Metabolite Cross-Feeding Enhances Virulence in a Model Polymicrobial Infection

Bergey's Manual of Determinative Bacteriology

S., F. A., Buchanan, R. E., Gibbons, N. E., & Bergey (1975) · Taxon · doi:10.2307/1218353 · Cited by 11,334 · see citing works

Site-directed mutagenesis by overlap extension using the polymerase chain reaction

Ho, S. N., Hunt, H. D., Horton, R. M., Pullen, J. K., & Pease, L. R. (1989) · Gene · doi:10.1016/0378-1119(89)90358-2 · Cited by 7,354 · see citing works

Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes

Kovach, M. E., Elzer, P. H., Hill, D. S., Robertson, G. T., Farris, M. A., Roop, R. M., & Peterson, K. M. (1995) · Gene · doi:10.1016/0378-1119(95)00584-1 · Cited by 3,355 · see citing works

Communication among Oral Bacteria

Kolenbrander, P. E., Andersen, R. N., Blehert, D. S., Egland, P. G., Foster, J. S., & Palmer, R. J. (2002) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.66.3.486-505.2002 · Cited by 1,022 · see citing works

Endocarditis Due to Rare and Fastidious Bacteria

Brouqui, P., & Raoult, D. (2001) · Clinical Microbiology Reviews · doi:10.1128/cmr.14.1.177-207.2001 · Cited by 750 · see citing works

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 747 · see citing works

The phenazine pyocyanin is a terminal signalling factor in the quorum sensing network of Pseudomonas aeruginosa

Dietrich, L. E. P., Price‐Whelan, A., Petersen, A., Whiteley, M., & Newman, D. K. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05306.x · Cited by 718 · see citing works

Actinobacillus actinomycetemcomitans in Human Periodontal Disease: a Cross-Sectional Microbiological Investigation

Slots, J., Reynolds, H. S., & Genco, R. J. (1980) · Infection and Immunity · doi:10.1128/iai.29.3.1013-1020.1980 · Cited by 650 · see citing works

The Prokaryotes: a handbook on the biology of bacteria

(2007) · Choice Reviews Online · doi:10.5860/choice.45-0025 · Cited by 638 · see citing works

Oral microbial communities in sickness and in health

Jenkinson, H. F., & Lamont, R. J. (2005) · Trends in Microbiology · doi:10.1016/j.tim.2005.09.006 · Cited by 630 · see citing works

Interspecies Interactions within Oral Microbial Communities

Kuramitsu, H. K., He, X., Lux, R., Anderson, M. H., & Shi, W. (2007) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00024-07 · Cited by 595 · see citing works

Bacteriology of severe periodontitis in young adult humans

Moore, W. E., Holdeman, L. V., Smibert, R. M., Hash, D. E., Burmeister, J. A., & Ranney, R. R. (1982) · Infection and Immunity · doi:10.1128/iai.38.3.1137-1148.1982 · Cited by 480 · see citing works

Human Atherosclerotic Plaque Contains Viable Invasive Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis

Kozarov, E. V., Dorn, B. R., Shelburne, C. E., Dunn, W. A., & Progulske‐Fox, A. (2005) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000155018.67835.1a · Cited by 476 · see citing works

Gram negative species associated with active destructive periodontal lesions

Dzink, J. L., Tanner, A. C. R., Haffajee, A. D., & Socransky, S. S. (1985) · Journal Of Clinical Periodontology · doi:10.1111/j.1600-051x.1985.tb00936.x · Cited by 470 · see citing works

Streptococcal Antagonism in Oral Biofilms: Streptococcus sanguinis and Streptococcus gordonii Interference with Streptococcus mutans

Kreth, J., Zhang, Y., & Herzberg, M. C. (2008) · Journal of Bacteriology · doi:10.1128/jb.00276-08 · Cited by 450 · see citing works

Bacteriology of Human Experimental Gingivitis: Effect of Plaque Age

Syed, S. A., & Loesche, W. J. (1978) · Infection and Immunity · doi:10.1128/iai.21.3.821-829.1978 · Cited by 320 · see citing works

Interspecies communication in Streptococcus gordonii–Veillonella atypica biofilms: Signaling in flow conditions requires juxtaposition

Egland, P. G., Palmer, R. J., Jr., & Kolenbrander, P. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407457101 · Cited by 256 · see citing works

Rat Model of Polymicrobial Infection, Immunity, and Alveolar Bone Resorption in Periodontal Disease

Kesavalu, L. N., Sathishkumar, S., Bakthavatchalu, V., Matthews, C. R., Dawson, D. R., Steffen, M. J., & Ebersole, J. L. (2007) · Infection and Immunity · doi:10.1128/iai.00733-06 · Cited by 246 · see citing works

Bacterial and Host Interactions of Oral Streptococci

Kreth, J., Merritt, J. L., & Qi, F. (2009) · DNA and Cell Biology · doi:10.1089/dna.2009.0868 · Cited by 241 · see citing works

Revisiting the host as a growth medium

Brown, S. A., Palmer, K. L., & Whiteley, M. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1955 · Cited by 208 · see citing works

Infection Due to Actinobacillus actinomycetemcomitans: 15 Cases and Review

Kaplan, A. H., Weber, D. J., Oddone, E. Z., & Perfect, J. R. (1989) · Clinical Infectious Diseases · doi:10.1093/clinids/11.1.46 · Cited by 197 · see citing works

Relationship between oxygen tension and subgingival bacterial flora in untreated human periodontal pockets

Loesche, W. J., Gusberti, F. A., Mettraux, G., Higgins, T., & Syed, S. A. (1983) · Infection and Immunity · doi:10.1128/iai.42.2.659-667.1983 · Cited by 196 · see citing works

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 168 · see citing works

Developing animal models for polymicrobial diseases

Bakaletz, L. O. (2004) · Nature Reviews Microbiology · doi:10.1038/nrmicro928 · Cited by 158 · see citing works

Phenotypic variation in Actinobacillus actionmycetemcomitans during laboratory growth: implications for virulence

Fine, D. H., Furgang, D., Schreiner, H. C., Goncharoff, P., Charlesworth, J. E., Ghazwan, G., Fitzgerald-Bocarsly, P. A., & Figurski, D. H. (1999) · Microbiology · doi:10.1099/13500872-145-6-1335 · Cited by 156 · see citing works

Population-Based Study of Salivary Carriage of Periodontal Pathogens in Adults

Könönen, E., Paju, S., Pussinen, P. J., Hyvönen, M., Tella, P. D., Suominen‐Taipale, L., & Knuuttila, M. L. E. (2007) · Journal of Clinical Microbiology · doi:10.1128/jcm.02560-06 · Cited by 144 · see citing works

Oral pathogens: from dental plaque to cardiac disease

Meyer, D. H., & Fives-Taylor, P. M. (1998) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(98)80147-1 · Cited by 129 · see citing works

Nitric Oxide Releasing Nanoparticles Are Therapeutic for Staphylococcus aureus Abscesses in a Murine Model of Infection

Han, G., Martinez, L. R., Mihu, M., Friedman, A., Friedman, J., & Nosanchuk, J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007804 · Cited by 125 · see citing works

Outer membrane protein 100, a versatile virulence factor of Actinobacillus actinomycetemcomitans

Asakawa, R., Komatsuzawa, H., Kawai, T., Yamada, S., Gonçalves, R. B., Izumi, S., Fujiwara, T., Nakano, Y., Suzuki, N., Uchida, Y., et al. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03748.x · Cited by 124 · see citing works

Aggregatibacter actinomycetemcomitans Builds Mutualistic Biofilm Communities with Fusobacterium nucleatum and Veillonella Species in Saliva

Periasamy, S., & Kolenbrander, P. E. (2009) · Infection and Immunity · doi:10.1128/iai.00345-09 · Cited by 122 · see citing works

Analytical investigation: Assay of d-lactate in diabetic plasma and urine

Talasniemi, J. P., Pennanen, S., Savolainen, H., NISKANEN, L. K., & Liesivuori, J. (2008) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2008.06.011 · Cited by 118 · see citing works

A Novel Exclusion Mechanism for Carbon Resource Partitioning in Aggregatibacter actinomycetemcomitans

Brown, S. A., & Whiteley, M. (2007) · Journal of Bacteriology · doi:10.1128/jb.00554-07 · Cited by 115 · see citing works

Tenacious adhesion of Actinobacillus actinomycetemcomitans strain CU1000 to salivary-coated hydroxyapatite

Fine, D. H., Furgang, D., Kaplan, J. B., Charlesworth, J. E., & Figurski, D. H. (1999) · Archives of Oral Biology · doi:10.1016/s0003-9969(99)00089-8 · Cited by 114 · see citing works

Biofilm formation by Porphyromonas gingivalis and Streptococcus gordonii

Cook, G. S., Costerton, J. W., & Lamont, R. J. (1998) · Journal of Periodontal Research · doi:10.1111/j.1600-0765.1998.tb02206.x · Cited by 110 · see citing works

Evaluation and modification of spectrophotometric procedures for analysis of lactate dehydrogenase, beta-glucuronidase and arylsulphatase in human gingival crevicular fluid collected with filter-paper strips

Lamster, I. B., Hartley, L. J., Oshrain, R. L., & Gordon, J. M. (1985) · Archives of Oral Biology · doi:10.1016/0003-9969(85)90039-1 · Cited by 98 · see citing works

Virulence of a polymicrobic complex, Treponema denticola and Porphyromonas gingivalis, in a murine model

Kesavalu, L. N., Holt, S. C., & Ebersole, J. L. (1998) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.1998.tb00694.x · Cited by 80 · see citing works

Comparative virulence of periodontopathogens in a mouse abscess model

Ebersole, J. L., Kesavaln, L., Schneider, S., Machen, R. L., & Holt, S. (1995) · Oral Diseases · doi:10.1111/j.1601-0825.1995.tb00174.x · Cited by 78 · see citing works

Detection of Functional Complement Components in Gingival Crevicular Fluid from Humans with Periodontal Disease

Courts, F. J., Boackle, R. J., Fudenberg, H. H., & Silverman, M. S. (1977) · Journal of Dental Research · doi:10.1177/00220345770560032001 · Cited by 73 · see citing works

The Genus Veillonella

Kolenbrander, P. E. (2006) · Springer eBooks · doi:10.1007/0-387-30744-3_36 · Cited by 72 · see citing works

Synergy in Polymicrobial Infections in a Mouse Model of Type 2 Diabetes

Mastropaolo, M. D., Evans, N. P., Byrnes, M. K., Stevens, A. M., Robertson, J. L., & Melville, S. B. (2005) · Infection and Immunity · doi:10.1128/iai.73.9.6055-6063.2005 · Cited by 62 · see citing works

Abscess Forming Ability of Streptococcus milleri Group: Synergistic Effect with Fusobacterium nucleatum

Nagashima, H., Takao, A., & Maeda, N. (1999) · Microbiology and Immunology · doi:10.1111/j.1348-0421.1999.tb02395.x · Cited by 60 · see citing works

Subgingival distribution of A. actinomycetemcomitans in periodontitis

Ebersole, J. L., Cappelli, D. P., & Sandoval, M. N. (1994) · Journal Of Clinical Periodontology · doi:10.1111/j.1600-051x.1994.tb00282.x · Cited by 58 · see citing works

Colonization and persistence of rough and smooth colony variants of Actinobacillus actinomycetemcomitans in the mouths of rats

Fine, D. H., Goncharoff, P., Schreiner, H. C., Chang, K. M., Furgang, D., & Figurski, D. H. (2001) · Archives of Oral Biology · doi:10.1016/s0003-9969(01)00067-x · Cited by 50 · see citing works

Lactate dehydrogenase activity in gingival crevicular fluid during orthodontic treatment

Serra, E., Perinetti, G., D’Attilio, M., Cordella, C., Paolantonio, M., Festa, F., & Spoto, G. (2003) · American Journal of Orthodontics and Dentofacial Orthopedics · doi:10.1016/s0889-5406(03)00407-4 · Cited by 50 · see citing works

Cross-Feeding of Lactate Between Streptococcus lactis and Bacteroides sp. Isolated from Termite Hindguts

Schultz, J. E., & Breznak, J. A. (1979) · Applied and Environmental Microbiology · doi:10.1128/aem.37.6.1206-1210.1979 · Cited by 48 · see citing works

Periodontopathic Bacteria in Young Healthy Subjects of Different Ethnic Backgrounds in Los Angeles

Sirinian, G., Shimizu, T., Sugar, C. A., Slots, J., & Chen, C. (2002) · Journal of Periodontology · doi:10.1902/jop.2002.73.3.283 · Cited by 43 · see citing works

Short protocols in molecular biology a compendium of methods from "Current protocols in molecular biology"

Ausubel, F. M. (1999) · Cited by 42 · see citing works

Genome Sequence of Naturally Competent Aggregatibacter actinomycetemcomitans Serotype a Strain D7S-1

Chen, C., Kittichotirat, W., Chen, W., Downey, J. S., Si, Y., & Bumgarner, R. E. (2010) · Journal of Bacteriology · doi:10.1128/jb.00157-10 · Cited by 40 · see citing works

Peripheral glucose appearance rate following fructose ingestion in normal subjects

NUTTAL, F. Q., Khan, M. A., & Gannon, M. C. (2000) · Metabolism · doi:10.1053/meta.2000.18553 · Cited by 39 · see citing works

Genome Sequence ofAggregatibacter actinomycetemcomitansSerotype c Strain D11S-1

Chen, C., Kittichotirat, W., Si, Y., & Bumgarner, R. E. (2009) · Journal of Bacteriology · doi:10.1128/jb.01203-09 · Cited by 37 · see citing works

imp A, a Gene Coding for an Inner Membrane Protein, Influences Colonial Morphology of Actinobacillus actinomycetemcomitans

Mintz, K. P., & Fives-Taylor, P. M. (2000) · Infection and Immunity · doi:10.1128/iai.68.12.6580-6586.2000 · Cited by 37 · see citing works

Non-invasive monitoring of gingival crevicular fluid for estimation of blood glucose level

Yamaguchi, M., Kawabata, Y., Kambe, S., W⇘rdell, K., Nystrom, F. H., Naitoh, K., & Yoshida, H. (2004) · Medical & Biological Engineering & Computing · doi:10.1007/bf02344706 · Cited by 36 · see citing works

Host responses induced by co‐infection with Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans in a murine model

Chen, P. B., Davern, L. B., Katz, J., Eldridge, J. H., & Michalek, S. M. (1996) · Oral Microbiology and Immunology · doi:10.1111/j.1399-302x.1996.tb00181.x · Cited by 29 · see citing works

A recombinase A-deficient strain ofActinobacillus actinomycetemcomitansconstructed by insertional mutagenesis using a mobilizable plasmid

Mintz, K. P., Brissette, C. A., & Fives-Taylor, P. M. (2002) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2002.tb10991.x · Cited by 29 · see citing works

Characterization of the L-Lactate Dehydrogenase from Aggregatibacter actinomycetemcomitans

Brown, S. A., & Whiteley, M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007864 · Cited by 25 · see citing works

Molecular characterization of the membrane‐bound quinol peroxidase functionally connected to the respiratory chain

Yamada, H., Takashima, E., & Konishi, K. (2007) · FEBS Journal · doi:10.1111/j.1742-4658.2006.05637.x · Cited by 22 · see citing works

Development of an in vitro microassay for glucose quantification in submicrolitre volumes of biological fluid

Ciantar, M., Spratt, D. A., Newman, H. N., & Wilson, M. (2002) · Journal of Periodontal Research · doi:10.1034/j.1600-0765.2001.00313.x · Cited by 20 · see citing works

Structural and Segregational Stability of Various Replicons inActinobacillus actinomycetemcomitans

Galli, D., Polan-Curtain, J. L., & LeBlanc, D. J. (1996) · Plasmid · doi:10.1006/plas.1996.0030 · Cited by 15 · see citing works

The Prokaryotes a handbook on the biology of bacteria

Dworkin, M. (2006) · Cited by 15 · see citing works

Comparison in a rat thigh abscess model of imipenem, meropenem and cefoperazone-sulbactam against Acinetobacter baumannii strains in terms of bactericidal efficacy and resistance selection

Fetiye, K., Karadenizli, A., Okay, E., Oz, S., Budak, F., Gündeş, S., & Vahaboğlu, H. (2004) · Annals of Clinical Microbiology and Antimicrobials · doi:10.1186/1476-0711-3-2 · Cited by 10 · see citing works

The Oral Microbiota: Dynamic Communities and Host Interactions

Lamont, R. J., Koo, H., & Hajishengallis, G. (2018) · Nature Reviews Microbiology · doi:10.1038/s41579-018-0089-x · Cited by 2,217 · see citing works

Beyond the red complex and into more complexity: the polymicrobial synergy and dysbiosis (PSD) model of periodontal disease etiology

Hajishengallis, G., & Lamont, R. J. (2012) · Molecular Oral Microbiology · doi:10.1111/j.2041-1014.2012.00663.x · Cited by 1,267 · see citing works

Immunomicrobial pathogenesis of periodontitis: keystones, pathobionts, and host response

Hajishengallis, G. (2014) · Trends in Immunology · doi:10.1016/j.it.2013.09.001 · Cited by 1,150 · see citing works

Biogeography of a human oral microbiome at the micron scale

Mark Welch, J. L., Rossetti, B. J., Rieken, C. W., Dewhirst, F. E., & Borisy, G. G. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522149113 · Cited by 968 · see citing works

The oral microbiome: Role of key organisms and complex networks in oral health and disease

Sedghi, L., DiMassa, V., Harrington, A., Lynch, S. V., & Kapila, Y. L. (2021) · Periodontology 2000 · doi:10.1111/prd.12393 · Cited by 755 · see citing works

Diversity, structure and convergent evolution of the global sponge microbiome

Thomas, T., Moitinho‐Silva, L., Lurgi, M., Björk, J. R., Easson, C., Astudillo‐García, C., Olson, J. B., Erwin, P. M., López‐Legentil, S., Luter, H. M., et al. (2016) · Nature Communications · doi:10.1038/ncomms11870 · Cited by 668 · see citing works

Polymicrobial synergy and dysbiosis in inflammatory disease

Lamont, R. J., & Hajishengallis, G. (2015) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2014.11.004 · Cited by 585 · see citing works

Ecology and evolution of metabolic cross-feeding interactions in bacteria

D’Souza, G. G., Shitut, S., Preußger, D., Yousif, G., Waschina, S., & Kost, C. (2018) · Natural Product Reports · doi:10.1039/c8np00009c · Cited by 556 · see citing works

From in vitro to in vivo Models of Bacterial Biofilm-Related Infections

Lebeaux, D., Chauhan, A., Rendueles, O., & Beloin, C. (2013) · Pathogens · doi:10.3390/pathogens2020288 · Cited by 551 · see citing works

Solving the etiology of dental caries

Simón‐Soro, Á., & Mira, Á. (2014) · Trends in Microbiology · doi:10.1016/j.tim.2014.10.010 · Cited by 509 · see citing works

The inflammophilic character of the periodontitis-associated microbiota

Hajishengallis, G. (2014) · Molecular Oral Microbiology · doi:10.1111/omi.12065 · Cited by 407 · see citing works

Community surveillance enhances <i>Pseudomonas aeruginosa</i> virulence during polymicrobial infection

Korgaonkar, A., Trivedi, U., Rumbaugh, K. P., & Whiteley, M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214550110 · Cited by 315 · see citing works

Staphylococcus aureus Shifts toward Commensalism in Response to Corynebacterium Species

Ramsey, M. M., Freire, M. O., Gabrilska, R. A., Rumbaugh, K. P., & Lemon, K. P. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01230 · Cited by 299 · see citing works

The polymicrobial nature of biofilm infection

Wolcott, R. D., Costerton, J. W., Raoult, D., & Cutler, S. J. (2012) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2012.04001.x · Cited by 302 · see citing works

Dancing with the Stars: How Choreographed Bacterial Interactions Dictate Nososymbiocity and Give Rise to Keystone Pathogens, Accessory Pathogens, and Pathobionts

Hajishengallis, G., & Lamont, R. J. (2016) · Trends in Microbiology · doi:10.1016/j.tim.2016.02.010 · Cited by 275 · see citing works

Microbial generalists and specialists differently contribute to the community diversity in farmland soils

Xu, Q., Vandenkoornhuyse, P., Li, L., Guo, J., Zhu, C., Guo, S., Ling, N., & Shen, Q. (2021) · Journal of Advanced Research · doi:10.1016/j.jare.2021.12.003 · Cited by 235 · see citing works

Oral polymicrobial communities: Assembly, function, and impact on diseases

Hajishengallis, G., Lamont, R. J., & Koo, H. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2023.02.009 · Cited by 221 · see citing works

Mechanisms of synergy in polymicrobial infections

Murray, J. L., Connell, J. L., Stacy, A., Turner, K. H., & Whiteley, M. (2014) · The Journal of Microbiology · doi:10.1007/s12275-014-4067-3 · Cited by 201 · see citing works

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

Stacy, A., Everett, J., Jorth, P., Trivedi, U., Rumbaugh, K. P., & Whiteley, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400586111 · Cited by 192 · see citing works

Candida Survival Strategies

Polke, M., Hube, B., & Jacobsen, I. D. (2015) · Advances in applied microbiology · doi:10.1016/bs.aambs.2014.12.002 · Cited by 188 · see citing works

Real-time monitoring of quorum sensing in 3D-printed bacterial aggregates using scanning electrochemical microscopy

Connell, J. L., Kim, J., Shear, J. B., Bard, A. J., & Whiteley, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421211111 · Cited by 181 · see citing works

Streptococcal co‐infection augments <i> <scp>C</scp> andida </i> pathogenicity by amplifying the mucosal inflammatory response

Xu, H., Sobue, T., Thompson, A., Xie, Z., Poon, K., Ricker, A., Cervantes, J., Diaz, P. I., & Dongari‐Bagtzoglou, A. (2014) · Cellular Microbiology · doi:10.1111/cmi.12216 · Cited by 179 · see citing works

Beyond the oral microbiome

Jenkinson, H. F. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02573.x · Cited by 172 · see citing works

Host microbiota can facilitate pathogen infection

Stevens, E. J., Bates, K. A., & King, K. C. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009514 · Cited by 161 · see citing works

Pathogens protection against the action of disinfectants in multispecies biofilms

Sanchez-Vizuete, P., Orgaz, B., Aymerich, S., Coq, D. L., & Briandet, R. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00705 · Cited by 156 · see citing works

Biofilm Models of Polymicrobial Infection

Gabrilska, R. A., & Rumbaugh, K. P. (2015) · Future Microbiology · doi:10.2217/fmb.15.109 · Cited by 152 · see citing works

Extracellular Metabolism Sets the Table for Microbial Cross-Feeding

Fritts, R. K., McCully, A. L., & McKinlay, J. B. (2021) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00135-20 · Cited by 150 · see citing works

Oral Commensal Streptococci: Gatekeepers of the Oral Cavity

Baty, J. J., Stoner, S. N., & Scoffield, J. A. (2022) · Journal of Bacteriology · doi:10.1128/jb.00257-22 · Cited by 168 · see citing works

Microbial protection and virulence in periodontal tissue as a function of polymicrobial communities: symbiosis and dysbiosis

Roberts, F. A., & Darveau, R. P. (2015) · Periodontology 2000 · doi:10.1111/prd.12087 · Cited by 151 · see citing works

Cross-feeding modulates antibiotic tolerance in bacterial communities

Adamowicz, E. M., Flynn, J. M., Hunter, R. C., & Harcombe, W. R. (2018) · The ISME Journal · doi:10.1038/s41396-018-0212-z · Cited by 142 · see citing works

Immune and regulatory functions of neutrophils in inflammatory bone loss

Hajishengallis, G., Moutsopoulos, N. M., Hajishengallis, E., & Chavakis, T. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.02.002 · Cited by 146 · see citing works

Bacterial Metabolism Shapes the Host–Pathogen Interface

Passalacqua, K. D., Charbonneau, M., & O’Riordan, M. X. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0027-2015 · Cited by 143 · see citing works

Polybacterial human disease: the ills of social networking

Short, F. L., Murdoch, S. L., & Ryan, R. P. (2014) · Trends in Microbiology · doi:10.1016/j.tim.2014.05.007 · Cited by 141 · see citing works

A Consortium of Aggregatibacter actinomycetemcomitans, Streptococcus parasanguinis, and Filifactor alocis Is Present in Sites Prior to Bone Loss in a Longitudinal Study of Localized Aggressive Periodontitis

Fine, D. H., Markowitz, K., Fairlie, K., Tischio‐Bereski, D., Ferrendiz, J., Furgang, D., Paster, B. J., & Dewhirst, F. E. (2013) · Journal of Clinical Microbiology · doi:10.1128/jcm.00729-13 · Cited by 140 · see citing works

Aggregatibacter actinomycetemcomitans (Aa) Under the Radar: Myths and Misunderstandings of Aa and Its Role in Aggressive Periodontitis

Fine, D. H., Patil, A. G., & Velusamy, S. K. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00728 · Cited by 136 · see citing works

Innocent until proven guilty: mechanisms and roles of S treptococcus– C andida interactions in oral health and disease

Xu, H., Jenkinson, H. F., & Dongari‐Bagtzoglou, A. I. (2014) · Molecular Oral Microbiology · doi:10.1111/omi.12049 · Cited by 131 · see citing works

Cross-protection and cross-feeding between Klebsiella pneumoniae and Acinetobacter baumannii promotes their co-existence

Semenec, L., Cain, A. K., Dawson, C. J., Liu, Q., Dinh, H., Lott, H., Penesyan, A., Maharjan, R. P., Short, F. L., Hassan, K. A., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36252-2 · Cited by 122 · see citing works

Discovery of a biofilm electrocline using real-time 3D metabolite analysis

Koley, D., Ramsey, M. M., Bard, A. J., & Whiteley, M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117298108 · Cited by 122 · see citing works

Oral Biofilms from Symbiotic to Pathogenic Interactions and Associated Disease –Connection of Periodontitis and Rheumatic Arthritis by Peptidylarginine Deiminase

Kriebel, K., Hieke, C., Müller-Hilke, B., Nakata, M., & Kreikemeyer, B. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00053 · Cited by 118 · see citing works

Mechanisms of Competition in Biofilm Communities

Rendueles, O., & Ghigo, J. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mb-0009-2014 · Cited by 118 · see citing works

Co-infecting microorganisms dramatically alter pathogen gene essentiality during polymicrobial infection

Ibberson, C. B., Stacy, A., Fleming, D. F., Dees, J. L., Rumbaugh, K. P., Gilmore, M. S., & Whiteley, M. (2017) · Nature Microbiology · doi:10.1038/nmicrobiol.2017.79 · Cited by 114 · see citing works

Metabolic Heterogeneity and Cross-Feeding in Bacterial Multicellular Systems

Evans, C. R., Kempes, C. P., Price‐Whelan, A., & Dietrich, L. E. P. (2020) · Trends in Microbiology · doi:10.1016/j.tim.2020.03.008 · Cited by 115 · see citing works

The pathogenic persona of community‐associated oral streptococci

Whitmore, S. E., & Lamont, R. J. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07707.x · Cited by 112 · see citing works

Community Interactions of Oral Streptococci

Jakubovics, N. S., Yassin, S. A., & Rickard, A. H. (2014) · Advances in Applied Microbiology · doi:10.1016/b978-0-12-800261-2.00002-5 · Cited by 107 · see citing works

Live and let die: Hydrogen peroxide production by the commensal flora and its role in maintaining a symbiotic microbiome

Redanz, S., Cheng, X., Giacaman, R. A., Pfeifer, C. S., Merritt, J. L., & Kreth, J. (2018) · Molecular Oral Microbiology · doi:10.1111/omi.12231 · Cited by 111 · see citing works

Polymicrobial infections reduce the cure rate in prosthetic joint infections: outcome analysis with two-stage exchange and follow-up ≥two years

Wimmer, M. D., Friedrich, M. J., Randau, T. M., Ploeger, M. M., Schmolders, J., Strauss, A. A., Hischebeth, G. T. R., Pennekamp, P. H., Vavken, P., & Gravius, S. (2015) · International Orthopaedics · doi:10.1007/s00264-015-2871-y · Cited by 110 · see citing works

A multidimensional perspective on microbial interactions

Pacheco, A. R., & Segrè, D. (2019) · FEMS Microbiology Letters · doi:10.1093/femsle/fnz125 · Cited by 110 · see citing works

Oral streptococci: modulators of health and disease

Bloch, S., Hager‐Mair, F. F., Andrukhov, O., & Schäffer, C. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1357631 · Cited by 107 · see citing works

Community interactions and spatial structure shape selection on antibiotic resistant lineages

Estrela, S., & Brown, S. P. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006179 · Cited by 103 · see citing works

Herpesvirus‐bacteria synergistic interaction in periodontitis

Chen, C., Feng, P., & Slots, J. (2019) · Periodontology 2000 · doi:10.1111/prd.12311 · Cited by 101 · see citing works

Antimicrobial photodynamic therapy (aPDT) for biofilm treatments. Possible synergy between aPDT and pulsed electric fields

Melo, W., Celiešiūtė-Germanienė, R., Šimonis, P., & Stirkė, A. (2021) · Virulence · doi:10.1080/21505594.2021.1960105 · Cited by 99 · see citing works

Individuality, Stability, and Variability of the Plaque Microbiome

Utter, D. R., Welch, J. L. M., & Borisy, G. G. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00564 · Cited by 94 · see citing works

Self-establishing communities enable cooperative metabolite exchange in a eukaryote

Campbell, K., Vowinckel, J., Mülleder, M., Malmsheimer, S., Lawrence, N. J., Calvani, E., Miller‐Fleming, L., Alam, M. T., Christen, S., Keller, M. A., et al. (2015) · eLife · doi:10.7554/elife.09943 · Cited by 93 · see citing works

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 · see citing works

The olive knot disease as a model to study the role of interspecies bacterial communities in plant disease

Buonaurio, R., Moretti, C., da Silva, D. P., Cortese, C., Ramos, C., & Venturi, V. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00434 · Cited by 90 · see citing works

Effect of chemotherapy on the microbiota and metabolome of human milk, a case report

Urbaniak, C., McMillan, A., Angelini, M., Gloor, G. B., Sumarah, M. W., Burton, J. P., & Reid, G. (2014) · Microbiome · doi:10.1186/2049-2618-2-24 · Cited by 88 · see citing works

Metabolic and Demographic Feedbacks Shape the Emergent Spatial Structure and Function of Microbial Communities

Estrela, S., & Brown, S. P. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003398 · Cited by 84 · see citing works

The enduring importance of animal modelsin understanding periodontal disease

Hajishengallis, G., Lamont, R. J., & Graves, D. T. (2015) · Virulence · doi:10.4161/21505594.2014.990806 · Cited by 84 · see citing works

Decoding molecular interactions in microbial communities

Abreu, N. A., & Taga, M. E. (2016) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuw019 · Cited by 76 · see citing works

Intercellular communications in multispecies oral microbial communities

Guo, L., He, X., & Shi, W. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00328 · Cited by 77 · see citing works

Host and bacterial factors linking periodontitis and rheumatoid arthritis

Kowalska, A., Strzelec, K., Dziedzic, A., Bereta, G. P., Łazarz‐Bartyzel, K., Potempa, J., & Gawron, K. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.980805 · Cited by 76 · see citing works

Bacterial short-chain fatty acid metabolites modulate the inflammatory response against infectious bacteria

Corrêa, R. O., Vieira, A. T., Sernaglia, E. M., Lancellotti, M., Vieira, A. T., Ávila-Campos, M. J., Rodrigues, H. G., & Vinolo, M. A. R. (2017) · Cellular Microbiology · doi:10.1111/cmi.12720 · Cited by 75 · see citing works

Critical roles of arginine in growth and biofilm development by S treptococcus gordonii

Jakubovics, N. S., Robinson, J. C., Samarian, D. S., Kolderman, E., Yassin, S. A., Bettampadi, D., Bashton, M., & Rickard, A. H. (2015) · Molecular Microbiology · doi:10.1111/mmi.13023 · Cited by 73 · see citing works

Complement Involvement in Periodontitis: Molecular Mechanisms and Rational Therapeutic Approaches

Hajishengallis, G., Maekawa, T., Abe, T., Hajishengallis, E., & Lambris, J. D. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-18603-0_4 · Cited by 73 · see citing works

Selective pressures during chronic infection drive microbial competition and cooperation

Baishya, J., & Wakeman, C. A. (2019) · npj Biofilms and Microbiomes · doi:10.1038/s41522-019-0089-2 · Cited by 70 · see citing works

S. oralis activates the Efg1 filamentation pathway in C. albicans to promote cross-kingdom interactions and mucosal biofilms

Xu, H., Sobue, T., Bertolini, M., Thompson, A. M., Vickerman, M. M., Nobile, C. J., & Dongari‐Bagtzoglou, A. I. (2017) · Virulence · doi:10.1080/21505594.2017.1326438 · Cited by 70 · see citing works

Streptococcus oralis maintains homeostasis in oral biofilms by antagonizing the cariogenic pathogen Streptococcus mutans

Thurnheer, T., & Belibasakis, G. N. (2018) · Molecular Oral Microbiology · doi:10.1111/omi.12216 · Cited by 69 · see citing works

Taking the Starch out of Oral Biofilm Formation: Molecular Basis and Functional Significance of Salivary α-Amylase Binding to Oral Streptococci

Nikitkova, A. E., Haase, E. M., & Scannapieco, F. A. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.02581-12 · Cited by 68 · see citing works

Dual lifestyle of Porphyromonas gingivalis in biofilm and gingival cells

Sakanaka, A., Takeuchi, H., Kuboniwa, M., & Amano, A. (2015) · Microbial Pathogenesis · doi:10.1016/j.micpath.2015.10.003 · Cited by 66 · see citing works

The Pseudomonas aeruginosa Complement of Lactate Dehydrogenases Enables Use of d - and l -Lactate and Metabolic Cross-Feeding

Lin, Y.-C., Cornell, W. C., Jo, J., Price‐Whelan, A., & Dietrich, L. E. P. (2018) · mBio · doi:10.1128/mbio.00961-18 · Cited by 63 · see citing works

Streptococcus gordonii glucosyltransferase promotes biofilm interactions with Candida albicans

Ricker, A., Vickerman, M. M., & Dongari‐Bagtzoglou, A. I. (2014) · Journal of Oral Microbiology · doi:10.3402/jom.v6.23419 · Cited by 64 · see citing works

Metabolic modeling of a chronic wound biofilm consortium predicts spatial partitioning of bacterial species

Phalak, P., Chen, J., Carlson, R. P., & Henson, M. A. (2016) · BMC Systems Biology · doi:10.1186/s12918-016-0334-8 · Cited by 63 · see citing works

Immune Modulation by Group B Streptococcus Influences Host Susceptibility to Urinary Tract Infection by Uropathogenic Escherichia coli

Kline, K. A., Schwartz, D. J., Gilbert, N. M., Hultgren, S. J., & Lewis, A. L. (2012) · Infection and Immunity · doi:10.1128/iai.00684-12 · Cited by 62 · see citing works

Cooperation and Conflict Within the Microbiota and Their Effects On Animal Hosts

Figueiredo, A. R. T., & Kramer, J. (2020) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2020.00132 · Cited by 61 · see citing works

From Metabolism to Ecology: Cross-Feeding Interactions Shape the Balance between Polymicrobial Conflict and Mutualism

Estrela, S., Trisos, C. H., & Brown, S. P. (2012) · The American Naturalist · doi:10.1086/667887 · Cited by 60 · see citing works

A commensal streptococcus hijacks a Pseudomonas aeruginosa exopolysaccharide to promote biofilm formation

Scoffield, J. A., Duan, D., Zhu, F., & Wu, H. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006300 · Cited by 57 · see citing works

Candida albicans Shields the Periodontal Killer Porphyromonas gingivalis from Recognition by the Host Immune System and Supports the Bacterial Infection of Gingival Tissue

Bartnicka, D., Gonzalez‐Gonzalez, M., Sykut, J., Kozieł, J., Ciastoń, I., Adamowicz, K., Braś, G., Zawrotniak, M., Karkowska‐Kuleta, J., Satała, D., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061984 · Cited by 59 · see citing works

Bacterial interactions in pathogenic subgingival plaque

Ng, H. M., Kin, L. X., Dashper, S. G., Slakeski, N., Butler, C. A., & Reynolds, E. C. (2015) · Microbial Pathogenesis · doi:10.1016/j.micpath.2015.10.022 · Cited by 61 · see citing works

Bacterial multispecies studies and microbiome analysis of a plant disease

da Silva, D. P., Castañeda‐Ojeda, M. P., Moretti, C., Buonaurio, R., Ramos, C., & Venturi, V. (2014) · Microbiology · doi:10.1099/mic.0.074468-0 · Cited by 56 · see citing works

Tracking Polymicrobial Metabolism in Cystic Fibrosis Airways: Pseudomonas aeruginosa Metabolism and Physiology Are Influenced by Rothia mucilaginosa-Derived Metabolites

Gao, B., Gallagher, T. M., Zhang, Y., Elbadawi-Sidhu, M., Lai, Z., Fiehn, O., & Whiteson, K. (2018) · mSphere · doi:10.1128/msphere.00151-18 · Cited by 55 · see citing works

Antimicrobial resistance three ways: healthcare crisis, major concepts and the relevance of biofilms

Jorge, P., Magalhães, A. P., Grainha, T., Alves, D. F., Sousa, A. M., Lopes, S. P., & Pereira, M. O. (2019) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiz115 · Cited by 56 · see citing works

Characterization of a bacterial tyrosine kinase in Porphyromonas gingivalis involved in polymicrobial synergy

Wright, C. J., Xue, P., Hirano, T., Liu, C., Whitmore, S. E., Hackett, M., & Lamont, R. J. (2014) · MicrobiologyOpen · doi:10.1002/mbo3.177 · Cited by 53 · see citing works

Probing Bacterial Metabolism during Infection Using High-Resolution Transcriptomics

Jorth, P. A., Trivedi, U., Rumbaugh, K. P., & Whiteley, M. (2013) · Journal of Bacteriology · doi:10.1128/jb.00875-13 · Cited by 52 · see citing works

Corncob structures in dental plaque reveal microhabitat taxon specificity

Morillo-López, V., Sjaarda, A., Islam, I., Borisy, G. G., & Welch, J. L. M. (2022) · Microbiome · doi:10.1186/s40168-022-01323-x · Cited by 51 · see citing works

Clinical Implications of Polymicrobial Synergism Effects on Antimicrobial Susceptibility

Little, W., Black, C., & Smith, A. C. (2021) · Pathogens · doi:10.3390/pathogens10020144 · Cited by 49 · see citing works

Proteomics of Streptococcus gordonii within a model developing oral microbial community

Hendrickson, E. L., Wang, T., Dickinson, B. C., Whitmore, S. E., Wright, C. J., Lamont, R. J., & Hackett, M. (2012) · BMC Microbiology · doi:10.1186/1471-2180-12-211 · Cited by 50 · see citing works

Selection of Potential Probiotic Lactobacillus with Inhibitory Activity Against Salmonella and Fecal Coliform Bacteria

Abhisingha, M., Dumnil, J., & Pitaksutheepong, C. (2017) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-017-9304-8 · Cited by 50 · see citing works

Quantitative Proteomics Reveal Distinct Protein Regulations Caused by Aggregatibacter actinomycetemcomitans within Subgingival Biofilms

Bao, K., Bostancı, N., Selevsek, N., Thurnheer, T., & Belibasakis, G. N. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119222 · Cited by 48 · see citing works

Proteomic profiling of host-biofilm interactions in an oral infection model resembling the periodontal pocket

Bao, K., Belibasakis, G. N., Selevsek, N., Grossmann, J., & Bostancı, N. (2015) · Scientific Reports · doi:10.1038/srep15999 · Cited by 47 · see citing works

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 46 · see citing works

Prevalence of two Entamoeba gingivalis ST1 and ST2-kamaktli subtypes in the human oral cavity under various conditions

Garcia, G., Ramos, F., Maldonado, J., Fernandez, A., Yáñez, J., Hernández, L., & Gaytán, P. (2018) · Parasitology Research · doi:10.1007/s00436-018-5990-8 · Cited by 46 · see citing works

Proteomics of Fusobacterium nucleatum within a model developing oral microbial community

Hendrickson, E. L., Wang, T., Beck, D. A. C., Dickinson, B. C., Wright, C. J., Lamont, R. J., & Hackett, M. (2014) · MicrobiologyOpen · doi:10.1002/mbo3.204 · Cited by 45 · see citing works

Large-scale identification of pathogen essential genes during coinfection with sympatric and allopatric microbes

Lewin, G. R., Stacy, A., Michie, K. L., Lamont, R. J., & Whiteley, M. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1907619116 · Cited by 41 · see citing works

Fracture Related Infections and Their Risk Factors for Treatment Failure—A Major Trauma Centre Perspective

Lu, V., Zhang, J., Patel, R., Zhou, A., Thahir, A., & Krkovič, M. (2022) · Diagnostics · doi:10.3390/diagnostics12051289 · Cited by 43 · see citing works

Strategies for controlling polymicrobial biofilms: A focus on antibiofilm agents

Jeong, G., Khan, F., Tabassum, N., Cho, K., & Kim, Y. (2024) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2024.107243 · Cited by 42 · see citing works

Exposure to pairs of Aeromonas strains enhances virulence in the Caenorhabditis elegans infection model

Mosser, T., Talagrand-Reboul, É., Colston, S. M., Graf, J., Figueras, M. J., Jumas‐Bilak, E., & Lamy, B. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01218 · Cited by 42 · see citing works

Marine sponge aquaculture towards drug development: An ongoing history of technical, ecological, chemical considerations and challenges

Maslin, M., Gaertner‐Mazouni, N., Debitus, C., de Voogd, N. J., & Ho, R. (2021) · Aquaculture Reports · doi:10.1016/j.aqrep.2021.100813 · Cited by 42 · see citing works

Cross-kingdom microbial interactions in dental implant-related infections: is Candida albicans a new villain?

Souza, J. G. S., Costa, R. C., Sampaio, A. A., Abdo, V. L., NAGAY, B. E., Castro, N., Retamal‐Valdes, B., Shibli, J. A., Feres, M., Barão, V. A. R., et al. (2022) · iScience · doi:10.1016/j.isci.2022.103994 · Cited by 42 · see citing works

16S rRNA gene sequencing reveals the relationship between gut microbiota and ovarian development in the swimming crab Portunus trituberculatus

Wei, H., Li, X., Tang, L., Yao, H., Ren, Z., Wang, C., Mu, C., Shi, C., & Wang, H. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.126891 · Cited by 40 · see citing works

Microbial Community Composition Impacts Pathogen Iron Availability during Polymicrobial Infection

Stacy, A., Abraham, N., Jorth, P. A., & Whiteley, M. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1006084 · Cited by 39 · see citing works

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 · see citing works

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 · see citing works

The effects of polymicrobial metabolism on pathogenesis and survival in Aggregatibacter actinomycetemcomitans

Ramsey, M. M. (2011) · Texas ScholarWorks (Texas Digital Library)

Competitive inhibition and mutualistic growth in co-infections: deciphering Staphylococcus aureus–Acinetobacter baumannii interaction dynamics

Timme, S., Wendler, S., Klassert, T. E., Saraiva, J., da Rocha, U. N., Wittchen, M., Schramm, S. T. J., Ehricht, R., Monecke, S., Edel, B., et al. (2024) · ISME Communications · doi:10.1093/ismeco/ycae077 · Cited by 12 · see citing works

Metabolic Modeling and Bidirectional Culturing of Two Gut Microbes Reveal Cross-Feeding Interactions and Protective Effects on Intestinal Cells

Hirmas, B., Gasaly, N., Orellana, G., Vega, M. A., Saa, P. A., Gotteland, M., & Garrido, D. A. (2022) · mSystems · doi:10.1128/msystems.00646-22 · Cited by 42 · see citing works