Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencing

The advent of high-throughput sequencing technologies, such as 16S rRNA amplicon sequencing, has enabled the characterization of microbial communities across diverse ecosystems including animal carrion. Although most studies on postmortem microbial communities focus on its application to human death...

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Main Authors: Jennifer L. Houtz, Joseph P. Receveur, Jennifer L. Pechal, M. Eric Benbow, Brent M. Horton, John R. Wallace
Format: Article
Language:English
Published: Elsevier 2022-12-01
Series:Forensic Science International: Animals and Environments
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666937422000130
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author Jennifer L. Houtz
Joseph P. Receveur
Jennifer L. Pechal
M. Eric Benbow
Brent M. Horton
John R. Wallace
author_facet Jennifer L. Houtz
Joseph P. Receveur
Jennifer L. Pechal
M. Eric Benbow
Brent M. Horton
John R. Wallace
author_sort Jennifer L. Houtz
collection DOAJ
description The advent of high-throughput sequencing technologies, such as 16S rRNA amplicon sequencing, has enabled the characterization of microbial communities across diverse ecosystems including animal carrion. Although most studies on postmortem microbial communities focus on its application to human death scene analysis, this technique holds great potential for wildlife crime investigations. We conducted a pilot study to characterize the spatial heterogeneity and temporal shifts between the perimortem (i.e., at time of death) and postmortem (i.e., after death) microbiomes associated with the gut tracts of decomposing European Starling (Sturnus vulgaris) nestlings over three days. We observed significant differences in microbial community structure among perimortem gut tract regions. The microbial communities converged across all gut tract regions within the first 24 h of death and remained stable between 24 and 72 h postmortem. A random forest classifier identified Lactococcus, Serratia, and Clostridium as the top three taxonomic predictors for predicting perimortem or postmortem microbial communities. Our findings provide preliminary data for considering the potential forensic utility of incorporating the postmortem gut microbiome in avian wildlife crimes.
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spelling doaj.art-4036f501134f460b8fc33948ffd938432022-12-22T03:53:41ZengElsevierForensic Science International: Animals and Environments2666-93742022-12-012100053Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencingJennifer L. Houtz0Joseph P. Receveur1Jennifer L. Pechal2M. Eric Benbow3Brent M. Horton4John R. Wallace5Department of Biology, Millersville University, P.O. Box 1002, Millersville, PA 17551-0302, USA; Corresponding authors.Department of Entomology, Michigan State University, 288 Farm Lane, East Lansing, MI 48824-1005, USADepartment of Entomology, Michigan State University, 288 Farm Lane, East Lansing, MI 48824-1005, USADepartment of Entomology, Michigan State University, 288 Farm Lane, East Lansing, MI 48824-1005, USA; Department of Osteopathic Medical Specialties, Michigan State University, 909 Wilson Road, East Lansing, MI 48824-1005, USADepartment of Biology, Millersville University, P.O. Box 1002, Millersville, PA 17551-0302, USADepartment of Biology, Millersville University, P.O. Box 1002, Millersville, PA 17551-0302, USA; Corresponding authors.The advent of high-throughput sequencing technologies, such as 16S rRNA amplicon sequencing, has enabled the characterization of microbial communities across diverse ecosystems including animal carrion. Although most studies on postmortem microbial communities focus on its application to human death scene analysis, this technique holds great potential for wildlife crime investigations. We conducted a pilot study to characterize the spatial heterogeneity and temporal shifts between the perimortem (i.e., at time of death) and postmortem (i.e., after death) microbiomes associated with the gut tracts of decomposing European Starling (Sturnus vulgaris) nestlings over three days. We observed significant differences in microbial community structure among perimortem gut tract regions. The microbial communities converged across all gut tract regions within the first 24 h of death and remained stable between 24 and 72 h postmortem. A random forest classifier identified Lactococcus, Serratia, and Clostridium as the top three taxonomic predictors for predicting perimortem or postmortem microbial communities. Our findings provide preliminary data for considering the potential forensic utility of incorporating the postmortem gut microbiome in avian wildlife crimes.http://www.sciencedirect.com/science/article/pii/S2666937422000130Gut microbiomeWildlife forensicsBirds, Sturnus vulgaris
spellingShingle Jennifer L. Houtz
Joseph P. Receveur
Jennifer L. Pechal
M. Eric Benbow
Brent M. Horton
John R. Wallace
Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencing
Forensic Science International: Animals and Environments
Gut microbiome
Wildlife forensics
Birds, Sturnus vulgaris
title Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencing
title_full Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencing
title_fullStr Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencing
title_full_unstemmed Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencing
title_short Characterization of the avian postmortem gut microbiome across space and time using 16S rRNA sequencing
title_sort characterization of the avian postmortem gut microbiome across space and time using 16s rrna sequencing
topic Gut microbiome
Wildlife forensics
Birds, Sturnus vulgaris
url http://www.sciencedirect.com/science/article/pii/S2666937422000130
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