Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1996 Mar;64(3):855–860. doi: 10.1128/iai.64.3.855-860.1996

Cloning and characterization of the galE locus of Pasteurella haemolytica A1.

M D Potter 1, R Y Lo 1
PMCID: PMC173848  PMID: 8641792

Abstract

The enzyme UDP-galactose 4-epimerase (GalE) is involved in one of the major steps of galactose metabolism in bacteria. In many cases, GalE is required for the biosynthesis of extracellular polysaccharide materials such as lipopolysaccharide (LPS) and capsule. Mutants defective in galE have been shown to exhibit reduced virulence. Here we describe the cloning and characterization of the galE gene from the bovine pathogen Pasteurella haemolytica A1. This was achieved by the complementation of a Salmonella typhimurium galE mutant with a P. haemolytica A1 plasmid bank. Analysis of six clones recovered on minimal media with galactose as the carbon source showed that they all contained the same recombinant plasmid with a 5-kbp DNA insert. The galE-complementing activity was localized to a 2.2-kbp DNA region by subcloning. Biochemical, immunological, and phage sensitivity analyses of the recombinant LPS in S. typhimurium showed that it is essentially identical to that of the wild type. In vivo expression studies showed that a 37-kDa protein is expressed from the complementing plasmids, and the presence of GalE activity was confirmed by an assay for epimerase activity. Nucleotide sequence analysis of the cloned DNA identified the galE gene. Comparison of the deduced amino acid sequence analysis of P. haemolytica A1 GalE with published data showed high-level homology, 81.6%, with the GalE of Haemophilus influenzae type b. However, the sequences flanking galE do not show similarity with any other gal gene, suggesting that P. haemolytica A1 galE is not linked to the other genes of the gal operon, as is the case for Neisseria meningitidis, Neisseria gonorrhoeae, and H. influenzae. The separation of galE from the classical gal operon genes was confirmed by Southern blot hybridization studies, and a physical map showing the relative positions of galE, galT, and galK was constructed.

Full Text

The Full Text of this article is available as a PDF (294.8 KB).

Selected References

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

  1. Bolivar F., Rodriguez R. L., Greene P. J., Betlach M. C., Heyneker H. L., Boyer H. W., Crosa J. H., Falkow S. Construction and characterization of new cloning vehicles. II. A multipurpose cloning system. Gene. 1977;2(2):95–113. [PubMed] [Google Scholar]
  2. Breider M. A., Kumar S., Corstvet R. E. Bovine pulmonary endothelial cell damage mediated by Pasteurella haemolytica pathogenic factors. Infect Immun. 1990 Jun;58(6):1671–1677. doi: 10.1128/iai.58.6.1671-1677.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Clarke R. C., Gyles C. L. Galactose epimeraseless mutants of Salmonella typhimurium as live vaccines for calves. Can J Vet Res. 1986 Apr;50(2):165–173. [PMC free article] [PubMed] [Google Scholar]
  4. Confer A. W., Simons K. R. Effects of Pasteurella haemolytica lipopolysaccharide on selected functions of bovine leukocytes. Am J Vet Res. 1986 Jan;47(1):154–157. [PubMed] [Google Scholar]
  5. Dolph P. J., Majerczak D. R., Coplin D. L. Characterization of a gene cluster for exopolysaccharide biosynthesis and virulence in Erwinia stewartii. J Bacteriol. 1988 Feb;170(2):865–871. doi: 10.1128/jb.170.2.865-871.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. FUKASAWA T., NIKAIDO H. Galactose-sensitive mutants of Salmonella. II. Bacteriolysis induced by galactose. Biochim Biophys Acta. 1961 Apr 15;48:470–483. doi: 10.1016/0006-3002(61)90045-2. [DOI] [PubMed] [Google Scholar]
  7. Germanier R., Fürer E. Characteristics of the attenuated oral vaccine strain "S. typhi" Ty 21a. Dev Biol Stand. 1983;53:3–7. [PubMed] [Google Scholar]
  8. Hammerschmidt S., Birkholz C., Zähringer U., Robertson B. D., van Putten J., Ebeling O., Frosch M. Contribution of genes from the capsule gene complex (cps) to lipooligosaccharide biosynthesis and serum resistance in Neisseria meningitidis. Mol Microbiol. 1994 Mar;11(5):885–896. doi: 10.1111/j.1365-2958.1994.tb00367.x. [DOI] [PubMed] [Google Scholar]
  9. Hanahan D. Studies on transformation of Escherichia coli with plasmids. J Mol Biol. 1983 Jun 5;166(4):557–580. doi: 10.1016/s0022-2836(83)80284-8. [DOI] [PubMed] [Google Scholar]
  10. Hone D. M., Attridge S. R., Forrest B., Morona R., Daniels D., LaBrooy J. T., Bartholomeusz R. C., Shearman D. J., Hackett J. A galE via (Vi antigen-negative) mutant of Salmonella typhi Ty2 retains virulence in humans. Infect Immun. 1988 May;56(5):1326–1333. doi: 10.1128/iai.56.5.1326-1333.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hone D., Morona R., Attridge S., Hackett J. Construction of defined galE mutants of Salmonella for use as vaccines. J Infect Dis. 1987 Jul;156(1):167–174. doi: 10.1093/infdis/156.1.167. [DOI] [PubMed] [Google Scholar]
  12. Houng H. S., Kopecko D. J., Baron L. S. Molecular cloning and physical and functional characterization of the Salmonella typhimurium and Salmonella typhi galactose utilization operons. J Bacteriol. 1990 Aug;172(8):4392–4398. doi: 10.1128/jb.172.8.4392-4398.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Jennings M. P., van der Ley P., Wilks K. E., Maskell D. J., Poolman J. T., Moxon E. R. Cloning and molecular analysis of the galE gene of Neisseria meningitidis and its role in lipopolysaccharide biosynthesis. Mol Microbiol. 1993 Oct;10(2):361–369. [PubMed] [Google Scholar]
  14. Johnson K. G., Perry M. B. Improved techniques for the preparation of bacterial lipopolysaccharides. Can J Microbiol. 1976 Jan;22(1):29–34. doi: 10.1139/m76-004. [DOI] [PubMed] [Google Scholar]
  15. KEISS R. E., WILL D. H., COLLIER J. R. SKIN TOXICITY AND HEMODYNAMIC PROPERTIES OF ENDOTOXIN DERIVED FROM PASTEURELLA HAMOLYTICA. Am J Vet Res. 1964 Jul;25:935–942. [PubMed] [Google Scholar]
  16. Karow M., Georgopoulos C. The essential Escherichia coli msbA gene, a multicopy suppressor of null mutations in the htrB gene, is related to the universally conserved family of ATP-dependent translocators. Mol Microbiol. 1993 Jan;7(1):69–79. doi: 10.1111/j.1365-2958.1993.tb01098.x. [DOI] [PubMed] [Google Scholar]
  17. Lee F. K., Stephens D. S., Gibson B. W., Engstrom J. J., Zhou D., Apicella M. A. Microheterogeneity of Neisseria lipooligosaccharide: analysis of a UDP-glucose 4-epimerase mutant of Neisseria meningitidis NMB. Infect Immun. 1995 Jul;63(7):2508–2515. doi: 10.1128/iai.63.7.2508-2515.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lemaire H. G., Müller-Hill B. Nucleotide sequences of the gal E gene and the gal T gene of E. coli. Nucleic Acids Res. 1986 Oct 10;14(19):7705–7711. doi: 10.1093/nar/14.19.7705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Levine M. M., Ferreccio C., Black R. E., Germanier R. Large-scale field trial of Ty21a live oral typhoid vaccine in enteric-coated capsule formulation. Lancet. 1987 May 9;1(8541):1049–1052. doi: 10.1016/s0140-6736(87)90480-6. [DOI] [PubMed] [Google Scholar]
  20. Lo R. Y., Strathdee C. A., Shewen P. E. Nucleotide sequence of the leukotoxin genes of Pasteurella haemolytica A1. Infect Immun. 1987 Sep;55(9):1987–1996. doi: 10.1128/iai.55.9.1987-1996.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. MacLachlan P. R., Sanderson K. E. Transformation of Salmonella typhimurium with plasmid DNA: differences between rough and smooth strains. J Bacteriol. 1985 Jan;161(1):442–445. doi: 10.1128/jb.161.1.442-445.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Maskell D. J., Szabo M. J., Butler P. D., Williams A. E., Moxon E. R. Molecular analysis of a complex locus from Haemophilus influenzae involved in phase-variable lipopolysaccharide biosynthesis. Mol Microbiol. 1991 May;5(5):1013–1022. doi: 10.1111/j.1365-2958.1991.tb01874.x. [DOI] [PubMed] [Google Scholar]
  23. Maskell D. J., Szabo M. J., Deadman M. E., Moxon E. R. The gal locus from Haemophilus influenzae: cloning, sequencing and the use of gal mutants to study lipopolysaccharide. Mol Microbiol. 1992 Oct;6(20):3051–3063. doi: 10.1111/j.1365-2958.1992.tb01763.x. [DOI] [PubMed] [Google Scholar]
  24. Metzger M., Bellemann P., Bugert P., Geider K. Genetics of galactose metabolism of Erwinia amylovora and its influence on polysaccharide synthesis and virulence of the fire blight pathogen. J Bacteriol. 1994 Jan;176(2):450–459. doi: 10.1128/jb.176.2.450-459.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Moreno F., Rodicio R., Herrero P. A new colorimetric assay for UDP-glucose 4-epimerase activity. Cell Mol Biol Incl Cyto Enzymol. 1981;27(6):589–592. [PubMed] [Google Scholar]
  26. NIKAIDO H. Galactose-sensitive mutants of Salmonella. I. Metabolism of galactose. Biochim Biophys Acta. 1961 Apr 15;48:460–469. doi: 10.1016/0006-3002(61)90044-0. [DOI] [PubMed] [Google Scholar]
  27. Paulsen D. B., Confer A. W., Clinkenbeard K. D., Mosier D. A. Pasteurella haemolytica lipopolysaccharide-induced arachidonic acid release from and neutrophil adherence to bovine pulmonary artery endothelial cells. Am J Vet Res. 1990 Oct;51(10):1635–1639. [PubMed] [Google Scholar]
  28. Paulsen D. B., Mosier D. A., Clinkenbeard K. D., Confer A. W. Direct effects of Pasteurella haemolytica lipopolysaccharide on bovine pulmonary endothelial cells in vitro. Am J Vet Res. 1989 Sep;50(9):1633–1637. [PubMed] [Google Scholar]
  29. Potter M. D., Lo R. Y. Cloning and characterization of a gene from Pasteurella haemolytica A1 involved in lipopolysaccharide biosynthesis. FEMS Microbiol Lett. 1995 Jun 1;129(1):75–81. doi: 10.1016/0378-1097(95)00140-Z. [DOI] [PubMed] [Google Scholar]
  30. Rimsay R. L., Coyle-Dennis J. E., Lauerman L. H., Squire P. G. Purification and biological characterizationof endotoxin fractions from Pasteruella haemolytica. Am J Vet Res. 1981 Dec;42(12):2134–2138. [PubMed] [Google Scholar]
  31. Roantree R. J., Kuo T. T., MacPhee D. G. The effect of defined lipopolysaccharide core defects upon antibiotic resistances of Salmonella typhimurium. J Gen Microbiol. 1977 Dec;103(2):223–234. doi: 10.1099/00221287-103-2-223. [DOI] [PubMed] [Google Scholar]
  32. Robertson B. D., Frosch M., van Putten J. P. The role of galE in the biosynthesis and function of gonococcal lipopolysaccharide. Mol Microbiol. 1993 May;8(5):891–901. doi: 10.1111/j.1365-2958.1993.tb01635.x. [DOI] [PubMed] [Google Scholar]
  33. Severn W. B., Richards J. C. Characterization of the O-polysaccharide of Pasteurella haemolytica serotype A1. Carbohydr Res. 1993 Feb 24;240:277–285. doi: 10.1016/0008-6215(93)84190-h. [DOI] [PubMed] [Google Scholar]
  34. Slocombe R. F., Mulks M., Killingsworth C. R., Derksen F. J., Robinson N. E. Effect of Pasteurella haemolytica-derived endotoxin on pulmonary structure and function in calves. Am J Vet Res. 1990 Mar;51(3):433–438. [PubMed] [Google Scholar]
  35. Whiteley L. O., Maheswaran S. K., Weiss D. J., Ames T. R. Immunohistochemical localization of Pasteurella haemolytica A1-derived endotoxin, leukotoxin, and capsular polysaccharide in experimental bovine Pasteurella pneumonia. Vet Pathol. 1990 May;27(3):150–161. doi: 10.1177/030098589002700302. [DOI] [PubMed] [Google Scholar]
  36. Wilkinson R. G., Gemski P., Jr, Stocker B. A. Non-smooth mutants of Salmonella typhimurium: differentiation by phage sensitivity and genetic mapping. J Gen Microbiol. 1972 May;70(3):527–554. doi: 10.1099/00221287-70-3-527. [DOI] [PubMed] [Google Scholar]
  37. Yanisch-Perron C., Vieira J., Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  38. Yates W. D. A review of infectious bovine rhinotracheitis, shipping fever pneumonia and viral-bacterial synergism in respiratory disease of cattle. Can J Comp Med. 1982 Jul;46(3):225–263. [PMC free article] [PubMed] [Google Scholar]
  39. Yoo H. S., Maheswaran S. K., Lin G., Townsend E. L., Ames T. R. Induction of inflammatory cytokines in bovine alveolar macrophages following stimulation with Pasteurella haemolytica lipopolysaccharide. Infect Immun. 1995 Feb;63(2):381–388. doi: 10.1128/iai.63.2.381-388.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES