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Updated: Dec 14, 2025

Identification of Rare Bacterial Pathogens by 16S rRNA Gene Sequencing and MALDI-TOF MS
Published on: July 11, 2016
Blood culture negative endocarditis in the modern era of 16S rRNA sequencing
Rebecca Godfrey1, Sally Curtis2, William Hk Schilling2
1Sussex Cardiac Centre, Brighton, UK.
Abstract:
Blood culture negative endocarditis (BCNE) accounts for up to 20% of infective endocarditis. While the most common cause of BCNE remains the initiation of antibiotics prior to culture, intracellular organisms such as Coxiella and Bartonella spp account for a significant proportion of cases. Identifying the infecting organism remains important to ensure optimal antimicrobial treatment. However, these organisms can be difficult to diagnose. We outline a systematic approach to BCNE. Over half of patients with infective endocarditis now undergo early surgery and 16S ribosomal ribonucleic acid (rRNA) polymerase chain reaction (PCR) of excised tissue can be vitally important to secure a diagnosis. Molecular testing is likely to become a key tool in improving outcomes from BCNE and contribute to an improved understanding of the aetiology. We advocate modifying the Duke criteria to incorporate organisms identified on molecular testing, including 16S rRNA PCR, in particular from explanted tissue.
Related Concept Videos
Endocarditis I: Introduction
Modern Molecular Taxonomy
Endocarditis II: Clinical Features of Infective Endocarditis
Endocarditis III: Medical Management
Applications of Molecular Taxonomy
Endocarditis IV: Nursing Management

