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The keystone-pathogen hypothesis
Open accessAbstract
Recent studies have highlighted the importance of the human microbiome in health and disease. However, for the most part the mechanisms by which the microbiome mediates disease, or protection from it, remain poorly understood. The keystone-pathogen hypothesis holds that certain low-abundance microbial pathogens can orchestrate inflammatory disease by remodelling a normally benign microbiota into a dysbiotic one. In this Opinion article, we critically assess the available literature that supports this hypothesis, which may provide a novel conceptual basis for the development of targeted diagnostics and treatments for complex dysbiotic diseases.
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“The genus Prevotella, including P. denticola, acts on the early and middle steps of oral biofilm formation with cellular adhesion for later colonizers and, in particular, supports the biofilm formation of Aggregatibacter actinomycetemcomitans [22,23].”
From Analysis of Chemical Structure and Antibiofilm Properties of Exopolysaccharides from Lactiplantibacillus plantarum EIR/IF-1 Postbiotics (2022) · cites this paper as [22]
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“The keystone-pathogen hypothesis88 and the α-bug hypothesis both state that certain, low abundance microbiota members (such as enterotoxigenic B. fragilis) possess unique virulence traits, which are pro-oncogenic and remodel the microbiome and in turn promote mucosal immune responses and colonic epithelial cell changes.89”
From The gut microbiota and host health: a new clinical frontier (2016) · cites this paper as [88]
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Cites
A human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624
Enterotypes of the human gut microbiome
MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548
Food Web Complexity and Species Diversity
Paine, R. T. (1966) · The American Naturalist · doi:10.1086/282400 · Cited by 5,361
Host-Bacterial Mutualism in the Human Intestine
Bäckhed, F., Ley, R. E., Sonnenburg, J. L., Peterson, D. A., & Gordon, J. I. (2005) · Science · doi:10.1126/science.1104816 · Cited by 5,277
Microbial complexes in subgingival plaque
Socransky, S. S., Haffajee, A. D., Cugini, M. A., Smith, C., & Kent, R. L. (1998) · Journal of Clinical Periodontology · doi:10.1111/j.1600-051x.1998.tb02419.x · Cited by 5,050
Pihlstrom, B. L., Michalowicz, B. S., & Johnson, N. W. (2005) · The Lancet · doi:10.1016/s0140-6736(05)67728-8 · Cited by 3,718
A microbial symbiosis factor prevents intestinal inflammatory disease
Mazmanian, S. K., Round, J. L., & Kasper, D. L. (2008) · Nature · doi:10.1038/nature07008 · Cited by 2,340
Metabolic Syndrome and Altered Gut Microbiota in Mice Lacking Toll-Like Receptor 5
Vijay-Kumar, M., Aitken, J. D., Carvalho, F. A., Cullender, T. C., Mwangi, S., Srinivasan, S., Sitaraman, S. V., Knight, R., Ley, R. E., & Gewirtz, A. T. (2010) · Science · doi:10.1126/science.1179721 · Cited by 2,068
Fusobacterium nucleatum infection is prevalent in human colorectal carcinoma
Castellarin, M., Warren, R. L., Freeman, J. D., Dreolini, L., Krzywinski, M., Strauss, J., Barnes, R., Watson, P., Allen-Vercoe, E., Moore, R. A., et al. (2012) · Genome Research · doi:10.1101/gr.126516.111 · Cited by 2,043
NLRP6 Inflammasome Regulates Colonic Microbial Ecology and Risk for Colitis
Elinav, E., Strowig, T., Kau, A. L., Henao-Mejia, J., Thaiss, C. A., Booth, C. J., Peaper, D. R., Bertin, J., Eisenbarth, S. C., Gordon, J. I., et al. (2011) · Cell · doi:10.1016/j.cell.2011.04.022 · Cited by 2,024
Challenges in the Quest for Keystones
Power, M. E., Tilman, D., Estes, J. A., Menge, B. A., Bond, W. J., Mills, L. S., Daily, G., Castilla, J. C., Lubchenco, J., & Paine, R. T. (1996) · BioScience · doi:10.2307/1312990 · Cited by 2,018
Genomic analysis identifies association of Fusobacterium with colorectal carcinoma
Kostic, A. D., Gevers, D., Pedamallu, C. S., Michaud, M., Duke, F., Earl, A. M., Ojesina, A. I., Jung, J., Bass, A. J., Tabernero, J., et al. (2012) · Genome Research · doi:10.1101/gr.126573.111 · Cited by 1,960
Intestinal homeostasis and its breakdown in inflammatory bowel disease
Maloy, K. J., & Powrie, F. M. (2011) · Nature · doi:10.1038/nature10208 · Cited by 1,911
Human gut microbiota in obesity and after gastric bypass
Zhang, H., DiBaise, J. K., Zuccolo, A., Kudrna, D., Braidotti, M., Yu, Y., Parameswaran, P., Crowell, M. D., Wing, R., Rittmann, B. E., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812600106 · Cited by 1,880
Crosstalk between cancer and immune cells: role of STAT3 in the tumour microenvironment
Yu, H., Kortylewski, M., & Pardoll, D. M. (2006) · Nature reviews. Immunology · doi:10.1038/nri1995 · Cited by 1,841
Wu, S., Rhee, K.-J., Albesiano, E., Rabizadeh, S., Wu, X., Yen, H.-R., Huso, D. L., Brancati, F. L., Wick, E., McAllister, F., et al. (2009) · Nature Medicine · doi:10.1038/nm.2015 · Cited by 1,812
A note on trophic complexity and community stability.
Paine, R. T. (1969) · The American Naturalist · doi:10.1086/282586 · Cited by 1,796
Periodontitis: a polymicrobial disruption of host homeostasis
Darveau, R. P. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2337 · Cited by 1,688
Self-citationH OW H OST -M ICROBIAL I NTERACTIONS S HAPE THE N UTRIENT E NVIRONMENT OF THE M AMMALIAN I NTESTINE
Hooper, L. V., Midtvedt, T., & Gordon, J. I. (2002) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.22.011602.092259 · Cited by 1,623
The Toll-like receptor 2 pathway establishes colonization by a commensal of the human microbiota
Round, J. L., Lee, S. M., Li, J., Tran, G., Jabri, B., Chatila, T. A., & Mazmanian, S. K. (2011) · Science · doi:10.1126/science.1206095 · Cited by 1,604
A Genomic View of the Human- Bacteroides thetaiotaomicron Symbiosis
Xu, J., Bjursell, M. K., Himrod, J., Deng, S., Carmichael, L. K., Chiang, H. C., Hooper, L. V., & Gordon, J. I. (2003) · Science · doi:10.1126/science.1080029 · Cited by 1,353
Lupp, C., Robertson, M. L., Wickham, M. E., Sekirov, I., Champion, O. L., Gaynor, E. C., & Finlay, B. B. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.06.010 · Cited by 1,310
Sea Otters: Their Role in Structuring Nearshore Communities
Estes, J. A., & Palmisano, J. F. (1974) · Science · doi:10.1126/science.185.4156.1058 · Cited by 1,187
Glycan foraging in vivo by an intestine-adapted bacterial symbiont
Sonnenburg, J. L., Xu, J., Leip, D. D., Chen, C.-H., Westover, B. P., Weatherford, J., Buhler, J. D., & Gordon, J. I. (2005) · Science · doi:10.1126/science.1109051 · Cited by 1,184
Hajishengallis, G., Liang, S., Payne, M. A., Hashim, A., Jotwani, R., Eskan, M. A., McIntosh, M. L., Alsam, A., Kirkwood, K. L., Lambris, J. D., et al. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.10.006 · Cited by 1,154
Self-citationEpithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut
Artis, D. (2008) · Nature reviews. Immunology · doi:10.1038/nri2316 · Cited by 1,136
Diabetes mellitus and periodontitis: a tale of two common interrelated diseases
Lalla, E., & Papapanou, P. N. (2011) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2011.106 · Cited by 1,063
Stecher, B., Robbiani, R., Walker, A. W., Westendorf, A. M., Barthel, M., Kremer, M., Chaffron, S., Macpherson, A. J., Buer, J., Parkhill, J., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050244 · Cited by 1,048
Kelly, D., Campbell, J. I., King, T. P., Grant, G., Jansson, E. Å., Coutts, A., Pettersson, S., & Conway, S. (2003) · Nature Immunology · doi:10.1038/ni1018 · Cited by 1,026
Angiogenins: a new class of microbicidal proteins involved in innate immunity
Hooper, L. V., Stappenbeck, T. S., Hong, C. V., & Gordon, J. I. (2003) · Nature Immunology · doi:10.1038/ni888 · Cited by 947
Holt, S. C., & Ebersole, J. L. (2005) · Periodontology 2000 · doi:10.1111/j.1600-0757.2005.00113.x · Cited by 932
Communicable Ulcerative Colitis Induced by T-bet Deficiency in the Innate Immune System
Garrett, W. S., Lord, G. M., Punit, S., Lugo‐Villarino, G., Mazmanian, S. K., Ito, S., Glickman, J. N., & Glimcher, L. H. (2007) · Cell · doi:10.1016/j.cell.2007.08.017 · Cited by 915
Armougom, F., Henry, M., Vialettes, B., Raccah, D., & Raoult, D. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007125 · Cited by 905
A bacterial driver–passenger model for colorectal cancer: beyond the usual suspects
Tjalsma, H., Boleij, A., Marchesi, J. R., & Dutilh, B. E. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2819 · Cited by 903
Escherichia coli induces DNA damage in vivo and triggers genomic instability in mammalian cells
Cuevas-Ramos, G., Petit, C. R., Marcq, I., Boury, M., Oswald, E., & Nougayrède, J.-P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001261107 · Cited by 855
Garrett, W. S., Gallini, C. A., Yatsunenko, T., Michaud, M., DuBois, A., Delaney, M. L., Punit, S., Karlsson, M., Bry, L., Glickman, J. N., et al. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2010.08.004 · Cited by 788
Martin, H., Campbell, B. J., Hart, C. A., Mpofu, C., Nayar, M. K., Singh, R., Englyst, H. N., Williams, H. F., & Rhodes, J. M. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.03.054 · Cited by 719
A humanized gnotobiotic mouse model of host-archaeal-bacterial mutualism
Samuel, B. S., & Gordon, J. I. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602187103 · Cited by 674
Intestinal Microbiota Promote Enteric Virus Replication and Systemic Pathogenesis
Kuss-Duerkop, S. K., Best, G. T., Etheredge, C. A., Pruijssers, A. J. P., Frierson, J. M., Hooper, L. V., Dermody, T. S., & Pfeiffer, J. K. (2011) · Science · doi:10.1126/science.1211057 · Cited by 631
Microbiology of Periodontal Disease—Present Status and Future Considerations
Socransky, S. S. (1977) · Journal of Periodontology · doi:10.1902/jop.1977.48.9.497 · Cited by 629
Role of the Commensal Microbiota in Normal and Pathogenic Host Immune Responses
Littman, D. R., & Pamer, E. G. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.10.004 · Cited by 568
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
Bacteriology of severe periodontitis in young adult humans
Moore, W. E., Holdeman, L. V., Smibert, R. M., Hash, D. E., Burmeister, J. A., & Ranney, R. R. (1982) · Infection and Immunity · doi:10.1128/iai.38.3.1137-1148.1982 · Cited by 480
Hastürk, H., Kantarcı, A., Goguet, E., Blackwood, A., Andry, C., Serhan, C. N., & Dyke, T. E. V. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.10.7021 · Cited by 470
Pathobionts of the gastrointestinal microbiota and inflammatory disease
Chow, J., Tang, H., & Mazmanian, S. K. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.07.010 · Cited by 466
Implantation of Bacteroides gingivalis in Nonhuman Primates Initiates Progression of Periodontitis
Holt, S. C., Ebersole, J. L., Felton, J. R., Brunsvold, M. A., & Kornman, K. S. (1988) · Science · doi:10.1126/science.3336774 · Cited by 464
A possible role of Bacteroides fragilis enterotoxin in the aetiology of colorectal cancer
Ulger Toprak, N., Yagci, A., Gulluoglu, B. M., Akin, M. L., Demirkalem, P., Celenk, T., & Soyletir, G. (2006) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2006.01494.x · Cited by 454
The Commensal Microbiota and Enteropathogens in the Pathogenesis of Inflammatory Bowel Diseases
Chassaing, B., & Darfeuille–Michaud, A. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.01.054 · Cited by 443
The leukocyte integrin antagonist Del-1 inhibits IL-17-mediated inflammatory bone loss
Eskan, M. A., Jotwani, R., Abe, T., Chmelar, J., Lim, J.-H., Liang, S., Ciero, P. A., Krauss, J. L., Li, F., Rauner, M., et al. (2012) · Nature Immunology · doi:10.1038/ni.2260 · Cited by 429
Self-citationEnterotoxigenic Bacteroides fragilis : a Rogue among Symbiotes
Sears, C. L. (2009) · Clinical Microbiology Reviews · doi:10.1128/cmr.00053-08 · Cited by 428
Modulation of the Intestinal Microbiota Alters Colitis-Associated Colorectal Cancer Susceptibility
Uronis, J. M., Mühlbauer, M., Herfarth, H. H., Rubinas, T. C., Jones, G. S., & Jobin, C. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006026 · Cited by 425
Gastrointestinal microbiology enters the metagenomics era
Frank, D. N., & Pace, N. R. (2008) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e3282f2b0e8 · Cited by 410
The impact of the microbiota on the pathogenesis of IBD: lessons from mouse infection models
Nell, S., Suerbaum, S., & Josenhans, C. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2403 · Cited by 407
Bacteroides fragilis enterotoxin induces c-Myc expression and cellular proliferation
Wu, S., Morin, P. J., Maouyo, D., & Sears, C. L. (2003) · Gastroenterology · doi:10.1053/gast.2003.50047 · Cited by 396
Successful Transmission of a Retrovirus Depends on the Commensal Microbiota
Kane, M., Case, L. K., Kopaskie, K., Kozlova, A., MacDearmid, C., Chervonsky, A. V., & Golovkina, T. V. (2011) · Science · doi:10.1126/science.1210718 · Cited by 360
Periodontitis in RA—the citrullinated enolase connection
Lundberg, K., Wegner, N., Yucel‐Lindberg, T., & Venables, P. J. (2010) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2010.139 · Cited by 344
Local Chemokine Paralysis, a Novel Pathogenic Mechanism forPorphyromonas gingivalis
Darveau, R. P., Belton, C. M., Reife, R. A., & Lamont, R. J. (1998) · Infection and Immunity · doi:10.1128/iai.66.4.1660-1665.1998 · Cited by 343
Self-citationGaffen, S. L., & Hajishengallis, G. (2008) · Journal of Dental Research · doi:10.1177/154405910808700908 · Cited by 334
Self-citationKumar, P., Leys, E. J., Bryk, J., Martinez, F. J., Moeschberger, M. L., & Griffen, A. L. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.00317-06 · Cited by 318
A Pathobiont of the Microbiota Balances Host Colonization and Intestinal Inflammation
Chow, J., & Mazmanian, S. K. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2010.03.004 · Cited by 312
Microbial manipulation of receptor crosstalk in innate immunity
Hajishengallis, G., & Lambris, J. D. (2011) · Nature reviews. Immunology · doi:10.1038/nri2918 · Cited by 307
Self-citationThe microflora of periodontal sites showing active destructive progression
Moore, W. E., Moore, L. H., Ranney, R. R., Smibert, R. M., Burmeister, J. A., & Schenkein, H. A. (1991) · Journal Of Clinical Periodontology · doi:10.1111/j.1600-051x.1991.tb00064.x · Cited by 265
Azcárate-Peril, M. A., Sikes, M. L., & Bruno-Bárcena, J. M. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00110.2011 · Cited by 260
Perspective: Alpha-Bugs, Their Microbial Partners, and the Link to Colon Cancer
Sears, C. L., & Pardoll, D. M. (2011) · The Journal of Infectious Diseases · doi:10.1093/jinfdis/jiq061 · Cited by 259
Microbial Hijacking of Complement–Toll-Like Receptor Crosstalk
Wang, M., Krauss, J. L., Domon, H., Hosur, K. B., Liang, S., Magotti, P., Triantafilou, M., Triantafilou, K., Lambris, J. D., & Hajishengallis, G. (2010) · Science Signaling · doi:10.1126/scisignal.2000697 · Cited by 229
Self-citationReducing the risk of CVD in patients with periodontitis
Genco, R. J., & Van Dyke, T. E. (2010) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2010.120 · Cited by 182
Liang, S., Krauss, J. L., Domon, H., McIntosh, M. L., Hosur, K. B., Qu, H., Li, F., Τζέκου, Α., Lambris, J. D., & Hajishengallis, G. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1003252 · Cited by 177
Self-citationDavic, R. D. (2003) · Conservation Ecology · doi:10.5751/es-00502-0701r11 · Cited by 164
The Oral Microbial Consortium's Interaction with the Periodontal Innate Defense System
Darveau, R. P. (2009) · DNA and Cell Biology · doi:10.1089/dna.2009.0864 · Cited by 150
Self-citationMaddocks, O. D. K., Short, A., Donnenberg, M. S., Bader, S. A., & Harrison, D. J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005517 · Cited by 150
Hoffmann, C., Hill, D. A., Minkah, N., Kirn, T., Troy, A., Artis, D., & Bushman, F. (2009) · Infection and Immunity · doi:10.1128/iai.00493-09 · Cited by 142
Inflammation and Cancer. I. Rodent models of infectious gastrointestinal and liver cancer.
Rogers, A., & Fox, J. (2004) · American Journal of Physiology - Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00499.2003 · Cited by 137
Porphyromonas gingivalis infection of oral epithelium inhibits neutrophil transepithelial migration
Madianos, P., Papapanou, P. N., & Sandros, J. (1997) · Infection and Immunity · doi:10.1128/iai.65.10.3983-3990.1997 · Cited by 124
Sporadic colorectal cancer – role of the commensal microbiota
Hope, M. E., Hold, G. L., Kain, R., & El-Omar, E. M. (2005) · FEMS Microbiology Letters · doi:10.1016/j.femsle.2005.01.029 · Cited by 112
Chaves, E. S., Jeffcoat, M. K., Ryerson, C. C., & Snyder, B. (2000) · Journal Of Clinical Periodontology · doi:10.1034/j.1600-051x.2000.027012897.x · Cited by 111
Effect of Periodontal Pathogens on the Metatranscriptome of a Healthy Multispecies Biofilm Model
Frias‐Lopez, J., & Duran-Pinedo, A. E. (2012) · Journal of Bacteriology · doi:10.1128/jb.06328-11 · Cited by 99
Kim, J. M., CHO, S. J., Oh, Y., JUNG, H.-Y., Kim, Y.-J., & KIM, N. (2002) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.2002.01921.x · Cited by 88
Methanogens outcompete sulphate reducing bacteria for H2 in the human colon.
Strocchi, A., Furne, J. K., Ellis, C., & Levitt, M. D. (1994) · Gut · doi:10.1136/gut.35.8.1098 · Cited by 86
Bry, L., Brigl, M., & Brenner, M. (2006) · Infection and Immunity · doi:10.1128/iai.74.1.673-681.2006 · Cited by 81
Bainbridge, B. W., Verma, R. K., Eastman, C., Yehia, B., Rivera, M. F., Moffatt, C. E., Bhattacharyya, I., Lamont, R. J., & Kesavalu, L. N. (2010) · Infection and Immunity · doi:10.1128/iai.00703-10 · Cited by 69
Doungudomdacha, S., Rawlinson, Ā., & Douglas, C. W. I. (2000) · Journal of Medical Microbiology · doi:10.1099/0022-1317-49-10-861 · Cited by 62
Page, R. C., Lantz, M. S., Darveau, R. P., Jeffcoat, M. K., Mancl, L., Houston, L. S., Braham, P. H., & Persson, G. R. (2007) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.2007.00337.x · Cited by 51
Self-citationPorphyromonas gingivalis Sinks Teeth into the Oral Microbiota and Periodontal Disease
Honda, K. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.10.008 · Cited by 46
Enterotoxigenic Bacteroides fragilis
Holton, J. (2008) · Current Infectious Disease Reports · doi:10.1007/s11908-008-0018-7 · Cited by 29
Say hello to our little friends
Walker, A. W. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1720 · Cited by 24
11. Community and Ecosystem Impacts of Single-Species Extinctions
Simberloff, D. (2003) · Princeton University Press eBooks · doi:10.1515/9781400866779-016 · Cited by 4
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Banerjee, S., Schlaeppi, K., & van der Heijden, M. G. A. (2018) · Nature Reviews Microbiology · doi:10.1038/s41579-018-0024-1 · Cited by 3,148
The gut microbiota and host health: a new clinical frontier
Marchesi, J. R., Adams, D. H., Fava, F., Hermes, G. D. A., Hirschfield, G. M., Hold, G., Quraishi, M. N., Kinross, J., Smidt, H., Tuohy, K. M., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-309990 · Cited by 2,302
“The keystone-pathogen hypothesis 88 and the α -bug hypothesis both state that certain, low abundance microbiota members (such as enterotoxigenic B. fragilis ) possess unique virulence traits, which are pro-oncogenic and remodel the microbiome and in turn promote mucosal immune responses and colonic…”
BackgroundThe Oral Microbiota: Dynamic Communities and Host Interactions
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Kamada, N., Seo, S.-U., Chen, G. Y., & Núñez, G. (2013) · Nature reviews. Immunology · doi:10.1038/nri3430 · Cited by 2,256
Metadata
- Authors
- Hajishengallis, G., Darveau, R. P., & Curtis, M. A.
- Affiliations
- University of Pennsylvania (US)
- University of Washington (US)
- Queen Mary University of London (GB)
- Corresponding author
- Hajishengallis, George
- Venue
- Nature Reviews Microbiology
- Published
- 2012-09-03
- Volume
- 10
- Issue
- 10
- Pages
- 717-725
- ISSN
- 1740-1526 (ISSN-L)
- 1740-1534
- PMC
- PMC3498498
- OpenAlex
- W2043248182
- Cited by
- 1,790
- References
- 86
- Citations by year
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- FWCI
- 5.89
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- Medical Research Council (MR/J011118/1)
- National Institute of Dental and Craniofacial Research (R01DE018292, DE-015254, R01DE015254, DE012768, DE021580, DE18274, DE021685, R01DE018274, DE018292, RC4DE021580, R01DE021685, R01DE012768)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Keywords
- human microbiome, dysbiosis, commensal microbiota, inflammatory diseases, targeted therapeutics
- MeSH terms
- Bacteria, Colonic Neoplasms, Humans, Inflammation, Models, Biological, Periodontitis, Inflammatory Bowel Diseases, Host-Pathogen Interactions, Metagenome, Microbial Interactions
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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