Evidence map›Paper›PMID 36828537›Full record

ArticleTropical medicine and infectious disease2023

Development and Optimization of an Unbiased, Metagenomics-Based Pathogen Detection Workflow for Infectious Disease and Biosurveillance Applications.

Kyle Parker, Hillary Wood, Joseph A Russell, David Yarmosh, Alan Shteyman, John Bagnoli, Brittany Knight, Jacob R Aspinwall, Jonathan Jacobs, Kristine Werking and 1 more

Open access · goldAbstract read
In one paragraph

Article in Tropical medicine and infectious disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Kyle ParkerMRIGlobal, 425 Dr. Martin Luther King Jr. Blvd, Kansas City, MO 64110, USA.
Hillary WoodMRIGlobal, 425 Dr. Martin Luther King Jr. Blvd, Kansas City, MO 64110, USA.
Joseph A RussellMRIGlobal, 65 West Watkins Mill Road, Gaithersburg, MD 20850, USA.
David YarmoshMRIGlobal, 65 West Watkins Mill Road, Gaithersburg, MD 20850, USA.ORCID 0000-0002-5012-8606
Alan ShteymanMRIGlobal, 65 West Watkins Mill Road, Gaithersburg, MD 20850, USA.
John BagnoliMRIGlobal, 65 West Watkins Mill Road, Gaithersburg, MD 20850, USA.ORCID 0000-0002-6124-9446
Brittany KnightMRIGlobal, 425 Dr. Martin Luther King Jr. Blvd, Kansas City, MO 64110, USA.
Jacob R AspinwallMRIGlobal, 425 Dr. Martin Luther King Jr. Blvd, Kansas City, MO 64110, USA.
Jonathan JacobsMRIGlobal, 65 West Watkins Mill Road, Gaithersburg, MD 20850, USA.ORCID 0000-0001-5608-4256
Kristine WerkingMRIGlobal, 425 Dr. Martin Luther King Jr. Blvd, Kansas City, MO 64110, USA.
Richard WinegarMRIGlobal, 425 Dr. Martin Luther King Jr. Blvd, Kansas City, MO 64110, USA.
MRIGlobal · US

Funding

the Defense Threat Reduction Agency-Joint Science and Technology Office for Chemical and Biological Defense HDTRA1-15-C-0013
6 · The paper itself

Abstract

Rapid, specific, and sensitive identification of microbial pathogens is critical to infectious disease diagnosis and surveillance. Classical culture-based methods can be applied to a broad range of pathogens but have long turnaround times. Molecular methods, such as PCR, are time-effective but are not comprehensive and may not detect novel strains. Metagenomic shotgun next-generation sequencing (NGS) promises specific identification and characterization of any pathogen (viruses, bacteria, fungi, and protozoa) in a less biased way. Despite its great potential, NGS has yet to be widely adopted by clinical microbiology laboratories due in part to the absence of standardized workflows. Here, we describe a sample-to-answer workflow called PanGIA (Pan-Genomics for Infectious Agents) that includes simplified, standardized wet-lab procedures and data analysis with an easy-to-use bioinformatics tool. PanGIA is an end-to-end, multi-use workflow that can be used for pathogen detection and related applications, such as biosurveillance and biothreat detection. We performed a comprehensive survey and assessment of current, commercially available wet-lab technologies and open-source bioinformatics tools for each workflow component. The workflow includes total nucleic acid extraction from clinical human whole blood and environmental microbial forensic swabs as sample inputs, host nucleic acid depletion, dual DNA and RNA library preparation, shotgun sequencing on an Illumina MiSeq, and sequencing data analysis. The PanGIA workflow can be completed within 24 h and is currently compatible with bacteria and viruses. Here, we present data from the development and application of the clinical and environmental workflows, enabling the specific detection of pathogens associated with bloodstream infections and environmental biosurveillance, without the need for targeted assay development.

Indexed as

biosurveillancehost depletioninfectious diseasenext-generation sequencing

Identifiers

PMID36828537
PMCPMC9966482
OpenAlexW4320917720

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.