared to animals dominated by Proteobacteria (median 1 month, range 1 day to 18 months; p = 0.003). CONCLUSIONS AND RELEVANCE: Lung microbiota composition is very similar in cat populations with spontaneous FA and CB besides small differences in some bacterial groups. However, with disease progression, the lung microbiome of cats with both diseases appears to shift away from dominantly Proteobacteria to a pattern more dominated by Bacteriodetes. A substantial proportion of cats tested positive for Mycoplasma spp. via sequencing, while none of them tested positive using classical PCR. Frontiers Media S.A. 2023-03-27 /pmc/articles/PMC10083293/ /pubmed/37051512 http://dx.doi.org/10.3389/fvets.2023.1148849 Text en Copyright © 2023 Werner, Weeger, Hörner-Schmid, Weber, Palić, Shih, Suchodolski, Pilla and Schulz. 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
Werner, Melanie
Weeger, Jasmin
Hörner-Schmid, Lina
Weber, Karin
Palić, Jelena
Shih, Jonathan
Suchodolski, Jan S.
Pilla, Rachel
Schulz, Bianka
Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis
title Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis
title_full Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis
title_fullStr Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis
title_full_unstemmed Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis
title_short Comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis
title_sort comparison of the respiratory bacterial microbiome in cats with feline asthma and chronic bronchitis
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083293/
https://www.ncbi.nlm.nih.gov/pubmed/37051512
http://dx.doi.org/10.3389/fvets.2023.1148849
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