Production of bioactive substances by intestinal bacteria as a basis for explaining probiotic mechanisms: Bacteriocins and conjugated linoleic acid

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 · see citing works

The gut microbiota as an environmental factor that regulates fat storage

Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245 · see citing works

Bacteriocins: Developing innate immunity for food

Cotter, P. D., Hill, C., & Ross, R. P. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1273 · Cited by 2,380 · see citing works

A microbial symbiosis factor prevents intestinal inflammatory disease

Mazmanian, S. K., Round, J. L., & Kasper, D. L. (2008) · Nature · doi:10.1038/nature07008 · Cited by 2,340 · see citing works

Complete genome sequence of <i>Lactobacillus plantarum</i> WCFS1

Kleerebezem, M., Boekhorst, J., van Kranenburg, R., Molenaar, D., Kuipers, O. P., Leer, R., Tarchini, R., Peters, S. A., Sandbrink, H. M., Fiers, M. W. E. J., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337704100 · Cited by 1,472 · see citing works

Dietary Sources of Conjugated Dienoic Isomers of Linoleic Acid, a Newly Recognized Class of Anticarcinogens

Chin, S. F., Liu, W., Storkson, J. M., Ha, Y. L., & Pariza, M. W. (1992) · Journal of Food Composition and Analysis · doi:10.1016/0889-1575(92)90037-k · Cited by 1,197 · see citing works

Effect of conjugated linoleic acid on body composition in mice

Park, Y., Albright, K. J., Liu, W., Storkson, J. M., Cook, M. E., & Pariza, M. W. (1997) · Lipids · doi:10.1007/s11745-997-0109-x · Cited by 1,163 · see citing works

Host interactions of probiotic bacterial surface molecules: comparison with commensals and pathogens

Lebeer, S., Vanderleyden, J., & De Keersmaecker, S. C. J. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2297 · Cited by 1,062 · see citing works

Conjugated Linoleic Acid Is Synthesized Endogenously in Lactating Dairy Cows by Δ9-Desaturase

Griinari, J. M., Nurmela, K., Corl, B. A., Lacy, S. H., Chouinard, P. Y., & Bauman, D. E. (2000) · Journal of Nutrition · doi:10.1093/jn/130.9.2285 · Cited by 1,054 · see citing works

Colicin Biology

Cascalès, E., Buchanan, S. K., Duché, D., Kleanthous, C., Lloubès, R., Postle, K., Riley, M. A., Slatin, S. L., & Cavard, D. (2007) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00036-06 · Cited by 1,023 · see citing works

Conjugated linoleic acid and atherosclerosis in rabbits

Lee, K. N., Kritchevsky, D., & Parizaa, M. W. (1994) · Atherosclerosis · doi:10.1016/0021-9150(94)90034-5 · Cited by 998 · see citing works

Anticarcinogens from fried ground beef: heat-altered derivatives of linoleic acid

Ha, Y. L., Grimm, N. K., & Pariza, M. W. (1987) · Carcinogenesis · doi:10.1093/carcin/8.12.1881 · Cited by 929 · see citing works

Once daily high dose probiotic therapy (VSL#3) for maintaining remission in recurrent or refractory pouchitis

Mimura, T., Rizzello, F., Helwig, U., Poggioli, G., Schreiber, S., Talbot, I. C., Nicholls, R. J., Gionchetti, P., Campieri, M., & Kamm, M. A. (2003) · Gut · doi:10.1136/gut.53.1.108 · Cited by 912 · 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

Soluble Proteins Produced by Probiotic Bacteria Regulate Intestinal Epithelial Cell Survival and Growth

Yan, F., Cao, H., Cover, T. L., Whitehead, R. H., Washington, M. K., & Polk, D. B. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.11.022 · Cited by 828 · see citing works

D IETARY C ONJUGATED L INOLEIC A CID IN H EALTH : Physiological Effects and Mechanisms of Action

Belury, M. A. (2002) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.22.021302.121842 · Cited by 815 · see citing works

Specific Binding of Nisin to the Peptidoglycan Precursor Lipid II Combines Pore Formation and Inhibition of Cell Wall Biosynthesis for Potent Antibiotic Activity

Wiedemann, I., Breukink, E. J., van Kraaij, C., Kuipers, O. P., Bierbaum, G., KRUIJFF, B. D., & Sahl, H. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006770200 · Cited by 793 · see citing works

The Continuing Story of Class IIa Bacteriocins

Drider, D., Fimland, G., Héchard, Y., McMullen, L. M., & Prévost, H. (2006) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00016-05 · Cited by 750 · see citing works

Intestinal microflora in early infancy: composition and development

Fanaro, S., Chierici, R., Guerrini, P., & Vigi, V. (2003) · Acta Paediatrica · doi:10.1111/j.1651-2227.2003.tb00646.x · Cited by 738 · see citing works

Intermediates and Products of the Biohydrogenation of Linoleic Acid by Butyrivibrio fibrisolvens

Kepler, C. R., Hirons, K. P., McNeill, J. J., & Tove, S. B. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96781-5 · Cited by 693 · see citing works

Dietary Conjugated Linoleic Acid Normalizes Impaired Glucose Tolerance in the Zucker Diabetic Fattyfa/faRat

Houseknecht, K. L., Heuvel, J. P. V., Moya-Camarena, S. Y., Portocarrero, C. P., Peck, L. W., Nickel, K. P., & Belury, M. A. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.8303 · Cited by 643 · see citing works

Lantibiotics: Peptides of Diverse Structure and Function

Willey, J. M., & van der Donk, W. A. (2007) · Annual Review of Microbiology · doi:10.1146/annurev.micro.61.080706.093501 · Cited by 621 · see citing works

Secreted bioactive factors from <i>Bifidobacterium infantis</i> enhance epithelial cell barrier function

Ewaschuk, J. B., Diaz, H., Meddings, L., Diederichs, B., Dmytrash, A., Backer, J., Looijer-van Langen, M., & Madsen, K. L. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90227.2008 · Cited by 590 · see citing works

Epithelial crosstalk at the microbiota–mucosal interface

Wells, J. M., Rossi, O., Meijerink, M., & van Baarlen, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000092107 · Cited by 574 · see citing works

Conjugated linoleic acid suppresses mammary carcinogenesis and proliferative activity of the mammary gland in the rat.

Ip, C., Singh, M., Thompson, H. J., & Scimeca, J. A. (1994) · PubMed · Cited by 555 · see citing works

Thuricin CD, a posttranslationally modified bacteriocin with a narrow spectrum of activity against <i>Clostridium difficile</i>

Rea, M. C., Sit, C. S., Clayton, E., O'Connor, P. M., Whittal, R. M., Zheng, J., Vederas, J. C., Ross, R. P., & Hill, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913554107 · Cited by 530 · see citing works

Bioconversion of vaccenic acid to conjugated linoleic acid in humans

Turpeinen, A. M., Mutanen, M., Aro, A., Salminen, I., Basu, S., Palmquist, D. L., & Griinari, J. M. (2002) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/76.3.504 · Cited by 495 · see citing works

The genome sequence of the probiotic intestinal bacterium Lactobacillus johnsonii NCC 533

Pridmore, R. D., Berger, B. W., Desiere, F., Vilanova, D., Barretto, C., Pittet, A.-C., Zwahlen, M.-C., Rouvet, M., Altermann, E., Barrangou, R., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307327101 · Cited by 485 · see citing works

Immune Modulation by Altered Nutrient Metabolism: Nutritional Control of Immune-Induced Growth Depression

COOK, M. E., MILLER, C. C., Park, Y., & Pariza, M. W. (1993) · Poultry Science · doi:10.3382/ps.0721301 · Cited by 477 · see citing works

Isolation of Bifidobacteria from Breast Milk and Assessment of the Bifidobacterial Population by PCR-Denaturing Gradient Gel Electrophoresis and Quantitative Real-Time PCR

Martı́n, R., Jiménez, E., Heilig, H. G. H. J., Fernández, L., Marín, M. L., Zoetendal, E. G., & Rodríguez, J. M. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.02063-08 · Cited by 434 · see citing works

Probiotic modulation of symbiotic gut microbial–host metabolic interactions in a humanized microbiome mouse model

Martin, F. J., Wang, Y., Sprenger, N., Yap, I. K. S., Lundstedt, T., Lek, P., Rezzi, S., Ramadan, Z., van Bladeren, P., Fay, L. B., et al. (2008) · Molecular Systems Biology · doi:10.1038/msb4100190 · Cited by 421 · see citing works

The dual role of bacteriocins as anti- and probiotics

Gillor, O., Etzion, A., & Riley, M. A. (2008) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-008-1726-5 · Cited by 418 · see citing works

Bifidobacterium strains from resident infant human gastrointestinal microflora exert antimicrobial activity

Liévin, V, Peiffer, I., Hudault, S., Rochat, F., Brassart, D., Neeser, J.-R., & Servin, A. L. (2000) · Gut · doi:10.1136/gut.47.5.646 · Cited by 397 · see citing works

Activation of PPAR γ and δ by conjugated linoleic acid mediates protection from experimental inflammatory bowel disease

Bassaganya-Riera, J., Reynolds, K., Martino‐Catt, S. J., Cui, Y., Hennighausen, L. G., Gonzalez, F. J., Rohrer, J., Uribe-Benninghoff, A., & Hontecillas, R. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.06.049 · Cited by 393 · see citing works

Microcins, gene-encoded antibacterial peptides from enterobacteria

Duquesne, S., Destoumieux‐Garzón, D., Péduzzi, J., & Rebuffat, S. (2007) · Natural Product Reports · doi:10.1039/b516237h · Cited by 389 · see citing works

Effect of broad- and narrow-spectrum antimicrobials on <i>Clostridium difficile</i> and microbial diversity in a model of the distal colon

Rea, M. C., Dobson, A., O'Sullivan, O., Crispie, F., Fouhy, F., Cotter, P. D., Shanahan, F., Kiely, B., Hill, C., & Ross, R. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001224107 · Cited by 377 · see citing works

Common mechanisms of target cell recognition and immunity for class II bacteriocins

Diep, D. B., Skaugen, M., Salehian, Z., Holo, H., & Nes, I. F. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608775104 · Cited by 374 · see citing works

Genetics of resistance to colicins in Escherichia coli K-12: cross-resistance among colicins of group A

Davies, J. K., & Reeves, P. R. (1975) · Journal of Bacteriology · doi:10.1128/jb.123.1.102-117.1975 · Cited by 351 · see citing works

Conjugated Linoleic Acid Isomers and Cancer ,

Kelley, N. S., Hubbard, N. E., & Erickson, K. L. (2007) · Journal of Nutrition · doi:10.1093/jn/137.12.2599 · Cited by 346 · see citing works

Human originated bacteria, Lactobacillus rhamnosus PL60, produce conjugated linoleic acid and show anti-obesity effects in diet-induced obese mice

Lee, H.-Y., Park, J.-H., Seok, S.-H., Baek, M.-W., Kim, D.-J., Lee, K.-E., Paek, K.-S., Lee, Y., & Park, J.-H. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2006.05.007 · Cited by 342 · see citing works

Microcin 25, a novel antimicrobial peptide produced by Escherichia coli

Salomón, R. A., & Farı́as, R. N. (1992) · Journal of Bacteriology · doi:10.1128/jb.174.22.7428-7435.1992 · Cited by 336 · see citing works

Gastrointestinal microflora, food components and colon cancer prevention

Davis, C. D., & Milner, J. A. (2009) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2009.06.001 · Cited by 335 · see citing works

Systemic multicompartmental effects of the gut microbiome on mouse metabolic phenotypes

Claus, S. P., Tsang, T. M., Wang, Y., Cloarec, O., Skordi, E., Martin, F., Rezzi, S., Ross, A., Kochhar, S., Holmes, E., et al. (2008) · Molecular Systems Biology · doi:10.1038/msb.2008.56 · Cited by 334 · see citing works

Lantibiotics—Ribosomally Synthesized Biologically Active Polypeptides containing Sulfide Bridges and α,β‐Didehydroamino Acids

Jung, G. (1991) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199110513 · Cited by 333 · see citing works

Culture-Independent Analyses of Temporal Variation of the Dominant Fecal Microbiota and Targeted Bacterial Subgroups in Crohn's Disease

Scanlan, P. D., Shanahan, F., O'Mahony, C., & Marchesi, J. R. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.00312-06 · Cited by 330 · see citing works

DNA from probiotic bacteria modulates murine and human epithelial and immune function

Jijon, H. B., Backer, J., Díaz, H., Yeung, H. P., Thiel, D., McKaigney, C. J., Simone, C. D., & Madsen, K. L. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.02.003 · Cited by 318 · see citing works

Probiotic and Gut Lactobacilli and Bifidobacteria: Molecular Approaches to Study Diversity and Activity

Kleerebezem, M., & Vaughan, E. E. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.091208.073341 · Cited by 315 · see citing works

Displacement of bacterial pathogens from mucus and Caco-2 cell surface by lactobacilli

Lee, Y. K., Puong, K.-Y., Ouwehand, A. C., & Salminen, S. (2003) · Journal of Medical Microbiology · doi:10.1099/jmm.0.05009-0 · Cited by 311 · see citing works

Clinical use of E. coli Nissle 1917 in inflammatory bowel disease

Schultz, M. (2008) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20377 · Cited by 310 · see citing works

Lactic acid bacteria secrete metabolites retaining anti-inflammatory properties after intestinal transport

Ménard, S., Candalh, C., Bambou, J. C., Terpend, K., Cerf–Bensussan, N., & Heyman, M. (2004) · Gut · doi:10.1136/gut.2003.026252 · Cited by 309 · see citing works

A preliminary study of the effect of probiotic Streptococcus salivarius K12 on oral malodour parameters

Burton, J. P., Chilcott, C. N., Moore, C. J., Speiser, G., & Tagg, J. R. (2006) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2006.02837.x · Cited by 307 · see citing works

Soluble factors from Lactobacillus GG activate MAPKs and induce cytoprotective heat shock proteins in intestinal epithelial cells

Tao, Y., Drabik, K., Waypa, T. S., Musch, M. W., Alverdy, J. C., Schneewind, O., Chang, E. B., & Petrof, E. O. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00131.2005 · Cited by 301 · see citing works

Conjugated linoleic acid biosynthesis by human-derived Bifidobacterium species

Coakley, M., Ross, R. P., Nordgren, M., Fitzgerald, G., Devery, R., & Stanton, C. (2003) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2003.01814.x · Cited by 299 · see citing works

Isolation of a Lactobacillus salivarius Strain and Purification of Its Bacteriocin, Which Is Inhibitory to Campylobacter jejuni in the Chicken Gastrointestinal System

Stern, N. J., Ea, S., Eruslanov, B. V., Perelygin, V. V., Mitsevich, E. V., Mitsevich, I. P., Pokhilenko, V. D., Levchuk, V. P., Svetoch, O. E., & Seal, B. S. (2006) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00259-06 · Cited by 297 · see citing works

Production of conjugated linoleic acid by dairy starter cultures

Jiang, Björck, & Fondén (1998) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.1998.00481.x · Cited by 295 · see citing works

Biochemical and Genetic Evidence that Enterococcus faecium L50 Produces Enterocins L50A and L50B, the sec -Dependent Enterocin P, and a Novel Bacteriocin Secreted without an N-Terminal Extension Termed Enterocin Q

Cintas, L. M., Casaus, P., Herranz, C., Håvarstein, L. S., Holo, H., Hernández, P. E., & Nes, I. F. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.23.6806-6814.2000 · Cited by 290 · see citing works

Production of conjugated fatty acids by lactic acid bacteria

Ogawa, J., Kishino, S., Ando, A., Sugimoto, S., Mihara, K., & Shimizu, S. (2005) · Journal of Bioscience and Bioengineering · doi:10.1263/jbb.100.355 · Cited by 289 · see citing works

Metabolism of Linoleic Acid by Human Gut Bacteria: Different Routes for Biosynthesis of Conjugated Linoleic Acid

Devillard, E., McIntosh, F. M., Duncan, S. H., & Wallace, R. J. (2007) · Journal of Bacteriology · doi:10.1128/jb.01359-06 · Cited by 285 · see citing works

Characterization of the genetic locus responsible for the production of ABP-118, a novel bacteriocin produced by the probiotic bacterium Lactobacillus salivarius subsp. salivarius UCC118 The GenBank accession number for the sequence reported in this paper is AF408405.

Flynn, S., van Sinderen, D., Thornton, G., Holo, H., Nes, I. F., & Collins, J. K. (2002) · Microbiology · doi:10.1099/00221287-148-4-973 · Cited by 264 · see citing works

Transport of Vitamin B 12 in Escherichia coli : Common Receptor Sites for Vitamin B 12 and the E Colicins on the Outer Membrane of the Cell Envelope

Masi, D. R. D., White, J. C., Schnaitman, C. A., & Bradbeer, C. (1973) · Journal of Bacteriology · doi:10.1128/jb.115.2.506-513.1973 · Cited by 263 · see citing works

Immunomodulatory properties of conjugated linoleic acid

O’Shea, M., Bassaganya-Riera, J., & Mohede, I. (2004) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/79.6.1199s · Cited by 262 · see citing works

Structure-Function Relationships of the Non-Lanthionine-Containing Peptide (class II) Bacteriocins Produced by Gram-Positive Bacteria

Nissen-Meyer, J., Rogne, P., Oppegård, C., Haugen, H., & Kristiansen, P. E. (2009) · Current Pharmaceutical Biotechnology · doi:10.2174/138920109787048661 · Cited by 256 · see citing works

Structure of Microcin J25, a Peptide Inhibitor of Bacterial RNA Polymerase, is a Lassoed Tail

Wilson, K.-A., Kalkum, M., Ottesen, J. J., Yuzenkova, Y., Chait, B. T., Landick, R. C., Muir, T. W., Severinov, K., & Darst, S. A. (2003) · Journal of the American Chemical Society · doi:10.1021/ja036756q · Cited by 240 · see citing works

Quorum sensing control of lantibiotic production; nisin and subtilin autoregulate their own biosynthesis

Kleerebezem, M. (2004) · Peptides · doi:10.1016/j.peptides.2003.10.021 · Cited by 234 · see citing works

The colicin G, H and X determinants encode microcins M and H47, which might utilize the catecholate siderophore receptors FepA, Cir, Fiu and IroN

Patzer, S. I., Baquero, M. R., Bravo, D., Moreno, F., & Hantke, K. (2003) · Microbiology · doi:10.1099/mic.0.26396-0 · Cited by 233 · see citing works

Identification of a Novel Two-Peptide Lantibiotic, Lichenicidin, following Rational Genome Mining for LanM Proteins

Begley, M., Cotter, P. D., Hill, C., & Ross, R. P. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00730-09 · Cited by 231 · see citing works

Production of Free Conjugated Linoleic Acid by Lactobacillus acidophilus and Lactobacillus casei of Human Intestinal Origin

Alonso, L., Cuesta, E. P., & Gilliland, S. E. (2003) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(03)73781-3 · Cited by 229 · see citing works

A Five-Strain Probiotic Combination Reduces Pathogen Shedding and Alleviates Disease Signs in Pigs Challenged with Salmonella enterica Serovar Typhimurium

Casey, P. G., Gardiner, G. E., Casey, G. D., Bradshaw, B., Lawlor, P. G., Lynch, P. B., Leonard, F. C., Stanton, C., Ross, R. P., Fitzgerald, G. F., et al. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01840-06 · Cited by 226 · see citing works

The probioticEscherichia colistrain Nissle 1917 interferes with invasion of human intestinal epithelial cells by different enteroinvasive bacterial pathogens

Altenhoefer, A., Oswald, S., Sonnenborn, U., Enders, C., Schulze, J., Hacker, J., & Oelschlaeger, T. A. (2004) · FEMS Immunology & Medical Microbiology · doi:10.1016/s0928-8244(03)00368-7 · Cited by 221 · see citing works

Labyrinthopeptins: A New Class of Carbacyclic Lantibiotics

Meindl, K., Schmiederer, T., Schneider, K., Reicke, A., Butz, D., Keller, S., Gühring, H., Vértesy, L., Wink, J. M., Hoffmann, H., et al. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200905773 · Cited by 217 · see citing works

Dietary Influences on Bovine Milk cis ‐9, trans ‐11‐Conjugated Linoleic Acid Content

Stanton, C., Lawless, F. N., KJELLMER, G., Harrington, D., Devery, R., Connolly, J. F., & Murphy, J. B. (1997) · Journal of Food Science · doi:10.1111/j.1365-2621.1997.tb15043.x · Cited by 214 · see citing works

High-Dose Probiotics for the Treatment of Active Pouchitis

Gionchetti, P., Rizzello, F., Morselli, C., Poggioli, G., Tambasco, R., Calabrese, C., Brigidi, P., Vitali, B., Straforini, G., & Campieri, M. (2007) · Diseases of the Colon & Rectum · doi:10.1007/s10350-007-9068-4 · Cited by 212 · see citing works

Bioproduction of Conjugated Linoleic Acid by Probiotic Bacteria Occurs In Vitro and In Vivo in Mice

Ewaschuk, J. B., Walker, J. W. T., Díaz, H., & Madsen, K. L. (2006) · Journal of Nutrition · doi:10.1093/jn/136.6.1483 · Cited by 209 · see citing works

Structural analysis and proteolytic activation of Enterococcus faecalis cytolysin, a novel lantibiotic

Booth, M. C., Bogie, C. P., Sahl, H., Siezen, R. J., Hatter, K. L., & Gilmore, M. S. (1996) · Molecular Microbiology · doi:10.1046/j.1365-2958.1996.831449.x · Cited by 206 · see citing works

Structure of Subtilosin A, a Cyclic Antimicrobial Peptide from Bacillus subtilis with Unusual Sulfur to α-Carbon Cross-Links: Formation and Reduction of α-Thio-α-Amino Acid Derivatives,

Kawulka, K. E., Sprules, T. J., Diaper, C. M., Whittal, R. M., McKay, R. T., Mercier, P., Zuber, P., & Vederas, J. C. (2004) · Biochemistry · doi:10.1021/bi0359527 · Cited by 205 · see citing works

The Group I Strain of Streptococcus mutans , UA140, Produces Both the Lantibiotic Mutacin I and a Nonlantibiotic Bacteriocin, Mutacin IV

Qi, F., Chen, P., & Caufield, P. W. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.1.15-21.2001 · Cited by 204 · see citing works

Peptide pheromone-dependent regulation of antimicrobial peptide production in Gram-positive bacteria: a case of multicellular behavior

Kleerebezem, M., & Quadri, L. E. N. (2001) · Peptides · doi:10.1016/s0196-9781(01)00493-4 · Cited by 202 · see citing works

Conjugated Linoleic Acid Accumulation via 10-Hydroxy-12-Octadecaenoic Acid during Microaerobic Transformation of Linoleic Acid by Lactobacillus acidophilus

Ogawa, J., Matsumura, K., Kishino, S., Omura, Y., & Shimizu, S. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.3.1246-1252.2001 · Cited by 202 · see citing works

The probiotic Escherichia coli strain Nissle 1917 (EcN) stops acute diarrhoea in infants and toddlers

Henker, J., Laass, M. W., Blokhin, B. M., Bolbot, Y. K., Maydannik, V. G., Elze, M., Wolff, C., & Schulze, J. (2007) · European Journal of Pediatrics · doi:10.1007/s00431-007-0419-x · Cited by 199 · see citing works

Metabolic activity of the enteric microbiota influences the fatty acid composition of murine and porcine liver and adipose tissues

Wall, R., Ross, R. P., Shanahan, F., O’Mahony, L., O’Mahony, C., Coakley, M., Hart, O. M., Lawlor, P. G., Quigley, E. M. M., Kiely, B., et al. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.27023 · Cited by 198 · see citing works

The peptide antibiotic microcin B17 induces double‐strand cleavage of DNA mediated by E. coli DNA gyrase.

Vizán, J. L., Hernández-Chico, C., del Castillo, I., & Moreno, F. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07969.x · Cited by 196 · see citing works

Antimicrobial activity of enterocins from Enterococcus faecalis SL-5 against Propionibacterium acnes, the causative agent in acne vulgaris, and its therapeutic effect

Kang, B. S., Seo, J., Lee, G.-S., Jung-Hwa, K., Kim, S. Y., Han, Y. W., Kang, H., Kim, H. O., Rhee, J. H., Chung, M.-J., et al. (2009) · The Journal of Microbiology · doi:10.1007/s12275-008-0179-y · Cited by 195 · see citing works

Conjugated linoleic acid production from linoleic acid by lactic acid bacteria

Kishino, S., Ogawa, J., Omura, Y., Matsumura, K., & Shimizu, S. (2002) · Journal of the American Oil Chemists Society · doi:10.1007/s11746-002-0451-4 · Cited by 194 · see citing works

The blp Bacteriocins of Streptococcus pneumoniae Mediate Intraspecies Competition both In Vitro and In Vivo

Dawid, S. R., Roche, A. M., & Weiser, J. N. (2006) · Infection and Immunity · doi:10.1128/iai.01775-05 · Cited by 188 · see citing works

Isolation and characterization of the lantibiotic salivaricin A and its structural gene salA from Streptococcus salivarius 20P3

Ross, K. F., Ronson, C. W., & Tagg, J. R. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.7.2014-2021.1993 · Cited by 186 · see citing works

Genetics of resistance to colicins in Escherichia coli K-12: cross-resistance among colicins of group B

Davies, J. K., & Reeves, P. R. (1975) · Journal of Bacteriology · doi:10.1128/jb.123.1.96-101.1975 · Cited by 186 · see citing works

Conjugated Linoleic Acid (9,11- and 10,12-Octadecadienoic Acid) Is Produced in Conventional but Not Germ-Free Rats Fed Linoleic Acid

Chin, S. F., STORKSON, J. M., Liu, W., ALBRIGHT, K. J., & Pariza, M. W. (1994) · Journal of Nutrition · doi:10.1093/jn/124.5.694 · Cited by 185 · see citing works

Antimicrobial activity of lacticin 3147 against clinical Clostridium difficile strains

Rea, M. C., Clayton, E. M., O’Connor, P. M., Shanahan, F., Kiely, B., Ross, R. P., & Hill, C. (2007) · Journal of Medical Microbiology · doi:10.1099/jmm.0.47085-0 · Cited by 185 · see citing works

Isomers of conjugated linoleic acids are synthesized via different mechanisms in ruminal digesta and bacteria

Wallace, R. J., McKain, N., Shingfield, K. J., & Devillard, E. (2007) · Journal of Lipid Research · doi:10.1194/jlr.m700271-jlr200 · Cited by 183 · see citing works

Comparative genomic analysis of the gut bacterium Bifidobacterium longum reveals loci susceptible to deletion during pure culture growth

Lee, J.-H., Karamychev, V., Kozyavkin, S. A., Mills, D. A., Pavlov, A., Pavlova, N. V., Polouchine, N., Richardson, P., Shakhova, V. V., Slesarev, A. I., et al. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-247 · Cited by 181 · see citing works

Conjugated Linoleic Acid in Humans: Regulation of Adiposity and Insulin Sensitivity

Brown, J. M., & McIntosh, M. (2003) · Journal of Nutrition · doi:10.1093/jn/133.10.3041 · Cited by 178 · see citing works

Ruminococcin A, a New Lantibiotic Produced by a Ruminococcus gnavu s Strain Isolated from Human Feces

Dabard, J., Bridonneau, C., Phillipe, C., Anglade, P., Mollé, D., Nardi, M., Ladiré, M., Girardin, H., Marcille, F., Gómez, A., et al. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.9.4111-4118.2001 · Cited by 178 · see citing works

Antiobesity effect of<i>trans</i>-10,<i>cis</i>-12-conjugated linoleic acid-producing<i>Lactobacillus plantarum</i>PL62 on diet-induced obese mice

Lee, K., Paek, K., Lee, H. Y., Park, J. H., & Lee, Y. (2007) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2007.03336.x · Cited by 175 · see citing works

Salivaricin A2 and the Novel Lantibiotic Salivaricin B Are Encoded at Adjacent Loci on a 190-Kilobase Transmissible Megaplasmid in the Oral Probiotic Strain Streptococcus salivarius K12

Hyink, O., Wescombe, P. A., Upton, M., Ragland, N. L., Burton, J. P., & Tagg, J. R. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.02265-06 · Cited by 173 · see citing works

The Two-Peptide Class II Bacteriocins: Structure, Production, and Mode of Action

Oppegård, C., Rogne, P., Emanuelsen, L., Kristiansen, P. E., Fimland, G., & Nissen-Meyer, J. (2007) · Microbial Physiology · doi:10.1159/000104750 · Cited by 170 · see citing works

Molecular Mechanism of Transcription Inhibition by Peptide Antibiotic Microcin J25

Adelman, K., Yuzenkova, J., Porta, A. L., Zenkin, N., Lee, J., Lis, J. T., Borukhov, S. I., Wang, M. D., & Severinov, K. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.05.017 · Cited by 169 · see citing works

Production of antibacterial substances by bifidobacterial isolates from infant stool active against Listeria monocytogenes

Toure, R., Kheadr, E., Lacroix, C., Moroni, O., & Fliss, I. (2003) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2003.02085.x · Cited by 167 · see citing works

Hydrogen peroxide production by Lactobacillus johnsonii NCC 533 and its role in anti-Salmonella activity

Pridmore, R. D., Pittet, A.-C., Praplan, F., & Cavadini, C. (2008) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2008.01176.x · Cited by 166 · see citing works

BAGEL2: mining for bacteriocins in genomic data

de Jong, A., van Heel, A. J., Kok, J., & Kuipers, O. P. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq365 · Cited by 165 · see citing works

Increase of Conjugated Linoleic Acid Content in Milk by Fermentation with Lactic Acid Bacteria

Kim, Y. J., & Liu, R. H. (2002) · Journal of Food Science · doi:10.1111/j.1365-2621.2002.tb08714.x · Cited by 164 · see citing works

Conjugated linoleic acid isomers: differences in metabolism and biological effects

Churruca, I., Fernández‐Quintela, A., & Portillo, M. P. (2009) · BioFactors · doi:10.1002/biof.13 · Cited by 160 · see citing works

Purification, amino acid sequence and mode of action of bifidocin B produced by Bifidobacterium bifidum NCFB 1454

Yıldırım, Z., Winters, D. K., & Johnson, M. G. (1999) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.1999.00629.x · Cited by 160 · see citing works

Microcin E492, a channel-forming bacteriocin from Klebsiella pneumoniae , induces apoptosis in some human cell lines

Hetz, C. A., Bono, M. R., Barros, L. F., & Lagos, R. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052709699 · Cited by 157 · see citing works

Relation between the intake of milk fat and the occurrence of conjugated linoleic acid in human adipose tissue

Jiang, J. Q., Wolk, A., & Vessby, B. O. (1999) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/70.1.21 · Cited by 154 · see citing works

Capacity of Human Nisin- and Pediocin-Producing Lactic Acid Bacteria To Reduce Intestinal Colonization by Vancomycin-Resistant Enterococci

Millette, M., Cornut, G., Dupont, C., Shareck, F., Archambault, D., & Lacroix, M. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.02150-07 · Cited by 153 · see citing works

Intra- and Interspecies Signaling between Streptococcus salivarius and Streptococcus pyogenes Mediated by SalA and SalA1 Lantibiotic Peptides

Upton, M., Tagg, J. R., Wescombe, P. A., & Jenkinson, H. F. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.13.3931-3938.2001 · Cited by 153 · see citing works

Elevation of Conjugated cis-9, trans-11-Octadecadienoic Acid in Bovine Milk Because of Dietary Supplementation

Lawless, F. N., Murphy, J. J., Harrington, D., Devery, R., & Stanton, C. (1998) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(98)75890-4 · Cited by 151 · see citing works

Aspartyl-tRNA Synthetase Is the Target of Peptide Nucleotide Antibiotic Microcin C

Metlitskaya, A. Z., Kazakov, T., Kommer, A., Pavlova, O., Prætorius-Ibba, M., Ibba, M., Krasheninnikov, I. A., Kolb, V. A., Khmel, I. A., & Severinov, K. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m513174200 · Cited by 151 · see citing works

Bacteriocin diversity and the frequency of multiple bacteriocin production in Escherichia coli

Gordon, D. M., & O’Brien, C. (2006) · Microbiology · doi:10.1099/mic.0.28690-0 · Cited by 151 · see citing works

To protect peptide pharmaceuticals against peptidases

Rink, R., Arkema-Meter, A., Baudoin, I., Post, E., Kuipers, A., Nelemans, S. A., Akanbi, M. H. J., & Moll, G. N. (2010) · Journal of Pharmacological and Toxicological Methods · doi:10.1016/j.vascn.2010.02.010 · Cited by 148 · see citing works

Functional Dairy Products

Mattila‐Sandholm, T., & Saarela, M. (2003) · CRC Press eBooks · doi:10.1201/9780203484661 · Cited by 142 · see citing works

Induction of Plantaricin Production inLactobacillus plantarumNC8 after Coculture with Specific Gram-Positive Bacteria Is Mediated by an Autoinduction Mechanism

Maldonado‐Barragán, A., Jiménez‐Díaz, R., & Ruiz-Barba, J. L. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.5.1556-1564.2004 · Cited by 139 · see citing works

Chemical Structure and Translation Inhibition Studies of the Antibiotic Microcin C7

Guijarro, J. I., González‐Pastor, J. E., Baleux, F., Millán, J. L. S., Castilla, M. A., Rico, M., Moreno, F., & Delepierre, M. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.40.23520 · Cited by 137 · 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

Expression of Toll-like receptor 9 and response to bacterial CpG oligodeoxynucleotides in human intestinal epithelium

Pedersen, G., Andresen, L. O., Matthiessen, M. W., Rask-Madsen, J., & Brynskov, J. (2005) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2005.02848.x · Cited by 134 · see citing works

Multiple Activities in Lantibiotics - Models for the Design of Novel Antibiotics?

Pag, U., & Sahl, H. (2002) · Current Pharmaceutical Design · doi:10.2174/1381612023395439 · Cited by 134 · see citing works

Conjugated linoleic acid concentration as affected by lactic cultures and added linoleic acid

Lin, T. Y., Lin, C., & Lee, C. (1999) · Food Chemistry · doi:10.1016/s0308-8146(99)00077-1 · Cited by 133 · see citing works

Classification of Bacteriocins from Gram-Positive Bacteria

Rea, M. C., Ross, R. P., Cotter, P. D., & Hill, C. (2011) · Springer eBooks · doi:10.1007/978-1-4419-7692-5_3 · Cited by 129 · see citing works

Conjugated Linoleic Acid Ameliorates Inflammation-Induced Colorectal Cancer in Mice through Activation of PPARγ

Evans, N. P., Misyak, S. A., Schmelz, E. M., Guri, A. J., Hontecillas, R., & Bassaganya-Riera, J. (2010) · Journal of Nutrition · doi:10.3945/jn.109.115642 · Cited by 129 · see citing works

In vivo study on the effectiveness of pediocin PA-1 and Pediococcus acidilactici UL5 at inhibiting Listeria monocytogenes

Dabour, N., Zihler, A., Kheadr, E., Lacroix, C., & Fliss, I. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.05.005 · Cited by 128 · see citing works

Colicin M Exerts Its Bacteriolytic Effect via Enzymatic Degradation of Undecaprenyl Phosphate-linked Peptidoglycan Precursors

Ghachi, M. E., Bouhss, A., Barreteau, H., Touzé, T., Auger, G., Blanot, D., & Mengin‐Lecreulx, D. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602834200 · Cited by 126 · see citing works

Genetically modified Streptococcus mutans for the prevention of dental caries

Hillman, J. D. (2002) · Springer eBooks · doi:10.1007/978-94-017-2029-8_25 · Cited by 125 · see citing works

Dose–response study of probiotic bacteria Bifidobacterium animalis subsp lactis BB-12 and Lactobacillus paracasei subsp paracasei CRL-341 in healthy young adults

Larsen, C. N., Nielsen, S., Kæstel, P., Brockmann, E., Bennedsen, M., Christensen, H. R., Eskesen, D. C., Jacobsen, B. L., & Michaelsen, K. F. (2006) · European Journal of Clinical Nutrition · doi:10.1038/sj.ejcn.1602450 · Cited by 124 · see citing works

Lactobacilli, bifidobacteriaandE. colinissle induce pro- and anti-inflammatory cytokines in peripheral blood mononuclear cells

Helwig, U. (2006) · World Journal of Gastroenterology · doi:10.3748/wjg.v12.i37.5978 · Cited by 124 · see citing works

Distribution and persistence of probiotic Streptococcus salivarius K12 in the human oral cavity as determined by real‐time quantitative polymerase chain reaction

Horz, H., Meinelt, A., Houben, B., & Conrads, G. (2007) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.2007.00334.x · Cited by 120 · see citing works

Pore-Forming Colicins and Their Relatives

Lakey, J. H., & Slatin, S. L. (2001) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-56508-3_7 · Cited by 119 · see citing works

Effect of Preventive Administration of a Nonpathogenic Escherichia coli Strain on the Colonization of the Intestine with Microbial Pathogens in Newborn Infants

LodÍnová‐ŽádnÍková, R., & Sonnenborn, U. (2009) · Biology of the Neonate · doi:10.1159/000244421 · Cited by 119 · see citing works

Structural and Functional Differences in Two Cyclic Bacteriocins with the Same Sequences Produced by Lactobacilli

Kawai, Y., Ishii, Y., Arakawa, K., Uemura, K., Saitoh, B., Nishimura, J., Kitazawa, H., Yamazaki, Y., Tateno, Y., Itoh, T., et al. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.5.2906-2911.2004 · Cited by 118 · see citing works

Class II one-peptide bacteriocins target a phylogenetically defined subgroup of mannose phosphotransferase systems on sensitive cells

Kjos, M., Nes, I. F., & Diep, D. B. (2009) · Microbiology · doi:10.1099/mic.0.030015-0 · Cited by 118 · see citing works

Genetic and Biochemical Analysis of Mutacin 1140, a Lantibiotic from Streptococcus mutans

Hillman, J. D., Novák, J., Sagura, E., Gutierrez, J. A., Brooks, T. A., Crowley, P. J., Hess, M. E., Azizi, A., Leung, K. ‐., Cvitkovitch, D. G., et al. (1998) · Infection and Immunity · doi:10.1128/iai.66.6.2743-2749.1998 · Cited by 118 · see citing works

Purification of Mutacin III from Group III Streptococcus mutans UA787 and Genetic Analyses of Mutacin III Biosynthesis Genes

Qi, F., Chen, P., & Caufield, P. W. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.9.3880-3887.1999 · Cited by 117 · see citing works

Human tumor cells are selectively inhibited by colicins

Chumchalová, J., & Šmarda, J. (2003) · Folia Microbiologica · doi:10.1007/bf02931286 · Cited by 114 · see citing works

Effect of natural commensal-origin DNA on toll-like receptor 9 (TLR9) signaling cascade, chemokine IL-8 expression, and barrier integritiy of polarized intestinal epithelial cells

Ghadimi, D., de Vrese, M., Heller, K. J., & Schrezenmeir, J. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21057 · Cited by 113 · see citing works

Structure of colicin I receptor bound to the R‐domain of colicin Ia: implications for protein import

Buchanan, S. K., Lukacik, P., Grizot, S., Ghirlando, R., Ali, M. M. U., Barnard, T. J., Jakes, K. S., Kienker, P. K., & Esser, L. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601693 · Cited by 113 · see citing works

Engineering of a novel thioether bridge and role of modified residues in the lantibiotic Pep5

Bierbaum, G., Szekat, C., Josten, M., Heidrich, C., Kempter, C., Jung, G., & Sahl, H. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.2.385-392.1996 · Cited by 113 · see citing works

Mechanisms Involved in Alleviation of Intestinal Inflammation by Bifidobacterium Breve Soluble Factors

Heuvelin, É., Lebreton, C., Grangette, C., Pot, B., Cerf–Bensussan, N., & Heyman, M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005184 · Cited by 113 · see citing works

Predominance of a bacteriocin-producing Lactobacillus salivarius component of a five-strain probiotic in the porcine ileum and effects on host immune phenotype

Walsh, M. C., Gardiner, G. E., Hart, O. M., Lawlor, P. G., Daly, M., Lynch, B., Richert, B. T., Radcliffe, J. S., Giblin, L. M., Hill, C., et al. (2008) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2008.00454.x · Cited by 113 · see citing works

Production of the Lantibiotic Salivaricin A and Its Variants by Oral Streptococci and Use of a Specific Induction Assay To Detect Their Presence in Human Saliva

Wescombe, P. A., Upton, M., Dierksen, K. P., Ragland, N. L., Sivabalan, S., Wirawan, R. E., Inglis, M. A., Moore, C. J., Walker, G. V., Chilcott, C. N., et al. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.2.1459-1466.2006 · Cited by 113 · see citing works

Construction and Characterization of an Effector Strain of Streptococcus mutans for Replacement Therapy of Dental Caries

Hillman, J. D., Brooks, T. A., Michalek, S. M., Harmon, C. C., Snoep, J. L., & van der Weijden, C. C. (2000) · Infection and Immunity · doi:10.1128/iai.68.2.543-549.2000 · Cited by 112 · see citing works

The synthesis of the bacteriocin sakacin A is a temperature-sensitive process regulated by a pheromone peptide through a three-component regulatory system

Diep, D. B., Axelsson, L. T., Grefsli, C., & Nes, I. F. (2000) · Microbiology · doi:10.1099/00221287-146-9-2155 · Cited by 110 · see citing works

In vitro inhibition of Escherichia coli O157:H7 by bifidobacterial strains of human origin

Gagnon, M., Kheadr, E., Blay, G. L., & Fliss, I. (2003) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2003.07.010 · Cited by 106 · see citing works

Isolation and characterization of microcin E 492 fromKlebsiella pneumoniae

de Lorenzo, V. (1984) · Archives of Microbiology · doi:10.1007/bf00692715 · Cited by 104 · see citing works

Production of plantaricin NC8 by Lactobacillus plantarum NC8 is induced in the presence of different types of gram-positive bacteria

Maldonado‐Barragán, A., Ruiz-Barba, J. L., & Jiménez‐Díaz, R. (2004) · Archives of Microbiology · doi:10.1007/s00203-003-0606-8 · Cited by 104 · see citing works

In vitro inhibition activity of nisin A, nisin Z, pediocin PA-1 and antibiotics against common intestinal bacteria

Blay, G. L., Lacroix, C., Zihler, A., & Fliss, I. (2007) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2007.02178.x · Cited by 104 · see citing works

Characterization of a bacteriocin produced by Enterococcus faecium GM-1 isolated from an infant

Kang, J.-H., & Lee, M. S. (2005) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2005.02556.x · Cited by 104 · see citing works

Antibacterial and Antitumorigenic Properties of Microcin E492, a Pore- Forming Bacteriocin

Lagos, R., Tello, M., Mercado, G., Garcia, V., & Monasterio, O. (2009) · Current Pharmaceutical Biotechnology · doi:10.2174/138920109787048643 · Cited by 104 · see citing works

Colonization of the Human Oral Cavity by a Streptococcus mutans Mutant Producing Increased Bacteriocin

Hillman, J. D., Dzuback, A. L., & Andrews, S. W. (1987) · Journal of Dental Research · doi:10.1177/00220345870660060101 · Cited by 103 · see citing works

Specific Interaction of the Unmodified Bacteriocin Lactococcin 972 with the Cell Wall Precursor Lipid II

Martı́nez, B., Böttiger, T., Schneider, T., Rodrı́guez, A., Sahl, H., & Wiedemann, I. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.00092-08 · Cited by 101 · see citing works

Probiotic Escherichia coli Nissle 1917 Versus Placebo for Treating Diarrhea of Greater Than 4 Days Duration in Infants and Toddlers

Henker, J., Laass, M. W., Blokhin, B. M., Maydannik, V. G., Bolbot, Y. K., Elze, M., Wolff, C., Schreiner, A., & Schulze, J. (2008) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0b013e318169034c · Cited by 100 · see citing works

Dietary Conjugated Linoleic Acid Alleviates Nonalcoholic Fatty Liver Disease in Zucker (fa/fa) Rats

Nagao, K., Inoue, N., Wang, Y., Shirouchi, B., & Yanagita, T. (2005) · Journal of Nutrition · doi:10.1093/jn/135.1.9 · Cited by 99 · see citing works

Genetically modified Streptococcus mutans for the prevention of dental caries

Hillman, J. D. (2002) · Antonie van Leeuwenhoek · doi:10.1023/a:1020695902160 · Cited by 99 · see citing works

Purification and Characterization of Streptin, a Type A1 Lantibiotic Produced by Streptococcus pyogenes

Wescombe, P. A., & Tagg, J. R. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.5.2737-2747.2003 · Cited by 96 · see citing works

Streptococcus rattus strain BHT produces both a class I two-component lantibiotic and a class II bacteriocin

Hyink, O., Balakrishnan, M., & Tagg, J. R. (2005) · FEMS Microbiology Letters · doi:10.1016/j.femsle.2005.09.003 · Cited by 95 · see citing works

Dietary conjugated linoleic acid and n-3 polyunsaturated fatty acids in inflammatory bowel disease

Bassaganya-Riera, J., & Hontecillas, R. (2010) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32833b648e · Cited by 94 · see citing works

Myosin-cross-reactive antigen (MCRA) protein from Bifidobacterium breve is a FAD-dependent fatty acid hydratase which has a function in stress protection

Rosberg-Cody, E., Liavonchanka, A., Göbel, C., Ross, R. P., O’Sullivan, Ó., Fitzgerald, G. F., Feußner, I., & Stanton, C. (2011) · BMC Biochemistry · doi:10.1186/1471-2091-12-9 · Cited by 93 · see citing works

Bacterial phospholipase A: structure and function of an integral membrane phospholipase

Snijder, A., & Dijkstra, B. W. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s1388-1981(00)00113-x · Cited by 93 · see citing works

Purification and structure of mutacin B‐Ny266: a new lantibiotic produced by Streptococcus mutans

Mota‐Meira, M., Lacroix, C., LaPointe, G., & Lavoie, M. C. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)00425-0 · Cited by 92 · see citing works

Plantaricin A Is an Amphiphilic α-Helical Bacteriocin-like Pheromone Which Exerts Antimicrobial and Pheromone Activities through Different Mechanisms

Hauge, H. H., Mantzilas, D., Moll, G. N., Konings, W. N., Driessen, A. J. M., Eijsink, V. G. H., & Nissen-Meyer, J. (1998) · Biochemistry · doi:10.1021/bi981532j · Cited by 91 · see citing works

Microbial diversity in the human intestine and novel insights from metagenomics

Ventura, M. (2009) · Frontiers in bioscience · doi:10.2741/3445 · Cited by 91 · see citing works

Isolation and characterization of a new bacteriocin from Lactobacillus gasseri KT7

Zhu, W., Liu, W., & Wu, D. (2000) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2000.01027.x · Cited by 91 · see citing works

Rapid screening method for analyzing the conjugated linoleic acid production capabilities of bacterial cultures

Barrett, E., Ross, R. P., Fitzgerald, G. F., & Stanton, C. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.01855-06 · Cited by 91 · see citing works

Top‐down systems biology integration of conditional prebiotic modulated transgenomic interactions in a humanized microbiome mouse model

Martin, F., Wang, Y., Sprenger, N., Yap, I. K. S., Rezzi, S., Ramadan, Z., Peré‐Trepat, E., Rochat, F., Cherbut, C., van Bladeren, P., et al. (2008) · Molecular Systems Biology · doi:10.1038/msb.2008.40 · Cited by 91 · see citing works

Induction of Colicin Production by High Temperature or Inhibition of Protein Synthesis

Kennedy, C. K. (1971) · Journal of Bacteriology · doi:10.1128/jb.108.1.10-19.1971 · Cited by 89 · see citing works

Killing of E. coli cells by E group nuclease colicins

James, R., Penfold, C. N., Moore, G. R., & Kleanthous, C. (2002) · Biochimie · doi:10.1016/s0300-9084(02)01450-5 · Cited by 88 · see citing works

Microcin E492 antibacterial activity: evidence for a TonB‐dependent inner membrane permeabilization on Escherichia coli

Destoumieux‐Garzón, D., Thomas, X., Santamaría, M., Goulard, C., Barthélémy, M., Boscher, B., Bessin, Y., Molle, G., Pons, A., Letellìer, L., et al. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03610.x · Cited by 88 · see citing works

Microcin H47, a chromosome-encoded microcin antibiotic of Escherichia coli

Laviña, M. D., Gaggero, C., & Moreno, F. (1990) · Journal of Bacteriology · doi:10.1128/jb.172.11.6585-6588.1990 · Cited by 87 · see citing works

Persistence of colicinogenic Escherichia coli in the mouse gastrointestinal tract

Gillor, O., Giladi, I., & Riley, M. A. (2009) · BMC Microbiology · doi:10.1186/1471-2180-9-165 · Cited by 87 · see citing works

Strain-specific inhibition of Helicobacter pylori by Lactobacillus salivarius and other lactobacilli

Ryan, K. A., Daly, P., Li, Y., Hooton, C., & O’Toole, P. W. (2008) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkn040 · Cited by 87 · see citing works

Prevention of streptococcal pharyngitis by anti-Streptococcus pyogenes bacteriocin-like inhibitory substances (BLIS) produced by Streptococcus salivarius.

Tagg, J. R. (2004) · PubMed · Cited by 86 · see citing works

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 · see citing works

Bacteriocin Production in Vancomycin-Resistant and Vancomycin-Susceptible Enterococcus Isolates of Different Origins

del Campo, R., Tenorio, C., Jiménez‐Díaz, R., Rubio, C., Gómez-Lus, R., Baquero, F., & Torres, C. (2001) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.45.3.905-912.2001 · Cited by 85 · see citing works

Megaplasmids encode differing combinations of lantibiotics in Streptococcus salivarius

Wescombe, P. A., Burton, J. P., Cadieux, P. A., Klesse, N. A., Hyink, O., Heng, N. C. K., Chilcott, C. N., Reid, G., & Tagg, J. R. (2006) · Antonie van Leeuwenhoek · doi:10.1007/s10482-006-9081-y · Cited by 84 · see citing works

Bacteriocin synthesis in uropathogenic and commensal Escherichia coli: colicin E1 is a potential virulence factor

Šmajs, D., Micenková, L., Šmarda, J., Vrba, M., Ševčíková, A., Vališová, Z., & Woznicová, V. (2010) · BMC Microbiology · doi:10.1186/1471-2180-10-288 · Cited by 83 · see citing works

Impact of Administered Bifidobacterium on Murine Host Fatty Acid Composition

Wall, R., Ross, R. P., Shanahan, F., O’Mahony, L., Kiely, B., Quigley, E. M. M., Dinan, T. G., Fitzgerald, G. F., & Stanton, C. (2010) · Lipids · doi:10.1007/s11745-010-3410-7 · Cited by 82 · see citing works

Mining the Microbiota of the Neonatal Gastrointestinal Tract for Conjugated Linoleic Acid-Producing Bifidobacteria

Rosberg-Cody, E., Ross, R. P., Hussey, S., Ryan, C. A., Murphy, B. P., Fitzgerald, G. F., Devery, R., & Stanton, C. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.8.4635-4641.2004 · Cited by 81 · see citing works

Cloning of the gene encoding Streptococcin A-FF22, a novel lantibiotic produced by Streptococcus pyogenes, and determination of its nucleotide sequence

Hynes, W. L., Ferretti, J. J., & Tagg, J. R. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.6.1969-1971.1993 · Cited by 79 · see citing works

Salivaricin P, One of a Family of Two-Component Antilisterial Bacteriocins Produced by Intestinal Isolates of Lactobacillus salivarius

Barrett, E., Hayes, M., O’Connor, P. M., Gardiner, G. E., Fitzgerald, G. F., Stanton, C., Ross, R. P., & Hill, C. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00666-06 · Cited by 79 · see citing works

Intestinal Bifidobacteria That Producetrans-9,trans-11 Conjugated Linoleic Acid: A Fatty Acid With Antiproliferative Activity Against Human Colon SW480 and HT-29 Cancer Cells

Coakley, M., Johnson, M. C., McGrath, E., Rahman, S., Ross, R. P., Fitzgerald, G. F., Devery, R., & Stanton, C. (2006) · Nutrition and Cancer · doi:10.1207/s15327914nc5601_13 · Cited by 77 · see citing works

Partial characterization of bacteriocins produced by human Lactococcus lactis and Pediococccus acidilactici isolates

Millette, M., Dupont, C., Archambault, D., & Lacroix, M. (2006) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2006.03044.x · Cited by 76 · see citing works

Class IIa bacteriocin resistance in Enterococcus faecalis V583: The mannose PTS operon mediates global transcriptional responses

Opsata, M., Nes, I. F., & Holo, H. (2010) · BMC Microbiology · doi:10.1186/1471-2180-10-224 · Cited by 76 · see citing works

Cis 9, trans 11- and trans 10, cis 12-conjugated linoleic acid isomers induce apoptosis in cultured SW480 cells.

Miller, Á., Stanton, C., & Devery, R. (2003) · PubMed · Cited by 76 · see citing works

Mode of Action of the Antimicrobial Peptide Aureocin A53 from Staphylococcus aureus

Netz, D. J. A., Bastos, M. D. C. D. F., & Sahl, H. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.11.5274-5280.2002 · Cited by 75 · see citing works

Trypsin-dependent production of an antibacterial substance by a human Peptostreptococcus strain in gnotobiotic rats and in vitro

Ramare, F., Nicoli, J. R., Dabard, J., Corring, T., Ladiré, M., Gueugneau, A.-M., & Raibaud, P. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.9.2876-2883.1993 · Cited by 74 · see citing works

Production of conjugated linoleic acid by isolated Bifidobacterium strains

Oh, D., Hong, G.-H., Lee, Y., Min, S., Sin, H., & Cho, S. K. (2003) · World Journal of Microbiology and Biotechnology · doi:10.1023/b:wibi.0000007313.90368.0c · Cited by 74 · see citing works

Isolation and characterization of genetically engineered gallidermin and epidermin analogs

Ottenwälder, B., Kupke, T. E., Brecht, S., Gnau, V., Metzger, J. W., Jung, G., & Götz, F. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.11.3894-3903.1995 · Cited by 73 · see citing works

Study of the physicochemical and biological stability of pediocin PA‐1 in the upper gastrointestinal tract conditions using a dynamic in vitro model

Kheadr, E., Zihler, A., Dabour, N., Lacroix, C., Blay, G. L., & Fliss, I. (2009) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2009.04644.x · Cited by 71 · see citing works

Primary Amino Acid and DNA Sequences of Gassericin T, a Lactacin F-Family Bacteriocin Produced byLactobacillus gasseriSBT2055

Kawai, Y., Saitoh, B., TAKAHASHI, O., Kitazawa, H., Saito, T., Nakajima, H., & Itoh, T. (2000) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.64.2201 · Cited by 71 · see citing works

Post‐Translational Heterocyclic Backbone Modifications in the 43‐Peptide Antibiotic Microcin B17

Bayer, A., Freund, S. M. V., & Jung, G. (1995) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1995.414_b.x · Cited by 69 · see citing works

Bactericidal Activity of both Secreted and Nonsecreted Microcin E492 Requires the Mannose Permease

Biéler, S., Silva, F., Soto, C. A., & Belin, D. (2006) · Journal of Bacteriology · doi:10.1128/jb.00688-06 · Cited by 69 · see citing works

Production of the Bsa Lantibiotic by Community-Acquired Staphylococcus aureus Strains

Daly, K. M., Upton, M., Sandiford, S. K., Draper, L. A., Wescombe, P. A., Jack, R. W., O’Connor, P. M., Rossney, A. S., Götz, F., Hill, C., et al. (2009) · Journal of Bacteriology · doi:10.1128/jb.01375-09 · Cited by 69 · see citing works

Molecular and Genetic Characterization of a Novel Bacteriocin Locus in Enterococcus avium Isolates from Infants

Birri, D. J., Brede, D. A., Forberg, T., Holo, H., & Nes, I. F. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01597-09 · Cited by 68 · see citing works

Cytotoxic effects of pyocin S2 produced by Pseudomonas aeruginosa on the growth of three human cell lines

Ali, A. A., Worobec, E. A., Deezagi, A., & Malekzadeh, F. (2004) · Canadian Journal of Microbiology · doi:10.1139/w04-019 · Cited by 65 · see citing works

Differences between human subjects in the composition of the faecal bacterial community and faecal metabolism of linoleic acid

Devillard, E., McIntosh, F. M., Paillard, D., Thomas, N. A., Shingfield, K. J., & Wallace, R. J. (2009) · Microbiology · doi:10.1099/mic.0.023416-0 · Cited by 65 · see citing works

Characterization of salivaricin CRL 1328, a two-peptide bacteriocin produced by Lactobacillus salivarius CRL 1328 isolated from the human vagina

Pingitore, E. V., Hebert, E. M., Nader-Macı́as, M. E., & Sesma, F. J. M. (2009) · Research in Microbiology · doi:10.1016/j.resmic.2009.06.009 · Cited by 64 · see citing works

Molecular nature of a novel bacterial toxin: the cytolysin of Enterococcus faecalis

Haas, W., & Gilmore, M. S. (1999) · Medical Microbiology and Immunology · doi:10.1007/s004300050091 · Cited by 62 · see citing works

Characterization of enterocin- and salivaricin-producing lactic acid bacteria from the mammalian gastrointestinal tract

O'Shea, E. F., Gardiner, G. E., O’Connor, P. M., Mills, S., Ross, R. P., & Hill, C. (2008) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2008.01427.x · Cited by 62 · see citing works

Specific Binding of Cinnamycin (Ro 09-0198) to Phosphatidylethanolamine. Comparison between Micellar and Membrane Environments

Machaidze, G., & Seelig, J. (2003) · Biochemistry · doi:10.1021/bi035225b · Cited by 62 · see citing works

Distribution of Megaplasmids inLactobacillus salivariusand Other Lactobacilli

Li, Y., Canchaya, C. A., Fang, F., Raftis, E. J., Ryan, K. A., van Pijkeren, J., van Sinderen, D., & O’Toole, P. W. (2007) · Journal of Bacteriology · doi:10.1128/jb.00447-07 · Cited by 61 · see citing works

Potential of Lactobacillus gasseri isolated from infant faeces to produce bacteriocin

Toba, T., Yoshioka, E., & Itoh, T. (1991) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.1991.tb00546.x · Cited by 58 · see citing works

Trypsin Mediates Growth Phase-Dependent Transcriptional Regulation of Genes Involved in Biosynthesis of Ruminococcin A, a Lantibiotic Produced by a Ruminococcus gnavus Strain from a Human Intestinal Microbiota

Gómez, A., Ladiré, M., Marcille, F., & Fons, M. (2002) · Journal of Bacteriology · doi:10.1128/jb.184.1.18-28.2002 · Cited by 58 · see citing works

Bacteriocins—A viable alternative to antibiotics?

Cotter, P. D., Ross, R. P., & Hill, C. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro2937 · Cited by 1,793 · see citing works

Probiotic Mechanisms of Action

Bermúdez-Brito, M., Plaza‐Díaz, J., Muñoz‐Quezada, S., Gómez‐Llorente, C., & Gil, Á. (2012) · Annals of Nutrition and Metabolism · doi:10.1159/000342079 · Cited by 1,276 · see citing works

Minireview: Gut microbiota: The neglected endocrine organ

Clarke, G., Stilling, R. M., Kennedy, P. J., Stanton, C., Cryan, J. F., & Dinan, T. G. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1108 · Cited by 1,192 · see citing works

Effects of probiotics on gut microbiota: mechanisms of intestinal immunomodulation and neuromodulation

Hemarajata, P., & Versalovic, J. (2013) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756283x12459294 · Cited by 1,083 · see citing works

Impact of antibiotics on the human microbiome and consequences for host health

Patangia, D. V., Ryan, C. A., Dempsey, E. M., Ross, R. P., & Stanton, C. (2022) · MicrobiologyOpen · doi:10.1002/mbo3.1260 · Cited by 806 · see citing works

Compositional and Functional Features of the Gastrointestinal Microbiome and Their Effects on Human Health

Hollister, E. B., Gao, C., & Versalovic, J. A. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.01.052 · Cited by 533 · see citing works

Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions

Zhang, L., & Davies, S. S. (2016) · Genome Medicine · doi:10.1186/s13073-016-0296-x · Cited by 499 · see citing works

Lactobacillus accelerates ISCs regeneration to protect the integrity of intestinal mucosa through activation of STAT3 signaling pathway induced by LPLs secretion of IL-22

Hou, Q., Ye, L., Liu, H., Huang, L., Yang, Q., Turner, J. R., & Yu, Q. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0070-2 · Cited by 403 · see citing works

Thirty Years of Lactobacillus rhamnosus GG

Capurso, L. (2019) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0000000000001170 · Cited by 384 · see citing works

Conjugated Linoleic Acid Effects on Cancer, Obesity, and Atherosclerosis: A Review of Pre-Clinical and Human Trials with Current Perspectives

den Hartigh, L. (2019) · Nutrients · doi:10.3390/nu11020370 · Cited by 371 · see citing works

Anti-Infective Activities of Lactobacillus Strains in the Human Intestinal Microbiota: from Probiotics to Gastrointestinal Anti-Infectious Biotherapeutic Agents

Moal, V. L.-L., & Servin, A. L. (2014) · Clinical Microbiology Reviews · doi:10.1128/cmr.00080-13 · Cited by 355 · see citing works

Molecular insights into probiotic mechanisms of action employed against intestinal pathogenic bacteria

van Zyl, W. F., Deane, S. M., & Dicks, L. M. T. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1831339 · Cited by 348 · see citing works

The Human Gut Microbiome and Body Metabolism: Implications for Obesity and Diabetes

Devaraj, S., Hemarajata, P., & Versalovic, J. (2013) · Clinical Chemistry · doi:10.1373/clinchem.2012.187617 · Cited by 321 · see citing works

Current status of probiotic and related health benefits

Das, T. K., Pradhan, S., Chakrabarti, S., Mondal, K. C., & Ghosh, K. (2022) · Applied Food Research · doi:10.1016/j.afres.2022.100185 · Cited by 294 · see citing works

International Society of Sports Nutrition Position Stand: Probiotics

Jäger, R., Mohr, A. E., Carpenter, K. C., Kerksick, C. M., Purpura, M., Moussa, A., Townsend, J. R., Lamprecht, M., West, N. P., Black, K., et al. (2019) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-019-0329-0 · Cited by 277 · see citing works

Lactic Acid Bacteria in Raw-Milk Cheeses: From Starter Cultures to Probiotic Functions

Coelho, M. C., Malcata, F. X., & Silva, C. C. G. (2022) · Foods · doi:10.3390/foods11152276 · Cited by 276 · see citing works

Effects of high doses of vitamin D3 on mucosa-associated gut microbiome vary between regions of the human gastrointestinal tract

Bashir, M., Prietl, B., Tauschmann, M., Mautner, S., Kump, P. K., Treiber, G. M., Wurm, P., Gorkiewicz, G., Högenauer, C., & Pieber, T. R. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-0966-2 · Cited by 258 · see citing works

Dietary supplementation of probiotic Bacillus coagulans ATCC 7050, improves the growth performance, intestinal morphology, microflora, immune response, and disease confrontation of Pacific white shrimp, Litopenaeus vannamei

Amoah, K., Huang, Q., Tan, B., Zhang, S., Chi, S., Yang, Q., Liu, H., & Dong, X. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.02.029 · Cited by 254 · see citing works

Antimicrobial activity, antibiotic susceptibility and virulence factors of Lactic Acid Bacteria of aquatic origin intended for use as probiotics in aquaculture

Muñoz-Atienza, E., Gómez‐Sala, B., Araújo, C., Campanero, C., del Campo, R., Hernández, P. E., Herranz, C., & Cintas, L. M. (2013) · BMC Microbiology · doi:10.1186/1471-2180-13-15 · Cited by 243 · see citing works

Bacteriocin production by Bifidobacterium spp. A review

Martinez, F. A. C., Balciunas, E. M., Converti, A., Cotter, P. D., & Oliveira, R. P. D. S. (2013) · Biotechnology Advances · doi:10.1016/j.biotechadv.2013.01.010 · Cited by 233 · see citing works

Gut Microbiota and Their Neuroinflammatory Implications in Alzheimer’s Disease

Giau, V. V., Wu, S., Jamerlan, A., An, S. S. A., Kim, S., & Hulme, J. (2018) · Nutrients · doi:10.3390/nu10111765 · Cited by 235 · see citing works

Antimicrobial Activity of Lactic Acid Bacteria in Dairy Products and Gut: Effect on Pathogens

Arqués, J. L., Rodrı́guez, E., Langa, S., Landete, J. M., & Médina, M. (2015) · BioMed Research International · doi:10.1155/2015/584183 · Cited by 211 · see citing works

Scientific evidence for health effects attributed to the consumption of probiotics and prebiotics: an update for current perspectives and future challenges

Martinez, R. C. R., Bedani, R., & Saad, S. M. I. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515003864 · Cited by 208 · see citing works

Bacteriocins: An Overview of Antimicrobial, Toxicity, and Biosafety Assessment by in vivo Models

Chao, D. F. B., León‐Buitimea, A., Lerma-Escalera, J. A., & Morones‐Ramírez, J. R. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.630695 · Cited by 199 · see citing works

Probiotics: How Effective Are They in the Fight against Obesity?

Mazloom, K., Siddiqi, I., & Covașă, M. (2019) · Nutrients · doi:10.3390/nu11020258 · Cited by 198 · see citing works

Lactobacillus rhamnosus GG Derived Extracellular Vesicles Modulate Gut Microbiota and Attenuate Inflammatory in DSS-Induced Colitis Mice

Tong, L., Zhang, X., Hao, H., Liu, Q., Zhou, Z., Liang, X., Liu, T., Gong, P., Zhang, L., Zhai, Z., et al. (2021) · Nutrients · doi:10.3390/nu13103319 · Cited by 189 · see citing works

Probiotics in the management of irritable bowel syndrome and inflammatory bowel disease

Whelan, K., & Quigley, E. M. M. (2013) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e32835d7bba · Cited by 183 · see citing works

Probiotic metabolites as epigenetic targets in the prevention of colon cancer

Kumar, M., Nagpal, R., Verma, V., Kumar, A., Kaur, N., Rajkumar, H., Gautam, S. K., & Singh, B. (2012) · Nutrition Reviews · doi:10.1111/j.1753-4887.2012.00542.x · Cited by 183 · see citing works

New perspectives on probiotics in health and disease

Daliri, E. B., & Lee, B. H. (2015) · Food Science and Human Wellness · doi:10.1016/j.fshw.2015.06.002 · Cited by 150 · see citing works

Probiotics as Complementary Treatment for Metabolic Disorders

Le Barz, M., Anhê, F. F., Varin, T. V., Desjardins, Y., Levy, E., Roy, D., Urdaci, M. C., & Marette, A. (2015) · Diabetes &amp; Metabolism Journal · doi:10.4093/dmj.2015.39.4.291 · Cited by 142 · see citing works

Current Trends of Enterococci in Dairy Products: A Comprehensive Review of Their Multiple Roles

Dapkevicius, M. D. L. E., Sgardioli, B. F., Câmara, S. P. D. A. E., Poeta, P. A. C. Q. D., & Malcata, F. X. (2021) · Foods · doi:10.3390/foods10040821 · Cited by 159 · see citing works

Concomitant memantine and Lactobacillus plantarum treatment attenuates cognitive impairments in APP/PS1 mice

Wang, Q., Shen, Y., Wang, X., Fu, S., Zhang, X., Zhang, Y., & Wang, R. (2020) · Aging · doi:10.18632/aging.102645 · Cited by 129 · see citing works

Microbiota and dietary interactions – an update to the hygiene hypothesis?

Frei, R., Lauener, R. P., Crameri, R., & O’Mahony, L. (2012) · Allergy · doi:10.1111/j.1398-9995.2011.02783.x · Cited by 127 · see citing works

Probiotics: an Antibiotic Replacement Strategy for Healthy Broilers and Productive Rearing

Neveling, D. P., & Dicks, L. M. T. (2020) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-020-09640-z · Cited by 127 · see citing works

Approaches to prevent and control Campylobacter spp. colonization in broiler chickens: a review

El-Hack, M. E. A., El‐Saadony, M. T., Shehata, A. M., Arif, M. A., Paswan, V. K., Batiha, G. E., Khafaga, A. F., & Elbestawy, A. R. (2020) · Environmental Science and Pollution Research · doi:10.1007/s11356-020-11747-3 · Cited by 121 · see citing works

Lipoteichoic Acid of Probiotic Lactobacillus plantarum Attenuates Poly I:C-Induced IL-8 Production in Porcine Intestinal Epithelial Cells

Kim, K. W., Kang, S., Woo, S., Park, O.-J., Ahn, K. B., Song, K., Lee, H., Yun, C., & Han, S. H. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01827 · Cited by 122 · see citing works

Short chain and polyunsaturated fatty acids in host gut health and foodborne bacterial pathogen inhibition

Peng, M., & Biswas, D. (2016) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2016.1203286 · Cited by 119 · see citing works

Diet Effects in Gut Microbiome and Obesity

Chen, J., He, X., & Huang, J. (2014) · Journal of Food Science · doi:10.1111/1750-3841.12397 · Cited by 116 · see citing works

Metabolic role of lactobacilli in weight modification in humans and animals

Drissi, F., Raoult, D., & Merhej, V. (2016) · Microbial Pathogenesis · doi:10.1016/j.micpath.2016.03.006 · Cited by 113 · see citing works

Microbiota regulate intestinal epithelial gene expression by suppressing the transcription factor Hepatocyte nuclear factor 4 alphaPreprint

Davison, J. M., Lickwar, C. R., Song, L., Breton, G., Crawford, G. E., & Rawls, J. F. (2017) · Genome Research · doi:10.1101/gr.220111.116 · Cited by 111 · see citing works

GABA-Producing Natural Dairy Isolate From Artisanal Zlatar Cheese Attenuates Gut Inflammation and Strengthens Gut Epithelial Barrier in vitro

Bajić, S. S., Đokić, J., Dinić, M., Veljović, K., Golić, N., Mihajlović, S., & Tolinački, M. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00527 · Cited by 109 · see citing works

Common occurrence of antibacterial agents in human intestinal microbiota

Drissi, F., Buffet, S., Raoult, D., & Merhej, V. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00441 · Cited by 108 · see citing works

The Role of Probiotics in Alleviating Postweaning Diarrhea in Piglets From the Perspective of Intestinal Barriers

Su, W., Gong, T., Jiang, Z., Lu, Z., & Wang, Y. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.883107 · Cited by 107 · see citing works

Lactic Acid Bacteria as Source of Functional Ingredients

Florou-Paneri, P. C., Christaki, E. V., & Bonos, E. (2013) · InTech eBooks · doi:10.5772/47766 · Cited by 103 · see citing works

Lactobacillus Dominate in the Intestine of Atlantic Salmon Fed Dietary Probiotics

Gupta, S., Fečkaninová, A., Lokesh, J., Koščová, J., Sørensen, M., Fernandes, J. M. O., & Kiron, V. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.03247 · Cited by 91 · see citing works

Unique genetic basis of the distinct antibiotic potency of high acetic acid production in the probiotic yeast Saccharomyces cerevisiae var. boulardiiPreprint

Offei, B., Vandecruys, P., Graeve, S. D., Foulquié-Moreno, M. R., & Thevelein, J. M. (2019) · Genome Research · doi:10.1101/gr.243147.118 · Cited by 92 · see citing works

Bacterial Production of Conjugated Linoleic and Linolenic Acid in Foods: A Technological Challenge

Gorissen, L., Leroy, F., Vuyst, L. D., SMET, S. D., & Raes, K. (2013) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2012.706243 · Cited by 90 · see citing works

Therapeutic Application of Synbiotics, a Fusion of Probiotics and Prebiotics, and Biogenics as a New Concept for Oral Candida Infections: A Mini Review

Ohshima, T., Kojima, Y., Seneviratne, C. J., & Maeda, N. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00010 · Cited by 87 · see citing works

Linoleic Acids Overproducing Lactobacillus casei Limits Growth, Survival, and Virulence of Salmonella Typhimurium and Enterohaemorrhagic Escherichia coli

Peng, M., Tabashsum, Z., Patel, P., Bernhardt, C. R., & Biswas, D. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02663 · Cited by 84 · see citing works

Environmental factors influencing the efficacy of probiotic bacteria

Marco, M. L., & Tachon, S. (2012) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2012.10.002 · Cited by 82 · see citing works

Role of the Lower and Upper Intestine in the Production and Absorption of Gut Microbiota-Derived PUFA Metabolites

Druart, C., Neyrinck, A. M., Vlaeminck, B., Fievez, V., Cani, P. D., & Delzenne, N. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087560 · Cited by 81 · see citing works

Gut Microbiota and Nonalcoholic Fatty Liver Disease: Insights on Mechanism and Application of Metabolomics

He, X., Ji, G., Jia, W. P., & Li, H. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030300 · Cited by 81 · see citing works

Influence of Probiotics Administration on Gut Microbiota Core

Falcinelli, S., Rodiles, A., Hatef, A., Picchietti, S., Cossignani, L., Merrifield, D. L., Unniappan, S., & Carnevali, O. (2018) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0000000000001064 · Cited by 79 · see citing works

Plant-Based Fat, Dietary Patterns Rich in Vegetable Fat and Gut Microbiota Modulation

Muralidharan, J., Galié, S., Hernández‐Alonso, P., Bulló, M., & Salas‐Salvadó, J. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00157 · Cited by 76 · see citing works

Probiotic Supplementation and Micronutrient Status in Healthy Subjects: A Systematic Review of Clinical Trials

Barkhidarian, B., Roldos, L., Iskandar, M. M., Saedisomeolia, A., & Kubow, S. J. (2021) · Nutrients · doi:10.3390/nu13093001 · Cited by 77 · see citing works

Identification and characterization of wild lactobacilli and pediococci from spontaneously fermented Mountain Cheese

Carafa, I., Nardin, T., Larcher, R., Viola, R., Tuohy, K. M., & Franciosi, E. (2014) · Food Microbiology · doi:10.1016/j.fm.2014.12.003 · Cited by 75 · see citing works

Gram-Positive Bacteria with Probiotic Potential for the Apis mellifera L. Honey Bee: The Experience in the Northwest of Argentina

Audisio, M. C. (2016) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-016-9231-0 · Cited by 72 · see citing works

Study of fermented feed by mixed strains and their effects on the survival, growth, digestive enzyme activity and intestinal flora of Penaeus vannamei

Zhang, M., Pan, L., Fan, D., He, J., Su, C., Gao, S., & Zhang, M. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735703 · Cited by 75 · see citing works

Optimization of probiotic therapeutics using machine learning in an artificial human gastrointestinal tract

Westfall, S., Carracci, F., Estill, M. S., Zhao, D., Wu, Q.-L., Shen, L., Simon, J. E., & Pasinetti, G. M. (2021) · Scientific Reports · doi:10.1038/s41598-020-79947-y · Cited by 71 · see citing works

Environmental Factors and the Risk of Developing Type 1 Diabetes—Old Disease and New Data

Zorena, K., Michalska, M., Kurpas, M., Jaskulak, M., Murawska, A., & Rostami, S. (2022) · Biology · doi:10.3390/biology11040608 · Cited by 80 · see citing works

Inflammatory Bowel Disease Therapeutics: A Focus on Probiotic Engineering

Mishra, J., Stubbs, M., Kuang, L., Vara, N., Kumar, P., & Kumar, N. (2022) · Mediators of Inflammation · doi:10.1155/2022/9621668 · Cited by 69 · see citing works

Ability of the gut microbiota to produce PUFA‐derived bacterial metabolites: Proof of concept in germ‐free versus conventionalized mice

Druart, C., Bindels, L. B., Schmaltz, R. J., Neyrinck, A. M., Cani, P. D., Walter, J., Ramer‐Tait, A. E., & Delzenne, N. M. (2015) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500014 · Cited by 69 · see citing works

Probiotics in human milk and probiotic supplementation in infant nutrition: a workshop report

Bergmann, H., Rodríguez, J. M., Salminen, S., & Szajewska, H. (2014) · British Journal Of Nutrition · doi:10.1017/s0007114514001949 · Cited by 67 · see citing works

Perspective: Fundamental Limitations of the Randomized Controlled Trial Method in Nutritional Research: The Example of Probiotics

Zeilstra, D., Younes, J. A., Brummer, R. J., & Kleerebezem, M. (2018) · Advances in Nutrition · doi:10.1093/advances/nmy046 · Cited by 67 · see citing works

Paenibacillus polymyxa improves the growth, immune and antioxidant activity, intestinal health, and disease resistance in Litopenaeus vannamei challenged with Vibrio parahaemolyticus

Amoah, K., Huang, Q., Dong, X., Tan, B., Zhang, S., Chi, S., Yang, Q., Liu, H., & Yang, Y. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.734563 · Cited by 66 · see citing works

Microbiota and body weight control: Weight watchers within?

Boscaini, S., Leigh, S., Lavelle, A., García‐Cabrerizo, R., Lipuma, T., Clarke, G. A., Schellekens, H., & Cryan, J. F. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101427 · Cited by 66 · see citing works

<i>In vivo</i> screening of multiple bacterial strains identifies <i>Lactobacillus rhamnosus</i> Lb102 and <i>Bifidobacterium animalis</i> ssp. <i>lactis</i> Bf141 as probiotics that improve metabolic disorders in a mouse model of obesity

Le Barz, M., Daniel, N., Varin, T. V., Naimi, S., Demers‐Mathieu, V., Pilon, G., Audy, J., Laurin, É., Roy, D., Urdaci, M. C., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201801672r · Cited by 63 · see citing works

Host gut-derived Bacillus probiotics supplementation improves growth performance, serum and liver immunity, gut health, and resistive capacity against Vibrio harveyi infection in hybrid grouper (♀Epinephelus fuscoguttatus × ♂Epinephelus lanceolatus)

Amoah, K., Tan, B., Zhang, S., Chi, S., Yang, Q., Liu, H., Yang, Y., Zhang, H., & Dong, X. (2023) · Animal nutrition · doi:10.1016/j.aninu.2023.05.005 · Cited by 63 · see citing works

Gut Microbial Metabolites of Polyunsaturated Fatty Acids Correlate with Specific Fecal Bacteria and Serum Markers of Metabolic Syndrome in Obese Women

Druart, C., Dewulf, E. M., Cani, P. D., Neyrinck, A. M., Thissen, J., & Delzenne, N. M. (2014) · Lipids · doi:10.1007/s11745-014-3881-z · Cited by 63 · see citing works

Adaptation of gut microbiome and host metabolic systems to lignocellulosic degradation in bamboo rats

Xiao, K., Liang, X., Lu, H., Li, X., Zhang, Z., Lu, X., Wang, H., Meng, Y., Roy, A., Luo, W., et al. (2022) · The ISME Journal · doi:10.1038/s41396-022-01247-2 · Cited by 59 · see citing works

Biochemical characterization and FAD-binding analysis of oleate hydratase from Macrococcus caseolyticus

Joo, Y., Jeong, K., Yeom, S., Kim, Y.-S., Kim, Y., & Oh, D. (2011) · Biochimie · doi:10.1016/j.biochi.2011.12.011 · Cited by 61 · see citing works

Inhibitory effect of biofilm-forming Lactobacillus kunkeei strains against virulent Pseudomonas aeruginosa in vitro and in honeycomb moth (Galleria mellonella) infection model

Berríos, P., Fuentes, J. A., Salas, D., Carreño, A., Aldea-Sánchez, P., Fernández, F., & Trombert, A. N. (2017) · Beneficial Microbes · doi:10.3920/bm2017.0048 · Cited by 57 · see citing works

Resource conflict and cooperation between human host and gut microbiota: implications for nutrition and health

Wasielewski, H., Alcock, J., & Aktipis, A. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13118 · Cited by 56 · see citing works

Conjugated linoleic acid production and probiotic assessment of Lactobacillus plantarum isolated from Pico cheese

Ribeiro, S. C., Stanton, C., Yang, B. K., Ross, R. P., & Silva, C. C. G. (2017) · LWT · doi:10.1016/j.lwt.2017.12.065 · Cited by 55 · see citing works

Microbiome modulation as a novel therapeutic approach in chronic kidney disease

Sumida, K., Lau, W. L., Kovesdy, C. P., Kalantar‐Zadeh, K., & Kalantar‐Zadeh, K. (2020) · Current Opinion in Nephrology & Hypertension · doi:10.1097/mnh.0000000000000661 · Cited by 57 · see citing works

Exploring the Gut Microbiome in Myasthenia Gravis

Thye, A. Y.-K., Law, J. W., Tan, L. T., Thurairajasingam, S., Chan, K., Letchumanan, V., & Lee, L. (2022) · Nutrients · doi:10.3390/nu14081647 · Cited by 57 · see citing works

Overview of conjugated linoleic acid formation and accumulation in animal products

Hur, S. J., Kim, H. S., Bahk, Y. Y., & Park, Y. (2016) · Livestock Science · doi:10.1016/j.livsci.2016.11.016 · Cited by 54 · see citing works

Microbes Central to Human Reproduction

Reid, G., Brigidi, P., Burton, J. P., Contractor, N., Duncan, S. H., Fargier, E., Hill, C., Lebeer, S., Martı́n, R., McBain, A. J., et al. (2014) · American Journal of Reproductive Immunology · doi:10.1111/aji.12319 · Cited by 53 · see citing works

Anti-infective activities of long-chain fatty acids against foodborne pathogens

Borreby, C., Lillebæk, E. M. S., & Kallipolitis, B. H. (2023) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuad037 · Cited by 53 · see citing works

Efficacy of Locally Isolated Lactic Acid Bacteria Against Antibiotic-Resistant Uropathogens

Manzoor, A., Haq, I. U., Baig, S., Qazi, J. I., & Seratlić, S. (2015) · Jundishapur Journal of Microbiology · doi:10.5812/jjm.18952 · Cited by 56 · see citing works

The anti-proliferative and pro-apoptotic effects of the trans9, trans11 conjugated linoleic acid isomer on MCF-7 breast cancer cells are associated with LXR activation

El Roz, A., Bard, J. M., Huvelin, J. M., & Nazih, H. (2013) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2012.12.006 · Cited by 52 · see citing works

The impact of aging-induced gut microbiome dysbiosis on dendritic cells and lung diseases

Malik, J. A., Zafar, M. A., Lamba, T., Nanda, S., Khan, M. A., & Agrewala, J. N. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2290643 · Cited by 51 · see citing works

Microbial modulation of the gut microbiome for treating autoimmune diseases

Balakrishnan, B., & Taneja, V. (2018) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2018.1517044 · Cited by 51 · see citing works

Combining prebiotics with probiotic bacteria can enhance bacterial growth and secretion of bacteriocins

Pranckutė, R., Kaunietis, A., Kuisienė, N., & Čitavičius, D. J. (2016) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2016.05.041 · Cited by 50 · see citing works

Pediocin-Like Antimicrobial Peptides of Bacteria

Баландин, С. В., Sheremeteva, E. V., & Ovchinnikova, T. V. (2019) · Biochemistry (Moscow) · doi:10.1134/s000629791905002x · Cited by 50 · see citing works

Ameliorating role of Tetrastigma hemsleyanum polysaccharides in antibiotic-induced intestinal mucosal barrier dysfunction in mice based on microbiome and metabolome analyses

Zhou, F., Lin, Y., Chen, S., Bao, X., Fu, S., Lv, Y., Zhou, M., Chen, Y., Zhu, B., Qian, C., et al. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.124419 · Cited by 49 · see citing works

The Role of Probiotics, Prebiotics, Synbiotics, and Postbiotics in Livestock and Poultry Gut Health: A Review

Yue, T., Yanan, L., Ding, W., Xu, B., Zhang, C., Li, L., Jian, F., & Huang, S. (2025) · Metabolites · doi:10.3390/metabo15070478 · Cited by 49 · see citing works

Bacteriocins and their applications for the treatment of bacterial diseases in aquaculture: a review

Sahoo, T. K., Jena, P. K., Patel, A. K., & Seshadri, S. (2014) · Aquaculture Research · doi:10.1111/are.12556 · Cited by 49 · see citing works

Competitive reduction of poultry-borne enteric bacterial pathogens in chicken gut with bioactive Lactobacillus casei

Tabashsum, Z., Peng, M., Alvarado‐Martinez, Z., Aditya, A., Bhatti, J., Romo, P. B., Young, A., & Biswas, D. (2020) · Scientific Reports · doi:10.1038/s41598-020-73316-5 · Cited by 47 · see citing works

Effects of heat-inactivated Bifidobacterium BB12 on cariogenicity of Streptococcus mutans in vitro

Schwendicke, F., Horb, K., Kneist, S., Dörfer, C. E., & Paris, S. (2014) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2014.08.012 · Cited by 47 · see citing works

In situ production of conjugated linoleic acid by Bifidobacterium lactis BB12 and Lactobacillus acidophilus LA5 in milk model medium

Amiri, S., Mokarram, R. R., Khiabani, M. S., Bari, M. R., & Alizadeh, M. (2020) · LWT · doi:10.1016/j.lwt.2020.109933 · Cited by 46 · see citing works

Effects of three probiotic strains (Bacillus coagulans, B. licheniformis and Paenibacillus polymyxa) on growth, immune response, gut morphology and microbiota, and resistance against Vibrio harveyi of northern whitings, Sillago sihama Forsskál (1775)

Amoah, K., Dong, X., Tan, B., Zhang, S., Chi, S., Yang, Q., Liu, H., Yang, Y., & Zhang, H. (2021) · Animal Feed Science and Technology · doi:10.1016/j.anifeedsci.2021.114958 · Cited by 46 · see citing works

Biosynthesis, classification, properties, and applications of Weissella bacteriocins

Singh, J. K., Devi, P. B., Reddy, G. B., Jaiswal, A. K., Kavitake, D., & Shetty, P. H. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1406904 · Cited by 45 · see citing works

Ileal and cecal microbial population and short-chain fatty acid profile in broiler chickens fed diets supplemented with lignocellulose.

Bogusławska‐Tryk, M., Szymeczko, R., Piotrowska‐Długosz, A., Burlikowska, K., & Śliżewska, K. (2015) · Digital Repository of UTP in Bydgoszcz (Uniwersytet Technologiczno-Przyrodniczy) · Cited by 45 · see citing works

In vitro evaluation of prebiotic activity, pathogen inhibition and enzymatic metabolism of intestinal bacteria in the presence of fructans extracted from agave: A comparison based on polymerization degree

Gamboa, R. G., Ortiz‐Basurto, R. I., Calderón‐Santoyo, M., Madrigal, J. B., Ruiz-Álvarez, B. E., & González‐Ávila, M. (2018) · LWT · doi:10.1016/j.lwt.2018.02.051 · Cited by 44 · see citing works

Gut microbiome modulation mediated by probiotics: Positive impact on growth and health status of Labeo rohita

Ghori, I., Tubassam, M., Ahmad, T., Zuberi, A., & Imran, M. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.949559 · Cited by 43 · see citing works

A representative of the dominant human colonic Firmicutes, Roseburia faecis M72/1, forms a novel bacteriocin-like substance

Hatziioanou, D., Mayer, M. J., Duncan, S. H., Flint, H. J., & Narbad, A. (2013) · Anaerobe · doi:10.1016/j.anaerobe.2013.07.006 · Cited by 43 · see citing works

Intraspecific difference of Latilactobacillus sakei in inflammatory bowel diseases: Insights into potential mechanisms through comparative genomics and metabolomics analyses

Liu, Y., Duan, H., Chen, Y., Zhang, C., Zhao, J., Narbad, A., Tian, F., Zhai, Q., Yu, L., & Chen, W. (2023) · iMeta · doi:10.1002/imt2.136 · Cited by 43 · see citing works

Unveiling and harnessing the human gut microbiome in the rising burden of non-communicable diseases during urbanization

Huang, Z., Li, Y., Park, H., Ho, M., Bhardwaj, K., Sugimura, N., Lee, H. W., Meng, H., Ebert, M. P., Chao, K., et al. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2237645 · Cited by 41 · 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

Specific metabolite production by gut microbiota as a basis for probiotic function

Ross, R. P., Mills, S., Hill, C., Fitzgerald, G. F., & Stanton, C. (2009) · International Dairy Journal · doi:10.1016/j.idairyj.2009.12.003 · Cited by 60 · see citing works

Metabolic activities and probiotic potential of bifidobacteria

Russell, D. A., Ross, R. P., Fitzgerald, G. F., & Stanton, C. (2011) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2011.06.003 · Cited by 265 · see citing works

Microbial production of bioactives : from fermented functional foods to probiotic mechanisms

Mills, S., Stanton, C., & Ross, R. P. (2009) · Australian Journal of Dairy Technology · Cited by 12 · see citing works

Bacteriocin Production: a Probiotic Trait?

Dobson, A., Cotter, P. D., Ross, R. P., & Hill, C. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.05576-11 · Cited by 690 · see citing works

Bioproduction of Conjugated Linoleic Acid by Probiotic Bacteria Occurs In Vitro and In Vivo in Mice

Ewaschuk, J. B., Walker, J. W. T., Díaz, H., & Madsen, K. L. (2006) · Journal of Nutrition · doi:10.1093/jn/136.6.1483 · Cited by 209 · see citing works