Isolation and culture of Methanobrevibacter smithii by co-culture with hydrogen-producing bacteria on agar plates

• Published in: Clinical microbiology and infection Vol. 25; no. 12; pp. 1561.e1 - 1561.e5
• Main Authors: Traore, S.I., Khelaifia, S., Armstrong, N., Lagier, J.C., Raoult, D.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.12.2019; Elsevier for the European Society of Clinical Microbiology and Infectious Diseases
• Subjects: Adult; Agar; Anaerobes; Anaerobiosis; Bacteria - classification; Bacteria - growth & development; Bacteria - metabolism; Bacteriology; Co-culture; Coculture Techniques; Culture Media; Feces - microbiology; Female; Healthy Volunteers; Humans; Hydrogen - metabolism; Hydrogen production; Life Sciences; Methane - analysis; Methane - biosynthesis; Methane production; Methanobrevibacter - growth & development; Methanobrevibacter - isolation & purification; Methanobrevibacter - metabolism; Methanobrevibacter smithii; Microbiology and Parasitology; Anaerobes; Co-culture; Methane production; Hydrogen production; Methanobrevibacter smithii
• ISSN: 1198-743X; 1469-0691
• DOI: 10.1016/j.cmi.2019.04.008

Methanogenic Archaea are considered as extremely oxygen-sensitive organisms, and their culture is fastidious, requiring specific equipment. We report here conditions allowing the cultivation of Methanobrevibacter smithii in an anaerobic chamber without the addition of hydrogen. We first enriched the stool sample in an anaerobic liquid medium. To cultivate M. smithii with Bacteroides thetaiotaomicron and other hydrogen-producing bacteria on solid medium in an anaerobic chamber, we divided the agar plates into two compartments and seeded each strain on each compartment. Methane production was assessed by gas chromatography, and the growing colonies were authenticated by MALDI-TOF MS. We successfully cultured M. smithii from a liquid culture medium inoculated with stool collected from a healthy donor in an anaerobic chamber. The isolation in pure culture permitted successful culture on agar medium by our performing a co-culture with B. thetaiotaomicron. We also successfully tested the co-cultivation of M. smithii with other known hydrogen-producing bacteria. Gas chromatographic tests showed that these strains produced hydrogen in different amounts. Agar colonies of methanogens were obtained by co-culture with these bacteria, and methane production was detected. We propose a new approach to isolate and cultivate new strains of M. smithii by using a co-culture–based technique that can facilitate and make available the isolation of new methanogenic Archaea strains in clinical microbiology laboratories.