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Postmortem succession of gut microbial communities in deceased human subjects

The human microbiome has demonstrated an importance for the health and functioning in living individuals. However, the fate of the microbiome after death is less understood. In addition to a better understanding of microbe-mediated decomposition processes, postmortem succession of human-associated m...

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Autores principales: DeBruyn, Jennifer M., Hauther, Kathleen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470579/
https://www.ncbi.nlm.nih.gov/pubmed/28626612
http://dx.doi.org/10.7717/peerj.3437
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author DeBruyn, Jennifer M.
Hauther, Kathleen A.
author_facet DeBruyn, Jennifer M.
Hauther, Kathleen A.
author_sort DeBruyn, Jennifer M.
collection PubMed
description The human microbiome has demonstrated an importance for the health and functioning in living individuals. However, the fate of the microbiome after death is less understood. In addition to a better understanding of microbe-mediated decomposition processes, postmortem succession of human-associated microbial communities has been suggested as a possible forensic tool for estimating time since death, or postmortem interval (PMI). The objective of our study was to document postmortem changes in human gut bacterial communities. Gut microflora were repeatedly sampled from the caeca of cadavers as they decayed under natural environmental conditions. 16S rRNA gene amplicon sequencing revealed that over time, bacterial richness significantly increased (r(s) = 0.449) while diversity decreased (r(s) =  − 0.701). The composition of gut bacterial communities changed in a similar manner over time towards a common decay community. OTUs belonging to Bacteroidales (Bacteroides, Parabacteroides) significantly declined while Clostridiales (Clostridium, Anaerosphaera) and the fly-associated Gammaproteobacteria Ignatzschineria and Wohlfahrtiimonas increased. Our examination of human caeca microflora in decomposing cadavers adds to the growing literature on postmortem microbial communities, which will ultimately contribute to a better understanding of decomposition processes.
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spelling pubmed-54705792017-06-16 Postmortem succession of gut microbial communities in deceased human subjects DeBruyn, Jennifer M. Hauther, Kathleen A. PeerJ Ecology The human microbiome has demonstrated an importance for the health and functioning in living individuals. However, the fate of the microbiome after death is less understood. In addition to a better understanding of microbe-mediated decomposition processes, postmortem succession of human-associated microbial communities has been suggested as a possible forensic tool for estimating time since death, or postmortem interval (PMI). The objective of our study was to document postmortem changes in human gut bacterial communities. Gut microflora were repeatedly sampled from the caeca of cadavers as they decayed under natural environmental conditions. 16S rRNA gene amplicon sequencing revealed that over time, bacterial richness significantly increased (r(s) = 0.449) while diversity decreased (r(s) =  − 0.701). The composition of gut bacterial communities changed in a similar manner over time towards a common decay community. OTUs belonging to Bacteroidales (Bacteroides, Parabacteroides) significantly declined while Clostridiales (Clostridium, Anaerosphaera) and the fly-associated Gammaproteobacteria Ignatzschineria and Wohlfahrtiimonas increased. Our examination of human caeca microflora in decomposing cadavers adds to the growing literature on postmortem microbial communities, which will ultimately contribute to a better understanding of decomposition processes. PeerJ Inc. 2017-06-12 /pmc/articles/PMC5470579/ /pubmed/28626612 http://dx.doi.org/10.7717/peerj.3437 Text en ©2017 DeBruyn and Hauther http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Ecology
DeBruyn, Jennifer M.
Hauther, Kathleen A.
Postmortem succession of gut microbial communities in deceased human subjects
title Postmortem succession of gut microbial communities in deceased human subjects
title_full Postmortem succession of gut microbial communities in deceased human subjects
title_fullStr Postmortem succession of gut microbial communities in deceased human subjects
title_full_unstemmed Postmortem succession of gut microbial communities in deceased human subjects
title_short Postmortem succession of gut microbial communities in deceased human subjects
title_sort postmortem succession of gut microbial communities in deceased human subjects
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470579/
https://www.ncbi.nlm.nih.gov/pubmed/28626612
http://dx.doi.org/10.7717/peerj.3437
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