Adaptive antimicrobial resistance, a description of microbial variants, and their relevance to periprosthetic joint infection.

Adaptive resistance Microbial variants PJI Periprosthetic joint infection Periprosthetic joint infection (PJI) Persister cells Phoenix colonies Small colony variants Transient antimicrobial resistance Transient hypermutability Variant selection antibiotic antimicrobial agents biofilms calcium sulphate clinicians organism(s) surgical debridement toxin

Journal

The bone & joint journal
ISSN: 2049-4408
Titre abrégé: Bone Joint J
Pays: England
ID NLM: 101599229

Informations de publication

Date de publication:
May 2022
Historique:
entrez: 2 5 2022
pubmed: 3 5 2022
medline: 4 5 2022
Statut: ppublish

Résumé

Periprosthetic joint infection (PJI) is a difficult complication requiring a comprehensive eradication protocol. Cure rates have essentially stalled in the last two decades, using methods of antimicrobial cement joint spacers and parenteral antimicrobial agents. Functional spacers with higher-dose antimicrobial-loaded cement and antimicrobial-loaded calcium sulphate beads have emphasized local antimicrobial delivery on the premise that high-dose local antimicrobial delivery will enhance eradication. However, with increasing antimicrobial pressures, microbiota have responded with adaptive mechanisms beyond traditional antimicrobial resistance genes. In this review we describe adaptive resistance mechanisms that are relevant to the treatment of PJI. Some mechanisms are well known, but others are new. The objective of this review is to inform clinicians of the known adaptive resistance mechanisms of microbes relevant to PJI. We also discuss the implications of these adaptive mechanisms in the future treatment of PJI. Cite this article:

Identifiants

pubmed: 35491584
doi: 10.1302/0301-620X.104B5.BJJ-2021-1759.R1
pmc: PMC9948434
doi:

Substances chimiques

Anti-Bacterial Agents 0
Anti-Infective Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

575-580

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM124436
Pays : United States
Organisme : NIAMS NIH HHS
ID : T32 AR059033
Pays : United States

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Auteurs

Christopher Hamad (C)

Department of Orthopaedic Surgery, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.

Madhav Chowdhry (M)

Nuffield Department of Primary Care Health Sciences, Kellogg College, University of Oxford, Oxford, UK.

Devin Sindeldecker (D)

Department of Microbial Infection and Immunity, The Ohio State University, Columbus, Ohio, USA.
Biomedical Sciences Graduate Program, The Ohio State University, Columbus, Ohio, USA.

Nicholas M Bernthal (NM)

Department of Orthopaedic Surgery, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.

Paul Stoodley (P)

Department of Microbial Infection and Immunity, The Ohio State University, Columbus, Ohio, USA.
Department of Orthopaedics, The Ohio State University, Columbus, Ohio, USA.
National Centre for Advanced Tribology at Southampton, Department of Mechanical Engineering, University of Southampton, Southampton, UK.

Edward J McPherson (EJ)

Department of Orthopaedic Surgery, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.

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Classifications MeSH