Cited by 761Gut microbiota and healthClostridium difficile and Clostridium perfringens researchAntibiotic Resistance in Bacteria

The DOI matches its Crossref record; 147 of the 147 references it cites were found in a registry or an index.

The intestinal microbiota: Antibiotics, colonization resistance, and enteric pathogens

Open access

Kim, Sohn, Covington, April, Pamer, Eric G.·2017·Immunological Reviews

DOI 10.1111/imr.12563PMC PMC6026851

Open this paper in CoChat — free account

Abstract

Summary: The human gastrointestinal tract hosts a diverse network of microorganisms, collectively known as the microbiota that plays an important role in health and disease. For instance, the intestinal microbiota can prevent invading microbes from colonizing the gastrointestinal tract, a phenomenon known as colonization resistance. Perturbations to the microbiota, such as antibiotic administration, can alter microbial composition and result in the loss of colonization resistance. Consequently, the host may be rendered susceptible to colonization by a pathogen. This is a particularly relevant concern in the hospital setting, where antibiotic use and antibiotic‐resistant pathogen exposure are more frequent. Many nosocomial infections arise from gastrointestinal colonization. Due to their resistance to antibiotics, treatment is often very challenging. However, recent studies have demonstrated that manipulating the commensal microbiota can prevent and treat various infections in the intestine. In this review, we discuss the members of the microbiota, as well as the mechanisms, that govern colonization resistance against specific pathogens. We also review the effects of antibiotics on the microbiota, as well as the unique epidemiology of immunocompromised patients that renders them a particularly high‐risk population to intestinal nosocomial infections.

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

Crossref · 10.1111/imr.12563

Cites

147 of 147 references verified0 citation errors · 0 not checkable

Statistics

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Structure, function and diversity of the healthy human microbiome
The Human Microbiome Project Consortium (2012) · Nature · doi:10.1038/nature11234 · Cited by 11,726
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
Diet rapidly and reproducibly alters the human gut microbiome
David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100
Changes of Intestinal Functions in Liver Cirrhosis
Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820
Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria?
Brogden, K. A. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1098 · Cited by 5,829
Diversity, stability and resilience of the human gut microbiota
Lozupone, C. A., Stombaugh, J. I., Gordon, J. I., Jansson, J. K., & Knight, R. (2012) · Nature · doi:10.1038/nature11550 · Cited by 5,533
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
Metagenomic Analysis of the Human Distal Gut Microbiome
Gill, S. R., Pop, M., DeBoy, R. T., Eckburg, P. B., Turnbaugh, P. J., Samuel, B. S., Gordon, J. I., Relman, D. A., Fraser-Liggett, C. M., & Nelson, K. E. (2006) · Science · doi:10.1126/science.1124234 · Cited by 4,699
Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis
Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251
Gut microbiota in health and disease
Sekirov, I., Russell, S. L., Antunes, L. C. M., & Finlay, B. B. (2010) · Physiological Reviews · doi:10.1152/physrev.00045.2009 · Cited by 4,182

Flagged first, then by citations

Show all 147 references

Research works printed but not linked: 2

Gilbert DN, 2013, The Sanford Guide to Antimicrobial Therapy 2013: 43rd edition, 71
Mandell GL, 2009, Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases: Seventh edition, 309

Sorted by citations

Items 701–761 of 761

Additional file 1 of Microbial signature in IgE-mediated food allergies
Goldberg, M. R., Mor, H., Neriya, D. M., Magzal, F., Muller, E., Appel, M. Y., Nachshon, L., Borenstein, E., Tamir, S., Louzoun, Y., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13151880
Additional file 6 of Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome
Zhou, A., Tang, B., Xie, Y., Li, S., Xiao, X., Wu, L., Tu, D., Wang, S., Feng, Y., Feng, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26647395
Additional file 1 of Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime
Ma, L., Song, Y., Lyu, W., Chen, Q., Xiao, X., Jin, Y., Yang, H., Wang, W., & Xiao, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26637600
Additional file 2 of Vibrio vulnificus induces the death of a major bacterial species in the mouse gut via cyclo-Phe-Pro
Kim, J.-A., Jang, B.-R., Kim, Y.-R., Jung, Y.-C., Kim, K.-S., & Lee, K.-H. (2021) · Figshare · doi:10.6084/m9.figshare.15026565
Additional file 7 of FMO3 deficiency of duck leads to decreased lipid deposition and increased antibacterial activity
Li, X., Song, J., Shi, X., Huang, M., Liu, L., Yi, G., Yang, N., Xu, G., & Zheng, J. (2022) · Figshare · doi:10.6084/m9.figshare.21564306
Additional file 11 of Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome
Zhou, A., Tang, B., Xie, Y., Li, S., Xiao, X., Wu, L., Tu, D., Wang, S., Feng, Y., Feng, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26647410
Additional file 4 of Large-scale causal analysis of gut microbiota and six common complications of diabetes: a mendelian randomization study
Wang, J., Teng, M., Feng, R., Su, X., Xu, K., Wang, J., Wang, G., Zhang, Y., & Xu, P. (2024) · Figshare · doi:10.6084/m9.figshare.26692777
Additional file 5 of Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome
Zhou, A., Tang, B., Xie, Y., Li, S., Xiao, X., Wu, L., Tu, D., Wang, S., Feng, Y., Feng, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26647392
Additional file 7 of Intensive antibiotic treatment of sows with parenteral crystalline ceftiofur and tulathromycin alters the composition of the nasal microbiota of their offspring
Bonillo-Lopez, L., Obregón-Gutierrez, P., Huerta, E., Correa‐Fiz, F., Sibila, M., & Aragón, V. (2024) · Figshare · doi:10.6084/m9.figshare.26645065
Additional file 13 of Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome
Zhou, A., Tang, B., Xie, Y., Li, S., Xiao, X., Wu, L., Tu, D., Wang, S., Feng, Y., Feng, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26647416
Additional file 3 of Intensive antibiotic treatment of sows with parenteral crystalline ceftiofur and tulathromycin alters the composition of the nasal microbiota of their offspring
Bonillo-Lopez, L., Obregón-Gutierrez, P., Huerta, E., Correa‐Fiz, F., Sibila, M., & Aragón, V. (2024) · Figshare · doi:10.6084/m9.figshare.26645053
Additional file 2 of Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome
Zhou, A., Tang, B., Xie, Y., Li, S., Xiao, X., Wu, L., Tu, D., Wang, S., Feng, Y., Feng, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.24709099
Additional file 5 of Large-scale causal analysis of gut microbiota and six common complications of diabetes: a mendelian randomization study
Wang, J., Teng, M., Feng, R., Su, X., Xu, K., Wang, J., Wang, G., Zhang, Y., & Xu, P. (2024) · Figshare · doi:10.6084/m9.figshare.26692780
Additional file 5 of Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime
Ma, L., Song, Y., Lyu, W., Chen, Q., Xiao, X., Jin, Y., Yang, H., Wang, W., & Xiao, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26637612
Additional file 8 of Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome
Zhou, A., Tang, B., Xie, Y., Li, S., Xiao, X., Wu, L., Tu, D., Wang, S., Feng, Y., Feng, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26647401
Additional file 1 of FMO3 deficiency of duck leads to decreased lipid deposition and increased antibacterial activity
Li, X., Song, J., Shi, X., Huang, M., Liu, L., Yi, G., Yang, N., Xu, G., & Zheng, J. (2022) · Figshare · doi:10.6084/m9.figshare.21564288
Additional file 7 of Changes of gut microbiota and short chain fatty acids in patients with Peutz–Jeghers syndrome
Zhou, A., Tang, B., Xie, Y., Li, S., Xiao, X., Wu, L., Tu, D., Wang, S., Feng, Y., Feng, X., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26647398
Additional file 4 of Intensive antibiotic treatment of sows with parenteral crystalline ceftiofur and tulathromycin alters the composition of the nasal microbiota of their offspring
Bonillo-Lopez, L., Obregón-Gutierrez, P., Huerta, E., Correa‐Fiz, F., Sibila, M., & Aragón, V. (2024) · Figshare · doi:10.6084/m9.figshare.26645056
Additional file 1 of Selective depletion of Campylobacter jejuni via T6SS dependent functionality: an approach for improving chickens gut health
Gupta, S., Biswas, P., Das, B., Mondal, S., Gupta, P., Das, D., & Mallick, A. I. (2024) · Figshare · doi:10.6084/m9.figshare.26289103
Additional file 1 of Intensive antibiotic treatment of sows with parenteral crystalline ceftiofur and tulathromycin alters the composition of the nasal microbiota of their offspring
Bonillo-Lopez, L., Obregón-Gutierrez, P., Huerta, E., Correa‐Fiz, F., Sibila, M., & Aragón, V. (2024) · Figshare · doi:10.6084/m9.figshare.26645047
Additional file 3 of Longitudinal metagenomic study reveals the dynamics of fecal antibiotic resistome in pigs throughout the lifetime
Ma, L., Song, Y., Lyu, W., Chen, Q., Xiao, X., Jin, Y., Yang, H., Wang, W., & Xiao, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26637606
Additional file 2 of Large-scale causal analysis of gut microbiota and six common complications of diabetes: a mendelian randomization study
Wang, J., Teng, M., Feng, R., Su, X., Xu, K., Wang, J., Wang, G., Zhang, Y., & Xu, P. (2024) · Figshare · doi:10.6084/m9.figshare.25406088
Additional file 2 of Intensive antibiotic treatment of sows with parenteral crystalline ceftiofur and tulathromycin alters the composition of the nasal microbiota of their offspring
Bonillo-Lopez, L., Obregón-Gutierrez, P., Huerta, E., Correa‐Fiz, F., Sibila, M., & Aragón, V. (2024) · Figshare · doi:10.6084/m9.figshare.26645050
Cheats can boost the success of an invading population
Lear, L., Buckling, A. G. J., & Hesse, E. (2025) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2025.2355 · Cited by 1
The Role of the Respiratory Microbiome in Pneumonia
Baker, J. M., & Dickson, R. P. (2026) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2025.12.004
Show Me the “Mino:” In Vitro Efficacy of Minocycline on Clinical Gram-Negative Bacterial Isolates
Crowley, P. D., Ranganath, N., Mira, P., Streck, N. T., Challener, D. W., Rivera, C. G., & AbuSaleh, O. (2026) · Microbial Drug Resistance · doi:10.1177/10766294261424485
Antibacterial activity of bioactive anthraquinones isolated from Cassia tora L. against pathogenic intestinal microorganisms
Balusamy, S. R., Lee, S., Anandapadmanaban, G., Samad, A., Shikder, M. R., Veeramani, C., Alsaif, M. A., Al‐Numair, K. S., Singh, P., & Perumalsamy, H. (2026) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-026-05084-4
A future perspective on upper respiratory tract diseases: diet and gut microbiota
Lei, Y., Sun, Z., Thanuphol, P., da Cruz, L. L., Li, S., & Zhu, Z. (2025) · International Journal of Food Science & Technology · doi:10.1093/ijfood/vvag030
Disease-Suppressive Phyllosphere Microbiomes: A Perspective on Microbiome Transplantation for Sustainable Agriculture
Kaur, L., Bell, T. H., Sadeghi, J., & Hockett, K. L. (2026) · Phytopathology · doi:10.1094/phyto-03-25-0116-per
Potential mechanism of glyphosate affecting Crohn’s disease by regulating metabolites of Bacteroides: a comprehensive analysis based on multi omics and machine learning
Yuan, T., Xing, J., Wang, Z., Song, X., & Liu, P. (2026) · International Journal of Surgery · doi:10.1097/js9.0000000000005017
Role of gut-brain axis in Glioblastoma: Therapeutic opportunities with nanotechnology
Arunsi, K., Pendse, S., & Misra, R. (2026) · Next research. · doi:10.1016/j.nexres.2026.101587
Association Between Clinical Frailty and Antibiotic Resistance Among Older Patients with Fever in the Emergency Department
Lim, J. Y., Lee, D. H., Chung, H. S., Choi, Y., Choi, Y. H., Kim, K., Hong, K.-H., & Bae, S. J. (2026) · Antibiotics · doi:10.3390/antibiotics15030296
Mapping 25 years of research on gut microbiota and antibiotic resistance: bibliometric insights and future directions
Heng, Y., Wang, M., Zhang, Z., Jian, E., Wu, C., Zhang, C., Chen, Q., Yu, X., Zhu, Y., & Cai, P. (2026) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-026-05455-y
Effects of Social Pairing on Measurable Disease Outcomes in Hospitalized Rhesus Macaques ( Macaca mulatta )
Burke, M. C., Haertel, A. J., Heagerty, A., & Dozier, B. L. (2026) · American Journal of Primatology · doi:10.1002/ajp.70144
Acquisition et transmission d'entérobactéries productrices de BLSE chez des sujets communautaires en zone de forte endémie
Maataoui, N. (2019) · doi:10.70675/7a53a548zef17z44d8zb1a5z5429d6ab96a0
Colonisation digestive par entérobactéries productrices de carbapénémase dans un modèle murin : aggravation de la pneumopathie à Pseudomonas aeruginosa
Guern, R. L. (2019) · theses.fr (ABES) · doi:10.70675/df8d5bddz7fd8z4510za8b0z2d2b5dd1b937
Mathematical modelling and simulation of the transmission, surveillance and control of human pathogens in healthcare settings
Smith, D. R. (2021) · theses.fr (ABES) · doi:10.70675/40b80716z75edz495ezaa7fz39000eea8928
Entérobactéries productrices de carbapénémases, comment maitriser le risque pandémique dans les pays à revenus moyens ou faibles ?
Saliba, R. (2022) · theses.fr (ABES) · doi:10.70675/b63c137fzd1b9z4199z875czba418bfb9966
Rôle des interactiοns hôte-micrοbiοte dans la physiοlοgie intestinale et dans les Τrοubles du Cοmpοrtement Alimentaire
Loison, L. (2024) · theses.fr (ABES) · doi:10.70675/820e1025z4df2z440cz9b11z786a8e3e4423
Gut microbiota and metabolic function in leeches with distinct feeding niches
Tong, X., Yang, D., Cao, X., Yang, X., Hu, Q., Fan, S., Chen, H., Cao, Y., Liu, J., & Liu, Z. (2026) · BMC Microbiology · doi:10.1186/s12866-026-05062-z
Prescripción farmacológica: inhaladores y antimicrobianos
Díez, I. B., & Ferré, A. M. R. (2026) · Atención Primaria · doi:10.1016/j.aprim.2026.103500
Effects of dietary turmeric powder on growth performance, antioxidant capacity, and intestinal health in juvenile large yellow croaker (Larimichthys crocea)
Wang, Y., Luo, S., Zhou, X., Huang, X., & Yan, M. (2026) · Aquaculture · doi:10.1016/j.aquaculture.2026.744181
A validated prediction model for intestinal vancomycin-resistant Enterococcus colonization in critically ill patients with sepsis: insights into risk stratification and clinical impact
Wang, Y.-H., Lee, Y., Lin, Y.-F., Huang, C.-C., Cheng, K.-C., Hsu, C.-C., Tsai, Y.-T., Lu, S., Jung, C., & Tai, Y. (2026) · BMC Infectious Diseases · doi:10.1186/s12879-026-13578-y
Enrofloxacin-loaded Zein nanoparticles combat E. coli O157:H7 in biomimetic 3D intestinal model
Herrera, G. J., Distor, N. T., Faria, L. U., Peña‐Bahamonde, J., Nguyen, H., & Rodrigues, D. F. (2026) · Health Nanotechnology · doi:10.1186/s44301-026-00031-x
Continuation of anti-tuberculosis therapy after Clostridioides difficile infection: a retrospective cohort study
Itogawa, K., Narumoto, O., Takeda, K., Kato, T., Sato, K., Maeda, M., Nakano, E., Usui, Y., Shimada, M., Morio, Y., et al. (2026) · Journal of Infection and Chemotherapy · doi:10.1016/j.jiac.2026.103016
Host immunity and recurrent Clostridioides difficile infection: a comprehensive review
Mirjalili, S., Hooshiar, M. H., Abbasabadarabi, S., & Aliramezani, A. (2026) · Pathogens and Global Health · doi:10.1080/20477724.2026.2686115
From Microbiota Correction to Host Protection: A New Therapeutic Target for the Prevention and Treatment of Postoperative Complications
Berikkhanov, Z. G. M., Pilipenko, M. O., Ermakova, E. D., Sukhanova, M. A., Ivanova, M. Y., Kotelnikov, A. G., Nikolaev, A., Razumovsky, V. S., Rakintsev, V. S., Shestakov, A. I., et al. (2026) · Journal of Clinical Medicine · doi:10.3390/jcm15135161
The influence of gut microbiota against ESKAPE pathogens
Shayista, H., Sathyanarayana, N. R., Nagalingaswamy, N. P. M., Kumar, M., & Baker, S. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-26726-0.00007-4
High prevalence and territorial heterogeneity of intestinal parasite detection in Ecuador: A large registry-based cross-sectional study using routine stool examinations
Ortiz‐Prado, E., Cadena, S., Durán, M., Larrea, X., Páez, N., Sarlabous, V., Sánchez, M., Toledo, P., Vergara, H., Vasconez-Gonzalez, J., et al. (2026) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2026.109026
Microbiome Engineering in Dairy Cattle: A Critical Review of Strategies for Disease Resistance, Productivity, and Sustainable Farming
Ashfaq, M. S., Tharwat, M., Ahmed, S., Shaukat, A., Nassar, N., Abid, S., Abid, M. A., & Alshanbari, F. A. (2026) · Veterinary Sciences · doi:10.3390/vetsci13080766
Early-life combined supplementation with lactoferrin and Bifidobacterium breve HH079 provides enhanced protection against Citrobacter rodentium infection in neonatal mice
Gu, Z., Xie, Z., Lu, Z., Xu, S., Huang, Q., Zhao, L., Liu, F., & Zhang, B. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.109712
Impact of the anti-inflammatory macrolide glasmacinal on the gut microbiota of healthy adults: an open-label trial
Sewunet, T., Razavi, M., Hanrott, K., Norris, V., Kricker, J., & Giske, C. G. (2026) · Nature Communications · doi:10.1038/s41467-026-76867-9
Multi-dimensional dynamic assessment revealed the antibiotic-induced pseudo-germ-free model in SD rats stabilized within 4 days
Zhao, Y., Wang, L., Zhang, K., Zhang, J., Guo, Z., Lu, X., & Li, J. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1930662
Effect of Nano- and Microparticulate Fermented Fish Protein Hydrolysate Diets on Growth, Digestive Function, Intestinal Development, and Gene Expression in Common Carp (Cyprinus carpio) Larvae
Noor, Z., Lodhi, F., Younas, W., Khan, F. U., Hassan, Z., Rizwan, M., Ullah, S., Khan, F. U., Bari, F., & Islam, M. F. (2026) · Biology · doi:10.3390/biology15191680
Fecal microbiota transplantation and peri-stoma microbiome management in patients with intestinal stomas: from mechanisms to clinical translation
Huang, Q., Huifei, X., Qiaoyun, L., Zhang, Y., Zou, J., Gao, Z., Yang, L., Zeng, H., & Liu, J. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1913974
Different gut microbiome dysbioses impact the evolutionary fate of hypervirulent Klebsiella pneumoniae
Lim, C., Zheng, J., Cheam, G., Yong, M., Chen, H., Ting, A., Chen, Y., Wang, Q., Nagarajan, N., & Gan, Y. (2026) · iMeta · doi:10.1002/imt2.70175
PBT2 potentiates carbapenem antibiotics against diverse Klebsiella pneumoniae strains
Tan, A., Hartono, A. R., Gunn, A. P., Gorrie, C. L., Oliveira, D. M. P. D., Short, F. L., Walker, M. J., Sherry, N. L., Howden, B. P., & McDevitt, C. A. (2026) · Microbiology Spectrum · doi:10.1128/spectrum.02109-26
Intestinal Responses to Short-Term Hexaflumuron Exposure in Grass Carp (Ctenopharyngodon idella): A Combined Physiological, Transcriptomic, and Gut Microbiota Perspective
Zhou, S., Li, J., Yang, Q., & Ai, X. (2026) · Animals · doi:10.3390/ani16193056
Gut Microbiome and Fecal Metabolome Analysis Reveal Potential Non-Invasive Biomarkers For Acute Myocardial Infarction
Khan, I., Xie, X., & Li, Z. (2026) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-026-11219-z
Within-host evolution and transmission of a human gut symbiont across ecological scales
Vasquez, K. S., Wong, D. P. G. H., Kotaka, K., McKeithen-Mead, S. A., Pedro, M. F., Yu, F. B., Jain, S., Meng, X., Higginbottom, S. K., DeFelice, B. C., et al. (2026) · Cell Host & Microbe · doi:10.1016/j.chom.2026.09.002 · Cited by 11
BindingDB Entry 50011353: Ultrapotent Inhibitor of
BindingDB (2022) · UC San Diego · doi:10.7270/q2k64np9

Authors: Kim, S., Covington, A., & Pamer, E. G.
Affiliations: Memorial Sloan Kettering Cancer Center (US)
Corresponding author: Pamer, Eric G.
ORCID: Kim, Sohn
Pamer, Eric G.
Venue: Immunological Reviews
Publisher: Wiley
Published: 2017-08-30
Volume: 279
Issue: 1
Pages: 90-105
ISSN: 0105-2896 (ISSN-L)
1600-065X
DOI: 10.1111/imr.12563
PMC: PMC6026851
OpenAlex: W2753747201
Cited by: 741
References: 147
Citations by year: 2026: 49 · 2025: 67 · 2024: 112 · 2023: 95 · 2022: 136 · 2021: 117 · 2020: 69 · 2019: 68 · 2018: 27 · 2017: 1
FWCI: 4.22
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Immunological Reviews (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Funders: National Cancer Institute (P01CA023766, P30CA008748)
National Institute of General Medical Sciences (T32GM007739)
National Institute of Allergy and Infectious Diseases (R01AI095706, U01AI124275, R01AI042135)
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
Health Sciences › Medicine › Microbiology (medical) › Antibiotic Resistance in Bacteria
Keywords: gut microbiota, colonization resistance, antibiotics, enteric pathogens, nosocomial infections, antibiotic resistance, immunocompromised patients, commensal microbiota, intestinal colonization
MeSH terms: Gastrointestinal Microbiome, Animals, Anti-Bacterial Agents, Bacterial Infections, Cross Infection, Drug Resistance, Humans, Immunocompromised Host, Host-Pathogen Interactions, Dysbiosis

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

The intestinal microbiota: Antibiotics, colonization resistance, and enteric pathogens

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks