Bacteriocin production: A relatively unharnessed probiotic trait?

An obesity-associated gut microbiome with increased capacity for energy harvest

Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444 · see citing works

Untitled work

Hill (2014) · doi:10.1038/nrgastro.2014.66 · Cited by 9,592 · see citing works

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762 · see citing works

Obesity alters gut microbial ecology

Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176 · see citing works

Richness of human gut microbiome correlates with metabolic markers

Le Chatelier, E., Nielsen, T., Qin, J., Prifti, E., Hildebrand, F., Falony, G., Almeida, M., Arumugam, M., Batto, J.-M., Kennedy, S., et al. (2013) · Nature · doi:10.1038/nature12506 · Cited by 4,662 · see citing works

Cross-talk between <i>Akkermansia muciniphila</i> and intestinal epithelium controls diet-induced obesity

Everard, A., Belzer, C., Geurts, L., Ouwerkerk, J. P., Druart, C., Bindels, L. B., Guiot, Y., Derrien, M., Muccioli, G. G., Delzenne, N. M., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219451110 · Cited by 4,511 · see citing works

Gut metagenome in European women with normal, impaired and diabetic glucose control

Karlsson, F. H., Tremaroli, V., Nookaew, I., Bergström, G., Behre, C. J., Fagerberg, B., Nielsen, J., & Bäckhed, F. (2013) · Nature · doi:10.1038/nature12198 · Cited by 3,115 · see citing works

Defining the normal bacterial flora of the oral cavity

Aas, J. A., Paster, B. J., Stokes, L. N., Olsen, I., & Dewhirst, F. E. (2005) · Journal of Clinical Microbiology · doi:10.1128/jcm.43.11.5721-5732.2005 · Cited by 3,092 · see citing works

Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults

Larsen, N., Vogensen, F. K., van den Berg, F. W. J., Nielsen, D. S., Andreasen, A. S., Pedersen, B. K., Al-Soud, W. A., Sørensen, S. J., Hansen, L. H., & Jakobsen, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009085 · Cited by 2,952 · see citing works

Diet-Induced Obesity Is Linked to Marked but Reversible Alterations in the Mouse Distal Gut Microbiome

Turnbaugh, P. J., Bäckhed, F., Fulton, L., & Gordon, J. I. (2008) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2008.02.015 · Cited by 2,915 · see citing works

Fusobacterium nucleatum Potentiates Intestinal Tumorigenesis and Modulates the Tumor-Immune Microenvironment

Kostic, A. D., Chun, E., Robertson, L., Glickman, J. N., Gallini, C. A., Michaud, M., Clancy, T. E., Chung, D. C., Lochhead, P., Hold, G. L., et al. (2013) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2013.07.007 · Cited by 2,718 · see citing works

Fusobacterium nucleatum Promotes Colorectal Carcinogenesis by Modulating E-Cadherin/β-Catenin Signaling via its FadA Adhesin

Rubinstein, M. R., Wang, X., Liu, W., Hao, Y., Cai, G., & Han, Y. W. (2013) · Cell Host &amp; Microbe · doi:10.1016/j.chom.2013.07.012 · Cited by 2,476 · see citing works

Microbiota and SCFA in lean and overweight healthy subjects

Schwiertz, A., Taras, D., Schäfer, K., Beijer, S., Bos, N. A., Donus, C., & Hardt, P. D. (2010) · Obesity · doi:10.1038/oby.2009.167 · Cited by 2,457 · 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

Occlusal Caries: Biological Approach for Its Diagnosis and Management

Carvalho, J. C., Dige, I., Mačhiulskienė, V., Qvist, V., Bakhshandeh, A., Parolo, C. C. F., & Maltz, M. (2016) · Caries Research · doi:10.1159/000448662 · Cited by 2,159 · see citing works

<i>Fusobacterium nucleatum</i> infection is prevalent in human colorectal carcinoma

Castellarin, M., Warren, R. L., Freeman, J. D., Dreolini, L., Krzywinski, M., Strauss, J., Barnes, R., Watson, P., Allen-Vercoe, E., Moore, R. A., et al. (2012) · Genome Research · doi:10.1101/gr.126516.111 · Cited by 2,043 · see citing works

<i>Akkermansia muciniphila</i> and improved metabolic health during a dietary intervention in obesity: relationship with gut microbiome richness and ecology

Dao, M. C., Everard, A., Aron-Wisnewsky, J., Sokolovska, N., Prifti, E., Verger, E. O., Kayser, B. D., Levenez, F., Chilloux, J., Hoyles, L., et al. (2016) · Gut · doi:10.1136/gutjnl-2014-308778 · Cited by 1,931 · 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

Binding of the Fap2 Protein of Fusobacterium nucleatum to Human Inhibitory Receptor TIGIT Protects Tumors from Immune Cell Attack

Gur, C., Ibrahim, Y., Isaacson, B., Yamin, R., Abed, J., Gamliel, M., Enk, J., Bar-On, Y., Stanietsky-Kaynan, N., Coppenhagen-Glazer, S., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.01.010 · Cited by 1,490 · see citing works

Gut Microbiota and Metabolic Endotoxemia in Young Obese Mexican Subjects

Radilla-Vázquez, R. B., Parra‐Rojas, I., Martínez-Hernández, N. E., Márquez‐Sandoval, F., Illades‐Aguiar, B., & Castro-Alarcón, N. (2016) · Obesity Facts · doi:10.1159/000442479 · Cited by 1,200 · 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

Functional cultures and health benefits

Shah, N. P. (2007) · International Dairy Journal · doi:10.1016/j.idairyj.2007.01.014 · Cited by 793 · see citing works

An opportunistic pathogen isolated from the gut of an obese human causes obesity in germfree mice

Fei, N., & Zhao, L.-P. (2012) · The ISME Journal · doi:10.1038/ismej.2012.153 · Cited by 713 · 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

Invasive potential of gut mucosa-derived fusobacterium nucleatum positively correlates with IBD status of the host

Strauss, J., Kaplan, G. G., Beck, P. L., Rioux, K. P., Panaccione, R., DeVinney, R., Lynch, T., & Allen‐Vercoe, E. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21606 · Cited by 574 · 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

An update on the use and investigation of probiotics in health and disease

Sanders, M. E., Guarner, F., Guerrant, R., Holt, P. R., Quigley, E. M., Sartor, R. B., Sherman, P. M., & Mayer, E. A. (2013) · Gut · doi:10.1136/gutjnl-2012-302504 · Cited by 503 · see citing works

Bacteriocin production augments niche competition by enterococci in the mammalian gastrointestinal tract

Kommineni, S., Bretl, D. J., Lam, V., Chakraborty, R., Hayward, M., Simpson, P., Cao, Y., Bousounis, P., Kristich, C. J., & Salzman, N. H. (2015) · Nature · doi:10.1038/nature15524 · Cited by 458 · see citing works

Acute appendicitis is characterised by local invasion with Fusobacterium nucleatum / necrophorum

Swidsinski, A. V., Dörffel, Y., Loening-Baucke, V. A., Theissig, F., Rueckert, J.-C., Ismail, M., Rau, W. A., Gaschler, D., Weizenegger, M., Kühn, S., et al. (2009) · Gut · doi:10.1136/gut.2009.191320 · Cited by 441 · see citing works

Invited Review: The Scientific Basis of Lactobacillus acidophilus NCFM Functionality as a Probiotic

Sanders, M. E., & Klaenhammer, T. R. (2001) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(01)74481-5 · Cited by 433 · see citing works

World Gastroenterology Organisation Global Guidelines: Probiotics and Prebiotics October 2011

Guarner, F., Khan, A. G., Garisch, J., Eliakim, R., Gangl, A., Thomson, A., Krabshuis, J., Lemair, T., Kaufmann, P., de Paula, J. A., et al. (2012) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e3182549092 · Cited by 418 · 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

Probiotics: from myth to reality. Demonstration of functionality in animal models of disease and in human clinical trials

Dunne, C. P., Murphy, L., Flynn, S., O’Mahony, L., O′Halloran, S., Feeney, M. B., Morrissey, D., Thornton, G., Fitzgerald, G. F., Daly, C., et al. (1999) · Antonie van Leeuwenhoek · doi:10.1023/a:1002065931997 · Cited by 399 · see citing works

Identification of Metabolic Signatures Linked to Anti-Inflammatory Effects of Faecalibacterium prausnitzii

Miquel, S., Leclerc, M., Martín, R., Chain, F., Lenoir, M., Raguideau, S., Hudault, S., Bridonneau, C., Northen, T. R., Bowen, B. P., et al. (2015) · mBio · doi:10.1128/mbio.00300-15 · Cited by 320 · 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

Nisin, an apoptogenic bacteriocin and food preservative, attenuates HNSCC tumorigenesis via CHAC 1

Joo, N. E., Ritchie, K., Kamarajan, P., Miao, D., & Kapila, Y. L. (2012) · Cancer Medicine · doi:10.1002/cam4.35 · Cited by 279 · see citing works

Divergent metabolic outcomes arising from targeted manipulation of the gut microbiota in diet-induced obesity

Murphy, E. F., Cotter, P. D., Hogan, A., O’Sullivan, Ó., Joyce, A., Fouhy, F., Clarke, S. F., Marques, T. M., O’Toole, P. W., Stanton, C., et al. (2012) · Gut · doi:10.1136/gutjnl-2011-300705 · Cited by 273 · see citing works

Bacteriocins as Potential Anticancer Agents

Kaur, S., & Kaur, S. (2015) · Frontiers in Pharmacology · doi:10.3389/fphar.2015.00272 · Cited by 270 · 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

Purification and characterization of the Lactobacillus acidophilus bacteriocin lactacin B

Barefoot, S. F., & Klaenhammer, T. R. (1984) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.26.3.328 · Cited by 246 · 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

Clostridium ramosum Promotes High-Fat Diet-Induced Obesity in Gnotobiotic Mouse Models

Woting, A., Pfeiffer, N., Loh, G., Klaus, S., & Blaut, M. (2014) · mBio · doi:10.1128/mbio.01530-14 · Cited by 224 · see citing works

Identification of Genetic Loci in Lactobacillus plantarum That Modulate the Immune Response of Dendritic Cells Using Comparative Genome Hybridization

Meijerink, M., van Hemert, S., Taverne, N., Wels, M., de Vos, P., Bron, P. A., Savelkoul, H. F. J., van Bilsen, J. H. M., Kleerebezem, M., & Wells, J. M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010632 · Cited by 207 · see citing works

Influence of the probiotic Streptococcus salivarius strain M18 on indices of dental health in children: a randomized double-blind, placebo-controlled trial

Burton, J. P., Drummond, B. K., Chilcott, C. N., Tagg, J. R., Thomson, W. M., Hale, J. D. F., & Wescombe, P. A. (2013) · Journal of Medical Microbiology · doi:10.1099/jmm.0.056663-0 · Cited by 199 · see citing works

Identification of Lactobacillus plantarum genes modulating the cytokine response of human peripheral blood mononuclear cells

van Hemert, S., Meijerink, M., Douwe Molenaar, B., Bron, P. A., de Vos, P., Kleerebezem, M., Wells, J. M., & Marco, M. L. (2010) · BMC Microbiology · doi:10.1186/1471-2180-10-293 · Cited by 196 · see citing works

Safety Assessment of the Oral Cavity Probiotic Streptococcus salivarius K12

Burton, J. P., Wescombe, P. A., Moore, C. J., Chilcott, C. N., & Tagg, J. R. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.4.3050-3053.2006 · Cited by 177 · see citing works

The life history ofLactobacillus acidophilusas a probiotic: a tale of revisionary taxonomy, misidentification and commercial success

Bull, M. J., Plummer, S. F., Marchesi, J. R., & Mahenthiralingam, E. (2013) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12293 · Cited by 171 · see citing works

Developing Oral Probiotics from Streptococcus Salivarius

Wescombe, P. A., Hale, J. D. F., Heng, N. C. K., & Tagg, J. R. (2012) · Future Microbiology · doi:10.2217/fmb.12.113 · Cited by 165 · see citing works

Identification of pioneer viridans streptococci in the oral cavity of human neonates

Pearce, C., Bowden, G. H., Evans, M., Fitzsimmons, S. P., Johnson, J., Sheridan, M. J., Wientzen, R. L., & Cole, M. F. (1995) · Journal of Medical Microbiology · doi:10.1099/00222615-42-1-67 · Cited by 158 · see citing works

High Frequency and Diversity of Antimicrobial Activities Produced by Nasal Staphylococcus Strains against Bacterial Competitors

Janek, D., Zipperer, A., Kulik, A., Krismer, B., & Peschel, A. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1005812 · Cited by 157 · see citing works

Modulation of Helicobacter pylori colonization with cranberry juice and Lactobacillus johnsonii La1 in children

Gotteland, M., Andrews, M., Toledo, M., Muñoz, L. A., Cáceres, P., Anziani, A., Wittig, E., Speisky, H., & Salazar, G. (2008) · Nutrition · doi:10.1016/j.nut.2008.01.007 · Cited by 146 · see citing works

In silico identification of bacteriocin gene clusters in the gastrointestinal tract, based on the Human Microbiome Project’s reference genome database

Walsh, C. J., Guinane, C. M., Hill, C., Ross, R. P., O’Toole, P. W., & Cotter, P. D. (2015) · BMC Microbiology · doi:10.1186/s12866-015-0515-4 · Cited by 146 · see citing works

Fusobacterium nucleatum

Allen‐Vercoe, E., Strauss, J., & Chadee, K. (2011) · Gut Microbes · doi:10.4161/gmic.2.5.18603 · Cited by 145 · see citing works

Comparative and Functional Analysis of Sortase-Dependent Proteins in the Predicted Secretome of Lactobacillus salivarius UCC118

van Pijkeren, J., Canchaya, C. A., Ryan, K. A., Li, Y., Claesson, M. J., Sheil, B., Steidler, L., O’Mahony, L., Fitzgerald, G. F., van Sinderen, D., et al. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.03023-05 · Cited by 141 · see citing works

Diversity and dynamics of bacteriocins from human microbiome

Zheng, J., Gänzle, M. G., Lin, X. B., Ruan, L., & Sun, M. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12662 · Cited by 138 · see citing works

Bacteriocins: Not Only Antibacterial Agents

Drider, D., Bendali, F., Naghmouchi, K., & Chikindas, M. L. (2016) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-016-9223-0 · Cited by 123 · see citing works

The rationale and potential for the reduction of oral malodour using Streptococcus salivarius probiotics

Burton, J. P., Chilcott, C., & Tagg, J. R. (2005) · Oral Diseases · doi:10.1111/j.1601-0825.2005.01084.x · 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

Isolation of Lactobacillus salivarius 1077 (NRRL B-50053) and Characterization of Its Bacteriocin, Including the Antimicrobial Activity Spectrum

Ea, S., Eruslanov, B. V., Levchuk, V. P., Perelygin, V. V., Mitsevich, E. V., Mitsevich, I. P., Stepanshin, J., Dyatlov, I. A., Seal, B. S., & Stern, N. J. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.02481-10 · Cited by 108 · see citing works

Persistence of the Oral Probiotic Streptococcus salivarius M18 Is Dose Dependent and Megaplasmid Transfer Can Augment Their Bacteriocin Production and Adhesion Characteristics

Burton, J. P., Wescombe, P. A., Macklaim, J. M., Chai, M. H. C., MacDonald, K. W., Hale, J. D. F., Tagg, J. R., Reid, G., Gloor, G. B., & Cadieux, P. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065991 · Cited by 87 · see citing works

Lactobacillus acidophilus La-5 increases lactacin B production when it senses live target bacteria

Tabasco, R., García‐Cayuela, T., Peláez, C., & Requena, T. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.04.004 · Cited by 84 · see citing works

Salivaricin 9, a new lantibiotic produced by Streptococcus salivarius

Wescombe, P. A., Upton, M., Renault, P., Wirawan, R. E., Power, D., Burton, J. P., Chilcott, C. N., & Tagg, J. R. (2011) · Microbiology · doi:10.1099/mic.0.044719-0 · Cited by 77 · see citing works

Bactofencin A, a New Type of Cationic Bacteriocin with Unusual Immunity

O'Shea, E. F., O’Connor, P. M., O’Sullivan, Ó., Cotter, P. D., Ross, R. P., & Hill, C. (2013) · mBio · doi:10.1128/mbio.00498-13 · Cited by 69 · see citing works

Production of Multiple Bacteriocins from a Single Locus by Gastrointestinal Strains of Lactobacillus salivarius

O'Shea, E. F., O’Connor, P. M., Raftis, E. J., O’Toole, P. W., Stanton, C., Cotter, P. D., Ross, R. P., & Hill, C. (2011) · Journal of Bacteriology · doi:10.1128/jb.06221-11 · Cited by 69 · see citing works

Salivaricin D, a Novel Intrinsically Trypsin-Resistant Lantibiotic from Streptococcus salivarius 5M6c Isolated from a Healthy Infant

Birri, D. J., Brede, D. A., & Nes, I. F. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.06588-11 · Cited by 68 · 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

Genome Sequence of the Bacteriocin-Producing Oral Probiotic Streptococcus salivarius Strain M18

Heng, N. C. K., Haji-Ishak, N. S., Kalyan, A., Wong, A. Y. C., Lovrić, M., Bridson, J. M., Artamonova, J., Stanton, J. L., Wescombe, P. A., Burton, J. P., et al. (2011) · Journal of Bacteriology · doi:10.1128/jb.06001-11 · Cited by 55 · see citing works

Influence of Adhesion and Bacteriocin Production by Lactobacillus salivarius on the Intestinal Epithelial Cell Transcriptional Response

O’Callaghan, J., Buttó, L. F., MacSharry, J. A., Nally, K., & O’Toole, P. W. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.00507-12 · Cited by 53 · see citing works

Streptococcus salivarius K12 Limits Group B Streptococcus Vaginal Colonization

Patras, K. A., Wescombe, P. A., Rösler, B., Hale, J. D. F., Tagg, J. R., & Doran, K. S. (2015) · Infection and Immunity · doi:10.1128/iai.00409-15 · Cited by 50 · see citing works

Growth, acid production and bacteriocin production by probiotic candidates under simulated colonic conditions

Fernandez, B., Lay, C., Jean, J., & Fliss, I. (2012) · Journal of Applied Microbiology · doi:10.1111/jam.12081 · Cited by 49 · see citing works

The bacteriocin bactofencin A subtly modulates gut microbial populations

Guinane, C. M., Lawton, E. M., O’Connor, P. M., O’Sullivan, Ó., Hill, C., Ross, R. P., & Cotter, P. D. (2016) · Anaerobe · doi:10.1016/j.anaerobe.2016.05.001 · Cited by 49 · see citing works

Salivaricin E and abundant dextranase activity may contribute to the anti-cariogenic potential of the probiotic candidate Streptococcus salivarius JH

Walker, G. V., Heng, N. C. K., Carne, A., Tagg, J. R., & Wescombe, P. A. (2016) · Microbiology · doi:10.1099/mic.0.000237 · Cited by 46 · 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

Impact of Environmental Factors on Bacteriocin Promoter Activity in Gut-Derived Lactobacillus salivarius

Guinane, C. M., Piper, C., Draper, L. A., O’Connor, P. M., Hill, C., Ross, R. P., & Cotter, P. D. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.02339-15 · Cited by 34 · see citing works

Influence of Environmental Factors on Bacteriocin Production by Human Isolates of Lactococcus lactis MM19 and Pediococcus acidilactici MM33

Turgis, M., Vu, K. D., Millette, M., Dupont, C., & Lacroix, M. (2015) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-015-9204-8 · Cited by 30 · see citing works

Probiotics and prebiotics in intestinal health and disease: from biology to the clinic

Sanders, M. E., Merenstein, D. J., Reid, G., Gibson, G. R., & Rastall, R. A. (2019) · Nature Reviews Gastroenterology &amp; Hepatology · doi:10.1038/s41575-019-0173-3 · Cited by 2,059 · see citing works

Microbial Biofilm: A Review on Formation, Infection, Antibiotic Resistance, Control Measures, and Innovative Treatment

Sharma, S. J., Mohler, J. L., Mahajan, S. D., Schwartz, S. A., Bruggemann, L., & Aalinkeel, R. (2023) · Microorganisms · doi:10.3390/microorganisms11061614 · Cited by 1,017 · see citing works

Functions and emerging applications of bacteriocins

Chikindas, M. L., Weeks, R. M., Drider, D., Chistyakov, V. A., & Dicks, L. M. T. (2017) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2017.07.011 · Cited by 574 · see citing works

Biofilms: Formation, drug resistance and alternatives to conventional approaches

Mirghani, R., Saba, T., Khaliq, H., Mitchell, J., Do, L., Chambi, L., Diaz, K., Kennedy, T., Alkassab, K., Huynh, T., et al. (2022) · AIMS Microbiology · doi:10.3934/microbiol.2022019 · Cited by 358 · 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

Fermented foods and gastrointestinal health: underlying mechanisms

Mukherjee, A., Breselge, S., Dimidi, E., Marco, M. L., & Cotter, P. D. (2023) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-023-00869-x · Cited by 264 · see citing works

Antimicrobials for food and feed; a bacteriocin perspective

O’Connor, P. M., Kuniyoshi, T. M., Oliveira, R. P., Hill, C., Ross, R. P., & Cotter, P. D. (2020) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2019.12.023 · Cited by 234 · see citing works

Fighting biofilms with lantibiotics and other groups of bacteriocins

Mathur, H., Field, D., Rea, M. C., Cotter, P. D., Hill, C., & Ross, R. P. (2018) · npj Biofilms and Microbiomes · doi:10.1038/s41522-018-0053-6 · Cited by 213 · 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

Occurrence and Dynamism of Lactic Acid Bacteria in Distinct Ecological Niches: A Multifaceted Functional Health Perspective

George, F., Daniel, C., Thomas, M., Singer, E., Guilbaud, A., Tessier, F. J., Revol-Junelles, A.-M., Borges, F., & Foligné, B. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02899 · Cited by 198 · see citing works

Pathogens, microbiome and the host: emergence of the ecological Koch's postulates

Vonaesch, P., Anderson, M. C., & Sansonetti, P. J. (2018) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuy003 · Cited by 170 · see citing works

Microbiome therapeutics: exploring the present scenario and challenges

Yadav, M., & Chauhan, N. S. (2021) · Gastroenterology report · doi:10.1093/gastro/goab046 · Cited by 157 · see citing works

Symbiosis-inspired approaches to antibiotic discovery

Adnani, N., Rajski, S. R., & Bugni, T. S. (2017) · Natural Product Reports · doi:10.1039/c7np00009j · Cited by 135 · see citing works

Colonization and development of the gut microbiome in calves

Du, Y., Gao, Y., Hu, M., Hou, J., Yang, L., Wang, X., Du, W., Liu, J., & Xu, Q. (2023) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-023-00856-x · Cited by 129 · see citing works

Evaluation of Probiotic Properties and Safety of Enterococcus faecium Isolated From Artisanal Tunisian Meat “Dried Ossban”

Zommiti, M., Cambronel, M., Maillot, O., Barreau, M., Sebei, K., Feuilloley, M. G. J., Ferchichi, M., & Connil, N. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01685 · Cited by 133 · 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

Discovery of a novel lantibiotic nisin O from Blautia obeum A2-162, isolated from the human gastrointestinal tract

Hatziioanou, D., Gherghisan-Filip, C., Saalbach, G., Horn, N., Wegmann, U., Duncan, S. H., Flint, H. J., Mayer, M. J., & Narbad, A. (2017) · Microbiology · doi:10.1099/mic.0.000515 · Cited by 113 · see citing works

Recent advances in microbial fermentation for dairy and health

Hill, D., Sugrue, I., Arendt, E. K., Hill, C., Stanton, C., & Ross, R. P. (2017) · F1000Research · doi:10.12688/f1000research.10896.1 · Cited by 108 · see citing works

Bacteriocins of lactic acid bacteria as biotechnological tools in food and pharmaceuticals: Current applications and future prospects

Daba, G. M., & Elkhateeb, W. A. (2020) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2020.101750 · Cited by 112 · see citing works

Probiotics at War Against Viruses: What Is Missing From the Picture?

Tiwari, S. K., Dicks, L. M. T., Popov, I. V., Karaseva, A. B., Ermakov, A. M., Suvorov, A. N., Tagg, J. R., Weeks, R. M., & Chikindas, M. L. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01877 · Cited by 108 · see citing works

Bacteriocins and Bacteriophages: Therapeutic Weapons for Gastrointestinal Diseases?

Lopetuso, L. R., Giorgio, M. E., Saviano, A., Scaldaferri, F., Gasbarrini, A., & Cammarota, G. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20010183 · Cited by 102 · see citing works

Bacilli as sources of agrobiotechnology: recent advances and future directions

Dame, Z. T., Rahman, M., & Islam, T. (2021) · Green Chemistry Letters and Reviews · doi:10.1080/17518253.2021.1905080 · Cited by 96 · see citing works

Immunomodulatory and prophylactic effects of Bifidobacterium bifidum probiotic strain on influenza infection in mice

Mahooti, M., Abdolalipour, E., Salehzadeh, A., Mohebbi, S. R., Gorji, A., & Ghaemi, A. (2019) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-019-2667-0 · Cited by 94 · see citing works

Recent advances and potentiality of postbiotics in the food industry: Composition, inactivation methods, current applications in metabolic syndrome, and future trends

Zhong, Y., Wang, T., Luo, R., Liu, J., Jin, R., & Peng, X. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2158174 · Cited by 96 · see citing works

Enterococcus spp. as a Producer and Target of Bacteriocins: A Double-Edged Sword in the Antimicrobial Resistance Crisis Context

Almeida-Santos, A. C., Novais, C., Peixe, L. M. S. V., & Freitas, A. R. (2021) · Antibiotics · doi:10.3390/antibiotics10101215 · Cited by 89 · see citing works

The Potential Impact of Probiotics on the Gut Microbiome of Athletes

Wosinska, L., Cotter, P. D., O’Sullivan, Ó., & Guinane, C. M. (2019) · Nutrients · doi:10.3390/nu11102270 · Cited by 86 · see citing works

Using Potential Lactic Acid Bacteria Biofilms and their Compounds to Control Biofilms of Foodborne Pathogens

Todhanakasem, T., & Kornkanok, K. (2020) · Biotechnology Reports · doi:10.1016/j.btre.2020.e00477 · Cited by 82 · see citing works

Colicins and Microcins Produced by Enterobacteriaceae: Characterization, Mode of Action, and Putative Applications

Mladenović, K., Grujović, M. Ž., Koraćević, M., Nikodijević, D. D., Milutinović, M. G., Semedo‐Lemsaddek, T., & Djilas, M. D. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph191811825 · Cited by 79 · see citing works

Effect of a synbiotic supplement on cecal microbial ecology, antioxidant status, and immune response of broiler chickens reared under heat stress

Mohammed, A. A., Jiang, S., Jacobs, J., & Cheng, H. W. (2019) · Poultry Science · doi:10.3382/ps/pez246 · Cited by 78 · see citing works

Co-Cultures of Lactobacillus acidophilus and Bacillus subtilis Enhance Mucosal Barrier by Modulating Gut Microbiota-Derived Short-Chain Fatty Acids

Xie, Z., Li, M., Qian, M., Yang, Z., & Han, X. (2022) · Nutrients · doi:10.3390/nu14214475 · Cited by 78 · see citing works

The Challenge of Applications of Probiotics in Gastrointestinal Diseases

Wolfe, W., Xiang, Z., Yu, X., Li, P., Chen, H., Yao, M., Fei, Y., Huang, Y., Yin, Y., & Xiao, H. (2023) · Advanced Gut & Microbiome Research · doi:10.1155/2023/1984200 · Cited by 73 · see citing works

Microbial metabolites as modulators of the infant gut microbiome and host-microbial interactions in early life

Roager, H. M., Stanton, C., & Hall, L. J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2192151 · Cited by 67 · see citing works

Recent advances in modulating the microbiome

Quigley, E. M. M., & Gajula, P. (2020) · F1000Research · doi:10.12688/f1000research.20204.1 · Cited by 68 · see citing works

Heterologous biosynthesis and characterization of a glycocin from a thermophilic bacterium

Kaunietis, A., Buivydas, A., Čitavičius, D. J., & Kuipers, O. P. (2019) · Nature Communications · doi:10.1038/s41467-019-09065-5 · Cited by 65 · see citing works

In Vitro and in Vivo Selection of Potentially Probiotic Lactobacilli From Nocellara del Belice Table Olives

Guantario, B., Zinno, P., Schifano, E., Roselli, M., Perozzi, G., Palleschi, C., Uccelletti, D., & Devirgiliis, C. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00595 · Cited by 61 · see citing works

Microbiological Sensing Technologies: A Review

Abbasian, F., Ghafar‐Zadeh, E., & Magierowski, S. (2018) · Bioengineering · doi:10.3390/bioengineering5010020 · Cited by 60 · see citing works

Production of multiple bacteriocins, including the novel bacteriocin gassericin M, by Lactobacillus gasseri LM19, a strain isolated from human milk

García-Gutiérrez, E., O’Connor, P. M., Colquhoun, I. J., Vior, N. M., Rodríguez, J. M., Mayer, M. J., Cotter, P. D., & Narbad, A. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10493-3 · Cited by 60 · see citing works

What Do We Know about the Microbiome in Cystic Fibrosis? Is There a Role for Probiotics and Prebiotics?

van Dorst, J. M., Tam, R. Y., & Ooi, C. Y. (2022) · Nutrients · doi:10.3390/nu14030480 · Cited by 60 · see citing works

Actinomyces Produces Defensin-Like Bacteriocins (Actifensins) with a Highly Degenerate Structure and Broad Antimicrobial Activity

Sugrue, I., O’Connor, P. M., Hill, C., Stanton, C., & Ross, R. P. (2019) · Journal of Bacteriology · doi:10.1128/jb.00529-19 · Cited by 58 · see citing works

Potential Novel Food-Related and Biomedical Applications of Nanomaterials Combined with Bacteriocins

Naskar, A., & Kim, K.-S. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13010086 · Cited by 56 · see citing works

Seeds, fermented foods, and agricultural by-products as sources of plant-derived antibacterial peptides

Chai, T., Tan, Y. N., Ee, K. Y., Xiao, J., & Wong, F. (2019) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1561418 · Cited by 53 · see citing works

Brazilian Journal of Development

(2021) · doi:10.34117/25258761 · Cited by 46 · see citing works

Use of Lactiplantibacillus plantarum ZJ316 as a starter culture for nitrite degradation, foodborne pathogens inhibition and microbial community modulation in pickled mustard fermentation

Zhang, X., Han, J., Zheng, X., Yan, J., Chen, X., Zhou, Q., Zhao, X., Gu, Q., & Li, P. (2022) · Food Chemistry X · doi:10.1016/j.fochx.2022.100344 · Cited by 45 · see citing works

Beneficial modulation of human health in the oral cavity and beyond using bacteriocin-like inhibitory substance-producing streptococcal probiotics

Tagg, J. R., Harold, L. K., Jain, R., & Hale, J. D. F. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1161155 · Cited by 45 · see citing works

Bacteriocin Occurrence and Activity in Escherichia coli Isolated from Bovines and Wastewater

Cameron, A., Zaheer, R., Adator, E. H., Barbieri, R., Reuter, T., & McAllister, T. A. (2019) · Toxins · doi:10.3390/toxins11080475 · Cited by 44 · see citing works

Food and gut originated bacteriocins involved in gut microbe-host interactions

Teng, K., Huang, F., Liu, Y., Wang, Y., Xia, T., Yun, F., & Zhong, J. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2022.2082860 · Cited by 40 · see citing works

Lactobacillus paracasei HII01 enhances lifespan and promotes neuroprotection in Caenorhabditis elegans

Kumaree, K. K., Prasanth, M. I., Sivamaruthi, B. S., Kesika, P., Tencomnao, T., Chaiyasut, C., & Prasansuklab, A. (2023) · Scientific Reports · doi:10.1038/s41598-023-43846-9 · Cited by 40 · see citing works

Probiotic-Based Bacteriocin: Immunity Supplementation Against Viruses. An Updated Review

Umair, M., Jabbar, S., Zhaoxin, L., Zhang, J., Abid, M., Khan, K.-U.-R., Korma, S. A., Alghamdi, M. A., El‐Saadony, M. T., El-Hack, M. E. A., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.876058 · Cited by 41 · see citing works

Postbiotics in inflammatory bowel disease: efficacy, mechanism, and therapeutic implications

Wang, S., Wang, P., Wang, D., Shen, S., Wang, S., Li, Y., & Chen, H. (2024) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.13721 · Cited by 41 · see citing works

Defining how microorganisms benefit human health

Marco, M. L. (2020) · Microbial Biotechnology · doi:10.1111/1751-7915.13685 · Cited by 37 · see citing works

Nanomedicine for drug resistant pathogens and COVID-19 using mushroom nanocomposite inspired with bacteriocin – A review

Srinivash, M., Krishnamoorthi, R., Mahalingam, P. U., Malaikozhundan, B., Bharathakumar, S., Gurushankar, K., Dhanapal, K., Samy, K. K., & Perumal, A. B. (2023) · Inorganic Chemistry Communications · doi:10.1016/j.inoche.2023.110682 · Cited by 37 · see citing works

The potency of the broad spectrum bacteriocin, bactofencin A, against staphylococci is highly dependent on primary structure, N-terminal charge and disulphide formation

Connor, P. M. O., Shea, E. F. O., Cotter, P. D., Hill, C., & Ross, R. P. (2018) · Scientific Reports · doi:10.1038/s41598-018-30271-6 · Cited by 37 · see citing works

Antimicrobial peptide production in response to gut microbiota imbalance

Cardoso, M. H. E. S., Meneguetti, B. T., Oliveira-Júnior, N. G., Macedo, M. L. R., & Franco, O. L. (2022) · Peptides · doi:10.1016/j.peptides.2022.170865 · Cited by 36 · see citing works

Bacteriocins: antibiotics in the age of the microbiome

Egan, K. M., Ross, R. P., & Hill, C. (2017) · Emerging Topics in Life Sciences · doi:10.1042/etls20160015 · Cited by 33 · see citing works

Colicin FY inhibits pathogenic Yersinia enterocolitica in mice

Bosák, J., Micenková, L., Hrala, M., Pomorská, K., Bosakova, M. K., Krejčı́, P., Göpfert, E., Faldyna, M., & Šmajs, D. (2018) · Scientific Reports · doi:10.1038/s41598-018-30729-7 · Cited by 33 · see citing works

The functional capacity of plantaricin-producing Lactobacillus plantarum SF9C and S-layer-carrying Lactobacillus brevis SF9B to withstand gastrointestinal transit

Butorac, K., Banić, M., Novak, J., Pavunc, A. L., Uroić, K., Durgo, K., Oršolić, N., Kukolj, M., Radović, S., Scalabrin, S., et al. (2020) · Microbial Cell Factories · doi:10.1186/s12934-020-01365-6 · Cited by 33 · see citing works

Probiotics and Prebiotics

Sanders, M. E., Goh, Y. J., & Klaenhammer, T. R. (2019) · ASM Press eBooks · doi:10.1128/9781555819972.ch32 · Cited by 32 · see citing works

Being a better version of yourself: genetically engineered probiotic bacteria as host defense enhancers in the control of intestinal pathogens

Carolak, E., Czajkowska, J., Stypułkowska, A., Waszczuk, W., Dutkiewicz, A., & Grzymajło, K. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2519696 · Cited by 31 · see citing works

Lactobacilli Isolated From Wild Boar (Sus scrofa) Antagonize Mycobacterium bovis Bacille Calmette-Guerin (BCG) in a Species-Dependent Manner

Bravo, M., Combes, T., Martínez, F. O., Cerrato, R., Rey, J., García‐Jiménez, W., Fernández‐Llario, P., Risco, D., & Gutierrez‐Merino, J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01663 · Cited by 30 · see citing works

Health benefits, antimicrobial activities, and potential applications of probiotics: A review

Sepehr, A., Miri, S. T., Aghamohammad, S., Rahimirad, N., Milani, M., Pourshafie, M. R., & Rohani, M. (2024) · Medicine · doi:10.1097/md.0000000000032412 · Cited by 32 · see citing works

Microcin J25 Exhibits Inhibitory Activity Against Salmonella Newport in Continuous Fermentation Model Mimicking Swine Colonic Conditions

Naimi, S., Zirah, S., Taher, M. B., Théolier, J., Fernandez, B., Rebuffat, S., & Fliss, I. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00988 · Cited by 29 · see citing works

Cell-free supernatant of Streptococcus salivarius M18 impairs the pathogenic properties of Pseudomonas aeruginosa and Klebsiella pneumonia

Tunçer, S., & Karaçam, S. (2020) · Archives of Microbiology · doi:10.1007/s00203-020-02005-8 · Cited by 29 · see citing works

Enterococcus faecium Regulates Honey Bee Developmental Genes

Du, Y., Luo, S., & Zhou, X. Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212105 · Cited by 29 · see citing works

The Role of Gut Microbiota, Nutrition, and Physical Activity in Depression and Obesity—Interdependent Mechanisms/Co-Occurrence

Sochacka, K., Kotowska, A., & Lachowicz, S. (2024) · Nutrients · doi:10.3390/nu16071039 · Cited by 33 · see citing works

Food, Health, and Environmental Impact of Lactic Acid Bacteria: The Superbacteria for Posterity

Akpoghelie, P. O., Edo, G. I., Mafe, A. N., Isoje, E. F., Igbuku, U. A., Ali, A. B. M., Yousif, E. A., Owheruo, J. O., Oberhiri, S. O., Essaghah, A. E. A., et al. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10546-x · Cited by 28 · see citing works

Acid lactic lactobacilli as a biotechnological toll to improve food quality and human health

de Sousa, M. A., Rama, G. R., de Souza, C. F. V., & Granada, C. E. (2019) · Biotechnology Progress · doi:10.1002/btpr.2937 · Cited by 28 · see citing works

Recent Innovations in Non-dairy Prebiotics and Probiotics: Physiological Potential, Applications, and Characterization

Khan, F. F., Sohail, A., Ghazanfar, S., Ahmad, A., Riaz, A., Abbasi, K. S., Ibrahim, M. S., Uzair, M., & Arshad, M. U. (2022) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-022-09983-9 · Cited by 26 · see citing works

Gut mucosal and adipose tissues as health targets of the immunomodulatory mechanisms of probiotics

Ashaolu, T. J., & Fernández‐Tomé, S. (2021) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2021.04.040 · Cited by 25 · see citing works

Complete Genome Sequence of the Newly Developed Lactobacillus acidophilus Strain With Improved Thermal Adaptability

Jeon, S., Kim, H., Choi, Y., Cho, S., Seo, M., & Kim, H. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.697351 · Cited by 23 · see citing works

Action and immunomodulatory mechanisms, formulations, and safety concerns of probiotics

Ashaolu, T. J., Greff, B., & Varga, L. (2024) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.2024-006 · Cited by 24 · see citing works

Impact of spatial proximity on territoriality among human skin bacteria

Hernandez‐Valdes, J. A., Zhou, L., de Vries, M. P., & Kuipers, O. P. (2020) · npj Biofilms and Microbiomes · doi:10.1038/s41522-020-00140-0 · Cited by 23 · see citing works

A Colicin M-Type Bacteriocin from Pseudomonas aeruginosa Targeting the HxuC Heme Receptor Requires a Novel Immunity Partner

Ghequire, M. G. K., & Öztürk, B. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.00716-18 · Cited by 22 · see citing works

Beyond biopreservatives, bacteriocins biotechnological applications: History, current status, and promising potentials

Daba, G. M., Elnahas, M. O., & Elkhateeb, W. A. (2021) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2021.102248 · Cited by 21 · see citing works

Human Systemic Immune Response to Ingestion of the Oral Probiotic Streptococcus salivarius BLIS K12

Laws, G., Hale, J. D. F., & Kemp, R. A. (2021) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-021-09822-3 · Cited by 20 · see citing works

Evaluation of the Potential Protective Effects of Lactobacillus Strains against Helicobacter pylori Infection: A Randomized, Double-Blinded, Placebo-Controlled Trial

Wang, S., Zhang, M., Yu, L., Tian, F., Lu, W., Wang, G., Chen, W., Wang, J., & Zhai, Q. (2022) · Canadian Journal of Infectious Diseases and Medical Microbiology · doi:10.1155/2022/6432750 · Cited by 20 · see citing works

BacSJ—Another Bacteriocin with Distinct Spectrum of Activity that Targets Man-PTS

Tymoszewska, A., Walczak, P., & Aleksandrzak‐Piekarczyk, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217860 · Cited by 20 · see citing works

Preventive Effect of Depolymerized Sulfated Galactans from Eucheuma serra on Enterotoxigenic Escherichia coli-Caused Diarrhea via Modulating Intestinal Flora in Mice

Ma, Y., Zhang, Q., Liu, W., Chen, Z., Zou, C., Fu, L., Wang, Y., & Liu, Y. (2021) · Marine Drugs · doi:10.3390/md19020080 · Cited by 19 · see citing works

Prebiotics and probiotics

Arruda, H. S., Geraldi, M. V., Cedran, M. F., Bicas, J. L., Maróstica, M. R., & Pastore, G. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823569-0.00006-0 · Cited by 20 · see citing works

Transporter Protein-Guided Genome Mining for Head-to-Tail Cyclized Bacteriocins

Major, D., Flanzbaum, L., Lussier, L., Davies, C., Caldo, K. M. P., & Acedo, J. Z. (2021) · Molecules · doi:10.3390/molecules26237218 · Cited by 17 · see citing works

Deciphering probiotic potential: a comprehensive guide to probiogenomic analyses

Sabino, Y. N. V., Paiva, A. D., Fonseca, B. R., Medeiros, J. D., & Machado, A. B. F. (2025) · Future Microbiology · doi:10.1080/17460913.2025.2492472 · Cited by 16 · see citing works

Characterization of the Biosynthetic Gene Cluster of Enterocin F4-9, a Glycosylated Bacteriocin

Maky, M. A., Ishibashi, N., Nakayama, J., & Zendo, T. (2021) · Microorganisms · doi:10.3390/microorganisms9112276 · Cited by 16 · see citing works

The ColM Family, Polymorphic Toxins Breaching the Bacterial Cell Wall

Ghequire, M. G. K., Buchanan, S. K., & Mot, R. D. (2018) · mBio · doi:10.1128/mbio.02267-17 · Cited by 16 · see citing works

Role Of Bacteriocin In Tackling The Global Problem Of Multi-Drug Resistance : An Updated Review

Bonhi, K. L. R., & Imran, S. (2019) · Bioscience Biotechnology Research Communications · doi:10.21786/bbrc/12.3/8 · Cited by 16 · see citing works

Bacteriocin production and distribution of bacteriocin-encoding genes in enterococci from dogs

Kubašová, I., Diep, D. B., Ovchinnikov, K. V., Lauková, A., & Strompfová, V. (2019) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2019.11.016 · Cited by 16 · see citing works

Nisin E Is a Novel Nisin Variant Produced by Multiple Streptococcus equinus Strains

Sugrue, I., Hill, D., O’Connor, P. M., Day, L., Stanton, C., Hill, C., & Ross, R. P. (2023) · Microorganisms · doi:10.3390/microorganisms11020427 · Cited by 16 · see citing works

Genomic analysis of Enterococcus durans LAB18S, a potential probiotic strain isolated from cheese

Comerlato, C. B., Prichula, J., Siqueira, F. M., Ritter, A. C., Varela, A. P. M., Mayer, F. Q., & Brandelli, A. (2022) · Genetics and Molecular Biology · doi:10.1590/1678-4685-gmb-2021-0201 · Cited by 14 · see citing works

Bioinformatic mining for RiPP biosynthetic gene clusters in Bacteroidales reveals possible new subfamily architectures and novel natural products

Fernández-Cantos, M. V., García-Morena, D., Yi, Y., Liang, L., Gómez, E., & Kuipers, O. P. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1219272 · Cited by 14 · see citing works

Thermophilin 109 is a naturally produced broad spectrum bacteriocin encoded within the blp gene cluster of Streptococcus thermophilus

Renye, J. A., Somkuti, G. A., & Steinberg, D. H. (2018) · Biotechnology Letters · doi:10.1007/s10529-018-02637-3 · Cited by 13 · see citing works

Production of Vitamins, Exopolysaccharides and Bacteriocins by Probiotic Bacteria

Linares, D. M., Fitzgerald, G. F., Hill, C., Stanton, C., & Ross, R. P. (2017) · doi:10.1002/9781119214137.ch9 · Cited by 13 · see citing works

Harnessing the probiotic properties and immunomodulatory effects of fermented food-derived Limosilactobacillus fermentum strains: implications for environmental enteropathy

Prakash, V., Madhavan, A., Veedu, A. P., Babu, P., Jothish, A., Nair, S. S., Suhail, A., Prabhakar, M., Sain, T., Rajan, R., et al. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1200926 · Cited by 12 · see citing works

Food Additives and Preservatives

Harshitha, T., Dasalkar, A. H., Parinitha, A., & Yannam, S. K. (2024) · Springer eBooks · doi:10.1007/978-981-97-3261-6_15 · Cited by 12 · see citing works

Proteus mirabilis Employs a Contact-Dependent Killing System against Competing Enterobacteriaceae

Kiani, D., Santus, W., Kiernan, K. A., & Behnsen, J. (2021) · mSphere · doi:10.1128/msphere.00321-21 · Cited by 12 · see citing works

Genomic analysis of Enterococcus durans LAB18S, a potential probiotic strain isolated from cheese

Comerlato, C. B., Prichula, J., Siqueira, F. M., Ritter, A. C., Varela, A. P. M., Mayer, F. Q., & Brandelli, A. (2022) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 12 · see citing works

Microbiome-based therapeutics for metabolic disorders: harnessing microbial intrusions for treatment

Ahmed, N., Gaur, V., Kamle, M., Chauhan, A., Chauhan, R., Kumar, P., & Singh, N. A. (2025) · Frontiers in Medical Technology · doi:10.3389/fmedt.2025.1695329 · Cited by 13 · see citing works

Selection of lactic acid bacteria as a probiotic and evaluated its performance on gnotobiotic catfish Clarias sp.

Turnip, E. R., Widanarni, W., & Meryandini, A. (2018) · Jurnal Akuakultur Indonesia · doi:10.19027/jai.17.1.68-80 · Cited by 11 · see citing works

Bacteriocins: Applications in Food Preservation and Therapeutics

Thapar, P., & Salooja, M. K. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.106871 · Cited by 11 · see citing works

Exploring regional variations in probiotics: Implications for efficacy and application

Abavisani, M., Khoshroo, N., Tafti, P., Moghadam, M. A., Kesharwani, P., & Sahebkar, A. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107963 · Cited by 8 · see citing works

The Role of Probiotics and Their Postbiotic Metabolites in Post-COVID-19 Syndrome

Jach, M. E., Sajnaga, E., Bumbul, M., Serefko, A., Borowicz, K. K., Golczyk, H., Kieliszek, M., & Wiater, A. (2025) · Molecules · doi:10.3390/molecules30204130 · Cited by 8 · see citing works

Mixed culture of Bacillus aerius B81e and Lactiplantibacillus paraplantarum L34b-2 derived from in vivo screening using hybrid catfish exhibits high probiotic effects on Pangasius bocourti

Meidong, R., Buatong, A., Nakao, M., Sakai, K., & Tongpim, S. (2021) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2021.06.006 · Cited by 7 · see citing works

Preventive Methods for Colorectal Cancer Through Dietary Interventions: A Focus on Gut Microbiota Modulation

Zhong, Y., Liu, Z., Wang, Y., Cai, S., Qiao, Z., Hu, X., Wang, T., & Yi, J. (2024) · Food Reviews International · doi:10.1080/87559129.2024.2414908 · Cited by 8 · 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

Lack of Heterogeneity in Bacteriocin Production Across a Selection of Commercial Probiotic Products

Hegarty, J. W., Guinane, C. M., Ross, R. P., Hill, C., & Cotter, P. D. (2017) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-017-9326-2 · Cited by 9 · see citing works

Probiotici – mit ili stvarnost?

Slović, A. (2011)

The Potential of Bacteriocin-Producing Probiotics and Associated Caveats

Gordon, D. M. (2009) · Future Microbiology · doi:10.2217/fmb.09.78 · Cited by 24 · see citing works

Enhancing the probiotic properties of escherichia coli nissle: when less is more

Bartram, E. (2023) · doi:10.25560/114519