Progress Report: Next-Generation Sequencing, Multiplex Polymerase Chain Reaction, and Broad-Range Molecular Assays as Diagnostic Tools for Fever of Unknown Origin Investigations in Adults.

16S rRNA gene PCR fever fever of unknown origin metagenomics multiplex PCR next-generation sequencing pyrexia pyrexia of unknown origin

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
09 03 2022
Historique:
received: 09 11 2020
pubmed: 20 2 2021
medline: 16 3 2022
entrez: 19 2 2021
Statut: ppublish

Résumé

Even well into the 21st century, infectious diseases still account for most causes of fever of unknown origin (FUO). Advances in molecular technologies, including broad-range polymerase chain reaction (PCR) of the 16S ribosomal RNA gene followed by Sanger sequencing, multiplex PCR assays, and more recently, next-generation sequencing applications, have transitioned from research methods to more commonplace in some clinical microbiology laboratories. They have the potential to supplant traditional microbial identification methods and antimicrobial susceptibility testing. Despite the remaining challenges with these technologies, publications in the past decade justify excitement about the potential to transform FUO investigations. We discuss available evidence using these molecular methods for FUO evaluations, including potential cost-benefits and future directions.

Identifiants

pubmed: 33606012
pii: 6144989
doi: 10.1093/cid/ciab155
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

924-932

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

William F Wright (WF)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Patricia J Simner (PJ)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Karen C Carroll (KC)

Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Paul G Auwaerter (PG)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

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Classifications MeSH