Could DNA uptake be a side effect of bacterial adhesion and twitching motility?
- M. Bakkali
- … show all 1 hide
Abstract
DNA acquisition promotes the spread of resistance to antibiotics and virulence among bacteria. It is also linked to several natural phenomena including recombination, genome dynamics, adaptation and speciation. Horizontal DNA transfer between bacteria occurs via conjugation, transduction or competence for natural transformation by DNA uptake. Among these, competence is the only mechanism of transformation initiated and entirely controlled by the chromosome of the recipient bacteria. While the molecular mechanisms allowing the uptake of extracellular DNA are increasingly characterized, the function of competence for natural transformation by DNA uptake, the selective advantage maintaining it and the reasons why bacteria take up DNA in the first place are still debated. In this synthesis, I review some of the literature and discuss the four hypotheses on how and why do bacteria take up DNA. I argue that DNA uptake by bacteria is an accidental by-product of bacterial adhesion and twitching motility. Adhesion and motility are generally increased in stressful conditions, which may explain why bacteria increase DNA uptake in these conditions. In addition to its fundamental scientific relevance, the new hypothesis suggested here has significant clinical implications and finds further support from the fact that antibiotics sometimes fail to eliminate the targeted bacterium while inevitably causing stress to others. The widespread misuse of antibiotics may thus not only be selecting for resistant strains, but may also be causing bacteria to take up more DNA with the consequent increase in the chances of acquiring drug resistance and virulence—a scenario in full concordance with the previously reported induction of competence genes by antibiotics in Streptococcus pneumoniae and Legionella pneumophila.
Related Content
Supplementary Material (0)
References (130)
- Auzat I et al (1999) The NADH oxidase of Streptococcus pneumoniae: its involvement in competence and virulence. Mol Microbiol 34:1018–1028 CrossRef
- Averhoff B (2004) DNA transport and natural transformation in mesophilic and thermophilic bacteria. J Bioenerg Biomembr 36:25–33 CrossRef
- Bakkali M (2007) Genome dynamics of short oligonucleotides: the example of bacterial DNA uptake enhancing sequences. PLoS ONE 2:e741 CrossRef
- Bakkali M, Chen TY, Lee HC, Redfield RJ (2004) Evolutionary stability of DNA uptake signal sequences in the Pasteurellaceae. Proc Natl Acad Sci USA 101:4513–4518 CrossRef
- Bartlett JG (2006) Narrative review: the new epidemic of Clostridium difficile-associated enteric disease. Ann Intern Med 145:758–764
- Berge M, Moscoso M, Prudhomme M, Martin B, Claverys JP (2002) Uptake of transforming DNA in Gram-positive bacteria: a view from Streptococcus pneumoniae. Mol Microbiol 45:411–421 CrossRef
- Bertolla F et al (2000) Plant genome complexity may be a factor limiting in situ the transfer of transgenic plant genes to the phytopathogen Ralstonia solanacearum. Appl Environ Microbiol 66:4161–4167 CrossRef
- Bhaya D, Bianco NR, Bryant D, Grossman A (2000) Type IV pilus biogenesis and motility in the cyanobacterium Synechocystis sp. PCC6803. Mol Microbiol 37:941–951 CrossRef
- Biswas GD, Sox T, Blackman E, Sparling PF (1977) Factors affecting genetic transformation of Neisseria gonorrhoeae. J Bacteriol 129:983–992
- Bradley DE (1975) The occurrence of pili associated with a plasmid of the W compatibility group. Biochem Biophys Res Commun 64:918–925 CrossRef
- Brener D, DeVoe IW (1983) Effects of culture pH on the expression of meningococcal pili. Curr Microbiol 8:57–61 CrossRef
- Brinkmann V et al (2004) Neutrophil extracellular traps kill bacteria. Science 303:1532–1535 CrossRef
- Burke WF Jr (1982) Bacillus subtilis extracellular nuclease production associated with the spoOH sporulation locus. J Gen Microbiol 128:1591–1597
- Catlin BW (1960) Transformation of Neisseria meningitidis by deoxyribonucleates from cells and from culture slime. J Bacteriol 79:579–590
- Chapuy-Regaud S, Duthoit F, Malfroy-Mastrorillo L, Gourdon P, Lindley ND, Trombe MC (2001) Competence regulation by oxygen availability and by Nox is not related to specific adjustment of central metabolism in Streptococcus pneumoniae. J Bacteriol 183:2957–2962 CrossRef
- Charpentier X, Kay E, Schneider D, Shuman HA (2011) Antibiotics and UV radiation induce competence for natural transformation in Legionella pneumophila. J Bacteriol 193:1114–1121 CrossRef
- Chen I, Dubnau D (2003) DNA transport during transformation. Front Biosci 8:s544–s556 CrossRef
- Chen I, Dubnau D (2004) DNA uptake during bacterial transformation. Nat Rev Microbiol 2:241–249 CrossRef
- Chen I, Christie PJ, Dubnau D (2005) The ins and outs of DNA transfer in bacteria. Science 310:1456–1460 CrossRef
- Chen I, Provvedi R, Dubnau D (2006) A macromolecular complex formed by a pilin-like protein in competent Bacillus subtilis. J Biol Chem 281:21720–21727 CrossRef
- Christie PJ, Atmakuri K, Krishnamoorthy V, Jakubowski S, Cascales E (2005) Biogenesis, architecture, and function of bacterial type IV secretion systems. Annu Rev Microbiol 59:451–485 CrossRef
- Claverys JP, Prudhomme M, Martin B (2006) Induction of competence regulons as a general response to stress in Gram-positive bacteria. Annu Rev Microbiol 60:451–475 CrossRef
- Claverys JP, Martin B, Polard P (2009) The genetic transformation machinery: composition, localization, and mechanism. FEMS Microbiol Rev 33:643–656 CrossRef
- Collins RF, Davidsen L, Derrick JP, Ford RC, Tonjum T (2001) Analysis of the PilQ secretin from Neisseria meningitidis by transmission electron microscopy reveals a dodecameric quaternary structure. J Bacteriol 183:3825–3832 CrossRef
- Courvalin P (2005) Antimicrobial drug resistance: “prediction is very difficult, especially about the future”. Emerg Infect Dis 11:1503–1506 CrossRef
- de Vries J, Meier P, Wackernagel W (2001) The natural transformation of the soil bacteria Pseudomonas stutzeri and Acinetobacter sp. by transgenic plant DNA strictly depends on homologous sequences in the recipient cells. FEMS Microbiol Lett 195:211–215
- Demaneche S, Kay E, Gourbiere F, Simonet P (2001) Natural transformation of Pseudomonas fluorescens and Agrobacterium tumefaciens in soil. Appl Environ Microbiol 67:2617–2621 CrossRef
- Diep BA, Carleton HA, Chang RF, Sensabaugh GF, Perdreau-Remington F (2006) Roles of 34 virulence genes in the evolution of hospital- and community-associated strains of methicillin-resistant Staphylococcus aureus. J Infect Dis 193:1495–1503 CrossRef
- Doran JL, Page WJ (1983) Heat sensitivity of Azotobacter vinelandii genetic transformation. J Bacteriol 155:159–168
- Dubnau D (1999) DNA uptake in bacteria. Annu Rev Microbiol 53:217–244 CrossRef
- Espinosa M, Joenje H, Venema G (1980) DNA binding and deoxyribonuclease activity in Bacillus subtilis during temperature-induced competence development. J Gen Microbiol 121:79–84
- Facius D, Meyer TF (1993) A novel determinant (comA) essential for natural transformation competence in Neisseria gonorrhoeae and the effect of a comA defect on pilin variation. Mol Microbiol 10:699–712 CrossRef
- Forest KT, Tainer JA (1997) Type-4 pilus-structure: outside to inside and top to bottom—a minireview. Gene 192:165–169 CrossRef
- Fraser C, Hanage WP, Spratt BG (2007) Recombination and the nature of bacterial speciation. Science 315:476–480 CrossRef
- Fyfe JA, Carrick CS, Davies JK (1995) The pilE gene of Neisseria gonorrhoeae MS11 is transcribed from a sigma 70 promoter during growth in vitro. J Bacteriol 177:3781–3787
- Glick BR, Brooks HE, Pasternak JJ (1985) Transformation of Azotobacter vinelandii with plasmid DNA. J Bacteriol 162:276–279
- Gomez–Gomez JM, Manfredi C, Alonso JC, Blazquez J (2007) A novel role for RecA under non-stress: promotion of swarming motility in Escherichia coli K-12. BMC Biol 5:14 CrossRef
- Goodgal SH, Herriott RM (1961) Studies on transformations of Hemophilus influenzae. I. Competence. J Gen Physiol 44:1201–1227 CrossRef
- Graves JF, Biswas GD, Sparling PF (1982) Sequence-specific DNA uptake in transformation of Neisseria gonorrhoeae. J Bacteriol 152:1071–1077
- Griffith F (1928) The significance of pneumococcal types. J Hyg 27:113–159 CrossRef
- Hahn J, Maier B, Haijema BJ, Sheetz M, Dubnau D (2005) Transformation proteins and DNA uptake localize to the cell poles in Bacillus subtilis. Cell 122:59–71 CrossRef
- Hahn J, Kramer N, Briley K Jr, Dubnau D (2009) McsA and B mediate the delocalization of competence proteins from the cell poles of Bacillus subtilis. Mol Microbiol 72:202–215 CrossRef
- Hamilton HL, Dominguez NM, Schwartz KJ, Hackett KT, Dillard JP (2005) Neisseria gonorrhoeae secretes chromosomal DNA via a novel type IV secretion system. Mol Microbiol 55:1704–1721 CrossRef
- Havarstein LS, Coomaraswamy G, Morrison DA (1995) An unmodified heptadecapeptide pheromone induces competence for genetic transformation in Streptococcus pneumoniae. Proc Natl Acad Sci USA 92:11140–11144 CrossRef
- Henrichsen J (1983) Twitching motility. Annu Rev Microbiol 37:81–93 CrossRef
- Herriott RM, Meyer EM, Vogt M (1970) Defined nongrowth media for stage II development of competence in Haemophilus influenzae. **J Bacteriol 101:517–524
- Jelsbak L, Sogaard-Andersen L (2000) Pattern formation: fruiting body morphogenesis in Myxococcus xanthus. Curr Opin Microbiol 3:637–642 CrossRef
- Johnsen PJ, Dubnau D, Levin BR (2009) Episodic selection and the maintenance of competence and natural transformation in Bacillus subtilis. Genetics 181:1521–1533 CrossRef
- Kaiser D (1979) Social gliding is correlated with the presence of pili in Myxococcus xanthus. Proc Natl Acad Sci USA 76:5952–5956 CrossRef
- Kaiser D (2000) Bacterial motility: how do pili pull? Curr Biol 10:R777–R780 CrossRef
- Karaolis DK, Somara S, Maneval DR Jr, Johnson JA, Kaper JB (1999) A bacteriophage encoding a pathogenicity island, a type-IV pilus and a phage receptor in cholera bacteria. Nature 399:375–379 CrossRef
- Kendall MM, Sperandio V (2007) Quorum sensing by enteric pathogens. Curr Opin Gastroenterol 23:10–15 CrossRef
- Kirchner M, Meyer TF (2005) The PilC adhesin of the Neisseria type IV pilus-binding specificities and new insights into the nature of the host cell receptor. Mol Microbiol 56:945–957 CrossRef
- Kozlovsky Y, Cohen I, Golding I, Ben-Jacob E (1999) Lubricating bacteria model for branching growth of bacterial colonies. Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics 59:7025–7035 CrossRef
- Kruger E, Msadek T, Ohlmeier S, Hecker M (1997) The Bacillus subtilis clpC operon encodes DNA repair and competence proteins. Microbiology 143(Pt 4):1309–1316 CrossRef
- Kubiet M, Ramphal R, Weber A, Smith A (2000) Pilus-mediated adherence of Haemophilus influenzae to human respiratory mucins. Infect Immun 68:3362–3367 CrossRef
- Kufryk GI, Sachet M, Schmetterer G, Vermaas WF (2002) Transformation of the cyanobacterium Synechocystis sp. PCC 6803 as a tool for genetic mapping: optimization of efficiency. FEMS Microbiol Lett 206:215–219 CrossRef
- Kupfer DM, McCarthy D (1992) rec-2-dependent phage recombination in Haemophilus influenzae. J Bacteriol 174:4960–4966
- Lacasta AM, Cantalapiedra IR, Auguet CE, Penaranda A, Ramirez-Piscina L (1999) Modeling of spatiotemporal patterns in bacterial colonies. Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics 59:7036–7041 CrossRef
- Lauer P, Albertson NH, Koomey M (1993) Conservation of genes encoding components of a type IV pilus assembly/two-step protein export pathway in Neisseria gonorrhoeae. Mol Microbiol 8:357–368 CrossRef
- Li YH, Lau PC, Lee JH, Ellen RP, Cvitkovitch DG (2001) Natural genetic transformation of Streptococcus mutans growing in biofilms. J Bacteriol 183:897–908 CrossRef
- Li YH et al (2002) A quorum-sensing signaling system essential for genetic competence in Streptococcus mutans is involved in biofilm formation. J Bacteriol 184:2699–2708 CrossRef
- Liles MR, Viswanathan VK, Cianciotto NP (1998) Identification and temperature regulation of Legionella pneumophila genes involved in type IV pilus biogenesis and type II protein secretion. Infect Immun 66:1776–1782
- Lin TL, Shun CT, Chang KC, Wang JT (2006) Isolation and characterization of a competence operon associated with transformation and adhesion in Helicobacter pylori. Microbes Infect 8:2756–2765 CrossRef
- Lopez P, Perez Urena MT, Espinosa M (1983) Influence of temperature-induced competence in the genetic transformation of Bacillus subtilis. Microbios 38:205–216
- Lorenz MG, Wackernagel W (1994) Bacterial gene transfer by natural genetic transformation in the environment. Microbiol Rev 58:563–602
- Lorenz MG, Gerjets D, Wackernagel W (1991) Release of transforming plasmid and chromosomal DNA from two cultured soil bacteria. Arch Microbiol 156:319–326 CrossRef
- Lorenz MG, Reipschlager K, Wackernagel W (1992) Plasmid transformation of naturally competent Acinetobacter calcoaceticus in non-sterile soil extract and groundwater. Arch Microbiol 157:355–360 CrossRef
- Love PE, Lyle MJ, Yasbin RE (1985) DNA-damage-inducible (din) loci are transcriptionally activated in competent Bacillus subtilis. Proc Natl Acad Sci USA 82:6201–6205 CrossRef
- Macfadyen LP, Dorocicz IR, Reizer J, Saier MH Jr, Redfield RJ (1996) Regulation of competence development and sugar utilization in Haemophilus influenzae Rd by a phosphoenolpyruvate:fructose phosphotransferase system. Mol Microbiol 21:941–952 CrossRef
- MacFadyen LP, Chen D, Vo HC, Liao D, Sinotte R, Redfield RJ (2001) Competence development by Haemophilus influenzae is regulated by the availability of nucleic acid precursors. Mol Microbiol 40:700–707 CrossRef
- Manetti AG et al (2010) Environmental acidification drives S. pyogenes pilus expression and microcolony formation on epithelial cells in a FCT-dependent manner. PLoS ONE 5:e13864 CrossRef
- Manning GS (2006) The persistence length of DNA is reached from the persistence length of its null isomer through an internal electrostatic stretching force. Biophys J 91:3607–3616 CrossRef
- Margolin W (2006) Gliding motility: anticipating the next move with a molecular clock. Curr Biol 16:R85–R87 CrossRef
- Mattick JS (2002) Type IV pili and twitching motility. Annu Rev Microbiol 56:289–314 CrossRef
- McBride MJ (2001) Bacterial gliding motility: multiple mechanisms for cell movement over surfaces. Annu Rev Microbiol 55:49–75 CrossRef
- Merz AJ, So M, Sheetz MP (2000) Pilus retraction powers bacterial twitching motility. Nature 407:98–102 CrossRef
- Messi P, Guerrieri E, de Niederhausern S, Sabia C, Bondi M (2006) Vancomycin-resistant enterococci (VRE) in meat and environmental samples. Int J Food Microbiol 107:218–222 CrossRef
- Michod RE, Wojciechowski MF, Hoelzer MA (1988) DNA repair and the evolution of transformation in the bacterium Bacillus subtilis. Genetics 118:31–39
- Mignot T, Merlie JP Jr, Zusman DR (2005) Regulated pole-to-pole oscillations of a bacterial gliding motility protein. Science 310:855–857 CrossRef
- Mignot T, Shaevitz JW, Hartzell PL, Zusman DR (2007) Evidence that focal adhesion complexes power bacterial gliding motility. Science 315:853–856 CrossRef
- Mongold JA (1992) DNA repair and the evolution of transformation in Haemophilus influenzae. Genetics 132:893–898
- Mortier-Barriere I, de Saizieu A, Claverys JP, Martin B (1998) Competence-specific induction of recA is required for full recombination proficiency during transformation in Streptococcus pneumoniae. Mol Microbiol 27:159–170 CrossRef
- Moscoso M, Claverys JP (2004) Release of DNA into the medium by competent Streptococcus pneumoniae: kinetics, mechanism and stability of the liberated DNA. Mol Microbiol 54:783–794 CrossRef
- Nachin L, Nannmark U, Nystrom T (2005) Differential roles of the universal stress proteins of Escherichia coli in oxidative stress resistance, adhesion, and motility. J Bacteriol 187:6265–6272 CrossRef
- Narra HP, Ochman H (2006) Of what use is sex to bacteria? Curr Biol 16:R705–R710 CrossRef
- Nijland R, Burgess JG, Errington J, Veening JW (2010) Transformation of environmental Bacillus subtilis isolates by transiently inducing genetic competence. PLoS ONE 5:e9724 CrossRef
- Nudleman E, Kaiser D (2004) Pulling together with type IV pili. J Mol Microbiol Biotechnol 7:52–62 CrossRef
- Oggioni MR et al (2004) Antibacterial activity of a competence-stimulating peptide in experimental sepsis caused by Streptococcus pneumoniae. Antimicrob Agents Chemother 48:4725–4732 CrossRef
- O’Rourke EJ, Pinto AV, Petroni EA, Tolmasky ME, Ielpi L (2004) Evidence for the active role of a novel nuclease from Helicobacter pylori in the horizontal transfer of genetic information. J Bacteriol 186:2586–2593 CrossRef
- Palchevskiy V, Finkel SE (2006) Escherichia coli competence gene homologs are essential for competitive fitness and the use of DNA as a nutrient. J Bacteriol 188:3902–3910 CrossRef
- Palmen R, Vosman B, Buijsman P, Breek CK, Hellingwerf KJ (1993) Physiological characterization of natural transformation in Acinetobacter calcoaceticus. J Gen Microbiol 139:295–305
- Provvedi R, Chen I, Dubnau D (2001) NucA is required for DNA cleavage during transformation of Bacillus subtilis. Mol Microbiol 40:634–644 CrossRef
- Prudhomme M, Attaiech L, Sanchez G, Martin B, Claverys JP (2006) Antibiotic stress induces genetic transformability in the human pathogen Streptococcus pneumoniae. Science 313:89–92 CrossRef
- Ranhand JM (1976) Effect of pH on competence development and deoxyribonucleic acid uptake in Streptococcus sanguis (Wicky). J Bacteriol 126:205–212
- Raymond-Denise A, Guillen N (1992) Expression of the Bacillus subtilis dinR and recA genes after DNA damage and during competence. J Bacteriol 174:3171–3176
- Redfield RJ (1988) Evolution of bacterial transformation: is sex with dead cells ever better than no sex at all? Genetics 119:213–221
- Redfield RJ (1991) Bacteria mating preferences. Nature 352:25–26 CrossRef
- Redfield RJ (1993a) Evolution of natural transformation: testing the DNA repair hypothesis in Bacillus subtilis and Haemophilus influenzae. Genetics 133:755–761
- Redfield RJ (1993b) Genes for breakfast: the have-your-cake-and-eat-it-too of bacterial transformation. J Hered 84:400–404
- Redfield RJ (2001) Do bacteria have sex? Nat Rev Genet 2:634–639 CrossRef
- Redfield RJ, Schrag MR, Dean AM (1997) The evolution of bacterial transformation: sex with poor relations. Genetics 146:27–38
- Redfield RJ, Findlay WA, Bosse J, Kroll JS, Cameron AD, Nash JH (2006) Evolution of competence and DNA uptake specificity in the Pasteurellaceae. BMC Evol Biol 6:82 CrossRef
- Roelants P, Konvalinkova V, Mergeay M, Lurquin PF, Ledoux L (1976) DNA uptake by Streptomyces species. Biochim Biophys Acta 442:117–122 CrossRef
- Rudel T, Scheurerpflug I, Meyer TF (1995a) Neisseria PilC protein identified as type-4 pilus tip-located adhesin. Nature 373:357–359 CrossRef
- Rudel T, Facius D, Barten R, Scheuerpflug I, Nonnenmacher E, Meyer TF (1995b) Role of pili and the phase-variable PilC protein in natural competence for transformation of Neisseria gonorrhoeae. Proc Natl Acad Sci USA 92:7986–7990 CrossRef
- Sabia C, Bondi M, Messi P, De Niederhausern S, Manicardi G (2005) Study of five penicillinase producing Neisseria gonorrhoeae isolated in Italy. New Microbiol 28:223–229
- Shafeeq S, Kloosterman TG, Kuipers OP (2011) CelR-mediated activation of the cellobiose-utilization gene cluster in Streptococcus pneumoniae. Microbiology 157:2854–2861 CrossRef
- Singh RN, Pitale MP (1968) Competence and deoxyribonucleic acid uptake in Bacillus subtilis. J Bacteriol 95:864–866
- Sisco KL, Smith HO (1979) Sequence-specific DNA uptake in Haemophilus transformation. Proc Natl Acad Sci USA 76:972–976 CrossRef
- Smeets LC, Becker SC, Barcak GJ, Vandenbroucke-Grauls CM, Bitter W, Goosen N (2006) Functional characterization of the competence protein DprA/Smf in Escherichia coli. FEMS Microbiol Lett 263:223–228 CrossRef
- Smith HO, Danner DB, Deich RA (1981) Genetic transformation. Annu Rev Biochem 50:41–68 CrossRef
- Steinmoen H, Knutsen E, Havarstein LS (2002) Induction of natural competence in Streptococcus pneumoniae triggers lysis and DNA release from a subfraction of the cell population. Proc Natl Acad Sci USA 99:7681–7686 CrossRef
- Sung P, Klein H (2006) Mechanism of homologous recombination: mediators and helicases take on regulatory functions. Nat Rev Mol Cell Biol 7:739–750 CrossRef
- Tang Y, Guest JR, Artymiuk PJ, Read RC, Green J (2004) Post-transcriptional regulation of bacterial motility by aconitase proteins. Mol Microbiol 51:1817–1826 CrossRef
- Thanassi JA, Hartman-Neumann SL, Dougherty TJ, Dougherty BA, Pucci MJ (2002) Identification of 113 conserved essential genes using a high-throughput gene disruption system in Streptococcus pneumoniae. Nucleic Acids Res 30:3152–3162 CrossRef
- Turgay K, Hamoen LW, Venema G, Dubnau D (1997) Biochemical characterization of a molecular switch involving the heat shock protein ClpC, which controls the activity of ComK, the competence transcription factor of Bacillus subtilis. Genes Dev 11:119–128 CrossRef
- Varga JJ, Nguyen V, O’Brien DK, Rodgers K, Walker RA, Melville SB (2006) Type IV pili-dependent gliding motility in the Gram-positive pathogen Clostridium perfringens and other Clostridia. Mol Microbiol 62:680–694 CrossRef
- Vazquez JA, Berron S, Gimenez MJ, de la Fuente L, Aguilar L (2001) In vitro susceptibility of Neisseria meningitidis isolates to gemifloxacin and ten other antimicrobial agents. Eur J Clin Microbiol Infect Dis 20:150–151
- Villar MT, Hirschberg RL, Schaefer MR (2001) Role of the Eikenella corrodens pilA locus in pilus function and phase variation. J Bacteriol 183:55–62 CrossRef
- Wang Y, Taylor DE (1990) Natural transformation in Campylobacter species. J Bacteriol 172:949–955
- Wang WB, Lai HC, Hsueh PR, Chiou RY, Lin SB, Liaw SJ (2006) Inhibition of swarming and virulence factor expression in Proteus mirabilis by resveratrol. J Med Microbiol 55:1313–1321 CrossRef
- Whitchurch CB, Tolker-Nielsen T, Ragas PC, Mattick JS (2002) Extracellular DNA required for bacterial biofilm formation. Science 295:1487 CrossRef
- Wolfgang M, Lauer P, Park HS, Brossay L, Hebert J, Koomey M (1998) PilT mutations lead to simultaneous defects in competence for natural transformation and twitching motility in piliated Neisseria gonorrhoeae. Mol Microbiol 29:321–330 CrossRef
- Wu SS, Kaiser D (1997) Regulation of expression of the pilA gene in Myxococcus xanthus. J Bacteriol 179:7748–7758
- Wu MC, Chen YC, Lin TL, Hsieh PF, Wang JT (2012) Cellobiose-specific phosphotransferase system of Klebsiella pneumoniae and its importance in biofilm formation and virulence. Infect Immun 80:2464–2472 CrossRef
- Yoshihara S, Geng X, Ikeuchi M (2002) pilG Gene cluster and split pilL genes involved in pilus biogenesis, motility and genetic transformation in the cyanobacterium Synechocystis sp. PCC 6803. Plant Cell Physiol 43:513–521 CrossRef
- Young FE, Spizizen J, Crawford IP (1963) Biochemical aspects of competence in the Bacillus subtilis transformation system. I. Chemical composition of cell walls. J Biol Chem 238:3119–3125
- Zeng L, Burne RA (2009) Transcriptional regulation of the cellobiose operon of Streptococcus mutans. J Bacteriol 191:2153–2162 CrossRef
- Zhu L, Zhang Y, Fan J, Herzberg MC, Kreth J (2011) Characterization of competence and biofilm development of a Streptococcus sanguinis endocarditis isolate. Mol Oral Microbiol 26:117–126 CrossRef
About this Article
- Title
- Could DNA uptake be a side effect of bacterial adhesion and twitching motility?
- Open Access
- Available under Open Access This content is freely available online to anyone, anywhere at any time.
- Journal
-
Archives of Microbiology
Volume 195, Issue 4 , pp 279-289 - Cover Date
- 2013-04-01
- DOI
- 10.1007/s00203-013-0870-1
- Print ISSN
- 0302-8933
- Online ISSN
- 1432-072X
- Publisher
- Springer-Verlag
- Additional Links
- Topics
- Keywords
-
- Competence
- DNA uptake
- Transformation
- Horizontal gene transfer
- Type IV pilus
- Twitching motility
- Social gliding
- Swarming
- Bacteria
- Industry Sectors
- Authors
-
-
M. Bakkali
(1)
-
M. Bakkali
- Author Affiliations
-
- 1. Departamento de Genética, Facultad de Ciencias, Universidad de Granada, Fuentenueva S/N, 18071, Granada, Spain