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Microbiota-mediated colonization resistance: mechanisms and regulation
Open accessAbstract
A dense and diverse microbial community inhabits the gut and many epithelial surfaces. Referred to as the microbiota, it co-evolved with the host and is beneficial for many host physiological processes. A major function of these symbiotic microorganisms is protection against pathogen colonization and overgrowth of indigenous pathobionts. Dysbiosis of the normal microbial community increases the risk of pathogen infection and overgrowth of harmful pathobionts. The protective mechanisms conferred by the microbiota are complex and include competitive microbial-microbial interactions and induction of host immune responses. Pathogens, in turn, have evolved multiple strategies to subvert colonization resistance conferred by the microbiota. Understanding the mechanisms by which microbial symbionts limit pathogen colonization should guide the development of new therapeutic approaches to prevent or treat disease.
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“The gut microbiota protects against intestinal colonization by pathogens via colonization resistance through both direct and indirect mechanisms.”
From Role of the gut microbiota in nutrient competition and protection against intestinal pathogen colonization (2023) · cites this paper as [34]
In the citing paper
“Examples of direct mechanisms of colonization resistance include nutrient competition between gut commensals and pathogens, production of inhibitory metabolites by gut commensals, production of bacteriocins by gut commensals, and the presence of bacteriophages [33, 34].”
From Role of the gut microbiota in nutrient competition and protection against intestinal pathogen colonization (2023) · cites this paper as [34]
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“Indirect mechanisms of colonization resistance include interactions between the gut microbiota and the host immune response, changes in the gut microbiota that influence oxygen availability, modulation of the mucus layer by the gut microbiota, and promotion of cytokine release by the gut microbiota [34].”
From Role of the gut microbiota in nutrient competition and protection against intestinal pathogen colonization (2023) · cites this paper as [34]
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Cites
A core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823
Dominguez-Bello, M. G., Costello, E. K., Contreras, M., Magris, M., Hidalgo, G., Fierer, N., & Knight, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002601107 · Cited by 4,774
Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554
Vaginal microbiome of reproductive-age women
Ravel, J., Gajer, P., Abdo, Z., Schneider, G. M., Koenig, S. S. K., McCulle, S. L., Karlebach, S., Gorle, R., Russell, J., Tacket, C. O., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002611107 · Cited by 4,254
The impact of the gut microbiota on human health: an integrative view
Clemente, J. C., Ursell, L. K., Parfrey, L. W., & Knight, R. (2012) · Cell · doi:10.1016/j.cell.2012.01.035 · Cited by 3,710
Duodenal Infusion of Donor Feces for Recurrent Clostridium difficile
van Nood, E., Vrieze, A., Nieuwdorp, M., Fuentes, S., Zoetendal, E. G., de Vos, W. M., Visser, C. E., Kuijper, E. J., Bartelsman, J. F. W. M., Tijssen, J. G. P., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1205037 · Cited by 3,708
Dynamics and Stabilization of the Human Gut Microbiome during the First Year of Life
Bäckhed, F., Roswall, J., Peng, Y., Feng, Q., Jia, H., Kovatcheva-Datchary, P., Li, Y., Xia, Y., Xie, H., Zhong, H., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.04.004 · Cited by 3,315
Topographical and Temporal Diversity of the Human Skin Microbiome
Grice, E. A., Kong, H. H., Conlan, S., Deming, C. B., Davis, J., Young, A. C., Program, N. C. S., Bouffard, G. G., Blakesley, R. W., Murray, P. R., et al. (2009) · Science · doi:10.1126/science.1171700 · Cited by 2,953
Desai, M. S., Seekatz, A. M., Koropatkin, N. M., Kamada, N., Hickey, C. A., Wolter, M., Pudlo, N. A., Kitamoto, S., Terrapon, N., Muller, A., et al. (2016) · Cell · doi:10.1016/j.cell.2016.10.043 · Cited by 2,805
Self-citationThe NIH Human Microbiome ProjectPreprint
The NIH HMP Working Group, Peterson, J. L., Garges, S., Giovanni, M. Y., McInnes, P., Wang, L., Schloss, J. A., Bonazzi, V. R., McEwen, J. E., Wetterstrand, K. A., et al. (2009) · Genome Research · doi:10.1101/gr.096651.109 · Cited by 2,168
Interleukin-22 mediates early host defense against attaching and effacing bacterial pathogens
Zheng, Y., Valdez, P. A., Danilenko, D. M., Hu, Y., Susan, M. L., Gong, Q., Abbas, A. R., Modrusan, Z. D., Ghilardi, N., de Sauvage, F. J., et al. (2008) · Nature Medicine · doi:10.1038/nm1720 · Cited by 1,972
Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile
Buffie, C. G., Bucci, V., Stein, R. R., McKenney, P. T., Ling, L., Gobourne, A., No, D., Liu, H., Kinnebrew, M., Viale, A., et al. (2015) · Nature · doi:10.1038/nature13828 · Cited by 1,872
Nod2-Dependent Regulation of Innate and Adaptive Immunity in the Intestinal Tract
Kobayashi, K. S., Chamaillard, M., Ogura, Y., Henegariu, O., Inohara, N., Núñez, G., & Flavell, R. A. (2005) · Science · doi:10.1126/science.1104911 · Cited by 1,834
Self-citationKelly, C. J., Zheng, L., Campbell, E. L., Saeedi, B., Scholz, C. C., Bayless, A. J., Wilson, K. E., Glover, L. E., Kominsky, D. J., Magnuson, A., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.03.005 · Cited by 1,716
Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease
Pickard, J. M., Zeng, M. Y., Caruso, R., & Núñez, G. (2017) · Immunological Reviews · doi:10.1111/imr.12567 · Cited by 1,699
Self-citationControl of pathogens and pathobionts by the gut microbiota
Kamada, N., Chen, G. Y., Inohara, N., & Núñez, G. (2013) · Nature Immunology · doi:10.1038/ni.2608 · Cited by 1,625
Self-citationSymbiotic bacteria direct expression of an intestinal bactericidal lectin
Cash, H. L., Whitham, C. V., Behrendt, C. L., & Hooper, L. V. (2006) · Science · doi:10.1126/science.1127119 · Cited by 1,432
Vaishnava, S., Yamamoto, M., Severson, K. M., Ruhn, K. A., Yu, X., Koren, O., Ley, R., Wakeland, E. K., & Hooper, L. V. (2011) · Science · doi:10.1126/science.1209791 · Cited by 1,412
Molecular Identification of Bacteria Associated with Bacterial Vaginosis
Fredricks, D. N., Fiedler, T. L., & Marrazzo, J. M. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa043802 · Cited by 1,303
Gut inflammation provides a respiratory electron acceptor for Salmonella
Winter, S., Thiennimitr, P., Winter, M. G., Butler, B. P., Huseby, D. L., Crawford, R. W., Russell, J. M., Bevins, C. L., Adams, L. G., Tsolis, R. M., et al. (2010) · Nature · doi:10.1038/nature09415 · Cited by 1,271
Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion
Byndloss, M. X., Olsan, E. E., Rivera-Chávez, F., Tiffany, C. R., Cevallos, S. A., Lokken, K. L., Torres, T. P., Byndloss, A. J., Faber, F., Gao, Y., et al. (2017) · Science · doi:10.1126/science.aam9949 · Cited by 1,260
A Primitive T Cell-Independent Mechanism of Intestinal Mucosal IgA Responses to Commensal Bacteria
Macpherson, A. J., Gatto, D., Sainsbury, E., Harriman, G. R., Hengartner, H., & Zinkernagel, R. M. (2000) · Science · doi:10.1126/science.288.5474.2222 · Cited by 1,113
Nakatsuji, T., Chen, T. H., Narala, S., Chun, K. A., Two, A. M., Yun, T., Shafiq, F., Kotol, P. F., Bouslimani, A., Melnik, A. V., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aah4680 · Cited by 1,095
Compartmentalized Control of Skin Immunity by Resident Commensals
Naik, S., Bouladoux, N., Wilhelm, C., Molloy, M. J., Salcedo, R., Kastenmuller, W., Deming, C., Quinones, M., Koo, L., Conlan, S., et al. (2012) · Science · doi:10.1126/science.1225152 · Cited by 1,092
Stunted microbiota and opportunistic pathogen colonization in caesarean-section birth
Shao, Y., Forster, S. C., Tsaliki, E., Vervier, K., Strang, A., Simpson, N., Kumar, N., Stares, M. D., Rodger, A., Brocklehurst, P., et al. (2019) · Nature · doi:10.1038/s41586-019-1560-1 · Cited by 1,088
Microbiota-liberated host sugars facilitate post-antibiotic expansion of enteric pathogens
Ng, K. M., Ferreyra, J. A., Higginbottom, S. K., Lynch, J. B., Kashyap, P. C., Gopinath, S., Naidu, N., Choudhury, B., Weimer, B. C., Monack, D. M., et al. (2013) · Nature · doi:10.1038/nature12503 · Cited by 1,035
Host-Derived Nitrate Boosts Growth of E. coli in the Inflamed Gut
Winter, S. E., Winter, M. G., Xavier, M. N., Thiennimitr, P., Poon, V., Keestra, A. M., Laughlin, R. C., Gomez, G., Wu, J., Lawhon, S. D., et al. (2013) · Science · doi:10.1126/science.1232467 · Cited by 1,019
Iwase, T., Uehara, Y., Shinji, H., Tajima, A., Seo, H., Takada, K., Agata, T., & Mizunoe, Y. (2010) · Nature · doi:10.1038/nature09074 · Cited by 991
(1958) · PubMed · Cited by 978
Theriot, C. M., Koenigsknecht, M. J., Carlson, P. E., Hatton, G. E., Nelson, A. M., Li, B., Huffnagle, G. B., Z. Li, J., & Young, V. B. (2014) · Nature Communications · doi:10.1038/ncomms4114 · Cited by 974
A Type VI Secretion System of Pseudomonas aeruginosa Targets a Toxin to Bacteria
Hood, R. D., Singh, P., Hsu, F., Güvener, T., Carl, M. A., Trinidad, R. R. S., Silverman, J. M., Ohlson, B. B., Hicks, K. B., Plemel, R. L., et al. (2010) · Cell Host & Microbe · doi:10.1016/j.chom.2009.12.007 · Cited by 971
Quorum Sensing in Staphylococci
Novick, R. P., & Geisinger, E. (2008) · Annual Review of Genetics · doi:10.1146/annurev.genet.42.110807.091640 · Cited by 953
Human commensals producing a novel antibiotic impair pathogen colonization
Zipperer, A., Konnerth, M. C., Laux, C., Berscheid, A., Janek, D., Weidenmaier, C., Burian, M., Schilling, N. A., Slavetinsky, C., Marschal, M., et al. (2016) · Nature · doi:10.1038/nature18634 · Cited by 938
Colonization resistance of the digestive tract in conventional and antibiotic-treated mice
van der Waaij, D., Vries, J. M. B.-D., & der Wees, J. E. C. L.-V. (1971) · Journal of Hygiene · doi:10.1017/s0022172400021653 · Cited by 907
Rivera-Chávez, F., Zhang, L. F., Faber, F., Lopez, C. A., Byndloss, M. X., Olsan, E. E., Xu, G., Velazquez, E. M., Lebrilla, C. B., Winter, S. E., et al. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.03.004 · Cited by 864
Skin microbiota–host interactions
Chen, Y. E., Fischbach, M. A., & Belkaid, Y. (2018) · Nature · doi:10.1038/nature25177 · Cited by 815
Bacterial Interference Caused by Autoinducing Peptide Variants
Ji, G., Beavis, R. C., & Novick, R. P. (1997) · Science · doi:10.1126/science.276.5321.2027 · Cited by 808
Review: microbial transformations of human bile acids
Guzior, D. V., & Quinn, R. A. (2021) · Microbiome · doi:10.1186/s40168-021-01101-1 · Cited by 795
Regulated virulence controls the ability of a pathogen to compete with the gut microbiota
Kamada, N., Kim, Y.-G., Sham, H. P., Vallance, B. A., Puente, J. L., Martens, E. C., & Núñez, G. (2012) · Science · doi:10.1126/science.1222195 · Cited by 682
Self-citationDysbiotic Proteobacteria expansion: a microbial signature of epithelial dysfunction
Litvak, Y., Byndloss, M. X., Tsolis, R. M., & Bäumler, A. J. (2017) · Current Opinion in Microbiology · doi:10.1016/j.mib.2017.07.003 · Cited by 658
Global Causes of Diarrheal Disease Mortality in Children <5 Years of Age: A Systematic Review
Lanata, C. F., Fischer-Walker, C. L., Olascoaga, A. C., Torres, C. X., Aryee, M. J., & Black, R. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072788 · Cited by 654
Gut microbiota utilize immunoglobulin A for mucosal colonization
Donaldson, G. P., Ladinsky, M. S., Yu, K. B., Sanders, J. G., Yoo, B. B., Chou, W., Conner, M. E., Earl, A. M., Knight, R. D., Björkman, P. J., et al. (2018) · Science · doi:10.1126/science.aaq0926 · Cited by 650
Bacterial colonization factors control specificity and stability of the gut microbiota
Lee, S. M., Donaldson, G. P., Mikulski, Z., Boyajian, S., Ley, K. F., & Mazmanian, S. K. (2013) · Nature · doi:10.1038/nature12447 · Cited by 640
Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits
Brandl, K., Plitas, G., Mihu, C. N., Ubeda, C., Jia, T., Fleisher, M., Schnabl, B., DeMatteo, R. P., & Pamer, E. G. (2008) · Nature · doi:10.1038/nature07250 · Cited by 631
Bergstrom, K. S. B., Kissoon-Singh, V., Gibson, D. L., Ma, C., Montero, M., Sham, H. P., Ryz, N., Huang, T., Velcich, A., Finlay, B. B., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000902 · Cited by 625
Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota
Thiennimitr, P., Winter, S., Winter, M. G., Byndloss, M. X., Tolstikov, V., Huseby, D. L., Sterzenbach, T., Tsolis, R. M., Roth, J. R., & Bäumler, A. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107857108 · Cited by 611
A Model of Host-Microbial Interactions in an Open Mammalian Ecosystem
Bry, L., Falk, P. G., Midtvedt, T., & Gordon, J. I. (1996) · Science · doi:10.1126/science.273.5280.1380 · Cited by 607
Deshmukh, H. S., Liu, Y., Menkiti, O. R., Mei, J., Dai, N., O'Leary, C. E., Oliver, P. M., Kolls, J. K., Weiser, J. N., & Worthen, G. S. (2014) · Nature Medicine · doi:10.1038/nm.3542 · Cited by 579
Zheng, L., Kelly, C. J., Battista, K. D., Schaefer, R., Lanis, J. M., Alexeev, E. E., Wang, R. X., Onyiah, J. C., Kominsky, D. J., & Colgan, S. P. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700105 · Cited by 574
Innate and Adaptive Humoral Responses Coat Distinct Commensal Bacteria with Immunoglobulin A
Bunker, J. J., Flynn, T. M., Koval, J., Shaw, D. G., Meisel, M., McDonald, B. D., Ishizuka, I. E., Dent, A. L., Wilson, P. C., Jabrì, B., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.08.007 · Cited by 561
Kristensen, N. B., Bryrup, T., Allin, K. H., Nielsen, T., Hansen, T. H., & Pedersen, O. (2016) · Genome Medicine · doi:10.1186/s13073-016-0300-5 · Cited by 561
Rapid fucosylation of intestinal epithelium sustains host–commensal symbiosis in sickness
Pickard, J. M., Maurice, C. F., Kinnebrew, M. A., Abt, M. C., Schenten, D., Golovkina, T. V., Bogatyrev, S. R., Ismagilov, R. F., Pamer, E. G., Turnbaugh, P. J., et al. (2014) · Nature · doi:10.1038/nature13823 · Cited by 550
Self-citationProbiotic Bacteria Reduce Salmonella Typhimurium Intestinal Colonization by Competing for Iron
Deriu, E., Liu, J. Z., Pezeshki, M., Edwards, R. A., Ochoa, R. J., Contreras, H., Libby, S. J., Fang, F. C., & Raffatellu, M. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.06.007 · Cited by 550
Normalization of host intestinal mucus layers requires long-term microbial colonization
Johansson, M. E. V., Jakobsson, H. E., Holmén-Larsson, J., Schütte, A., Ermund, A., Rodríguez-Piñeiro, A. M., Arike, L., Wising, C., Svensson, F., Bäckhed, F., et al. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.10.007 · Cited by 549
Microcins mediate competition among Enterobacteriaceae in the inflamed gut
Sassone-Corsi, M., Nuccio, S.-P., Liu, H., Hernandez, D., Vu, C. T., Takahashi, A. A., Edwards, R. A., & Raffatellu, M. (2016) · Nature · doi:10.1038/nature20557 · Cited by 549
An enteric virus can replace the beneficial function of commensal bacteria
Kernbauer, E., Ding, Y., & Cadwell, K. (2014) · Nature · doi:10.1038/nature13960 · Cited by 527
Raffatellu, M., George, M. D., Akiyama, Y., Hornsby, M. J., Nuccio, S.-P., Paixao, T. A., Butler, B. P., Chu, H., Santos, R. L., Berger, T., et al. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.03.011 · Cited by 525
Brugiroux, S., Beutler, M., Pfann, C., Garzetti, D., Ruscheweyh, H., Ring, D., Diehl, M., Herp, S., Loetscher, Y., Hussain, S., et al. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.215 · Cited by 490
Theriot, C. M., Bowman, A. A., & Young, V. B. (2016) · mSphere · doi:10.1128/msphere.00045-15 · Cited by 481
Bajaj, V., Lucas, R. L., Hwang, C., & Lee, C. A. (1996) · Molecular Microbiology · doi:10.1046/j.1365-2958.1996.d01-1718.x · Cited by 477
Natural polyreactive IgA antibodies coat the intestinal microbiota
Bunker, J. J., Erickson, S. A., Flynn, T. M., Henry, C., Koval, J., Meisel, M., Jabrì, B., Antonopoulos, D. A., Wilson, P. C., & Bendelac, A. S. (2017) · Science · doi:10.1126/science.aan6619 · Cited by 470
Sorbara, M. T., & Pamer, E. G. (2022) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00667-9 · Cited by 468
Kommineni, S., Bretl, D. J., Lam, V., Chakraborty, R., Hayward, M., Simpson, P., Cao, Y., Bousounis, P., Kristich, C. J., & Salzman, N. H. (2015) · Nature · doi:10.1038/nature15524 · Cited by 458
Bacterial Community Mapping of the Mouse Gastrointestinal Tract
Gu, S., Chen, D., Zhang, J., Lv, X., Wang, K., Duan, L.-P., Nie, Y., & Wu, X. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074957 · Cited by 455
Cogen, A. L., Yamasaki, K., Sanchez, K. M., Dorschner, R. A., Lai, Y., MacLeod, D. T., Torpey, J. W., Otto, M., Nizet, V., Kim, J. E., et al. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2009.243 · Cited by 432
Challenges in infant immunity: implications for responses to infection and vaccines
PrabhuDas, M., Adkins, B., Gans, H. A., King, C. L., Levy, O., Ramilo, O., & Siegrist, C. (2011) · Nature Immunology · doi:10.1038/ni0311-189 · Cited by 430
Stecher, B., Chaffron, S., Käppeli, R., Hapfelmeier, S., Freedrich, S., Weber, T. C., Kirundi, J., Suar, M., McCoy, K. D., von Mering, C., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000711 · Cited by 427
Control of the Microbial Flora of the Vagina by H202-Generating Lactobacilli
Klebanoff, S. J., Hillier, S. L., Eschenbach, D. A., & Waltersdorph, A. M. (1991) · The Journal of Infectious Diseases · doi:10.1093/infdis/164.1.94 · Cited by 420
Smillie, C. S., Sauk, J. S., Gevers, D., Friedman, J., Sung, J., Youngster, I., Hohmann, E. L., Staley, C. M., Khoruts, A., Sadowsky, M. J., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.01.003 · Cited by 418
Contact-Dependent Inhibition of Growth in Escherichia coli
Aoki, S. K., Pamma, R., Hernday, A. D., Bickham, J. E., Braaten, B. A., & Low, D. A. (2005) · Science · doi:10.1126/science.1115109 · Cited by 417
Zeng, M. Y., Cisalpino, D., Varadarajan, S., Hellman, J., Warren, H. S., Cascalho, M., Inohara, N., & Núñez, G. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.006 · Cited by 417
Self-citationThe microbiome-shaping roles of bacteriocins
Heilbronner, S., Krismer, B., Brötz‐Oesterhelt, H., & Peschel, A. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-021-00569-w · Cited by 416
Franchi, L., Kamada, N., Nakamura, Y., Burberry, A., Kuffa, P., Suzuki, S., Shaw, M. H., Kim, Y., & Núñez, G. (2012) · Nature Immunology · doi:10.1038/ni.2263 · Cited by 414
Self-citationHigh-avidity IgA protects the intestine by enchaining growing bacteria
Moor, K., Diard, M., Sellin, M. E., Felmy, B., Wotzka, S. Y., Toska, A., Bakkeren, E., Arnoldini, M., Bansept, F., Co, A. D., et al. (2017) · Nature · doi:10.1038/nature22058 · Cited by 411
Brandl, K., Plitas, G., Schnabl, B., DeMatteo, R. P., & Pamer, E. G. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070563 · Cited by 385
Importance and regulation of the colonic mucus barrier in a mouse model of colitis
Petersson, J., Schreiber, O., Hansson, G. C., Gendler, S. J., Velcich, A., Lundberg, J. O., Roos, S., Holm, L., & Phillipson, M. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00422.2010 · Cited by 384
A Type VI Secretion-Related Pathway in Bacteroidetes Mediates Interbacterial Antagonism
Russell, A. B., Wexler, A. G., Harding, B. N., Whitney, J. C. C., Bohn, A., Goo, Y. A., Tran, B. Q., Barry, N. A., Zheng, H., Peterson, S. B., et al. (2014) · Cell Host & Microbe · doi:10.1016/j.chom.2014.07.007 · Cited by 380
An exclusive metabolic niche enables strain engraftment in the gut microbiota
Shepherd, E. S., DeLoache, W. C., Pruss, K. M., Whitaker, W. R., & Sonnenburg, J. L. (2018) · Nature · doi:10.1038/s41586-018-0092-4 · Cited by 367
Effect of Streptomycin on Susceptibility of Intestinal Tract to Experimental Salmonella Infection.
Bohnhoff, M., Drake, B. L., & Miller, C. P. (1954) · Experimental Biology and Medicine · doi:10.3181/00379727-86-21030 · Cited by 354
Salmonella Typhimurium utilizes a T6SS-mediated antibacterial weapon to establish in the host gut
Sana, T. G., Flaugnatti, N., Lugo, K., Lam, L. H., Jacobson, A. R., Baylot, V., Durand, É., Journet, L., Cascalès, E., & Monack, D. M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608858113 · Cited by 348
Freter, R., Brickner, H., Botney, M. D., Cleven, D., & Aranki, A. (1983) · Infection and Immunity · doi:10.1128/iai.39.2.676-685.1983 · Cited by 340
Bomar, L., Brugger, S. D., Yost, B. H., Davies, S. S., & Lemon, K. P. (2016) · mBio · doi:10.1128/mbio.01725-15 · Cited by 332
Liu, J. Z., Jellbauer, S., Poe, A. J., Ton, V., Pesciaroli, M., Kehl-Fie, T. E., Restrepo, N. A., Hosking, M. P., Edwards, R. A., Battistoni, A., et al. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.01.017 · Cited by 328
Modulation of Shigella virulence in response to available oxygen in vivo
Marteyn, B., West, N. P., Browning, D. F., Cole, J. A., Shaw, J. G., Palm, F., Mounier, J., Prévost, M., Sansonetti, P. J., & Tang, C. M. (2010) · Nature · doi:10.1038/nature08970 · Cited by 323
Mucispirillum schaedleri Antagonizes Salmonella Virulence to Protect Mice against Colitis
Herp, S., Brugiroux, S., Garzetti, D., Ring, D., Jochum, L. M., Beutler, M., Eberl, C., Hussain, S., Walter, S., Gerlach, R. G., et al. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2019.03.004 · Cited by 322
A widespread family of polymorphic contact-dependent toxin delivery systems in bacteria
Aoki, S. K., Diner, E. J., de Roodenbeke, C. T., Burgess, B. R., Poole, S. J., Braaten, B. A., Jones, A. M., Webb, J., Hayes, C. S., Cotter, P. A., et al. (2010) · Nature · doi:10.1038/nature09490 · Cited by 308
Cooperating Commensals Restore Colonization Resistance to Vancomycin-Resistant Enterococcus faecium
Caballero, S., Kim, S., Carter, R. A., Leiner, I. M., Sušac, B., Miller, L., Kim, G. J., Ling, L., & Pamer, E. G. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.04.002 · Cited by 308
Williams, M. R., Costa, S. K., Zaramela, L. S., Khalil, S., Todd, D. A., Winter, H. L., Sanford, J. A., O’Neill, A. M., Liggins, M. C., Nakatsuji, T., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aat8329 · Cited by 292
Microbiota-derived lantibiotic restores resistance against vancomycin-resistant Enterococcus
Kim, S. G., Becattini, S., Moody, T. U., Shliaha, P. V., Littmann, E. R., Seok, R., Gjonbalaj, M., Eaton, V. P., Fontana, E., Amoretti, L. A., et al. (2019) · Nature · doi:10.1038/s41586-019-1501-z · Cited by 290
Maltby, R., Leatham-Jensen, M. P., Gibson, T., Cohen, P. S., & Conway, T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053957 · Cited by 285
Fransen, F., Zagato, E., Mazzini, E., Fosso, B., Manzari, C., Aidy, S. E., Chiavelli, A., D’Erchia, A. M., Sethi, M. K., Pabst, O., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.08.011 · Cited by 284
The Cytokine IL-22 Promotes Pathogen Colonization by Suppressing Related Commensal Bacteria
Behnsen, J., Jellbauer, S., Wong, C. P., Edwards, R. A., George, M. D., Ouyang, W., & Raffatellu, M. (2014) · Immunity · doi:10.1016/j.immuni.2014.01.003 · Cited by 279
Microbial ecology perturbation in human IgA deficiency
Fadlallah, J., Kafsi, H. E., Sterlin, D., Juste, C., Parizot, C., Dorgham, K., Autaa, G., Gouas, D. A., Almeida, M., Lepage, P., et al. (2018) · Science Translational Medicine · doi:10.1126/scitranslmed.aan1217 · Cited by 277
Bacterial killing via a type IV secretion system
de Souza, D. P., Oka, G. U., Alvarez‐Martinez, C. E., Bisson‐Filho, A. W., Dunger, G., Hobeika, L., Cavalcante, N. G. S., Alegria, M. C., Barbosa, L. R. S., Salinas, R. K., et al. (2015) · Nature Communications · doi:10.1038/ncomms7453 · Cited by 275
Neonatal acquisition of Clostridia species protects against colonization by bacterial pathogens
Kim, Y., Sakamoto, K., Seo, S., Pickard, J. M., Gillilland, M. G., Pudlo, N. A., Hoostal, M. J., Li, X., Wang, T. D., Feehley, T., et al. (2017) · Science · doi:10.1126/science.aag2029 · Cited by 271
Self-citationSpatial organization of intestinal microbiota in the mouse ascending colon
Nava, G. M., Friedrichsen, H. J., & Stappenbeck, T. S. (2010) · The ISME Journal · doi:10.1038/ismej.2010.161 · Cited by 270
Commensal Enterobacteriaceae Protect against Salmonella Colonization through Oxygen Competition
Litvak, Y., Mon, K. K. Z., Nguyen, H., Chanthavixay, G., Liou, M. J., Velazquez, E. M., Kutter, L., Alcantara, M. A., Byndloss, M. X., Tiffany, C. R., et al. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2018.12.003 · Cited by 261
Sugimoto, S., Iwamoto, T., Takada, K., Okuda, K.-I., Tajima, A., Iwase, T., & Mizunoe, Y. (2013) · Journal of Bacteriology · doi:10.1128/jb.01672-12 · Cited by 259
Sorbara, M. T., Dubin, K., Littmann, E. R., Moody, T. U., Fontana, E., Seok, R., Leiner, I. M., Taur, Y., Peled, J. U., van den Brink, M. R. M., et al. (2019) · Journal of Experimental Medicine · doi:10.1084/jem.20181639 · Cited by 259
Innate secretory antibodies protect against natural Salmonella typhimurium infection
Wijburg, O. L. C., Uren, T. K., Simpfendorfer, K. R., Johansen, F., Brandtzæg, P., & Strugnell, R. A. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20052093 · Cited by 253
The aetiology of bacterial vaginosis
Turovskiy, Y., Noll, K. S., & Chikindas, M. L. (2011) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2011.04977.x · Cited by 250
RESISTANCE OF THE MOUSE'S INTESTINAL TRACT TO EXPERIMENTAL SALMONELLA INFECTION
Bohnhoff, M., Miller, C. P., & Martin, W. R. (1964) · The Journal of Experimental Medicine · doi:10.1084/jem.120.5.805 · Cited by 246
Spees, A. M., Wangdi, T., Lopez, C. A., Kingsbury, D. D., Byndloss, M. X., Winter, S., Tsolis, R. M., & Bäumler, A. J. (2013) · mBio · doi:10.1128/mbio.00430-13 · Cited by 245
Lopez, C. A., Winter, S., Rivera-Chávez, F., Byndloss, M. X., Poon, V., Nuccio, S., Tsolis, R. M., & Bäumler, A. J. (2012) · mBio · doi:10.1128/mbio.00143-12 · Cited by 242
Paharik, A. E., Parlet, C. P., Chung, N., Todd, D. A., Rodriguez, E. I., Dyke, M. J. V., Cech, N. B., & Horswill, A. R. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.11.001 · Cited by 242
Chatzidaki‐Livanis, M., Geva‐Zatorsky, N., & Comstock, L. E. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522510113 · Cited by 241
Commensal Microbes Induce Serum IgA Responses that Protect against Polymicrobial Sepsis
Wilmore, J. R., Gaudette, B. T., Gómez, D., Hashemi, T., Jones, D. D., Gardner, C. A., Cole, S. D., Misic, A. M., Beiting, D. P., & Allman, D. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.01.005 · Cited by 235
In vivo IgA coating of anaerobic bacteria in human faeces.
van der Waaij, L. A., Limburg, P. C., Mesander, G., & van der Waaij, D. (1996) · Gut · doi:10.1136/gut.38.3.348 · Cited by 227
Nagao‐Kitamoto, H., Leslie, J. L., Kitamoto, S., Jin, C., Thomsson, K. A., Gillilland, M. G., Kuffa, P., Goto, Y., Jenq, R. R., Ishii, C., et al. (2020) · Nature Medicine · doi:10.1038/s41591-020-0764-0 · Cited by 225
Human symbionts inject and neutralize antibacterial toxins to persist in the gut
Wexler, A. G., Bao, Y., Whitney, J. C. C., Bobay, L., Xavier, J. B., Schofield, W. B., Barry, N. A., Russell, A. B., Tran, B. Q., Goo, Y. A., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1525637113 · Cited by 220
Adaptive immunity induces mutualism between commensal eukaryotes
Ost, K. S., O’Meara, T. R., Stephens, W. Z., Chiaro, T. R., Zhou, H., Penman, J., Bell, R. S., Catanzaro, J., Song, D., Singh, S., et al. (2021) · Nature · doi:10.1038/s41586-021-03722-w · Cited by 212
The nasal cavity microbiota of healthy adults
Bassis, C. M., Tang, A. L., Young, V. B., & Pynnonen, M. A. (2014) · Microbiome · doi:10.1186/2049-2618-2-27 · Cited by 209
Studer, N., Desharnais, L., Beutler, M., Brugiroux, S., Miani, M. A. T., Menin, L., Schürch, C. M., McCoy, K. D., Kuehne, S. A., Minton, N. P., et al. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00191 · Cited by 209
Zarepour, M., Bhullar, K., Montero, M., Ma, C., Huang, T., Velcich, A., Xia, L., & Vallance, B. A. (2013) · Infection and Immunity · doi:10.1128/iai.00854-13 · Cited by 206
Virulence factors enhance Citrobacter rodentium expansion through aerobic respiration
Lopez, C. A., Miller, B. M., Rivera-Chávez, F., Velazquez, E. M., Byndloss, M. X., Chávez-Arroyo, A., Lokken, K. L., Tsolis, R. M., Winter, S. E., & Bäumler, A. J. (2016) · Science · doi:10.1126/science.aag3042 · Cited by 201
Endogenous Enterobacteriaceae underlie variation in susceptibility to Salmonella infection
Velazquez, E. M., Nguyen, H., Heasley, K. T., Saechao, C. H., Gil, L. M., Rogers, A. W. L., Miller, B. M., Rolston, M. R., Lopez, C. A., Litvak, Y., et al. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0407-8 · Cited by 201
Antagonism toward the intestinal microbiota and its effect on Vibrio cholerae virulence
Zhao, W., Caro, F., Robins, W. P., & Mekalanos, J. J. (2018) · Science · doi:10.1126/science.aap8775 · Cited by 198
Freter, R. (1955) · The Journal of Infectious Diseases · doi:10.1093/infdis/97.1.57 · Cited by 194
Coyne, M. J., Roelofs, K., & Comstock, L. E. (2016) · BMC Genomics · doi:10.1186/s12864-016-2377-z · Cited by 193
Strain competition restricts colonization of an enteric pathogen and prevents colitis
Hecht, A. L., Casterline, B. W., Earley, Z. M., Goo, Y. A., Goodlett, D. R., & Wardenburg, J. B. (2016) · EMBO Reports · doi:10.15252/embr.201642282 · Cited by 193
Transition Metal Sequestration by the Host-Defense Protein Calprotectin
Zygiel, E. M., & Nolan, E. M. (2018) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-062917-012312 · Cited by 193
Respiration of Microbiota-Derived 1,2-propanediol Drives Salmonella Expansion during Colitis
Faber, F., Thiennimitr, P., Spiga, L., Byndloss, M. X., Litvak, Y., Lawhon, S. D., Andrews‐Polymenis, H. L., Winter, S., & Bäumler, A. J. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006129 · Cited by 188
Whitney, J. C. C., Peterson, S. B., Kim, J., Pazos, M., Verster, A. J., Radey, M. C., Kulasekara, H. D., Ching, M. Q., Bullen, N. P., Bryant, D., et al. (2017) · eLife · doi:10.7554/elife.26938 · Cited by 187
Host-mediated sugar oxidation promotes post-antibiotic pathogen expansion
Faber, F., Tran, L., Byndloss, M. X., Lopez, C. A., Velazquez, E. M., Kerrinnes, T., Nuccio, S., Wangdi, T., Fiehn, O., Tsolis, R. M., et al. (2016) · Nature · doi:10.1038/nature18597 · Cited by 186
In Vitro Antibacterial Activity of Unconjugated and Conjugated Bile Salts on Staphylococcus aureus
Sannasiddappa, T. H., Lund, P. A., & Clarke, S. R. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01581 · Cited by 186
Host Selection of Microbiota via Differential Adhesion
McLoughlin, K. G., Schlüter, J., Rakoff-Nahoum, S., Smith, A. L., & Foster, K. R. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.02.021 · Cited by 185
Shigella sonnei Encodes a Functional T6SS Used for Interbacterial Competition and Niche Occupancy
Anderson, M. C., Vonaesch, P., Saffarian, A., Marteyn, B., & Sansonetti, P. J. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.05.004 · Cited by 181
Microbiota-Derived Hydrogen Fuels Salmonella Typhimurium Invasion of the Gut Ecosystem
Maier, L., Vyas, R., Cordova, C. D., Lindsay, H. A., Schmidt, T., Brugiroux, S., Periaswamy, B., Bauer, R., Sturm, A., Schreiber, F., et al. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.11.002 · Cited by 179
Probiotics for prevention of Clostridium difficile infection
Mills, J., Rao, K. K., & Young, V. B. (2017) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000000410 · Cited by 178
O'Sullivan, J. N., Rea, M. C., O’Connor, P. M., Hill, C., & Ross, R. P. (2018) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiy241 · Cited by 171
Diaz-Ochoa, V. E., Lam, D., Lee, C. S., Klaus, S., Behnsen, J., Liu, J. Z., Chim, N., Nuccio, S.-P., Rathi, S. G., Mastroianni, J. R., et al. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.05.005 · Cited by 164
Hung, C., Garner, C. D., Slauch, J. M., Dwyer, Z. W., Lawhon, S. D., Frye, J. G., McClelland, M., Ahmer, B. M. M., & Altier, C. (2013) · Molecular Microbiology · doi:10.1111/mmi.12149 · Cited by 163
Human gut bacteria contain acquired interbacterial defence systems
Ross, B. D., Verster, A. J., Radey, M. C., Schmidtke, D. T., Pope, C. E., Hoffman, L. R., Hajjar, A. M., Peterson, S. B., Borenstein, E., & Mougous, J. D. (2019) · Nature · doi:10.1038/s41586-019-1708-z · Cited by 163
The role of iron in host–microbiota crosstalk and its effects on systemic glucose metabolism
Mayneris‐Perxachs, J., Moreno‐Navarrete, J. M., & Fernández‐Real, J. M. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-022-00721-3 · Cited by 161
Regulation of virulence by butyrate sensing in enterohaemorrhagic Escherichia coli
Nakanishi, N., Tashiro, K., Kuhara, S., Hayashi, T., Sugimoto, N., & Tobe, T. (2009) · Microbiology · doi:10.1099/mic.0.023499-0 · Cited by 160
Segmented Filamentous Bacteria Prevent and Cure Rotavirus Infection
Shi, Z., Zou, J., Zhang, Z., Zhao, X., Noriega, J., Zhang, B., Zhao, C., Ingle, H., Bittinger, K. L., Mattei, L. M., et al. (2019) · Cell · doi:10.1016/j.cell.2019.09.028 · Cited by 159
Microbiota-targeted maternal antibodies protect neonates from enteric infection
Zheng, W., Zhao, W., Wu, M., Song, X., Caro, F., Sun, X., Gazzaniga, F., Stefanetti, G., Oh, S., Mekalanos, J. J., et al. (2020) · Nature · doi:10.1038/s41586-019-1898-4 · Cited by 158
Janek, D., Zipperer, A., Kulik, A., Krismer, B., & Peschel, A. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005812 · Cited by 157
Xu, Z., Takizawa, F., Casadei, E., Shibasaki, Y., Ding, Y., Sauters, T. J. C., Yu, Y., Salinas, I., & Sunyer, J. O. (2020) · Science Immunology · doi:10.1126/sciimmunol.aay3254 · Cited by 154
Osbelt, L., Wende, M., Almási, É. D. H., Derksen, E., Muthukumarasamy, U., Lesker, T. R., Gálvez, E. J. C., Pils, M. C., Schalk, E., Chhatwal, P., et al. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.09.003 · Cited by 153
Bitschar, K., Sauer, B., Focken, J., Dehmer, H., Moos, S., Konnerth, M. C., Schilling, N. A., Grond, S., Kalbacher, H., Kurschus, F. C., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10646-7 · Cited by 151
Liu, Q., Liu, Q., Meng, H., Lv, H., Liu, Y., Liu, J., Wang, H., He, L., Qin, J., Wang, Y., et al. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2019.11.003 · Cited by 148
Preventing dysbiosis of the neonatal mouse intestinal microbiome protects against late-onset sepsis
Singer, J. R., Blosser, E. G., Zindl, C. L., Silberger, D. J., Conlan, S., Laufer, V. A., Ditoro, D. F., Deming, C., Kumar, R., Morrow, C. D., et al. (2019) · Nature Medicine · doi:10.1038/s41591-019-0640-y · Cited by 145
Role of volatile fatty acids in colonization resistance to Clostridium difficile
Rolfe, R. D. (1984) · Infection and Immunity · doi:10.1128/iai.45.1.185-191.1984 · Cited by 142
Watanabe, M., Fukiya, S., & Yokota, A. (2017) · Journal of Lipid Research · doi:10.1194/jlr.m075143 · Cited by 142
Dsouza, M., Menon, R., Crossette, E. M., Bhattarai, S. K., Schneider, J., Kim, Y., Reddy, S., Caballero, S., Felix, C. R., Cornacchione, L. P., et al. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.03.016 · Cited by 142
Guo, X., Liang, Y., Zhang, Y., Lasorella, A., Kee, B. L., & Fu, Y.-X. (2015) · Immunity · doi:10.1016/j.immuni.2015.03.012 · Cited by 138
Sequeira, R. P., McDonald, J. A. K., Marchesi, J. R., & Clarke, T. B. (2020) · Nature Microbiology · doi:10.1038/s41564-019-0640-1 · Cited by 136
Vancomycin-Resistant Enterococci
Reyes, K., Bardossy, A. C., & Zervos, M. (2016) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2016.07.009 · Cited by 128
Durant, J. A., Corrier, D. E., & Ricke, S. C. (2000) · Journal of Food Protection · doi:10.4315/0362-028x-63.5.573 · Cited by 118
Singh, V., Yeoh, B. S., Chassaing, B., Zhang, B., Saha, P., Xiao, X., Awasthi, D., Shashidharamurthy, R., Dikshit, M., Gewirtz, A., et al. (2016) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2016.03.007 · Cited by 117
Intestinally Secreted C-Type Lectin Reg3b Attenuates Salmonellosis but Not Listeriosis in Mice
van Ampting, M. T. J., Loonen, L., Schonewille, A., Konings, I. B. M., Vink, C., Iovanna, J., Chamaillard, M., Dekker, J., van der Meer, R. V. D., Wells, J., et al. (2012) · Infection and Immunity · doi:10.1128/iai.06165-11 · Cited by 108
Ryouichi, S. H. I. N., Suzuki, M., & Morishita, Y. (2002) · Journal of Medical Microbiology · doi:10.1099/0022-1317-51-3-201 · Cited by 106
Osbelt, L., Thiemann, S., Smit, N., Lesker, T. R., Schröter, M., Gálvez, E. J. C., Schmidt‐Hohagen, K., Pils, M. C., Mühlen, S., Dersch, P., et al. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008448 · Cited by 106
Antagonistic activity against pathogenic bacteria by human vaginal lactobacilli
Voravuthikunchai, S. P., Bilasoi, S., & Supamala, O. (2006) · Anaerobe · doi:10.1016/j.anaerobe.2006.06.003 · Cited by 104
Mechanisms and Biological Roles of Contact-Dependent Growth Inhibition SystemsPreprint
Hayes, C. S., Koskiniemi, S., Ruhe, Z. C., Poole, S. J., & Low, D. A. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a010025 · Cited by 102
Chen, J., Waddell, A., Lin, Y.-D., & Cantorna, M. T. (2014) · Mucosal Immunology · doi:10.1038/mi.2014.94 · Cited by 101
Murphy, K., & Mitchell, C. M. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw140 · Cited by 101
Siderophore-mediated zinc acquisition enhances enterobacterial colonization of the inflamed gut
Behnsen, J., Zhi, H., Aron, A. T., Subramanian, V., Santus, W., Lee, M. H., Gerner, R. R., Petras, D., Liu, J. Z., Green, K. D., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27297-2 · Cited by 101
IFN-I and IL-22 mediate protective effects of intestinal viral infection
Neil, J. A., Matsuzawa, Y., Kernbauer, E., Schuster, S. L., Sota, S., Venzon, M., Dallari, S., Neto, A. G., Hine, A. M., Hudesman, D. P., et al. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0470-1 · Cited by 98
Zhou, P., Zhou, Y., Liu, B., Jin, Z., Zhuang, X., Dai, W., Yang, Z., Feng, X., Zhou, Q., Liu, Y., et al. (2020) · mSphere · doi:10.1128/msphere.00984-19 · Cited by 95
Bile acid-independent protection against Clostridioides difficile infection
Aguirre, A. M., Yalçınkaya, N., Wu, Q., Swennes, A. G., Tessier, M. E. M., Roberts, P., Miyajima, F., Savidge, T., & Sorg, J. A. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1010015 · Cited by 95
Abt, M. C., Buffie, C. G., Sušac, B., Becattini, S., Carter, R. A., Leiner, I., Keith, J. W., Artis, D., Osborne, L. C., & Pamer, E. G. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad6663 · Cited by 94
Roelofs, K., Coyne, M. J., Gentyala, R. R., Chatzidaki‐Livanis, M., & Comstock, L. E. (2016) · mBio · doi:10.1128/mbio.01055-16 · Cited by 94
A family of anti-Bacteroidales peptide toxins wide-spread in the human gut microbiota
Coyne, M. J., Béchon, N., Matano, L. M., McEneany, V. L., Chatzidaki‐Livanis, M., & Comstock, L. E. (2019) · Nature Communications · doi:10.1038/s41467-019-11494-1 · Cited by 88
Persistence of colicinogenic Escherichia coli in the mouse gastrointestinal tract
Gillor, O., Giladi, I., & Riley, M. A. (2009) · BMC Microbiology · doi:10.1186/1471-2180-9-165 · Cited by 87
Microbiota-Derived Metabolic Factors Reduce Campylobacteriosis in Mice
Sun, X., Winglee, K., Gharaibeh, R. Z., Gauthier, J., He, Z., Tripathi, P., Avram, D., Bruner, S. D., Fodor, A. A., & Jobin, C. (2018) · Gastroenterology · doi:10.1053/j.gastro.2018.01.042 · Cited by 87
Salmonella effector driven invasion of the gut epithelium: breaking in and setting the house on fire
Fattinger, S. A., Sellin, M. E., & Hardt, W. (2021) · Current Opinion in Microbiology · doi:10.1016/j.mib.2021.08.007 · Cited by 84
Neumann, M., Steimle, A., Grant, E. T., Wolter, M., Parrish, A., Willième, S., Brenner, D., Martens, E. C., & Desai, M. S. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1966263 · Cited by 80
Caballero-Flores, G. G., Pickard, J. M., Fukuda, S., Inohara, N., & Núñez, G. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.06.018 · Cited by 79
Self-citationGenetic Ablation of Butyrate Utilization Attenuates Gastrointestinal Salmonella Disease
Bronner, D. N., Faber, F., Olsan, E. E., Byndloss, M. X., Sayed, N. A., Xu, G., Yoo, W., Kim, D., Ryu, S., Lebrilla, C. B., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.01.004 · Cited by 78
Kohli, N., Crisp, Z., Riordan, R., Li, M., Alaniz, R. C., & Jayaraman, A. (2018) · PLoS ONE · doi:10.1371/journal.pone.0190613 · Cited by 75
Jimenez, A. G., Ellermann, M., Abbott, D. W., & Sperandio, V. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0641-0 · Cited by 75
Sweeney, N. J., Klemm, P., McCormick, B. A., Nielsen, E. M., Utley, M., Schembri, M. A., Laux, D. C., & Cohen, P. S. (1996) · Infection and Immunity · doi:10.1128/iai.64.9.3497-3503.1996 · Cited by 72
Pathogenic E. coli Extracts Nutrients from Infected Host Cells Utilizing Injectisome Components
Pal, R. R., Baidya, A. K., Mamou, G., Bhattacharya, S., Socol, Y., Kobi, S., Katsowich, N., Ben-Yehuda, S., & Rosenshine, I. (2019) · Cell · doi:10.1016/j.cell.2019.02.022 · Cited by 72
Miller, B. M., Liou, M. J., Zhang, L. F., Nguyen, H., Litvak, Y., Schorr, E., Jang, K. K., Tiffany, C. R., Butler, B. P., & Bäumler, A. J. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.10.009 · Cited by 71
Flaugnatti, N., Isaac, S., Rocha, L. F. L., Stutzmann, S., Rendueles, O., Stoudmann, C., Vesel, N., Garcia‐Garcerà, M., Nucci, A., Sana, T. G., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26041-0 · Cited by 69
Type VI secretion systems of pathogenic and commensal bacteria mediate niche occupancy in the gut
Serapio-Palacios, A., Woodward, S. E., Vogt, S. L., Deng, W., Creus-Cuadros, A., Huus, K. E., Cirstea, M. S., Gerrie, M., Barcik, W., Yu, H., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110731 · Cited by 68
Shelton, C. D., Yoo, W., Shealy, N. G., Torres, T. P., Zieba, J. K., Calcutt, M. W., Foegeding, N. J., Kim, D., Kim, J., Ryu, S., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110180 · Cited by 66
Centenary of the death of Elie Metchnikoff: a visionary and an outstanding team leader
Cavaillon, J., & Legout, S. (2016) · Microbes and Infection · doi:10.1016/j.micinf.2016.05.008 · Cited by 65
Lewis, B. B., Carter, R. A., Ling, L., Leiner, I. M., Taur, Y., Kamboj, M., Dubberke, E. R., Xavier, J. B., & Pamer, E. G. (2017) · mBio · doi:10.1128/mbio.00885-17 · Cited by 65
Leatham-Jensen, M. P., Frimodt-Møller, J., Adediran, J., Mokszycki, M. E., Banner, M., Caughron, J. E., Krogfelt, K. A., Conway, T., & Cohen, P. S. (2012) · Infection and Immunity · doi:10.1128/iai.06193-11 · Cited by 62
Connolly, J. P. R., Slater, S. L., O’Boyle, N., Goldstone, R. J., Crepin, V. F., Ruano‐Gallego, D., Herzyk, P., Smith, D. G., Douce, G. R., Frankel, G. M., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06701-4 · Cited by 60
Pheromone killing of multidrug-resistant Enterococcus faecalis V583 by native commensal strains
Gilmore, M. S., Rauch, M., Ramsey, M. M., Himes, P., Varahan, S., Manson, J. M., Lebreton, F., & Hancock, L. E. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1500553112 · Cited by 58
Host cells subdivide nutrient niches into discrete biogeographical microhabitats for gut microbes
Liou, M. J., Miller, B. M., Litvak, Y., Nguyen, H., Natwick, D. E., Savage, H. P., Rixon, J. A., Mahan, S. P., Hiyoshi, H., Rogers, A. W. L., et al. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2022.04.012 · Cited by 57
Antimicrobial Peptides in Gut Health: A Review
Gong, T., Fu, J., Shi, L., Chen, X., & Zong, X. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.751010 · Cited by 52
Antimicrobial Peptides—or How Our Ancestors Learned to Control the Microbiome
Bosch, T. C. G., & ZASLOFF, M. A. (2021) · mBio · doi:10.1128/mbio.01847-21 · Cited by 43
Stecher, B. (2021) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2021.151484 · Cited by 41
Leslie, J. L., Jenior, M. L., Vendrov, K. C., Standke, A. K., Barron, M. R., O’Brien, T. J., Unverdorben, L. V., Thaprawat, P., Bergin, I. L., Schloss, P. D., et al. (2021) · mBio · doi:10.1128/mbio.00522-21 · Cited by 35
Zhang, T., Sasabe, J., Hullahalli, K., Sit, B., & Waldor, M. K. (2021) · Infection and Immunity · doi:10.1128/iai.00667-20 · Cited by 32
Kafkova, L. R., Brokešová, D., Křupka, M., Stehlíková, Z., Dvořák, J., Coufal, Š., Fajstová, A., Šrůtková, D., Štěpánová, K., Hermanová, P. P., et al. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-00345-8 · Cited by 31
Klüber, P., Meurer, S. K., Lambertz, J., Schwarz, R., Zechel-Gran, S., Braunschweig, T. A., Hurka, S., Domann, E., & Weiskirchen, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222313156 · Cited by 31
Waldschmitt, N., Kitamoto, S., Sécher, T., Zacharioudaki, V., Boulard, O., Floquet, E., Delacre, M., Lamas, B., Pham, H., Six, A., et al. (2018) · Gut · doi:10.1136/gutjnl-2018-316757 · Cited by 22
Bile acid sensitivity and in vivo virulence of clinical Clostridium difficile isolates
Lewis, B. B., Carter, R. A., & Pamer, E. G. (2016) · Anaerobe · doi:10.1016/j.anaerobe.2016.05.010 · Cited by 21
Citrobacter amalonaticus Inhibits the Growth of Citrobacter rodentium in the Gut Lumen
Mullineaux-Sanders, C., Carson, D., Hopkins, E. G. D., Glegola-Madejska, I., Escobar‐Zepeda, A., Browne, H. P., Lawley, T. D., & Frankel, G. M. (2021) · mBio · doi:10.1128/mbio.02410-21 · Cited by 20
Betz, K. J., Maier, E. A., Amarachintha, S. P., Wu, D. X.-Y., Karmele, E. P., Kinder, J. M., Steinbrecher, K. A., McNeal, M., Luzader, D., Hogan, S. P., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0198434 · Cited by 13
Research works printed but not linked: 1
- Hutchinson, G. E. An Introduction to Population Ecology (Yale Univ. Press, 1978).
Cited by
Sorted by citations
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Martín, R., Ríos-Covián, D., Huillet, E., Auger, S., Khazaal, S., Bermúdez‐Humarán, L. G., Sokol, H., Chatel, J., & Langella, P. (2023) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuad039 · Cited by 630
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Metadata
- Authors
- Caballero-Flores, G., Pickard, J. M., & Núñez, G.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Caballero-Flores, Gustavo
- Núñez, Gabriel
- Venue
- Nature Reviews Microbiology
- Published
- 2022-12-20
- Volume
- 21
- Issue
- 6
- Pages
- 347-360
- ISSN
- 1740-1526 (ISSN-L)
- 1740-1534
- PMC
- PMC10249723
- OpenAlex
- W4312065785
- Cited by
- 474
- References
- 196
- Citations by year
- 2026: 160 · 2025: 182 · 2024: 100 · 2023: 32
- FWCI
- 8.16
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature Reviews Microbiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (K99-R00)
- National Institute of Allergy and Infectious Diseases (K99AI159620, R00AI159620)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK095782)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Infectious Diseases › Clostridium difficile and Clostridium perfringens research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
- Keywords
- gut microbiota, colonization resistance, pathogen colonization, dysbiosis, pathobionts, microbial competition, host immune response, host-microbe interactions, microbiota-based therapy
- MeSH terms
- Immunity, Microbiota
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