Clinical Metagenomic Sequencing for Species Identification and Antimicrobial Resistance Prediction in Orthopedic Device Infection.


Journal

Journal of clinical microbiology
ISSN: 1098-660X
Titre abrégé: J Clin Microbiol
Pays: United States
ID NLM: 7505564

Informations de publication

Date de publication:
20 04 2022
Historique:
pubmed: 1 4 2022
medline: 23 4 2022
entrez: 31 3 2022
Statut: ppublish

Résumé

Diagnosis of orthopedic device-related infection is challenging, and causative pathogens may be difficult to culture. Metagenomic sequencing can diagnose infections without culture, but attempts to detect antimicrobial resistance (AMR) determinants using metagenomic data have been less successful. Human DNA depletion may maximize the amount of microbial DNA sequence data available for analysis. Human DNA depletion by saponin was tested in 115 sonication fluid samples generated following revision arthroplasty surgery, comprising 67 where pathogens were detected by culture and 48 culture-negative samples. Metagenomic sequencing was performed on the Oxford Nanopore Technologies GridION platform. Filtering thresholds for detection of true species versus contamination or taxonomic misclassification were determined. Mobile and chromosomal genetic AMR determinants were identified in Staphylococcus aureus-positive samples. Of 114 samples generating sequence data, species-level positive percent agreement between metagenomic sequencing and culture was 50/65 (77%; 95% confidence interval [CI], 65 to 86%) and negative percent agreement was 103/114 (90%; 95% CI, 83 to 95%). Saponin treatment reduced the proportion of human bases sequenced in comparison to 5-μm filtration from a median (interquartile range [IQR]) of 98.1% (87.0% to 99.9%) to 11.9% (0.4% to 67.0%), improving reference genome coverage at a 10-fold depth from 18.7% (0.30% to 85.7%) to 84.3% (12.9% to 93.8%). Metagenomic sequencing predicted 13/15 (87%) resistant and 74/74 (100%) susceptible phenotypes where sufficient data were available for analysis. Metagenomic nanopore sequencing coupled with human DNA depletion has the potential to detect AMR in addition to species detection in orthopedic device-related infection. Further work is required to develop pathogen-agnostic human DNA depletion methods, improving AMR determinant detection and allowing its application to other infection types.

Identifiants

pubmed: 35354286
doi: 10.1128/jcm.02156-21
pmc: PMC9020354
doi:

Substances chimiques

Anti-Bacterial Agents 0
Saponins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0215621

Subventions

Organisme : Wellcome Trust
ID : 200205/Z/15/Z
Pays : United Kingdom
Organisme : NIHR | NIHR Oxford Biomedical Research Centre (OxBRC)
ID : BRC-1215-20008

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Auteurs

Teresa L Street (TL)

Nuffield Department of Medicine, University of Oxfordgrid.4991.5, John Radcliffe Hospital, Oxford, United Kingdom.
NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom.

Nicholas D Sanderson (ND)

Nuffield Department of Medicine, University of Oxfordgrid.4991.5, John Radcliffe Hospital, Oxford, United Kingdom.
NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom.

Camille Kolenda (C)

Department of Bacteriology, Lyon University Hospital, Lyon, France.

James Kavanagh (J)

Nuffield Department of Medicine, University of Oxfordgrid.4991.5, John Radcliffe Hospital, Oxford, United Kingdom.

Hayleah Pickford (H)

Nuffield Department of Medicine, University of Oxfordgrid.4991.5, John Radcliffe Hospital, Oxford, United Kingdom.

Sarah Hoosdally (S)

Nuffield Department of Medicine, University of Oxfordgrid.4991.5, John Radcliffe Hospital, Oxford, United Kingdom.
NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom.

Jack Cregan (J)

Nuffield Department of Medicine, University of Oxfordgrid.4991.5, John Radcliffe Hospital, Oxford, United Kingdom.

Carol Taunt (C)

Microbiology Laboratory, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Emma Jones (E)

Microbiology Laboratory, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Sarah Oakley (S)

Microbiology Laboratory, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Bridget L Atkins (BL)

Microbiology Laboratory, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
Bone Infection Unit, Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Maria Dudareva (M)

Microbiology Laboratory, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
Bone Infection Unit, Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Martin A McNally (MA)

Bone Infection Unit, Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Justin O'Grady (J)

Quadram Institute Bioscience, Norwich, United Kingdom.

Derrick W Crook (DW)

Nuffield Department of Medicine, University of Oxfordgrid.4991.5, John Radcliffe Hospital, Oxford, United Kingdom.
NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom.

David W Eyre (DW)

NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom.
Big Data Institute, Nuffield Department of Population Health, University of Oxfordgrid.4991.5, Oxford, United Kingdom.

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Classifications MeSH