Cited by 601Anaerobic Digestion and Biogas ProductionGut microbiota and healthMicrobial Fuel Cells and Bioremediation

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Methanomassiliicoccus luminyensis gen. nov., sp. nov., a methanogenic archaeon isolated from human faeces

Dridi, Bédis, Fardeau, Marie-Laure, Ollivier, Bernard, Raoult, Didier, Drancourt, Michel·2012·International Journal of Systematic and Evolutionary Microbiology

DOI 10.1099/ijs.0.033712-0

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Abstract

During attempts to obtain novel, human-associated species of the domain Archaea , a coccoid micro-organism, designated strain B10 T , was isolated in pure culture from a sample of human faeces collected in Marseille, France. On the basis of its phenotypic characteristics and 16S rRNA and mcr A gene sequences, the novel strain was classified as a methanogenic archaeon. Cells of the strain were non-motile, Gram-staining-positive cocci that were approximately 850 nm in diameter and showed autofluorescence at 420 nm. Cells were lysed by 0.1 % (w/v) SDS. With hydrogen as the electron donor, strain B10 T produced methane by reducing methanol. The novel strain was unable to produce methane when hydrogen or methanol was the sole energy source. In an atmosphere containing CO 2 , strain B10 T could not produce methane from formate, acetate, trimethylamine, 2-butanol, 2-propanol, cyclopentanol, 2-pentanol, ethanol, 1-propanol or 2,3-butanediol. Strain B10 T grew optimally with 0.5–1.0 % (w/v) NaCl, at pH 7.6 and at 37 °C. It required tungstate-selenite for growth. The complete genome of the novel strain was sequenced; the size of the genome was estimated to be 2.05 Mb and the genomic DNA G+C content was 59.93 mol%. In phylogenetic analyses based on 16S rRNA gene sequences, the highest sequence similarities (98.0–98.7 %) were seen between strain B10 T and several uncultured, methanogenic Archaea that had been collected from the digestive tracts of a cockroach, a chicken and mammals. In the same analysis, the non-methanogenic ‘ Candidatus Aciduliprofundum boonei’ DSM 19572 was identified as the cultured micro-organism that was most closely related to strain B10 T (83.0 % 16S rRNA gene sequence similarity). Each of the three treeing algorithms used in the analysis of 16S rRNA gene sequences indicated that strain B10 T belongs to a novel order that is distinct from the Thermoplasmatales . The novel strain also appeared to be distinct from Methanosphaera stadtmanae DSM 3091 T (72.9 % 16S rRNA gene sequence similarity), another methanogenic archaeon that was isolated from human faeces and can use methanol in the presence of hydrogen. Based on the genetic and phenotypic evidence, strain B10 T represents a novel species of a new genus for which the name Methanomassiliicoccus luminyensis gen. nov., sp. nov. is proposed. The type strain of the type species is B10 T ( = DSM 24529 T = CSUR P135 T ).

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16S ribosomal DNA amplification for phylogenetic study
Weisburg, W. G., Barns, S. M., Pelletier, D. A., & Lane, D. J. (1991) · Journal of Bacteriology · doi:10.1128/jb.173.2.697-703.1991 · Cited by 11,970
Genome sequencing in microfabricated high-density picolitre reactors
Margulies, M., Egholm, M., Altman, W. E., Attiya, S., Bader, J. S., Bemben, L. A., Berka, J., Braverman, M. S., Chen, Y.-J., Chen, Z., et al. (2005) · Nature · doi:10.1038/nature03959 · Cited by 7,693
MEGA: A biologist-centric software for evolutionary analysis of DNA and protein sequences
Kumar, S., Nei, M., Dudley, J. T., & Tamura, K. (2008) · Briefings in Bioinformatics · doi:10.1093/bib/bbn017 · Cited by 3,511
Methanogens: reevaluation of a unique biological group
Balch, W. E., Fox, G. E., Magrum, L. J., Woese, C. R., & WOLFE, R. S. (1979) · Microbiological Reviews · doi:10.1128/mr.43.2.260-296.1979 · Cited by 2,918
The mcrA gene as an alternative to 16S rRNA in the phylogenetic analysis of methanogen populations in landfill b bThe GenBank accession numbers for the mcrA sequences reported in this paper are AF414034–AF414051 (see Fig. 2) and AF414007–AF414033 (environmental isolates in Fig. 3).
Luton, P. E., Wayne, J. M., Sharp, R. J., & Riley, P. W. (2002) · Microbiology · doi:10.1099/00221287-148-11-3521 · Cited by 875
Genomic and metabolic adaptations of Methanobrevibacter smithii to the human gut
Samuel, B. S., Hansen, E. E., Manchester, J. K., Coutinho, P. M., Henrissat, B., Fulton, R., Latreille, P., Kim, K., Wilson, R. K., & Gordon, J. I. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704189104 · Cited by 549
High Prevalence of Methanobrevibacter smithii and Methanosphaera stadtmanae Detected in the Human Gut Using an Improved DNA Detection Protocol
Dridi, B., Henry, M., Khéchine, A. E., Raoult, D., & Drancourt, M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007063 · Cited by 401
Self-citation
Identification of Methyl Coenzyme M Reductase A ( mcrA ) Genes Associated with Methane-Oxidizing Archaea
Hallam, S., Girguis, P. R., Preston, C. M., Richardson, P. M., & DeLong, E. F. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.9.5483-5491.2003 · Cited by 385
Methanosphaera stadtmaniae gen. nov., sp. nov.: a species that forms methane by reducing methanol with hydrogen
Miller, T. L., & Wolin, M. J. (1985) · Archives of Microbiology · doi:10.1007/bf00423270 · Cited by 362
Isolation of Methanobrevibacter smithii from human feces
Miller, T. L., Wolin, M. J., de Macario, E. C., & Macario, A. J. L. (1982) · Applied and Environmental Microbiology · doi:10.1128/aem.43.1.227-232.1982 · Cited by 287

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Authors: Dridi, B., Fardeau, M.-L., Ollivier, B., Raoult, D., & Drancourt, M.
Affiliations: Centre National de la Recherche Scientifique (FR)
Aix-Marseille Université (FR)
ORCID: Fardeau, Marie-Laure
Ollivier, Bernard
Raoult, Didier
Drancourt, Michel
Venue: International Journal of Systematic and Evolutionary Microbiology
Publisher: Microbiology Society
Published: 2012-08-01
Volume: 62
Issue: Pt_8
Pages: 1902-1907
ISSN: 1466-5026 (ISSN-L)
1466-5034
DOI: 10.1099/ijs.0.033712-0
OpenAlex: W2076631370
Cited by: 596
References: 32
Citations by year: 2026: 14 · 2025: 19 · 2024: 36 · 2023: 38 · 2022: 40 · 2021: 49 · 2020: 61 · 2019: 63 · 2018: 66 · 2017: 42 · 2016: 45 · 2015: 53 · 2014: 28 · 2013: 31 · 2012: 11
FWCI: 76.70
Type: journal article
Language: en
Open access: closed
Locations: INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY (publishedVersion)
PubMed (publishedVersion)
HAL (submittedVersion)
Funders: Aix-Marseille Université
Topics: Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Anaerobic Digestion and Biogas Production
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Physical Sciences › Environmental Science › Environmental Engineering › Microbial Fuel Cells and Bioremediation
MeSH terms: Aged, 80 and over, Archaea, Base Composition, Feces, Humans, Male, Methane, Molecular Sequence Data, Phylogeny, RNA, Ribosomal, 16S, Sequence Analysis, DNA, DNA, Archaeal, Genome, Archaeal

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Methanomassiliicoccus luminyensis gen. nov., sp. nov., a methanogenic archaeon isolated from human faeces

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