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PMID: 2707857 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

lcrH, a gene necessary for virulence of Yersinia pestis and for the normal response of Y. pestis to ATP and calcium.

Infection and immunity ·Vol. 57 ·No. 5 ·1989-05-00 ·Pages 1491-8

Price SB, Straley SC

Abstract

We are investigating the functions of the three proteins encoded by the V operon (lcrGVH) of the low-calcium response virulence plasmid pCD1 of Yersinia pestis KIM5. The purpose of this study was to define the role of the 18-kilodalton protein encoded by lcrH, the third gene of the V operon. Using marker exchange mutagenesis, we constructed a Y. pestis mutant that failed to express the LcrH protein. This LcrH- mutant was "ATP blind" in that it failed to show altered growth and V-antigen expression at 37 degrees C when 18 mM ATP was present. It also showed only a partial response to 2.5 mM Ca2+. The parental Y. pestis strain showed full growth yield at 37 degrees C and depressed expression of V antigen and of yop (yersinial pCD1-encoded outer membrane protein) genes in response to ATP or Ca2+. In contrast, the LcrH- mutant failed to grow at 37 degrees C in the presence of ATP and showed only limited growth when Ca2+ was present. V-antigen expression in the mutant was not depressed by ATP and only partially depressed by Ca2+. These findings show that LcrH is necessary for the normal response of Y. pestis to ATP and that LcrH contributes to Ca2+ responsiveness. The mutant also showed abnormal yopJ expression, indicating that LcrH also is necessary for normal yop regulation. The LcrH- mutant was avirulent in mice, probably because of its compromised growth at 37 degrees C. These findings indicate that the responses of Y. pestis to ATP and Ca2+ are distinct and that lcrH encodes a protein that is an important mediator of Ca2+ and ATP regulation of pCD1-encoded virulence determinant(s) in Y. pestis.

MeSH Terms
Adenosine Triphosphate/pharmacology Antigens, Bacterial/genetics Bacterial Outer Membrane Proteins/genetics Calcium/pharmacology Chloramphenicol O-Acetyltransferase/genetics DNA Mutational Analysis Electrophoresis, Gel, Two-Dimensional Gene Expression Regulation Genes, Bacterial Genes, Regulator Isoelectric Point Molecular Weight Operon Restriction Mapping Yersinia pestis/genetics,growth & development,pathogenicity
Chemicals
Antigens, Bacterial Bacterial Outer Membrane Proteins Adenosine Triphosphate Chloramphenicol O-Acetyltransferase Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Price S B
Department of Microbiology and Immunology, Chandler Medical Center, University of Kentucky, Lexington 40536.
Straley S C
References (33)
33 references, click to expand
  1. Characterization of common virulence plasmids in Yersinia species and their role in the expression of outer membrane proteins.
    Infect Immun. 1984 Jan;43(1):108-14 PMID: 6317562
  2. Consequences of Ca2+ deficiency on macromolecular synthesis and adenylate energy charge in Yersinia pestis.
    J Bacteriol. 1979 Sep;139(3):792-9 PMID: 479109
  3. Essential virulence determinants of different Yersinia species are carried on a common plasmid.
    Plasmid. 1981 Mar;5(2):183-7 PMID: 7243971
  4. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  5. Effect of exogenous nucleotides on Ca2+ dependence and V antigen synthesis in Yersinia pestis.
    Infect Immun. 1982 Dec;38(3):953-9 PMID: 7152680
  6. Expression of the temperature-inducible outer membrane proteins of yersiniae.
    Infect Immun. 1985 Apr;48(1):234-40 PMID: 3980086
  7. In vivo repackaging of recombinant cosmid molecules for analyses of Salmonella typhimurium, Streptococcus mutans, and mycobacterial genomic libraries.
    Infect Immun. 1986 Apr;52(1):101-9 PMID: 2937735
  8. In vivo comparison of avirulent Vwa- and Pgm- or Pstr phenotypes of yersiniae.
    Infect Immun. 1984 Mar;43(3):895-900 PMID: 6365786
  9. Regulation of expression of V antigen and outer membrane proteins in Yersinia pestis.
    Contrib Microbiol Immunol. 1987;9:173-8 PMID: 3665495
  10. THE EFFECT OF CA++ AND MG++ ON LYSIS, GROWTH, AND PRODUCTION OF VIRULENCE ANTIGENS BY PASTEURELLA PESTIS.
    J Infect Dis. 1964 Feb;114:13-25 PMID: 14118042
  11. Temperature-controlled plasmid regulon associated with low calcium response in Yersinia pestis.
    J Bacteriol. 1986 Feb;165(2):443-7 PMID: 3944056
  12. Analysis of recombinant DNA using Escherichia coli minicells.
    Methods Enzymol. 1983;101:347-62 PMID: 6350817
  13. Molecular cloning and expression of calcium-regulated, plasmid-coded proteins of Y. pseudotuberculosis.
    Microb Pathog. 1987 Feb;2(2):123-37 PMID: 3507554
  14. The virulence protein Yop5 of Yersinia pseudotuberculosis is regulated at transcriptional level by plasmid-plB1-encoded trans-acting elements controlled by temperature and calcium.
    Mol Microbiol. 1988 Jan;2(1):121-33 PMID: 2835586
  15. Genetic analysis of the low calcium response in Yersinia pestis mu d1(Ap lac) insertion mutants.
    J Bacteriol. 1984 Dec;160(3):842-8 PMID: 6094509
  16. Mutation rate to nonpigmentation in Pasteurella pestis.
    J Bacteriol. 1969 Jun;98(3):1404-6 PMID: 5788712
  17. Transduction of Pasteurella pestis.
    Virology. 1972 Feb;47(2):513-6 PMID: 4550902
  18. A rapid alkaline extraction procedure for screening recombinant plasmid DNA.
    Nucleic Acids Res. 1979 Nov 24;7(6):1513-23 PMID: 388356
  19. Construction and characterization of new cloning vehicles. II. A multipurpose cloning system.
    Gene. 1977;2(2):95-113 PMID: 344137
  20. High resolution two-dimensional electrophoresis of basic as well as acidic proteins.
    Cell. 1977 Dec;12(4):1133-41 PMID: 23215
  21. The basis of virulence in Pasteurella pestis: an antigen determining virulence.
    Br J Exp Pathol. 1956 Oct;37(5):481-93 PMID: 13374206
  22. Growth in mouse peritoneal macrophages of Yersinia pestis lacking established virulence determinants.
    Infect Immun. 1984 Sep;45(3):649-54 PMID: 6469351
  23. Plasmids in Yersinia pestis.
    Infect Immun. 1981 Feb;31(2):839-41 PMID: 7216478
  24. Plasmids of Escherichia coli as cloning vectors.
    Methods Enzymol. 1979;68:245-67 PMID: 232214
  25. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  26. High resolution two-dimensional electrophoresis of proteins.
    J Biol Chem. 1975 May 25;250(10):4007-21 PMID: 236308
  27. The genus Yersinia: biochemistry and genetics of virulence.
    Curr Top Microbiol Immunol. 1972;57:111-58 PMID: 4554354
  28. Plasmid insertion mutagenesis and lac gene fusion with mini-mu bacteriophage transposons.
    J Bacteriol. 1984 May;158(2):488-95 PMID: 6327606
  29. Plaque formation and isolation of pure lines with poliomyelitis viruses.
    J Exp Med. 1954 Feb;99(2):167-82 PMID: 13130792
  30. Virulence genes regulated at the transcriptional level by Ca2+ in Yersinia pestis include structural genes for outer membrane proteins.
    Infect Immun. 1986 Feb;51(2):445-54 PMID: 3002984
  31. Studies on the nutrition and physiology of Pasteurella pestis. III. Effects of calcium ions on the growth of virulent and avirulent strains of Pasteurella pestis.
    J Bacteriol. 1959 Mar;77(3):317-21 PMID: 13641190
  32. Isolation and characterization of Ca2+-blind mutants of Yersinia pestis.
    J Bacteriol. 1985 Nov;164(2):704-11 PMID: 2997127
  33. A low-Ca2+ response operon encodes the V antigen of Yersinia pestis.
    Infect Immun. 1986 Nov;54(2):428-34 PMID: 3021629
Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1989-05-00
Pages
1491-8
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC313304
Subset
IM
Grants
NIAID NIH HHS · AI 21017 · United States
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