Lactobacillaceae and Cell Adhesion: Genomic and Functional Screening

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

Thompson, J. D., Higgins, D. G., & Gibson, T. J. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.22.4673 · Cited by 64,617 · see citing works

Primer3 on the WWW for General Users and for Biologist Programmers

Rozen, S., & Skaletsky, H. (2003) · Humana Press eBooks · doi:10.1385/1-59259-192-2:365 · Cited by 14,952 · see citing works

Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA

Muyzer, G., de Waal, E. C., & Uitterlinden, A. G. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.3.695-700.1993 · Cited by 11,455 · see citing works

TM4: a free, open-source system for microarray data management and analysis

Saeed, A. I., Sharov, V., White, J., Li, J., Liang, W., Bhagabati, N., Braisted, J., Klapa, M., Currier, T., Thiagarajan, M., et al. (2003) · BioTechniques · doi:10.2144/03342mt01 · Cited by 4,837 · see citing works

Stem cells, self-renewal, and differentiation in the intestinal epithelium.

van der Flier, L. G., & Clevers, H. (2009) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163145 · Cited by 1,859 · 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

Comparative genomics of the lactic acid bacteria.

Makarova, K., Slesarev, A., Wolf, Y., Sorokin, A., Mirkin, B., Koonin, E., Pavlov, A., Pavlova, N., Karamychev, V., Polouchine, N., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607117103 · Cited by 1,391 · see citing works

Genes and Molecules of Lactobacilli Supporting Probiotic Action

Lebeer, S., Vanderleyden, J., & De Keersmaecker, S. C. J. (2008) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00017-08 · Cited by 1,013 · see citing works

Extracellular MUC3 mucin secretion follows adherence of Lactobacillus strains to intestinal epithelial cells in vitro

Mack, D. R., Ahrné, S., Hyde, L., Wei, S. H., & Hollingsworth, M. A. (2003) · Gut · doi:10.1136/gut.52.6.827 · Cited by 666 · see citing works

Complete genome sequence of the probiotic lactic acid bacterium Lactobacillus acidophilus NCFM

Altermann, E., Russell, W. M., Azcárate-Peril, M. A., Barrangou, R., Buck, B. L., McAuliffe, O. E., Souther, N. E., Dobson, A., Duong, T., Callanan, M. J., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409188102 · Cited by 594 · see citing works

Determination of the Core of a Minimal Bacterial Gene Set

Gil, R., Silva, F. J., Peretó, J., & Moya, A. (2004) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.68.3.518-537.2004 · Cited by 573 · see citing works

Mucin-bacterial interactions in the human oral cavity and digestive tract

Derrien, M., van Passel, M. W. J., van de Bovenkamp, J. H. B., Schipper, R., de Vos, W., & Dekker, J. (2010) · Gut Microbes · doi:10.4161/gmic.1.4.12778 · Cited by 556 · see citing works

Probiotics inhibit enteropathogenic E. coliadherence in vitro by inducing intestinal mucin gene expression.

Mack, D., Michail, S., Wei, S., McDougall, L., & Hollingsworth, M. (1999) · American Journal of Physiology - Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.276.4.g941 · Cited by 544 · see citing works

The VSL#3 probiotic formula induces mucin gene expression and secretion in colonic epithelial cells

Caballero‐Franco, C., Keller, K., Simone, C. D., & Chadee, K. (2006) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00265.2006 · Cited by 493 · 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

Cell Surface-Associated Elongation Factor Tu Mediates the Attachment of <i>Lactobacillus johnsonii</i> NCC533 (La1) to Human Intestinal Cells and Mucins

Granato, D., Bergonzelli, G. E., Pridmore, R. D., Marvin, L., Rouvet, M., & Corthésy-Theulaz, I. E. (2004) · Infection and Immunity · doi:10.1128/iai.72.4.2160-2169.2004 · Cited by 410 · see citing works

Functional Analysis of Putative Adhesion Factors in <i>Lactobacillus acidophilus</i> NCFM

Buck, B. L., Altermann, E., Svingerud, T., & Klaenhammer, T. R. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.12.8344-8351.2005 · Cited by 390 · see citing works

A high-molecular-mass cell-surface protein from Lactobacillus reuteri 1063 adheres to mucus components The GenBank accession number for the sequence reported in this paper is AF120104.

Roos, S., & Jonsson, H. (2002) · Microbiology · doi:10.1099/00221287-148-2-433 · Cited by 376 · see citing works

Mucin gene structure and expression: protection vs. adhesion

van Klinken, B. J., Dekker, J. P., Büller, H. A., & Einerhand, A. W. C. (1995) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1995.269.5.g613 · Cited by 319 · see citing works

Biodiversity-Based Identification and Functional Characterization of the Mannose-Specific Adhesin of<i>Lactobacillus plantarum</i>

Pretzer, G., Snel, J., Molenaar, D., Wiersma, A., Bron, P. A., Lambert, J., de Vos, W. M., van der Meer, R., Smits, M. A., & Kleerebezem, M. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.17.6128-6136.2005 · Cited by 316 · see citing works

Comparative Genome Analysis of Lactobacillus reuteri and Lactobacillus fermentum Reveal a Genomic Island for Reuterin and Cobalamin Production

Morita, H., Toh, H., Fukuda, S., Horikawa, H., Oshima, K., Suzuki, T., Murakami, M., Hisamatsu, S., Kato, Y., Takizawa, T., et al. (2008) · DNA Research · doi:10.1093/dnares/dsn009 · Cited by 305 · see citing works

Microbial adhesins to gastrointestinal mucus

Juge, N. (2011) · Trends in Microbiology · doi:10.1016/j.tim.2011.10.001 · Cited by 304 · see citing works

Characterization and probiotic potential of Lactobacillus plantarum strains isolated from cheeses

Zago, M., Fornasari, M. E., Carminati, D., Burns, P., Suárez, V., Vinderola, G., Reinheimer, J. A., & Giraffa, G. (2011) · Food Microbiology · doi:10.1016/j.fm.2011.02.009 · Cited by 298 · see citing works

Functional and Probiotic Attributes of an Indigenous Isolate of Lactobacillus plantarum

Kaushik, J. K., Kumar, A., Duary, R. K., Mohanty, A. K., Grover, S., & Batish, V. K. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008099 · Cited by 295 · see citing works

Differential expression of the human mucin genes MUC1 to MUC5 in relation to growth and differentiation of different mucus-secreting HT-29 cell subpopulations

Lesuffleur, T., Porchet, N., Aubert, J., Swallow, D. M., Gum, J. R., Kim, Y. S., & Real, F. X. (1993) · Journal of Cell Science · doi:10.1242/jcs.106.3.771 · Cited by 278 · see citing works

Mucosal Adhesion Properties of the Probiotic Lactobacillus rhamnosus GG SpaCBA and SpaFED Pilin Subunits

von Ossowski, I., Reunanen, J., Satokari, R. M., Vesterlund, S., Kankainen, M., Huhtinen, H., Tynkkynen, S., Salminen, S., de Vos, W. M., & Palva, A. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.01958-09 · Cited by 216 · see citing works

Strain-specific diversity of mucus-binding proteins in the adhesion and aggregation properties of Lactobacillus reuteri

MacKenzie, D. A., Jeffers, F., Parker, M. L., Vibert-Vallet, A., Bongaerts, R. J., Roos, S., Walter, J., & Juge, N. (2010) · Microbiology · doi:10.1099/mic.0.043265-0 · Cited by 202 · see citing works

Comparative analysis of proteins with a mucus-binding domain found exclusively in lactic acid bacteria

Boekhorst, J., Helmer, Q., Kleerebezem, M., & Siezen, R. J. (2005) · Microbiology · doi:10.1099/mic.0.28415-0 · Cited by 191 · see citing works

Comparison ofin vitromodels to study bacterial adhesion to the intestinal epithelium

Laparra, J. M., & Sanz, Y. (2009) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2009.02729.x · Cited by 189 · see citing works

GeneFisher--software support for the detection of postulated genes.

Giegerich, R., Meyer, F., & Schleiermacher, C. (1996) · PubMed · Cited by 181 · see citing works

Potential probiotic lactic acid bacteria Lactobacillus rhamnosus (HN001), Lactobacillus acidophilus (HN017) and Bifidobacterium lactis (HN019) do not degrade gastric mucin in vitro

Zhou, J. S., Gopal, P. K., & Gill, H. S. (2001) · International Journal of Food Microbiology · doi:10.1016/s0168-1605(00)00398-6 · Cited by 178 · see citing works

Cell surface Lactobacillus plantarum LA 318 glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH) adheres to human colonic mucin

Kinoshita, H., Uchida, H., Kawai, Y., Kawasaki, T., Wakahara, N., Matsuo, H., Watanabe, M., Kitazawa, H., Ohnuma, S., Miura, K., et al. (2008) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2007.03679.x · Cited by 163 · see citing works

Drastic changes in fecal and mucosa-associated microbiota in adult patients with short bowel syndrome

Joly, F., Mayeur, C., Bruneau, A., Noordine, M.-L., Meylheuc, T., Langella, P., Messing, B., Duée, P., Cherbuy, C., & Thomas, M. (2010) · Biochimie · doi:10.1016/j.biochi.2010.02.015 · Cited by 155 · see citing works

Genetic Screening of Functional Properties of Lactic Acid Bacteria in a Fermented Pearl Millet Slurry and in the Metagenome of Fermented Starchy Foods

Turpin, W., Humblot, C., & Guyot, J. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.05988-11 · Cited by 152 · see citing works

Functional Roles of Aggregation-Promoting-Like Factor in Stress Tolerance and Adherence of <i>Lactobacillus acidophilus</i> NCFM

Goh, Y. J., & Klaenhammer, T. R. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.00030-10 · Cited by 149 · see citing works

Surface displaced alfa-enolase of Lactobacillus plantarum is a fibronectin binding protein

Castaldo, C., Vastano, V., Siciliano, R. A., Candela, M., Vici, M., Muscariello, L., Marasco, R., & Sacco, M. (2009) · Microbial Cell Factories · doi:10.1186/1475-2859-8-14 · Cited by 146 · see citing works

Inhibition of Escherichia coli O157:H7 attachment by interactions between lactic acid bacteria and intestinal epithelial cells.

Kim, Y., Kim, S. H., Whang, K. Y., Kim, Y. J., & Oh, S. (2008) · PubMed · Cited by 142 · 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

A Mucus Adhesion Promoting Protein, MapA, Mediates the Adhesion ofLactobacillus reuterito Caco-2 Human Intestinal Epithelial Cells

MIYOSHI, Y., Okada, S., Uchimura, T., & Satoh, E. (2006) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.50688 · Cited by 139 · see citing works

Fusobacterium nucleatum Infection of Colonic Cells Stimulates MUC2 Mucin and Tumor Necrosis Factor Alpha

Dharmani, P., Strauss, J., Ambrose, C., Allen‐Vercoe, E., & Chadee, K. (2011) · Infection and Immunity · doi:10.1128/iai.05118-11 · Cited by 139 · see citing works

A Collagen-Binding S-Layer Protein in Lactobacillus crispatus

Toba, T., Virkola, R., Westerlund‐Wikström, B., Björkman, Y., Sillanpää, J., VARTIO, T., Kalkkinen, N., & Korhonen, T. K. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.7.2467-2471.1995 · Cited by 136 · see citing works

Rapid PCR-based procedure to identify lactic acid bacteria: application to six common Lactobacillus species

Chagnaud, P., Machinis, K., Coutte, L., Marecat, A., & Mercenier, A. (2001) · Journal of Microbiological Methods · doi:10.1016/s0167-7012(00)00244-x · Cited by 131 · see citing works

Isolation and physiological study of an amylolytic strain of Lactobacillus plantarum

Giraud, É., Brauman, A., Keleke, S., Lelong, B., & Raimbault, M. (1991) · Applied Microbiology and Biotechnology · doi:10.1007/bf00208160 · Cited by 127 · see citing works

Lactobacilli as multifaceted probiotics with poorly disclosed molecular mechanisms

Turpin, W., Humblot, C., Thomas, M., & Guyot, J. (2010) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2010.07.032 · Cited by 119 · see citing works

Extracellular proteins of Lactobacillus crispatus enhance activation of human plasminogen

Kainulainen, V., Edelman, S., Antikainen, J., Baumann, M., Lähteenmäki, K., & Korhonen, T. (2007) · Microbiology · doi:10.1099/mic.0.2006/000901-0 · Cited by 119 · see citing works

Isolation and characterization of new amylolytic strains of Lactobacillus fermentum from fermented maize doughs (mawè and ogi) from Benin

Agati, V., Morlon‐Guyot, J., Morlon‐Guyot, J., Talamond, P., & Hounhouigan, J. D. (1998) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.1998.853527.x · Cited by 114 · see citing works

Lactobacillus manihotivorans sp. nov., a new starch-hydrolysing lactic acid bacterium isolated during cassava sour starch fermentation

MORLON-GUYOT, J., GUYOT, J. P., POT, B., DE HAUT, I. J., & RAIMBAULT, M. (1998) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-48-4-1101 · Cited by 112 · see citing works

Expression of the mucus adhesion genes Mub and MapA, adhesion-like factor EF-Tu and bacteriocin gene plaA of Lactobacillus plantarum 423, monitored with real-time PCR

Ramiah, K., van Reenen, C. A., & Dicks, L. M. T. (2007) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2007.02.011 · Cited by 110 · see citing works

Functional Characterization of a Mucus-Specific LPXTG Surface Adhesin from Probiotic Lactobacillus rhamnosus GG

von Ossowski, I., Satokari, R. M., Reunanen, J., Lebeer, S., Keersmaecker, S. C. J. D., Vanderleyden, J., de Vos, W. M., & Palva, A. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.02497-10 · Cited by 107 · see citing works

2‐DE and MS analysis of key proteins in the adhesion of Lactobacillus plantarum, a first step toward early selection of probiotics based on bacterial biomarkers

Izquierdo, E., Horvatovich, P. L., Marchioni, E., Werner, D., Sanz, Y., & Ennahar, S. (2009) · Electrophoresis · doi:10.1002/elps.200800399 · Cited by 106 · see citing works

Lactobacillus sakei: recent developments and future prospects

Champomier‐Vergès, M., Chaillou, S., Cornet, M., & Zagorec, M. (2001) · Research in Microbiology · doi:10.1016/s0923-2508(01)01267-0 · Cited by 105 · see citing works

Functional Analysis of the p40 and p75 Proteins from Lactobacillus casei BL23

Bäuerl, C., Pérez‐Martínez, G., Yan, F., Polk, D. B., & Monedero, V. (2010) · Microbial Physiology · doi:10.1159/000322233 · Cited by 103 · see citing works

Characterization of a Mucin cDNA Clone Isolated from HT-29 Mucus-secreting Cells.

Lesuffleur, T., Roche, F., Hill, A. S., Lacasa, M., Fox, M., Swallow, D. M., Zweibaum, A., & Real, F. X. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.23.13665 · Cited by 102 · see citing works

Comparative High-Density Microarray Analysis of Gene Expression during Growth of <i>Lactobacillus helveticus</i> in Milk versus Rich Culture Medium

Smeianov, V. V., Wechter, P., Broadbent, J. R., Hughes, J. E., Rodríguez, B. T., Christensen, T. K., Ardö, Y., & Steele, J. L. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00005-07 · Cited by 97 · see citing works

Lactobacillus plantarum Reduces the In Vitro Secretory Response of Intestinal Epithelial Cells to Enteropathogenic Escherichia coli Infection

Michail, S., & Abernathy, F. (2002) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-200209000-00021 · Cited by 96 · see citing works

Probiotic Properties of the 2-Substituted (1,3)-β- d -Glucan-Producing Bacterium Pediococcus parvulus 2.6

de Palencia, P. F., Werning, M. L., Sierra‐Filardi, E., Dueñas, M. T., Irastorza, A., Corbí, A. L., & López, P. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00394-09 · Cited by 95 · see citing works

Characterization of MabA, a modulator ofLactobacillus rhamnosusGG adhesion and biofilm formation

Vélez, M. P., Petrova, M., Lebeer, S., Verhoeven, T. L. A., Claes, I. J. J., Lambrichts, I., Tynkkynen, S., Vanderleyden, J., & Keersmaecker, S. C. J. D. (2010) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2010.00680.x · Cited by 94 · see citing works

Role of Transporter Proteins in Bile Tolerance ofLactobacillus acidophilus

Pfeiler, E. A., & Klaenhammer, T. R. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00495-09 · Cited by 91 · see citing works

Benefits and pitfalls of using microarrays to monitor bacterial gene expression during infection.

HINTON, J., HAUTEFORT, I., ERIKSSON, S., THOMPSON, A., & RHEN, M. (2004) · Current Opinion in Microbiology · doi:10.1016/j.mib.2004.04.009 · Cited by 85 · see citing works

Expression of fibronectin-binding protein FbpA modulates adhesion in Streptococcus gordonii The GenBank accession number for the sequence reported in this paper is X65164.

Christie, J., McNab, R., & Jenkinson, H. F. (2002) · Microbiology · doi:10.1099/00221287-148-6-1615 · Cited by 77 · see citing works

Functional and phenotypic characterization of a protein from Lactobacillus acidophilus involved in cell morphology, stress tolerance and adherence to intestinal cells

O’Flaherty, S., & Klaenhammer, T. R. (2010) · Microbiology · doi:10.1099/mic.0.043158-0 · Cited by 60 · see citing works

Identification of a new adhesin-like protein from Lactobacillus mucosae ME-340 with specific affinity to the human blood group A and B antigens

Watanabe, M., Kinoshita, H., Nitta, M., Yukishita, R., Kawai, Y., Kimura, K., Taketomo, N., Yamazaki, Y., Tateno, Y., Miura, K., et al. (2010) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2010.04719.x · Cited by 54 · see citing works

Impact of the Metabolic Activity of Streptococcus thermophilus on the Colon Epithelium of Gnotobiotic Rats

Rul, F., Ben-Yahia, L., Chegdani, F., Wrzosek, L., Thomas, S., Noordine, M.-L., Gitton, C., Cherbuy, C., Langella, P., & Thomas, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.168666 · Cited by 51 · see citing works

Lactobacillus plantarum Extracellular Chitin-Binding Protein and Its Role in the Interaction between Chitin, Caco-2 Cells, and Mucin

Sánchez, B., González-Tejedo, C., Ruas‐Madiedo, P., Urdaci, M. C., & Margollés, A. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.02080-10 · Cited by 50 · see citing works

Characterization of intestinal bacteria tightly bound to the human ileal epithelium

Fakhry, S. S., Manzo, N., D’Apuzzo, E., Pietrini, L., Sorrentini, I., Ricca, E., Felice, M. D., & Baccigalupi, L. (2009) · Research in Microbiology · doi:10.1016/j.resmic.2009.09.009 · Cited by 49 · see citing works

Lectin Microarray Reveals Binding Profiles of Lactobacillus casei Strains in a Comprehensive Analysis of Bacterial Cell Wall Polysaccharides

Yasuda, E., Tateno, H., Hirabarashi, J., Iino, T., & Sako, T. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.00240-11 · Cited by 47 · see citing works

Global transcriptional response of Lactobacillus reuteri to the sourdough environment

Hüfner, E., Britton, R. A., Roos, S., Jonsson, H., & Hertel, C. (2008) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2008.06.005 · Cited by 45 · see citing works

Two Atypical Enteropathogenic Escherichia coli Strains Induce the Production of Secreted and Membrane-Bound Mucins To Benefit Their Own Growth at the Apical Surface of Human Mucin-Secreting Intestinal HT29-MTX Cells

Vieira, M. A. M., Gomes, T. A. T., Ferreira, A. J. P., Knöbl, T., Servin, A. L., & Moal, V. L.-L. (2010) · Infection and Immunity · doi:10.1128/iai.01115-09 · Cited by 43 · see citing works

Adhesion characteristics of lactobacillus is a criterion of the probiotic choice

Георгиевич, К. Э., Ермолаев, А. В., Викторовна, А. И., Yashina, N. V., Чеснокова, В. Л., & Далин, М. В. (2008) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-008-0058-x · Cited by 42 · see citing works

Interactive transcriptome analysis of enterohemorrhagic Escherichia coli (EHEC) O157:H7 and intestinal epithelial HT-29 cells after bacterial attachment

Kim, Y., Oh, S., Park, S., & Kim, S. H. (2009) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2009.03.002 · Cited by 40 · see citing works

Carbohydrate Metabolism Is Essential for the Colonization of Streptococcus thermophilus in the Digestive Tract of Gnotobiotic Rats

Thomas, M., Wrzosek, L., Ben-Yahia, L., Noordine, M.-L., Gitton, C., Chevret, D., Langella, P., Mayeur, C., Cherbuy, C., & Rul, F. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028789 · Cited by 39 · see citing works

Lactobacillus and Bifidobacterium species do not secrete protease that cleaves the MUC2 mucin which organises the colon mucus

Subramani, D. B., Johansson, M., Dahlén, G., & Hansson, G. C. (2010) · Beneficial Microbes · doi:10.3920/bm2010.0039 · Cited by 32 · see citing works

Adhesive Properties, Extracellular Protein Production, and Metabolism in the Lactobacillus rhamnosus GG Strain when Grown in the Presence of Mucin

Sánchez, B. (2010) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.0911.11007 · Cited by 30 · see citing works

Adhesion of human enterotoxigenic Escherichia coli to human mucus secreting HT-29 cell subpopulations in culture.

Kernéis, S. M., Bernet‐Camard, M., Coconnier, M. H., & Servin, A. L. (1994) · Gut · doi:10.1136/gut.35.10.1449 · Cited by 30 · see citing works

Bactéries lactiques et probiotiques

Luquet, F. M., Corrieu, G., & Marteau, P. R. (2006) · Acta Endoscopica · doi:10.1007/bf03006054 · Cited by 16 · see citing works

Discovering probiotic microorganisms: in vitro, in vivo, genetic and omics approaches

Papadimitriou, K., Ζουμποπούλου, Γ., Foligné, B., Alexandraki, V., Κάζου, Μ., Pot, B., & Tsakalidou, E. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00058 · Cited by 388 · see citing works

African fermented foods and probiotics

Franz, C. M. A. P., Huch, M., Mathara, J. M., Abriouel, H., Benomar, N., Reid, G., Gálvez, A., & Holzapfel, W. H. (2014) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2014.08.033 · Cited by 265 · see citing works

The effect of cell surface components on adhesion ability of Lactobacillus rhamnosus

Polak‐Berecka, M., Waśko, A. D., Paduch, R., Skrzypek, T., & Sroka‐Bartnicka, A. (2014) · Antonie van Leeuwenhoek · doi:10.1007/s10482-014-0245-x · Cited by 150 · see citing works

In vitro evaluation of the mucin-adhesion ability and probiotic potential of Lactobacillus mucosae LM1

Valeriano, V. D., Parungao-Balolong, M. M., & Kang, D. K. (2014) · Journal of Applied Microbiology · doi:10.1111/jam.12539 · Cited by 147 · see citing works

Lactic Acid Bacteria Isolated from Bovine Mammary Microbiota: Potential Allies against Bovine Mastitis

Bouchard, D. S., Seridan, B., Saraoui, T., Rault, L., Germon, P., Gonzalez-Moreno, C., Nader-Macias, F. M. E., Baud, D., François, P., Chuat, V., et al. (2015) · PLOS ONE · doi:10.1371/journal.pone.0144831 · Cited by 144 · see citing works

Isolation of lactic acid bacteria with probiotic potentials from kimchi, traditional Korean fermented vegetable

Lee, K. W., Shim, J. M., Park, S.-K., Heo, H. J., Kim, H., Ham, K., & Kim, J. H. (2016) · LWT · doi:10.1016/j.lwt.2016.03.029 · Cited by 133 · see citing works

Intestinal in vitro cell culture models and their potential to study the effect of food components on intestinal inflammation

de León-Rodríguez, M. D. C. P., Guyot, J., & Laurent-Babot, C. (2018) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2018.1506734 · 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

Genome Analysis of Lactobacillus plantarum Isolated From Some Indian Fermented Foods for Bacteriocin Production and Probiotic Marker Genes

Goel, A., Halami, P. M., & Tamang, J. P. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00040 · Cited by 125 · see citing works

Structural basis for adaptation of lactobacilli to gastrointestinal mucus

Etzold, S., Coleman, O. I., MacKenzie, D. A., Tailford, L. E., Gunning, A. P., Walshaw, J., Hemmings, A. M., & Juge, N. (2013) · Environmental Microbiology · doi:10.1111/1462-2920.12377 · Cited by 111 · see citing works

Surface proteins of Propionibacterium freudenreichii are involved in its anti-inflammatory properties

Maréchal, C. L., Péton, V., Plé, C., Vroland, C., Jardin, J., Briard‐Bion, V., Durant, G., Chuat, V., Loux, V., Foligné, B., et al. (2014) · Journal of Proteomics · doi:10.1016/j.jprot.2014.07.018 · Cited by 107 · see citing works

Evaluation of the Function of Probiotics, Emphasizing the Role of their Binding to the Intestinal Epithelium in the Stability and their Effects on the Immune System

Javanshir, N., Hosseini, G. N. G., Sadeghi, M., Esmaeili, R., Satarikia, F., Ahmadian, G., & Fard, N. A. (2021) · Biological Procedures Online · doi:10.1186/s12575-021-00160-w · Cited by 109 · see citing works

Probiotic attributes of Lactobacillus fermentum isolated from human feces and dairy products

Archer, A. C., & Halami, P. M. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-6679-x · Cited by 101 · see citing works

Preliminary probiotic and technological characterization of Pediococcus pentosaceus strain KID7 and in vivo assessment of its cholesterol-lowering activity

Damodharan, K., Lee, Y. S., Palaniyandi, S. A., Yang, S. H., & Suh, J. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00768 · Cited by 97 · see citing works

Zebrafish gut colonization by mCherry-labelled lactic acid bacteria

Russo, P., Iturria, I., Mohedano, M. L., Caggianiello, G., Rainieri, S., Fiocco, D., Pardo, M. Á., López, P., & Spano, G. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-6351-x · Cited by 92 · see citing works

Functional properties of Lactobacillus plantarum strains: A multivariate screening study

Guidone, A., Zotta, T., Ross, R. P., Stanton, C., Rea, M. C., Parente, E., & Ricciardi, A. (2013) · LWT · doi:10.1016/j.lwt.2013.10.036 · Cited by 85 · see citing works

Probiotic properties of Pediococcus strains isolated from jeotgals, salted and fermented Korean sea-food

Lee, K. W., Park, J. Y., Sa, H. D., Jeong, J. H., Jin, D. E., Heo, H. J., & Kim, J. H. (2014) · Anaerobe · doi:10.1016/j.anaerobe.2014.06.013 · Cited by 77 · see citing works

Screening of cell surface properties of potential probiotic lactobacilli isolated from human milk

Rokana, N., Singh, B. P., Thakur, N., Sharma, C., Gulhane, R. D., & Panwar, H. (2018) · Journal of Dairy Research · doi:10.1017/s0022029918000432 · Cited by 73 · see citing works

Identification of novel anti-inflammatory probiotic strains isolated from pulque

Torres-Maravilla, E., Lenoir, M., Mayorga-Reyes, L., Allain, T., Sokol, H., Langella, P., Sánchez-Pardo, M. E., & Bermúdez‐Humarán, L. G. (2015) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-015-7049-4 · Cited by 73 · see citing works

Comprehensive pan‐genome analysis of <i>Lactiplantibacillus plantarum</i> complete genomes

Carpi, F. M., Coman, M. M., Silvi, S., Picciolini, M., Verdenelli, M. C., & Napolioni, V. (2022) · Journal of Applied Microbiology · doi:10.1111/jam.15199 · Cited by 72 · see citing works

Food-grade TiO2 is trapped by intestinal mucus in vitro but does not impair mucin O-glycosylation and short-chain fatty acid synthesis in vivo: implications for gut barrier protection

Talbot, P., Radziwill-Bienkowska, J. M., Kamphuis, J. B. J., Steenkeste, K., Bettini, S., Robert, V., Noordine, M.-L., Mayeur, C., Gaultier, E., Langella, P., et al. (2018) · Journal of Nanobiotechnology · doi:10.1186/s12951-018-0379-5 · Cited by 65 · see citing works

Isolation and characterization of potential probiotic Lactobacilli from leaves of food plants for possible additives in pellet feeding

Samedi, L., & Charles, A. L. (2019) · Annals of Agricultural Sciences · doi:10.1016/j.aoas.2019.05.004 · Cited by 59 · see citing works

A proposed framework for an appropriate evaluation scheme for microorganisms as novel foods with a health claim in Europe

Miquel, S., Beaumont, M., Martín, R., Langella, P., Braesco, V., & Thomas, M. (2015) · Microbial Cell Factories · doi:10.1186/s12934-015-0229-1 · Cited by 58 · see citing works

Alterations in gut bacterial and fungal microbiomes are associated with bacterial Keratitis, an inflammatory disease of the human eye

Jayasudha, R., Chakravarthy, S. K., Prashanthi, G. S., Sharma, S., Garg, P., Murthy, S. I., & Shivaji, S. (2018) · Journal of Biosciences · doi:10.1007/s12038-018-9798-6 · Cited by 56 · see citing works

Probiotic properties of Weissella cibaria and Leuconostoc citreum isolated from tejuino – A typical Mexican beverage

Silva, M. S., Ramos, C. L., González‐Ávila, M., Gschaedler, A., Arrizón, J., Schwan, R. F., & Dias, D. R. (2017) · LWT · doi:10.1016/j.lwt.2017.08.009 · Cited by 56 · see citing works

Galacto-Oligosaccharides Modulate the Juvenile Gut Microbiome and Innate Immunity To Improve Broiler Chicken Performance

Richards, P. J., Lafontaine, G. M. F., Connerton, P. L., Liang, L., Asiani, K., Fish, N. M., & Connerton, I. F. (2020) · mSystems · doi:10.1128/msystems.00827-19 · Cited by 48 · see citing works

AggLb Is the Largest Cell-Aggregation Factor from Lactobacillus paracasei Subsp. paracasei BGNJ1-64, Functions in Collagen Adhesion, and Pathogen Exclusion In Vitro

Miljković, M., Strahinić, I., Tolinački, M., Živković, M., Kojić, S., Golić, N., & Kojić, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126387 · Cited by 48 · see citing works

Local domestication of lactic acid bacteria via cassava beer fermentation

Colehour, A., Meadow, J. F., Cepon‐Robins, T. J., Gildner, T. E., Liebert, M. A., Urlacher, S. S., Bohannan, B. J. M., Snodgrass, J. J., & Sugiyama, L. S. (2014) · PeerJ · doi:10.7717/peerj.479 · Cited by 48 · see citing works

Functional in vitro screening of Lactobacillus strains isolated from Tunisian camel raw milk toward their selection as probiotic

Mahmoudi, I., Moussa, O. B., Khaldi, T. E. M., Kebouchi, M., Soligot, C., Roux, Y. L., & Hassouna, M. (2016) · Small Ruminant Research · doi:10.1016/j.smallrumres.2016.03.016 · Cited by 46 · see citing works

In vitro adhesion and anti-inflammatory properties of native Lactobacillus fermentum and Lactobacillus delbrueckii spp.

Archer, A. C., Kurrey, N. K., & Halami, P. M. (2018) · Journal of Applied Microbiology · doi:10.1111/jam.13757 · Cited by 44 · see citing works

Screening, Characterization and In Vitro Evaluation of Probiotic Properties Among Lactic Acid Bacteria Through Comparative Analysis

Devi, S. M., Archer, A. C., & Halami, P. M. (2015) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-015-9195-5 · Cited by 42 · see citing works

Eczema-protective probiotic alters infant gut microbiome functional capacity but not composition: sub-sample analysis from a RCT

Murphy, R., Morgan, X. C., Wang, C., Wickens, K. L., Purdie, G., Fitzharris, P., Otal, A., Lawley, B., Stanley, T., Barthow, C. A., et al. (2018) · Beneficial Microbes · doi:10.3920/bm2017.0191 · Cited by 40 · see citing works

Structural and molecular insights into novel surface‐exposed mucus adhesins from L actobacillus reuteri human strains

Etzold, S., MacKenzie, D. A., Jeffers, F., Walshaw, J., Roos, S., Hemmings, A. M., & Juge, N. (2014) · Molecular Microbiology · doi:10.1111/mmi.12574 · Cited by 40 · see citing works

Whole genome sequencing and analysis of probiotic characteristics for Lactiplantibacillus plantarum EL2 isolated from yak yogurt

Zheng, X., Liang, Q., Zhao, B., Song, X., & Zhang, Y. (2024) · LWT · doi:10.1016/j.lwt.2024.116039 · Cited by 39 · see citing works

Formation of <i>In Vitro</i> Mixed-Species Biofilms by Lactobacillus pentosus and Yeasts Isolated from Spanish-Style Green Table Olive Fermentations

León-Romero, Á., Domínguez-Manzano, J., Garrido-Fernández, A., Arroyo-López, F. N., & Jiménez-Díaz, R. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.02727-15 · Cited by 38 · see citing works

Novel Aggregation Promoting Factor AggE Contributes to the Probiotic Properties of Enterococcus faecium BGGO9-28

Veljović, K., Popović, N., Miljković, M., Tolinački, M., Terzić-Vidojević, A., & Kojić, M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01843 · Cited by 38 · see citing works

Health-Promoting Nature of Lactococcus lactis IBB109 and Lactococcus lactis IBB417 Strains Exhibiting Proliferation Inhibition and Stimulation of Interleukin-18 Expression in Colorectal Cancer Cells

Sałański, P., Kowalczyk, M., Bardowski, J. K., & Szczepankowska, A. K. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.822912 · Cited by 37 · see citing works

Implication of sortase-dependent proteins of Streptococcus thermophilus in adhesion to human intestinal epithelial cell lines and bile salt tolerance

Kebouchi, M., Galia, W., Genay, M., Soligot, C., Lecomte, X., Awussi, A. A., Perrin, C., Roux, É., Dary, A., & Roux, Y. L. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7322-1 · Cited by 36 · see citing works

A large scale in vitro screening of Streptococcus thermophilus strains revealed strains with a high anti-inflammatory potential

Junjua, M., Kechaou, N., Chain, F., Awussi, A. A., Roussel, Y., Perrin, C., Roux, É., Langella, P., Bermúdez‐Humarán, L. G., Roux, Y. L., et al. (2016) · LWT · doi:10.1016/j.lwt.2016.02.006 · Cited by 35 · see citing works

Comparative genomics and functional analysis of a highly adhesive dairy Lactobacillus paracasei subsp. paracasei IBB3423 strain

Koryszewska-Bagińska, A., Gawor, J., Nowak, A., Grynberg, M., & Aleksandrzak‐Piekarczyk, T. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10010-1 · Cited by 35 · see citing works

Probiotic Properties of Lactobacillus Strains Isolated from Table Olive Biofilms

Benítez‐Cabello, A., Torres-Maravilla, E., Bermúdez‐Humarán, L. G., Langella, P., Martín, R., Jiménez‐Díaz, R., & Arroyo‐López, F. N. (2019) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-019-09604-y · Cited by 32 · see citing works

Probiotic properties of lactic acid bacteria isolated from traditionally prepared dry starters of the Eastern Himalayas

Pradhan, P., & Tamang, J. P. (2021) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-020-02975-3 · Cited by 32 · see citing works

In vitro and genetic screening of probiotic properties of lactic acid bacteria isolated from naturally fermented cow-milk and yak-milk products of Sikkim, India

Rai, R., & Tamang, J. P. (2022) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-021-03215-y · Cited by 32 · see citing works

Systematic evaluation of genome-wide metabolic landscapes in lactic acid bacteria reveals diet- and strain-specific probiotic idiosyncrasies

Koduru, L., Lakshmanan, M., Lee, Y. Q., Ho, P. L., Lim, P. Y., Ler, W. X., Ng, S. K., Kim, D., Park, D., Banu, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111735 · Cited by 31 · see citing works

Contribution of plasmid-encoded peptidase S8 (PrtP) to adhesion and transit in the gut of Lactococcus lactis IBB477 strain.

Radziwill-Bienkowska, J. M., Robert, V., Drabot, K., Chain, F., Cherbuy, C., Langella, P., Thomas, M., Bardowski, J. K., Mercier-Bonin, M., & Kowalczyk, M. (2017) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-017-8334-1 · Cited by 30 · see citing works

First Insight into the Probiotic Properties of Ten Streptococcus thermophilus Strains Based on In Vitro Conditions

Zhang, J., Liu, M., Xu, J., Qi, Y., Zhao, N., & Fan, M. (2019) · Current Microbiology · doi:10.1007/s00284-019-01840-3 · Cited by 27 · see citing works

Determination of expression and activity of genes involved in starch metabolism in Lactobacillus plantarum A6 during fermentation of a cereal-based gruel

Humblot, C., Turpin, W., Chevalier, F., Picq, C., Rochette, I., & Guyot, J. (2014) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2014.05.016 · Cited by 26 · see citing works

Probiogenomics of Lactobacillus delbrueckii subsp. lactis CIDCA 133: In Silico, In Vitro, and In Vivo Approaches

de Jesus, L. C. L., Drumond, M. M., Aburjaile, F. F., Sousa, T. J., Coelho-Rocha, N. D., Profeta, R., Brenig, B., Mancha-Agresti, P. D. C., & Azevedo, V. (2021) · Microorganisms · doi:10.3390/microorganisms9040829 · Cited by 26 · see citing works

Probiotic Properties of Bifidobacterium longum KABP042 and Pediococcus pentosaceus KABP041 Show Potential to Counteract Functional Gastrointestinal Disorders in an Observational Pilot Trial in Infants

Astó, E., Huedo, P., Altadill, T., Aguiló, M., Sticco, M., Pérez, M., & Espadaler, J. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.741391 · Cited by 26 · see citing works

In VitroandIn VivoSurvival and Colonic Adhesion ofPediococcus acidilacticiMTCC5101 in Human Gut

Balgir, P. P., Kaur, B., Kaur, T., Daroch, N., & Kaur, G. (2013) · BioMed Research International · doi:10.1155/2013/583850 · Cited by 26 · see citing works

Characterization of two new strains of Lactococcus lactis for their probiotic efficacy over commercial synbiotics consortia

Bandyopadhyay, B., Das, S., Mitra, P. K., Kundu, A., Mandal, V., Adhikary, R., Mandal, V., & Mandal, N. C. (2022) · Brazilian Journal of Microbiology · doi:10.1007/s42770-022-00685-6 · Cited by 25 · see citing works

Characterization of Mucus-Related Properties of Streptococcus thermophilus: From Adhesion to Induction

Fernandez, N., Wrzosek, L., Radziwill-Bienkowska, J. M., Ringot-Destrez, B., Duviau, M.-P., Noordine, M.-L., Laroute, V., Robert, V., Cherbuy, C., Daveran‐Mingot, M., et al. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00980 · Cited by 25 · see citing works

Antioncogenic potential of probiotics: Challenges and future prospective

Chattaraj, S., Mitra, D., Chattaraj, A., Chattaraj, M., Kundu, M., Ganguly, A., & MOHAPATRA, P. K. D. (2023) · Indian Journal of Microbiology Research · doi:10.18231/j.ijmr.2023.001 · Cited by 24 · see citing works

Whole‐genome based validation of the adaptive properties of Indian origin probiotic Lactobacillus helveticus MTCC 5463

Suja Rani, S., Prajapati, J. B., & Joshi, C. G. (2014) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.6721 · Cited by 24 · see citing works

PCR of crtNM combined with analytical biochemistry: An efficient way to identify carotenoid producing lactic acid bacteria

Turpin, W., Renaud, C., Avallone, S., Hammoumi, A., Guyot, J., & Humblot, C. (2015) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2015.12.003 · Cited by 24 · see citing works

High‐sugar diet intake, physical activity, and gut microbiota crosstalk: Implications for obesity in rats

Neves, V. G. D. O., de Oliveira, D. T., Oliveira, D. C., Perucci, L. O., dos Santos, T. A. P., Fernandes, I. D. C., de Sousa, G. G., Barboza, N. R., & Guerra‐Sá, R. (2020) · Food Science & Nutrition · doi:10.1002/fsn3.1842 · Cited by 24 · see citing works

Isolation of Yeasts from Some Homemade Fermented Cow-Milk Products of Sikkim and Their Probiotic Characteristics

Lama, S., & Tamang, J. P. (2022) · Fermentation · doi:10.3390/fermentation8120664 · Cited by 23 · see citing works

The Administration Matrix Modifies the Beneficial Properties of a Probiotic Mix of Bifidobacterium animalis subsp. lactis BB-12 and Lactobacillus acidophilus LA-5

Pápai, G., Torres-Maravilla, E., Chain, F., Varga-Visi, É., Antal, O., Naár, Z., Bermúdez‐Humarán, L. G., Langella, P., & Martín, R. (2020) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-020-09702-2 · Cited by 22 · see citing works

Anti-inflammation and adhesion enhancement properties of the multifunctional LPxTG-motif surface protein derived from the Lactobacillus reuteri DSM 8533

Xu, H., Lao, L., Ji, C., Lü, Q., Guo, Y., Pan, D., & Wu, Z. F. (2022) · Molecular Immunology · doi:10.1016/j.molimm.2022.04.004 · Cited by 21 · see citing works

Structure and Immunomodulatory Activity of a Recombinant Mucus-Binding Protein of <i>Lactobacillus Acidophilus</i>

Xiong, R., Pan, D., Wu, Z., Guo, Y., Zeng, X., & Lian, L. (2018) · Future Microbiology · doi:10.2217/fmb-2018-0222 · Cited by 20 · see citing works

Behavior of Lactobacilli Isolated from Fermented Slurry (ben-saalga) in Gnotobiotic Rats

Turpin, W., Humblot, C., Noordine, M.-L., Wrzosek, L., Tomas, J., Mayeur, C., Cherbuy, C., Guyot, J., & Thomas, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057711 · Cited by 20 · see citing works

Prospecting of potentially probiotic lactic acid bacteria from bovine mammary ecosystem: imminent partners from bacteriotherapy against bovine mastitis

Steinberg, R. S., Silva, L. C. S. E., de Souza, M. R., Reis, R. B., Bicalho, A. F., Nunes, J. P. S., Dias, A. A. M., Nicoli, J. R., Neumann, E., & Nunes, Á. C. (2021) · International Microbiology · doi:10.1007/s10123-021-00209-6 · Cited by 20 · see citing works

Fermentation of Shiikuwasha (Citrus depressa Hayata) pomace by lactic acid bacteria to generate new functional materials

Kimoto‐Nira, H., Moriya, N., Nogata, Y., Sekiyama, Y., & Toguchi, Y. (2018) · International Journal of Food Science & Technology · doi:10.1111/ijfs.13980 · Cited by 17 · see citing works

Lactobacillus fermentum strains of dairy-product origin adhere to mucin and survive digestive juices

Aziz, K., Zaidi, A., Fatima, H. N., & Tariq, M. (2019) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001090 · Cited by 17 · see citing works

Metagenomics and metagenome-assembled genomes mining of health benefits in jalebi batter, a naturally fermented cereal-based food of India

Shangpliang, H. N. J., & Tamang, J. P. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113130 · Cited by 16 · see citing works

Over-production of exopolysaccharide by Lacticaseibacillus rhamnosus CNCM I-3690 strain cutbacks its beneficial effect on the host

Martín, R., Benítez‐Cabello, A., Kulakauskas, S., Viana, M. V. C., Chamignon, C., Courtin, P., Carbonne, C., Chain, F., Pham, H., Derrien, M., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-32116-3 · Cited by 14 · see citing works

Metagenome-assembled genomes for biomarkers of bio-functionalities in Laal dahi, an Indian ethnic fermented milk product

Shangpliang, H. N. J., & Tamang, J. P. (2023) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2023.110300 · Cited by 13 · see citing works

Immunomodulation and Intestinal Morpho-Functional Aspects of a Novel Gram-Negative Bacterium Rouxiella badensis subsp. acadiensis

Yahfoufi, N., Alsadi, N., Mallet, J., Kulshreshtha, G., Hincke, M. T., Ismail, N., & Matar, C. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.569119 · Cited by 13 · see citing works

Potentially probioticLimosilactobacillus reuterifrom human milk strengthens the gut barrier in T84 cells and a murine enteroid model

Anjum, J., Quach, A., Wongkrasant, P., Nazir, S., Tariq, M., Barrett, K. E., & Zaidi, A. (2022) · Journal of Applied Microbiology · doi:10.1093/jambio/lxac029 · Cited by 12 · see citing works

LES ASPECTS TECHNOLOGIQUES, MICROBIOLOGIQUES ET NUTRITIONNELS DES ALIMENTS FERMENTES A BASE DE LAIT ET DE MIL EN AFRIQUE DE L’OUEST.

Université Ouaga I Professeur Joseph Ki-Zerbo, U. D. F. E. D. R. E. S. D. L. V. E. D. L. T., Tankoano, A., Diop, M. B., Université Gaston Berger, U. D. F. E. D. R. D. S. A., Sawadogo‐Lingani, H., Kaoré, D., IJAR, Savadogo, A., & Université Ouaga I Professeur Joseph Ki-Zerbo, U. D. F. E. D. R. E. S. D. L. V. E. D. L. T. (2017) · International Journal of Advanced Research · doi:10.21474/ijar01/5211 · Cited by 12 · see citing works

Safety assessment of probiotic Lactiplantibacillus plantarum MCC5231 and its persistence in gastrointestinal tract

Goel, A., & Halami, P. M. (2024) · Microbial Pathogenesis · doi:10.1016/j.micpath.2024.106824 · Cited by 11 · see citing works

Compositional Quality and Possible Gastrointestinal Performance of Marketed Probiotic Supplements

Aziz, G., Zaidi, A., & Tariq, M. (2022) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-022-09931-7 · Cited by 11 · see citing works

Cottage cheese enriched with lactobacilli encapsulated in alginate–chitosan microparticles forestalls perishability and augments probiotic activity

Ahmed, S. A., Muhammad, T., & Zaidi, A. (2021) · Journal of Food Processing and Preservation · doi:10.1111/jfpp.15473 · Cited by 11 · see citing works

iTRAQ proteomic analysis of N‐acetylmuramic acid mediated anti‐inflammatory capacity in LPS‐induced RAW 264.7 cells

Wu, Z. F., Pan, D., Guo, Y., Zeng, X., & Sun, Y. (2015) · PROTEOMICS · doi:10.1002/pmic.201400580 · Cited by 10 · see citing works

Synthetic Mucins as Glycan-Defined Prebiotics

Alty, J. W., Barnes, C. E., Nicoli, A. M., Turner, B. S., Beneman, E. A., Dugan, A. E., Brucks, S. D., Kruger, A. G., Schrock, R. R., Ribbeck, K., et al. (2025) · ACS Central Science · doi:10.1021/acscentsci.5c00317 · Cited by 10 · see citing works

An Isolate of Streptococcus mitis Displayed In Vitro Antimicrobial Activity and Deleterious Effect in a Preclinical Model of Lung Infection

Mathieu, E., Marquant, Q., Chain, F., Bouguyon, E., Saint‐Criq, V., Goffic, R. L., Descamps, D., Langella, P., Tompkins, T. A., Binda, S., et al. (2023) · Nutrients · doi:10.3390/nu15020263 · Cited by 9 · see citing works

Gemcitabine and docetaxel in metastatic breast cancer.

Seidman, A. D. (2004) · PubMed · Cited by 9 · see citing works

Probiogenomic analysis of Limosilactobacillus fermentum SD7, a probiotic candidate with remarkable aggregation abilities

Yaikhan, T., Wonglapsuwan, M., Pahumunto, N., Nokchan, N., Teanpaisan, R., & Surachat, K. (2025) · Heliyon · doi:10.1016/j.heliyon.2025.e42451 · Cited by 8 · see citing works

Genomic and Phenotypic Insight into the Probiotic Potential of Lactic Acid Bacterial spp. Associated with the Human Gut Mucosa

Aziz, K., Gilbert, J. A., & Zaidi, A. (2023) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10193-0 · Cited by 8 · see citing works

Probiotic Validation of a Non-native, Thermostable, Phytase-Producing Bacterium: Streptococcus thermophilus

Paul, P., & Balaji, S. (2020) · Current Microbiology · doi:10.1007/s00284-020-01957-w · Cited by 8 · see citing works

Mining indigenous honeybee gut microbiota for Lactobacillus with probiotic potential

Aziz, G., Tariq, M., & Zaidi, A. (2021) · Microbiology · doi:10.1099/mic.0.001032 · Cited by 8 · see citing works

Microbiome and Colorectal Cancer Management

Alrahawy, M., Javed, S., Atif, H., ElSanhoury, K., Mekhaeil, K., & Eskander, G. H. (2022) · Cureus · doi:10.7759/cureus.30720 · Cited by 8 · see citing works

Next-Generation Probiotics Their Molecular Taxonomy and Health Benefits

Khan, S. T., & Malik, A. R. A. (2019) · Springer eBooks · doi:10.1007/978-3-030-24903-8_16 · Cited by 7 · see citing works

Streptococcus macedonicus strains isolated from traditional fermented milks: resistance to gastrointestinal environment and adhesion ability

Khaldi, T. E. M., Kebouchi, M., Soligot, C., Gomri, M. A., Kharroub, K., Roux, Y. L., & Roux, É. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09651-z · Cited by 7 · see citing works

The functional microbiota of on- and off-year moso bamboo (Phyllostachys edulis) influences the development of the bamboo pest Pantana phyllostachysae

Li, J., Zhao, Q., Huang, J., Jia, J.-Y., Zhu, T., Hong, T., & Su, J. (2022) · BMC Plant Biology · doi:10.1186/s12870-022-03680-z · Cited by 7 · see citing works

Diversity of probiotic adhesion genes in the gastrointestinal tract of goats

Subramaniyan, V., & Gurumurthy, K. (2019) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28508 · Cited by 7 · see citing works

Decreased mucosal adhesion of Lactobacillus species in patients with inflammatory bowel disease.

Najafi, S., Sotoodehnejadnematalahi, F., Amiri, M. M., Pourshafie, M. R., & Rohani, M. (2022) · PubMed Central · doi:10.22088/cjim.13.4.71 · Cited by 6 · see citing works

Potential Use of Lactiplantibacillus plantarum BCC 4352 as a Functional Starter Culture for Fermenting Thai Pork Sausage (Nham)

Kingcha, Y., Pumpuang, L., Adunphatcharaphon, S., Chantarasakha, K., Santiyanont, P., Klomtun, M., Janyaphisan, T., Kongtong, K., Phonsatta, N., Panya, A., et al. (2024) · Fermentation · doi:10.3390/fermentation10030145 · Cited by 6 · see citing works

Fighting Off Human Infections: A New Role for Bacteriocin Molecules

(2014) · CRC Press eBooks · doi:10.1201/b16439-4 · Cited by 6 · see citing works

Novel L-asparaginase from Paucilactobacillus vaccinostercus: Insights into anti-cancer potential using metagenomic, molecular docking and molecular dynamics simulation

Das, R., Tamang, B., Bhattarai, A., & Najar, I. N. (2025) · The Microbe · doi:10.1016/j.microb.2025.100390 · Cited by 6 · see citing works

Protective effects of metabolites from lactic acid bacteria against infections of mastitis pathogen in bovine cells

Kaewkod, T., Cheepchirasuk, N., Suriyaprom, S., Suriyasathaporn, W., Chitov, T., Panya, A., & Tragoolpua, Y. (2025) · Scientific Reports · doi:10.1038/s41598-025-05355-9 · Cited by 4 · see citing works

Probiotics

Novik, G. I., Sidarenka, A. V., Kiseleva, E. P., Kolomiets, E. I., & Dey, E. S. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8005-1_9 · Cited by 4 · see citing works

Evaluation of Rye Bran Enzymatic Hydrolysate Effect on Gene Expression and Bacteriocinogenic Activity of Lactic Acid Bacteria

Epishkina, J. M., Romanova, M., Chalenko, M. A., Khromova, N. Y., Karetkin, B. A., Beloded, A. V., Kornienko, M. A., Averina, Y. M., Shakir, I. V., & Panfilov, V. I. (2022) · Fermentation · doi:10.3390/fermentation8120752 · Cited by 3 · see citing works

Metataxonomic analysis of microbiota from Pakistani dromedary camelids milk and characterization of a newly isolated Lactobacillus fermentum strain with probiotic and bio-yogurt starter traits

Aziz, K., Farooq, Z., Tariq, M., & Zaidi, A. (2021) · Folia Microbiologica · doi:10.1007/s12223-021-00855-3 · Cited by 3 · see citing works

Human Intestinal Microbial Biofilm and its Correlation with Intestinal Mucin Secretion

Williams, K., Bekele, A. Z., Gokulan, K., & Khare, S. (2015) · doi:10.1002/9781118864036.ch9 · Cited by 3 · see citing works

Studies on the Probiotic, Adhesion, and Induction Properties of Artisanal Lactic Acid Bacteria: to Customize a Gastrointestinal Niche to Trigger Anti-obesity Functions

KAMBER, A., Albayrak, Ç. B., & Harsa, Ş. (2024) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-024-10357-6 · Cited by 2 · see citing works

Assessing lactococcal and enterococcal strains derived from traditionally fermented kefir and nabeez for their prospects as probiotics

Aziz, G., & Zaidi, A. (2025) · Microbiology · doi:10.1099/mic.0.001616 · Cited by 1 · see citing works

Oral Intake of Klebsiella oxytoca Disrupts Murine Intestinal Bacteriota and Anti-K. oxytoca Compound Baicalin by In Silico and In Vitro Analysis

Ma, Y., Qin, X., Wang, Y., Xie, L., & Chen, L. (2025) · Microbiology Research · doi:10.3390/microbiolres16080189 · Cited by 1 · see citing works

Current Status and Prospects of Various Methods used for Screening Probiotic Microorganisms

Kim, D., Kim, H. S., Jeong, D., Chon, J.-W., Kim, H., Kim, Y.-J., Kang, I.-B., Lee, S., Song, K., Park, J.-H., et al. (2016) · Journal of Dairy Science and Biotechnology · doi:10.22424/jmsb.2016.34.4.203 · Cited by 1 · see citing works

Novel bifidobacteria strains isolated from nonconventional sources. Technological, antimicrobial and biological characterization for their use as probiotics

Sarquis, A., Siroli, L., Modesto, M., Patrignani, F., Lanciotti, R., Mattarelli, P., Reinheimer, J. A., & Burns, P. (2019) · Journal of Applied Microbiology · doi:10.1111/jam.14367 · Cited by 1 · see citing works

Genes encoding for intestinal mucus adhesion factors in lactobacillus mucosae strains isolated from brazilian goat milk.

de Moraes, G. M. D., de Abreu, L. R., do Egito, A. S., Todorov, S. D., & dos Santos, K. M. O. (2016) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

New lactic acid bacterial strains from traditional M ongolian fermented milk products have altered adhesion to porcine gastric mucin depending on the carbon source

Kimoto‐Nira, H., Yamasaki, S., Sasaki, K., Moriya, N., Takénaka, A., & Suzuki, C. (2014) · Animal Science Journal · doi:10.1111/asj.12270 · Cited by 11 · see citing works

Lactobacillus acidophilusbinds to MUC3 component of cultured intestinal epithelial cells with highest affinity

Das, J. K., Mahapatra, R. K., Patro, S., Goswami, C., & Suar, M. (2016) · FEMS Microbiology Letters · doi:10.1093/femsle/fnw050 · Cited by 13 · see citing works

Functional Genomics of Probiotic Lactobacilli

Klaenhammer, T. R., Altermann, E., Pfeiler, E. A., Buck, B. L., Goh, Y. J., O’Flaherty, S., Barrangou, R., & Duong, T. (2008) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e31817da140 · Cited by 81 · see citing works

Evaluation of adhesion properties of lactobacilli probiotic candidates

Sepová, H. K., Florová, B., Bilková, A., Drobná, E., & Březina, V. (2018) · Monatshefte für Chemie - Chemical Monthly · doi:10.1007/s00706-017-2135-1 · Cited by 8 · see citing works