Cargando…
Microbial succession from a subsequent secondary death event following mass mortality
BACKGROUND: Each death event can be characterized by its associated microbes – a living community of bacteria composed of carcass, soil, and insect-introduced bacterial species – a necrobiome. With the possibility for close succession of these death events, it may be beneficial to characterize how t...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557037/ https://www.ncbi.nlm.nih.gov/pubmed/33050884 http://dx.doi.org/10.1186/s12866-020-01969-3 |
_version_ | 1783594333875732480 |
---|---|
author | Harrison, Lindsay Kooienga, Emilia Speights, Cori Tomberlin, Jeffery Lashley, Marcus Barton, Brandon Jordan, Heather |
author_facet | Harrison, Lindsay Kooienga, Emilia Speights, Cori Tomberlin, Jeffery Lashley, Marcus Barton, Brandon Jordan, Heather |
author_sort | Harrison, Lindsay |
collection | PubMed |
description | BACKGROUND: Each death event can be characterized by its associated microbes – a living community of bacteria composed of carcass, soil, and insect-introduced bacterial species – a necrobiome. With the possibility for close succession of these death events, it may be beneficial to characterize how the magnitude of an initial death event may impact the decomposition and necrobiomes of subsequent death events in close proximity. In this paper we hope to characterize the microbial communities associated with a proximate subsequent death event, and distinguish any changes within those communities based on the magnitude of an initial death event and the biomass of preexisting carcass (es) undergoing decomposition. For this experiment, 6 feral swine carcasses in containers were placed in the vicinity of preexisting and ongoing carcass decomposition at sites of three different scales of decomposing carcass biomass. Swab samples were collected from the skin and eye sockets of the container pigs and subjected to 16 s rRNA sequencing and OTU assignment. RESULTS: PERMANOVA analysis of the bacterial taxa showed that there was no significant difference in the bacterial communities based on initial mortality event biomass size, but we did see a change in the bacterial communities over time, and slight differences between the skin and ocular cavity communities. Even without soil input, necrobiome communities can change rapidly. Further characterization of the bacterial necrobiome included utilization of the Random Forest algorithm to identify the most important predictors for time of decomposition. Sample sets were also scanned for notable human and swine-associated pathogens. CONCLUSIONS: The applications from this study are many, ranging from establishing the environmental impacts of mass mortality events to understanding the importance of scavenger, and scavenger microbial community input on decomposition. |
format | Online Article Text |
id | pubmed-7557037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75570372020-10-15 Microbial succession from a subsequent secondary death event following mass mortality Harrison, Lindsay Kooienga, Emilia Speights, Cori Tomberlin, Jeffery Lashley, Marcus Barton, Brandon Jordan, Heather BMC Microbiol Research Article BACKGROUND: Each death event can be characterized by its associated microbes – a living community of bacteria composed of carcass, soil, and insect-introduced bacterial species – a necrobiome. With the possibility for close succession of these death events, it may be beneficial to characterize how the magnitude of an initial death event may impact the decomposition and necrobiomes of subsequent death events in close proximity. In this paper we hope to characterize the microbial communities associated with a proximate subsequent death event, and distinguish any changes within those communities based on the magnitude of an initial death event and the biomass of preexisting carcass (es) undergoing decomposition. For this experiment, 6 feral swine carcasses in containers were placed in the vicinity of preexisting and ongoing carcass decomposition at sites of three different scales of decomposing carcass biomass. Swab samples were collected from the skin and eye sockets of the container pigs and subjected to 16 s rRNA sequencing and OTU assignment. RESULTS: PERMANOVA analysis of the bacterial taxa showed that there was no significant difference in the bacterial communities based on initial mortality event biomass size, but we did see a change in the bacterial communities over time, and slight differences between the skin and ocular cavity communities. Even without soil input, necrobiome communities can change rapidly. Further characterization of the bacterial necrobiome included utilization of the Random Forest algorithm to identify the most important predictors for time of decomposition. Sample sets were also scanned for notable human and swine-associated pathogens. CONCLUSIONS: The applications from this study are many, ranging from establishing the environmental impacts of mass mortality events to understanding the importance of scavenger, and scavenger microbial community input on decomposition. BioMed Central 2020-10-13 /pmc/articles/PMC7557037/ /pubmed/33050884 http://dx.doi.org/10.1186/s12866-020-01969-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Harrison, Lindsay Kooienga, Emilia Speights, Cori Tomberlin, Jeffery Lashley, Marcus Barton, Brandon Jordan, Heather Microbial succession from a subsequent secondary death event following mass mortality |
title | Microbial succession from a subsequent secondary death event following mass mortality |
title_full | Microbial succession from a subsequent secondary death event following mass mortality |
title_fullStr | Microbial succession from a subsequent secondary death event following mass mortality |
title_full_unstemmed | Microbial succession from a subsequent secondary death event following mass mortality |
title_short | Microbial succession from a subsequent secondary death event following mass mortality |
title_sort | microbial succession from a subsequent secondary death event following mass mortality |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557037/ https://www.ncbi.nlm.nih.gov/pubmed/33050884 http://dx.doi.org/10.1186/s12866-020-01969-3 |
work_keys_str_mv | AT harrisonlindsay microbialsuccessionfromasubsequentsecondarydeatheventfollowingmassmortality AT kooiengaemilia microbialsuccessionfromasubsequentsecondarydeatheventfollowingmassmortality AT speightscori microbialsuccessionfromasubsequentsecondarydeatheventfollowingmassmortality AT tomberlinjeffery microbialsuccessionfromasubsequentsecondarydeatheventfollowingmassmortality AT lashleymarcus microbialsuccessionfromasubsequentsecondarydeatheventfollowingmassmortality AT bartonbrandon microbialsuccessionfromasubsequentsecondarydeatheventfollowingmassmortality AT jordanheather microbialsuccessionfromasubsequentsecondarydeatheventfollowingmassmortality |