Evidence map›Paper›PMID 31563940›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

Investigating Transfusion-related Sepsis Using Culture-Independent Metagenomic Sequencing.

Emily Crawford, Jack Kamm, Steve Miller, Lucy M Li, Saharai Caldera, Amy Lyden, Deborah Yokoe, Amy Nichols, Nam K Tran, Sarah E Barnard and 13 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Metagenomic next-generation sequencing: new horizons in microbiology.Frontiers in cellular and infection microbiology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Whole-genome sequencing rule-out of suspected hospital-onsetInfection control and hospital epidemiology · 2023
    Article
  13. Review
  14. In host evolution of beta lactam resistance during active treatment forFrontiers in cellular and infection microbiology · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

23 authors.

Emily CrawfordChan Zuckerberg Biohub, San Francisco, California, USA.
Jack KammChan Zuckerberg Biohub, San Francisco, California, USA.
Steve MillerDepartment of Laboratory Medicine, University of California-San Francisco, San Francisco, California, USA.
Lucy M LiChan Zuckerberg Biohub, San Francisco, California, USA.
Saharai CalderaChan Zuckerberg Biohub, San Francisco, California, USA.
Amy LydenChan Zuckerberg Biohub, San Francisco, California, USA.
Deborah YokoeDivision of Infectious Diseases, Department of Medicine, University of California-San Francisco, San Francisco, California, USA.
Amy NicholsDepartment of Hospital Epidemiology and Infection Prevention, University of California-San Francisco, San Francisco, California, USA.
Nam K TranDepartment of Pathology and Laboratory Medicine, University of California-Davis, Davis, California, USA.
Sarah E BarnardDepartment of Pathology and Laboratory Medicine, University of California-Davis, Davis, California, USA.
Peter M ConnerDepartment of Pathology and Laboratory Medicine, University of California-Davis, Davis, California, USA.
Ashok NambiarDepartment of Laboratory Medicine, University of California-San Francisco, San Francisco, California, USA.
Matt S ZinterDivision of Pulmonary and Critical Care Medicine, Department of Pediatrics, University of California-San Francisco, San Francisco, California, USA.
Morvarid MoayeriDepartment of Laboratory Medicine, University of California-San Francisco, San Francisco, California, USA.
Paula Hayakawa SerpaChan Zuckerberg Biohub, San Francisco, California, USA.
Brian C PrinceDivision of Infectious Diseases, Department of Medicine, University of California-San Francisco, San Francisco, California, USA.
Jenai QuanNorthwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Rene SitChan Zuckerberg Biohub, San Francisco, California, USA.
Michelle TanChan Zuckerberg Biohub, San Francisco, California, USA.
Maira PhelpsChan Zuckerberg Biohub, San Francisco, California, USA.
Joseph L DerisiChan Zuckerberg Biohub, San Francisco, California, USA.
Cristina M TatoChan Zuckerberg Biohub, San Francisco, California, USA.
Charles LangelierChan Zuckerberg Biohub, San Francisco, California, USA.

Funding

Profiling the Lung Transcriptome for Precision Diagnosis of Respiratory Infections using Host/Pathogen Metagenomic SequencingK23HL138461 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LANGELIER, CHARLES · 2018 to 2021
$718k
NHLBI NIH HHS K23 HL138461
6 · The paper itself

Abstract

backgroundTransfusion-related sepsis remains an important hospital infection control challenge. Investigation of septic transfusion events is often restricted by the limitations of bacterial culture in terms of time requirements and low yield in the setting of prior antibiotic administration.

methodsIn 3 gram-negative septic transfusion cases, we performed metagenomic next-generation sequencing (mNGS) of direct clinical blood specimens in addition to standard culture-based approaches utilized for infection control investigations. Pathogen detection leveraged IDSeq, a new open-access microbial bioinformatics portal. Phylogenetic analysis was performed to assess microbial genetic relatedness and understand transmission events.

resultsmNGS of direct clinical blood specimens afforded precision detection of pathogens responsible for each case of transfusion-related sepsis and enabled discovery of a novel Acinetobacter species in a platelet product that had become contaminated despite photochemical pathogen reduction. In each case, longitudinal assessment of pathogen burden elucidated the temporal sequence of events associated with each transfusion-transmitted infection. We found that informative data could be obtained from culture-independent mNGS of residual platelet products and leftover blood specimens that were either unsuitable or unavailable for culture or that failed to grow due to prior antibiotic administration. We additionally developed methods to enhance accuracy for detecting transfusion-associated pathogens that share taxonomic similarity to contaminants commonly found in mNGS library preparations.

conclusionsCulture-independent mNGS of blood products afforded rapid and precise assessment of pathogen identity, abundance, and genetic relatedness. Together, these challenging cases demonstrated the potential for metagenomics to advance existing methods for investigating transfusion-transmitted infections.

Indexed as

MetagenomicsSepsisHigh-Throughput Nucleotide SequencingHumansMetagenomePhylogenyhealthcare infectionsmetagenomic sequencingmNGSplatelet transfusionseptic transfusion

Identifiers

PMID31563940
PMCPMC7442849

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.