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Community-wide transcriptome of the oral microbiome in subjects with and without periodontitis
Open accessAbstract
Despite increasing knowledge on phylogenetic composition of the human microbiome, our understanding of the in situ activities of the organisms in the community and their interactions with each other and with the environment remains limited. Characterizing gene expression profiles of the human microbiome is essential for linking the role of different members of the bacterial communities in health and disease. The oral microbiome is one of the most complex microbial communities in the human body and under certain circumstances, not completely understood, the healthy microbial community undergoes a transformation toward a pathogenic state that gives rise to periodontitis, a polymicrobial inflammatory disease. We report here the in situ genome-wide transcriptome of the subgingival microbiome in six periodontally healthy individuals and seven individuals with periodontitis. The overall picture of metabolic activities showed that iron acquisition, lipopolysaccharide synthesis and flagellar synthesis were major activities defining disease. Unexpectedly, the vast majority of virulence factors upregulated in subjects with periodontitis came from organisms that are not considered major periodontal pathogens. One of the organisms whose gene expression profile was characterized was the uncultured candidate division TM7, showing an upregulation of putative virulence factors in the diseased community. These data enhance understanding of the core activities that are characteristic of periodontal disease as well as the role that individual organisms in the subgingival community play in periodontitis.
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“Application of transcriptomic approaches has proved extremely significant for delineating both microbial and host gene expression in the context of oral health and pathology.14, 68, 94”
From The oral microbiome: Role of key organisms and complex networks in oral health and disease (2021) · cites this paper as [68]
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“Culture‐independent methods have improved our understanding of microbial diversity in the oral cavity.”
From The oral microbiome: Role of key organisms and complex networks in oral health and disease (2021) · cites this paper as [68]
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Ram-Mohan, N., & Meyer, M. M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/847889
Moderne mikrobiologisk diagnostik
Kilian, M. (2020) · Aktuel nordisk odontologi · doi:10.18261/issn.2058-7538-2020-01-02
Parallelized Pipeline for Whole Genome Shotgun Metagenomics with GHOSTZ-GPU and MEGAN
Ohue, M., Yamasawa, M., Izawa, K., & Akiyama, Y. (2019) · IEEE International Conference on Bioinformatics and Bioengineering (BIBE) · doi:10.1109/bibe.2019.00035
Ecological Approaches to Periodontal Therapy
Diaz, P. I., & Hoare, A. (2020) · Springer eBooks · doi:10.1007/978-3-030-42990-4_13
Besteht ein Zusammenhang zwischen der peripheren arteriellen Verschlusskrankheit und Parodontitis?
Aarabi, G., Jacobi, N., Kaschwich, M., Walther, C., Raedel, M., Debus, E. S., Larena-Avellaneda, A. A., Seedorf, U., Heydecke, G., & Behrendt, C. (2020) · Gefässchirurgie · doi:10.1007/s00772-020-00689-2
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“59 In particular, multiple separate cohort studies have probed the functional potential of 60 periodontitis-associated microbiota via metagenome (15, 18, 19, 24, 25) or metatranscriptome 61 (26, 27).”
BackgroundEcological Perturbations Impact Species-Specific Gene Expression of the Oral MicrobiotaPreprint
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Stress Hormones and the Gut Microbiota Composition and Function
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Self-citationEcological Therapeutic Opportunities for Oral Diseases
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The evolving microbial taxonomy
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“[1,5,16] ]”
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The Oral Biofilm Microenvironment
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Oral Microbiome in Periodontal Disease: Where Are We Now?
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“…study by Duran-Pinedo et al., it was observed that, in the context of periodontal disease, there was an upregulation in the expression of genes and related metabolic activities involved in iron uptake, lipopolysaccharide synthesis, fla - gella synthesis, and beta-lactam degradation processes [ 71].”
Metadata
- Authors
- Duran-Pinedo, A. E., Chen, T., Teles, R., Starr, J. R., Wang, X., Krishnan, K., & Frias-Lopez, J.
- Affiliations
- The Forsyth Institute (US)
- Harvard University (US)
- Department of Microbiology, Forsyth Institute , Cambridge, MA, USA
- Venue
- The ISME Journal
- Publisher
- Oxford University Press (OUP)
- Published
- 2014-03-06
- Volume
- 8
- Issue
- 8
- Pages
- 1659-1672
- ISSN
- 1751-7362 (ISSN-L)
- 1751-7370
- PMC
- PMC4817619
- OpenAlex
- W2080580603
- Cited by
- 327
- References
- 92
- Citations by year
- 2026: 15 · 2025: 19 · 2024: 17 · 2023: 21 · 2022: 36 · 2021: 42 · 2020: 38 · 2019: 26 · 2018: 25 · 2017: 28 · 2016: 21 · 2015: 26 · 2014: 12
- FWCI
- 38.27
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The ISME Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Dental and Craniofacial Research (DE021127, U01DE021127, DE021553, R01DE021553)
- Topics
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- periodontitis, oral microbiota, subgingival microbiota, microbial gene expression, virulence factors, iron acquisition, lipopolysaccharide biosynthesis, flagellar synthesis, polymicrobial disease, microbial interactions
- MeSH terms
- Adult, Bacteria, Humans, Periodontitis, Phylogeny, Virulence Factors, Metagenome, Transcriptome, Microbiota
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