The DOI matches its Crossref record; 104 of the 106 references it cites were found in a registry or an index.
Healthy hosts rule within: ecological forces shaping the gut microbiota
Open accessAbstract
A balanced gut microbiota is important for human health, but the mechanisms that maintain homeostasis are incompletely understood. Recent insights suggest the host plays a key role in shaping its gut microbiota to be beneficial. While host control in the small intestine curbs bacterial numbers to avoid competition for simple sugars and amino acids, the host limits oxygen availability in the large intestine to obtain microbial fermentation products from fiber. Epithelial cells are major players in imposing ecological control mechanisms, which involves the release of antimicrobial peptides by small-intestinal Paneth cells and maintenance of luminal anaerobiosis by epithelial hypoxia in the colon. Harnessing these epithelial control mechanisms for therapeutic means could provide a novel lynchpin for strategies to remediate dysbiosis.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“For example, the availability of oxygen during inflammation drives a disruption, or dysbiosis, of the microbiota by favoring Enterobacteriaceae expansion through respiration (Byndloss et al., 2018).”
From The Impact of Dietary Transition Metals on Host-Bacterial Interactions (2018) · cites this paper as Byndloss et al., 2018
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Diversity of the Human Intestinal Microbial Flora
Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913
Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease
Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597
Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells
Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549
The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis
Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413
den Besten, G., van Eunen, K., Groen, A. K., Venema, K., Reijngoud, D.-J., & Bakker, B. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r036012 · Cited by 5,048
The gut microbiota shapes intestinal immune responses during health and disease
Round, J. L., & Mazmanian, S. K. (2009) · Nature Reviews Immunology · doi:10.1038/nri2515 · Cited by 5,029
Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation
Arpaia, N., Campbell, C., Fan, X., Dikiy, S., van der Veeken, J., deRoos, P., Liu, H., Cross, J. R., Pfeffer, K., Coffer, P. J., et al. (2013) · Nature · doi:10.1038/nature12726 · Cited by 4,838
Environmental genome shotgun sequencing of the sargasso sea
Venter, J. C., Remington, K., Heidelberg, J. F., Halpern, A. L., Rusch, D., Eisen, J. A., Wu, D., Paulsen, I., Nelson, K. E., Nelson, W., et al. (2004) · Science · doi:10.1126/science.1093857 · Cited by 4,376
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
Proteobacteria: Microbial signature of dysbiosis in gut microbiota
Shin, N.-R., Whon, T. W., & Bae, J.-W. (2015) · Trends in Biotechnology · doi:10.1016/j.tibtech.2015.06.011 · Cited by 3,954
Research works printed but not linked: 1
- Koch, 1882, Die Aetiologie derTuberkulose, Berl. Klin. Wochenschr., 15, 221
Cited by
Sorted by citations
Fassarella, M., Blaak, E. E., Penders, J., Nauta, A., Smidt, H., & Zoetendal, E. G. (2020) · Gut · doi:10.1136/gutjnl-2020-321747 · Cited by 806
“54 Additionally, the acidic pH found in the stomach is considered a first line of protection against foreign microbes, 55 and the bile acids, secreted at the proximal end of the small intestine, are bactericidal to certain species and known to broadly shape the composition of the microbiota.”
BackgroundThe microbiome and gut homeostasis
Lee, J., Tsolis, R. M., & Bäumler, A. J. (2022) · Science · doi:10.1126/science.abp9960 · Cited by 444
Bile acids as modulators of gut microbiota composition and function
Larabi, A. B., Masson, H. L. P., & Bäumler, A. J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2172671 · Cited by 437
The 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
The Healthy Microbiome—What Is the Definition of a Healthy Gut Microbiome?
Shanahan, F., Ghosh, T. S., & O’Toole, P. W. (2021) · Gastroenterology · doi:10.1053/j.gastro.2020.09.057 · Cited by 383
The Association between Early-Life Gut Microbiota and Long-Term Health and Diseases
Sarkar, A., Yoo, J. Y., Dutra, S. V. O., Morgan, K. H., & Groer, M. E. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10030459 · Cited by 368
“Changes in bacteria composition and diversity can lead to disruption in the epithelial barrier and increase susceptibility to infections and immune disorders [94-96].”
BackgroundAdvancing human gut microbiota research by considering gut transit time
Procházková, N., Falony, G., Dragsted, L. O., Licht, T. R., Raes, J., & Roager, H. M. (2022) · Gut · doi:10.1136/gutjnl-2022-328166 · Cited by 338
Mining the microbiota for microbial and metabolite-based immunotherapies
Skelly, A. N., Sato, Y., Kearney, S., & Honda, K. (2019) · Nature Reviews Immunology · doi:10.1038/s41577-019-0144-5 · Cited by 306
Zhang, W., Xu, J., Yu, T., & Chen, Q. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109131 · Cited by 247
RetractedThe Impact of Dietary Transition Metals on Host-Bacterial Interactions
Lopez, C. A., & Skaar, E. P. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.05.008 · Cited by 190
“, 2002; Janakiraman and Slauch, 2000), in part by providing iron to iron-sulfur (FeS) clusters necessary for respiration (Byndloss et al., 2018).”
BackgroundSynthetic ecology of the human gut microbiota
Vrancken, G., Gregory, A., Huys, G. R. B., Faust, K., & Raes, J. (2019) · Nature Reviews Microbiology · doi:10.1038/s41579-019-0264-8 · Cited by 194
Gut dysbiosis: Ecological causes and causative effects on human disease
Winter, S., & Bäumler, A. J. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2316579120 · Cited by 160
“This paradigm shift suggests that dysbiosis represents a state of weakened host control over the microbial environment, whereas gut homeostasis defines a state where these host functions operate normally (24, 63, 65, 68).”
BackgroundPrenatal and postnatal contributions of the maternal microbiome on offspring programming
Jašarević, E., & Bale, T. L. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100797 · Cited by 131
Zhu, W., Miyata, N., Winter, M. G., Arenales, A., Hughes, E. R., Spiga, L., Kim, J., Sifuentes-Dominguez, L., Starokadomskyy, P., Gopal, P., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20181939 · Cited by 125
Dysbiosis: from fiction to function
Tiffany, C. R., & Bäumler, A. J. (2019) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00230.2019 · Cited by 127
“ota, which is shaped by the human host (10, 17).”
BackgroundWiles, T. J., Schlomann, B. H., Wall, E. S., Betancourt, R., Parthasarathy, R., & Guillemin, K. J. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000661 · Cited by 95
Jašarević, E., Hill, E. M., Kane, P. J., Rutt, L., Gyles, T. M., Folts, L. M., Rock, K. D., Howard, C. D., Morrison, K. E., Ravel, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26634-9 · Cited by 86
Xiao, S., Jiang, S., Qian, D., & Duan, J. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10312-4 · Cited by 88
Diet-Microbe-Host Interactions That Affect Gut Mucosal Integrity and Infection Resistance
Forgie, A. J., Fouhse, J. M., & Willing, B. P. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01802 · Cited by 87
Huda, M., Ahmad, S. M., Kalanetra, K., Taft, D. H., Alam, M. J., Khanam, A., Raqib, R., Underwood, M. A., Mills, D., & Stephensen, C. B. (2019) · Journal of NutriLife · doi:10.1093/jn/nxz034 · Cited by 58
“It is also possible that VAS could promote normal development of the colonic epithelial barrier (9–12), or enhance its repair after damage (14–16), to maintain an appropriate, low oxygen tension in the colonic lumen (59).”
BackgroundDeciphering the gut microbiome of grass carp through multi-omics approach
Li, M., Liang, H., Yang, H., Ding, Q., Xia, R., Chen, J., Zhou, W., Yang, Y., Zhang, Z., Yao, Y., et al. (2024) · Microbiome · doi:10.1186/s40168-023-01715-7 · Cited by 79
“The important role of the commensal microbiota in immune homeostasis, disease and 42 health has been demonstrated in humans [7-9], and a comprehensive gut microbiome gene 43”
BackgroundMiller, 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
“By supplying the habitat, the host wields a prominent influence over microbial growth at body surfaces (Byndloss et al., 2018; Foster et al., 2017).”
BackgroundYee, A. L., Miller, E. M., Dishaw, L. J., Gordon, J. M., Ji, M., Dutra, S. V. O., Ho, T. T. B., Gilbert, J. A., & Groer, M. E. (2019) · mSystems · doi:10.1128/msystems.00229-18 · Cited by 73
Impact of the mother's gut microbiota on infant microbiome and brain development
Mady, E. A., Doghish, A. S., El‐Dakroury, W. A., Elkhawaga, S. Y., Ismail, A., El‐Mahdy, H. A., Elsakka, E. G. E., & El‐Husseiny, H. M. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105195 · Cited by 73
Beneficial effects of seaweed-derived dietary fiber: Highlights of the sulfated polysaccharides
Huang, W., Tan, H., & Nie, S. (2021) · Food Chemistry · doi:10.1016/j.foodchem.2021.131608 · Cited by 70
Dual functional roles of the MyD88 signaling in colorectal cancer development
Wang, L., Yu, K., Zhang, X., & Yu, S. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.07.139 · Cited by 61
The human gut microbiome in health and disease: time for a new chapter?
Lee, J., Bays, D. J., Savage, H. P., & Bäumler, A. J. (2024) · Infection and Immunity · doi:10.1128/iai.00302-24 · Cited by 62
“The resulting shift from an anoxic to an oxic environment sets the stage for colonic domination by facultatively anaerobic microorganisms (75–77, 101–103) (Fig.”
Gastrointestinal host-pathogen interaction in the age of microbiome research
Tsolis, R. M., & Bäumler, A. J. (2020) · Current Opinion in Microbiology · doi:10.1016/j.mib.2020.03.002 · Cited by 56
McKinney, C. A., Bedenice, D., PACHECO, A. P. D. S., Oliveira, B. C. M., Paradis, M. R., Mazan, M. R., & Widmer, G. (2021) · PLoS ONE · doi:10.1371/journal.pone.0244381 · Cited by 52
“Of particular interest would be to examine whether WCHB-1 abundance promotes recovery from colitis or is simply a consequence of the re-establishment of anaerobic conditions following an episode of diarrhea [52].”
BackgroundSynthetic gut microbiome: Advances and challenges
Mabwi, H. A., Kim, E., Song, D., Yoon, H. S., Pan, C., Komba, E. V. G., Ko, G., & Cha, K. H. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.12.029 · Cited by 53
“As these variations include immunological differences, transit time, intestinal structure, and functional caecum presence [58,59], cur-”
BackgroundZhang, W., Tan, B., Deng, J., & Zhang, H. (2021) · Scientific Reports · doi:10.1038/s41598-021-02278-z · Cited by 50
Microbial Control of Intestinal Homeostasis via Enteroendocrine Cell Innate Immune Signaling
Watnick, P. I., & Jugder, B. (2019) · Trends in Microbiology · doi:10.1016/j.tim.2019.09.005 · Cited by 49
Chikina, A. S., & Vignjevic, D. M. (2021) · Cells and Development · doi:10.1016/j.cdev.2021.203712 · Cited by 51
Sun, Y., Vornhagen, J., Breen, P. A., Forsyth, V. S., Zhao, L., Mobley, H. L. T., & Bachman, M. A. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1008010 · Cited by 48
Modulation of the gut microbiota to improve innate resistance
Schnupf, P., Gaboriau‐Routhiau, V., & Cerf–Bensussan, N. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.08.003 · Cited by 50
Microbiota-Nourishing Immunity: A Guide to Understanding Our Microbial Self
Litvak, Y., & Bäumler, A. J. (2019) · Immunity · doi:10.1016/j.immuni.2019.08.003 · Cited by 43
Seike, K., Kiledal, E. A., Fujiwara, H., Henig, I. J., da Silva, M. B., van den Brink, M. R. M., Hein, R., Hoostal, M. J., Liu, C., Oravecz-Wilson, K. I., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.01.007 · Cited by 42
Coorens, M., Rao, A., Gräfe, S. K., Unelius, D., Lindforss, U., Agerberth, B., Mjösberg, J., & Bergman, P. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.007290 · Cited by 39
“Enterobacteriaceae is a large family of Gram-negative bacteria that are commonly found as part of the human intestinal microbiota and include species such as Escherichia coli and Klebsiella pneumoniae (1, 2).”
BackgroundThe longitudinal and cross-sectional heterogeneity of the intestinal microbiota
Miller, B. M., Liou, M. J., Lee, J., & Bäumler, A. J. (2021) · Current Opinion in Microbiology · doi:10.1016/j.mib.2021.08.004 · Cited by 44
Liu, Y., Zhang, H., Xie, A., Sun, J., Yang, H., Li, J., Li, Y., Chen, F., Mei, Y., & Liang, Y. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202200340 · Cited by 36
Maier, L., Stein‐Thoeringer, C. K., Ley, R. E., Brötz‐Oesterhelt, H., Link, H., Ziemert, N., Wagner, S., & Peschel, A. (2024) · The Lancet Microbe · doi:10.1016/s2666-5247(24)00049-1 · Cited by 38
Colonization resistance against multi-drug-resistant bacteria: a narrative review
Guern, R. L., Stabler, S., Gosset, P., Pichavant, M., Grandjean, T., Faure, E., Karaca, Y., Faure, K., Kipnis, É., & Dessein, R. (2021) · Journal of Hospital Infection · doi:10.1016/j.jhin.2021.09.001 · Cited by 38
Safety assessment of monosodium glutamate based on intestinal function and flora in mice
Xu, J., Tang, M., Liu, Y., Xu, J., & Xu, X. (2021) · Food Science and Human Wellness · doi:10.1016/j.fshw.2021.07.016 · Cited by 36
Mohr, A. E., Mach, N., Pugh, J. N., Grosicki, G. J., Allen, J. M., Karl, J. P., & Whisner, C. M. (2025) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaf037 · Cited by 37
“Ecologically, diet exerts strong selective pressures on gut microbial communities (Byndloss et al. 2018 ), driven by competition for nutrients and increased fitness through cross-feeding interactions (Morris et al. 2013 ).”
Microbiota-nourishing Immunity and Its Relevance for Ulcerative Colitis
Byndloss, M. X., Litvak, Y., & Bäumler, A. J. (2019) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izz004 · Cited by 33
The Habitat Filters of Microbiota-Nourishing Immunity
Miller, B. M., & Bäumler, A. J. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101819-024945 · Cited by 35
Lyu, Y., Li, D. X., Yuan, X., Li, Z., Zhang, J., Ming, X., Shaw, P. C., Zhang, C., Kong, A. P. S., & Zuo, Z. (2022) · Phytomedicine · doi:10.1016/j.phymed.2022.154099 · Cited by 32
Contributors to Dysbiosis in Very-Low-Birth-Weight Infants
Groer, M. E., Miller, E. M., D’Agata, A. L., Ho, T. T. B., Dutra, S. V. O., Yoo, J. Y., Yee, A. L., Gilbert, J. A., & Dishaw, L. J. (2020) · Journal of Obstetric, Gynecologic & Neonatal Nursing · doi:10.1016/j.jogn.2020.02.003 · Cited by 30
The Metallome as a Link Between the “Omes” in Autism Spectrum Disorders
Stanton, J. E., Malijauskaite, S., McGourty, K., & Grabrucker, A. M. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.695873 · Cited by 16
Enabling oxygen-controlled microfluidic cultures for spatiotemporal microbial single-cell analysis
Kasahara, K., Leygeber, M., Seiffarth, J., Ruzaeva, K., Drepper, T., Nöh, K., & Kohlheyer, D. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1198170 · Cited by 17
Sun, P., Wang, M., Zheng, W., Li, S., Zhu, X., Chai, X., & Zhao, S. (2023) · Stress Biology · doi:10.1007/s44154-023-00098-x · Cited by 17
“In ecological terms, diet habit is one of the most important selection pressures on the gut microbiota, partly caused by competition for nutrients (Byndloss et al. 2018).”
BackgroundNikolenko, V. N., Oganesyan, M. V., Sankova, M. V., Bulygin, K. V., Vovkogon, A. D., Rizaeva, N. A., & Sinelnikov, M. Y. (2020) · BioEssays · doi:10.1002/bies.202000180 · Cited by 18
Tang-Fichaux, M., Branchu, P., Nougayrède, J., & Oswald, É. (2021) · Toxins · doi:10.3390/toxins13120897 · Cited by 18
“In addition to ROS, less oxygen consumption by IECs during inflammation also elevates mucosal oxygenation [64].”
BackgroundMarißen, J., Reichert, L., Härtel, C., Fortmann, M. I., Faust, K., Msanga, D. R., Harder, J., Zemlin, M., de Agüero, M. G., Masjosthusmann, K., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126684 · Cited by 19
Ghannoum, M. A., Long, L. A., Bunick, C. G., Rosso, J. Q. D., Gamal, A., Tyring, S. K., McCormick, T. S., & Grada, A. A. (2022) · Antibiotics · doi:10.3390/antibiotics11030324 · Cited by 13
“The composition of the human microbiome varies across body sites with the greatest concentration and diversity of microorganisms found in the gastrointestinal tract [1].”
BackgroundWei, J., Xiao, H., Wei, Y., Tsopmejio, I. S. N., Sun, C. L., Wu, H., Jin, Z., & Song, H. (2022) · mSystems · doi:10.1128/msystems.00835-22 · Cited by 14
“It is also called an equilibrium state or steady state (9, 10).”
BackgroundNagler‐Anderson, C. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20191642 · Cited by 13
“The short chain fatty acid butyrate, in particular, is an important energy source for colonic epithelial cells (Byndloss et al., 2018).”
BackgroundWang, X., Zhang, Z., Wang, X., Bao, Q., Wang, R., & Duan, Z. (2021) · Biology · doi:10.3390/biology10080769 · Cited by 12
“According to the point of ecological view, diet could select microbial communities within the gut ecosystem [17], but the effect of dietary components on the stability of the gut microbiota has been poorly addressed [18].”
BackgroundPerinatal exposure to tetracycline contributes to lasting developmental effects on offspring
Hill, E. M., Howard, C. D., Bale, T. L., & Jašarević, E. (2021) · Animal Microbiome · doi:10.1186/s42523-021-00099-z · Cited by 13
“A bloom of Proteobacteria in the gut has been implicated in weight gain and inflammation, and an increase of this taxa early in life may contribute to the weight gain that was observed in the C57Bl/6J male[40, 41].”
BackgroundRibeiro, T. R. M., Salgaço, M. K., Adorno, M. Â. T., da Silva, M. A., Piazza, R. M. F., Sivieri, K., & Moreira, C. G. (2021) · BMC Microbiology · doi:10.1186/s12866-021-02220-3 · Cited by 11
Systematic optimization of fermentation conditions for in vitro fermentations with fecal inocula
Poppe, J., Vieira‐Silva, S., Raes, J., Verbeke, K., & Falony, G. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1198903 · Cited by 10
“In vitro, where the outcome of inter-taxon competition is not subjected to host control mechanisms such as immune surveillance, the end result of the community maturation process initiated by inoculum dilution unfortunately differed substantially from what has been observed in vivo, due to the unhampered overgrowth of…”
BackgroundLu, H., Zhang, W., Sun, S., Mei, Y., Zhao, G., & Kailun, Y. (2023) · Animals · doi:10.3390/ani13152415 · Cited by 11
“However, the relationship between WCHB1-41 and intestinal inflammation remains to be determined [62].”
BackgroundLauder, E., Kiledal, E. A., Maneix, L., Furnholm, T., Santibanez, A., Zhao, D., Sun, Y., Dick, G. J., & Reddy, P. R. (2025) · Blood · doi:10.1182/blood.2024025924 · Cited by 9
How Microbial Food Fermentation Supports a Tolerant Gut
Poppe, J., van Baarle, L., Matteoli, G., & Verbeke, K. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000036 · Cited by 9
Parente, I. A., Xavier, M., Roupar, D., Amado, I. R., Berni, P. R. D. A., Botelho, C., Teixeira, J. A., Pastrana, L. M., Nobre, C., & Gonçalves, C. (2022) · Journal of Functional Foods · doi:10.1016/j.jff.2022.105200 · Cited by 9
Hargarten, J. C., Vaughan, M. J., Lampe, A. T., Jones, R. M., Ssebambulidde, K., Nickerson, K. W., Williamson, P. R., Atkin, A. L., & Brown, D. M. (2023) · Infection and Immunity · doi:10.1128/iai.00384-23 · Cited by 8
“Under homeostatic conditions, oxygen is excluded from the gastrointestinal tract and Candida is excluded from the peritoneum (47).”
BackgroundZheng, Z.-L., Zheng, Q.-F., Wang, L., & Liu, Y. (2024) · World Journal of Gastroenterology · doi:10.3748/wjg.v31.i2.100589 · Cited by 9
“This is of great significance for maintaining the dominance of obligate anaerobic bacteria in the gut microbiota[129].”
The effect of intrinsic factors and mechanisms in shaping human gut microbiota
Wang, H., Li, J., Wu, G., Zhang, F., Jia, Y., & He, Y. (2022) · Medicine in Microecology · doi:10.1016/j.medmic.2022.100054 · Cited by 9
Dual stressors of infection and warming can destabilize host microbiomes
Li, J., Gao, Y. Y., Stevens, E. J., & King, K. C. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0069 · Cited by 6
“We revealed that parasite infection and warming, independently and simultaneously destabilized host microbiomes, as shown by an increase in dispersion ([28,69,70]; figure 6).”
BackgroundIshii, Y., Matsunaga, T., Yasui, T., Rini, D. M., Inoüe, R., Yamamoto, Y., & Suzuki, T. (2024) · Nutraceuticals · doi:10.3390/nutraceuticals4020019 · Cited by 7
“Antimicrobial proteins exhibit a site-specific spectrum of antimicrobial activity and expression in the small and large intestines [11].”
BackgroundPhillips, S., Watt, R., Atkinson, T., Savva, G. M., Hayhoe, A., Hall, L. J., on behalf of the PEARL study team, Hall, L. J., Philips, S., Watt, R., et al. (2021) · BMC Pediatrics · doi:10.1186/s12887-021-02835-5 · Cited by 6
“tion of additional nutrients and energy from dietary components, optimised development of the immune system, and resistance against pathogens [1, 2].”
BackgroundGarcía-Pérez, P., Tomaş, M., Giuberti, G., Çapanoğlu, E., Callegari, M. L., Lucini, L., & Patrone, V. (2025) · Microbiological Research · doi:10.1016/j.micres.2025.128226 · Cited by 6
Conceptual Exchanges for Understanding Free-Living and Host-Associated Microbiomes
Pfister, C. A., Light, S. H., Bohannan, B. J. M., Schmidt, T. M., Martiny, A. C., Hynson, N. A., Devkota, S., David, L. A., & Whiteson, K. (2022) · mSystems · doi:10.1128/msystems.01374-21 · Cited by 6
“Although studies of human gut health indicate the importance of classifying aerobic and anaerobic bacteria and their interactions (83), an understanding of the redox environment across different human tissue types will likely enhance our understanding of pathogenesis and dysbiosis.”
BackgroundThe concept of balance in microbiome research
O’Malley, M. A. (2024) · BioEssays · doi:10.1002/bies.202400050 · Cited by 5
The role of probiotics in adolescents’ obesity
Chen, X., Li, Y., & Jia, Y. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1546627 · Cited by 7
“Their primary function is to regulate gut microbiota and maintain intestinal ecological balance, thereby promoting digestion, enhancing immunity, and preventing various diseases (Byndloss et al., 2018; Ezzaidi et al., 2019).”
Wu, Q., Liu, B., Yu, R., Sun, X., Wang, Z., Zhou, J., Lu, C., Wan, H., Zhang, J., Han, J., et al. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.102661 · Cited by 5
Huo, F., Liu, Q., Zhang, S., Liu, X., Lv, S., Zhao, M., Liu, Y., Zhu, X., Huang, C., Feng, S., et al. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01552-8 · Cited by 4
Liu, Y., Kou, C., Chen, J., Li, Y., & Li, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25137425 · Cited by 4
“These physiological changes may be considered as feedback from the significant increase in the abundance of intestinal pathogens [42].”
BackgroundOrganic Acids: Key Products of Fermented Foods and Sources of Anti-Inflammatory Potential
Li, W., Ghamry, M., Xu, X., Zhang, L., & Li, J. (2025) · Food Reviews International · doi:10.1080/87559129.2025.2529546 · Cited by 3
“[207,210] Additionally, short-chain fatty acids can promote T-cell production of IL-10 through GPR43, thereby alleviating colitis, [211] and regulate glucose, lipid, and cholesterol metabolism in the liver and muscles via the AMPK pathway, thereby indirectly influencing gut homeostasis.”
Rodakova, K. S., Gancarčíková, S., Demečková, V., Lauko, S., Rynikova, M., Andrejčáková, Z., Spišáková, D., Fusek, M., Vlčková, R., Strompfová, V., et al. (2026) · Applied Sciences · doi:10.3390/app16115529 · Cited by 3
Tanca, A., & Uzzau, S. (2025) · Expert Review of Proteomics · doi:10.1080/14789450.2025.2580644 · Cited by 3
Host control and species interactions jointly determine microbiome community structure
Abbasi, E., & Akçay, E. (2024) · Theoretical Population Biology · doi:10.1016/j.tpb.2024.06.006 · Cited by 3
Wiles, T. J., Schlomann, B. H., Wall, E. S., Betancourt, R., Parthasarathy, R., & Guillemin, K. J. (2019) · SSRN Electronic Journal · doi:10.2139/ssrn.3467155 · Cited by 3
Ishiguro, E. E., Haskey, N., & Campbell, K. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91387-4.00001-6 · Cited by 3
Vasa, S. R., Gardiner, G. E., Cormican, P., O’Driscoll, K., Bee, G., & Lawlor, P. G. (2024) · Journal of Animal Science · doi:10.1093/jas/skae380 · Cited by 2
Li, M., Liang, H., Xia, R., Zhang, J., Chen, J., Zhou, W., Ding, Q., Yang, Y., Zhang, Z., Yao, Y., et al. (2024) · Aquaculture Reports · doi:10.1016/j.aqrep.2024.102604 · Cited by 2
Houghton, C. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820593-8.00014-8 · Cited by 3
Genetic Modification and Sequence Analysis of Probiotic Microorganisms
Akçelik, M., Akçelik, N., Şanlıbaba, P., & TEZEL, B. U. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822909-5.00006-x · Cited by 2
Tjaden, N. E. B., Liou, M. J., Sax, S. E., Lassoued, N., Lou, M., Schneider, S., Beigel, K., Eisenberg, J. D., Loeffler, E., Anderson, S. E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.10.637436 · Cited by 2
The gut microbiome in personalized precision medicine
Buschmann, M. M., & Gilbert, J. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-98808-7.00012-6 · Cited by 1
Bian, X., Xu, H., Li, J., Kuang, J., Shi, F., Li, X., & Li, J. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1668148 · Cited by 1
McDermott, K. (2018) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York) · Cited by 1
Jašarević, E., Hill, E. M., Kane, P. J., Rutt, L., Gyles, T. M., Folts, L. M., Rock, K. D., Howard, C. D., Morrison, K. E., Ravel, J., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.01.429213 · Cited by 1
“…with previous work showing loss of intestinal hypoxia due to high-fat low-fiber diet consumption, we found decreased expression of the hypoxia-inducible factor 1-alpha in the colon of HFt-LFb relative to LFt-HFb females (Figure 3E) (Byndloss et al., 2018; Faber and Bäumler, 2014; Lee et al., 2020).”
MethodDevelopment and dynamics of the normal gut microbiota
Olsson, L. M. (2020) · Gothenburg University Publications Electronic Archive (Gothenburg University)
The microbiome in preterm infants and implications in health
Wang, A. Z., & Claud, E. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820602-7.00004-0
The Role of High Sugar Diets in Colitis
Rajaruban, S. (2020) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-tthe-t208
van der Meer, J. R., & Carraro, N. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737594052.793576386
Keskey, R. C., Nicholson, S. E., & Alverdy, J. C. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-69787-3.00111-8
Liu, Y., Kou, C., Chen, J., Li, Y., Zhu, L., & Li, J. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4777228
Huo, F., Liu, Q., Lv, S., Liu, Y., Zhu, X., Huang, C., Feng, S., Wang, H., Xu, S., Shen, J., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4388330/v1
Metadata
- Authors
- Byndloss, M. X., Pernitzsch, S. R., & Bäumler, A. J.
- Affiliations
- University of California, Davis (US)
- Corresponding author
- Bäumler, Andreas J.
- Venue
- Mucosal Immunology
- Publisher
- Elsevier BV
- Published
- 2018-09
- Volume
- 11
- Issue
- 5
- Pages
- 1299-1305
- ISSN
- 1933-0219 (ISSN-L)
- OpenAlex
- W2800529903
- Cited by
- 109
- References
- 106
- Citations by year
- 2026: 4 · 2025: 11 · 2024: 17 · 2023: 13 · 2022: 8 · 2021: 20 · 2020: 16 · 2019: 16 · 2018: 4
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Mucosal Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
- Keywords
- gut microbiota, host-microbe interactions, microbial homeostasis, Paneth cells, antimicrobial peptides, dietary fiber fermentation, small intestine, large intestine, dysbiosis
- MeSH terms
- Gastrointestinal Microbiome, Host Microbial Interactions, Animals, Ecology, Epithelial Cells, Homeostasis, Humans, Intestinal Mucosa, Intestines, Microbiota
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 ›
Are you an author, or do you see a problem with this page? Request a review