Impact of Probiotics on Colonizing Microbiota of the Gut

Sanders, Mary Ellen

doi:10.1097/mcg.0b013e318227414a

Cited by 153Probiotics and Fermented FoodsGut microbiota and healthInfant Nutrition and Health

Impact of Probiotics on Colonizing Microbiota of the Gut

Sanders, Mary Ellen·2011·Journal of Clinical Gastroenterology

DOI 10.1097/mcg.0b013e318227414a

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Abstract

Although precise mechanisms responsible for all demonstrations of probiotic health benefits are not known, many lines of evidence suggest that probiotics function through direct or indirect impact on colonizing microbiota of the gut. Probiotics can directly influence colonizing microbes through multiple mechanisms, including the production of inhibitory compounds (bacteriocins, short chain fatty acids, and others), by producing substrates that might promote the growth of colonizing microbes (secreted exopolysaccharides, vitamins, fatty acids, sugars from undigested carbohydrates and others), and by promoting immune responses against specific microbes. Indirectly, probiotics can influence colonizing microbes by inhibiting attachment through stimulated mucin production, reinforcing gut barrier effects, and downregulation of gut inflammation, thereby promoting microbes that are associated with a healthier gut physiology. Although the value of targeted changes in populations of gut bacteria is a matter of debate, increased levels of Bifidobacterium and Lactobacillus in the gut correlate with numerous health endpoints. Microbiota changes due to probiotic intake include increased numbers of related phylotypes, decreasing pathogens and their toxins, altering bacterial community structure to enhance evenness, stabilizing bacterial communities when perturbed (eg, with antibiotics), or promoting a more rapid recovery from a perturbation. Further research will provide insight into the degree of permanence of probiotic-induced changes, although research to date suggests that continued probiotic consumption is needed for sustained impact.

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Administering a probiotic may change gut community structure in unexpected ways, and these changes may or may not alter community function.
“It may change community structure in unexpected ways, and these changes may or may not alter community function.138”
From The Gut Microbiome and the Brain (2014) · cites this paper as [138]

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 · see citing works
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 · see citing works
Enterotypes of the human gut microbiome
MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548 · see citing works
Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa
De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579 · see citing works
Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases
Frank, D. N., St. Amand, A. L., Feldman, R. A., Boedeker, E. C., Harpaz, N., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706625104 · Cited by 4,611 · see citing works
<i>Faecalibacterium prausnitzii</i> is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients
Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413 · see citing works
Bifidobacteria can protect from enteropathogenic infection through production of acetate
Fukuda, S., Toh, H., Hase, K., Oshima, K., Nakanishi, Y., Yoshimura, K., Tobe, T., Clarke, J. M., Topping, D. L., Suzuki, T., et al. (2011) · Nature · doi:10.1038/nature09646 · Cited by 2,387 · see citing works
Reduced diversity of faecal microbiota in Crohn’s disease revealed by a metagenomic approach
Manichanh, C., Rigottier-Gois, L., Bonnaud, E., Gloux, K., Pelletier, E., Frangeul, L., Nalin, R., Jarrin, C., Chardon, P., Marteau, P., et al. (2006) · Gut · doi:10.1136/gut.2005.073817 · Cited by 2,277 · see citing works
Innate immunity and intestinal microbiota in the development of Type 1 diabetes
Wen, L., Ley, R. E., Volchkov, P. Y., Stranges, P. B., Avanesyan, L., Stonebraker, A. C., Hu, C., Wong, F. S., Szot, G. L., Bluestone, J. A., et al. (2008) · Nature · doi:10.1038/nature07336 · Cited by 1,921 · see citing works
Host-Mediated Inflammation Disrupts the Intestinal Microbiota and Promotes the Overgrowth of Enterobacteriaceae
Lupp, C., Robertson, M. L., Wickham, M. E., Sekirov, I., Champion, O. L., Gaynor, E. C., & Finlay, B. B. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.06.010 · Cited by 1,310 · see citing works
Regulation of Tight Junction Permeability by Intestinal Bacteria and Dietary Components1,2
Ulluwishewa, D., Anderson, R. C., McNabb, W. C., Moughan, P. J., Wells, J. M., & Roy, N. C. (2011) · The Journal of Nutrition · doi:10.3945/jn.110.135657 · Cited by 1,177 · see citing works
Salmonella enterica serovar typhimurium exploits inflammation to compete with the intestinal microbiota
Stecher, B., Robbiani, R., Walker, A. W., Westendorf, A. M., Barthel, M., Kremer, M., Chaffron, S., Macpherson, A. J., Buer, J., Parkhill, J., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050244 · Cited by 1,048 · see citing works
The Fecal Microbiota of Irritable Bowel Syndrome Patients Differs Significantly From That of Healthy Subjects
Kassinen, A., Krogius-Kurikka, L., Mäkivuokko, H., Rinttilä, T., Paulin, L., Corander, J., Malinen, E., Apajalahti, J., & Palva, A. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.04.005 · Cited by 1,002 · see citing works
Bacteriocin production as a mechanism for the antiinfective activity of <i>Lactobacillus salivarius</i> UCC118
Corr, S. C., Li, Y., Riedel, C. U., O'Toole, P. W., Hill, C., & Gahan, C. G. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700440104 · Cited by 853 · see citing works
Dietary prebiotics: current status and new definition
Gibson, G. R., Scott, K. P., Rastall, R. A., Tuohy, K. M., Hotchkiss, A. T., Dubert‐Ferrandon, A., Gareau, M. G., Murphy, E. F., Saulnier, D. M. A., Loh, G., et al. (2010) · Food Science & Technology Bulletin Functional Foods · doi:10.1616/1476-2137.15880 · Cited by 783 · see citing works
Bacterial metabolism and health-related effects of galacto-oligosaccharides and other prebiotics
Macfarlane, G. T., Steed, H., & Macfarlane, S. (2007) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2007.03520.x · Cited by 771 · see citing works
A meta‐analysis of the association between Caesarean section and childhood asthma
Thavagnanam, S., Fleming, J., Bromley, A., Shields, M. D., & Cardwell, C. R. (2008) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2007.02780.x · Cited by 651 · see citing works
16S rRNA gene-based analysis of fecal microbiota from preterm infants with and without necrotizing enterocolitis
Wang, Y., Hoenig, J. D., Malin, K. J., Qamar, S., Petrof, E. O., Sun, J., Antonopoulos, D. A., Chang, E. B., & Claud, E. C. (2009) · The ISME Journal · doi:10.1038/ismej.2009.37 · Cited by 598 · see citing works
Probiotics inhibit enteropathogenic E. coliadherence in vitro by inducing intestinal mucin gene expression.
Mack, D., Michail, S., Wei, S., McDougall, L., & Hollingsworth, M. (1999) · American Journal of Physiology - Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.276.4.g941 · Cited by 544 · see citing works
Probiotics—compensation for lactase insufficiency
de Vrese, M., Stegelmann, A., Richter, B., Fenselau, S., Laue, C., & Schrezenmeir, J. (2001) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/73.2.421s · Cited by 521 · see citing works
Host-Mediated Inflammation Disrupts the Intestinal Microbiota and Promotes the Overgrowth of Enterobacteriaceae
Lupp, C., Robertson, M. L., Wickham, M. E., Sekirov, I., Champion, O. L., Gaynor, E. C., & Finlay, B. B. (2007) · Cell Host & Microbe · doi:10.1016/j.chom.2007.08.002 · Cited by 501 · see citing works
Gut microbiota modulation with norfloxacin and ampicillin enhances glucose tolerance in mice
Membrez, M., Blancher, F., Jaquet, M., Bibiloni, R., Cani, P. D., Burcelin, R. G., Corthesy, I., Macé, K., & Chou, C. J. (2008) · The FASEB Journal · doi:10.1096/fj.07-102723 · Cited by 493 · see citing works
Twin studies reveal specific imbalances in the mucosa-associated microbiota of patients with ileal Crohnʼs disease
Willing, B., Halfvarson, J., Dicksved, J., Rosenquist, M., Järnerot, G., Engstrand, L., Tysk, C., & Jansson, J. K. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20783 · Cited by 455 · see citing works
Fecal microbiota in early rheumatoid arthritis.
Vaahtovuo, J., Munukka, E., Korkeamäki, M., Luukkainen, R., & Toivanen, P. (2008) · PubMed · Cited by 426 · see citing works
Role of the gut microbiota in defining human health
Fujimura, K. E., Slusher, N. A., Cabana, M. D., & Lynch, S. V. (2010) · Expert Review of Anti-infective Therapy · doi:10.1586/eri.10.14 · Cited by 408 · see citing works
Imbalance in the composition of the duodenal microbiota of children with coeliac disease
Nadal, I., Donant, E., Ribes‐Koninckx, C., Calabuig, M., & Sanz, Y. (2007) · Journal of Medical Microbiology · doi:10.1099/jmm.0.47410-0 · Cited by 396 · see citing works
A probiotic mixture alleviates symptoms in irritable bowel syndrome patients: a controlled 6‐month intervention
KAJANDER, K., HATAKKA, K., POUSSA, T., FÄRKKILÄ, M., & KORPELA, R. (2005) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2005.02579.x · Cited by 361 · see citing works
Mucosal damage and neutropenia are required for Candida albicans dissemination
Koh, A. Y., Köhler, J. R., Coggshall, K. T., Van Rooijen, N., & Pier, G. B. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.0040035 · Cited by 360 · see citing works
Metagenomics, biotechnology with non-culturable microbes
Schmeisser, C., Steele, H. L., & Streit, W. R. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-0945-5 · Cited by 315 · see citing works
Early Impairment of Gut Function and Gut Flora Supporting a Role for Alteration of Gastrointestinal Mucosa in Human Immunodeficiency Virus Pathogenesis
Gori, A., Tincati, C., Rizzardini, G., Torti, C., Quirino, T., Haarman, M., Amor, K. B., van Schaik, J., Vriesema, A. J. M., Knol, J., et al. (2007) · Journal of Clinical Microbiology · doi:10.1128/jcm.01729-07 · Cited by 232 · see citing works
Bifidobacterium animalis subsp. lactis fermented milk product reduces inflammation by altering a niche for colitogenic microbes
Veiga, P., Gallini, C. A., Beal, C., Michaud, M., Delaney, M. L., DuBois, A. M., Khlebnikov, A., Vlieg, J. E. T. V. H., Punit, S., Glickman, J. N., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011737107 · Cited by 220 · see citing works
Probiotic Bacteria Influence the Composition and Function of the Intestinal Microbiota
O’Toole, P. W., & Cooney, J. C. (2008) · Interdisciplinary Perspectives on Infectious Diseases · doi:10.1155/2008/175285 · Cited by 201 · see citing works
Immunomodulation by commensal and probiotic bacteria
Forsythe, P., & Bienenstock, J. (2010) · Immunological Investigations · doi:10.3109/08820131003667978 · Cited by 189 · see citing works
Dietary Modulation of Gut Functional Ecology Studied by Fecal Metabonomics
Martin, F., Sprenger, N., Montoliu, I., Rezzi, S., Kochhar, S., & Nicholson, J. K. (2010) · Journal of Proteome Research · doi:10.1021/pr100554m · Cited by 137 · see citing works
Effects of a probiotic fermented milk beverage containing Lactobacillus casei strain Shirota on defecation frequency, intestinal microbiota, and the intestinal environment of healthy individuals with soft stools
Matsumoto, K., Takada, T., Shimizu, K., Moriyama, K., Kawakami, K., Hirano, K., Kajimoto, O., & Nomoto, K. (2010) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2010.05.016 · Cited by 134 · see citing works
Lactobacillus casei Abundance Is Associated with Profound Shifts in the Infant Gut Microbiome
Cox, M. J., Huang, Y. J., Fujimura, K. E., Liu, J. T., McKean, M., Boushey, H. A., Segal, M. R., Brodie, E., Cabana, M. D., & Lynch, S. V. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008745 · Cited by 126 · see citing works
The putative role of the intestinal microbiota in the irritable bowel syndrome
Collins, S. M., Denou, E., Verdu, E. F., & Berčík, P. (2009) · Digestive and Liver Disease · doi:10.1016/j.dld.2009.07.023 · Cited by 124 · see citing works
Effect of a multispecies probiotic supplement on quantity of irritable bowel syndrome-related intestinal microbial phylotypes
Lyra, A., Krogius-Kurikka, L., Nikkilä, J., Malinen, E., Kajander, K., Kurikka, K., Korpela, R., & Palva, A. (2010) · BMC Gastroenterology · doi:10.1186/1471-230x-10-110 · Cited by 86 · see citing works
Probiotic Intervention in the First Months of Life
Rinne, M., Kalliomäki, M. A., Salminen, S., & Isolauri, E. (2006) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/01.mpg.0000228106.91240.5b · Cited by 78 · see citing works
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 · see citing works
Lactobacillus strains stabilize intestinal microbiota in Japanese cedar pollinosis patients
Kubota, A., He, F., Kawase, M., Harata, G., Hiramatsu, M., Salminen, S., & Iino, H. (2009) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2009.00113.x · Cited by 22 · see citing works

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Inamura, K. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.06.006 · Cited by 62 · see citing works
Healthy human aging: intrinsic and environmental factors
Sgarbieri, V. C., & Pacheco, M. T. B. (2017) · Brazilian journal of food technology/Brazilian Journal of Food Technology · doi:10.1590/1981-6723.00717 · Cited by 62 · see citing works
Effects of probiotic Enterococcus faecium NCIMB 11181 administration on swine fecal microbiota diversity and composition using barcoded pyrosequencing
Pajarillo, E. A. B., Chae, J. P., Balolong, M. P., Kim, H. B., Park, C.-S., & Kang, D. (2015) · Animal Feed Science and Technology · doi:10.1016/j.anifeedsci.2015.01.011 · Cited by 58 · see citing works
Pre-, pro- and synbiotics in cancer prevention and treatment—a review of basic and clinical research
Scott, A. J., Merrifield, C. A., Younes, J. A., & Pekelharing, E. P. (2018) · ecancermedicalscience · doi:10.3332/ecancer.2018.869 · Cited by 58 · see citing works
Synbiotic Lactobacillus acidophilus NCFM and cellobiose does not affect human gut bacterial diversity but increases abundance of lactobacilli, bifidobacteria and branched-chain fatty acids: a randomized, double-blinded cross-over trial
van Zanten, G. C., Krych, Ł., Röytiö, H., Forssten, S. D., Lahtinen, S. J., Al‐Soud, W. A., Sørensen, S. J., Svensson, B., Jespersen, L., & Jakobsen, M. (2014) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12397 · Cited by 57 · see citing works
Restitution of gut microbiota in Ugandan children administered with probiotics (Lactobacillus rhamnosus GG and Bifidobacterium animalis subsp. lactis BB-12) during treatment for severe acute malnutrition
Castro-Mejía, J. L., O’Ferrall, S., Krych, Ł., O’Mahony, E., Namusoke, H., Lanyero, B., Kot, W., Nabukeera‐Barungi, N., Michaelsen, K. F., Mølgaard, C., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1712982 · Cited by 55 · see citing works
Dietary administration of probiotic Lactobacillus rhamnosus modulates the neurological toxicities of perfluorobutanesulfonate in zebrafish
Liu, M., Song, S., Hu, C., Tang, L., Lam, J. C. W., Lam, P. K. S., & Chen, L. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.114832 · Cited by 55 · see citing works
Glycosynthases as tools for the production of glycan analogs of natural products
Cobucci‐Ponzano, B., & Moracci, M. (2012) · Natural Product Reports · doi:10.1039/c2np20032e · Cited by 52 · see citing works
Ability of Lactobacillus kefiri LKF01 (DSM32079) to colonize the intestinal environment and modify the gut microbiota composition of healthy individuals
Toscano, M., Grandi, R. D., Miniello, V. L., Mattina, R., & Drago, L. (2016) · Digestive and Liver Disease · doi:10.1016/j.dld.2016.11.011 · Cited by 51 · see citing works
Cellular and molecular mechanisms of probiotics effects on colorectal cancer
Faghfoori, Z., Gargari, B. P., Gharamaleki, A. S., Bagherpour, H., & Khosroushahi, A. Y. (2015) · Journal of Functional Foods · doi:10.1016/j.jff.2015.08.013 · Cited by 44 · see citing works
Effect of prebiotic and probiotic supplementation on neurodevelopment in preterm very low birth weight infants: findings from a meta-analysis
Upadhyay, R. P., Taneja, S., Chowdhury, R., Strand, T. A., & Bhandari, N. (2018) · Pediatric Research · doi:10.1038/s41390-018-0211-9 · Cited by 40 · see citing works
Microbial Activation of Gut Dendritic Cells and the Control of Mucosal Immunity
Owen, J. L., & Mohamadzadeh, M. (2013) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2013.0046 · Cited by 41 · see citing works
The gut microbiome and frailty
Piggott, D. A., & Tuddenham, S. (2020) · Translational research · doi:10.1016/j.trsl.2020.03.012 · Cited by 41 · see citing works
In Ovo and Oral Administration of Probiotic Lactobacilli Modulate Cell- and Antibody-Mediated Immune Responses in Newly Hatched Chicks
Alizadeh, M., Bavananthasivam, J., Shojadoost, B., Astill, J., Taha-Abdelaziz, K., Alqazlan, N. M., Boodhoo, N., Doost, J. S., & Sharif, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.664387 · Cited by 38 · see citing works
Frailty syndrome: A target for functional nutrients?
Davinelli, S., Corbi, G., & Scapagnini, G. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111441 · Cited by 38 · see citing works
Lactic acid bacteria-containing chocolate as a practical probiotic product with increased acid tolerance
Yonejima, Y., Hisa, K., Kawaguchi, M., Ashitani, H., Koyama, T., Usamikrank, Y., Kishida, N., Kishino, S., & Ogawa, J. (2015) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2015.09.001 · Cited by 36 · see citing works
Effect of Probiotic E. coli Nissle 1917 Supplementation on the Growth Performance, Immune Responses, Intestinal Morphology, and Gut Microbes of Campylobacter jejuni Infected Chickens
Helmy, Y. A., Closs, G., Jung, K., Kathayat, D., Vlasova, A. N., & Rajashekara, G. (2022) · Infection and Immunity · doi:10.1128/iai.00337-22 · Cited by 35 · see citing works
Interspecies comparison of probiotics isolated from different animals
Abdou, A. M., Hedia, R. H., Omara, S. T., Mahmoud, M. A. E.-F., Kandil, M. M., & Bakry, M. A. (2018) · Veterinary World · doi:10.14202/vetworld.2018.227-230 · Cited by 33 · see citing works
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Torun, A., Hupalowska, A., Trzonkowski, P., Kierkuś, J., & Pyrzyńska, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.642166 · Cited by 34 · see citing works
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Gaspardo, A., Zannoni, A., Turroni, S., Barone, M., Sabetti, M. C., Zanoni, R. G., Forni, M., Brigidi, P., & Pietra, M. (2020) · Frontiers in Veterinary Science · doi:10.3389/fvets.2020.00146 · Cited by 32 · see citing works
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Sanders, M. E., Goh, Y. J., & Klaenhammer, T. R. (2019) · ASM Press eBooks · doi:10.1128/9781555819972.ch32 · Cited by 32 · see citing works
Self-citation
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Chen, Z., Jin, X., Gao, F.-X., Gui, J., Zhao, Z., & Shi, Y. (2022) · Aquaculture · doi:10.1016/j.aquaculture.2022.738366 · Cited by 31 · see citing works
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Lin, F., Wu, H., Zeng, M., Yu, G., Dong, S., & Yang, H. (2018) · Food & Function · doi:10.1039/c7fo00990a · Cited by 30 · see citing works
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Martinello, F., Roman, C. F., & de Souza, P. A. (2017) · Arquivos de Gastroenterologia · doi:10.1590/s0004-2803.201700000-07 · Cited by 30 · see citing works
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Xie, G., Chen, X., Feng, Y., Yu, Z., Lu, Q., Li, M., Ye, Z., Lin, H., Yu, W., & Shu, H. (2024) · Microorganisms · doi:10.3390/microorganisms12071358 · Cited by 28 · see citing works
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Ahire, J. J., Neelamraju, J., & Madempudi, R. S. (2020) · LWT · doi:10.1016/j.lwt.2020.109196 · Cited by 28 · see citing works
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Jiang, Y., Kong, Q., Roland, K. L., Wolf, A., & Curtiss, R. (2014) · Pathogens and Disease · doi:10.1111/2049-632x.12153 · Cited by 26 · see citing works
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Zeng, J., Ji, Y., Liang, B., Zhang, G., Chen, D., Zhu, M., Wu, S., & Kuang, W. (2021) · Complementary Therapies in Clinical Practice · doi:10.1016/j.ctcp.2021.101370 · Cited by 25 · see citing works
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Tesfaye, W., Suárez-Lepe, J. A., Loira, I., Palomero, F., & Morata, A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-815504-2.00014-1 · Cited by 25 · see citing works
Gut microbiome engineering with probiotics: current trends and future directions
Duhan, P., Gupta, B., Ahmed, M. M. M., & Bansal, P. (2025) · Discover Applied Sciences · doi:10.1007/s42452-025-07622-w · Cited by 24 · see citing works
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Möller, C. M., Olsa, E. J. A., Ginty, A. T., Rapelje, A. L., Tindall, C. L., Holesh, L. A., Petersen, K. L., & Conklin, S. M. (2017) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000489 · Cited by 24 · see citing works
Short-term daily intake of 6 billion live probiotic cells can be insufficient in healthy adults to modulate the intestinal bifidobacteria and lactobacilli
Taverniti, V., Scabiosi, C., Arioli, S., Mora, D., & Guglielmetti, S. (2014) · Journal of Functional Foods · doi:10.1016/j.jff.2013.11.014 · Cited by 23 · see citing works
The influence of the gastrointestinal microbiome on infant colic
Chaib, A. O., Levy, E. I., Chaib, M. O., & Vandenplas, Y. (2020) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2020.1791702 · Cited by 23 · see citing works
Gut microbiota in very early systemic sclerosis: the first case-control taxonomic and functional characterisation highlighting an altered butyric acid profile
Bellando-Randone, S., Russo, E., Gloria, L. D., Lepri, G., Baldi, S., Fioretto, B. S., Romano, E., Ghezzi, G., Bertorello, S., Aoufy, K. E., et al. (2024) · RMD Open · doi:10.1136/rmdopen-2024-004647 · Cited by 22 · see citing works
Scope of Archaea in Fish Feed: a New Chapter in Aquafeed Probiotics?
Chuphal, N., Singha, K. P., Sardar, P., Sahu, N. P., Shamna, N., & Kumar, V. (2021) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-021-09778-4 · Cited by 22 · see citing works
Effect of antibiotic, probiotic, and human rotavirus infection on colonisation dynamics of defined commensal microbiota in a gnotobiotic pig model
Huang, H., Vlasova, A. N., Kumar, A., Kandasamy, S., Fischer, D. D., Deblais, L., Paim, F. C., Langel, S. N., Alhamo, M. A., Rauf, A., et al. (2017) · Beneficial Microbes · doi:10.3920/bm2016.0225 · Cited by 22 · see citing works
Biochemical, functional and genomic characterization of a new probiotic Ligilactobacillus salivarius F14 from the gut of tribes of Odisha
Dash, J., Sethi, M., Deb, S., Parida, D., Kar, S., Mahapatra, S., Minz, A. P., Pradhan, B., Prasad, P., & Senapati, S. (2023) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-023-03626-z · Cited by 17 · see citing works
Effects of probiotics on neurocognitive outcomes in infants and young children: a meta-analysis
Lin, F.-L., Chen, C.-M., Sun, C., Cheng, Y., Tzang, R., Chiu, H., Wang, M., Cheng, Y., & Hung, K.-C. (2023) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1323511 · Cited by 17 · see citing works
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Shi, Y., Peng, H., Liao, Y., Li, J., Yin, Y., Peng, H., Wang, L., Tan, Y., Li, C., Bai, H., et al. (2023) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10145-8 · Cited by 16 · see citing works
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Giglione, E., Prodam, F., Bellone, S., Monticone, S., Beux, S., Marolda, A., Pagani, A., Gioia, D. D., Piano, M. D., Mogna, G., et al. (2016) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0000000000000693 · Cited by 17 · see citing works
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Barbuti, R. C., Schiavon, L. D. L., de Oliveira, C. P. M. S., Álvares‐da‐Silva, M. R., Sassaki, L. Y., Passos, M. D. C. F., Farias, A. Q., Barros, L. L., Barreto, B. A. P., de Albuquerque, G. B. D. M. L., et al. (2020) · Arquivos de Gastroenterologia · doi:10.1590/s0004-2803.202000000-72 · Cited by 14 · see citing works
Changes in the metabolome of probiotics during the stationary phase increase resistance to lyophilization
Jeon, H. J., Kim, J., Seok, W. Y., Kim, G.-S., Choi, B., Shin, M., Lee, J.-H., Kim, Y., Yang, J., & Jung, Y. H. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.102499 · Cited by 13 · see citing works
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Song, Y., Shi, M., & Wang, Y. (2024) · Molecular Medicine · doi:10.1186/s10020-024-00976-8 · Cited by 12 · see citing works
Nutrition – facts and myths
Verbanac, D., Maleš, Ž., & Barišić, K. (2019) · Acta Pharmaceutica · doi:10.2478/acph-2019-0051 · Cited by 12 · see citing works
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Kosek, M. N., Yori, P. P., Olórtegui, M. P., Lefante, J. J., Ramal-Asayag, C., Zamora-Babilonia, M., Meza‐Sánchez, G., & Oberhelman, R. A. (2018) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0000000000002267 · Cited by 11 · see citing works
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Khoury, S. E., Gauthier, J., Mercier, P.-L., Moïse, S., Giovenazzo, P., & Derôme, N. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.00578-24 · Cited by 12 · see citing works
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Kim, Y. I., Lee, E.-S., Song, E., Shin, D., Eom, J.-E., Shin, H. S., Kim, J. E., Oh, J. Y., Nam, Y., & Lee, S. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105404 · Cited by 10 · see citing works
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van der Goot, E., van Spronsen, F. J., Salles, J. F., & van der Zee, E. A. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00611 · Cited by 9 · see citing works
The Gut-Brain-Microbe Interaction: Relevance in Inflammation and Depression
Parletta, N. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811073-7.00013-1 · Cited by 8 · see citing works
Effects of Lactobacillus plantarum supplementation on growth performance, digestive enzyme activity, antioxidant capacity, immune response, and intestinal health in red claw crayfish (Cherax quadricarinatus)
Zhang, Q., Li, L. X., Lu, H., Meng, L., Zeng, Q., Wang, R., Wang, D., Tong, T., Liu, Y., & Yang, H. (2025) · Aquaculture Reports · doi:10.1016/j.aqrep.2025.103077 · Cited by 9 · see citing works
Clinical trials for foods and supplements: Guidance for industry symposium report
O’Connor, E. M. (2013) · Nutrition Bulletin · doi:10.1111/nbu.12032 · Cited by 7 · see citing works
Evaluation of skin cancer prevention properties of probiotics
Torabi, S., Nahidi, Y., Ghasemi, S. Z., Reihani, A., Samadi, A., Ramezanghorbani, N., Nazari, E., & Davoudi, S. (2025) · Genes & Nutrition · doi:10.1186/s12263-025-00770-z · Cited by 6 · see citing works
Impact of a novel synbiotic supplementation during gestation and lactation on immune responses in the Swiss albino mice offspring
Nallagatla, H., Rajkumar, H., Kondapalli, N. B., & Mohammed, S. (2016) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.8059 · Cited by 6 · see citing works
A Phase One Safety Study of Lactobacillus reuteri Conducted in the Peruvian Amazon: Observations from the Field
Oberhelman, R. A., Kosek, M. N., Yori, P. P., Olórtegui, M. P., & Connolly, E. (2014) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.13-0639 · Cited by 6 · see citing works
Synergistic Effect of Nanoparticles with Probiotics on Gastrointestinal Regenerative Medicine
Kouhbananinejad, S. M., Farsinejad, A., Shahabi, A., Satarzadeh, N., Sadeghifar, A., Mahmoudi-Meymand, F., Bardsiri, M. S., & Dousari, A. S. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10707-y · Cited by 5 · see citing works
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Naimi, M., Abid, A., & Khaled, M. B. (2021) · Journal of Microbiology Biotechnology and Food Sciences · doi:10.15414/jmbfs.2937 · Cited by 5 · see citing works
An adaptable and non-invasive method for tracking Bifidobacterium animalis subspecies lactis 420 in the mouse gut
Lopez‐Pier, M. A., Koppinger, M. P., Harris, P. R., Cannon, D. K., Skaria, R. S., Hurwitz, B. L., Watts, G. S., Aras, S. G., Slepian, M. J., & Konhilas, J. P. (2021) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2021.106302 · Cited by 5 · see citing works
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Ngene, A. C., Musa, S., Egbere, O. J., Odu, C. E., Danladi, M. M. A., Onyimba, I. A., Dashen, M. M., Ochiheche, E., Nguhemen, H., & Ogaji, A. O. (2023) · Microbes and Infectious Diseases /Microbes and Infectious Diseases · doi:10.21608/mid.2023.175533.1418 · Cited by 6 · see citing works
Microbiome and Immunotherapy for Melanoma
Haddad, A., & Holder, A. M. (2024) · Hematology/Oncology Clinics of North America · doi:10.1016/j.hoc.2024.05.010 · Cited by 4 · see citing works

Authors: Sanders, M. E.
Corresponding author: Sanders, Mary Ellen
ORCID: Sanders, Mary Ellen
Venue: Journal of Clinical Gastroenterology
Publisher: Ovid Technologies (Wolters Kluwer Health)
Published: 2011-11
Volume: 45
Pages: S115-S119
ISSN: 0192-0790 (ISSN-L)
DOI: 10.1097/mcg.0b013e318227414a
OpenAlex: W1966668014
Cited by: 153
References: 41
Citations by year: 2026: 4 · 2025: 9 · 2024: 10 · 2023: 12 · 2022: 6 · 2021: 10 · 2020: 23 · 2019: 11 · 2018: 12 · 2017: 10 · 2016: 9 · 2015: 5 · 2014: 14 · 2013: 7 · 2012: 10
FWCI: 1.38
Type: journal article
Language: en
Open access: closed
Locations: Journal of Clinical Gastroenterology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Health Sciences › Nursing › Nutrition and Dietetics › Infant Nutrition and Health
Keywords: probiotics, gut microbiota, bacteriocins, short-chain fatty acids, exopolysaccharides, mucin production, intestinal barrier, intestinal inflammation, Bifidobacterium, Lactobacillus, bacterial community structure, health benefits of probiotics
MeSH terms: Bacteria, Bifidobacterium, Humans, Intestines, Lactobacillus, Probiotics, Metagenome

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