Colonization resistance

Pseudomembraneous enterocolitis: mechanism for restoring floral homeostasis.

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Colonization, suprainfection and superinfection: major microbiologic and clinical problems.

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Changes in the oropharyngeal and colon microflora in relation to antimicrobial concentrations in saliva and faeces.

Heimdahl, A., Kager, L., & Ce, N. (1985) · PubMed · Cited by 16

Intake of Lactobacillus plantarum Reduces Certain Gastrointestinal Symptoms During Treatment With Antibiotics

Lönnermark, E., Friman, V., Lappas, G., Sandberg, T., Berggren, A., & Adlerberth, I. (2010) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e3181b2683f · Cited by 110

Probiotic/Synbiotic Therapy for Treating Critically Ill Patients from a Gut Microbiota Perspective

Shimizu, K., Ogura, H., Asahara, T., Nomoto, K., Morotomi, M., Tasaki, O., Matsushima, A., Kuwagata, Y., Shimazu, T., & Sugimoto, H. (2012) · Digestive Diseases and Sciences · doi:10.1007/s10620-012-2334-x · Cited by 109

Clostridium difficile infection: molecular pathogenesis and novel therapeutics

Rineh, A., Kelso, M. J., Vatansever, F., Tegos, G. P., & Hamblin, M. R. (2014) · Expert Review of Anti-infective Therapy · doi:10.1586/14787210.2014.866515 · Cited by 120

A bacteriophage cocktail targeting Escherichia coli reduces E. coli in simulated gut conditions, while preserving a non-targeted representative commensal normal microbiota

Cieplak, T., Soffer, N., Sulakvelidze, A., & Nielsen, D. S. (2018) · Gut Microbes · doi:10.1080/19490976.2018.1447291 · Cited by 108

State of the Art on Functional Virgin Olive Oils Enriched with Bioactive Compounds and Their Properties

Reboredo‐Rodríguez, P., Figueiredo-González, M., González‐Barreiro, C., Simal‐Gándara, J., Salvador, M. D., Cancho-Grande, B., & Fregapane, G. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18030668 · Cited by 111

In vivo production of hydroxyl radical by enterococcus faecalis colonizing the intestinal tract using aromatic hydroxylation

Huycke, M. M., & Moore, D. R. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00977-2 · Cited by 106

Comparative Effects of Moxifloxacin and Clarithromycin on the Normal Intestinal Microflora

Edlund, G. B. C. (2000) · Scandinavian Journal of Infectious Diseases · doi:10.1080/00365540050164272 · Cited by 106

Structural and functional changes in the gut microbiota associated to Clostridium difficile infection

Pérez‐Cobas, A. E., Artacho, A., Ott, S. J., Moyá, A., Gosalbes, M. J., & Latorre, A. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00335 · Cited by 109

Gut microbiome and liver disease

Betrapally, N. S., Gillevet, P. M., & Bajaj, J. S. (2016) · Translational research · doi:10.1016/j.trsl.2016.07.005 · Cited by 106

In Vitro Activities of Ramoplanin, Teicoplanin, Vancomycin, Linezolid, Bacitracin, and Four Other Antimicrobials against Intestinal Anaerobic Bacteria

Citron, D. M., Merriam, C. V., Tyrrell, K. L., Warren, Y. A., Fernandez, H. T., & Goldstein, E. J. C. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.7.2334-2338.2003 · Cited by 100

Saccharomyces boulardiieffects on gastrointestinal diseases

Zanello, G., Meurens, F., Berri, M., & Salmon, H. (2009) · Current Issues in Molecular Biology · doi:10.21775/cimb.011.047 · Cited by 100

Clostridium difficile Alters the Structure and Metabolism of Distinct Cecal Microbiomes during Initial Infection To Promote Sustained Colonization

Jenior, M. L., Leslie, J. L., Young, V. B., & Schloss, P. D. (2018) · mSphere · doi:10.1128/msphere.00261-18 · Cited by 96

Effects of anti-Helicobacter pylori treatment and probiotic supplementation on intestinal microbiota

Myllyluoma, E., Ahlroos, T., Veijola, L., Rautelin, H., Tynkkynen, S., & Korpela, R. (2006) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2006.08.034 · Cited by 95

Gastrointestinal dysmotility is associated with altered gut flora and septic mortality in patients with severe systemic inflammatory response syndrome: a preliminary study

Shimizu, K., Ogura, H., Asahara, T., Nomoto, K., Morotomi, M., Nakahori, Y., Osuka, A., Yamano, S., Goto, M., Matsushima, A., et al. (2010) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2010.01653.x · Cited by 94

Recurrent Clostridium difficile infection: From colonization to cure

Shields, K. S., Araujo-Castillo, R. V., Theethira, T. G., Alonso, C. D., & Kelly, C. P. (2015) · Anaerobe · doi:10.1016/j.anaerobe.2015.04.012 · Cited by 98

Risk-factors for acquisition of extended-spectrum β-lactamase-producing Escherichia coli among hospitalised patients

Peña, C., Gudiol, C., Tubau, F., Saballs, M., Pujol, M., Domínguez, M. Á., Calatayud, L., Ariza, J., & Gudiol, F. (2006) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2005.01358.x · Cited by 92

All great truths are iconoclastic: selective decontamination of the digestive tract moves from heresy to level 1 truth

van Saene, H. K. F., Petros, A., Ramsay, G., & Baxby, D. (2003) · Intensive Care Medicine · doi:10.1007/s00134-003-1722-2 · Cited by 91

Clostridium difficile infection in horses: A review

Diab, S. S., Songer, G., & Uzal, F. A. (2013) · Veterinary Microbiology · doi:10.1016/j.vetmic.2013.03.032 · Cited by 90

DNA replication proteins as potential targets for antimicrobials in drug-resistant bacterial pathogens

van Eijk, E., Wittekoek, B., Kuijper, E., & Smits, W. K. (2017) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkw548 · Cited by 94

Digestive tract colonization by multidrug-resistant Enterobacteriaceae in travellers: An update

Ruppé, É., Andremont, A., & Armand-Lefèvre, L. (2017) · Travel Medicine and Infectious Disease · doi:10.1016/j.tmaid.2017.11.007 · Cited by 81

Exoproducts of the Escherichia coli strain H22 inhibiting some enteric pathogens both in vitro and in vivo

Cursino, L., Šmajs, D., Šmarda, J., Nardi, R. M. D., Nicoli, J. R., Chartone‐Souza, E., & Nascimento, A. M. A. (2006) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2006.02834.x · Cited by 86

Antimicrobial activity of quinoxaline 1,4-dioxide with 2- and 3-substituted derivatives

Vieira, M., Pinheiro, C., Fernandes, R., Noronha, J. P., & Prudêncio, C. (2013) · Microbiological Research · doi:10.1016/j.micres.2013.06.015 · Cited by 85

Synbiotics Decrease the Incidence of Septic Complications in Patients with Severe SIRS: A Preliminary Report

Shimizu, K., Ogura, H., Goto, M., Asahara, T., Nomoto, K., Morotomi, M., Matsushima, A., Tasaki, O., Fujita, K., Hosotsubo, H., et al. (2008) · Digestive Diseases and Sciences · doi:10.1007/s10620-008-0460-2 · Cited by 87

From natural product to marketed drug: the tiacumicin odyssey

Erb, W., & Zhu, J. (2012) · Natural Product Reports · doi:10.1039/c2np20080e · Cited by 85

Lactobacillus rhamnosus GG treatment improves intestinal permeability and modulates microbiota dysbiosis in an experimental model of sepsis

Chen, L., Li, H., Li, J., Chen, Y., & Yang, Y. (2019) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2019.4050 · Cited by 84

A Multi-Omic View of Host-Pathogen-Commensal Interplay in Salmonella-Mediated Intestinal Infection

Kaiser, B. L. D., Li, J., Sanford, J. A., Kim, Y., Kronewitter, S. R., Jones, M. B., Peterson, C. T., Peterson, S. N., Frank, B. C., Purvine, S. O., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067155 · Cited by 83

Selective digestive decontamination in patients in intensive care

Bonten, M. J. M. (2000) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/46.3.351 · Cited by 83

Approaches in the safety evaluations of veterinary antimicrobial agents in food to determine the effects on the human intestinal microflora

Cerniglia, C. E., & Kotarski, S. F. (2005) · Journal of Veterinary Pharmacology and Therapeutics · doi:10.1111/j.1365-2885.2004.00595.x · Cited by 82

In situ ESBL conjugation from avian to human Escherichia coli during cefotaxime administration

Smet, A., Rasschaert, G., Martel, A., Persoons, D., Dewulf, J., Butaye, P., Catry, B., Haesebrouck, F., Herman, L., & Heyndrickx, M. (2011) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2010.04907.x · Cited by 86

Safety and tolerance of the human milk probiotic strain Lactobacillus salivarius CECT5713 in 6-month-old children

Maldonado, J., Lara‐Villoslada, F., Sierra, S., Sempere, L., Gómez, M., Rodríguez, J. M., Bozá, J., Xaus, J., & Olivares, M. M. (2009) · Nutrition · doi:10.1016/j.nut.2009.08.023 · Cited by 81

Coexistence of Vancomycin-Resistant Enterococci and Staphylococcus aureus in the Intestinal Tracts of Hospitalized Patients

Ray, A. J., Pultz, N. J., Bhalla, A., Aron, D. C., & Donskey, C. J. (2003) · Clinical Infectious Diseases · doi:10.1086/377451 · Cited by 82

Microbial and metabolic interactions between the gastrointestinal tract and Clostridium difficile infection

Theriot, C. M., & Young, V. B. (2013) · Gut Microbes · doi:10.4161/gmic.27131 · Cited by 83

Escherichia coli Isolate for Studying Colonization of the Mouse Intestine and Its Application to Two-Component Signaling Knockouts

Lasaro, M. A., Liu, Z., Bishar, R. A., Kelly, K., Chattopadhyay, S., Paul, S., Sokurenko, E. V., Zhu, J., & Goulian, M. (2014) · Journal of Bacteriology · doi:10.1128/jb.01296-13 · Cited by 81

Dietary Calcium Phosphate Stimulates Intestinal Lactobacilli and Decreases the Severity of a Salmonella Infection in Rats

Bovee-Oudenhoven, I. M. J., Lettink-Wissink, M. L. G., Wouters, J. T., & van der Meer, R. (1999) · Journal of Nutrition · doi:10.1093/jn/129.3.607 · Cited by 80

Colonization of the Cecal Mucosa by Helicobacter hepaticus Impacts the Diversity of the Indigenous Microbiota

Kuehl, C. J., Wood, H. D., Marsh, T. L., Schmidt, T. M., & Young, V. B. (2005) · Infection and Immunity · doi:10.1128/iai.73.10.6852-6961.2005 · Cited by 79

Role of intestinal microbiota in transplantation outcomes

Taur, Y., Jenq, R. R., Úbeda, C., van den Brink, M. R. M., & Pamer, E. G. (2015) · Best Practice & Research Clinical Haematology · doi:10.1016/j.beha.2015.10.013 · Cited by 79

Protective role of the vulture facial skin and gut microbiomes aid adaptation to scavenging

Mendoza, M. L. Z., Graves, G. R., Roggenbuck, M., Vargas, K. M., Hansen, L. H., Brunak, S., Gilbert, M. T. P., & Sicheritz‐Pontén, T. (2018) · Acta veterinaria Scandinavica · doi:10.1186/s13028-018-0415-3 · Cited by 78

Evaluation of Veterinary Drug Residues in Food for Their Potential to Affect Human Intestinal Microflora

Cerniglia, C. E., & Kotarski, S. F. (1999) · Regulatory Toxicology and Pharmacology · doi:10.1006/rtph.1999.1300 · Cited by 79

Fecal Microbiota Transplantation for the Management of Clostridium difficile Infection

Rao, K. K., & Young, V. B. (2015) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2014.11.009 · Cited by 79

Complex intestinal bacterial communities in three species of planorbid snails

Horn, D. J., Garcia, J. R., Loker, E. S., Mitchell, K. R., Mkoji, G. M., Adema, C. M., & Takacs‐Vesbach, C. D. (2011) · Journal of Molluscan Studies · doi:10.1093/mollus/eyr038 · Cited by 78

Methicillin-Resistant Staphylococcus aureus as a Causative Agent of Postoperative Intra-abdominal Infection: Relation to Nasal Colonization

Fierobe, L., Decré, D., Muller‐Serieys, C., Lucet, J. C., Marmuse, J., Mantz, J., & Desmonts, J.-M. (1999) · Clinical Infectious Diseases · doi:10.1086/313454 · Cited by 78

Diarrhea-associated pathogens, lactobacilli and cellulolytic bacteria in equine feces: Responses to antibiotic challenge

Harlow, B. E., LAWRENCE, L. M., & Flythe, M. D. D. (2013) · Veterinary Microbiology · doi:10.1016/j.vetmic.2013.05.003 · Cited by 79

Intercellular communications in multispecies oral microbial communities

Guo, L., He, X., & Shi, W. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00328 · Cited by 80

Antianaerobic Antibiotic Therapy Promotes Overgrowth of Antibiotic-Resistant, Gram-Negative Bacilli and Vancomycin-Resistant Enterococci in the Stool of Colonized Patients

Bhalla, A., Pultz, N. J., Ray, A. J., Hoyen, C. K., Eckstein, E. C., & Donskey, C. J. (2003) · Infection Control and Hospital Epidemiology · doi:10.1086/502267 · Cited by 75

Probiotication of Nutritious Fruit and Vegetable Juices: An Alternative to Dairy-Based Probiotic Functional Products

Mojikon, F. D., Kasimin, M. E., Molujin, A. M., Gansau, J. A., & Jawan, R. (2022) · Nutrients · doi:10.3390/nu14173457 · Cited by 81

The Clostridium difficile cpr Locus Is Regulated by a Noncontiguous Two-Component System in Response to Type A and B Lantibiotics

Suárez, J. M., Edwards, A. N., & McBride, S. M. (2013) · Journal of Bacteriology · doi:10.1128/jb.00166-13 · Cited by 74

Antimicrobial Use, Human Gut Microbiota and Clostridium difficile Colonization and Infection

Vincent, C., & Manges, A. R. (2015) · Antibiotics · doi:10.3390/antibiotics4030230 · Cited by 76

Antimicrobial resistance risk factors and characterisation of faecal E. coli isolated from healthy Labrador retrievers in the United Kingdom

Schmidt, V. M., Pinchbeck, G. L., Nuttall, T., McEwan, N., Dawson, S., & Williams, N. J. (2015) · Preventive Veterinary Medicine · doi:10.1016/j.prevetmed.2015.01.013 · Cited by 67

Recurrent Clostridium difficile infection: causality and therapeutic approaches

Johnson, S. (2009) · International Journal of Antimicrobial Agents · doi:10.1016/s0924-8579(09)70014-7 · Cited by 72

Fecal microbiota transplantation for the treatment of Clostridium difficile infection

Rao, K. K., & Safdar, N. (2015) · Journal of Hospital Medicine · doi:10.1002/jhm.2449 · Cited by 69

Fecal microbiota in patients receiving enteral feeding are highly variable and may be altered in those who develop diarrhea

Whelan, K., Judd, P. A., Tuohy, K. M., Gibson, G. R., Preedy, V. R., & Taylor, M. A. (2008) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.26219 · Cited by 70

Pediatric Carbapenem-resistant Enterobacteriaceae in Los Angeles, California, a High-prevalence Region in the United States

Pannaraj, P. S., Bard, J. D., Cerini, C., & Weissman, S. J. (2014) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0000000000000471 · Cited by 69

Lactobacillus plantarum 299v Enhances the Concentrations of Fecal Short-Chain Fatty Acids in Patients with Recurrent Clostridium difficile-Associated Diarrhea

Wullt, M., Hagslätt, M.-L. J., Odenholt, I., & Berggren, A. (2007) · Digestive Diseases and Sciences · doi:10.1007/s10620-006-9123-3 · Cited by 68

Mining zebrafish microbiota reveals key community-level resistance against fish pathogen infection

Stressmann, F. A., Bernal-Bayard, J., Pérez-Pascual, D., Audrain, B., Rendueles, O., Briolat, V., Bruchmann, S., Volant, S., Ghozlane, A., Häußler, S., et al. (2020) · The ISME Journal · doi:10.1038/s41396-020-00807-8 · Cited by 68

Clostridium difficileinfections in animals with special reference to the horse. A review

Båverud, V. (2002) · Veterinary Quarterly · doi:10.1080/01652176.2002.9695137 · Cited by 66

Modulation of Rat Cecal Microbiota by Administration of Raffinose and Encapsulated Bifidobacterium breve

Dinoto, A., Suksomcheep, A., Ishizuka, S., Tsuchihashi, H., Hanada, S., Kamagata, Y., Asano, K., Tomita, F., & Yokota, A. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.1.784-792.2006 · Cited by 65

DNA microarray analysis of predominant human intestinal bacteria in fecal samples

Wang, R., Beggs, M. L., Erickson, B. D., & Cerniglia, C. E. (2004) · Molecular and Cellular Probes · doi:10.1016/j.mcp.2004.03.002 · Cited by 65

Adherence to Streptococci Facilitates Fusobacterium nucleatum Integration into an Oral Microbial Community

He, X., Hu, W., Kaplan, C. W., Guo, L., Shi, W., & Lux, R. (2011) · Microbial Ecology · doi:10.1007/s00248-011-9989-2 · Cited by 64

Transcriptional interactions suggest niche segregation among microorganisms in the human gut

Plichta, D. R., Juncker, A. S., Bertalan, M., Rettedal, E. A., Gautier, L., Varela, E., Manichanh, C., Fouqueray, C., Levenez, F., Nielsen, T., et al. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.152 · Cited by 61

Design and evaluation of group-specific oligonucleotide probes for quantitative analysis of intestinal ecosystems: their application to assessment of equine colonic microflora

Daly, K., & Shirazi‐Beechey, S. P. (2003) · FEMS Microbiology Ecology · doi:10.1016/s0168-6496(03)00032-1 · Cited by 63

Antibiotic Pressure Is a Major Risk Factor for Rectal Colonization by Multidrug-Resistant Pseudomonas aeruginosa in Critically Ill Patients

Gómez-Zorrilla, S., Camoez, M., Tubau, F., Periche, E., Cañizares, R., Domínguez, M. Á., Ariza, J., & Peña, C. (2014) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.03419-14 · Cited by 62

Intestinal transit of an orally administered streptomycin-rifampicin-resistant variant ofBifidobacterium longumSBT2928: its long-term survival and effect on the intestinal microflora and metabolism

Fujiwara, S., Seto, Y., Kimura, A., & Hashiba, H. (2001) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2001.01205.x · Cited by 61

Antibiotic effect and microbiome persistence vary along the European seabass gut

Kokou, F., Sasson, G., Mizrahi, I., & Cnaani, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-66622-5 · Cited by 62

Targeted and Intracellular Antibacterial Activity against S. agalactiae of the Chimeric Peptides Based on Pheromone and Cell-Penetrating Peptides

Li, J., Shang, L., Lan, J. Q., Chou, S., Feng, X., Shi, B., Wang, J., Lyu, Y., & Shan, A. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c12226 · Cited by 59

Effects of lactitol on intestinal microflora and plasma endotoxin in patients with chronic viral hepatitis

Chen, C., Li, L., Wu, Z., Chen, H., & Fu, S. (2006) · Journal of Infection · doi:10.1016/j.jinf.2005.11.013 · Cited by 60

BIOTHERAPEUTIC AGENTS IN THE TREATMENT OF INFECTIOUS DIARRHEA

Elmer, G. W., & McFarland, L. V. (2001) · Gastroenterology Clinics of North America · doi:10.1016/s0889-8553(05)70213-2 · Cited by 60

Clostridium difficile diarrhea: infection control in horses

Båverud, V. (2004) · Veterinary Clinics of North America Equine Practice · doi:10.1016/j.cveq.2004.07.005 · Cited by 59

Reuterin disrupts Clostridioides difficile metabolism and pathogenicity through reactive oxygen species generation

Engevik, M. A., Danhof, H. A., Shrestha, R., Chang‐Graham, A. L., Hyser, J. M., Haag, A. M., Mohammad, M. A., Britton, R. A., Versalovic, J. A., Sorg, J. A., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1795388 · Cited by 59

Repairing gut barrier by traditional Chinese medicine: roles of gut microbiota

Zhou, Y., Zhang, D., Cheng, H., Wu, J., Liu, J., Feng, W., & Peng, C. Y. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1389925 · Cited by 66

Comparative In Vitro Activities of LFF571 against Clostridium difficile and 630 Other Intestinal Strains of Aerobic and Anaerobic Bacteria

Citron, D. M., Tyrrell, K. L., Merriam, C. V., & Goldstein, E. J. C. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.06305-11 · Cited by 57

Enhanced preservation of the human intestinal microbiota by ridinilazole, a novel Clostridium difficile-targeting antibacterial, compared to vancomycin

Thorpe, C. M., Kane, A. V., Chang, J. H., Tai, A., Vickers, R. J., & Snydman, D. R. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199810 · Cited by 56

Veterinary Drug Residues in Meat and Meat Products: Occurrence, Detection and Implications

Falowo, A. B., & Akinmoladun, O. F. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.83616 · Cited by 55

Gut Microbiota and Probiotics/Synbiotics for Modulation of Immunity in Critically Ill Patients

Shimizu, K., Ojima, M., & Ogura, H. (2021) · Nutrients · doi:10.3390/nu13072439 · Cited by 56

Emergence of quinolone resistance in the microbiota of hospitalized patients treated or not with a fluoroquinolone

LASTOURS, V. D., Chau, F., Roy, C., Larroque, B., & Fantin, B. (2014) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dku283 · Cited by 54

Analysis of Anti-Clostridium difficile Activity of Thuricin CD, Vancomycin, Metronidazole, Ramoplanin, and Actagardine, both Singly and in Paired Combinations

Mathur, H., O’Connor, P. M., Hill, C., Cotter, P. D., & Ross, R. P. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00261-13 · Cited by 53

Bacterial microbiota of Aedes aegypti mosquito larvae is altered by intoxication with Bacillus thuringiensis israelensis

Tetreau, G., Grizard, S., Patil, C. D., Tran, F. H., Van, V. T., Stalinski, R., Laporte, F., Mavingui, P., Després, L., & Moro, C. V. (2018) · Parasites & Vectors · doi:10.1186/s13071-018-2741-8 · Cited by 53

Effect of Parenteral Antibiotic Administration on Establishment of Intestinal Colonization in Mice by Klebsiella pneumoniae Strains Producing Extended-Spectrum β-Lactamases

Hoyen, C. K., Pultz, N. J., Paterson, D. L., Aron, D. C., & Donskey, C. J. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.11.3610-3612.2003 · Cited by 53

The intestinal microbiota predisposes to traveler’s diarrhea and to the carriage of multidrug-resistant Enterobacteriaceae after traveling to tropical regions

Léo, S., Lazarević, V., Gaïa, N., Estellat, C., Girard, M., Matheron, S., Armand-Lefèvre, L., Andremont, A., The VOYAG-R Study Group, Andremont, A., et al. (2019) · Gut Microbes · doi:10.1080/19490976.2018.1564431 · Cited by 54

Effects of Antibiotics on Bacterial Species Composition and Metabolic Activities in Chemostats Containing Defined Populations of Human Gut Microorganisms

Newton, D. F., Macfarlane, S., & Macfarlane, G. T. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00079-13 · Cited by 50

Impact of the Microbiota on Bacterial Infections during Cancer Treatment

Galloway-Peña, J., Brumlow, C., & Shelburne, S. A. (2017) · Trends in Microbiology · doi:10.1016/j.tim.2017.06.006 · Cited by 52

Travel and acquisition of multidrug-resistant Enterobacteriaceae

Armand-Lefèvre, L., Andremont, A., & Ruppé, É. (2018) · Médecine et Maladies Infectieuses · doi:10.1016/j.medmal.2018.02.005 · Cited by 55

Comparative Effects of Levofloxacin and Ofloxacin on the Normal Oral and Intestinal Microflora

Edlund, C., Sjöstedt, S., & Nord, C. E. (1997) · Scandinavian Journal of Infectious Diseases · doi:10.3109/00365549709011835 · Cited by 50

Influence of antibiotic pressure on multi-drug resistant Klebsiella pneumoniae colonisation in critically ill patients

Ramos, J. R., Gordón, M., Villarreal, E., Frasquet, J., Sánchez, M. Á., Cerezuela, M. M., Castellanos, Á., & Ramírez, P. (2019) · Antimicrobial Resistance and Infection Control · doi:10.1186/s13756-019-0484-8 · Cited by 48

Causes, consequences, and perspectives in the variations of intestinal density of colonization of multidrug-resistant enterobacteria

Ruppé, É., & Andremont, A. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00129 · Cited by 51

Prebiotics, faecal transplants and microbial network units to stimulate biodiversity of the human gut microbiome

den Abbeele, P. V., Verstraete, W., Aidy, S. E., Geirnaert, A., & de Wiele, T. V. (2013) · Microbial Biotechnology · doi:10.1111/1751-7915.12049 · Cited by 50

Bacterial colonization and intestinal mucosal barrier development

Huang, X. (2013) · World Journal of Clinical Pediatrics · doi:10.5409/wjcp.v2.i4.46 · Cited by 50

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