Growth in mouse peritoneal macrophages of Yersinia pestis lacking established virulence determinants

Cultured mouse resident peritoneal macrophages were challenged with strains of Yersinia pestis differing only with respect to the absence of one or more of the virulence determinants established for the species. Guanine-auxotrophic (Pur-) yersiniae were unable to survive within the macrophages; exogenous hypoxanthine and guanosine permitted intracellular growth. This finding supports the idea that Pur- yersiniae are avirulent due to inability to obtain sufficient free purines in host tissues for growth and maintenance and indicates that net biosynthesis is necessary to counteract the intracellular microbicidal environment of macrophages. Yersiniae unable to pigment in medium containing the dye Congo red (Pgm-) or lacking either of the plasmids associated with the pesticin or calcium dependence virulence determinants (Pst- and Vwa-, respectively) were taken up as efficiently into macrophages and grew as well within these cells as did bacteria having all invasive virulence determinants intact. Opsonization with 100% homologous normal serum before infection of macrophages did not affect the ability of Pgm- or Vwa- Pgm- yersiniae to grow within macrophages. Accordingly, attributes independent of these virulence determinants mediate the survival and growth of yersiniae in serum and within resident macrophages, and components of the mammalian environment other than serum and macrophages must interact with Pgm-, Pst- and Vwa- yersiniae to cause their avirulence in vivo.

[1]  C. Wisseman,et al.  Mechanisms of Immunity in Typhus Infections III. Influence of Human Immune Serum and Complement on the Fate of Rickettsia mooseri Within Human Macrophages , 1973, Infection and immunity.

[2]  S. Lebedeva,et al.  Transmission of a bacteriocinogenic factor in Pasteurella pestis. , 1971, Soviet genetics.

[3]  T. Burrows,et al.  The virulence-enhancing effect of iron on nonpigmented mutants of virulent strains of Pasteurella pestis. , 1956, British journal of experimental pathology.

[4]  E. N. Fox,et al.  SYNTHESIS OF THE FRACTION I ANTIGENIC PROTEIN BY PASTEURELLA PESTIS , 1958, Journal of bacteriology.

[5]  M. Surgalla,et al.  THE PATHOGENESIS OF PLAGUE. I. A STUDY OF THE CORRELATION BETWEEN VIRULENCE AND RELATIVE PHAGOCYTOSIS RESISTANCE OF SOME STRAINS OF PASTEURELLA PESTIS. , 1963, The Journal of infectious diseases.

[6]  M. Surgalla,et al.  Congo red-agar plating medium for detecting pigmentation in Pasteurella pestis. , 1969, Applied microbiology.

[7]  R. Brubaker,et al.  PESTICINOGENY AND BACTERIAL VIRULENCE , 1965 .

[8]  R. Brubaker,et al.  THE EFFECT OF CA++ AND MG++ ON LYSIS, GROWTH, AND PRODUCTION OF VIRULENCE ANTIGENS BY PASTEURELLA PESTIS. , 1964, The Journal of infectious diseases.

[9]  T. Burrows,et al.  The effects of loss of different virulence determinants on the virulence and immunogenicity of strains of Pasteurella pestis. , 1958, British journal of experimental pathology.

[10]  S. Curtis CHROMOSOMAL ABERRATIONS ASSOCIATED WITH MUTATIONS TO BACTERIOPHAGE RESISTANCE IN ESCHERICHIA COLI. , 1965, Journal of bacteriology.

[11]  R. Brubaker,et al.  Pasteurella pestis: Role of Pesticin I and Iron in Experimental Plague , 1965, Science.

[12]  T. Burrows,et al.  V and W antigens in strains of Pasteurella pseudotuberculosis. , 1960, British journal of experimental pathology.

[13]  JAMES L. Smith,et al.  STUDIES ON THE NUTRITION AND PHYSIOLOGY OF PASTEURELLA PESTIS VI. A , 1961 .

[14]  R. Brubaker,et al.  Localization in Yersinia pestis of peptides associated with virulence , 1982, Infection and immunity.

[15]  S. Straley,et al.  Yersinia pestis grows within phagolysosomes in mouse peritoneal macrophages , 1984, Infection and immunity.

[16]  R. Brubaker,et al.  Vwa+ phenotype of Yersinia enterocolitica , 1983, Infection and immunity.

[17]  T. Burrows,et al.  The effects of biochemical mutation on the virulence of Bacterium typhosum; the loss of virulence of certain mutants. , 1951, British journal of experimental pathology.

[18]  A. Maurelli,et al.  Use of UV-irradiated bacteriophage T6 to kill extracellular bacteria in tissue culture infectivity assays. , 1983, Journal of immunological methods.

[19]  R. Brubaker,et al.  In vivo comparison of avirulent Vwa- and Pgm- or Pstr phenotypes of yersiniae , 1984, Infection and immunity.

[20]  L. Bertalanffy,et al.  A new and rapid method for diagnosis of vaginal and cervical cancer by fluorescence microscopy , 1958, Cancer.

[21]  T. Burrows,et al.  The basis of virulence in Pasteurella pestis: an antigen determining virulence. , 1956, British journal of experimental pathology.

[22]  T. Burrows,et al.  The basis of virulence in Pasteurella pestis: comparative behaviour of virulent and avirulent strains in vivo. , 1954, British journal of experimental pathology.

[23]  R. Brubaker,et al.  Plasmids in Yersinia pestis , 1981, Infection and immunity.

[24]  A. Hackett,et al.  The Virulence of Biochemical Mutants of Klebsiella Pneumoniae. , 1952, Proceedings of the National Academy of Sciences of the United States of America.

[25]  R. Brubaker Mutation rate to nonpigmentation in Pasteurella pestis , 1969, Journal of bacteriology.

[26]  D. Shaw,et al.  Thioglycollate-elicited mouse peritoneal macrophages are less efficient than resident macrophages in antibody-dependent cell-mediated cytolysis. , 1982, Journal of immunology.

[27]  A. Dobozy,et al.  The growth of purine mutants of Bacillus anthracis in the body of the mouse. , 1968, Journal of general microbiology.

[28]  K. F. Meyer,et al.  Avirulent Strains of Pasteurella pestis. , 1943 .

[29]  D. Rowley,et al.  Transduction of virulence within the species Salmonella typhimurium. , 1956, Journal of general microbiology.

[30]  D. Ham,et al.  Role of the capsule of Pasteurella pestis in bubonic plague in the guinea pig. , 1961, The Journal of infectious diseases.

[31]  R. Brubaker,et al.  Cytoplasmic and membrane proteins of yersiniae cultivated under conditions simulating mammalian intracellular environment. , 1981, Proceedings of the National Academy of Sciences of the United States of America.