The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
Dictyostelium as host model for pathogenesis
Open accessAbstract
The haploid social soil amoeba Dictyostelium discoideum has been established as a host model for several pathogens including Pseudomonas aeruginosa, Cryptococcus neoformans, Mycobacterium spp. and Legionella pneumophila. The research areas presently pursued include (i) the use of Dictyostelium wild-type cells as screening system for virulence of extracellular and intracellular pathogens and their corresponding mutants, (ii) the use of Dictyostelium mutant cells to identify genetic host determinants of susceptibility and resistance to infection and (iii) the use of reporter systems in Dictyostelium cells which allow the dissection of the complex host-pathogen cross-talk. The body of information presented in this review demonstrates that the availability of host cell markers, the knowledge of cell signalling pathways, the completion of the genome sequencing project and the tractability for genetic studies qualifies Dictyostelium for the study of fundamental cellular processes of pathogenesis.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Several bacterial pathogens for humans, such as legionella, mycobacteria and salmonella, are pathogenic also for Dictyostelium, favouring the use of this model to study host-pathogen interactions [9-19].”
From Genome-wide transcriptional changes induced by phagocytosis or growth on bacteria in Dictyostelium (2008) · cites this paper as [15]
Citations
Cites
A kingdom-level phylogeny of eukaryotes based on combined protein data.
Baldauf, S., Roger, A., Wenk-Siefert, I., & Doolittle, W. (2000) · Science · doi:10.1126/science.290.5493.972 · Cited by 1,243
Microorganisms Resistant to Free-Living Amoebae
Greub, G., & Raoult, D. (2004) · Clinical Microbiology Reviews · doi:10.1128/cmr.17.2.413-433.2004 · Cited by 1,066
Tan, M., Mahajan‐Miklos, S., & Ausubel, F. M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.2.715 · Cited by 1,008
Macromolecular Architecture in Eukaryotic Cells Visualized by Cryoelectron Tomography
Medalia, O., Weber, I. T., Frangakis, A. S., Nicastro, D., Gerisch, G., & Baumeister, W. P. (2002) · Science · doi:10.1126/science.1076184 · Cited by 841
Legionella PneumophilaPathogenesis: A Fateful Journey from Amoebae to Macrophages
Swanson, M. S., & Hammer, B. K. (2000) · Annual Review of Microbiology · doi:10.1146/annurev.micro.54.1.567 · Cited by 402
Tzou, P., Gregorio, E. D., & Lemaître, B. (2002) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(02)00294-1 · Cited by 399
Differentiate to thrive: lessons from the Legionella pneumophila life cycle
Molofsky, A. B., & Swanson, M. S. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04129.x · Cited by 338
Legionella Effectors That Promote Nonlytic Release from Protozoa
Chen, J. Y.-S., de Felipe, K. S., Clarke, M., Lu, H. X., Anderson, O. R., Segal, G., & Shuman, H. A. (2004) · Science · doi:10.1126/science.1094226 · Cited by 294
Legionella pneumophila: an aquatic microbe goes astray
Steinert, M., Hentschel, U., & Hacker, J. H. (2002) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2002.tb00607.x · Cited by 292
Self-citationPukatzki, S., Kessin, R. H., & Mekalanos, J. J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052704399 · Cited by 289
Research works printed but not linked: 2
- Steinert M., 2002, FEMS Microbiol Rev, 743, 1
- Steinert M., 2002, Legionella - 5th International Conference on Legionella., 161
Cited by
Sorted by citations
Pukatzki, S. U., Ma, A. T., Sturtevant, D., Krastins, B., Sarracino, D. A., Nelson, W. C., Heidelberg, J. F., & Mekalanos, J. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510322103 · Cited by 1,116
Current and Past Strategies for Bacterial Culture in Clinical Microbiology
Lagier, J., Edouard, S., Pagnier, I., Mediannikov, O., Drancourt, M., & Raoult, D. (2015) · Clinical Microbiology Reviews · doi:10.1128/cmr.00110-14 · Cited by 657
Molecular Pathogenesis of Infections Caused by Legionella pneumophila
Newton, H. J., Ang, D. K. Y., van Driel, I. R., & Hartland, E. L. (2010) · Clinical Microbiology Reviews · doi:10.1128/cmr.00052-09 · Cited by 522
Functional role of bacterial multidrug efflux pumps in microbial natural ecosystems
Martínez, J. L., Sánchez, M. B., Martínez‐Solano, L., Hernandez, A., Garmendia, L., Fajardo-Lubian, A., & Alvarez‐Ortega, C. (2009) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2008.00157.x · Cited by 506
The phagosome: compartment with a license to kill
Haas, A. (2007) · Traffic · doi:10.1111/j.1600-0854.2006.00531.x · Cited by 450
Eat, kill or die: when amoeba meets bacteria
Cosson, P., & Soldati, T. (2008) · Current Opinion in Microbiology · doi:10.1016/j.mib.2008.05.005 · Cited by 250
Do Free-Living Amoebae in Treated Drinking Water Systems Present an Emerging Health Risk?
Thomas, J., & Ashbolt, N. J. (2010) · Environmental Science & Technology · doi:10.1021/es102876y · Cited by 226
Ragaz, C., Pietsch, H., Urwyler, S., Tiaden, A. N., Weber, S. S., & Hilbi, H. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01219.x · Cited by 222
Environmental predators as models for bacterial pathogenesis
Hilbi, H., Weber, S. S., Ragaz, C., Nyfeler, Y., & Urwyler, S. (2007) · Environmental Microbiology · doi:10.1111/j.1462-2920.2007.01238.x · Cited by 206
Tiaden, A. N., Spirig, T., Weber, S. S., Brüggemann, H., Bosshard, R., Buchrieser, C., & Hilbi, H. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.01005.x · Cited by 185
Dictyostelium discoideum—a model for many reasons
Annesley, S. J., & Fisher, P. R. (2009) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-009-0111-8 · Cited by 166
Using non-mammalian hosts to study fungal virulence and host defense
Fuchs, B. B., & Mylonakis, E. E. (2006) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.06.004 · Cited by 154
Free-living amoebae, a training field for macrophage resistance of mycobacteria
Salah, I. B., Ghigo, É., & Drancourt, M. (2009) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2009.03011.x · Cited by 155
Mycobacterium marinum: ubiquitous agent of waterborne granulomatous skin infections
Petrini, B. (2006) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-006-0201-4 · Cited by 142
From Grazing Resistance to Pathogenesis: The Coincidental Evolution of Virulence Factors
Adiba, S., Nizak, C., van Baalen, M., Denamur, É., & Depaulis, F. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011882 · Cited by 142
Weber, S. S., Ragaz, C., & Hilbi, H. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2008.01266.x · Cited by 145
Aubert, D., Flannagan, R. S., & Valvano, M. A. (2008) · Infection and Immunity · doi:10.1128/iai.01338-07 · Cited by 132
Biggins, J. B., Ternei, M. A., & Brady, S. F. (2012) · Journal of the American Chemical Society · doi:10.1021/ja3052156 · Cited by 125
Towards a molecular understanding of human diseases using Dictyostelium discoideum
Williams, R. S. B., Boeckeler, K., Gräf, R., Müller‐Taubenberger, A., Li, Z., Isberg, R. R., Wessels, D. J., Soll, D. R., Alexander, H., & Alexander, S. (2006) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2006.07.003 · Cited by 125
The Professional Phagocyte Dictyostelium discoideum as a Model Host for Bacterial Pathogens
Bozzaro, S., & Eichinger, L. (2011) · Current Drug Targets · doi:10.2174/138945011795677782 · Cited by 122
Genomic and Functional Analysis of the Type VI Secretion System in Acinetobacter
Weber, B. S., Miyata, S. T., Iwashkiw, J. A., Mortensen, B. L., Skaar, E. P., Pukatzki, S. U., & Feldman, M. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055142 · Cited by 117
Free-living amoebae and squatters in the wild: ecological and molecular features
Samba‐Louaka, A., Delafont, V., Rodier, M., Cateau, E., & Héchard, Y. (2019) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuz011 · Cited by 116
DiSalvo, S., Haselkorn, T. S., Bashir, U., Jimenez, D., Brock, D. A., Queller, D. C., & Strassmann, J. E. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1511878112 · Cited by 113
Dictyostelium transcriptional host cell response upon infection with Legionella
Farbrother, P., Wagner, C., Na, J., Tunggal, B., Morio, T., Urushihara, H., Tanaka, Y., Schleicher, M., Steinert, M., & Eichinger, L. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00633.x · Cited by 112
Self-citationLegionella spp. outdoors: colonization, communication and persistence
Hilbi, H., Hoffmann, C., & Harrison, C. F. (2011) · Environmental Microbiology Reports · doi:10.1111/j.1758-2229.2011.00247.x · Cited by 117
Acanthamoeba and Dictyostelium as Cellular Models for Legionella Infection
Swart, A. L., Harrison, C. F., Eichinger, L., Steinert, M., & Hilbi, H. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00061 · Cited by 113
Self-citationLegionella pathogenicity: Genome structure, regulatory networks and the host cell response
Steinert, M., Heuner, K., Buchrieser, C., Albert-Weißenberger, C., & Glöckner, G. (2007) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2007.03.009 · Cited by 118
Self-citationTung, S. M., Ünal, C., Ley, A., Peña, C., Tunggal, B., Noegel, A. A., Krut, O., Steinert, M., & Eichinger, L. (2010) · Cellular Microbiology · doi:10.1111/j.1462-5822.2010.01432.x · Cited by 106
Self-citationLive-Cell Imaging of Phosphoinositide Dynamics and Membrane Architecture during Legionella Infection
Weber, S., Wagner, M. A., & Hilbi, H. (2014) · mBio · doi:10.1128/mbio.00839-13 · Cited by 110
Proteomics Fingerprinting of Phagosome Maturation and Evidence for the Role of a Gα during Uptake
Gotthardt, D., Blancheteau, V., Bosserhoff, A., Ruppert, T., Delorenzi, M., & Soldati, T. (2006) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m600113-mcp200 · Cited by 98
Type VI Secretion Effectors: Methodologies and Biology
Lien, Y., & Lai, E. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00254 · Cited by 98
Autophagy in Dictyostelium: Genes and pathways, cell death and infection
Calvo‐Garrido, J., Carilla-Latorre, S., Kubohara, Y., Santos-Rodrigo, N., Mesquita, A., Soldati, T., Golstein, P., & Escalante, R. (2010) · Autophagy · doi:10.4161/auto.6.6.12513 · Cited by 99
Steiner, B., Weber, S., & Hilbi, H. (2017) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2017.08.004 · Cited by 98
Chapter 6 Phagocytosis and Host–Pathogen Interactions in Dictyostelium with a Look at Macrophages
Bozzaro, S., Bucci, C., & Steinert, M. (2008) · International review of cytology · doi:10.1016/s1937-6448(08)01206-9 · Cited by 96
Self-citationAnimal models: an important tool in mycology
Capilla, J., Clemons, K. V., & Stevens, D. A. (2007) · Medical Mycology · doi:10.1080/13693780701644140 · Cited by 94
Dictyostelium Finds New Roles to Model
Williams, J. G. (2010) · Genetics · doi:10.1534/genetics.110.119297 · Cited by 95
Pathogen–host interactions in Dictyostelium, Legionella, Mycobacterium and other pathogens
Steinert, M. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.11.003 · Cited by 94
Self-citationProteomic analysis of Legionella-containing phagosomes isolated from Dictyostelium
Shevchuk, O., Batzilla, C. F., Hägele, S., Kusch, H., Engelmann, S., Hecker, M., Haas, A., Heuner, K., Glöckner, G., & Steinert, M. (2009) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2009.03.006 · Cited by 88
Self-citationThe Cold War of the Social Amoebae
Shaulsky, G., & Kessin, R. H. (2007) · Current Biology · doi:10.1016/j.cub.2007.06.024 · Cited by 84
Anchors for Effectors: Subversion of Phosphoinositide Lipids by Legionella
Hilbi, H., Weber, S., & Finsel, I. (2011) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00091 · Cited by 88
Modulation of phosphoinositide metabolism by pathogenic bacteria
Hilbi, H. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00793.x · Cited by 80
Autophagy in Inflammatory Diseases
Choi, A. J. S., & Ryter, S. W. (2011) · International Journal of Cell Biology · doi:10.1155/2011/732798 · Cited by 72
Genome-wide transcriptional changes induced by phagocytosis or growth on bacteria in Dictyostelium
Sillo, A., Bloomfield, G., Balest, A., Balbo, A., Pergolizzi, B., Peracino, B., Skelton, J., Ivens, A., & Bozzaro, S. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-291 · Cited by 69
Bacterial–protozoa interactions; an update on the role these phenomena play towards human illness
Snelling, W. J., Moore, J. E., McKenna, J. P., Lecky, D. M., & Dooley, J. S. G. (2005) · Microbes and Infection · doi:10.1016/j.micinf.2005.09.001 · Cited by 69
Infection in a dish: high-throughput analyses of bacterial pathogenesis
Kurz, C. L., & Ewbank, J. J. (2006) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.12.001 · Cited by 66
Modelling infectious disease — time to think outside the box?
Wiles, S., Hanage, W. P., Frankel, G. M., & Robertson, B. D. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1386 · Cited by 65
Häuslein, I., Manske, C., Goebel, W., Eisenreich, W., & Hilbi, H. (2015) · Molecular Microbiology · doi:10.1111/mmi.13313 · Cited by 65
Synergistic activity of cosecreted natural products from amoebae-associated bacteria
Arp, J., Götze, S., Mukherji, R., Mattern, D. J., García‐Altares, M., Klapper, M., Brock, D. A., Brakhage, A. A., Strassmann, J. E., Queller, D. C., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1721790115 · Cited by 63
A silkworm model of pathogenic bacterial infection.
Kaito, C., & Sekimizu, K. (2007) · PubMed · Cited by 58
Bayer‐Santos, E., Lima, L. D. P., Ceseti, L. D. M., RATAGAMI, C. Y., de Santana, E. S., da Silva, A. M., Farah, C. S., & Alvarez‐Martinez, C. E. (2018) · Environmental Microbiology · doi:10.1111/1462-2920.14085 · Cited by 56
Choosing an Appropriate Infection Model to Study Quorum Sensing Inhibition in Pseudomonas Infections
Papaioannou, E., Utari, P. D., & Quax, W. J. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140919309 · Cited by 52
Carilla-Latorre, S., Calvo‐Garrido, J., Bloomfield, G., Skelton, J., Kay, R. R., Ivens, A. C., Martínez, J. L., & Escalante, R. (2008) · BMC Microbiology · doi:10.1186/1471-2180-8-109 · Cited by 43
Hasselbring, B. M., Patel, M. K., & Schell, M. A. (2011) · Infection and Immunity · doi:10.1128/iai.01233-10 · Cited by 44
Dictyostelium discoideum as a non‐mammalian biomedical model
Martín‐González, J., Montero‐Bullón, J., & Lacal, J. (2020) · Microbial Biotechnology · doi:10.1111/1751-7915.13692 · Cited by 43
The Genealogic Tree of Mycobacteria Reveals a Long-Standing Sympatric Life into Free-Living Protozoa
Lamrabet, O., Merhej, V., Pontarotti, P., Raoult, D., & Drancourt, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034754 · Cited by 40
Dictyostelium discoideum —a promising expression system for the production of eukaryotic proteins
Arya, R., Bhattacharya, A., & Saini, K. S. (2008) · The FASEB Journal · doi:10.1096/fj.08-110544 · Cited by 44
Setting Up and Monitoring an Infection of Dictyostelium discoideum with Mycobacteria
Arafah, S., Kicka, S., Trofimov, V., Hagedorn, M., Andreu, N., Wiles, S., Robertson, B. D., & Soldati, T. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-302-2_22 · Cited by 39
Kicka, S., Trofimov, V., Harrison, C. F., Ouertatani-Sakouhi, H., McKinney, J. D., Scapozza, L., Hilbi, H., Cosson, P., & Soldati, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087834 · Cited by 39
Tools to study molecular mechanisms of Aspergillus pathogenicity
Krappmann, S. (2006) · Trends in Microbiology · doi:10.1016/j.tim.2006.06.005 · Cited by 33
Exploring Anti-Bacterial Compounds against Intracellular Legionella
Harrison, C. F., Kicka, S., Trofimov, V., Berschl, K., Ouertatani-Sakouhi, H., Ackermann, N., Hedberg, C., Cosson, P., Soldati, T., & Hilbi, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074813 · Cited by 31
Dictyostelium discoideum : A Model System for Cell and Developmental Biology
Mathavarajah, S., Flores, A., & Huber, R. J. (2017) · Current Protocols Essential Laboratory Techniques · doi:10.1002/cpet.15 · Cited by 31
Aragão, K. S., Satre, M., Imberty, A., & Varrot, A. (2008) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.22038 · Cited by 31
Edwards, S., & Kjellerup, B. V. (2012) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2012.00975.x · Cited by 31
Smati, M., Magistro, G., Adiba, S., Wieser, A., Picard, B., Schubert, S., & Denamur, É. (2016) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2016.11.004 · Cited by 32
Treasure hunt in an amoeba: non-coding RNAs in Dictyostelium discoideum
Hinas, A., & Söderbom, F. (2006) · Current Genetics · doi:10.1007/s00294-006-0112-z · Cited by 26
Non-vertebrate hosts in the analysis of host–pathogen interactions
Dorer, M. S., & Isberg, R. R. (2006) · Microbes and Infection · doi:10.1016/j.micinf.2005.11.020 · Cited by 26
What can Dictyostelium bring to the study of Pseudomonas infections?
de Lima, W. C., Lelong, E., & Cosson, P. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.11.006 · Cited by 24
Pathogen vacuole membrane contact sites – close encounters of the fifth kind
Vormittag, S., Ende, R. J., Derré, I., & Hilbi, H. (2023) · microLife · doi:10.1093/femsml/uqad018 · Cited by 24
Subversion of Cell-Autonomous Immunity and Cell Migration by Legionella pneumophila Effectors
Simon, S., & Hilbi, H. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00447 · Cited by 23
Yan, Y., Jiang, L., Aufderheide, K. J., Wright, G. A., Terekhov, A. Y., Costa, L. A., Qin, K. H., McCleery, W. T., Fellenstein, J., Ustione, A., et al. (2014) · Microscopy and Microanalysis · doi:10.1017/s1431927613014037 · Cited by 22
Sattler, N., Bosmani, C., Barisch, C., Guého, A., Gopaldass, N., Dias, M., Leuba, F., Brückert, F., Cosson, P., & Soldati, T. (2018) · Journal of Cell Science · doi:10.1242/jcs.218040 · Cited by 22
Richter, A., Shapira, T., & Av‐Gay, Y. (2019) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01601-19 · Cited by 22
Efficient inactivation of intracellular bacteria in dormant amoeba spores by FeP
He, Z., Zheng, N., Zhang, L., Tian, Y., Hu, Z., & Shu, L. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2021.127996 · Cited by 22
Vlahou, G., Schmidt, O., Wagner, B., Uenlue, H., Dersch, P., Rivero, F., & Weissenmayer, B. (2009) · BMC Microbiology · doi:10.1186/1471-2180-9-138 · Cited by 22
Kin Discrimination in Dictyostelium Social Amoebae
Strassmann, J. E. (2016) · Journal of Eukaryotic Microbiology · doi:10.1111/jeu.12307 · Cited by 23
Endocytosis and the Actin Cytoskeleton in Dictyostelium discoideum
Rivero, F. (2008) · International review of cytology · doi:10.1016/s1937-6448(08)00633-3 · Cited by 21
Developmental changes in transcriptional profiles
Loomis, W. F., & Shaulsky, G. (2011) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2010.01241.x · Cited by 20
DiSalvo, S., Brock, D. A., Smith, J. S., Queller, D. C., & Strassmann, J. E. (2014) · BMC Microbiology · doi:10.1186/s12866-014-0328-x · Cited by 19
Tapping lipid droplets: A rich fat diet of intracellular bacterial pathogens
Hüsler, D., Stauffer, P., & Hilbi, H. (2023) · Molecular Microbiology · doi:10.1111/mmi.15120 · Cited by 17
The Dictyostelium model for mitochondrial biology and disease
Pearce, X. G., Annesley, S. J., & Fisher, P. R. (2019) · The International Journal of Developmental Biology · doi:10.1387/ijdb.190233pf · Cited by 18
Lefrançois, L. H., Nitschke, J., Wu, H., Panis, G., Prados, J., Butler, R. E., Mendum, T. A., Hanna, N., Stewart, G. R., & Soldati, T. (2024) · mSystems · doi:10.1128/msystems.01326-23 · Cited by 17
Hanna, N., Kicka, S., Chiriano, G., Harrison, C. F., Ouertatani-Sakouhi, H., Trofimov, V., Kranjc, A., Nitschke, J., Pagni, M., Cosson, P., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00266 · Cited by 16
Haselkorn, T. S., Jimenez, D., Bashir, U., Sallinger, E., Queller, D. C., Strassmann, J. E., & DiSalvo, S. (2021) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12985 · Cited by 17
Decreased virulence of cystic fibrosis Pseudomonas aeruginosa in Dictyostelium discoideum
Bradbury, R. S., Reid, D. W., Inglis, T. J. J., & Champion, A. C. (2011) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2011.00314.x · Cited by 16
Reassessing the Role of DotF in the Legionella pneumophila Type IV Secretion System
Sutherland, M. C., Binder, K. A., Cualing, P. Y., & Vogel, J. P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065529 · Cited by 16
A vesicle surface tyrosine kinase regulates phagosome maturation
Fang, J., Brzostowski, J. A., Ou, S., Isik, N., Nair, V., & Jin, T. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200701023 · Cited by 16
Bozzaro, S., Peracino, B., & Eichinger, L. (2012) · Methods in molecular biology · doi:10.1007/978-1-62703-161-5 · Cited by 14
Host as the Variable: Model Hosts Approach the Immunological Asymptote
Casadevall, A. (2005) · Infection and Immunity · doi:10.1128/iai.73.7.3829-3832.2005 · Cited by 14
Hanna, N., Burdet, F., Melotti, A., Bosmani, C., Kicka, S., Hilbi, H., Cosson, P., Pagni, M., & Soldati, T. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/590810 · Cited by 15
Immunomagnetic Purification of Fluorescent Legionella-Containing Vacuoles
Finsel, I., Hoffmann, C., & Hilbi, H. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-302-2_24 · Cited by 13
Pathogenese, Diagnostik und Therapie der Legionella-Infektion
Lück, P. C., & Steinert, M. (2006) · Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz · doi:10.1007/s00103-006-1254-3 · Cited by 13
Self-citationShevchuk, O., & Steinert, M. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-204-5_4 · Cited by 11
Self-citationde Oliveira, A. L., Barbieri, N. L., Newman, D. M., Young, M. M., Nolan, L. K., & Logue, C. M. (2021) · PeerJ · doi:10.7717/peerj.12631 · Cited by 10
Coincidental Loss of Bacterial Virulence in Multi-Enemy Microbial Communities
Zhang, J., Ketola, T., Örmälä‐Odegrip, A., Mappes, J., & Laakso, J. T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111871 · Cited by 10
Noh, S., Peck, R. F., Larson, E. R., Covitz, R., Chen, A., Roy, P., Hamilton, M. C., & Dettmann, R. A. (2024) · Evolution Letters · doi:10.1093/evlett/qrae001 · Cited by 9
Hayes, A. C., Stupak, J., Li, J., & Cox, A. D. (2012) · Journal of Lipid Research · doi:10.1194/jlr.m032219 · Cited by 9
Shina, M. C., & Noegel, A. A. (2008) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-0-387-09595-0_8 · Cited by 9
Single Cell Analysis of Legionella and Legionella-Infected Acanthamoeba by Agarose Embedment
Personnic, N., Striednig, B., & Hilbi, H. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9048-1_12 · Cited by 8
Woods, A. L., Parker, D. T., Glick, M., Peng, Y., Lenoir, F., Mulligan, E. A., Yu, V., Piizzi, G., Lister, T., Lilly, M.-D., et al. (2022) · ACS Omega · doi:10.1021/acsomega.1c06633 · Cited by 8
Koonce, M. P., & Gräf, R. (2010) · Methods in cell biology · doi:10.1016/s0091-679x(10)96009-3 · Cited by 9
Metadata
- Authors
- Steinert, M., & Heuner, K.
- Affiliations
- University of Würzburg (DE)
- Corresponding author
- Steinert, Michael
- ORCID
- Steinert, Michael
- Venue
- Cellular Microbiology
- Publisher
- Hindawi Limited
- Published
- 2005-03
- Volume
- 7
- Issue
- 3
- Pages
- 307-314
- ISSN
- 1462-5814 (ISSN-L)
- 1462-5822
- OpenAlex
- W2035399581
- Cited by
- 144
- References
- 51
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 5 · 2023: 5 · 2022: 2 · 2021: 3 · 2020: 6 · 2019: 7 · 2018: 6 · 2017: 4 · 2016: 2 · 2015: 5 · 2014: 9 · 2013: 6 · 2012: 5
- FWCI
- 1.46
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cellular Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (STE 838/3-2)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Legionella and Acanthamoeba research
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Slime Mold and Myxomycetes Research
- Life Sciences › Immunology and Microbiology › Immunology › Invertebrate Immune Response Mechanisms
- Keywords
- Dictyostelium discoideum, host-pathogen interaction, pathogenesis, virulence screening, host resistance and susceptibility, reporter system, cell signalling pathways, Pseudomonas aeruginosa, Cryptococcus neoformans, Mycobacterium, Legionella pneumophila, intracellular pathogens, extracellular pathogens
- MeSH terms
- Animals, Cryptococcus neoformans, Dictyostelium, Mutation, Mycobacterium, Phagocytosis, Pseudomonas aeruginosa, Virulence, Legionella pneumophila, Models, Animal
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review