Bacterial fight-and-flight responses enhance virulence in a polymicrobial infection

Bacterial biofilms: from the Natural environment to infectious diseases

Hall‐Stoodley, L., Costerton, J. W., & Stoodley, P. (2004) · Nature Reviews Microbiology · doi:10.1038/nrmicro821 · Cited by 7,133

Bacterial competition: surviving and thriving in the microbial jungle

Hibbing, M. E., Fuqua, C., Parsek, M. R., & Peterson, S. B. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2259 · Cited by 2,765

Pathways of Oxidative Damage

Imlay, J. A. (2003) · Annual Review of Microbiology · doi:10.1146/annurev.micro.57.030502.090938 · Cited by 2,201

Periodontitis: a polymicrobial disruption of host homeostasis

Darveau, R. P. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2337 · Cited by 1,688

Oral multispecies biofilm development and the key role of cell–cell distance

Kolenbrander, P. E., Palmer, R. J., Periasamy, S., & Jakubovics, N. S. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2381 · Cited by 1,309

Molecular basis of intercellular adhesion in the biofilm‐forming Staphylococcus epidermidis

Heilmann, C., Schweitzer, O., Gerke, C., Vanittanakom, N., Mack, D., & Götz, F. (1996) · Molecular Microbiology · doi:10.1111/j.1365-2958.1996.tb02548.x · Cited by 912

Short protocols in molecular biology. A compendium of methods from current protocols in molecular biology

(1990) · Gene · doi:10.1016/0378-1119(90)90070-8 · Cited by 741

Polymicrobial Interactions: Impact on Pathogenesis and Human Disease

Peters, B. M., Jabra‐Rizk, M. A., O’May, G. A., Costerton, J. W., & Shirtliff, M. E. (2012) · Clinical Microbiology Reviews · doi:10.1128/cmr.00013-11 · Cited by 733

Bacterial diversity in the oral cavity of 10 healthy individuals

Bik, E. M., Long, C. D., Armitage, G. C., Loomer, P., Emerson, J., Mongodin, E. F., Nelson, K. E., Gill, S. R., Fraser-Liggett, C. M., & Relman, D. A. (2010) · The ISME Journal · doi:10.1038/ismej.2010.30 · Cited by 651

daime , a novel image analysis program for microbial ecology and biofilm research

Daims, H., Lücker, S., & Wagner, M. (2005) · Environmental Microbiology · doi:10.1111/j.1462-2920.2005.00880.x · Cited by 606

Aggregatibacter actinomycetemcomitans colonization and persistence in a primate model

Velusamy, S. K., Sampathkumar, V., Ramasubbu, N., Paster, B. J., & Fine, D. H. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905238116 · Cited by 22

Spoils of war: iron at the crux of clinical and ecological fitness of Pseudomonas aeruginosa

Nguyen, A. T., & Oglesby, A. G. (2015) · BioMetals · doi:10.1007/s10534-015-9848-6 · Cited by 23

Sustained release of CIP from TiO2‐PVDF/starch nanocomposite mats with potential application in wound dressing

Ansarizadeh, M., Haddadi, S. A., Amini, M., Hasany, M., & A., A. R. S. (2020) · Journal of Applied Polymer Science · doi:10.1002/app.48916 · Cited by 21

Essential Fitness Repertoire of Staphylococcus aureus during Co-infection with Acinetobacter baumannii In Vivo

Li, G., Shen, W., Gong, Y., Li, M., Rao, X., Liu, Q., Yu, Y., Zhou, J., Zhu, K., Yuan, M., et al. (2022) · mSystems · doi:10.1128/msystems.00338-22 · Cited by 17

Redox-mediated quorum sensing in plants

Fuller, A. W., Young, P., Pierce, B. D., Kitson-Finuff, J., Jain, P., Schneider, K., Lazar, S., Taran, O., Palmer, A. G., & Lynn, D. G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182655 · Cited by 18

Terpinen-4-ol and carvacrol affect multi-species biofilm composition

Maquera-Huacho, P. M., Herrero, E. R., Verspecht, T., Pauwels, M., Marcantônio, É., Spolidório, D. M. P., & Teughels, W. (2019) · Biofouling · doi:10.1080/08927014.2019.1630386 · Cited by 17

Bacterial supernatants elevate glucose-dependent insulin secretion in rat pancreatic INS-1 line and islet β-cells via PI3K/AKT signaling

Ramenzoni, L. L., Zuellig, R. A., Hussain, A., Lehmann, R., Heumann, C., Attin, T., & Schmidlin, P. R. (2018) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-018-3408-7 · Cited by 16

Illuminating the oral microbiome and its host interactions: tools and approaches for molecular ecological studies

Kreth, J., & Merritt, J. L. (2022) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuac052 · Cited by 15

Rv1717 Is a Cell Wall - Associated β-Galactosidase of Mycobacterium tuberculosis That Is Involved in Biofilm Dispersion

Bharti, S., Maurya, R. K., Venugopal, U., Singh, R., Akhtar, M. S., & Krishnan, M. Y. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.611122 · Cited by 15

Bacterial metabolism and pathogenesis intimate intertwining: time for metabolic modelling to come into action

Nogales, J., & Garmendia, J. (2021) · Microbial Biotechnology · doi:10.1111/1751-7915.13942 · Cited by 12

Metabolism of periodontal pathobionts: Their regulatory roles in the dysbiotic microbiota

Ding, J., Zhao, C., & Gao, L. (2023) · Molecular Oral Microbiology · doi:10.1111/omi.12409 · Cited by 15

A Literature Review and Framework Proposal for Halitosis Assessment in Cigarette Smokers and Alternative Nicotine-Delivery Products Users

Zanetti, F., Semren, T. Ž., Battey, J. N. D., Guy, P. A., Ivanov, N. V., van der Plas, A., & Hoeng, J. (2021) · Frontiers in Oral Health · doi:10.3389/froh.2021.777442 · Cited by 13

Small molecule reaction networks that model the ROS dynamics of the rhizosphere

Taran, O., Patel, V., & Lynn, D. G. (2019) · Chemical Communications · doi:10.1039/c8cc08940j · Cited by 13

Signaling Systems in Oral Bacteria

Miller, D. P., & Lamont, R. J. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-28524-1_3 · Cited by 13

Metatranscriptomics-based metabolic modeling of patient-specific urinary microbiome during infection

Josephs‐Spaulding, J., Rettig, H. C., Zimmermann, J., Chkonia, M., Mischnik, A., Franzenburg, S., Graspeuntner, S., Rupp, J., & Kaleta, C. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00823-6 · Cited by 13

Unravelling the intricacies of Porphyromonas gingivalis: virulence factors, lifecycle dynamics and phytochemical interventions for periodontal disease management

Nadaf, R., Kumbar, V., & Ghagane, S. C. (2024) · Apmis · doi:10.1111/apm.13440 · Cited by 11

Commensal bacteria contribute to the growth of multidrug-resistant Avibacterium paragallinarum in chickens

Zhu, J., Chen, Y., Wu, Y., Wang, Y., & Zhu, K. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1010584 · Cited by 9

Evolution of Bacterial “Frenemies”

Darch, S. E., Ibberson, C. B., & Whiteley, M. (2017) · mBio · doi:10.1128/mbio.00675-17 · Cited by 10

A novel heterologous expression strategy for the quorum-quenching enzyme MomL in Lysobacter enzymogenes to the inhibit pathogenicity of Pectobacterium

Wang, Y., Feng, T., Li, H., Yu, Y., Han, Y. C., Zhang, J., Li, X., Li, Y., & Zhang, X. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10166-w · Cited by 9

Biofilms of pathogenic bacteria in pig industry

Kolchyk, O. V., Buzun, А. І., & Paliy, А. (2020) · Ukrainian Journal of Ecology · doi:10.15421/2020_189 · Cited by 9

ccdC Regulates Biofilm Dispersal in Bacillus velezensis FZB42

Shao, L., Shen, Z., Li, M., Guan, C., Fan, B., Chai, Y., & Zhao, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105201 · Cited by 8

Facemask acne attenuation through modulation of indirect microbiome interactions

Na, H.-H., Kim, S., Kim, J., Lee, S., Kim, Y.-S., Kim, S., Lee, C.-H., Kim, D., Yoon, S. H., Jeong, H., et al. (2024) · npj Biofilms and Microbiomes · doi:10.1038/s41522-024-00512-w · Cited by 9

Experimental Inoculation of Aggregatibacter actinomycetemcomitans and Streptococcus gordonii and Its Impact on Alveolar Bone Loss and Oral and Gut Microbiomes

Rocha, C. M., Kawamoto, D., Martins, F. H., Bueno, M. R., Ishikawa, K. H., Ando‐Suguimoto, E. S., Carlucci, A. R., Arroteia, L. S., Casarin, R. C. V., Saraiva, L. M., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158090 · Cited by 8

Identification and functional characterization of type II toxin/antitoxin systems in Aggregatibacter actinomycetemcomitans

Schneider, B., Weigel, W., Sztukowska, M. N., & Demuth, D. R. (2018) · Molecular Oral Microbiology · doi:10.1111/omi.12215 · Cited by 8

Intrageneric and Intergeneric Interactions Developed by Oral Streptococci: Pivotal Role in the Pathogenesis of Oral Diseases

Chen, Y., Li, Y., & Zou, J. (2019) · Current Issues in Molecular Biology · doi:10.21775/cimb.032.377 · Cited by 9

Negative interactions and virulence differences drive the dynamics in multispecies bacterial infections

Schmitz, D. A., Allen, R. C., & Kümmerli, R. (2023) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2023.1119 · Cited by 7

Saliva as the Sole Nutritional Source in the Development of Multispecies Communities in Dental Plaque

Jakubovics, N. S. (2015) · ASM Press eBooks · doi:10.1128/9781555818883.ch12 · Cited by 8

Microbial interactions impact stress tolerance in a model oral community

Lewin, G. R., Evans, E., & Whiteley, M. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.01005-24 · Cited by 7

Structural and functional analysis of de‐N‐acetylase PgaB from periodontopathogen Aggregatibacter actinomycetemcomitans

Parthiban, C., Varudharasu, D., Shanmugam, M., Gopal, P., Ragunath, C., Thomas, L. M., Nitz, M., & Ramasubbu, N. (2016) · Molecular Oral Microbiology · doi:10.1111/omi.12175 · Cited by 7

The events that may contribute to subgingival dysbiosis: a focus on the interplay between iron, sulfide and oxygen

Chathoth, K., Martin, B., Cornélis, P., Yvenou, S., Bonnaure‐Mallet, M., & Baysse, C. (2020) · FEMS Microbiology Letters · doi:10.1093/femsle/fnaa100 · Cited by 7

Exploring the Microbiome of Diabetic Foot Ulcers: A Focus on Cases with a Clinical Worse Outcome

Soldevila‐Boixader, L., Carrera-Salinas, A., Mur, I., Morata, L., Rivera, A., Bosch, J., Montero, A., Castillejo, J. M., Benito, N., Martí, S., et al. (2025) · Antibiotics · doi:10.3390/antibiotics14070724 · Cited by 6

Elongation factor Tu promotes the onset of periodontitis through mediating bacteria adhesion

Xiao, L., Pu, Y., Cui, Y., Chen, C., Xiao, Q., Wang, Y., Wei, Y., Feng, M., Zhang, T., Yang, S., et al. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00680-3 · Cited by 7

[The origin of hydrogen peroxide in oral cavity and its role in oral microecology balance].

Keke, Z., Zhou, X., & Xu, X. (2017) · PubMed · doi:10.7518/hxkq.2017.02.020 · Cited by 7

The polymicrobial synergy and dysbiosis model of periodontal disease pathogenesis

Hajishengallis, G., & Lamont, R. J. (2016) · doi:10.1002/9781118982907.ch14 · Cited by 6

Development of a Versatile, Low-Cost Electrochemical System to Study Biofilm Redox Activity at the Micron Scale

Klementiev, A., & Whiteley, M. (2022) · Applied and Environmental Microbiology · doi:10.1128/aem.00434-22 · Cited by 5

Induction of Periodontitis Using Bacterial Strains Isolated from the Human Oral Microbiome in an Experimental Rat Model

Ancuța, D.-L., Alexandru, D. M., Coman, C., & Crivineanu, M. (2023) · Biomedicines · doi:10.3390/biomedicines11082098 · Cited by 5

Mapping Reaction-Diffusion Networks at the Plant Wound Site With Pathogens

Liu, S., Lin, Y.-H., Murphy, A., Anderson, J., Walker, N., Lynn, D. G., Binns, A. N., & Pierce, B. D. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.01074 · Cited by 5

Lactobacillus acidophilus LA-5 Ameliorates Inflammation and Alveolar Bone Loss Promoted by A. actinomycetemcomitans and S. gordonii in Mice and Impacts Oral and Gut Microbiomes

Bueno, M. R., Martins, F. H., Rocha, C. M., Kawamoto, D., Ishikawa, K. H., Ando‐Suguimoto, E. S., Carlucci, A. R., Arroteia, L. S., Casarin, R. C. V., & Mayer, M. P. A. (2024) · Microorganisms · doi:10.3390/microorganisms12040836 · Cited by 5

Impact of Polymicrobial Infection on Fitness of Streptococcus gordonii In Vivo

Pandey, S. D., Perpich, J. D., Stocke, K. S., Mansfield, J. M., Kikuchi, Y., Yakoumatos, L., Muszyński, A., Azadi, P., Tettelin, H., Whiteley, M., et al. (2023) · mBio · doi:10.1128/mbio.00658-23 · Cited by 4

Microbial Biofilms and Pathobiology of Gingivitis and Periodontitis

Miller, D. P. (2025) · Springer series on biofilms · doi:10.1007/978-3-031-82202-5_10 · Cited by 4

Community lifespan, niche expansion and the evolution of interspecific cooperation

Rodrigues, A. M. M., Estrela, S., & Brown, S. P. (2020) · Journal of Evolutionary Biology · doi:10.1111/jeb.13739 · Cited by 4

Tools for the Real-Time Assessment of a Pseudomonas aeruginosa Infection Model

Gannon, A. D., & Darch, S. E. (2021) · Journal of Visualized Experiments · doi:10.3791/62420 · Cited by 4

Commentary: The Evolution of Periodontology: Science Always Wins

Genco, R. J. (2014) · Journal of Periodontology · doi:10.1902/jop.2014.140346 · Cited by 4

From Global to Nano: A Geographical Perspective of Aggregatibacter actinomycetemcomitans

Ryder, M. I., Fine, D. H., & Barron, A. E. (2024) · Pathogens · doi:10.3390/pathogens13100837 · Cited by 3

Utilization and control of ecological interactions in polymicrobial infections and community-based microbial cell factories

Wigneswaran, V., Amador, C. I., Jelsbak, L., Sternberg, C., & Jelsbak, L. (2016) · F1000Research · doi:10.12688/f1000research.7876.1 · Cited by 3

Electrochemical sensors for oral biofilm–biomaterials interface characterization: A review

Koley, D. (2022) · Molecular Oral Microbiology · doi:10.1111/omi.12396 · Cited by 4

Strain-dependent interactions of Streptococcus suis and Glaesserella parasuis in co-culture.

Bujold, A. R., Barre, A. M. E., Kunkel, E., & MacInnes, J. I. (2023) · PubMed Central · Cited by 3

Recent progress in understanding the role of bacterial extracellular DNA: focus on dental biofilm

Geng, F., Liu, J., Liu, J., Lu, Z., & Pan, Y. (2024) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2024.2438117 · Cited by 3

Cyclic di-GMP and the Regulation of Biofilm Dispersion

Sauer, K. (2020) · Springer eBooks · doi:10.1007/978-3-030-33308-9_31 · Cited by 3

A phylogeographic approach of three species of Clinostomum Leidy, 1856, (Trematoda: Clinostomidae) from the Neotropical region of Mexico, with the description of a new species from Ardea herodias (Ardeidae)

Sereno-Uribe, A. L., López-Jiménez, A., González-García, M. T., Ortega-Olivares, M. P., & García‐Varela, M. (2025) · Parasitology International · doi:10.1016/j.parint.2025.103067 · Cited by 2

Hyphal growth determines spatial organization and coexistence in a pathogenic polymicrobial community in a spatially structured environment

Mancini, L., Saliekh, L., Claydon, R., Kotar, J., Bényei, É. B., Munro, C. A., Shendruk, T. N., Brown, A. T., Welch, M., & Cicuta, P. (2025) · The ISME Journal · doi:10.1093/ismejo/wraf279 · Cited by 3

Exploring aggregation genes in a P. aeruginosa chronic infection model

Gannon, A. D., Matlack, J. K., & Darch, S. E. (2024) · Journal of Bacteriology · doi:10.1128/jb.00429-24 · Cited by 2

Bacteria choose to fight and flee

Kåhrström, C. T. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3294 · Cited by 2

Microbial Biofilms ☆

Scoffield, J. A., & Wu, H. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.99205-5 · Cited by 4

Comparative investigation of the Diabetic foot ulcer microbiomePreprint

Saeb, A. T. M., Tayeb, H. T., Ouizi, S., Nassar, M. S., Alfadda, A. A., Gk, U. R., Mani, B., Youssef, A. M., & Alsuabeyl, M. S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.21.427721 · Cited by 2

Author response: Interactions between metabolism and growth can determine the co-existence of Staphylococcus aureus and Pseudomonas aeruginosa

Pajon, C., Fortoul, M. C., Diaz-Tang, G., Meneses, E. M., Kalifa, A. R., Sevy, E., Mariah, T., Toscan, B., Marcelin, M., Hernandez, D. M., et al. (2023) · eLife · doi:10.7554/elife.83664.sa2 · Cited by 2

MOB rules: Antibiotic Exposure Reprograms Metabolism to Mobilize Bacillus subtilis in Competitive InteractionsPreprint

Liu, Y. C., LaBonte, S. A., Brake, C. N., LaFayette, C., Rosebrock, A. P., Caudy, A. A., & Straight, P. D. (2024) · eLife · doi:10.7554/elife.98078 · Cited by 2

MOB rules: Antibiotic Exposure Reprograms Metabolism to Mobilize Bacillus subtilis in Competitive InteractionsPreprint

Liu, Y. C., LaBonte, S. A., Brake, C. N., LaFayette, C., Rosebrock, A. P., Caudy, A. A., & Straight, P. D. (2024) · eLife · doi:10.7554/elife.98078.1 · Cited by 2

PTA-DFS study: design of a randomised controlled trial assessing the effects of early percutaneous transluminal angioplasty on the healing of diabetic foot ulcers in persons with type 2 diabetes

Bódis, K. B., Florea, D.-I., Goh, S., Kramser, N., Wienemann, T., Binsch, C., Stern, M. E., Pfeffer, K., Kelm, M., Roden, M., et al. (2025) · BMC Cardiovascular Disorders · doi:10.1186/s12872-025-05288-1 · Cited by 1

Genomic integration and expression of the Aggregatibacter actinomycetemcomitans catalase gene in Aggregatibacter aphrophilus

Yang, Y. A., Cheng, Y.-A., & Chen, C. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.12.002 · Cited by 1

Identification of a glutathione transporter in A. actinomycetemcomitans

Klementiev, A., Garg, N., & Whiteley, M. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.03511-23 · Cited by 1

Mast cells exhibit intracellular microbicidal activity against Aggregatibacter actinomycetemcomitans

de Lima, H. G., Pinke, K. H., Lopes, M. M. R., Peres‐Buzalaf, C., Campanelli, A. P., & Lara, V. S. (2020) · Journal of Periodontal Research · doi:10.1111/jre.12763 · Cited by 1

MOB rules: Antibiotic Exposure Reprograms Metabolism to Mobilize Bacillus subtilis in Competitive InteractionsPreprint

Liu, Y. C., LaBonte, S. A., Brake, C. N., LaFayette, C., Rosebrock, A. P., Caudy, A. A., & Straight, P. D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.20.585991 · Cited by 1

Hyphal growth determines spatial organization and coexistence in a pathogenic polymicrobial community within alveoli-like geometriesPreprint

Mancini, L., Saliekh, L., Claydon, R., Kotar, J., Bényei, É. B., Munro, C. A., Shendruk, T. N., Brown, A. T., Welch, M., & Cicuta, P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.22.644766 · Cited by 1

SUBGİNGİVAL PLAK İÇİNDE BAKTERİYEL ETKİLEŞİMLER

Aytekin, Z., & Arabacı, T. (2016) · Atatürk Üniversitesi Diş Hekimliği Fakültesi Dergisi · doi:10.17567/ataunidfd.290456

Clinical Implications of Interkingdom Fungal and Bacterial Biofilms

Ramage, G., O’Donnell, L. E., Kean, R., Townsend, E. R., & Rajendran, R. (2017) · CRC Press eBooks · doi:10.4324/9781315120119-2 · Cited by 1

Mecanismos de defesa dos mastócitos contra o periodontopatógeno Aggregatibacter actinomycetemcomitans: atividade microbicida intracelular

de Lima, H. G. (2016) · doi:10.11606/t.25.2016.tde-03022016-152747

Interactions between microbial community members

Rice, S. A. (2017) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12571

The Molecular and Microbial Microenvironments in Chronically Diseased LungsPreprint

Melnik, A. V., Vázquez‐Baeza, Y., Aksenov, A. A., Hyde, E. R., McAvoy, A. C., Wang, M., Silva, R., Protsyuk, I., Wu, J. V., Bouslimani, A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/676148

Ecological Approaches to Periodontal Therapy

Diaz, P. I., & Hoare, A. (2020) · Springer eBooks · doi:10.1007/978-3-030-42990-4_13

Bacterial Peptides Targeting Periodontal Pathogens in Communities

Xie, H., & Lamont, R. J. (2020) · Springer eBooks · doi:10.1007/978-3-030-42990-4_11

A Comparison between Scaling and Root Planning (SRP), Antibiotic and Diode Laser Application in Treatment of Localized Juvenile Periodontitis (Microscopical Study)

Hazeem, M. I. (2018) · Tikrit Journal for Dental Sciences · doi:10.25130/tjds.6.1.1

Epithelial responses to Porphyromonas gingivalis in the community context.

Fitzsimonds, Z. R. (2020) · doi:10.18297/etd/3508

Oral Microbiology

Jakubovics, N. S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.99216-x

Aggregatibacter actinomycetemcomitans exploits and modulates the immune response by human neutrophils for survival in the anaerobic environment.

Ozuna, H. (2022) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/3808

Efeito da infecção experimental por Aggregatibacter actinomycetemcomitans e Streptococcus gordonii sobre a expressão de genes associados à barreira intestinal e inflamação, níveis séricos de LPS e reabsorção do osso alveolar em modelo murino

Rocha, C. M. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.23.2022.tde-30012023-111435

Microorganism Carrier-Surface Method as an Efficient Model for Microscopic Characterization of Biofilm Structure and Dispersion in Dairy Associated Spore-Forming Bacteria

Malek, F. (2023) · Journal of Food Engineering and Technology · doi:10.32732/jfet.2023.12.1.21

The Matrix Proteome: Protein Actors in the Extracellular Bacterial Biofilm

Cassin, E. K., & Tseng, B. S. (2024) · Springer series on biofilms · doi:10.1007/978-3-031-70476-5_3

Resistance phenotypes and genomic features of Mycobacterium seoulense isolates

Zhao, J., Shen, X., Jin, L., Ji, S., & Pan, X. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1553591

Additional file 1 of The mediating roles of the oral microbiome in saliva and subgingival sites between e-cigarette smoking and gingival inflammation

Park, B., Koh, H., Patatanian, M., Reyes-Caballero, H., Zhao, N., Meinert, J. L., Holbrook, J. T., Leinbach, L. I., & Biswal, S. (2024) · Figshare · doi:10.6084/m9.figshare.26565806

Additional file 4 of The mediating roles of the oral microbiome in saliva and subgingival sites between e-cigarette smoking and gingival inflammation

Park, B., Koh, H., Patatanian, M., Reyes-Caballero, H., Zhao, N., Meinert, J. L., Holbrook, J. T., Leinbach, L. I., & Biswal, S. (2024) · Figshare · doi:10.6084/m9.figshare.26565815

Additional file 3 of The mediating roles of the oral microbiome in saliva and subgingival sites between e-cigarette smoking and gingival inflammation

Park, B., Koh, H., Patatanian, M., Reyes-Caballero, H., Zhao, N., Meinert, J. L., Holbrook, J. T., Leinbach, L. I., & Biswal, S. (2024) · Figshare · doi:10.6084/m9.figshare.26565812

Additional file 5 of The mediating roles of the oral microbiome in saliva and subgingival sites between e-cigarette smoking and gingival inflammation

Park, B., Koh, H., Patatanian, M., Reyes-Caballero, H., Zhao, N., Meinert, J. L., Holbrook, J. T., Leinbach, L. I., & Biswal, S. (2024) · Figshare · doi:10.6084/m9.figshare.26565818

Additional file 2 of The mediating roles of the oral microbiome in saliva and subgingival sites between e-cigarette smoking and gingival inflammation

Park, B., Koh, H., Patatanian, M., Reyes-Caballero, H., Zhao, N., Meinert, J. L., Holbrook, J. T., Leinbach, L. I., & Biswal, S. (2024) · Figshare · doi:10.6084/m9.figshare.26565809

Revealing community dynamics in polymicrobial infections through a quantitative framework

Adekoya, A. E., Boggs, T. E., & Ibberson, C. B. (2026) · ISME Communications · doi:10.1093/ismeco/ycag061

Submerged biofilms of Bacillus subtilis : architecture, resistance to biocides and pathogens protection

Vizuete, M. D. P. S. (2014) · theses.fr (ABES) · doi:10.70675/04549528z27e1z425bz9398z0023e7d1fdd8

Une étude de la flore bactérienne et virale infectant la plaie du pied diabétique par approche culturomique

Jneid, J. (2018) · theses.fr (ABES) · doi:10.70675/79b91b1dzc327z4120z8bbcz69fc1e75ba42

Deciphering Biotic Interactions and Their Role in Soil Microbial Community Assembly and Functions

Huet, S. (2022) · doi:10.70675/c6538dc2z0818z4f4bza0f7z517316e633f7

Overview of head & neck microbiota

Jayasinghe, R., Gunawardhana, K. S. N. D., & Senevirathna, K. (2026) · Advances in immunology · doi:10.1016/bs.ai.2026.04.003

Architectural intelligence: toward a spatial framework for interpreting microbiome-associated human disease

Parappalliyalil, H., Padmakumar, A., Ghosal, D., & Reynolds, E. C. (2026) · The ISME Journal · doi:10.1093/ismejo/wrag180

No strain, no gain: within-host bacterial microdiversity and human health

Wojtkowiak, A., Shinfuku, M. S., & Lewin, G. R. (2026) · Infection and Immunity · doi:10.1128/iai.00062-26

Fight and flight fortifies pathogen

(2014) · Nature · doi:10.1038/509537e

A Commensal Bacterium Promotes Virulence of an Opportunistic Pathogen via Cross-Respiration

Stacy, A., Fleming, D. F., Lamont, R. J., Rumbaugh, K. P., & Whiteley, M. (2016) · mBio · doi:10.1128/mbio.00782-16 · Cited by 93

Oxygen as a Virulence Determinant in Polymicrobial Infections

Selleck, E. M., & Gilmore, M. S. (2016) · mBio · doi:10.1128/mbio.01249-16 · Cited by 5

Polymicrobial interactions stimulate resistance to host innate immunity through metabolite perception

Ramsey, M. M., & Whiteley, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809533106 · Cited by 171

Fine‐tuned production of hydrogen peroxide promotes biofilm formation of Streptococcus parasanguinis by a pathogenic cohabitant Aggregatibacter actinomycetemcomitans

Duan, D., Scoffield, J. A., Zhou, X., & Wu, H. (2016) · Environmental Microbiology · doi:10.1111/1462-2920.13425 · Cited by 49