Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1996 Mar;178(6):1623–1630. doi: 10.1128/jb.178.6.1623-1630.1996

Aeromonas salmonicida possesses two genes encoding homologs of the major outer membrane protein, OmpA.

G M Costello 1, R Vipond 1, S MacIntyre 1
PMCID: PMC177847  PMID: 8626290

Abstract

Two homologs of the outer membrane protein OmpA were identified in Aeromonas salmonicida by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, immunoblotting, and amino-terminal sequence analyses. An A. salmonicida genomic DNA library was constructed by using lambda GEM-11 and recombinant phage carrying both genes ompAI and ompAII) selected by immunoscreening. A 5.0-kb BamHI fragment containing the two genes in tandem was subcloned in pBluescript and used for further subcloning and sequencing of the genes. The encoded proteins (Mr = 33,564 and 32,536 for mature OmpAI and OmpAII, respectively) had only 64% identity with each other and otherwise had the highest level of homology to OmpA proteins from the members of the family Enterobacteriaceae. Based on the Escherichia coli OmpA model, an eight-stranded amphipathic beta-barrel model for the membrane assembly of the N-terminal half of OmpAI and OmpAII was predicted. Most variation between the two proteins was localized to the predicted surface loops and periplasmic turns, while the transmembrane strands and C-terminals domains were highly conserved. Expression of ompAI and ompAII separately in E. coli indicated that both genes could be independently transcribed from their own promoters and that both gene products were assembled into the E. coli outer membrane. A survey of different Aeromonas spp. by PCR revealed that possession of two tandem ompA genes was widespread among this genus. This is the first report of any bacterial species possessing two genes for homologs of this major outer membrane protein.

Full Text

The Full Text of this article is available as a PDF (403.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arnold W., Pühler A. A family of high-copy-number plasmid vectors with single end-label sites for rapid nucleotide sequencing. Gene. 1988 Oct 15;70(1):171–179. doi: 10.1016/0378-1119(88)90115-1. [DOI] [PubMed] [Google Scholar]
  2. Beher M. G., Schnaitman C. A., Pugsley A. P. Major heat-modifiable outer membrane protein in gram-negative bacteria: comparison with the ompA protein of Escherichia coli. J Bacteriol. 1980 Aug;143(2):906–913. doi: 10.1128/jb.143.2.906-913.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Braun G., Cole S. T. DNA sequence analysis of the Serratia marcescens ompA gene: implications for the organisation of an enterobacterial outer membrane protein. Mol Gen Genet. 1984;195(1-2):321–328. doi: 10.1007/BF00332766. [DOI] [PubMed] [Google Scholar]
  4. Chou P. Y., Fasman G. D. Empirical predictions of protein conformation. Annu Rev Biochem. 1978;47:251–276. doi: 10.1146/annurev.bi.47.070178.001343. [DOI] [PubMed] [Google Scholar]
  5. Cole S. T., Bremer E., Hindennach I., Henning U. Characterisation of the promoters for the ompA gene which encodes a major outer membrane protein of Escherichia coli. Mol Gen Genet. 1982;188(3):472–479. doi: 10.1007/BF00330051. [DOI] [PubMed] [Google Scholar]
  6. Darveau R. P., MacIntyre S., Buckley J. T., Hancock R. E. Purification and reconstitution in lipid bilayer membranes of an outer membrane, pore-forming protein of Aeromonas salmonicida. J Bacteriol. 1983 Dec;156(3):1006–1011. doi: 10.1128/jb.156.3.1006-1011.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. De Mot R., Proost P., Van Damme J., Vanderleyden J. Homology of the root adhesin of Pseudomonas fluorescens OE 28.3 with porin F of P. aeruginosa and P. syringae. Mol Gen Genet. 1992 Feb;231(3):489–493. doi: 10.1007/BF00292721. [DOI] [PubMed] [Google Scholar]
  8. De Mot R., Vanderleyden J. The C-terminal sequence conservation between OmpA-related outer membrane proteins and MotB suggests a common function in both gram-positive and gram-negative bacteria, possibly in the interaction of these domains with peptidoglycan. Mol Microbiol. 1994 Apr;12(2):333–334. doi: 10.1111/j.1365-2958.1994.tb01021.x. [DOI] [PubMed] [Google Scholar]
  9. Dodsworth S. J., Bennett A. J., Coleman G. Molecular cloning and nucleotide sequence analysis of the maltose-inducible porin gene of Aeromonas salmonicida. FEMS Microbiol Lett. 1993 Sep 1;112(2):191–197. doi: 10.1111/j.1574-6968.1993.tb06447.x. [DOI] [PubMed] [Google Scholar]
  10. Duchêne M., Schweizer A., Lottspeich F., Krauss G., Marget M., Vogel K., von Specht B. U., Domdey H. Sequence and transcriptional start site of the Pseudomonas aeruginosa outer membrane porin protein F gene. J Bacteriol. 1988 Jan;170(1):155–162. doi: 10.1128/jb.170.1.155-162.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Freudl R., Schwarz H., Klose M., Movva N. R., Henning U. The nature of information, required for export and sorting, present within the outer membrane protein OmpA of Escherichia coli K-12. EMBO J. 1985 Dec 16;4(13A):3593–3598. doi: 10.1002/j.1460-2075.1985.tb04122.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Freudl R., Schwarz H., Stierhof Y. D., Gamon K., Hindennach I., Henning U. An outer membrane protein (OmpA) of Escherichia coli K-12 undergoes a conformational change during export. J Biol Chem. 1986 Aug 25;261(24):11355–11361. [PubMed] [Google Scholar]
  13. Gotschlich E. C., Seiff M., Blake M. S. The DNA sequence of the structural gene of gonococcal protein III and the flanking region containing a repetitive sequence. Homology of protein III with enterobacterial OmpA proteins. J Exp Med. 1987 Feb 1;165(2):471–482. doi: 10.1084/jem.165.2.471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hardham J. M., Stamm L. V. Identification and characterization of the Treponema pallidum tpn50 gene, an ompA homolog. Infect Immun. 1994 Mar;62(3):1015–1025. doi: 10.1128/iai.62.3.1015-1025.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Henning U., Schwarz H., Chen R. Radioimmunological screening method for specific membrane proteins. Anal Biochem. 1979 Aug;97(1):153–157. doi: 10.1016/0003-2697(79)90339-7. [DOI] [PubMed] [Google Scholar]
  16. Jeanteur D., Gletsu N., Pattus F., Buckley J. T. Purification of Aeromonas hydrophila major outer-membrane proteins: N-terminal sequence analysis and channel-forming properties. Mol Microbiol. 1992 Nov;6(22):3355–3363. doi: 10.1111/j.1365-2958.1992.tb02203.x. [DOI] [PubMed] [Google Scholar]
  17. Karlyshev A. V., MacIntyre S. Cloning and study of the genetic organization of the exe gene cluster of Aeromonas salmonicida. Gene. 1995 May 26;158(1):77–82. doi: 10.1016/0378-1119(95)00139-w. [DOI] [PubMed] [Google Scholar]
  18. Lutwyche P., Exner M. M., Hancock R. E., Trust T. J. A conserved Aeromonas salmonicida porin provides protective immunity to rainbow trout. Infect Immun. 1995 Aug;63(8):3137–3142. doi: 10.1128/iai.63.8.3137-3142.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. MacIntyre S., Eschbach M. L., Mutschler B. Export incompatibility of N-terminal basic residues in a mature polypeptide of Escherichia coli can be alleviated by optimising the signal peptide. Mol Gen Genet. 1990 May;221(3):466–474. doi: 10.1007/BF00259413. [DOI] [PubMed] [Google Scholar]
  20. MacIntyre S., Trust T. J., Buckley J. T. Identification and characterization of outer membrane fragments released by Aeromonas sp. Can J Biochem. 1980 Oct;58(10):1018–1025. doi: 10.1139/o80-138. [DOI] [PubMed] [Google Scholar]
  21. Mizuno T., Chou M. Y., Inouye M. A comparative study on the genes for three porins of the Escherichia coli outer membrane. DNA sequence of the osmoregulated ompC gene. J Biol Chem. 1983 Jun 10;258(11):6932–6940. [PubMed] [Google Scholar]
  22. Morona R., Krämer C., Henning U. Bacteriophage receptor area of outer membrane protein OmpA of Escherichia coli K-12. J Bacteriol. 1985 Nov;164(2):539–543. doi: 10.1128/jb.164.2.539-543.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Movva N. R., Nakamura K., Inouye M. Gene structure of the OmpA protein, a major surface protein of Escherichia coli required for cell-cell interaction. J Mol Biol. 1980 Nov 5;143(3):317–328. doi: 10.1016/0022-2836(80)90193-x. [DOI] [PubMed] [Google Scholar]
  24. Nakamura K., Pirtle R. M., Inouye M. Homology of the gene coding for outer membrane lipoprotein within various Gram-negative bacteria. J Bacteriol. 1979 Jan;137(1):595–604. doi: 10.1128/jb.137.1.595-604.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Paul C., Rosenbusch J. P. Folding patterns of porin and bacteriorhodopsin. EMBO J. 1985 Jun;4(6):1593–1597. doi: 10.1002/j.1460-2075.1985.tb03822.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Rice P. A., Vayo H. E., Tam M. R., Blake M. S. Immunoglobulin G antibodies directed against protein III block killing of serum-resistant Neisseria gonorrhoeae by immune serum. J Exp Med. 1986 Nov 1;164(5):1735–1748. doi: 10.1084/jem.164.5.1735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Ried G., Koebnik R., Hindennach I., Mutschler B., Henning U. Membrane topology and assembly of the outer membrane protein OmpA of Escherichia coli K12. Mol Gen Genet. 1994 Apr;243(2):127–135. doi: 10.1007/BF00280309. [DOI] [PubMed] [Google Scholar]
  28. Sirakova T., Kolattukudy P. E., Murwin D., Billy J., Leake E., Lim D., DeMaria T., Bakaletz L. Role of fimbriae expressed by nontypeable Haemophilus influenzae in pathogenesis of and protection against otitis media and relatedness of the fimbrin subunit to outer membrane protein A. Infect Immun. 1994 May;62(5):2002–2020. doi: 10.1128/iai.62.5.2002-2020.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Sonntag I., Schwarz H., Hirota Y., Henning U. Cell envelope and shape of Escherichia coli: multiple mutants missing the outer membrane lipoprotein and other major outer membrane proteins. J Bacteriol. 1978 Oct;136(1):280–285. doi: 10.1128/jb.136.1.280-285.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Struyvé M., Moons M., Tommassen J. Carboxy-terminal phenylalanine is essential for the correct assembly of a bacterial outer membrane protein. J Mol Biol. 1991 Mar 5;218(1):141–148. doi: 10.1016/0022-2836(91)90880-f. [DOI] [PubMed] [Google Scholar]
  31. Sugawara E., Nikaido H. OmpA protein of Escherichia coli outer membrane occurs in open and closed channel forms. J Biol Chem. 1994 Jul 8;269(27):17981–17987. [PubMed] [Google Scholar]
  32. Vogel H., Jähnig F. Models for the structure of outer-membrane proteins of Escherichia coli derived from raman spectroscopy and prediction methods. J Mol Biol. 1986 Jul 20;190(2):191–199. doi: 10.1016/0022-2836(86)90292-5. [DOI] [PubMed] [Google Scholar]
  33. Weiser J. N., Gotschlich E. C. Outer membrane protein A (OmpA) contributes to serum resistance and pathogenicity of Escherichia coli K-1. Infect Immun. 1991 Jul;59(7):2252–2258. doi: 10.1128/iai.59.7.2252-2258.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES