First description of bacteremia caused by Oscillibacter valericigenes in a patient hospitalized for leg amputation

• Published in: Anaerobe Vol. 64; p. 102244
• Main Authors: Broutin, Lauranne, Deroche, Luc, Michaud, Anthony, Le Moal, Gwenaël, Burucoa, Christophe, Gayet, Louis-Etienne, Plouzeau, Chloé, Pichon, Maxime
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 01-08-2020; Elsevier Masson
• Subjects: 16S sequencing; Joint and bone infection; Life Sciences; Molecular diagnosis; Oscillibacter; Pharmaceutical sciences; Molecular diagnosis; Oscillibacter; Joint and bone infection; 16S sequencing
• ISSN: 1075-9964; 1095-8274
• DOI: 10.1016/j.anaerobe.2020.102244

Initially isolated from the alimentary canal of a Japanese corbicula clam, Oscillibacter valericigenes is a Gram-negative rod, of which culture remains very difficult. Herein we present the first case of bacteremia due to Oscillibacter valericigenes, in humans.
A 55-year-old man was hospitalized for clinical management of multiple neglected leg wounds (colonized with maggots) that had occurred during a motorcycle accident. Following radiological confirmation of the bone infection, a transfemoral amputation was performed to limit the risk of extended infection.
During hospitalization, before the amputation, the patient experienced fever, biological inflammation justifying the sampling of multiple blood cultures. Anaerobic blood culture was positive after 34 hours, without identification by routine procedure (MALDI-TOF), justifying identification by 16S DNA sequencing. In the absence of possible subculture, antibiotic sensitivity testing could not be performed. A pre-emptive treatment by piperacillin-tazobactam was introduced for 14 days. The evolution was good, except for a local disunion.
Complete phylogenic analysis of the clinical strain showed that it significantly differed from the reference strain, which is distantly related to the Clostridia cluster IV. Due to the culture conditions and specialized identification method by sequencing, prevalence of O. valericigenes may be underestimated. Optimization of blood culture procedures and utilization of 16S rRNA gene sequencing are tools needed for identification of rare pathogens that could help to optimize clinical management of infected patients.
•Culture of Oscillibacter valericigenes, a Gram-negative rod, remains very difficult.•This Bacterium was, for the first time, isolated during bacteremia.•16S rDNA sequencing is not of interest to predict disease severity.