Functions of Bacterial Flagella

References

• Thomashow L. S., Rittenberg S. C. Isolation and composition of sheathed flagella from Bdellovibrio bacteriovorus 109J. J. Bacteriol. 1985; 163: 1047
   PubMed Web of Science ®Google Scholar
• Sjobald Emala R. D.C.W., Doetsch R. N. Bacterial flagellar sheaths: structures in search of a function. Cell. Motil. 1983; 3: 93
   PubMedGoogle Scholar
• Geis Leying G., Suerbaum H., Mai S.U., Opferkuch W. Ultrastructure and chemical analysis of Campylobacter pylori flagella. J. Clin. Microbiol. 1989; 27: 436
   PubMed Web of Science ®Google Scholar
• Hirota Kitada N.M., Imae Y. Flagellar motors of alkalophilic Bacillus are powered by an electrochemical potential gradient of Na+. FEBS Lett. 1981; 132: 278
   Web of Science ®Google Scholar
• Larsen Adler S. H., Gargus J.J.J., Hogg R. W. Chemomechanical coupling without ATP: the source of energy for motility and chemotaxis in bacteria. Proc. Natl. Acad. Sci. U.S.A. 1974; 71: 1239
   PubMed Web of Science ®Google Scholar
• Allen R. D., Baumann P. Structure and arrangement of flagella in species of the genus Beneckea and. Photobacterium fischeri, J. Bacteriol. 1971; 107: 295
   PubMed Web of Science ®Google Scholar
• Tarrand Krieg J. J.N.R., Döbereiner J. A taxonomic study of the Spirillum lipoferum group with description of a new genus. Azospirillum gen. nov. and two species Azospirillum lipoferum (Beijerinck) comb. nov. and Azospirillum brasilense sp. nov. Can. J. Microbiol 1978; 24: 967
   PubMed Web of Science ®Google Scholar
• Aizawa S.-I. Flagellar assembly in. Salmonella typhimurium, Mol. Microbiol. 1996; 19: 1
   Google Scholar
• Blair D. F. How bacteria sense and swim. Annu. Rev. Microbiol. 1995; 49: 489
   PubMed Web of Science ®Google Scholar
• Macnab R. M. Genetics and biogenesis of bacterial flagella. Annu. Rev. Genet. 1992; 26: 131
   PubMed Web of Science ®Google Scholar
• Shapiro L. The bacterial flagellum: from genetic network to complex architecture. Cell 1995; 80: 525
   PubMed Web of Science ®Google Scholar
• Henrichsen J. Bacterial surface translocation: a survey and a classification. Bacteriol Rev. 1972; 36: 478
   PubMedGoogle Scholar
• Bradley D. E. A function of Pseudomonas aeruginosa PAO polar pili: twitching motility. Can. J. Microbiol. 1980; 26: 146
   PubMed Web of Science ®Google Scholar
• O'Rear Alberti J.L., Harshey R. M. Mutations that impair swarming motility in Serratia marcescens 274 include but are not limited to those affecting chemotaxis of flagellar function. J. Bacterioi 1992; 174: 6125
   PubMed Web of Science ®Google Scholar
• Macnab R. M. Motility and chemotaxis. Escherichia coli and Salmonella typhimurium, Cellular and Molecular Biology, F. C. Neidhardt Ingraham, J. Low, K. B. Magasanik, B.M. Schaechter, H. E. Umbarger. ASM Publications, Washington, D.C. 1987; Vol. I: 732
   Google Scholar
• Charon Greenberg N. W., Koopman E. P.M.B.H., Limberger R. J. Spirochete chemotaxis, motility, and the structure of the spirochetal periplasmic flagella. Res. Microbiol. 1992; 143: 597
   PubMed Web of Science ®Google Scholar
• Holt S. C. Anatomy and chemistry of spirochetes. Microbiol. Rev. 1978; 38: 114
   Google Scholar
• Goldstein Charon S. F.N.W., Kreiling J. A. Borrelia burgdorferi swims with a planar waveform similar to that of eukaryotic flagella. Proc. Natl. Acad. Sci. U.S.A. 1994; 91: 3433
   PubMed Web of Science ®Google Scholar
• Götz Limmer R., Ober N.K., Schmitt R. Motility and chemotaxis in two strains of Rhizobium with complex flagella. J. Gen. Microbiol. 1982; 128: 789
   Google Scholar
• Krupski G., Götz Ober R., Pleier K.E., Schmitt R. Structure of complex flagellar filaments in. Rhizobium meliloti, J. Bacteriol. 1985; 162: 361
   PubMed Web of Science ®Google Scholar
• Belas R. The swarming phenomenon of. Proteus mirabilis, ASM News 1992; 58: 15
   Google Scholar
• Williams F. D., Schwarzkopf R. H. Nature of the swarming phenomenon in. Proteus, Annu. Rev. Microbiol. 1978; 32: 101
   PubMed Web of Science ®Google Scholar
• Allison Lai C.H., Gygi C.D., Hughes C. Cell differentiation of Proteus mirabilis is initiated by glutamine, a specific chemoattractant for swarming cells. Mol. Microbiol. 1993; 8: 53
   PubMed Web of Science ®Google Scholar
• Gygi Rahman D., Lai M. M.H., Carlson C., Guard-Petter R.J., Hughes C. A cell surface polysaccharide that facilitates rapid population migration by differentiated swarm cells of. Proteus mirabilis, Mol. Microbiol. 1995; 17: 1167
   PubMed Web of Science ®Google Scholar
• Alberti L., Harshey R. M. Differentiation of Serratia marcescens 274 into swimmer and swarmer cells. J. Bacteriol. 1990; 172: 4322
   PubMed Web of Science ®Google Scholar
• Eberl Christiansen L., Molin G.S., Givskov M. Differentiation of Serratia liquefaciens into swarm cells is controlled by the expression of the flhD master operon. J. Bacteriol 1996; 178: 554
   PubMed Web of Science ®Google Scholar
• Ulitzer S. Induction of swarming in. Vibrio parahaemolyticus, Arch. Microbiol. 1974; 101: 357
   PubMed Web of Science ®Google Scholar
• Ulitzer S. The mechanism of swarming in. Vibrio alginolyticus, Arch. Microbiol. 1975; 104: 67
   PubMed Web of Science ®Google Scholar
• Harshey R. M., Matsuyama T. Dimorphic transition in Escherichia coli, Salmonella typhimurium: surface-induced differentiation into hyperflagellate swarmer cells. Proc. Natl Acad. Sci. U.S.A 1994; 91: 8631
   PubMed Web of Science ®Google Scholar
• Ragatz Jiang L.Z., Bauer Y.C.E., Gest H. Macroscopic phototactic behavior of the purple photosynthetic bacterium. Rhodospirillum centenum, Arch. Microbiol. 1995; 163: 1
   PubMed Web of Science ®Google Scholar
• Hall P. G., Krieg N. R. Swarming of Azospirillum brasilense on solid media. Can. J. Microbiol. 1983; 29: 1592
   Web of Science ®Google Scholar
• Harshey R. M. Bees aren't the only ones: swarming in Gram-negative bacteria. Mol. Microbiol. 1994; 13: 389
   PubMed Web of Science ®Google Scholar
• Belas Simon R.M., Silverman M. Regulation of lateral flagella gene transcription in. Vibrio parahaemolyticus, J. Bacteriol. 1986; 167: 210
   PubMed Web of Science ®Google Scholar
• McCarter L., Silverman M. Surface-induced swarmer cell differentiation of. Vibrio parahaemolyticus, Mol. Microbiol. 1990; 4: 1057
   PubMed Web of Science ®Google Scholar
• Shinoda S., Okamoto K. Formation and function of Vibrio parahaemolyticus lateral flagella. J. Bacteriol. 1977; 129: 1266
   PubMed Web of Science ®Google Scholar
• Atsumi McCarter T.L., Imae Y. Polar and lateral flagella motors of marine Vibrio are driven by different ion membrane forces. Nature (London 1992; 355: 182
   PubMed Web of Science ®Google Scholar
• Sar McCarter N., Simon L.M., Silverman M. Chemotactic control of the two flagellar systems of. Vibrio parahaemolyticus, J. Bacteriol. 1990; 172: 334
   PubMed Web of Science ®Google Scholar
• McCarter Hilmen L.M.L., Silverman M. Flagellar dynamometer controls swarmer cell differentiation of. V. parahaemolyticus, Cell 1988; 54: 345
   PubMed Web of Science ®Google Scholar
• McCarter L., Silverman M. Iron regulation of swarmer cell differentiation of. Vibrio parahaemolyticus, J. Bacteriol. 1989; 171: 731
   PubMed Web of Science ®Google Scholar
• Tomita T., Kanegasaki S. Enhanced phagocytic response of macrophages to bacteria by physical impact caused by bacterial motility or centrifugation. Infect. Immun. 1982; 38: 865
   PubMed Web of Science ®Google Scholar
• Drake D., Montie T. C. Protection against Pseudomonas aeruginosa infection by passive transfer of anti-flagellar serum. Can. J. Microbiol. 1987; 33: 755
   PubMed Web of Science ®Google Scholar
• Drake D., Montie T. C. Flagella, motility and invasive virulence of. Pseudomonas aeruginosa, J. Gen. Microbiol. 1988; 134: 43
   PubMed Web of Science ®Google Scholar
• Holder Wheeler I. A.R., Montie T. C. Flagellar preparations from Pseudomonas aeruginosa: animal protection studies. Infect. Immun. 1982; 35: 276
   PubMed Web of Science ®Google Scholar
• Landsperger Kelly-Wintenberg W. J., Montie K. D., Knight T. C., Hansen L. S., Huntenburg M. B.C.C., Schneidkraut M. J. Inhibition of bacterial motility with human antiflagellar monoclonal antibodies attenuates Pseudomonas aeruginosa-induced pneumonia in the immunocompetent rat. Infect. Immun. 1994; 62: 4825
   PubMed Web of Science ®Google Scholar
• Ochi Ohtsuka H., Yokota H.S., Uezumi I., Terashima I., Irie M.K., Noguchi H. Inhibitory activity on bacterial motility and in vivo protective activity of human monoclonal antibodies against flagella of. Pseudomonas aeruginosa, Infect. Immun. 1991; 59: 550
   PubMed Web of Science ®Google Scholar
• Rosok Stebbins M. J., Connelly M. R., Lostrom K.M.E., Siadak A. W. Generation and characterization of murine antiflagellum antibodies that are protective against lethal challenge with. Pseudomonas aeruginosa, Infect. Immun. 1990; 58: 3819
   PubMed Web of Science ®Google Scholar
• Rudner Hazlett X. L.L.D., Berk R. S. Systemic and topical protection studies using Pseudomonas aeruginosa flagella in an ocular model of infection. Curr. Eye Res. 1992; 11: 727
   PubMed Web of Science ®Google Scholar
• Weigelt Schneider W.T., Lange R. Sequence homology between spirochaete flagellin and human myelin basic protein. Immunol. Today 1992; 13: 279
   PubMedGoogle Scholar
• Acero-Reyes J. R., Newton S. M. C. Expression of cholera toxin epitopes inserted in flagellin by attenuated Salmonella strains. Rev. Bras. Genet. 1994; 17: 249
   Google Scholar
• Newton Joys S. M. C., Anderson T. M., Kennedy S. A., Hovi R. C.M.E., Stocker B. A. D. Expression and immunogenicity of an 18-residue epitope of HIVI gp41 inserted in the flagellar protein of a Salmonella live vaccine. Res. Microbiol. 1995; 146: 203
   PubMed Web of Science ®Google Scholar
• Taylor D. E. Genetics of Campylobacter and. Helicobacter, Annu. Rev. Microbiol. 1992; 46: 35
   PubMed Web of Science ®Google Scholar
• Seidler R. J., Starr M. P. Structure of the flagellum of. Bdellovibrio bacteriovorus, J. Bacteriol. 1968; 95: 1952
   PubMed Web of Science ®Google Scholar
• Abram D., Duvis B. K. Structural properties and features of parasitic. Bdellovibrio bacteriovorus, J. Bacteriol. 1970; 104: 948
   PubMed Web of Science ®Google Scholar
• Burnham Hashimoto J. C.T., Conti S. F. Electron microscopic observations on the penetration of Bdellovibrio bacteriovorus into Gram-negative hosts. J. Bacteriol. 1968; 96: 1366
   PubMed Web of Science ®Google Scholar
• Stolp H., Petzold H. Untersuchungen über einen obligat parasitischen Mikroorganismus mit lytischer Aktivität für Pseudomonas-Bakterien. Phytopathol Z 1962; 45: 364
   Google Scholar
• Stolp H., Starr M. P. Bdellovibrio bacteriovorus gen. et sp. n. a predatory, ectoparasitic, and bacteriolytic microorganism, Antonie VanLeeuwenhoek. J. Microbiol. Serol. 1963; 29: 217
   PubMed Web of Science ®Google Scholar
• Varon M., Shilo M. Interaction of Bdellovibrio bacteriovorus and host bacteria. I. Kinetic studies of attachment and invasion of Escherichia coli. B by. Bdellovibrio bacteriovorus, J. Bacteriol 1968; 95: 744
   PubMed Web of Science ®Google Scholar
• Chandler Thomason F. W.B.M., Hebert G. A. Flagella on Legionnaires' disease bacteria in the human lung. Ann. Intern. Med. 1980; 93: 715
   PubMed Web of Science ®Google Scholar
• Winn W. C. Legionnaires disease, historical perspective. Clin. Microbiol. Rev. 1988; 1: 60
   PubMedGoogle Scholar
• Chandler Roth F. W., Callaway I. L., Bump C. L., Thomason J. L.B.M., Weaver R. E. Flagella on Legionnaires' disease bacteria. Ann. Intern. Med. 1980; 93: 711
   PubMed Web of Science ®Google Scholar
• Rodgers Greaves F. G., Macrae P. W.A.D., Lewis M. J. Electronmicroscopic evidence of flagella and pili on. Legionella pneumophila, J. Clin. Pathol. 1980; 33: 1184
   PubMed Web of Science ®Google Scholar
• Elliott J. A., Johnson W. Virulence conversion of Legionella pneumophila serogroup 1 by passage in guinea pigs and embryonated eggs. Infect. Immun. 1982; 35: 943
   PubMed Web of Science ®Google Scholar
• Ott Messner M., Heesemann P., Marre J.R., Hacker J. Temperature-dependent expression of flagella in. Legionella, J. Gen. Microbiol. 1991; 137: 1955
   PubMed Web of Science ®Google Scholar
• Pruckler Benson J. M., Moyenuddin R. F., Martin M.W.T., Fields B. S. Association of flagellum expression and intracellular growth of. Legionella pneumophila, Infect. Immun. 1995; 63: 4928
   PubMed Web of Science ®Google Scholar
• Leben C., Whitmoyer R. E. Adherence of bacteria to leaves. Can. J. Microbiol. 1979; 25: 896
   PubMed Web of Science ®Google Scholar
• Hattermann D. R., Ries S. M. Motility of Pseudomonas syringae pv. glycinea and its role in infection. Phytopathology 1989; 79: 284
   Web of Science ®Google Scholar
• Panopoulos N. J., Schroth M. N. Role of flagellar motility in the invasion of bean leaves by. Pseudomonas phaseolicola, Phytopathology 1974; 64: 1389
   Web of Science ®Google Scholar
• Billing Baker E., Crosse L. A. E.J.E., Garrett C. M. E. Characteristics of English isolates of Erwinia amylovora (Burr.) Winslow, et al. J. Appl. Bacteriol. 1961; 24: 195
   Google Scholar
• Huang J. J., Goodman R. N. Morphology and ultrastructure of normal rodshaped and filamentous forms of Erwinia amylovora. J. Bacteriol. 1970; 102: 862
   PubMed Web of Science ®Google Scholar
• Bayot R. G., Ries S. M. Role of motility in apple blossom infection by Erwinia amylovora and studies of fire blight control with attractant and repellent compounds. Phytopathology 1986; 76: 441
   Web of Science ®Google Scholar
• Raymundo A. K., Ries S. M. Motility of. Erwinia amylovora, Phytopathology 1981; 71: 45
   Web of Science ®Google Scholar
• Bradbury J. F. Xanthomonas Dowson1939, in Bergey's Manual of Systematic Bacteriology, N. R. Krieg, J. G. Holt. Williams & Wilkins, Baltimore. 1984; Vol. 1: 199
   Google Scholar
• Zoller B. G. Ph.D. dissertation. University of California, Davis. 1972
   Google Scholar
• Kamoun S., Kado C. I. Phenotypic switching affecting chemotaxis, xanthan production, and virulence in. Xanthomonas campestris, Appl. Environ. Microbiol. 1990; 56: 3855
   PubMed Web of Science ®Google Scholar
• Kelman A. The relationship of pathogenicity in Pseudomonas solanacearum to colony appearance on a tetrazolium medium. Phytopathology 1954; 44: 693
   Web of Science ®Google Scholar
• Kelman A., Hruschka J. The role of motility and aerotaxis in the selective increase of avirulent bacteria in still broth cultures of. Pseudomonas solanacearum, J. Gen. Microbiol. 1973; 76: 177
   PubMed Web of Science ®Google Scholar
• Feng T. Y., Kuo T. G. Bacterial leaf blight of rice plants. VI. Chemotactic responses of Xanthomonas oryzae to water droplets exudated from water pores on the leaves of rice plants. Bot. Bull. Acad. Sin. 1975; 16: 126
   Google Scholar
• Pirhonen Saarilahti M., Karlsson H.M.-B., Palva E. T. Identification of pathogenicity determinants of Erwinia carotovora subsp. carotovora by transposon mutagenesis. Mol. Plant-Microb. Interact 1991; 4: 276
   Web of Science ®Google Scholar
• Mulholland Hinton V., Sidebotham J. C. D., Toth J., Hyman I. K., Pérombelon Reeves L. J. M. C. M.P.J., Salmond G. P. C. A pleiotropic reduced virulence (Rvi) mutant of Erwinia carotovora subspecies atroseptica is defective in flagella assembly proteins that are conserved in plant and animal bacterial pathogens. Mol. Microbiol 1993; 9: 343
   PubMed Web of Science ®Google Scholar
• VanGijsegem Gough F., Zischek C., Niqueux C., Arlat E., Genin M., Barberis S., German P., Castello S.P., Boucher C. The hrp locus of Pseudomonas solanacearum which controls the production of a type III secretion system, encodes eight proteins related to components of the bacterial flagellar biogenesis complex. Mol. Microbiol 1995; 15: 1095
   PubMed Web of Science ®Google Scholar
• Haefele D. M., Lindow S. E. Flagellar motility confers epiphytic fitness advantages upon. Pseudomonas syringae, Appl. Environ. Microbiol. 1987; 53: 2528
   PubMed Web of Science ®Google Scholar
• Lindow S. E. The role of bacterial ice nucleation in frost injury to plants. Annu. Rev. Phytopathol. 1983; 21: 363
   Web of Science ®Google Scholar
• Shaw Loake C. H., Brown G. J., Garrett A. P., Deakin C. S., Alton W., Hall G., Jones M.S.A., O'Leary M., Primavesi L. Isolation and characterization of behavioural mutants and genes of. Agrobacterium tumefaciens, J. Gen. Microbiol. 1991; 137: 1939
   Google Scholar
• Bradley Douglas D. E.C.J., Peschon J. Flagella-specific bacteriophages of Agrobacterium tumefaciens: demonstration of virulence of nonmotile mutants. Can. J. Microbiol. 1984; 30: 676
   PubMed Web of Science ®Google Scholar
• Douglas Halperin C. J.W., Nester E. W. Agrobacterium tumefaciens mutants affected in attachment to plant cells. J. Bacteriol. 1982; 152: 1265
   PubMed Web of Science ®Google Scholar
• Hawes M. C., Smith L. Y. Requirement for chemotaxis in pathogenicity of Agrobacterium tumefaciens on roots of soilgrown pea plants. J. Bacteriol. 1989; 171: 5668
   PubMed Web of Science ®Google Scholar
• Hawes Smith M. C.L.Y., Howarth A. J. Agrobacterium tumefaciens mutants deficient in chemotaxis to root exudates. Mol. Plant-Microb. Interact. 1988; 1: 182
   Google Scholar
• Heierson A., Sidén Kivaisi I.A., Boman H. G. Bacteriophage-resistant mutants of Bacillus thuringiensis with decreased virulence in pupae of. Hyalophora cecropia, J. Bacteriol. 1986; 167: 18
   PubMed Web of Science ®Google Scholar
• Lövgren Zhang A.M.-Y., Engström A., Landén R. Identification of two expressed flagellin genes in the insect pathogen Bacillus thuringiensis subsp. alesti, J. Gen. Microbiol. 1993; 139: 21
   PubMed Web of Science ®Google Scholar
• Samakovlis Asling C., Boman B., Gateff H. G.E., Hultmark D. In vitro induction of cecropin genes — an immune response in a Drosophila blood cell line. Biochem. Biophys. Res. Commun 1992; 188: 1169
   PubMed Web of Science ®Google Scholar
• Zhang M.-Y., LövgrenLow A.M.G., Landén R. Characterization of an avirulent pleiotropic mutant of the insect pathogen Bacillus thuringiensis: reduced expression of flagellin and phospholipases. Infect. Immun. 1993; 61: 4947
   PubMed Web of Science ®Google Scholar
• Zhang M.-Y., Lövgren A., Landén R. Adhesion and cytotoxicity of Bacillus thuringiensis to cultured Spodoptera, Drosophila cells. J. Invertebr. Pathol 1995; 66: 46
   PubMed Web of Science ®Google Scholar
• Maxwell Dunphy P. W.G.B., Niven D. F. Effects of bacterial age and method of culture on the interaction of Xenorhabdus nematophilus (Enterobacteriaceae) with hematocytes of nonimmune Galleria mellonella (Insecta) larvae. J. Gen. Appl. Microbiol 1995; 41: 207
   Web of Science ®Google Scholar
• Jarrell K. F., Kropinski A. M. The virulence of protease and cell surface mutants of Pseudomonas aeruginosa for larvae of. Galleria mellonella, J. Invertebr. Pathol. 1982; 39: 395
   PubMed Web of Science ®Google Scholar
• Thomas Navab D. D., Haake M., Fogelman D. A., Miller A. M.J.N., Lovett M. A. Treponema pallidum invades intercellular junctions of endothelial cell monolayers. Proc. Natl. Acad. Sci. U.S.A. 1988; 85: 3608
   PubMed Web of Science ®Google Scholar
• Kennedy Rosnick M. J., Ulrich D. K.R.G., Yancey R. J., Jr. Association of Treponema hyodysenteriae with porcine intestinal mucosa. J. Gen. Microbiol. 1988; 134: 1565
   PubMedGoogle Scholar
• Sadziene Thomas A., Bundoc D. D., Holt V. G.S.C., Barbour A. G. A flagellaless mutant of. Borrelia burgdorferi, J. Clin. Invest. 1991; 88: 82
   PubMed Web of Science ®Google Scholar
• Kaiser G. E., Doetch R. N. Enhanced translational motion of Leptospira in viscous environments. Nature 1975; 255: 656, (London)
   PubMed Web of Science ®Google Scholar
• Taraura Y., Tanaka S. Effect of antiflagellar serum in the protection of mice against. Clostridium chauvoei, Infect. Immun. 1984; 43: 612
   PubMed Web of Science ®Google Scholar
• Tamura Minamoto Y.N., Tanaka S. Demonstration of protective antigen carried by flagella of. Clostridium chauvoei, Microbiol. Immunol. 1984; 28: 1325
   PubMed Web of Science ®Google Scholar
• Tanaka Hirayama M.N., Tamura Y. Production, characterization, and protective effect of monoclonal antibodies to. Clostridium chauvoei, Infect. Immun. 1987; 55: 1779
   PubMed Web of Science ®Google Scholar
• Tamura Kijima-Tanaka Y., Aoki M., Ogikubo A.Y., Takahashi T. Reversible expression of motility and flagella in Clostridium chauvoei and their relationship to virulence. Microbiology. 1995; 141: 605
   PubMed Web of Science ®Google Scholar
• Leifson E., Palen M. I. Variations and spontaneous mutations in the genus Listeria in respect to flagellation and motility. J. Bacteriol. 1955; 70: 233
   PubMed Web of Science ®Google Scholar
• Peel Donachie M.W., Shaw A. Temperature-dependent expression of flagella of Listeria monocytogenes studied by electron microscopy, SDS-PAGE and Western blotting. J. Gen. Microbiol. 1988; 134: 2171
   PubMedGoogle Scholar
• Dons Rasmussen L.O.F., Olsen J. E. Cloning and characterization of a gene encoding flagellin of. Listeria monocytogenes, Mol. Microbiol. 1992; 6: 2919
   PubMed Web of Science ®Google Scholar
• Czuprynski Brown C. J.J.F., Roll J. T. Growth at reduced temperatures increases the virulence of Listeria monocytogenes for intravenously but not intragastrically inoculated mice. Microbial Pathogen. 1989; 7: 213
   PubMed Web of Science ®Google Scholar
• Stephens Roberts J. C., Jones I. S.D., Andrew P. W. Effect of growth temperature on virulence of strains of Listeria monocytogenes in the mouse: evidence for a dose dependence. J. Appl. Bacteriol. 1991; 70: 239
   PubMedGoogle Scholar
• Kathariou Kanenaka S., Allen R., Fok R. D.A.K., Mizumoto C. Repression of motility and flagellin production at 37°C is stronger in Listeria monocytogenes than in the nonpathogenic species. Listeria innocua, Can. J. Microbiol. 1995; 41: 572
   PubMed Web of Science ®Google Scholar
• Cossart P. Actin-based bacterial motility. Curr. Opin. Cell Biol. 1995; 7: 94
   PubMed Web of Science ®Google Scholar
• Portnoy Chakraborty D. A., Goebel T.W., Cossart P. Molecular determinants of Listeria monocytogenes pathogenesis. J. Bacteriol. 1992; 60: 1263
   Google Scholar
• Benson Kar L. A., McLaughlin S.G., Ihler G. M. Entry of Bartonella bacilliformis into erythrocytes. Infect. Immun. 1986; 54: 347
   PubMed Web of Science ®Google Scholar
• Mernaugh G., Ihler G. M. Deformation factor: an extracellular protein synthesized by Bartonella bacilliformis that deforms erythrocyte membranes. Infect. Immun. 1992; 60: 937
   PubMed Web of Science ®Google Scholar
• Scherer D. C., De Buron-Connors I., Minnick M. F. Characterization of Bartonella bacilliformis flagella and effect of antiflagellin antibodies on invasion of human erythrocytes. Infect. Immun. 1993; 61: 4962
   PubMed Web of Science ®Google Scholar
• Carpenter Zuberi P. B.A.R., Ordal G. W. Bacillus subtilis flagellar proteins FliP, FliQ, FliR and FlhB are related to Shigella flexneri virulence factors. Gene 1993; 137: 243
   PubMed Web of Science ®Google Scholar
• Hughes Gillen K. T., Semon K. L.M.J., Karlinsey J. E. Sensing structural intermediates in bacterial flagellar assembly by export of a negative regulator. Science 1993; 262: 1277
   PubMed Web of Science ®Google Scholar
• Schmitt Darnell C. K., Tesh S. C., Stocker V. L.B.A.D., O'Brien A. D. Mutation of flgM attenuates virulence of Salmonella typhimurium and mutation of fliA represses the attenuated phenotype. J. Bacteriol 1994; 176: 368
   PubMed Web of Science ®Google Scholar
• Tominaga Mahmoud A., Mukaihara M. A. H.T., Enomoto M. Molecular characterization of intact, but cryptic, flagellin genes in the genus. Shigella, Mol. Microbiol. 1994; 12: 277
   PubMed Web of Science ®Google Scholar
• Girón J. A. Expression of flagella and motility by. Shigella, Mol. Microbiol. 1995; 18: 63
   PubMed Web of Science ®Google Scholar
• Arico Miller B., Roy J. F., Stibitz C., Monack S., Falkow D., Gross S.R., Rappuoli R. Sequences required for expression of Bordetella pertussis virulence factors share homology with prokaryotic signal transduction proteins. Proc. Natl. Acad. Sci. U.S.A. 1989; 86: 6671
   PubMed Web of Science ®Google Scholar
• Uhl M. A., Miller J. F. Autophosphorylation and phosphotransfer in the Bordetella pertussis BvgAS signal transduction cascade. Proc. Natl. Acad. Sci. U.S.A. 1994; 91: 1163
   PubMed Web of Science ®Google Scholar
• Akerley Cotter B. J.P.A., Miller J. F. Ectopic expression of the flagellar regulon alters development of the Bordetella host interaction. Cell 1995; 80: 611
   PubMed Web of Science ®Google Scholar
• Akerley B. J., Miller J. F. Flagellin gene transcription in Bordetella bronchiseptica is regulated by the BvgAS virulence control system. J. Bacteriol. 1993; 175: 3468
   PubMed Web of Science ®Google Scholar
• Akerley Monack B. J., Falkow D. M.S., Miller J. F. The bvgAS locus negatively controls motility and synthesis of flagella in. Bordetella bronchiseptica, J. Bacteriol. 1992; 174: 980
   PubMed Web of Science ®Google Scholar
• Cotter P. A., Miller J. F. BvgAS-mediated signal transduction: analysis of phase-locked regulatory mutants of Bordetella bronchiseptica in a rabbit model. Infect. Immun. 1994; 62: 3381
   PubMed Web of Science ®Google Scholar
• Cornelis G. Yersiniae, finely tuned pathogens. Molecular Biology of Bacterial Infection: Current Status and Future Perspectives, C. E.C.W. Hormaeche Penn, C. J. Smyth. Cambridge University Press, Cambridge 1992; 231
   Google Scholar
• Kapatral V., Minnich S. A. Co-ordinate, temperature-sensitive regulation of the three Yersinia enterocolitica flagellin genes. Mol. Microbiol. 1995; 17: 49
   PubMed Web of Science ®Google Scholar
• Iriarte Stainier M., Mikulskis I.A.V., Cornelis G. R. The fliA gene encoding σ28 in. Yersinia enterocolitica, J. Bacteriol 1995; 177: 2299
   PubMed Web of Science ®Google Scholar
• Grimont P. A. D., Grimont F. The genus. Serratia, Annu. Rev. Microbiol. 1978; 32: 221
   PubMed Web of Science ®Google Scholar
• Daschner F. D. The epidemiology of Serratia marcescens. The Genus Serratia, A. von Graevenitz, S. J. Rubin. CRC Press, Boca Raton, FL. 1980; 187
   Google Scholar
• Paruchuri D. K., Harshey R. M. Flagellar variation in Serratia marcescens is associated with color variation. J. Bacteriol. 1987; 169: 61
   PubMed Web of Science ®Google Scholar
• Givskov Eberl M., Christiansen L., Benedik G.M.J., Molin S. Induction of phospholipase- and flagellar synthesis in Serratia liquefaciens is controlled by expression of the flagellar master operon. flhD, Mol. Microbiol. 1995; 15: 445
   PubMed Web of Science ®Google Scholar
• Allison Lai C.H.-C., Hughes C. Co-ordinate expression of virulence genes during swarm-cell differentiation and population migration of. Proteus mirabilis, Mol. Microbiol. 1992; 6: 1583
   PubMed Web of Science ®Google Scholar
• Harmon Rutherford R. C., Wu R. L.H.M., Collins M. S. Monoclonal antibody-mediated protection and neutralization of motility in experimental Proteus mirabilisinfection. Infect. Immun. 1989; 57: 1936
   PubMed Web of Science ®Google Scholar
• Pazin G. J., Braude A. I. Immobilizing antibodies in pyelonephritis. J. Immunol. 1969; 102: 454
   Web of Science ®Google Scholar
• Pazin G. J., Braude A. I. Immobilizing antibodies in urine: prevention of ascending spread of. Proteus mirabilis. Invest. Urol. 1974; 12: 129
   PubMed Web of Science ®Google Scholar
• Allison C., Emödy Coleman L.N., Hughes C. The role of swarm cell differentiation and multicellular migration in the uropathogenicity of. Proteus mirabilis, J. Infect. Dis. 1994; 169: 1155
   PubMed Web of Science ®Google Scholar
• Allison Coleman C., Jones N.P.L., Hughes C. Ability of Proteus mirabilis to invade human urothelial cells is coupled to motility and swarming differentiation. Infect. Immun. 1992; 60: 4740
   PubMed Web of Science ®Google Scholar
• Nuijten VanAsten P. J. M.A., Gaastra J. A. M.W., Vander Zeijst B. A. M. Structural and functional analysis of two Campylobacter jejuni flagellin genes. J. Biol. Chem. 1990; 265: 17798
   PubMed Web of Science ®Google Scholar
• Nuijten P. J.M., Vander Zeijst B. A. M., Newell D. G. Localization of immunogenic regions on the flagellin proteins of Campylobacter jejuni 81116. Infect. Immun. 1991; 59: 1100
   PubMed Web of Science ®Google Scholar
• Nuijten Bleumink-Pluym P. J. M., Gaastra N. M. C.W., Vander Zeijst B. A. M. Flagellin gene expression in Campylobacter jejuni is regulated at the transcriptional level. Infect. Immun. 1989; 57: 1084
   PubMed Web of Science ®Google Scholar
• Wassenaar Bleumink-Pluym T. M., Newell N. M. C., Nuijten D. G.P.J.M., Vander Zeijst B. A. M. Differential flagellin expression in a flaA flaB+ mutant of. Campylobacter jejuni, Infect. Immun 1994; 62: 3901
   PubMed Web of Science ®Google Scholar
• Ferrero R. L., Lee A. Motility of Campylobacter jejuni in a viscous environment: comparison with conventional rodshaped bacteria. J. Gen. Microbiol. 1988; 134: 53
   PubMedGoogle Scholar
• Szymanski King C. M., Haardt M.M., Armstrong G. D. Campylobacter jejuni motility and invasion of Caco-2 cells. Infect. Immun. 1995; 63: 4295
   PubMed Web of Science ®Google Scholar
• Caldwell Guerry M. B., Lee P., Burans E. C.J.P., Walker R. I. Reversible expression of flagella in. Campylobacter jejuni, Infect. Immun. 1985; 50: 941
   PubMed Web of Science ®Google Scholar
• Newell McBride D. G.H., Dolby J. M. Investigations on the role of flagella in the colonization of infant mice with Campylobacter jejuni and attachment of Campylobacter jejuni to human epithelial cell lines. J. Hyg. Camb 1985; 95: 217
   PubMedGoogle Scholar
• Aguero-Rosenfeld Yang M. E.X.-H., Nachamkin I. Infection of adult Syrian hamsters with flagellar variants of. Campylobacter jejuni, Infect. Immun. 1990; 58: 2214
   PubMed Web of Science ®Google Scholar
• Pavlovskis Rollins O. R., Haberberger D. M.R.L., Jr., Green Habash A. E., Strocko L.S., Walker R. I. Significance of flagella in colonization resistance of rabbits immunized with Campylobacter spp. Infect. Immun. 1991; 59: 2259
   PubMed Web of Science ®Google Scholar
• Morooka Umeda T.A., Amako K. Motility as an intestinal colonization factor for. Campylobacter jejuni, J. Gen. Microbiol. 1985; 131: 1973
   PubMedGoogle Scholar
• Nachamkin Yang I.X.-H., Stern N. J. Role of Campylobacter jejuni flagella as colonization factors for three-day-old chicks: analysis with flagellar mutants. Appl. Environ. Microbiol. 1993; 59: 1269
   PubMed Web of Science ®Google Scholar
• Wassenaar T. M., Vander Zeijst Ayling B. A. M.R., Newell D. G. Colonization of chicks by motility mutants of Campylobacter jejuni demonstrates the importance of flagellin A expression. J. Gen. Microbiol. 1993; 139: 1171
   PubMedGoogle Scholar
• Newell D. G. Monoclonal antibodies directed against the flagella of Campylobacter jejuni: production, characterization and lack of effect on the colonization of infant mice. J. Hyg. Camb. 1986; 96: 131
   PubMedGoogle Scholar
• Black Levine R. E., Clements M. M., Hughes M. L.T.P., Blaser M. J. Experimental Campylobacter jejuni infection in humans. J. Infect. Dis. 1988; 157: 472
   PubMed Web of Science ®Google Scholar
• Field Underwood L. H., Payne J. L.S.M., Berry L. J. Characteristics of an avirulent Campylobacter jejuni strain and its virulence-enhanced variants. J. Med. Microbiol. 1993; 38: 293
   PubMed Web of Science ®Google Scholar
• McSweegan E., Walker R. I. Identification and characterization of two Campylobacter jejuni adhesins for cellular and mucous substrates. Infect. Immun. 1986; 53: 141
   PubMed Web of Science ®Google Scholar
• Wassenaar Bleumink-Pluym T. M.N.M.C., Vander Zeijst B. A. M. Inactivation of Campylobacter jejuni flagellin genes by homologous recombination demonstrates that flaA but not flaB is required for invasion. EMBO J 1991; 10: 2055
   PubMed Web of Science ®Google Scholar
• Grant Konkel C. C. R., Cieplak M. E.W., Jr., Tompkins L. S. Role of flagella in adherence, internalization, and translocation of Campylobacter jejuni in nonpolarized and polarized epithelial cell cultures. Infect. Immun. 1993; 61: 1764
   PubMed Web of Science ®Google Scholar
• Yao Burr R., Doig D. H., Trust P., Niu T. J.H., Guerry P. Isolation of motile and non-motile insertional mutants of Campylobacter jejuni: the role of motility in adherence and invasion of eukaryotic cells. Mol. Microbiol. 1994; 14: 883
   PubMed Web of Science ®Google Scholar
• Konkel M. E., Cieplak W., Jr. Altered synthetic response of Campylobacter jejuni to cocultivation with human epithelial cells is associated with enhanced internalization. Infect. Immun. 1992; 60: 4945
   PubMed Web of Science ®Google Scholar
• Russell R. G., Blake D. C., Jr. Cell association and invasion of Caco-2 cells by. Campylobacter jejuni, Infect. Immun. 1994; 62: 3773
   PubMed Web of Science ®Google Scholar
• Vandamme Falsen P.E., Rossau R. Revision of Campylobacter, Helicobacter, Wolinella taxonomy: emendations of generic descriptions and proposals of Arcobacter gen. nov. Int. J. Syst. Bacteriol 1991; 41: 88
   PubMedGoogle Scholar
• Geis Suerbaum G., Forsthoff S., Leying B.H., Opferkuch W. Ultrastructure and biochemical studies of the flagellar sheath of. Helicobacter pylori, J. Med. Microbiol. 1993; 38: 371
   PubMed Web of Science ®Google Scholar
• Luke C. J., Penn C. W. Identification of a 29 kDa flagellar sheath protein in Helicobacter pylori using a murine monoclonal antibody. Microbiology 1995; 144: 597
   Google Scholar
• Josenhans Labigne C.A., Suerbaum S. Comparative ultrastructural and functional studies of Helicobacter pylori, Helicobacter mustelae flagellin mutants: both flagellin units, FlaA and FlaB, are necessary for full motility in Helicobacter species. J. Bacteriol 1995; 177: 3010
   PubMed Web of Science ®Google Scholar
• Hazell Lee S. L., Brady A.L., Hennessy W. Campylobacter pyloridis and gastritis: association with intercellular spaces and adaptation to an environment of mucus as important factors in colonization of the gastric epithelium. J. Infect. Dis. 1986; 153: 658
   PubMed Web of Science ®Google Scholar
• Eaton Morgan K. A.D.R., Krakowka S. Campylobacter pylori virulence factors in gnotobiotic piglets. Infect. Immun. 1989; 57: 1119
   PubMed Web of Science ®Google Scholar
• Eaton Morgan K. A.D.R., Krakowka S. Motility as a factor in the colonisation of gnotobiotic piglets by. Helicobacter pylori, J. Med. Microbiol. 1992; 37: 123
   PubMed Web of Science ®Google Scholar
• Koch C., Hoiby N. Pathogenesis of cystic fibrosis. Lancet 1993; 341: 1065
   PubMed Web of Science ®Google Scholar
• Poggio Glynn E. C., Schein R. J., Seddon O. D., Shannon J. M., Scardino M. J.V.A., Kenyon K. R. The incidence of ulcerative keratitis among users of daily-wear and extended-wear soft contact lenses. N. Engl. J. Med. 1989; 321: 779
   PubMed Web of Science ®Google Scholar
• Schein Glynn O. D., Poggio R. J., Seddon E. C.J.M., Kenyon K. R. The relative risk of ulcerative keratitis among users of daily-wear and extended-wear soft contact lenses. A case-control study. N. Engl. J. Med. 1989; 321: 1773
   PubMed Web of Science ®Google Scholar
• Benerjee Emori S. S., Culver T. G., Gaynes D. H., Jarvis R. P., Horan W. R., Edwards T., Tolson J. R., Henderson J.T., Martone W. J. Secular trends in nosocomial primary bloodstream infections in the United States, 1980–1989. Am. J. Med 1991; 91((Suppl. 3B))86S
   Google Scholar
• Bodey Bolivar G. P., Feinstein R.V., Jodega L. Infections caused by. Pseudomonas aeruginosa, Rev. Infect. Dis. 1983; 5: 279
   PubMed Web of Science ®Google Scholar
• Deitch Xu E. A., Qi D. Z.L., Berg R. D. Bacterial translocation from the gut impairs systemic immunity. Surgery 1991; 109: 269
   PubMed Web of Science ®Google Scholar
• Wells Jechorek C. L.R.P., Gillingham K. J. Relative contributions of host and microbial factors in bacterial translocation. Arch. Surg. 1991; 126: 247
   PubMedGoogle Scholar
• Allison Dawson J. S., Drake M.D., Montie T. C. Electrophoretic separation and molecular weight characterization of Pseudomonas aeruginosa H-antigen flagellins. Infect. Immun. 1985; 49: 770
   PubMed Web of Science ®Google Scholar
• Montie Doyle-Huntzinger T. C., Craven D.R., Holder I. A. Loss of virulence associated with absence of flagellum in an isogenic mutant of Pseudomonas aeruginosa in the burned mouse model. Infect. Immun. 1982; 38: 1296
   PubMed Web of Science ®Google Scholar
• Luzar Thomassen M. A.M.J., Montie T. C. Flagella and motility alterations in Pseudomonas aeruginosa strains from patients with cystic fibrosis: relationship to patient clinical condition. Infect. Immun. 1985; 50: 577
   PubMed Web of Science ®Google Scholar
• Mahenthiralingam Campbell E.M.E., Speert D. P. Nonmotility and phagocytic resistance of Pseudomonas aeruginosa isolates from chronically colonized patients with cystic fibrosis. Infect. Immun. 1994; 62: 596
   PubMed Web of Science ®Google Scholar
• Mahenthiralingam E., Speert D. P. Nonopsonic phagocytosis of Pseudomonas aeruginosa by macrophages and polymorphonuclear leukocytes requires the presence of the bacterial flagellum. Infect. Immun. 1995; 63: 4519
   PubMed Web of Science ®Google Scholar
• Ritchings Almira B. W., Lory E. C.S., Ramphal R. Cloning and phenotypic characterization of fleS, fleR new response regulators of Pseudomonas aeruginosa which regulate motility and adhesion to mucin. Infect. Immun 1995; 63: 4868
   PubMed Web of Science ®Google Scholar
• Simpson Ramphal D. A.R., Lory S. Genetic analysis of Pseudomonas aeruginosa adherence: distinct genetic loci control attachment to epithelial cells and mucins. Infect. Immun. 1992; 60: 3771
   PubMed Web of Science ®Google Scholar
• Simpson Ramphal D. A.R., Lory S. Characterization of Pseudomonas aeruginosa fliO a gene involved in flagellar biosynthesis and adherence. Infect. Immun. 1995; 63: 2950
   PubMed Web of Science ®Google Scholar
• Totten P. A., Lory S. Characterization of the type a flagellin gene from Pseudomonas aeruginosa PAK. J. Bacteriol. 1990; 172: 7188
   PubMed Web of Science ®Google Scholar
• Hazlett L. D., Rudner X. L. Investigations on the role of flagella in adhesion of Pseudomonas aeruginosa to mouse and human corneal epithelial proteins. Ophthal. Res. 1994; 26: 375
   PubMed Web of Science ®Google Scholar
• Wachsmuth Blake I. K.P.A., Olsvik O. Vibrio cholerae and Cholera: Molecular to Global Perspectives. American Society for Microbiology, Washington, D.C. 1994
   Google Scholar
• Gill D. M. Mechanism of action of cholera toxin. Adv. Cyclic Nucleotide Res. 1977; 8: 85
   PubMedGoogle Scholar
• DiRita Parsot V. J., Jander C.G., Mekalanos J. J. Regulatory cascade controls virulence in. Vibrio cholerae, Proc. Natl. Acad. Sci. U.S.A. 1991; 88: 5403
   PubMed Web of Science ®Google Scholar
• Peterson K. M., Mekalanos J. J. Characterization of the Vibrio cholerae ToxR regulon: identification of novel genes involved in intestinal colonization. Infect. Immun. 1988; 56: 2822
   PubMed Web of Science ®Google Scholar
• Camilli A., Mekalanos J. J. Use of recombinase gene fusion to identify Vibrio cholerae genes induced during infection. Mol. Microbiol. 1995; 18: 671
   PubMed Web of Science ®Google Scholar
• Gardel C. L., Mekalanos J. J. Modus operandi of Vibrio cholerae: swim to arrive stop to kill. The relationship among chemotaxis, motility and virulence. J. Cell Biochem 1994; 18A: 65
   Google Scholar
• Harkey Everiss C. W.K.D., Peterson K. M. The Vibrio cholerae toxin-co-regulated-pilus gene tcpI encodes a homolog of methyl-accepting chemotaxis proteins. Infect. Immun 1994; 62: 2669
   PubMed Web of Science ®Google Scholar
• Guentzel M. N., Berry L. J. Motility as a virulence factor for. Vibrio cholerae, Infect. Immun. 1975; 11: 890
   PubMed Web of Science ®Google Scholar
• Freter Allweiss P., O'Brien Halstead B. P. C. M.S.A., Macsai M. S. The role of chemotaxis in the association of motile bacteria with intestinal mucosa: in vitro studies. Infect. Immun. 1981; 34: 241
   PubMed Web of Science ®Google Scholar
• Freter P., O'Brien P. C. M., Macsai M. S. The role of chemotaxis in the association of motile bacteria with intestinal mucosa: in vivo studies. Infect. Immun. 1981; 34: 234
   PubMed Web of Science ®Google Scholar
• Attridge S. R., Rowley D. The role of the flagellum in the adherence of. Vibrio cholerae, J. Infect. Dis. 1983; 147: 864
   PubMed Web of Science ®Google Scholar
• Richardson K. Role of motility and flagellar structure in pathogenicity of Vibrio cholerae: analysis of motility mutants in three animal models. Infect. Immun. 1991; 59: 2727
   PubMed Web of Science ®Google Scholar
• Freter R., O'Brien P. C. M. The role of chemotaxis in the association of motile bacteria with intestinal mucosa: fitness and virulence of non-chemotactic Vibrio cholerae mutants in infant mice. Infect. Immun. 1981; 34: 222
   PubMed Web of Science ®Google Scholar
• Jones G. W., Freter R. Adhesive properties of Vibrio cholerae: nature of the interaction with isolated rabbit brush border membranes and human erythrocytes. Infect. Immun. 1976; 14: 240
   PubMed Web of Science ®Google Scholar
• Freter R., O'Brien P. C. M. The role of chemotaxis in the association of motile bacteria with intestinal mucosa: chemotactic responses of Vibrio cholerae and description of motile nonchemotactic mutants. Infect. Immun. 1981; 34: 215
   PubMed Web of Science ®Google Scholar
• Mostow P., Richardson K. High-frequency spontaneous mutation of classical Vibrio cholerae to a nonmotile phenotype. Infect. Immun. 1990; 58: 3633
   PubMed Web of Science ®Google Scholar
• Joseph Colwell S. W.R.R., Kaper J. B. Vibrio parahemolyticus and related halophilic vibrios. Crit. Rev. Microbiol. 1983; 10: 77
   Web of Science ®Google Scholar
• Belas M. R., Colwell R. R. Adsorption kinetics of laterally and polarly flagellated. Vibrio, J. Bacteriol. 1982; 151: 1568
   PubMed Web of Science ®Google Scholar
• Iijima Yamada Y.H., Shinoda S. Adherence of Vibrio parahaemolyticus and its relation to pathogenicity. Can. J. Microbiol. 1981; 27: 1252
   PubMed Web of Science ®Google Scholar
• Merrell Walker B. R.R.I., Joseph S. W. In vitro, in vivo pathologic effects of Vibrio parahaemolyticus on human epithelial cells. Can. J. Microbiol 1984; 30: 381
   PubMed Web of Science ®Google Scholar
• Chart H. Multiflagellate variants of. Vibrio anguillarum, J. Gen. Microbiol. 1983; 129: 2196
   Google Scholar
• Milton D. L., O'Toole R., Hörstedt P., Wolf-Watz H. Flagellin A is essential for the virulence of. Vibrio anguillarum, J. Bacteriol. 1996; 178: 1310
   PubMed Web of Science ®Google Scholar
• O'Toole Milton R.D.L., Wolf-Watz H. Chemotactic motility is required for invasion of the host by the fish pathogen. Vibrio anguillarum, Mol. Microbiol. 1996; 19: 625
   PubMed Web of Science ®Google Scholar
• Cantey J. R., Blake R. K. Diarrhea due to Escherichia coli in the rabbit: a novel mechanism. J. Infect. Dis. 1977; 135: 454
   PubMed Web of Science ®Google Scholar
• Ritter Blum A., Emödy Kerenyi G.L., Böck Neuhierl M.A., Rabsch B., Scheutz W.F., Hacker J. tRNA genes and pathogenicity islands: influence on virulence and metabolic properties of uropathogenic. Escherichia coli, Mol. Microbiol. 1995; 17: 109
   PubMed Web of Science ®Google Scholar
• Finlay B. B., Falkow S. Salmonella as an intracellular parasite. Mol. Microbiol. 1989; 3: 1833
   PubMed Web of Science ®Google Scholar
• Carsiotis Weinstein M., Karch D. L., Holder H.I.A., O'Brien A. D. Flagella of Salmonella typhimurium are a virulence factor in infected C57BL/6J mice. Infect. Immun. 1984; 46: 814
   PubMed Web of Science ®Google Scholar
• Weinstein Carsiotis D. L., Lissner M.C.C., O'Brien A. D. Flagella help Salmonella typhimurium survive within murine macrophages. Infect. Immun. 1984; 46: 819
   PubMed Web of Science ®Google Scholar
• Carsiotis Stocker M., Weinstein B. A. D.D.L., O'Brien A. D. A Salmonella typhimurium virulence gene linked to. flg, Infect. Immun. 1989; 57: 3276
   PubMed Web of Science ®Google Scholar
• Lockman H. A., Curtiss R., III. Salmonella typhimurium mutants lacking flagella or motility remain virulent in BALB/c mice. Infect. Immun. 1990; 58: 137
   PubMed Web of Science ®Google Scholar
• Betts J., Finlay B. B. Identification of Salmonella typhimurium invasiveness loci. Can. J. Microbiol. 1992; 38: 852
   PubMed Web of Science ®Google Scholar
• Jones Richardson G. W.L.A., Uhlman D. The invasion of HeLa cells by Salmonella typhimurium: reversible and irreversible bacterial attachment and the role of bacterial motility. J. Gen. Microbiol. 1981; 127: 351
   PubMedGoogle Scholar
• Jones Lee B. D.C.A., Falkow S. Invasion by Salmonella typhimurium is affected by the direction of flagellar rotation. Infect. Immun. 1992; 60: 2475
   PubMed Web of Science ®Google Scholar
• Fields Swanson P. I., Haidaris R. V.C.G., Heffron F. Mutants of Salmonella typhimurium that cannot survive within the macrophage are avirulent. Proc. Natl. Acad. Sci. U.S.A. 1986; 83: 5189
   PubMed Web of Science ®Google Scholar
• Liu S.-Ezaki L., Miura T., Matsui H.K., Yabuuchi E. Intact motility as a Salmonella typhi invasion-related factor. Infect. Immun. 1988; 56: 1967
   PubMed Web of Science ®Google Scholar
• Lawrence Delaquis J. R., Korber P. J.D.R., Caldwell D. E. Behavior of Pseudomonas fluorescens within the hydrodynamic boundary layers of surface microenvironments. Microb. Ecol. 1987; 14: 1
   PubMed Web of Science ®Google Scholar
• Marshall Stout K. C.R., Mitchell R. Mechanisms of the initial events in the sorption of marine bacteria to solid surfaces. J. Gen. Microbiol. 1971; 68: 337
   Google Scholar
• Meadows P. S. The attachment of bacteria to solid surfaces. Arch. Microbiol. 1971; 75: 374
   Google Scholar
• Korber Lawrence D. R., Sutton J. R.B., Caldwell D. E. Effect of laminar flow velocity on the kinetics of surface recolonization by Mot+ and Mot. Pseudomonas fluorescens, Microb. Ecol 1989; 18: 1
   Google Scholar
• Stanley P. M. Factors affecting the irreversible attachment of Pseudomonas aeruginosa to stainless steel. Can. J. Microbiol. 1983; 29: 1493
   PubMed Web of Science ®Google Scholar
• Dufrěne Vermeiren Y. F., Vanderleyden H.J., Rouxhet P. G. Direct evidence for the involvement of extracellular proteins in the adhesion of Azospirillum brasilense. Microbiology, in press
   Web of Science ®Google Scholar
• Butler Stewart J. L., Vanderzant J. C., Carpenter C.Z.L., Smith G. C. Attachment of microorganisms to pork skin and surfaces of beef and lamb carcasses. J. Food Prot. 1979; 42: 401
   PubMed Web of Science ®Google Scholar
• Farber J. M., Idziak E. S. Attachment of psychrotrophic meat spoilage bacteria to muscle surfaces. J. Food Prot. 1984; 47: 92
   PubMed Web of Science ®Google Scholar
• Firstenberg-Eden R. Attachment of bacteria to meat surfaces: a review. J. Food Prot. 1981; 44: 602
   PubMed Web of Science ®Google Scholar
• Lillard H. S. Bacterial cell characteristics and conditions influencing their adhesion to poultry skin. J. Food Prot. 1985; 48: 803
   PubMed Web of Science ®Google Scholar
• McMeekin T. A., Thomas C. J. Retention of bacteria on chicken skin after immersion in bacterial suspensions. J. Appl. Bacteriol. 1978; 45: 383
   PubMedGoogle Scholar
• Notermans Firstenberg-Eden S.R., VanSchothorst M. Attachment of bacteria to teats of cows. J. Food Prot. 1979; 42: 228
   PubMed Web of Science ®Google Scholar
• Notermans S., Kampelmacher E. H. Attachment of some bacterial strains to the skin of broiler chickens. Br. Poult. Sci. 1974; 15: 573
   PubMed Web of Science ®Google Scholar
• Notermans Dufrenne S.J., VanSchothorst M. The effect of cultural procedures on the attachment of bacteria to chicken breast meat. J. Appl. Bacteriol. 1980; 49: 273
   PubMedGoogle Scholar
• Lillard H. S. Role of fimbriae and flagella in the attachment of Salmonella typhimurium to poultry skin. J. Food Sci. 1986; 51: 54
   Web of Science ®Google Scholar
• Piette J.-P.G., Idziak E. S. New method to study bacterial adhesion to meat. Appl. Environ. Microbiol. 1989; 55: 1531
   PubMed Web of Science ®Google Scholar
• Piette J.-P. G., Idziak E. S. Role of flagella in adhesion of Pseudomonas fluorescens to tendon slices. Appl. Environ. Microbiol. 1991; 57: 1635
   PubMed Web of Science ®Google Scholar
• Ray D. L. Agglutination of bacteria: a feeding mechanism in the soil amoeba. Hartmanella sp. J. Exp. Zool. 1951; 118: 442
   Google Scholar
• Preston T. M., King C. A. Binding sites for bacterial flagella at the surface of the soil amoeba. Acanthamoeba, J. Gen. Microbiol. 1984; 130: 1449
   Google Scholar
• McCormick Laux B. A.D.C., Cohen P. S. Neither motility nor chemotaxis play a role in the ability of Escherichia coli F-18 to colonize the streptomycin-treated mouse large intestine. Infect. Immun. 1990; 58: 2957
   PubMed Web of Science ®Google Scholar
• Stanton T. B., Savage D. C. Colonization of gnotobiotic mice by Roseburia cecicola a motile, obligately anaerobic bacterium from murine ceca. Appl. Environ. Microbiol. 1983; 45: 1677
   PubMed Web of Science ®Google Scholar
• Stanton T. B., Savage D. C. Roseburia cecicola gen. nov. sp. nov. a motile, obligately anaerobic bacterium from a murine cecum. Int. J. Syst. Bacteriol. 1983; 33: 618
   Google Scholar
• Stanton T. B., Savage D. C. Motility as a factor in bowel colonization by Roseburia cecicola an obligately anaerobic bacterium from the mouse caecum. J. Gen. Microbiol. 1984; 130: 173
   PubMedGoogle Scholar
• Arora Filinow D. K.A.B., Lockwood J. L. Bacterial chemotaxis to fungal propagules in vitro and in soil. Can. J. Microbiol. 1983; 29: 1104
   Web of Science ®Google Scholar
• Bashan Y. Migration of the rhizosphere bacteria Azospirillum brasilense, Pseudomonas fluorescens toward wheat roots in the soil. J. Gen. Microbiol 1986; 132: 3407
   Google Scholar
• Soby S., Bergman K. Motility and chemotaxis of Rhizobium meliloti in soil. Appl. Environ. Microbiol. 1983; 46: 995
   PubMed Web of Science ®Google Scholar
• Wong P. T. W., Griffin D. M. Bacterial movement at high matric potentials. I. In artificial and natural soils. Soil Biol. Biochem. 1976; 8: 215
   Web of Science ®Google Scholar
• DeFlaun Tanzer M. F., McAteer A. S., Marshall A. L.B.M., Levy S. B. Development of an adhesion assay and characterization of an adhesion-deficient mutant of. Pseudomonas fluorescens, Appl. Environ. Microbiol. 1990; 56: 112
   PubMed Web of Science ®Google Scholar
• DeFlaun Marshall M. F., Kulle B. M.E.-P., Levy S. B. Tn5 insertion mutants of Pseudomonas fluorescens defective in adhesion to soil and seeds. Appl. Environ. Microbiol. 1994; 60: 2637
   PubMed Web of Science ®Google Scholar
• Misaghi Olsen I. J., Billotte M. W.J.M., Sonoda R. M. The importance of rhizobacterial mobility in biocontrol of bacterial wilt of tomato. Soil Biol. Biochem. 1992; 24: 287
   Web of Science ®Google Scholar
• Scher Kloepper F. M., Singleton J. W., Zaleska C.I., Laliberte M. Colonization of soybean roots by Pseudomonas, Serratia species: relationship to bacterial motility, chemotaxis, and generation time. Phytopathology 1988; 78: 1055
   Web of Science ®Google Scholar
• Howie Cook W. J.R.J., Weller D. M. Effects of soil matric potential and cell motility on wheat root colonization by fluorescent pseudomonads suppressive to take-all. Phytopathology 1987; 77: 286
   Web of Science ®Google Scholar
• De Weger L. A., Vander Vlugt Wijfjes C. I. M., Bakker A. H. M.P., Schippers A. H. M.B., Lugtenberg B. Flagella of a plant-growth-stimulating Pseudomonas fluorescens strain are required for colonization of potato roots. J. Bacteriol. 1987; 169: 2769
   PubMed Web of Science ®Google Scholar
• Bashan Y., Levanony H. Horizontal and vertical movement of Azospirillum brasilense Cd in the soil and along the rhizosphere of wheats and weeds in controlled and field environments. J. Gen. Microbiol. 1987; 133: 3473
   Google Scholar
• Bashan Y., Holguin G. Root-to-root travel of the beneficial bacterium. Azospirillum brasilense, Appl. Environ. Microbiol. 1994; 60: 2120
   PubMed Web of Science ®Google Scholar
• Bashan Y., Holguin G. Inter-root movement of Azospirillum brasilense and subsequent root colonization of crop and weed seedlings growing in soil. Microb. Ecol. 1995; 29: 269
   PubMed Web of Science ®Google Scholar
• Michiels Croes K. W.C.L., Vanderleyden J. Two different modes of attachment of Azospirillum brasilense Sp7 to wheat roots. J. Gen. Microbiol. 1991; 137: 2241
   Google Scholar
• Croes Moens C. L., VanBastelaere S., Vanderleyden E.J., Michiels K. W. The polar flagellum mediates Azospirillum brasilense adsorption to wheat roots. J. Gen. Microbiol. 1993; 139: 2261
   Google Scholar
• De Ley J., Rassel A. DNA base composition, flagellation and taxonomy of the genus. Rhizobium, J. Gen. Microbiol. 1965; 41: 85
   PubMedGoogle Scholar
• Tsien H.-C. Ultrastructure of free-living cells. Nitrogen Fixation, Rhizobium, W. J. Broughton. Clarendon Press, Oxford 1982; Vol 2: 192
   Google Scholar
• Smit Kijne G.J.W., Lugtenberg B. J. J. Involvement of both cellulose fibrils and a Ca2+-dependent adhesin in the attachment of Rhizobium leguminosarum to pea root hair tips. J. Bacteriol 1987; 169: 4294
   PubMed Web of Science ®Google Scholar
• Smit Kijne G.J.W., Lugtenberg B. J. J. Roles of flagella, lipopolysaccharide, and a Ca2+-dependent cell surface protein in attachment of Rhizobium leguminosarum biovar viciae to pea root hair tips. J. Bacteriol 1989; 171: 569
   PubMed Web of Science ®Google Scholar
• Napoli C., Albersheim P. Infection and nodulation of clover by nonmotile. Rhizobium trifolii, J. Bacteriol. 1980; 141: 979
   PubMed Web of Science ®Google Scholar
• Mellor Glenn H. Y., Arwas A. R.R., Dilworth M. J. Symbiotic and competitive properties of motility mutants of Rhizobium trifolii TA1. Arch. Microbiol. 1987; 148: 34
   Web of Science ®Google Scholar
• Ames Schluederberg P.S.A., Bergman K. Behavioral mutants of. Rhizobium meliloti, J. Bacteriol. 1980; 141: 722
   PubMed Web of Science ®Google Scholar
• Ames P., Bergman K. Competitive advantage provided by bacterial motility in the formation of nodules by. Rhizobium meliloti, J. Bacteriol. 1981; 148: 728
   PubMed Web of Science ®Google Scholar
• Caetano-Anollés Wall G., De Micheli Macchi L.G.A.T., Bauer E. M.W.D., Favelukes G. Role of motility and chemotaxis in efficiency of nodulation by. Rhizobium meliloti, Plant Physiol. 1988; 86: 1228
   PubMed Web of Science ®Google Scholar
• Malek W. The role of motility in the efficiency of nodulation by. Rhizobium meliloti, Arch. Microbiol. 1992; 158: 26
   Web of Science ®Google Scholar
• Liu Tran R.V.M., Schmidt E. L. Nodulating competitiveness of a nonmotile Tn7 mutant of Bradyrhizobium japonicum in nonsterile soil. Appl Environ. Microbiol. 1989; 55: 1895
   PubMed Web of Science ®Google Scholar
• Ruby E. G., Asato L. M. Growth and flagellation of Vibrio fischeri during initiation of the sepiolid squid light organ symbiosis. Arch. Microbiol. 1993; 159: 160
   PubMed Web of Science ®Google Scholar
• Tebo Linthicum B. M.D.S., Nealson K. H. Luminous bacteria and light-emitting fish: ultrastructure of the symbiosis. BioSystems 1979; 11: 269
   PubMed Web of Science ®Google Scholar
• Vincent J. M. Factors controlling the legume-Rhizobium symbiosis. Nitrogen Fixation, W. E. Newton, W. H. Orme-Johnson. University Park Press, Baltimore 1980; Vol. 2: 103
   Google Scholar
• Wilson D. R., Beveridge T. J. Bacterial flagellar filaments and their component flagellins. Can. J. Microbiol. 1993; 39: 451
   PubMed Web of Science ®Google Scholar
• Beveridge T. J. The bacterial surface: general considerations towards design and function. Can. J. Microbiol. 1988; 34: 363
   PubMed Web of Science ®Google Scholar
• Sugiyama S. Na+-driven flagellar motors as a likely Na+ re-entry pathway in alkalophilic bacteria. Mol. Microbiol 1995; 15: 592
   PubMed Web of Science ®Google Scholar
• Allaloui Woestyn A., Sluiters S.C., Cornelis G. R. YscU, a Yersinia enterocolitica inner membrane protein involved in Yop secretion. J. Bacteriol. 1994; 176: 4534
   PubMed Web of Science ®Google Scholar
• Dreyfus Williams G., Kawagishi A. W.I., Macnab R. M. Genetic and biochemical analysis of Salmonella typhimurium FliI, a flagellar protein related to the catalytic subunit of the F0F1 ATPase and to virulence proteins of mammalian and plant pathogens. J. Bacteriol 1993; 175: 3131
   PubMed Web of Science ®Google Scholar
• Fenselau S., Bonas U. Sequence and expression analysis of the hrpB pathogenicity operon of Xanthomonas campestris pv. vesicatoria which encodes eight proteins with similarity to components of the Hrp, Ysc, Spa, and Fli secretion systems. Mol. Plant Microb. Interact 1995; 8: 845
   PubMed Web of Science ®Google Scholar
• Lidell M. C., Hutcheson S. W. Characterization of the hrpJ, hrpU operons of Pseudomonas syringae pv. syringae Pss61: similarity with components of enteric bacteria involved in flagellar biogenesis and demonstration of their role in HarpinPss secretion. Mol. Plant. Microb. Interact 1994; 7: 488
   PubMed Web of Science ®Google Scholar
• Miller Pesci S.E.C., Pickett C. L. A Campylobacter jejuni homolog of the LcrD/FlbF family of proteins is necessary for flagellar biogenesis. Infect. Immun. 1993; 61: 2930
   PubMed Web of Science ®Google Scholar
• Plano Barve G. V.S.S., Straley S. C. LcrD: a membrane-bound regulatory protein of the Yersinia pestis low-Ca2+ response. J. Bacteriol 1991; 173: 7293
   PubMed Web of Science ®Google Scholar
• Ramakrishnan Zhao G.J.L., Newton A. The cell cycle-regulated flagellar gene flbF of Caulobacter crescentus is homologous to a virulence locus (IcrD) of. Yersinia pestis, J. Bacteriol 1991; 173: 7283
   PubMed Web of Science ®Google Scholar
• Sanders VanWay L. A.S., Mullin D. A. Characterization of the Caulobacter crescentus flbF product as a homolog of the LcrD protein from. Yersinia enterocolitica, J. Bacteriol. 1992; 174: 857
   PubMed Web of Science ®Google Scholar
• Venkatesan Buysse M. M.J.M., Oaks E. V. Surface presentation of Shigella flexneri invasion plasmid antigens requires the products of the spa locus. J. Bacteriol 1992; 174: 1990
   PubMed Web of Science ®Google Scholar