The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
The Pic Protease of Enteroaggregative Escherichia coli Promotes Intestinal Colonization and Growth in the Presence of Mucin
Open accessAbstract
Enteroaggregative Escherichia coli (EAEC) is increasingly being recognized as a cause of diarrheal disease in diverse populations. No small animal model is currently available to study this pathogen. We report here that conventional mice orally inoculated with prototype EAEC strain 042 generally became colonized, though the abundance of organisms cultured from their stool varied substantially among individual animals. In contrast, mice whose water contained 5 g/liter streptomycin consistently became colonized at high levels (ca. 10 8 CFU/g of stool). Neither conventional nor streptomycin-treated mice developed clinical signs or histopathologic abnormalities. Using specific mutants in competition with the wild-type strain, we evaluated the contribution of several putative EAEC virulence factors to colonization of streptomycin-treated mice. Our data suggest that the dispersin surface protein and Pic, a serine protease autotransporter secreted by EAEC and Shigella flexneri , promote colonization of the mouse. In contrast, we found no role for the aggregative adherence fimbriae, the transcriptional activator AggR, or the surface factor termed Air (entero a ggregative i mmunoglobulin r epeat protein). To study Pic further, we constructed a single nucleotide mutation in strain 042 which altered only the Pic catalytic serine (strain 042PicS258A). Fractionation of the tissue at 24 h and 3 days demonstrated an approximate 3-log 10 difference between 042 and 042PicS258A in the lumen and mucus layer and adherent to tissue. Strains 042 and 042PicS258A adhered similarly to mouse tissue ex vivo. While no growth differences were observed in a continuous-flow anaerobic intestinal simulator system, the wild-type strain exhibited a growth advantage over 042PicS258A in a culture of cecal mucus and in cecal contents in vitro; this difference was manifest only after 6 h of growth. Moreover, enhanced growth of the wild type was observed in comparison with that of the mutant in minimal medium containing mucin but not in the absence of mucin. The data suggest a novel metabolic role for the Pic mucinase in EAEC colonization.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Proteases from different infectious agents such as Pic in diarrheagenic E. coli and Shigella, or vibriolysin in V. cholera, degrade the colonic mucus, which is a key step facilitating epithelium invasion.10,68,69,71”
From The emerging roles of bacterial proteases in intestinal diseases (2023) · cites this paper as [71]
Experimental — accuracy not yet measuredIn the citing paper
“the serine protease Pic produced by E. coli (EAEC), Citrobacter and Shigella flexneri is a virulence factor associated with adherence, colonization and evasion of the innate immune system.68–71”
From The emerging roles of bacterial proteases in intestinal diseases (2023) · cites this paper as [71]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Donnenberg, M. S., & Kaper, J. B. (1991) · Infection and Immunity · doi:10.1128/iai.59.12.4310-4317.1991 · Cited by 1,051
Carbon nutrition of Escherichia coli in the mouse intestine
Chang, D., Smalley, D. J., Tucker, D. L., Leatham, M. P., Norris, W. E., Stevenson, S. J., Anderson, A. B., Grissom, J. E., Laux, D. C., Cohen, P. S., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307888101 · Cited by 513
Self-citationVirulence Functions of Autotransporter Proteins
Henderson, I. R., & Nataro, J. P. (2001) · Infection and Immunity · doi:10.1128/iai.69.3.1231-1243.2001 · Cited by 448
Self-citationAsmar, R. E., Panigrahi, P., Bamford, P. D., Berti, I., Not, T., Coppa, G. V., Catassi, C., & Fasano, A. (2002) · Gastroenterology · doi:10.1053/gast.2002.36578 · Cited by 369
Henderson, I. R., Czeczulin, J., Eslava, C., Noriega, F., & Nataro, J. P. (1999) · Infection and Immunity · doi:10.1128/iai.67.11.5587-5596.1999 · Cited by 357
Self-citationHeterogeneity of Enteroaggregative Escherichia Coli Virulence Demonstrated
Nataro, J. P., Yikang, D., Cookson, S., Cravioto, A., Savarino, S. J., Guers, L., Levine, M. M., & Tacket, C. O. (1995) · The Journal of Infectious Diseases · doi:10.1093/infdis/171.2.465 · Cited by 326
Self-citationBhan, M. K., Raj, P., Levine, M. M., Kaper, J. B., Bhandari, N., Srivastava, R., Kumar, R., & Sazawal, S. (1989) · The Journal of Infectious Diseases · doi:10.1093/infdis/159.6.1061 · Cited by 323
Nataro, J. P., Deng, Y., Maneval, D. R., German, A. L., Martin, W. C., & Levine, M. M. (1992) · Infection and Immunity · doi:10.1128/iai.60.6.2297-2304.1992 · Cited by 303
Self-citationCzeczulin, J. R., Balepur, S., Hicks, S., Phillips, A. D., HALL, R. H., Kothary, M. H., Navarro‐García, F., & Nataro, J. P. (1997) · Infection and Immunity · doi:10.1128/iai.65.10.4135-4145.1997 · Cited by 279
Self-citationA novel dispersin protein in enteroaggregative Escherichia coli
Sheikh, J., Czeczulin, J. R., Harrington, S. M., Hicks, S., Henderson, I. R., Bouguénec, C. L., Gounon, P., Phillips, A. D., & Nataro, J. P. (2002) · Journal of Clinical Investigation · doi:10.1172/jci16172 · Cited by 255
Self-citation
Cited by
Sorted by citations
Origins of the E. coli Strain Causing an Outbreak of Hemolytic–Uremic Syndrome in Germany
Rasko, D. A., Webster, D. R., Sahl, J. W., Bashir, A., Boisen, N., Scheutz, F., Paxinos, E. E., Sebra, R., Chin, C.-S., Iliopoulos, D., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1106920 · Cited by 835
Self-citationRoles and regulation of the mucus barrier in the gut
Cornick, S., Tawiah, A., & Chadee, K. (2015) · Tissue Barriers · doi:10.4161/21688370.2014.982426 · Cited by 556
Interactions of Intestinal Bacteria with Components of the Intestinal Mucus
Sicard, J.-F., Bihan, G. L., Vogeleer, P., Jacques, M., & Harel, J. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00387 · Cited by 481
Infection strategies of enteric pathogenic Escherichia coli
Clements, A., Young, J. C., Constantinou, N., & Frankel, G. M. (2012) · Gut Microbes · doi:10.4161/gmic.19182 · Cited by 375
The host selects mucosal and luminal associations of coevolved gut microorganisms: a novel concept
den Abbeele, P. V., de Wiele, T. V., Verstraete, W., & Possemiers, S. (2011) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2011.00270.x · Cited by 273
How Do the Virulence Factors of Shigella Work Together to Cause Disease?
Mattock, E., & Blocker, A. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00064 · Cited by 253
Th17 Cytokines and the Gut Mucosal Barrier
Blaschitz, C., & Raffatellu, M. (2010) · Journal of Clinical Immunology · doi:10.1007/s10875-010-9368-7 · Cited by 258
Pokharel, P., Dhakal, S., & Dozois, C. M. (2023) · Microorganisms · doi:10.3390/microorganisms11020344 · Cited by 252
Shiga Toxin-Producing Escherichia coli O104:H4: a New Challenge for Microbiology
Muniesa, M., Hammerl, J. A., Hertwig, S. T., Appel, B., & Brüssow, H. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.00217-12 · Cited by 197
Genomic Characterization of Enteroaggregative Escherichia coli From Children in Mali
Boisen, N., Scheutz, F., Rasko, D. A., Redman, J. C., Persson, S., Simon, J. K., Kotloff, K. L., Levine, M. M., Sow, S. O., Tamboura, B., et al. (2011) · The Journal of Infectious Diseases · doi:10.1093/infdis/jir757 · Cited by 189
Self-citationChaudhuri, R. R., Sebaihia, M., Hobman, J. L., Webber, M. A., Leyton, D. L., Goldberg, M. D., Cunningham, A. F., Scott-Tucker, A., Ferguson, P., Thomas, C. M., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008801 · Cited by 196
Self-citationCrossman, L. C., Chaudhuri, R. R., Beatson, S. A., Wells, T. J., Desvaux, M., Cunningham, A. F., Petty, N. K., Mahon, V., Brinkley, C., Hobman, J. L., et al. (2010) · Journal of Bacteriology · doi:10.1128/jb.00710-10 · Cited by 185
Self-citationRuiz-Perez, F., & Nataro, J. P. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1355-8 · Cited by 149
Self-citationLuo, Q., Kumar, P., Vickers, T. J., Sheikh, A., Lewis, W. G., Rasko, D. A., Sistrunk, J., & Fleckenstein, J. M. (2014) · Infection and Immunity · doi:10.1128/iai.01106-13 · Cited by 139
Ahmed, S. A., Awosika, J. A., Baldwin, C. D., Bishop‐Lilly, K. A., Biswas, B., Broomall, S. M., Chain, P., Chertkov, O., Chokoshvili, O., Coyne, S. R., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048228 · Cited by 130
Enteroaggregative Escherichia coli : An Emerging Enteric Food Borne Pathogen
Kaur, P., Chakraborti, A., & Asea, A. A. A. (2010) · Interdisciplinary Perspectives on Infectious Diseases · doi:10.1155/2010/254159 · Cited by 124
Serine Protease Autotransporters of Enterobacteriaceae (SPATEs): Biogenesis and Function
Dautin, N. (2010) · Toxins · doi:10.3390/toxins2061179 · Cited by 113
Okhuysen, P. C., & DuPont, H. L. (2010) · The Journal of Infectious Diseases · doi:10.1086/654895 · Cited by 112
Ramírez-Larrota, J. S., & Eckhard, U. (2022) · Biomolecules · doi:10.3390/biom12020306 · Cited by 122
Ruı́z-Pérez, F., Wahid, R., Faherty, C. S., Kolappaswamy, K., Rodriguez, L., Santiago, A. E., Murphy, E., Cross, A. S., Sztein, M. B., & Nataro, J. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1101006108 · Cited by 114
Self-citationBai, X.-N., Fu, S., Zhang, J., Fan, R.-Y., Xu, Y.-M., Sun, H., He, X., Xu, J.-G., & Xiong, Y.-W. (2018) · Scientific Reports · doi:10.1038/s41598-018-25233-x · Cited by 91
Navarro‐García, F., Gutiérrez-Jiménez, J., García-Tovar, C. G., Castro‐Sánchez, L., Salazar-González, H., & Cordova, V. (2010) · Infection and Immunity · doi:10.1128/iai.00523-10 · Cited by 104
Stecher, B., Berry, D., & Loy, A. (2013) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12024 · Cited by 106
Virulent Bacteriophages Can Target O104:H4 Enteroaggregative Escherichia coli in the Mouse Intestine
Maura, D., Galtier, M., Bouguénec, C. L., & Debarbieux, L. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00602-12 · Cited by 104
Autotransporter secretion: varying on a theme
Grijpstra, J., Arenas, J., Rutten, L., & Tommassen, J. (2013) · Research in Microbiology · doi:10.1016/j.resmic.2013.03.010 · Cited by 95
Lima, I. F. N., Boisen, N., Quetz, J. D. S., Havt, A., de Carvalho, E. B., Soares, A. M., Lima, N. L., Mota, R. M. S., Nataro, J. P., Guerrant, R. L., et al. (2013) · Journal of Medical Microbiology · doi:10.1099/jmm.0.054262-0 · Cited by 96
Self-citationThe emerging roles of bacterial proteases in intestinal diseases
Caminero, A., Guzman, M., Libertucci, J., & Lomax, A. E. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2181922 · Cited by 92
Sevrin, G., Massier, S., Chassaing, B., Agus, A., Delmas, J., Denizot, J., Billard, E., & Barnich, N. (2018) · Gut Microbes · doi:10.1080/19490976.2017.1421886 · Cited by 98
Gibold, L., Garénaux, E., Dalmasso, G., Gallucci, C., Cia, D., Mottet-Auselo, B., Faïs, T., Darfeuille–Michaud, A., Nguyen, H. T. T., Barnich, N., et al. (2015) · Cellular Microbiology · doi:10.1111/cmi.12539 · Cited by 111
Th17 cytokines and host-pathogen interactions at the mucosa: Dichotomies of help and harm
Liu, J. Z., Pezeshki, M., & Raffatellu, M. (2009) · Cytokine · doi:10.1016/j.cyto.2009.07.005 · Cited by 83
Navarro‐García, F. (2014) · Microbiology Spectrum · doi:10.1128/microbiolspec.ehec-0008-2013 · Cited by 89
Rajan, A., Vela, L., Zeng, X., Yu, X., Shroyer, N. F., Blutt, S. E., Poole, N. M., Carlin, L. G., Nataro, J. P., Estes, M. K., et al. (2018) · mBio · doi:10.1128/mbio.02419-17 · Cited by 81
Self-citationEnteric bacterial proteases in inflammatory bowel disease- pathophysiology and clinical implications
Carroll, I. M. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i43.7531 · Cited by 82
Mucosal Inflammatory Response to Salmonella typhimurium Infection
Patel, S. N., & McCormick, B. A. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00311 · Cited by 85
Lara, F. B. M., Nery, D. R., de Oliveira, P. M., Araujo, M., Carvalho, F. R. Q., Messias-Silva, L. C. F., Ferreira, L. B., Faria-Junior, C., & Pereira, A. L. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00146 · Cited by 66
Role of Enteroaggregative Escherichia coli Virulence Factors in Uropathogenesis
Boll, E. J., Struve, C., Boisen, N., Olesen, B. R. S., Stahlhut, S. G., & Krogfelt, K. A. (2013) · Infection and Immunity · doi:10.1128/iai.01376-12 · Cited by 77
Allaire, J. M., Morampudi, V., Crowley, S. M., Stahl, M., Yu, H., Bhullar, K., Knodler, L. A., Bressler, B. L., Jacobson, K., & Vallance, B. A. (2018) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00181.2017 · Cited by 79
Classification, structural biology, and applications of mucin domain-targeting proteases
Shon, D. J., Kuo, A., Ferracane, M. J., & Malaker, S. A. (2021) · Biochemical Journal · doi:10.1042/bcj20200607 · Cited by 72
Safadi, R., Abu-Ali, G., Sloup, R. E., Rudrik, J. T., Waters, C. M., Eaton, K. A., & Manning, S. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041628 · Cited by 75
An innate antiviral pathway acting before interferons at epithelial surfaces
Iversen, M. B., Reinert, L. S., Thomsen, M. K., Bagdonaite, I., Nandakumar, R., Cheshenko, N., Prabakaran, T., Vakhrushev, S. Y., Krzyżowska, M., Kratholm, S. K., et al. (2015) · Nature Immunology · doi:10.1038/ni.3319 · Cited by 71
Richter, A. M., Povolotsky, T. L., Wieler, L. H., & Hengge, R. (2014) · EMBO Molecular Medicine · doi:10.15252/emmm.201404309 · Cited by 65
Autotransporters and virulence of enteroaggregativeE. coli
Navarro‐García, F., & Elias, W. P. (2011) · Gut Microbes · doi:10.4161/gmic.2.1.14933 · Cited by 64
Pereira, W. A., Pereira, C. D. D. S., Assunção, R. G., da Silva, I. S. C., Rego, F. S., Alves, L. S. R., Santos, J., Nogueira, F. J. R., Zagmignan, A., Thomsen, T. T., et al. (2021) · Biomolecules · doi:10.3390/biom11020302 · Cited by 60
Ageorges, V., Monteiro, R., Léroy, S., Burgess, C. M., Pizza, M., Chaucheyras‐Durand, F., & Desvaux, M. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa008 · Cited by 65
Cyclic di-GMP Signaling Regulates Invasion by Ehrlichia chaffeensis of Human Monocytes
Kumagai, Y., Matsuo, J., Hayakawa, Y., & Rikihisa, Y. (2010) · Journal of Bacteriology · doi:10.1128/jb.00132-10 · Cited by 59
Shigella depends on SepA to destabilize the intestinal epithelial integrity via cofilin activation
Maldonado-Contreras, A., Birtley, J. R., Boll, E., Zhao, Y., Mumy, K. L., Toscano, J., Ayehunie, S., Reinecker, H.-C., Stern, L. J., & McCormick, B. A. (2017) · Gut Microbes · doi:10.1080/19490976.2017.1339006 · Cited by 57
Kida, Y., Shimizu, T., & Kuwano, K. (2010) · Infection and Immunity · doi:10.1128/iai.01053-10 · Cited by 57
Abreu, A. G., Fraga, T. R., Martinez, A. P. G., Kondo, M. Y., Juliano, M. A., Juliano, L., Navarro‐García, F., Isaac, L., Barbosa, A. S., & Elias, W. P. (2015) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiv013 · Cited by 57
Mucus layer modeling of human colonoids during infection with enteroaggragative E. coli
Liu, L., Saitz, W., Smith, R., Gonyar, L. A., In, J., Kovbasnjuk, O. N., Zachos, N. C., Donowitz, M., Nataro, J. P., & Ruı́z-Pérez, F. (2020) · Scientific Reports · doi:10.1038/s41598-020-67104-4 · Cited by 58
Self-citationEnteric Pathogens Exploit the Microbiota-generated Nutritional Environment of the Gut
Pacheco, A. R., & Sperandio, V. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mbp-0001-2014 · Cited by 55
Navarro‐García, F., Serapio-Palacios, A., Ugalde‐Silva, P., Tapia-Pastrana, G., & Chávez‐Dueñas, L. (2012) · BioMed Research International · doi:10.1155/2013/374395 · Cited by 54
Autotransporter passenger proteins: virulence factors with common structural themes
Nishimura, K., Tajima, N., Yoon, Y.-H., Park, S., & Tame, J. R. H. (2010) · Journal of Molecular Medicine · doi:10.1007/s00109-010-0600-y · Cited by 52
Autoactivation of the AggR regulator of enteroaggregativeEscherichia coli in vitroandin vivo
Morin, N. P., Tirling, C., Ivison, S. M., Kaur, A. P., Nataro, J. P., & Steiner, T. S. (2009) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2009.00645.x · Cited by 49
Self-citationBoll, E. J., Ayala-Luján, J. L., Szabady, R. L., Louissaint, C., Smith, R., Krogfelt, K. A., Nataro, J. P., Ruı́z-Pérez, F., & McCormick, B. A. (2017) · mBio · doi:10.1128/mbio.00717-17 · Cited by 52
Self-citationPokharel, P., Habouria, H., Bessaiah, H., & Dozois, C. M. (2019) · Microorganisms · doi:10.3390/microorganisms7120594 · Cited by 48
Munera, D., Ritchie, J. M., Hatzios, S. K., Bronson, R. T., Fang, G., Schadt, E. E., Davis, B. M., & Waldor, M. K. (2014) · Nature Communications · doi:10.1038/ncomms4080 · Cited by 45
Bolick, D. T., Roche, J. K., Hontecillas, R., Bassaganya-Riera, J., Nataro, J. P., & Guerrant, R. L. (2013) · Journal of Medical Microbiology · doi:10.1099/jmm.0.046300-0 · Cited by 43
Self-citationVieira, M. A. M., Gomes, T. A. T., Ferreira, A. J. P., Knöbl, T., Servin, A. L., & Moal, V. L.-L. (2010) · Infection and Immunity · doi:10.1128/iai.01115-09 · Cited by 44
Escherichia coli O104:H4 outbreak--have we learnt a lesson from it?
Bloch, S., Felczykowska, A., & Nejman-Faleńczyk, B. (2012) · Acta Biochimica Polonica · doi:10.18388/abp.2012_2081 · Cited by 42
Zangari, T., Melton‐Celsa, A. R., Panda, A., Boisen, N., Smith, M. A., Tatarov, I., Tolla, L. J. D., Nataro, J. P., & O’Brien, A. D. (2013) · Infection and Immunity · doi:10.1128/iai.01310-12 · Cited by 43
Self-citationA generalised module for the selective extracellular accumulation of recombinant proteins
Sevastsyanovich, Y. R., Leyton, D. L., Wells, T. J., Wardius, C. A., Tveen‐Jensen, K., Morris, F. C., Knowles, T. J., Cunningham, A. F., Cole, J. A., & Henderson, I. R. (2012) · Microbial Cell Factories · doi:10.1186/1475-2859-11-69 · Cited by 41
Self-citationEllis, S., Crossman, L. C., McGrath, C. J., Chattaway, M. A., Hölken, J. M., Brett, B. T., Bundy, L., Kay, G. L., Wain, J. R., & Schüller, S. (2020) · Scientific Reports · doi:10.1038/s41598-020-64424-3 · Cited by 40
The serine protease Pic as a virulence factor of atypical enteropathogenic Escherichia coli
Abreu, A. G., Abe, C. M., Nunes, K. O., Moraes, C. T. P., Chavez-Dueñas, L., Navarro-Garcia, F., Barbosa, A. S., Piazza, R. M. F., & Elias, W. P. (2016) · Gut Microbes · doi:10.1080/19490976.2015.1136775 · Cited by 39
Myoviridae phage PDX kills enteroaggregative Escherichia coli without human microbiome dysbiosis
Cepko, L. C. S., Garling, E. E., Dinsdale, M. J., Scott, W. P., Bandy, L., Nice, T. J., Faber-Hammond, J. J., & Mellies, J. L. (2020) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001162 · Cited by 39
Jensen, B. H., Poulsen, A., Rasmussen, S. H. R., Struve, C., Engberg, J., Friis‐Møller, A., Boisen, N., Jønsson, R., Petersen, R. F., Petersen, A. M., et al. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00230 · Cited by 38
Serine proteases at the cutting edge of IBD: Focus on gastrointestinal inflammation
Kriaa, A., Jablaoui, A., Mkaouar, H., Akermi, N., Maguin, E., & Rhimi, M. (2020) · The FASEB Journal · doi:10.1096/fj.202000031rr · Cited by 38
Rajan, A., Robertson, M. J., Carter, H. E., Poole, N. M., Clark, J. R., Green, S. I., Criss, Z. K., Zhao, B., Karandikar, U. C., Xing, Y., et al. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008851 · Cited by 38
The 2011 German Enterohemorrhagic Escherichia Coli O104:H4 Outbreak—The Danger Is Still Out There
Kampmeier, S., Berger, M., Mellmann, A., Karch, H., & Berger, P. (2018) · Current topics in microbiology and immunology · doi:10.1007/82_2018_107 · Cited by 38
Petro, C. D., Duncan-Lowey, J. K., Seldina, Y. I., Allué‐Guardia, A., Eppinger, M., Riddle, M. S., Tribble, D. R., Johnson, R. C., Dalgard, C. L., Sukumar, G., et al. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00200 · Cited by 33
Boll, E. J., Struve, C., Sander, A., Demma, Z., Nataro, J. P., McCormick, B. A., & Krogfelt, K. A. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis417 · Cited by 33
Self-citationde Andrade, F. B., Abreu, A. G., Nunes, K. O., Gomes, T. A. T., Piazza, R. M. F., & Elias, W. P. (2017) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2017.02.018 · Cited by 30
Toloza, L., Gíménez, R., Fábrega, M.-J., Álvarez-Villagómez, C. S., Aguilera, L., Cañas, M. A., Martín-Venegas, R., Badı́a, J., & Baldomà, L. (2015) · BMC Microbiology · doi:10.1186/s12866-015-0591-5 · Cited by 30
Bhullar, K., Zarepour, M., Yu, H., Yang, H., Croxen, M., Stahl, M., Finlay, B. B., Turvey, S. E., & Vallance, B. A. (2015) · Infection and Immunity · doi:10.1128/iai.00025-15 · Cited by 29
de Medeiros, P. H. Q. S., Lima, A. Â. M., Guedes, M. M., Havt, A., Bona, M. D., Rey, L. C., Soares, A. M., Guerrant, R. L., Weigl, B. H., & Lima, I. F. N. (2017) · Diagnostic Microbiology and Infectious Disease · doi:10.1016/j.diagmicrobio.2017.11.002 · Cited by 29
Nasser, A., Mosadegh, M., Azimi, T., & Shariati, A. (2022) · Molecular and Cellular Pediatrics · doi:10.1186/s40348-022-00145-z · Cited by 29
Navarro‐García, F., Sonnested, M., & Teter, K. (2010) · Toxins · doi:10.3390/toxins2051134 · Cited by 27
França, F. L. S., Wells, T. J., Browning, D. F., Nogueira, R. T., Sarges, F. S., Pereira, A. C. M., Cunningham, A. F., Lucheze, K., Rosa, A. C. P., Henderson, I. R., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069971 · Cited by 27
Self-citationFirst clinical isolate of Escherichia coli harboring mcr-1 gene in Mexico
Mérida-Vieyra, J., Ranero, A. D. C., Arzate-Barbosa, P., de la Garza, E. A., Méndez-Tenorio, A., Murcia-Garzón, J., & Aquino-Andrade, A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0214648 · Cited by 26
Gonyar, L. A., Smith, R. M., Girón, J. A., Zachos, N. C., Ruı́z-Pérez, F., & Nataro, J. P. (2020) · Infection and Immunity · doi:10.1128/iai.00176-20 · Cited by 26
Self-citationEffects of different doses lipopolysaccharides on the mucosal barrier in mouse intestine
Li, C. L., Ma, D., Zhou, H., Zhang, M., An, L., Wang, Y., & Wu, C. (2020) · Research in Veterinary Science · doi:10.1016/j.rvsc.2020.09.005 · Cited by 26
Broad Spectrum Activity of a Lectin-Like Bacterial Serine Protease Family on Human Leukocytes
Ayala-Luján, J. L., Vijayakumar, V., Gong, M., Smith, R., Santiago, A. E., & Ruı́z-Pérez, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107920 · Cited by 26
Animal models of enteroaggregativeEscherichia coliinfection
Philipson, C. W., Bassaganya-Riera, J., & Hontecillas, R. (2013) · Gut Microbes · doi:10.4161/gmic.24826 · Cited by 25
McGuire, M. K., Randall, A. Z., Seppo, A., Järvinen, K. M., Meehan, C. L., Gindola, D. K., Williams, J. E., Sellen, D., Kamau‐Mbuthia, E. W., Kamundia, E. W., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.614372 · Cited by 25
Prevalence, Biogenesis, and Functionality of the Serine Protease Autotransporter EspP
Weiss, A., & Brockmeyer, J. (2012) · Toxins · doi:10.3390/toxins5010025 · Cited by 22
Rossiter, A. E., Godfrey, R. E., Connolly, J. A., Busby, S. J. W., Henderson, I. R., & Browning, D. F. (2014) · Biochemical Journal · doi:10.1042/bj20141315 · Cited by 22
Self-citationNutrition of Escherichia coli within the intestinal microbiome
Doranga, S., Krogfelt, K. A., Cohen, P. S., & Conway, T. (2024) · EcoSal Plus · doi:10.1128/ecosalplus.esp-0006-2023 · Cited by 23
Self-citationSantiago, A. E., Yan, M. B., Hazen, T. H., Sauder, B., Meza-Segura, M., Rasko, D. A., Kendall, M. M., Ruı́z-Pérez, F., & Nataro, J. P. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006545 · Cited by 21
Self-citationBorgersen, Q., Bolick, D. T., Kolling, G. L., Aijuka, M., Ruı́z-Pérez, F., Guerrant, R. L., Nataro, J. P., & Santiago, A. E. (2018) · Gut Microbes · doi:10.1080/19490976.2018.1429877 · Cited by 21
Self-citationEnteroaggregative Escherichia coli (EAEC)
Elias, W. P., & Navarro‐García, F. (2016) · Springer eBooks · doi:10.1007/978-3-319-45092-6_2 · Cited by 22
Bueris, V., Sellera, F. P., Fuga, B., Sano, E., de Carvalho, M. P. N., Couto, S. C. F., Moura, Q., & Lincopán, N. (2022) · Scientific Reports · doi:10.1038/s41598-022-09598-8 · Cited by 19
Flores-Sánchez, F., Chávez‐Dueñas, L., Sanchez-Villamil, J. I., & Navarro‐García, F. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.564953 · Cited by 21
Mg2+ binding affects the structure and activity of ovomucin
Shan, Y., Xu, Q., & Ma, M. (2014) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2014.06.056 · Cited by 19
Navarro‐García, F. (2023) · Molecular Microbiology · doi:10.1111/mmi.15116 · Cited by 18
Role of Class 1 Serine Protease Autotransporter in the Pathogenesis of Citrobacter rodentium Colitis
Vijayakumar, V., Santiago, A. E., Smith, R. M., Smith, M., Robins-Browne, R. M., Nataro, J. P., & Ruı́z-Pérez, F. (2014) · Infection and Immunity · doi:10.1128/iai.01518-13 · Cited by 18
Self-citationSaile, N., Schwarz, L., Eißenberger, K., Klumpp, J., Fricke, W. F., & Schmidt, H. (2018) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2018.03.006 · Cited by 18
Organization and architecture of AggR‐dependent promoters from enteroaggregative Escherichia coli
Yasir, M., Icke, C., AbdelWahab, R. A., Haycocks, J. R. J., Godfrey, R. E., Sazinas, P., Pallen, M. J., Henderson, I. R., Busby, S. J. W., & Browning, D. F. (2018) · Molecular Microbiology · doi:10.1111/mmi.14172 · Cited by 17
Self-citationThe proteolytic activity in inflammatory bowel disease: insight from gut microbiota
Hou, J., Ding, L., Yang, T., Yang, Y.-F., Jin, Y., Zhang, X., Ma, A.-H., & Qin, Y. (2024) · Microbial Pathogenesis · doi:10.1016/j.micpath.2024.106560 · Cited by 20
Belmont-Monroy, L., Saitz, W., Soria‐Bustos, J., Mickey, A. S., Sherman, N. E., Orsburn, B. C., Ruı́z-Pérez, F., & Santiago, A. E. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008776 · Cited by 16
What’s for dinner? How Citrobacter rodentium’s metabolism helps it thrive in the competitive gut
Liang, Q., & Vallance, B. A. (2021) · Current Opinion in Microbiology · doi:10.1016/j.mib.2021.06.004 · Cited by 17
Hernández‐Chiñas, U., Gazarian, T. G., Gazaryan, K., Mendoza‐Hernández, G., Xicohtencatl‐Cortés, J., & Carlos, E. (2009) · Peptides · doi:10.1016/j.peptides.2009.09.019 · Cited by 16
Metadata
- Authors
- Harrington, S. M., Sheikh, J., Henderson, I. R., Ruiz-Perez, F., Cohen, P. S., & Nataro, J. P.
- Affiliations
- Center for Vaccine Development, University of Maryland School of Medicine, and Departments of Microbiology and Immunology
- University of Maryland, Baltimore (US)
- University of Rhode Island (US)
- Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland 21201
- Venue
- Infection and Immunity
- Publisher
- American Society for Microbiology
- Published
- 2009-06
- Volume
- 77
- Issue
- 6
- Pages
- 2465-2473
- ISSN
- 0019-9567 (ISSN-L)
- 1098-5522
- PMC
- PMC2687332
- OpenAlex
- W2161414686
- Cited by
- 156
- References
- 47
- Citations by year
- 2026: 5 · 2025: 10 · 2024: 6 · 2023: 6 · 2022: 5 · 2021: 6 · 2020: 13 · 2019: 6 · 2018: 12 · 2017: 10 · 2016: 6 · 2015: 10 · 2014: 11 · 2013: 16 · 2012: 11
- FWCI
- 7.17
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Infection and Immunity (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Journal of Media Literacy Education (submittedVersion, cc-by)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (R56AI048945, R01AI033096, R01AI043615, R01AI048945, AI33096, AI43615, AI48945, AI03615, R56AI043615)
- Topics
- Life Sciences › Immunology and Microbiology › Microbiology › Escherichia coli research studies
- Life Sciences › Immunology and Microbiology › Microbiology › Enterobacteriaceae and Cronobacter Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- enteroaggregative Escherichia coli, mucinase, intestinal colonization, mucin, aggregative adherence fimbriae, aggR, virulence factors, diarrheal disease
- MeSH terms
- Animals, Cecum, Child, Escherichia coli, Feces, Female, Humans, Intestinal Mucosa, Mice, Inbred BALB C, Mucins, Polysaccharide-Lyases, Serine Endopeptidases, Shigella flexneri, Virulence, Colony Count, Microbial, Mutagenesis, Site-Directed, Gene Deletion, Amino Acid Substitution, Catalytic Domain, Escherichia coli Proteins, Virulence Factors, Mice
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