1887

Abstract

Mutants of serovar Typhimurium lacking DNA adenine (Dam) methylase show reduced secretion of invasion effectors encoded in the -pathogenicity island 1 (SPI-1). Concomitant with this alteration, a high number and quantity of extracellular proteins are detected in cultures of Dam mutants. This study shows by subcellular fractionation analysis that the presence of numerous extracellular proteins in cultures of Dam mutants is linked to an exacerbated release of membrane particulate material. The membrane ‘leaky’ phenotype and the impaired functionality of type III secretion systems were, however, unrelated since exacerbated release of proteins to the medium was evident in Dam strains carrying mutations in either SPI-1 (, ) or flagellar () genes. This result supports the view that Dam methylation controls a plethora of cellular processes. Electron microscopy analysis demonstrated that the accumulation of membrane particulate material occurs preferentially as vesicles in stationary cultures of Dam strains. In addition, a reduction in the relative amount of peptidoglycan-associated lipoprotein (PAL), TolB, OmpA and murein lipoprotein (Lpp) bound to peptidoglycan was observed in actively growing Dam mutants. The existence of an envelope defect was further confirmed by the increased sensitivity to deoxycholate exhibited by Dam mutants, mostly during exponential growth. Unexpectedly, lack of Dam methylation neither increased envelope instability nor impaired the association of PAL-Tol-Lpp proteins to the peptidoglycan in . Accordingly, Dam mutants did not show sensitivity to deoxycholate. Altogether, these results indicate that, besides its role in modulating the secretion of effectors by the SPI-1-encoded type III apparatus, Dam methylation controls cell envelope integrity in

Loading

Article metrics loading...

/content/journal/micro/10.1099/00221287-148-4-1171
2002-04-01
2024-04-19
Loading full text...

Full text loading...

/deliver/fulltext/micro/148/4/1481171a.html?itemId=/content/journal/micro/10.1099/00221287-148-4-1171&mimeType=html&fmt=ahah

References

  1. Barras F., Marinus M. G. 1989; The great GATC: DNA methylation in E. coli . Trends Genet 5:139–143 [CrossRef]
    [Google Scholar]
  2. Bernadac A., Gavioli M., Lazzaroni J. C., Raina S., Lloubes R. 1998; Escherichia coli tol-pal mutants form outer membrane vesicles. J Bacteriol 180:4872–4878
    [Google Scholar]
  3. Bolker M., Kahmann R. 1989; The Escherichia coli regulatory protein OxyR discriminates between methylated and unmethylated states of the phage Mu mom promoter. EMBO J 8:2403–2410
    [Google Scholar]
  4. Bouveret E., Derouiche R., Rigal A., Lloubes R., Lazdunski C., Benedetti H. 1995; Peptidoglycan-associated lipoprotein-TolB interaction. A possible key to explaining the formation of contact sites between the inner and outer membranes of Escherichia coli . J Biol Chem 270:11071–11077 [CrossRef]
    [Google Scholar]
  5. Bouveret E., Benedetti H., Rigal A., Loret E., Lazdunski C. 1999; In vitro characterization of peptidoglycan-associated lipoprotein (PAL)-peptidoglycan and PAL-TolB interactions. J Bacteriol 181:6306–6311
    [Google Scholar]
  6. Boye E., Lobner-Olesen A. 1990; The role of dam methyltransferase in the control of DNA replication in E. coli . Cell 62:981–989 [CrossRef]
    [Google Scholar]
  7. Braaten B. A., Nou X., Kaltenbach L. S., Low D. A. 1994; Methylation patterns in pap regulatory DNA control pyelonephritis-associated pili phase variation in E. coli . Cell 76:577–588 [CrossRef]
    [Google Scholar]
  8. Campbell J. L., Kleckner N. 1990; E. coli oriC and the dnaA gene promoter are sequestered from Dam methyltransferase following the passage of the chromosomal replication fork. Cell 62:967–979 [CrossRef]
    [Google Scholar]
  9. Casadesús J., Torreblanca J. 1996; Methylation-related epigenetic signals in bacterial DNA. In Epigenetic Mechanisms of Gene Regulation . pp 141–153 Edited by Russo V. E. A., Martienssen R. A., Riggs A. D. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory;
  10. Clavel T., Germon P., Vianney A., Portalier R., Lazzaroni J. C. 1998; TolB protein of Escherichia coli K-12 interacts with the outer membrane peptidoglycan-associated proteins Pal, Lpp and OmpA. Mol Microbiol 29:359–367 [CrossRef]
    [Google Scholar]
  11. Collazo C. M., Galán J. E. 1997; The invasion-associated type III system of Salmonella typhimurium directs the translocation of Sip proteins into the host cell. Mol Microbiol 24:747–756 [CrossRef]
    [Google Scholar]
  12. Collazo C. M., Zierler M. K., Galán J. E. 1995; Functional analysis of the Salmonella typhimurium invasion genes invl and invJ and identification of a target of the protein secretion apparatus encoded in the inv locus. Mol Microbiol 15:25–38 [CrossRef]
    [Google Scholar]
  13. Garcia-del Portillo F., Pucciarelli M. G., Casadesus J. 1999; DNA adenine methylase mutants of Salmonella typhimurium show defects in protein secretion, cell invasion, and M cell cytotoxicity. Proc Natl Acad Sci USA 96:11578–11583 [CrossRef]
    [Google Scholar]
  14. Glauner B. 1988; Separation and quantification of muropeptides with high-performance liquid chromatography. Anal Biochem 172:451–464 [CrossRef]
    [Google Scholar]
  15. Hattman S., Brooks J. E., Masurekar M. 1978; Sequence specificity of the P1 modification methylase (M.Eco P1) and the DNA methylase (M.Eco dam) controlled by the Escherichia coli dam gene. J Mol Biol 126:367–380 [CrossRef]
    [Google Scholar]
  16. Heithoff D. M., Sinsheimer R. L., Low D. A., Mahan M. J. 1999; An essential role for DNA adenine methylation in bacterial virulence. Science 284:967–970 [CrossRef]
    [Google Scholar]
  17. Heithoff D. M., Enioutina E. Y., Daynes R. A., Sinsheimer R. L., Low D. A., Mahan M. J. 2001; Salmonella DNA adenine methylase mutants confer cross-protective immunity. Infect Immun 69:6725–6730 [CrossRef]
    [Google Scholar]
  18. Hellman J., Loiselle P. M., Tehan M. M., Allaire J. E., Boyle L. A., Kurnick J. T., Andrews D. M., Sik Kim K., Warren H. S. 2000a; Outer membrane protein A, peptidoglycan-associated lipoprotein, and murein lipoprotein are released by Escherichia coli bacteria into serum. Infect Immun 68:2566–2572 [CrossRef]
    [Google Scholar]
  19. Hellman J., Loiselle P. M., Zanzot E. M., Allaire J. E., Tehan M. M., Boyle L. A., Kurnick J. T., Warren H. S. 2000b; Release of gram-negative outer-membrane proteins into human serum and septic rat blood and their interactions with immunoglobulin in antiserum to Escherichia coli J5. J Infect Dis 181:1034–1043 [CrossRef]
    [Google Scholar]
  20. Hilbert F., Garcia-del Portillo F., Groisman E. A. 1999; A periplasmic d-alanyl-d-alanine dipeptidase in the gram-negative bacterium Salmonella enterica . J Bacteriol 181:2158–2165
    [Google Scholar]
  21. Hoiseth S. K., Stocker B. A. 1981; Aromatic-dependent Salmonella typhimurium are non-virulent and effective as live vaccines. Nature 291:238–239 [CrossRef]
    [Google Scholar]
  22. Kadurugamuwa J. L., Beveridge T. J. 1995; Virulence factors are released from Pseudomonas aeruginosa in association with membrane vesicles during normal growth and exposure to gentamicin: a novel mechanism of enzyme secretion. J Bacteriol 177:3998–4008
    [Google Scholar]
  23. Kadurugamuwa J. L., Beveridge T. J. 1997; Natural release of virulence factors in membrane vesicles by Pseudomonas aeruginosa and the effect of aminoglycoside antibiotics on their release. J Antimicrob Chemother 40:615–621 [CrossRef]
    [Google Scholar]
  24. Kadurugamuwa J. L., Beveridge T. J. 1999; Membrane vesicles derived from Pseudomonas aeruginosa and Shigella flexneri can be integrated into the surfaces of other gram-negative bacteria. Microbiology 145:2051–2060 [CrossRef]
    [Google Scholar]
  25. Kaniga K., Trollinger D., Galán J. E. 1995; Identification of two targets of the type III protein secretion system encoded by the inv and spa loci of Salmonella typhimurium that have homology to the Shigella IpaD and IpaA proteins. J Bacteriol 177:7078–7085
    [Google Scholar]
  26. Keenan J., Day T., Neal S., Cook B., Perez-Perez G., Allardyce R., Bagshaw P. 2000; A role for the bacterial outer membrane in the pathogenesis of Helicobacter pylori infection. FEMS Microbiol Lett 182:259–264 [CrossRef]
    [Google Scholar]
  27. Koebnik R. 1995; Proposal for a peptidoglycan-associating alpha-helical motif in the C-terminal regions of some bacterial cell-surface proteins. Mol Microbiol 16:1269–1270 [CrossRef]
    [Google Scholar]
  28. Komoriya K., Shibano N., Higano T., Azuma N., Yamaguchi S., Aizawa S. I. 1999; Flagellar proteins and type III-exported virulence factors are the predominant proteins secreted into the culture media of Salmonella typhimurium . Mol Microbiol 34:767–779 [CrossRef]
    [Google Scholar]
  29. Lacks S., Greenberg B. 1977; Complementary specificity of restriction endonucleases of Diplococcus pneumoniae with respect to DNA methylation. J Mol Biol 114:153–168 [CrossRef]
    [Google Scholar]
  30. Lazzaroni J. C., Portalier R. 1992; The excC gene of Escherichia coli K-12 required for cell envelope integrity encodes the peptidoglycan-associated lipoprotein (PAL). Mol Microbiol 6:735–742 [CrossRef]
    [Google Scholar]
  31. Lazzaroni J. C., Germon P., Ray M. C., Vianney A. 1999; The Tol proteins of Escherichia coli and their involvement in the uptake of biomolecules and outer membrane stability. FEMS Microbiol Lett 177:191–197 [CrossRef]
    [Google Scholar]
  32. Li Z., Clarke A. J., Beveridge T. J. 1998; Gram-negative bacteria produce membrane vesicles which are capable of killing other bacteria. J Bacteriol 180:5478–5483
    [Google Scholar]
  33. Low D. A., Weyand N. J., Mahan M. J. 2001; Roles of DNA adenine methylation in regulating bacterial gene expression and virulence. Infect Immun 69:7197–7204 [CrossRef]
    [Google Scholar]
  34. Marinus M. G. others 1996; Methylation of DNA. In Escherichia coli and Salmonella: Cellular and Molecular Biology . , 2nd edn. pp 782–791 Edited by Neidhardt F. C. Washington, DC: American Society for Microbiology;
  35. Meno Y., Fujimoto S., Horikawa K., Yoshida S. 2000; Release of membrane vesicles containing endotoxic lipopolysaccharide in Escherichia coli O157: H7 clinical isolates. Microbiol Immunol 44:271–274 [CrossRef]
    [Google Scholar]
  36. Mirlashari M. R., Hoiby E. A., Holst J., Lyberg T. 2001; Outer membrane vesicles from Neisseria meningitidis : effects on cytokine production in human whole blood. Cytokine 13:91–97 [CrossRef]
    [Google Scholar]
  37. Nicholson B., Low D. 2000; DNA methylation-dependent regulation of pef expression in Salmonella typhimurium . Mol Microbiol 35:728–742 [CrossRef]
    [Google Scholar]
  38. Ogden G. B., Pratt M. J., Schaechter M. 1988; The replicative origin of the E. coli chromosome binds to cell membranes only when hemimethylated. Cell 54:127–135 [CrossRef]
    [Google Scholar]
  39. Parsot C., Menard R., Gounon P., Sansonetti P. J. 1995; Enhanced secretion through the Shigella flexneri Mxi-Spa translocon leads to assembly of extracellular proteins into macromolecular structures. Mol Microbiol 16:291–300 [CrossRef]
    [Google Scholar]
  40. Radman M., Wagner R. 1986; Mismatch repair in Escherichia coli . Annu Rev Genet 20:523–538 [CrossRef]
    [Google Scholar]
  41. Reisenauer A., Kahng L. S., McCollum S., Shapiro L. 1999; Bacterial DNA methylation: a cell cycle regulator?. J Bacteriol 181:5135–5139
    [Google Scholar]
  42. Rigal A., Bouveret E., Lloubes R., Lazdunski C., Benedetti H. 1997; The TolB protein interacts with the porins of Escherichia coli . J Bacteriol 179:7274–7279
    [Google Scholar]
  43. Roberts D., Hoopes B. C., McClure W. R., Kleckner N. 1985; IS 10 transposition is regulated by DNA adenine methylation. Cell 43:117–130 [CrossRef]
    [Google Scholar]
  44. Shägger H., von Jagow G. 1987; Tricine-sodium docecyl sulphate-polyacrylamide gel electrophoresis for the separation of proteins in the range of 1 to 100 kDa. Anal Biochem 166:368–379 [CrossRef]
    [Google Scholar]
  45. Sternberg N. 1985; Evidence that adenine methylation influences DNA-protein interactions in Escherichia coli . J Bacteriol 164:490–493
    [Google Scholar]
  46. Torreblanca J., Casadesus J. 1996; DNA adenine methylase mutants of Salmonella typhimurium and a novel dam -regulated locus. Genetics 144:15–26
    [Google Scholar]
  47. Torreblanca J., Marques S., Casadesus J. 1999; Synthesis of FinP RNA by plasmids F and pSLT is regulated by DNA adenine methylation. Genetics 152:31–45
    [Google Scholar]
  48. van der Woude M. W., Low D. A. 1994; Leucine-responsive regulatory protein and deoxyadenosine methylase control the phase variation and expression of the sfa and daa pili operons in Escherichia coli . Mol Microbiol 11:605–618 [CrossRef]
    [Google Scholar]
  49. van der Woude M., Braaten B., Low D. 1996; Epigenetic phase variation of the pap operon in Escherichia coli . Trends Microbiol 4:5–9 [CrossRef]
    [Google Scholar]
  50. Wai S. N., Takade A., Amako K. 1995; The release of outer membrane vesicles from the strains of enterotoxigenic Escherichia coli . Microbiol Immunol 39:451–456 [CrossRef]
    [Google Scholar]
  51. Whitmire W. M., Garon C. F. 1993; Specific and nonspecific responses of murine B cells to membrane blebs of Borrelia burgdorferi . Infect Immun 61:1460–1467
    [Google Scholar]
  52. Yokoyama K., Horii T., Yamashino T., Hashikawa S., Barua S., Hasegawa T., Watanabe H., Ohta M. 2000; Production of shiga toxin by Escherichia coli measured with reference to the membrane vesicle-associated toxins. FEMS Microbiol Lett 192:139–144 [CrossRef]
    [Google Scholar]
  53. Zhou L., Srisatjaluk R., Justus D. E., Doyle R. J. 1998; On the origin of membrane vesicles in gram-negative bacteria. FEMS Microbiol Lett 163:223–228 [CrossRef]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/00221287-148-4-1171
Loading
/content/journal/micro/10.1099/00221287-148-4-1171
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error