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Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway

BACKGROUND: A severe form of acute hemorrhagic diarrhea syndrome (AHDS) occurred in dogs in the Oslo region of Norway during autumn 2019. OBJECTIVES: To characterize the fecal microbiota of dogs with AHDS during the outbreak and compare it to that of healthy dogs from the same period and before the...

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Autores principales: Herstad, Kristin M. V., Trosvik, Pål, Haaland, Anita Haug, Haverkamp, Thomas H.A., de Muinck, Eric J., Skancke, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478063/
https://www.ncbi.nlm.nih.gov/pubmed/34288148
http://dx.doi.org/10.1111/jvim.16201
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author Herstad, Kristin M. V.
Trosvik, Pål
Haaland, Anita Haug
Haverkamp, Thomas H.A.
de Muinck, Eric J.
Skancke, Ellen
author_facet Herstad, Kristin M. V.
Trosvik, Pål
Haaland, Anita Haug
Haverkamp, Thomas H.A.
de Muinck, Eric J.
Skancke, Ellen
author_sort Herstad, Kristin M. V.
collection PubMed
description BACKGROUND: A severe form of acute hemorrhagic diarrhea syndrome (AHDS) occurred in dogs in the Oslo region of Norway during autumn 2019. OBJECTIVES: To characterize the fecal microbiota of dogs with AHDS during the outbreak and compare it to that of healthy dogs from the same period and before the outbreak. ANIMALS: Dogs with AHDS (n = 50), dogs with nonhemorrhagic diarrhea (n = 3), and healthy dogs (n = 11) were sampled during the outbreak. In addition, 78 healthy dogs from the same region were sampled before the outbreak between 2017 and 2018. METHODS: Retrospective case‐control study. The fecal microbiotas were characterized using 16S rRNA gene amplicon sequencing. RESULTS: Dogs with AHDS had significantly different microbiota composition (R (2) = .07, P < .001) and decreased intestinal diversity relative to healthy dogs from the outbreak period (median, 2.7; range, 0.9‐3.5 vs median, 3.2; range, 2.6‐4.0; P < .001). The microbiota in dogs with AHDS was characterized by a decrease of Firmicutes and an outgrowth of Proteobacteria, with increased numbers of Clostridium perfringens and Providencia spp. Among the Providencia spp., 1 showed 100% sequence identity with a Providencia alcalifaciens strain that was cultivated and isolated from the same outbreak. No Providencia spp. was found in healthy dogs sampled before the outbreak. CONCLUSIONS AND CLINICAL IMPORTANCE: Dogs with AHDS had marked changes in fecal microbiota including increased numbers of Providencia spp. and C. perfringens, which may have contributed to the severity of this illness.
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spelling pubmed-84780632021-10-04 Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway Herstad, Kristin M. V. Trosvik, Pål Haaland, Anita Haug Haverkamp, Thomas H.A. de Muinck, Eric J. Skancke, Ellen J Vet Intern Med SMALL ANIMAL BACKGROUND: A severe form of acute hemorrhagic diarrhea syndrome (AHDS) occurred in dogs in the Oslo region of Norway during autumn 2019. OBJECTIVES: To characterize the fecal microbiota of dogs with AHDS during the outbreak and compare it to that of healthy dogs from the same period and before the outbreak. ANIMALS: Dogs with AHDS (n = 50), dogs with nonhemorrhagic diarrhea (n = 3), and healthy dogs (n = 11) were sampled during the outbreak. In addition, 78 healthy dogs from the same region were sampled before the outbreak between 2017 and 2018. METHODS: Retrospective case‐control study. The fecal microbiotas were characterized using 16S rRNA gene amplicon sequencing. RESULTS: Dogs with AHDS had significantly different microbiota composition (R (2) = .07, P < .001) and decreased intestinal diversity relative to healthy dogs from the outbreak period (median, 2.7; range, 0.9‐3.5 vs median, 3.2; range, 2.6‐4.0; P < .001). The microbiota in dogs with AHDS was characterized by a decrease of Firmicutes and an outgrowth of Proteobacteria, with increased numbers of Clostridium perfringens and Providencia spp. Among the Providencia spp., 1 showed 100% sequence identity with a Providencia alcalifaciens strain that was cultivated and isolated from the same outbreak. No Providencia spp. was found in healthy dogs sampled before the outbreak. CONCLUSIONS AND CLINICAL IMPORTANCE: Dogs with AHDS had marked changes in fecal microbiota including increased numbers of Providencia spp. and C. perfringens, which may have contributed to the severity of this illness. John Wiley & Sons, Inc. 2021-07-21 2021 /pmc/articles/PMC8478063/ /pubmed/34288148 http://dx.doi.org/10.1111/jvim.16201 Text en © 2021 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle SMALL ANIMAL
Herstad, Kristin M. V.
Trosvik, Pål
Haaland, Anita Haug
Haverkamp, Thomas H.A.
de Muinck, Eric J.
Skancke, Ellen
Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway
title Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway
title_full Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway
title_fullStr Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway
title_full_unstemmed Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway
title_short Changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in Norway
title_sort changes in the fecal microbiota in dogs with acute hemorrhagic diarrhea during an outbreak in norway
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478063/
https://www.ncbi.nlm.nih.gov/pubmed/34288148
http://dx.doi.org/10.1111/jvim.16201
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