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Nanoscale imaging of Bacillus thuringiensis flagella using atomic force microscopy

Bibliographic reference Gillis, Annika ; Dupres, Vincent ; Delestrait, Guillaume ; Mahillon, Jacques ; Dufrêne, Yves. Nanoscale imaging of Bacillus thuringiensis flagella using atomic force microscopy. In: Nanoscale, Vol. 4, p. 1585-1591 (2012)
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  1. Jarrell Ken F., McBride Mark J., The surprisingly diverse ways that prokaryotes move, 10.1038/nrmicro1900
  2. Kearns Daniel B., A field guide to bacterial swarming motility, 10.1038/nrmicro2405
  3. Berg Howard C., The Rotary Motor of Bacterial Flagella, 10.1146/annurev.biochem.72.121801.161737
  4. Erhardt M., Namba K., Hughes K. T., Bacterial Nanomachines: The Flagellum and Type III Injectisome, 10.1101/cshperspect.a000299
  5. Lidstrom Mary E, Konopka Michael C, The role of physiological heterogeneity in microbial population behavior, 10.1038/nchembio.436
  6. Kearns D. B., Cell population heterogeneity during growth of Bacillus subtilis, 10.1101/gad.1373905
  7. Wei Y., Wang X., Liu J., Nememan I., Singh A. H., Weiss H., Levin B. R., The population dynamics of bacteria in physically structured habitats and the adaptive virtue of random motility, 10.1073/pnas.1013499108
  8. Nielubowicz Greta R., Mobley Harry L. T., Host–pathogen interactions in urinary tract infection, 10.1038/nrurol.2010.101
  9. Roy Koushik, Hilliard George M., Hamilton David J., Luo Jiwen, Ostmann Marguerite M., Fleckenstein James M., Enterotoxigenic Escherichia coli EtpA mediates adhesion between flagella and host cells, 10.1038/nature07568
  10. Costerton J. W., Bacterial Biofilms: A Common Cause of Persistent Infections, 10.1126/science.284.5418.1318
  11. Ghelardi E., Celandroni F., Salvetti S., Beecher D. J., Gominet M., Lereclus D., Wong A. C. L., Senesi S., Requirement of flhA for Swarming Differentiation, Flagellin Export, and Secretion of Virulence-Associated Proteins in Bacillus thuringiensis, 10.1128/jb.184.23.6424-6433.2002
  12. Salamone Gabriela V, Petracca Yanina, Bass Juan I Fuxman, Rumbo Martín, Nahmod Karen A, Gabelloni Maria L, Vermeulen Mónica E, Matteo Mario J, Geffner Jorge R, Trevani Analia S, Flagellin delays spontaneous human neutrophil apoptosis, 10.1038/labinvest.2010.77
  13. Arora S. K., Neely A. N., Blair B., Lory S., Ramphal R., Role of Motility and Flagellin Glycosylation in the Pathogenesis of Pseudomonas aeruginosa Burn Wound Infections, 10.1128/iai.73.7.4395-4398.2005
  14. Leifson, J. Bacteriol., 20, 203 (1930)
  15. West, J. Clin. Microbiol., 6, 414 (1977)
  16. Turner L., Zhang R., Darnton N. C., Berg H. C., Visualization of Flagella during Bacterial Swarming, 10.1128/jb.00083-10
  17. Blair K. M., Turner L., Winkelman J. T., Berg H. C., Kearns D. B., A Molecular Clutch Disables Flagella in the Bacillus subtilis Biofilm, 10.1126/science.1157877
  18. Copeland M. F., Flickinger S. T., Tuson H. H., Weibel D. B., Studying the Dynamics of Flagella in Multicellular Communities of Escherichia coli by Using Biarsenical Dyes, 10.1128/aem.02153-09
  19. Jensen G. B., Hansen B. M., Eilenberg J., Mahillon J., The hidden lifestyles of Bacillus cereus and relatives : The hidden lifestyles of B. cereus and relatives, 10.1046/j.1462-2920.2003.00461.x
  20. de Maagd R, How Bacillus thuringiensis has evolved specific toxins to colonize the insect world, 10.1016/s0168-9525(01)02237-5
  21. Vilas-Bôas G.T., Peruca A.P.S., Arantes O.M.N., Biology and taxonomy ofBacillus cereus,Bacillus anthracis, andBacillus thuringiensis, 10.1139/w07-029
  22. Houry A., Briandet R., Aymerich S., Gohar M., Involvement of motility and flagella in Bacillus cereus biofilm formation, 10.1099/mic.0.034827-0
  23. Ghelardi E., Celandroni F., Salvetti S., Ceragioli M., Beecher D. J., Senesi S., Wong A. C. L., Swarming Behavior of and Hemolysin BL Secretion by Bacillus cereus, 10.1128/aem.02345-06
  24. Ramarao Nalini, Lereclus Didier, Adhesion and cytotoxicity of Bacillus cereus and Bacillus thuringiensis to epithelial cells are FlhA and PlcR dependent, respectively, 10.1016/j.micinf.2006.01.005
  25. Müller Daniel J, Helenius Jonne, Alsteens David, Dufrêne Yves F, Force probing surfaces of living cells to molecular resolution, 10.1038/nchembio.181
  26. Dufrêne Yves F, Atomic force microscopy and chemical force microscopy of microbial cells, 10.1038/nprot.2008.101
  27. Andre Guillaume, Kulakauskas Saulius, Chapot-Chartier Marie-Pierre, Navet Benjamine, Deghorain Marie, Bernard Elvis, Hols Pascal, Dufrêne Yves F., Imaging the nanoscale organization of peptidoglycan in living Lactococcus lactis cells, 10.1038/ncomms1027
  28. Doktycz M.J., Sullivan C.J., Hoyt P.R., Pelletier D.A., Wu S., Allison D.P., AFM imaging of bacteria in liquid media immobilized on gelatin coated mica surfaces, 10.1016/s0304-3991(03)00045-7
  29. Beckmann M.A., Venkataraman S., Doktycz M.J., Nataro J.P., Sullivan C.J., Morrell-Falvey J.L., Allison D.P., Measuring cell surface elasticity on enteroaggregative Escherichia coli wild type and dispersin mutant by AFM, 10.1016/j.ultramic.2006.02.006
  30. Telford John L., Barocchi Michèle A., Margarit Immaculada, Rappuoli Rino, Grandi Guido, Pili in Gram-positive pathogens, 10.1038/nrmicro1443
  31. Ton-That Hung, Schneewind Olaf, Assembly of pili in Gram-positive bacteria, 10.1016/j.tim.2004.03.004
  32. Andrup, J. Bacteriol., 175, 6530 (1993)
  33. Jensen Gert B., Andrup Lars, Wilcks Andrea, Smidt Lasse, Poulsen Otto M., The aggregation-mediated conjugation system of Bacillus thuringiensis subsp. israelensis: Host range and kinetics of transfer, 10.1007/s002849900105
  34. Branda S. S., Gonzalez-Pastor J. E., Dervyn E., Ehrlich S. D., Losick R., Kolter R., Genes Involved in Formation of Structured Multicellular Communities by Bacillus subtilis, 10.1128/jb.186.12.3970-3979.2004