Evidence map›Paper›PMID 33363519›Full record

ArticleFrontiers in microbiology2020

Effects of Extended Postmortem Interval on Microbial Communities in Organs of the Human Cadaver.

Holly Lutz, Alexandria Vangelatos, Neil Gottel, Antonio Osculati, Silvia Visona, Sheree J Finley, Jack A Gilbert, Gulnaz T Javan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Microbiology and postmortem interval: a systematic review.Forensic science, medicine, and pathology · 2024
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  9. RedefiningFrontiers in microbiology · 2025
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  14. Impact ofJournal of clinical medicine · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Holly LutzDepartment of Pediatrics, University of California, San Diego, La Jolla, CA, United States.
Alexandria VangelatosBiological Sciences Division, University of Chicago, Chicago, IL, United States.
Neil GottelDepartment of Pediatrics, University of California, San Diego, La Jolla, CA, United States.
Antonio OsculatiDepartment of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Silvia VisonaDepartment of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Sheree J FinleyPhysical Sciences Department, Forensic Science Programs, Alabama State University, Montgomery, AL, United States.
Jack A GilbertDepartment of Pediatrics, University of California, San Diego, La Jolla, CA, United States.
Gulnaz T JavanPhysical Sciences Department, Forensic Science Programs, Alabama State University, Montgomery, AL, United States.
Alabama State University · USUniversity of California, San Diego · USUniversity of Pavia · ITScripps Institution of Oceanography · USUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human thanatomicrobiota studies have shown that microorganisms inhabit and proliferate externally and internally throughout the body and are the primary mediators of putrefaction after death. Yet little is known about the source and diversity of the thanatomicrobiome or the underlying factors leading to delayed decomposition exhibited by reproductive organs. The use of the V4 hypervariable region of bacterial 16S rRNA gene sequences for taxonomic classification ("barcoding") and phylogenetic analyses of human postmortem microbiota has recently emerged as a possible tool in forensic microbiology. The goal of this study was to apply a 16S rRNA barcoding approach to investigate variation among different organs, as well as the extent to which microbial associations among different body organs in human cadavers can be used to predict forensically important determinations, such as cause and time of death. We assessed microbiota of organ tissues including brain, heart, liver, spleen, prostate, and uterus collected at autopsy from criminal casework of 40 Italian cadavers with times of death ranging from 24 to 432 h. Both the uterus and prostate had a significantly higher alpha diversity compared to other anatomical sites, and exhibited a significantly different microbial community composition from non-reproductive organs, which we found to be dominated by the bacterial orders MLE1-12, Saprospirales, and Burkholderiales. In contrast, reproductive organs were dominated by Clostridiales, Lactobacillales, and showed a marked decrease in relative abundance of MLE1-12. These results provide insight into the observation that the uterus and prostate are the last internal organs to decay during human decomposition. We conclude that distinct community profiles of reproductive versus non-reproductive organs may help guide the application of forensic microbiology tools to investigations of human cadavers.

Indexed as

16S rRNAcadaverinternal organsmanner of deaththanatomicrobiome

Identifiers

PMID33363519
PMCPMC7752770
OpenAlexW3111092087

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.