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Human Thanatomicrobiome Succession and Time Since Death

The thanatomicrobiome (thanatos, Greek for death) is a relatively new term and is the study of the microbes colonizing the internal organs and orifices after death. Recent scientific breakthroughs in an initial study of the thanatomicrobiome have revealed that a majority of the microbes within the h...

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Autores principales: Javan, Gulnaz T., Finley, Sheree J., Can, Ismail, Wilkinson, Jeremy E., Hanson, J. Delton, Tarone, Aaron M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944132/
https://www.ncbi.nlm.nih.gov/pubmed/27412051
http://dx.doi.org/10.1038/srep29598
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author Javan, Gulnaz T.
Finley, Sheree J.
Can, Ismail
Wilkinson, Jeremy E.
Hanson, J. Delton
Tarone, Aaron M.
author_facet Javan, Gulnaz T.
Finley, Sheree J.
Can, Ismail
Wilkinson, Jeremy E.
Hanson, J. Delton
Tarone, Aaron M.
author_sort Javan, Gulnaz T.
collection PubMed
description The thanatomicrobiome (thanatos, Greek for death) is a relatively new term and is the study of the microbes colonizing the internal organs and orifices after death. Recent scientific breakthroughs in an initial study of the thanatomicrobiome have revealed that a majority of the microbes within the human body are the obligate anaerobes, Clostridium spp., in the internal postmortem microbial communities. We hypothesized that time-dependent changes in the thanatomicrobiome within internal organs can estimate the time of death as a human body decays. Here we report a cross-sectional study of the sampling of 27 human corpses from criminal cases with postmortem intervals between 3.5–240 hours. The impetus for examining microbial communities in different internal organs is to address the paucity of empirical data on thanatomicrobiomic succession caused by the limited access to these organs prior to death and a dearth of knowledge regarding the movement of microbes within remains. Our sequencing results of 16S rRNA gene amplicons of 27 postmortem samples from cadavers demonstrated statistically significant time-, organ-, and sex-dependent changes. These results suggest that comprehensive knowledge of the number and abundance of each organ’s signature microorganisms could be useful to forensic microbiologists as a new source of data for estimating postmortem interval.
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spelling pubmed-49441322016-07-20 Human Thanatomicrobiome Succession and Time Since Death Javan, Gulnaz T. Finley, Sheree J. Can, Ismail Wilkinson, Jeremy E. Hanson, J. Delton Tarone, Aaron M. Sci Rep Article The thanatomicrobiome (thanatos, Greek for death) is a relatively new term and is the study of the microbes colonizing the internal organs and orifices after death. Recent scientific breakthroughs in an initial study of the thanatomicrobiome have revealed that a majority of the microbes within the human body are the obligate anaerobes, Clostridium spp., in the internal postmortem microbial communities. We hypothesized that time-dependent changes in the thanatomicrobiome within internal organs can estimate the time of death as a human body decays. Here we report a cross-sectional study of the sampling of 27 human corpses from criminal cases with postmortem intervals between 3.5–240 hours. The impetus for examining microbial communities in different internal organs is to address the paucity of empirical data on thanatomicrobiomic succession caused by the limited access to these organs prior to death and a dearth of knowledge regarding the movement of microbes within remains. Our sequencing results of 16S rRNA gene amplicons of 27 postmortem samples from cadavers demonstrated statistically significant time-, organ-, and sex-dependent changes. These results suggest that comprehensive knowledge of the number and abundance of each organ’s signature microorganisms could be useful to forensic microbiologists as a new source of data for estimating postmortem interval. Nature Publishing Group 2016-07-14 /pmc/articles/PMC4944132/ /pubmed/27412051 http://dx.doi.org/10.1038/srep29598 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Javan, Gulnaz T.
Finley, Sheree J.
Can, Ismail
Wilkinson, Jeremy E.
Hanson, J. Delton
Tarone, Aaron M.
Human Thanatomicrobiome Succession and Time Since Death
title Human Thanatomicrobiome Succession and Time Since Death
title_full Human Thanatomicrobiome Succession and Time Since Death
title_fullStr Human Thanatomicrobiome Succession and Time Since Death
title_full_unstemmed Human Thanatomicrobiome Succession and Time Since Death
title_short Human Thanatomicrobiome Succession and Time Since Death
title_sort human thanatomicrobiome succession and time since death
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944132/
https://www.ncbi.nlm.nih.gov/pubmed/27412051
http://dx.doi.org/10.1038/srep29598
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