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. 1988 Aug;56(8):2036–2046. doi: 10.1128/iai.56.8.2036-2046.1988

A 36-kilodalton Brucella abortus cell envelope protein is encoded by repeated sequences closely linked in the genomic DNA.

T A Ficht 1, S W Bearden 1, B A Sowa 1, L G Adams 1
PMCID: PMC259520  PMID: 3135269

Abstract

Recombinant bacteriophage expressing Brucella abortus antigens have been isolated from a lambda gt11 expression library by using antibody raised against a sodium dodecyl sulfate-polyacrylamide gel electrophoresis-purified cell envelope protein of 36 kilodaltons. Fusion products expressed by these recombinants vary in apparent molecular mass by sodium dodecyl sulfate-polyacrylamide gel electrophoresis but only slightly exceed the size of beta-galactosidase. Western blot (immunoblot) analysis of crude lysates derived from lambda gt11 lysogens indicates that the fusion products react specifically with the original antisera used for recombinant selection and selectively bind antibody directed against the 36-kilodalton cell envelope protein. Analysis of the DNA inserts from 11 independently selected recombinants reveals similar-size EcoRI fragments which range in size from 150 to 300 base pairs (bp), all of which cross-hybridize via Southern blot analysis. Three independently selected EcoRI inserts ranging in size from 200 to 270 bp have been subcloned into M13mp18 and sequenced; all three contain a common region of about 200 bp. Southern blot analysis of B. abortus genomic DNAs digested with EcoRI, PstI, or DdeI indicates the presence of two fragments which hybridize to these DNA probes while single BamHI and HindIII fragments hybridize. The absence of these sites from the internal DNA sequence of the cloned probes suggests the presence of more than one copy of these sequences within the B. abortus genome. The same DNA probes have been used to select genomic clones of approximately 20 kbp from a lambda 2001 library. The lambda 2001 recombinants contain single BamHI fragments and two PstI fragments which hybridize to these oligonucleotide probe constructed on the basis of the amino-terminal sequence of the mature gene product hybridizes to the same BamHI and PstI fragments as the lambda gt11-derived DNA probe. Although the relative positions of the oligonucleotide sequences and the lambda gt11 insert within the genes is not known, the two sequences flank a region which corresponds to at least 40% of the size of the predicted gene. Additional experimentation must be performed to determine whether these sequences represent either two complete structural genes encoding major cell envelope proteins or repetitive sequences within a single structural gene.

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Selected References

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  1. Aiba H., Matsuyama S., Mizuno T., Mizushima S. Function of micF as an antisense RNA in osmoregulatory expression of the ompF gene in Escherichia coli. J Bacteriol. 1987 Jul;169(7):3007–3012. doi: 10.1128/jb.169.7.3007-3012.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Anderson S. Shotgun DNA sequencing using cloned DNase I-generated fragments. Nucleic Acids Res. 1981 Jul 10;9(13):3015–3027. doi: 10.1093/nar/9.13.3015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baldwin C. L., Verstreate D. R., Winter A. J. Immune response of cattle to Brucella abortus outer membrane proteins measured by lymphocyte blastogenesis. Vet Immunol Immunopathol. 1985 Aug;9(4):383–396. doi: 10.1016/0165-2427(85)90067-4. [DOI] [PubMed] [Google Scholar]
  4. Baldwin C. L., Winter A. J. Blastogenic response of bovine lymphocytes to Brucella abortus lipopolysaccharide. Infect Immun. 1985 Feb;47(2):570–572. doi: 10.1128/iai.47.2.570-572.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Beckwith J., Ferro-Novick S. Genetic studies on protein export in bacteria. Curr Top Microbiol Immunol. 1986;125:5–27. doi: 10.1007/978-3-642-71251-7_2. [DOI] [PubMed] [Google Scholar]
  6. Benson S. A., Hall M. N., Silhavy T. J. Genetic analysis of protein export in Escherichia coli K12. Annu Rev Biochem. 1985;54:101–134. doi: 10.1146/annurev.bi.54.070185.000533. [DOI] [PubMed] [Google Scholar]
  7. Blake M. S., Johnston K. H., Russell-Jones G. J., Gotschlich E. C. A rapid, sensitive method for detection of alkaline phosphatase-conjugated anti-antibody on Western blots. Anal Biochem. 1984 Jan;136(1):175–179. doi: 10.1016/0003-2697(84)90320-8. [DOI] [PubMed] [Google Scholar]
  8. Brown M. R., Williams P. The influence of environment on envelope properties affecting survival of bacteria in infections. Annu Rev Microbiol. 1985;39:527–556. doi: 10.1146/annurev.mi.39.100185.002523. [DOI] [PubMed] [Google Scholar]
  9. Chappel R. J., Hayes J., Rogerson B. A., Shenfield L. J. The serological response of cattle to vaccines against brucellosis, as measured by the brucellosis radioimmunoassay and other tests. J Hyg (Lond) 1982 Feb;88(1):11–19. doi: 10.1017/s0022172400069849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Douglas J. T., Rosenberg E. Y., Nikaido H., Verstreate D. R., Winter A. J. Porins of Brucella species. Infect Immun. 1984 Apr;44(1):16–21. doi: 10.1128/iai.44.1.16-21.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Fensterbank R., Plommet M. Vaccination against bovine brucellosis with a low dose of strain 19 administered by the conjunctival route. IV. Comparison between two methods of vaccination. Ann Rech Vet. 1979;10(1):131–139. [PubMed] [Google Scholar]
  12. Finch J. E., Brown M. R. Effect of growth environment on Pseudomonas aeruginosa killing by rabbit polymorphonuclear leudocytes and cationic proteins. Infect Immun. 1978 May;20(2):340–346. doi: 10.1128/iai.20.2.340-346.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gilleland H. E., Jr, Parker M. G., Matthews J. M., Berg R. D. Use of a purified outer membrane protein F (porin) preparation of Pseudomonas aeruginosa as a protective vaccine in mice. Infect Immun. 1984 Apr;44(1):49–54. doi: 10.1128/iai.44.1.49-54.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hohn B. In vitro packaging of lambda and cosmid DNA. Methods Enzymol. 1979;68:299–309. doi: 10.1016/0076-6879(79)68021-7. [DOI] [PubMed] [Google Scholar]
  15. Hohn B., Murray K. Packaging recombinant DNA molecules into bacteriophage particles in vitro. Proc Natl Acad Sci U S A. 1977 Aug;74(8):3259–3263. doi: 10.1073/pnas.74.8.3259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hu N., Messing J. The making of strand-specific M13 probes. Gene. 1982 Mar;17(3):271–277. doi: 10.1016/0378-1119(82)90143-3. [DOI] [PubMed] [Google Scholar]
  17. Hunkapiller M. W., Lujan E., Ostrander F., Hood L. E. Isolation of microgram quantities of proteins from polyacrylamide gels for amino acid sequence analysis. Methods Enzymol. 1983;91:227–236. doi: 10.1016/s0076-6879(83)91019-4. [DOI] [PubMed] [Google Scholar]
  18. Ito K., Wittekind M., Nomura M., Shiba K., Yura T., Miura A., Nashimoto H. A temperature-sensitive mutant of E. coli exhibiting slow processing of exported proteins. Cell. 1983 Mar;32(3):789–797. doi: 10.1016/0092-8674(83)90065-x. [DOI] [PubMed] [Google Scholar]
  19. JONES L. M., MONTGOMERY V., WILSON J. B. CHARACTERISTICS OF CARBON DIOXIDE-INDEPENDENT CULTURES OF BRUCELLA ABORTUS ISOLATED FROM CATTLE VACCINATED WITH STRAIN 19. J Infect Dis. 1965 Jun;115:312–320. doi: 10.1093/infdis/115.3.312. [DOI] [PubMed] [Google Scholar]
  20. Kaneene J. M., Anderson R. K., Johnson D. W., Angus R. D., Muscoplat C. C., Pietz D. E., Vanderwagon L. C., Sloane E. E. Cell-mediated immune responses in swine from a herd infected with Brucella suis. Am J Vet Res. 1978 Oct;39(10):1607–1611. [PubMed] [Google Scholar]
  21. Kaneene J. M., Anderson R. K., Johnson D. W., Muscoplat C. C., Meyer M. E., Gibbons R., Sloane E. D. Cell-mediated immune responses in cattle vaccinated with killed Brucella melitensis strain H-38 vaccine or infected with viable Brucella abortus strain 2308 organisms, or both. Am J Vet Res. 1979 Jan;40(1):40–47. [PubMed] [Google Scholar]
  22. Kaneene J. M., Nicoletti P., Anderson R. K., Muscoplat C. C., Johnson D. W. Cell-mediated immune responses in cattle adult-vaccinated with Brucella abortus strain 19 and in cattle infected with Brucella abortus field strain. Am J Vet Res. 1979 Nov;40(11):1503–1509. [PubMed] [Google Scholar]
  23. Karn J., Matthes H. W., Gait M. J., Brenner S. A new selective phage cloning vector, lambda 2001, with sites for XbaI, BamHI, HindIII, EcoRI, SstI and XhoI. Gene. 1984 Dec;32(1-2):217–224. doi: 10.1016/0378-1119(84)90049-0. [DOI] [PubMed] [Google Scholar]
  24. Kiczka W., Szkaradkiewicz A., Wolko K. Mechanizmy immunologiczne w przebiegu brucelozy przewlekłej u ludzi. I. Odpornoś komórkowa w brucelozie przewlekłej. Pol Arch Med Wewn. 1978 Feb;59(2):135–141. [PubMed] [Google Scholar]
  25. Klesius P. H., Kramer T. T., Swann A. I., Christenberry C. C. Cell-mediated immune response after Brucella abortus S19 vaccination. Am J Vet Res. 1978 May;39(5):883–886. [PubMed] [Google Scholar]
  26. Kreutzer D. L., Dreyfus L. A., Robertson D. C. Interaction of polymorphonuclear leukocytes with smooth and rough strains of Brucella abortus. Infect Immun. 1979 Mar;23(3):737–742. doi: 10.1128/iai.23.3.737-742.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Kuusi N., Nurminen M., Saxen H., Valtonen M., Mäkelä P. H. Immunization with major outer membrane proteins in experimental salmonellosis of mice. Infect Immun. 1979 Sep;25(3):857–862. doi: 10.1128/iai.25.3.857-862.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  29. Lugtenberg B., Peters R., Bernheimer H., Berendsen W. Influence of cultural conditions and mutations on the composition of the outer membrane proteins of Escherichia coli. Mol Gen Genet. 1976 Sep 23;147(3):251–262. doi: 10.1007/BF00582876. [DOI] [PubMed] [Google Scholar]
  30. Lutkenhaus J. F. Role of a major outer membrane protein in Escherichia coli. J Bacteriol. 1977 Aug;131(2):631–637. doi: 10.1128/jb.131.2.631-637.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Maniatis T., Hardison R. C., Lacy E., Lauer J., O'Connell C., Quon D., Sim G. K., Efstratiadis A. The isolation of structural genes from libraries of eucaryotic DNA. Cell. 1978 Oct;15(2):687–701. doi: 10.1016/0092-8674(78)90036-3. [DOI] [PubMed] [Google Scholar]
  32. Martin A., Le Garrec Y., Dazord L., Toujas L. Modulation of immune response by killed Brucella abortus organisms: comparison of the effects of smooth and rough strains on T-dependent responses. Infect Immun. 1978 Sep;21(3):1027–1028. doi: 10.1128/iai.21.3.1027-1028.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Meinkoth J., Wahl G. Hybridization of nucleic acids immobilized on solid supports. Anal Biochem. 1984 May 1;138(2):267–284. doi: 10.1016/0003-2697(84)90808-x. [DOI] [PubMed] [Google Scholar]
  34. Messing J., Vieira J. A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments. Gene. 1982 Oct;19(3):269–276. doi: 10.1016/0378-1119(82)90016-6. [DOI] [PubMed] [Google Scholar]
  35. 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]
  36. Mizuno T., Chou M. Y., Inouye M. A unique mechanism regulating gene expression: translational inhibition by a complementary RNA transcript (micRNA). Proc Natl Acad Sci U S A. 1984 Apr;81(7):1966–1970. doi: 10.1073/pnas.81.7.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Nicoletti P. The epidemiology of bovine brucellosis. Adv Vet Sci Comp Med. 1980;24:69–98. [PubMed] [Google Scholar]
  38. Nicoletti P. Vaccination of cattle with Brucella abortus strain 19 administered by differing routes and doses. Vaccine. 1984 Jun;2(2):133–135. doi: 10.1016/0264-410x(84)90004-5. [DOI] [PubMed] [Google Scholar]
  39. Raybould T. J. Antigens of diagnostic significance in Brucella abortus. Can J Microbiol. 1982 Jun;28(6):557–566. doi: 10.1139/m82-084. [DOI] [PubMed] [Google Scholar]
  40. SPINK W. W., THOMPSON H. Human brucellosis caused by Brucella abortus, strain 19. J Am Med Assoc. 1953 Nov 28;153(13):1162–1165. doi: 10.1001/jama.1953.02940300020006. [DOI] [PubMed] [Google Scholar]
  41. Samra Y., Shaked Y., Hertz M., Altman G. Brucellosis: difficulties in diagnosis and a report on 38 cases. Infection. 1983 Nov-Dec;11(6):310–312. doi: 10.1007/BF01641353. [DOI] [PubMed] [Google Scholar]
  42. Santos J. M., Verstreate D. R., Perera V. Y., Winter A. J. Outer membrane proteins from rough strains of four Brucella species. Infect Immun. 1984 Oct;46(1):188–194. doi: 10.1128/iai.46.1.188-194.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Schurig G. G., Jones L. M., Speth S. L., Berman D. T. Antibody response to antigens distinct from smooth lipopolysaccharide complex in Brucella infection. Infect Immun. 1978 Sep;21(3):994–1002. doi: 10.1128/iai.21.3.994-1002.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Smith H. O. Recovery of DNA from gels. Methods Enzymol. 1980;65(1):371–380. doi: 10.1016/s0076-6879(80)65048-4. [DOI] [PubMed] [Google Scholar]
  45. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  46. Sowa B. A., Moore D., Ippen-Ihler K. Physiology of F-pilin synthesis and utilization. J Bacteriol. 1983 Feb;153(2):962–968. doi: 10.1128/jb.153.2.962-968.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Sulitzeanu D. Mechanism of immunity against brucella. Nature. 1965 Mar 13;205(976):1086–1088. doi: 10.1038/2051086a0. [DOI] [PubMed] [Google Scholar]
  48. Sutherland S. S., Le Cras D. V., Robertson A. G., Johnston J. M., Evans R. J. Serological response of cattle after vaccination and challenge with Brucella abortus. Vet Microbiol. 1982 May;7(2):165–175. doi: 10.1016/0378-1135(82)90028-1. [DOI] [PubMed] [Google Scholar]
  49. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Vaitukaitis J. L. Production of antisera with small doses of immunogen: multiple intradermal injections. Methods Enzymol. 1981;73(Pt B):46–52. doi: 10.1016/0076-6879(81)73055-6. [DOI] [PubMed] [Google Scholar]
  51. Verstreate D. R., Creasy M. T., Caveney N. T., Baldwin C. L., Blab M. W., Winter A. J. Outer membrane proteins of Brucella abortus: isolation and characterization. Infect Immun. 1982 Mar;35(3):979–989. doi: 10.1128/iai.35.3.979-989.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Verstreate D. R., Winter A. J. Comparison of sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles and antigenic relatedness among outer membrane proteins of 49 Brucella abortus strains. Infect Immun. 1984 Oct;46(1):182–187. doi: 10.1128/iai.46.1.182-187.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Wickner W. T., Lodish H. F. Multiple mechanisms of protein insertion into and across membranes. Science. 1985 Oct 25;230(4724):400–407. doi: 10.1126/science.4048938. [DOI] [PubMed] [Google Scholar]
  54. Woodard L. F., Toone N. M., McLaughlin C. A. Immunogenic properties of soluble antigens or whole cells of Brucella abortus strain 45/20 associated with immunoadjuvants. I. Soluble antigens. Can J Comp Med. 1980 Oct;44(4):453–455. [PMC free article] [PubMed] [Google Scholar]
  55. Woodard L. F., Toone N. M., McLaughlin C. A. Immunogenic properties of soluble antigens or whole cells of Brucella abortus strain 45/20 associated with immunoadjuvants. II. Whole cells. Can J Comp Med. 1980 Oct;44(4):456–458. [PMC free article] [PubMed] [Google Scholar]
  56. Young E. J. Human brucellosis. Rev Infect Dis. 1983 Sep-Oct;5(5):821–842. doi: 10.1093/clinids/5.5.821. [DOI] [PubMed] [Google Scholar]
  57. Young R. A., Davis R. W. Efficient isolation of genes by using antibody probes. Proc Natl Acad Sci U S A. 1983 Mar;80(5):1194–1198. doi: 10.1073/pnas.80.5.1194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Young R. A., Davis R. W. Yeast RNA polymerase II genes: isolation with antibody probes. Science. 1983 Nov 18;222(4625):778–782. doi: 10.1126/science.6356359. [DOI] [PubMed] [Google Scholar]

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