Blood culture negative endocarditis in the modern era of 16S rRNA sequencing

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.

Keywords: 16S rRNA; Bartonella henselae; Endocarditis; PCR; culture negative.

Fig 1.

A pragmatic approach to determining the causative organism in suspected endocarditis. ANA = anti-nuclear antibody; anti-dsDNA = anti-double-stranded deoxyribonucleic acid; BSAC = British Society for Antimicrobial Chemotherapy; ESC = European Society of Cardiology; PCR = polymerase chain reaction; RF rheumatoid factor; rRNA = ribosomal ribonucleic acid.