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Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis

Next generation sequencing has demonstrated that alpha diversity of the fecal microbiota is significantly altered in horses with typhlocolitis. The objective of this study was to evaluate the bacterial composition of the cecum content of horses with and without typhlocolitis through direct and cultu...

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Autores principales: Zakia, Luiza S., Gomez, Diego E., Caddey, Benjamin B., Boerlin, Patrick, Surette, Michael G., Arroyo, Luis G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101396/
https://www.ncbi.nlm.nih.gov/pubmed/37053174
http://dx.doi.org/10.1371/journal.pone.0284193
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author Zakia, Luiza S.
Gomez, Diego E.
Caddey, Benjamin B.
Boerlin, Patrick
Surette, Michael G.
Arroyo, Luis G.
author_facet Zakia, Luiza S.
Gomez, Diego E.
Caddey, Benjamin B.
Boerlin, Patrick
Surette, Michael G.
Arroyo, Luis G.
author_sort Zakia, Luiza S.
collection PubMed
description Next generation sequencing has demonstrated that alpha diversity of the fecal microbiota is significantly altered in horses with typhlocolitis. The objective of this study was to evaluate the bacterial composition of the cecum content of horses with and without typhlocolitis through direct and culture-enriched 16S gene sequencing of six healthy horses and six horses with acute typhlocolitis; a case-control study design. Cecal content was collected after euthanasia. An aliquot was used for direct 16S gene sequencing. Another was serially diluted with brain heart infusion (BHI) and plated onto five different agar media. All culture medias, except for MacConkey, were incubated anaerobically. Bacterial colonies were harvested in bulk and used for DNA extraction, 16S PCR amplification, and sequenced using the Illumina MiSeq platform. Predominant phyla in healthy and diseased horses were Firmicutes, followed by Bacteroidetes in all cultured medias, except for MacConkey agar, in which Proteobacteria was the dominant phylum. Greater bacterial richness was identified in sequenced cecal contents as compared to cultured plates (P < 0.05). Culture-enriched molecular profiling combined with 16S rRNA gene sequencing offer an alternative method for the study of the gut microbiota of horses. For direct cecum content 16S gene amplification, the alpha diversity indices were lower in diarrheic horses compared to healthy horses (P < 0.05). A higher relative abundance of Fusobacteriota was found in 2/6 samples from diarrheic horses. The role of Fusobacteriota in equine colitis deserves investigation.
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spelling pubmed-101013962023-04-14 Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis Zakia, Luiza S. Gomez, Diego E. Caddey, Benjamin B. Boerlin, Patrick Surette, Michael G. Arroyo, Luis G. PLoS One Research Article Next generation sequencing has demonstrated that alpha diversity of the fecal microbiota is significantly altered in horses with typhlocolitis. The objective of this study was to evaluate the bacterial composition of the cecum content of horses with and without typhlocolitis through direct and culture-enriched 16S gene sequencing of six healthy horses and six horses with acute typhlocolitis; a case-control study design. Cecal content was collected after euthanasia. An aliquot was used for direct 16S gene sequencing. Another was serially diluted with brain heart infusion (BHI) and plated onto five different agar media. All culture medias, except for MacConkey, were incubated anaerobically. Bacterial colonies were harvested in bulk and used for DNA extraction, 16S PCR amplification, and sequenced using the Illumina MiSeq platform. Predominant phyla in healthy and diseased horses were Firmicutes, followed by Bacteroidetes in all cultured medias, except for MacConkey agar, in which Proteobacteria was the dominant phylum. Greater bacterial richness was identified in sequenced cecal contents as compared to cultured plates (P < 0.05). Culture-enriched molecular profiling combined with 16S rRNA gene sequencing offer an alternative method for the study of the gut microbiota of horses. For direct cecum content 16S gene amplification, the alpha diversity indices were lower in diarrheic horses compared to healthy horses (P < 0.05). A higher relative abundance of Fusobacteriota was found in 2/6 samples from diarrheic horses. The role of Fusobacteriota in equine colitis deserves investigation. Public Library of Science 2023-04-13 /pmc/articles/PMC10101396/ /pubmed/37053174 http://dx.doi.org/10.1371/journal.pone.0284193 Text en © 2023 Zakia et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zakia, Luiza S.
Gomez, Diego E.
Caddey, Benjamin B.
Boerlin, Patrick
Surette, Michael G.
Arroyo, Luis G.
Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis
title Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis
title_full Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis
title_fullStr Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis
title_full_unstemmed Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis
title_short Direct and culture-enriched 16S rRNA sequencing of cecal content of healthy horses and horses with typhlocolitis
title_sort direct and culture-enriched 16s rrna sequencing of cecal content of healthy horses and horses with typhlocolitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101396/
https://www.ncbi.nlm.nih.gov/pubmed/37053174
http://dx.doi.org/10.1371/journal.pone.0284193
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