An Extracellular Serine/Threonine-Rich Protein from Lactobacillus plantarum NCIMB 8826 Is a Novel Aggregation-Promoting Factor with Affinity to Mucin

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961 · 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

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

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

Quorum sensing-controlled gene expression in lactic acid bacteria

Kuipers, O. P., de Ruyter, P. G. G. A., Kleerebezem, M., & de Vos, W. M. (1998) · Journal of Biotechnology · doi:10.1016/s0168-1656(98)00100-x · Cited by 682 · see citing works

10 years of the nisin-controlled gene expression system (NICE) in Lactococcus lactis

Mierau, I., & Kleerebezem, M. (2005) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-005-0107-6 · Cited by 591 · see citing works

Lactobacillus plantarum—survival, functional and potential probiotic properties in the human intestinal tract

de Vries, M. C., Vaughan, E. E., Kleerebezem, M., & de Vos, W. M. (2006) · International Dairy Journal · doi:10.1016/j.idairyj.2005.09.003 · Cited by 516 · see citing works

Molecular dialogue between the human gut microbiota and the host: a Lactobacillus and Bifidobacterium perspective

Turroni, F., Ventura, M., Buttó, L. F., Duranti, S., O’Toole, P. W., Motherway, M. O., & van Sinderen, D. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1318-0 · Cited by 336 · see citing works

Probiotics in foods not containing milk or milk constituents, with special reference to Lactobacillus plantarum 299v

Molin, G. (2001) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/73.2.380s · Cited by 261 · see citing works

Role of SraP, a Serine-Rich Surface Protein of Staphylococcus aureus , in Binding to Human Platelets

Siboo, I. R., Chambers, H. F. “., & Sullam, P. M. (2005) · Infection and Immunity · doi:10.1128/iai.73.4.2273-2280.2005 · Cited by 241 · see citing works

A serine‐rich glycoprotein of <i>Streptococcus sanguis</i> mediates adhesion to platelets via GPIb

Plummer, C., Wu, H., Kerrigan, S. W., Meade, G., Cox, D., & Ian Douglas, C. W. (2005) · British Journal of Haematology · doi:10.1111/j.1365-2141.2005.05421.x · Cited by 192 · 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

Characterization of Lactobacillus coryniformis DSM 20001 T Surface Protein Cpf Mediating Coaggregation with and Aggregation among Pathogens

Schachtsiek, M., Hammes, W. P., & Hertel, C. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.12.7078-7085.2004 · Cited by 175 · see citing works

Stability of Integrated Plasmids in the Chromosome of Lactococcus lactis

Leenhouts, K. J., Kok, J., & Venema, G. (1990) · Applied and Environmental Microbiology · doi:10.1128/aem.56.9.2726-2735.1990 · Cited by 157 · see citing works

Transformation of Lactobacillus strains used in meat and vegetable fermentations

Aukrust, T. W., & Blom, H. (1992) · Food Research International · doi:10.1016/0963-9969(92)90121-k · Cited by 149 · 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

Glucosyltransferase A (GtfA) and inulosucrase (Inu) of Lactobacillus reuteri TMW1.106 contribute to cell aggregation, in vitro biofilm formation, and colonization of the mouse gastrointestinal tract

Walter, J., Schwab, C., Loach, D. M., Gänzle, M. G., & Tannock, G. W. (2008) · Microbiology · doi:10.1099/mic.0.2007/010637-0 · Cited by 148 · see citing works

Identification and Characterization of hsa , the Gene Encoding the Sialic Acid-Binding Adhesin of Streptococcus gordonii DL1

Takahashi, Y., Konishi, K., Cisar, J. O., & Yoshikawa, M. (2002) · Infection and Immunity · doi:10.1128/iai.70.3.1209-1218.2002 · Cited by 145 · see citing works

Molecular Characterization of a Novel Staphylococcus Aureus Surface Protein (SasC) Involved in Cell Aggregation and Biofilm Accumulation

Schroeder, K., Jularic, M., Horsburgh, S. M., Nina, H., Neumann, C., Bertling, A., Schulte, A., Foster, S. J., Kehrel, B. E., Peters, G., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007567 · Cited by 143 · see citing works

Exported proteins in probiotic bacteria: adhesion to intestinal surfaces, host immunomodulation and molecular cross-talking with the host

Sánchez, B., Bressollier, P., & Urdaci, M. C. (2008) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2008.00454.x · Cited by 141 · see citing works

Characterization of the aggregation promoting factor from Lactobacillus gasseri , avaginal isolate

Boris, S., Suárez, J. E., & Barbés, C. (1997) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.1997.00250.x · Cited by 139 · see citing works

Strain- and matrix-dependent adhesion of Lactobacillus plantarum is mediated by proteinaceous bacterial compounds

Tallon, R., Arias, S., Bressollier, P., & Urdaci, M. C. (2006) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2006.03086.x · Cited by 138 · see citing works

High frequency of conjugation in Lactobacillus mediated by an aggregation-promoting factor

Reniero, R., Cocconcelli, P. S., Bottazzi, V., & Morelli, L. (1992) · Journal of General Microbiology · doi:10.1099/00221287-138-4-763 · Cited by 137 · see citing works

A unique serine-rich repeat protein (Srr-2) and novel surface antigen (ε) associated with a virulent lineage of serotype III Streptococcus agalactiae

Seifert, K., Adderson, E. E., Whiting, A. A., Bohnsack, J. F., Crowley, P. J., & Brady, L. J. (2006) · Microbiology · doi:10.1099/mic.0.28516-0 · Cited by 123 · see citing works

Identification and Characterization of Novel Surface Proteins in Lactobacillus johnsonii and Lactobacillus gasseri

Ventura, M., Janković, I., Walker, D. C., Pridmore, R. D., & Zink, R. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.12.6172-6181.2002 · Cited by 116 · see citing works

Identification of surface proteins involved in the adhesion of a probiotic Bacillus cereus strain to mucin and fibronectin

Sánchez, B., Arias, S., Chaignepain, S., Denayrolles, M., Schmitter, J., Bressollier, P., & Urdaci, M. C. (2009) · Microbiology · doi:10.1099/mic.0.025288-0 · Cited by 92 · see citing works

Identification of dipeptide repeats and a cell wall sorting signal in the fimbriae‐associated adhesin, Fap1, of Streptococcus parasanguis

Wu, H., & Fives-Taylor, P. M. (1999) · Molecular Microbiology · doi:10.1046/j.1365-2958.1999.01670.x · Cited by 90 · see citing works

Beneficial effect of auto-aggregating Lactobacillus crispatus on experimentally induced colitis in mice

Castagliuolo, I., Galeazzi, F., Ferrari, S., Elli, M., Brun, P., Cavaggioni, A., Tormen, D., Sturniolo, G. C., Morelli, L., & Palù, G. (2004) · FEMS Immunology & Medical Microbiology · doi:10.1016/j.femsim.2004.08.011 · Cited by 86 · see citing works

Microbiota/Host Crosstalk Biomarkers: Regulatory Response of Human Intestinal Dendritic Cells Exposed to Lactobacillus Extracellular Encrypted Peptide

Bernardo, D., Sánchez, B., Al-Hassi, H. O., Mann, E. R., Urdaci, M. C., Knight, S. C., & Margollés, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036262 · Cited by 83 · see citing works

Specific Lactobacillus/Mutans Streptococcus Co-aggregation

Lang, C., Böttner, M., Holz, C., Veen, M., Ryser, M., Reindl, A., Pompejus, M., & Tanzer, J. M. (2010) · Journal of Dental Research · doi:10.1177/0022034509356246 · Cited by 83 · see citing works

Major Role of NAD-Dependent Lactate Dehydrogenases in Aerobic Lactate Utilization in Lactobacillus plantarum during Early Stationary Phase

Goffin, P., Lorquet, F., Kleerebezem, M., & Pascal Hols, A. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.19.6661-6666.2004 · Cited by 82 · see citing works

Contribution of Aggregation-Promoting Factor to Maintenance of Cell Shape in <i>Lactobacillus</i> <i>gasseri</i> 4B2

Jankovic, I., Ventura, M., Meylan, V., Rouvet, M., Elli, M., & Zink, R. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.11.3288-3296.2003 · Cited by 82 · see citing works

Enteroaggregative Escherichia coli flagellin‐induced interleukin‐8 secretion requires Toll‐like receptor 5‐dependent p38 MAP kinase activation

Khan, M. A., Kang, J., & Steiner, T. S. (2004) · Immunology · doi:10.1111/j.1365-2567.2004.01923.x · Cited by 81 · see citing works

Characterization of the Lactococcus lactis pepN gene encoding an aminopeptidase homologous to mammalian aminopeptidase N

Tan, P. S. T., Boerrigter, I. J., Poolman, B., Siezen, R. J., de Vos, W. M., & Konings, W. N. (1992) · FEBS Letters · doi:10.1016/0014-5793(92)80827-4 · Cited by 75 · see citing works

Characterization of pig colonic mucins

Fogg, F. J. J., Hutton, D. A., Jumel, K., Pearson, J. P., Harding, S. E., & Allen, A. (1996) · Biochemical Journal · doi:10.1042/bj3160937 · Cited by 73 · see citing works

Proteomic analysis of cell surface-associated proteins from probioticLactobacillus plantarum

Beck, H. C., Madsen, S. ̧. M., Glenting, J., Petersen, J., Israelsen, H., ̧rrelykke, M. R. N., Antonsson, M., & Hansen, A. M. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2009.01662.x · Cited by 63 · see citing works

A 35-kDa co-aggregation factor is a hemin binding protein in Porphyromonas gingivalis

Shibata, Y., Hiratsuka, K., Hayakawa, M., Shiroza, T., Takiguchi, H., Nagatsuka, Y., & Abiko, Y. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02826-7 · Cited by 63 · see citing works

Molecular Characterization of a Novel Bacteriocin and an Unusually Large Aggregation Factor of Lactobacillus paracasei subsp. paracasei BGSJ2-8, a Natural Isolate from Homemade Cheese

Lozo, J., Jovčić, B., Kojić, M., Dalgalarrondo, M., Chobert, J., Haertlé, T., & Topisirović, L. (2007) · Current Microbiology · doi:10.1007/s00284-007-0159-1 · Cited by 57 · see citing works

Association of a novel high molecular weight, serine‐rich protein (SrpA) with fibril‐mediated adhesion of the oral biofilm bacterium Streptococcus cristatus

Handley, P. S., CORREIA, F. F., Russell, K., Rosan, B., & DiRienzo, J. M. (2005) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.2004.00190.x · Cited by 57 · see citing works

Aggregation-promoting factor in human vaginal Lactobacillus strains

Kmeť, V., & Lucchini, F. (2006) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.1997.tb01079.x · Cited by 53 · see citing works

Determination of chromosome size and number ofrrnloci inLactobacillus plantarumby pulsed-field gel electrophoresis

Chevallier, B., Hubert, J., & Kammerer, B. (1994) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1994.tb07006.x · Cited by 52 · 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

Glycine Residues in the Hydrophobic Core of the GspB Signal Sequence Route Export toward the Accessory Sec Pathway

Bensing, B. A., Siboo, I. R., & Sullam, P. M. (2007) · Journal of Bacteriology · doi:10.1128/jb.00027-07 · Cited by 46 · see citing works

Identification of Novel Proteins Secreted by Lactobacillus plantarum That Bind to Mucin and Fibronectin

Sánchez, B., Schmitter, J., & Urdaci, M. C. (2009) · Microbial Physiology · doi:10.1159/000233579 · Cited by 45 · see citing works

Proteomic investigation of the aggregation phenomenon in Lactobacillus crispatus

Siciliano, R. A., Cacace, G., Mazzeo, M. F., Morelli, L., Elli, M., Rossi, M., & Malorni, A. (2007) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2007.11.007 · Cited by 36 · see citing works

The aggregation-promoting factor of Lactobacillus crispatus M247 and its genetic locus

Marcotte, H., Ferrari, S., Cesena, C., Hammarström, L. L. G., Morelli, L., Pozzi, G., & Oggioni, M. R. (2004) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2004.02364.x · Cited by 33 · see citing works

Aggregation-promoting factor in pig intestinal Lactobacillus strains

Kmeť, V., Callegari, M. L., Bottazzi, V., & Morelli, L. (1995) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.1995.tb01079.x · Cited by 31 · see citing works

Controlled expression of CluA in Lactococcus lactis and its role in conjugation

Stentz, R., Jury, K. L., Eaton, T. J., Parker, M. L., Narbad, A., Gasson, M. J., & Shearman, C. A. (2004) · Microbiology · doi:10.1099/mic.0.27149-0 · Cited by 18 · see citing works

Cell surface-associated glycolytic enzymes from Lactobacillus plantarum 299v mediate adhesion to human epithelial cells and extracellular matrix proteins

Madsen, S. M., Glenting, J., Vrang, A., Ravn, P., Riemann, H., Israelsson, H., Nørrelykke, M. R., Hansen, A. M., Antonsson, M., Ahrné, S., et al. (2005) · Lund University Publications (Lund University) · Cited by 4 · see citing works

Bacterial autoaggregation

Trunk, T., Bacterial Cell Surface Group, S. F. G. A. E. B., S. Khalil, H., & C. Leo, J. (2018) · AIMS Microbiology · doi:10.3934/microbiol.2018.1.140 · Cited by 444 · see citing works

Paraprobiotics and Postbiotics of Probiotic Lactobacilli, Their Positive Effects on the Host and Action Mechanisms: A Review

Teame, T., Wang, A., Xie, M., Zhang, Z., Yang, Y., Ding, Q., Gao, C., Olsen, R. E., Ran, C., & Zhou, Z. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.570344 · Cited by 407 · see citing works

Adhesion abilities of dairy Lactobacillus plantarum strains showing an aggregation phenotype

García-Cayuela, T., Korany, A. M., Bustos, I., P. Gómez de Cadiñanos, L., Requena, T., Peláez, C., & Martínez-Cuesta, M. C. (2014) · Food Research International · doi:10.1016/j.foodres.2014.01.010 · Cited by 286 · see citing works

A planarian nidovirus expands the limits of RNA genome size

Saberi, A., Gulyaeva, A. A., Brubacher, J. L., Newmark, P. A., & Gorbalenya, A. E. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007314 · Cited by 138 · see citing works

Lactobacillus plantarum WCFS 1 and its host interaction: a dozen years after the genome

van den Nieuwboer, M., van Hemert, S., Claassen, E., & de Vos, W. M. (2016) · Microbial Biotechnology · doi:10.1111/1751-7915.12368 · Cited by 136 · see citing works

Molecular Players Involved in the Interaction Between Beneficial Bacteria and the Immune System

Hevia, A., Delgado, S., Sánchez, B., & Margollés, A. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01285 · Cited by 125 · see citing works

Antimicrobial activity of Lactobacillus salivarius and Lactobacillus fermentum against Staphylococcus aureus

Kang, M., Lim, H.-S., Oh, J., Lim, Y.-J., Wuertz‐Kozak, K., Harro, J. M., Shirtliff, M. E., & Achermann, Y. (2017) · Pathogens and Disease · doi:10.1093/femspd/ftx009 · Cited by 123 · see citing works

Lactobacillus gasseri SBT2055 Reduces Infection by and Colonization of Campylobacter jejuni

Nishiyama, K., Seto, Y., Yoshioka, K., Kakuda, T., Takaı̈, S., Yamamoto, Y., & Mukai, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108827 · Cited by 77 · see citing works

Polymicrobial interaction between Lactobacillus and Saccharomyces cerevisiae: coexistence-relevant mechanisms

Xu, Z., Lu, Z., Soteyome, T., Ye, Y., Huang, T., Liu, J., Harro, J. M., Kjellerup, B. V., & Peters, B. M. (2021) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2021.1893265 · Cited by 64 · see citing works

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

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

Cell surface‐associated aggregation‐promoting factor from L actobacillus gasseri SBT 2055 facilitates host colonization and competitive exclusion of C ampylobacter jejuni

Nishiyama, K., Nakazato, A., Ueno, S., Seto, Y., Kakuda, T., Takaı̈, S., Yamamoto, Y., & Mukai, T. (2015) · Molecular Microbiology · doi:10.1111/mmi.13153 · Cited by 49 · see citing works

Extracellular molecular effectors mediating probiotic attributes

Ruíz, L., Hevia, A., Bernardo, D., Margollés, A., & Sánchez, B. (2014) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12576 · Cited by 46 · see citing works

Bistable auto-aggregation phenotype in Lactiplantibacillus plantarum emerges after cultivation in in vitro colonic microbiota

Isenring, J., Geirnaert, A., Lacroix, C., & Stevens, M. J. A. (2021) · BMC Microbiology · doi:10.1186/s12866-021-02331-x · Cited by 42 · see citing works

Aggregation of Lactobacillus brevis associated with decrease in pH by glucose fermentation

Saito, K., Tomita, S., & Nakamura, T. (2019) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2019.1584522 · Cited by 33 · see citing works

Natural Aggregation of Lactobacillus: Mechanisms and Influencing Factors

Wang, S., Li, L., Yu, L., Tian, F., Zhao, J., Zhai, Q., & Chen, W. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.105007 · Cited by 34 · see citing works

Genome Sequence and Assessment of Safety and Potential Probiotic Traits of Lactobacillus johnsonii CNCM I-4884

Boucard, A.-S., Florent, I., Polack, B., Langella, P., & Bermúdez‐Humarán, L. G. (2022) · Microorganisms · doi:10.3390/microorganisms10020273 · Cited by 24 · see citing works

New insights into the role of plasmids from probiotic Lactobacillus pentosus MP-10 in Aloreña table olive brine fermentation

Abriouel, H., Pérez Montoro, B., de la Fuente Ordoñez, J. J., Lavilla Lerma, L., Knapp, C. W., & Benomar, N. (2019) · Scientific Reports · doi:10.1038/s41598-019-47384-1 · Cited by 22 · see citing works

Molecular identification and in vitro evaluation of probiotic functional properties of some Egyptian lactic acid bacteria and yeasts

Ahmed, A.-S. I., Moghazy, G. M. E., Elsayed, T. R., Goda, H. A., & Khalafalla, G. M. (2021) · Journal of Genetic Engineering and Biotechnology · doi:10.1186/s43141-021-00212-4 · Cited by 23 · see citing works

Effects of potential synbiotic interaction between Lactobacillus rhamnosus GG and salicylic acid on human colon and prostate cancer cells

Çelebioğlu, H. U. (2021) · Archives of Microbiology · doi:10.1007/s00203-021-02200-1 · Cited by 21 · see citing works

From One-Size-Fits-All to Precision Medicine: The Promise of Personalized Probiotics

Montazeri‐Najafabady, N. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10815-9 · Cited by 14 · see citing works

Mucolytic bacteria: prevalence in various pathological diseases

Selwal, K. K., Selwal, M. K., & Yu, Z. (2021) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-021-03145-9 · Cited by 14 · see citing works

Effects of Lactobacillus plantarum Postbiotics on Growth Performance, Immune Status, and Intestinal Microflora of Growing Minks

Li, Y., Zhen, S., Cao, L., Sun, F., & Wang, L. (2023) · Animals · doi:10.3390/ani13182958 · Cited by 13 · see citing works

Complete genome sequence of Lactobacillus helveticus CAUH18, a potential probiotic strain originated from koumiss

Yang, Y., An, H., Zhai, Z., Wang, G., Li, J., & Hao, Y. (2016) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2016.03.004 · Cited by 13 · see citing works

Autoaggregation and adhesion abilities in bacteria associated with colonies of Microcystis

Zhang, P., Chen, M., Zhang, Y., Li, Y.-Y., Lu, S., & Li, P. (2018) · Hydrobiologia · doi:10.1007/s10750-018-3706-9 · Cited by 13 · see citing works

Butanol Tolerance of Lactiplantibacillus plantarum: A Transcriptome Study

Petrov, K. K., Arsov, A., & Petrova, P. M. (2021) · Genes · doi:10.3390/genes12020181 · Cited by 12 · see citing works

Limosilactobacillus allomucosae sp. nov., a novel species isolated from wild boar faecal samples as a potential probiotic for domestic pigs

Chen, B., Silvaraju, S., Almunawar, S. N. A., Heng, Y. C., Lee, J. K. Y., & Kittelmann, S. (2024) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2024.126556 · Cited by 10 · see citing works

Development of a Limosilactobacillus reuteri therapeutic delivery platform with reduced colonization potential

Alexander, L. M., Khalid, S., Gallego-López, G. M., Astmann, T. J., Oh, J., Heggen, M., Huss, P., Fisher, R., Mukherjee, A., Raman, S., et al. (2024) · Applied and Environmental Microbiology · doi:10.1128/aem.00312-24 · Cited by 6 · see citing works

Isolation and Characterization of β-Phenylethylamine-Producing Lactic Acid Bacteria from Dairy Products

Casado, A., Fernández, E., González‐Iglesias, H., Fernández, M., Álvarez, M. A., & Ladero, V. (2025) · Microorganisms · doi:10.3390/microorganisms13050966 · Cited by 5 · see citing works

Laboratory domestication of Lactiplantibacillus plantarum alters some phenotypic traits but causes non-novel genomic impact

Surve, S. V., Shinde, D. B., Fernandes, J. M., Sharma, S., Vijayvargiya, M., Kadam, K., & Kulkarni, R. S. (2024) · Journal of Applied Microbiology · doi:10.1093/jambio/lxae035 · Cited by 3 · see citing works

In vitro analysis on the adhesion potential of Lactiplantibacillus plantarum from infant faeces and its gastrointestinal localization, growth promotion, and immunomodulation in Wistar rats: a preliminary study

Narayanan, R., & Keerthi, T. R. (2024) · Letters in Applied Microbiology · doi:10.1093/lambio/ovae034 · Cited by 3 · see citing works

Adhesion Abilities of Lactobacillus Plantarum Strains Isolated from Nigerian Fermented Maize Food - Akamu

Obinna-Echem, P. C. (2017) · Journal of Food Research · doi:10.5539/jfr.v6n5p50 · Cited by 2 · see citing works

Infection-induced elevation of gut glycosaminoglycans fosters microbiota expansion in Drosophila melanogaster

Arias-Rojas, A., Rubinić, M., Albiez, J., Frahm, D., HURWITZ, R. M., & Iatsenko, I. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116598 · Cited by 1 · see citing works

Development of a Nigerian fermented maize food “Akamu” as a functional food

Obinna-Echem, P. C. (2014) · PEARL (University of Plymouth) · doi:10.24382/1413 · Cited by 1 · see citing works

Biomaterials for bacterial recruitment function: A review

Fu, J., Chen, W., Zhang, Y., Li, X., Lu, K. Y., Wang, A., Chen, S., & Zhang, P. (2026) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2026.115707

Prospecting and characterization of potential probiotic lactobacilli from animal gut and food sources

Asiegbu, C. V., & Tabit, F. T. (2026) · Scientific Reports · doi:10.1038/s41598-026-47302-2

Aggregation-promoting factor in pig intestinal Lactobacillus strains

Kmeť, V., Callegari, M. L., Bottazzi, V., & Morelli, L. (1995) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.1995.tb01079.x · Cited by 31 · see citing works

The aggregation-promoting factor of Lactobacillus crispatus M247 and its genetic locus

Marcotte, H., Ferrari, S., Cesena, C., Hammarström, L. L. G., Morelli, L., Pozzi, G., & Oggioni, M. R. (2004) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2004.02364.x · Cited by 33 · see citing works

A novel type of autoaggregation in lactic acid bacteria promoted by new AggS aggregation factor from Streptococcus thermophilus CC40-4S

Tsibulskaya, D., Slavić, M. Š., Terzić-Vidojević, A., Zivkovic, I. P., Blagojević, V., Prodanović, M., Serrano, M., & Kojić, M. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.146517 · Cited by 2 · see citing works

Aggregation-promoting factor in human vaginal Lactobacillus strains

Kmeť, V., & Lucchini, F. (2006) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.1997.tb01079.x · Cited by 53 · see citing works

Bistable auto-aggregation phenotype in Lactiplantibacillus plantarum emerges after cultivation in in vitro colonic microbiota

Isenring, J., Geirnaert, A., Lacroix, C., & Stevens, M. J. A. (2021) · BMC Microbiology · doi:10.1186/s12866-021-02331-x · Cited by 42 · see citing works