Abstract
A virulent strain of Legionella pneumophila serogroup 1, subgroup Pontiac, was grown in continuous culture at a constant growth rate under iron-replete and iron-limited conditions. Iron limitation was achieved by the removal of ferrous sulfate and hemin from the chemically defined medium. Residual contaminating iron, 0.45 microM, was sufficient to support iron-limited growth. Typical iron-replete cultures metabolized 3.3 microM iron. Serine provided the principal source of carbon and energy for both cultures, although iron-replete cultures also depleted a number of other amino acids. There was a 40% decrease in culture biomass under iron-restricted conditions. Iron limitation did not significantly affect carbohydrate metabolism, with the molar growth yield for carbon (Ycarbon) comparable for both cultures. However, under iron-limited conditions a sixfold increase in Yiron correlated with a significant decrease in the iron content of the biomass, as the culture utilized the available iron more efficiently. Highly pleomorphic iron-replete cultures became uniform cultures of short fine rods when adapted to iron-deficient conditions. In addition to the morphological and physiological changes, iron limitation had a critical effect on culture virulence. The virulence of this strain was significantly (P < 0.05) reduced when the culture was subjected to iron-limited conditions. This phenomenon was reversible, with a significant increase in culture virulence upon reversion to iron-replete conditions. When compared in an in vitro macrophage assay, the number of culturable avirulent iron-limited cells located intracellularly after infection was significantly lower than for the virulent replete and control cultures. These results further support the role of environmental parameters in regulating the virulence of L. pneumophila.
Full Text
The Full Text of this article is available as a PDF (344.7 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Abu Kwaik Y., Eisenstein B. I., Engleberg N. C. Phenotypic modulation by Legionella pneumophila upon infection of macrophages. Infect Immun. 1993 Apr;61(4):1320–1329. doi: 10.1128/iai.61.4.1320-1329.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barker J., Lambert P. A., Brown M. R. Influence of intra-amoebic and other growth conditions on the surface properties of Legionella pneumophila. Infect Immun. 1993 Aug;61(8):3503–3510. doi: 10.1128/iai.61.8.3503-3510.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baskerville A., Fitzgeorge R. B., Broster M., Hambleton P., Dennis P. J. Experimental transmission of legionnaires' disease by exposure to aerosols of Legionella pneumophila. Lancet. 1981 Dec 19;2(8260-61):1389–1390. doi: 10.1016/s0140-6736(81)92803-8. [DOI] [PubMed] [Google Scholar]
- Bortner C. A., Miller R. D., Arnold R. R. Bactericidal effect of lactoferrin on Legionella pneumophila. Infect Immun. 1986 Feb;51(2):373–377. doi: 10.1128/iai.51.2.373-377.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brener D., DeVoe I. W., Holbein B. E. Increased virulence of Neisseria meningitidis after in vitro iron-limited growth at low pH. Infect Immun. 1981 Jul;33(1):59–66. doi: 10.1128/iai.33.1.59-66.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Byrd T. F., Horwitz M. A. Interferon gamma-activated human monocytes downregulate transferrin receptors and inhibit the intracellular multiplication of Legionella pneumophila by limiting the availability of iron. J Clin Invest. 1989 May;83(5):1457–1465. doi: 10.1172/JCI114038. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cianciotto N. P., Eisenstein B. I., Mody C. H., Engleberg N. C. A mutation in the mip gene results in an attenuation of Legionella pneumophila virulence. J Infect Dis. 1990 Jul;162(1):121–126. doi: 10.1093/infdis/162.1.121. [DOI] [PubMed] [Google Scholar]
- Cianciotto N. P., Fields B. S. Legionella pneumophila mip gene potentiates intracellular infection of protozoa and human macrophages. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):5188–5191. doi: 10.1073/pnas.89.11.5188. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dowling J. N., Saha A. K., Glew R. H. Virulence factors of the family Legionellaceae. Microbiol Rev. 1992 Mar;56(1):32–60. doi: 10.1128/mr.56.1.32-60.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Edelstein P. H. Improved semiselective medium for isolation of Legionella pneumophila from contaminated clinical and environmental specimens. J Clin Microbiol. 1981 Sep;14(3):298–303. doi: 10.1128/jcm.14.3.298-303.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Feeley J. C., Gorman G. W., Weaver R. E., Mackel D. C., Smith H. W. Primary isolation media for Legionnaires disease bacterium. J Clin Microbiol. 1978 Sep;8(3):320–325. doi: 10.1128/jcm.8.3.320-325.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fitzgeorge R. B., Baskerville A., Broster M., Hambleton P., Dennis P. J. Aerosol infection of animals with strains of Legionella pneumophila of different virulence: comparison with intraperitoneal and intranasal routes of infection. J Hyg (Lond) 1983 Feb;90(1):81–89. doi: 10.1017/s0022172400063877. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fitzgeorge R. B. The effect of antibiotics on the growth of Legionella pneumophila in guinea-pig alveolar phagocytes infected in vivo by an aerosol. J Infect. 1985 May;10(3):189–193. doi: 10.1016/s0163-4453(85)92413-2. [DOI] [PubMed] [Google Scholar]
- Fliermans C. B., Cherry W. B., Orrison L. H., Smith S. J., Tison D. L., Pope D. H. Ecological distribution of Legionella pneumophila. Appl Environ Microbiol. 1981 Jan;41(1):9–16. doi: 10.1128/aem.41.1.9-16.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gebran S. J., Newton C., Yamamoto Y., Widen R., Klein T. W., Friedman H. Macrophage permissiveness for Legionella pneumophila growth modulated by iron. Infect Immun. 1994 Feb;62(2):564–568. doi: 10.1128/iai.62.2.564-568.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- George J. R., Pine L., Reeves M. W., Harrell W. K. Amino acid requirements of Legionella pneumophila. J Clin Microbiol. 1980 Mar;11(3):286–291. doi: 10.1128/jcm.11.3.286-291.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goldberg M. B., Boyko S. A., Calderwood S. B. Transcriptional regulation by iron of a Vibrio cholerae virulence gene and homology of the gene to the Escherichia coli fur system. J Bacteriol. 1990 Dec;172(12):6863–6870. doi: 10.1128/jb.172.12.6863-6870.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gordon S. A., Fleck A., Bell J. Optimal conditions for the estimation of ammonium by the Berthelot reaction. Ann Clin Biochem. 1978 Sep;15(5):270–275. doi: 10.1177/000456327801500164. [DOI] [PubMed] [Google Scholar]
- Gross R. Signal transduction and virulence regulation in human and animal pathogens. FEMS Microbiol Rev. 1993 Apr;10(3-4):301–326. doi: 10.1111/j.1574-6968.1993.tb05873.x. [DOI] [PubMed] [Google Scholar]
- Hickey E. K., Cianciotto N. P. Cloning and sequencing of the Legionella pneumophila fur gene. Gene. 1994 May 27;143(1):117–121. doi: 10.1016/0378-1119(94)90615-7. [DOI] [PubMed] [Google Scholar]
- Horwitz M. A. Characterization of avirulent mutant Legionella pneumophila that survive but do not multiply within human monocytes. J Exp Med. 1987 Nov 1;166(5):1310–1328. doi: 10.1084/jem.166.5.1310. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jepras R. I., Fitzgeorge R. B., Baskerville A. A comparison of virulence of two strains of Legionella pneumophila based on experimental aerosol infection of guinea-pigs. J Hyg (Lond) 1985 Aug;95(1):29–38. doi: 10.1017/s0022172400062252. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jepras R. I., Fitzgeorge R. B. The effect of oxygen-dependent antimicrobial systems on strains of Legionella pneumophila of different virulence. J Hyg (Lond) 1986 Aug;97(1):61–69. doi: 10.1017/s0022172400064354. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson W., Varner L., Poch M. Acquisition of iron by Legionella pneumophila: role of iron reductase. Infect Immun. 1991 Jul;59(7):2376–2381. doi: 10.1128/iai.59.7.2376-2381.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keevil C. W., Davies D. B., Spillane B. J., Mahenthiralingam E. Influence of iron-limited and replete continuous culture on the physiology and virulence of Neisseria gonorrhoeae. J Gen Microbiol. 1989 Apr;135(4):851–863. doi: 10.1099/00221287-135-4-851. [DOI] [PubMed] [Google Scholar]
- Mauchline W. S., Araujo R., Wait R., Dowsett A. B., Dennis P. J., Keevil C. W. Physiology and morphology of Legionella pneumophila in continuous culture at low oxygen concentration. J Gen Microbiol. 1992 Nov;138(11):2371–2380. doi: 10.1099/00221287-138-11-2371. [DOI] [PubMed] [Google Scholar]
- Mauchline W. S., James B. W., Fitzgeorge R. B., Dennis P. J., Keevil C. W. Growth temperature reversibly modulates the virulence of Legionella pneumophila. Infect Immun. 1994 Jul;62(7):2995–2997. doi: 10.1128/iai.62.7.2995-2997.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mengaud J. M., Horwitz M. A. The major iron-containing protein of Legionella pneumophila is an aconitase homologous with the human iron-responsive element-binding protein. J Bacteriol. 1993 Sep;175(17):5666–5676. doi: 10.1128/jb.175.17.5666-5676.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Otto B. R., Verweij-van Vught A. M., MacLaren D. M. Transferrins and heme-compounds as iron sources for pathogenic bacteria. Crit Rev Microbiol. 1992;18(3):217–233. doi: 10.3109/10408419209114559. [DOI] [PubMed] [Google Scholar]
- POWELL E. O. Criteria for the growth of contaminants and mutants in continuous culture. J Gen Microbiol. 1958 Feb;18(1):259–268. doi: 10.1099/00221287-18-1-259. [DOI] [PubMed] [Google Scholar]
- Pine L., George J. R., Reeves M. W., Harrell W. K. Development of a chemically defined liquid medium for growth of Legionella pneumophila. J Clin Microbiol. 1979 May;9(5):615–626. doi: 10.1128/jcm.9.5.615-626.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pine L., Hoffman P. S., Malcolm G. B., Benson R. F., Franzus M. J. Role of keto acids and reduced-oxygen-scavenging enzymes in the growth of Legionella species. J Clin Microbiol. 1986 Jan;23(1):33–42. doi: 10.1128/jcm.23.1.33-42.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prince R. W., Storey D. G., Vasil A. I., Vasil M. L. Regulation of toxA and regA by the Escherichia coli fur gene and identification of a Fur homologue in Pseudomonas aeruginosa PA103 and PA01. Mol Microbiol. 1991 Nov;5(11):2823–2831. doi: 10.1111/j.1365-2958.1991.tb01991.x. [DOI] [PubMed] [Google Scholar]
- Reeves M. W., Pine L., Hutner S. H., George J. R., Harrell W. K. Metal requirements of Legionella pneumophila. J Clin Microbiol. 1981 Apr;13(4):688–695. doi: 10.1128/jcm.13.4.688-695.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reeves M. W., Pine L., Neilands J. B., Balows A. Absence of siderophore activity in Legionella species grown in iron-deficient media. J Bacteriol. 1983 Apr;154(1):324–329. doi: 10.1128/jb.154.1.324-329.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rogers J., Keevil C. W. Immunogold and fluorescein immunolabelling of Legionella pneumophila within an aquatic biofilm visualized by using episcopic differential interference contrast microscopy. Appl Environ Microbiol. 1992 Jul;58(7):2326–2330. doi: 10.1128/aem.58.7.2326-2330.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simonson C., Brener D., DeVoe I. W. Expression of a high-affinity mechanism for acquisition of transferrin iron by Neisseria meningitidis. Infect Immun. 1982 Apr;36(1):107–113. doi: 10.1128/iai.36.1.107-113.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Staggs T. M., Perry R. D. Identification and cloning of a fur regulatory gene in Yersinia pestis. J Bacteriol. 1991 Jan;173(2):417–425. doi: 10.1128/jb.173.2.417-425.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tesh M. J., Morse S. A., Miller R. D. Intermediary metabolism in Legionella pneumophila: utilization of amino acids and other compounds as energy sources. J Bacteriol. 1983 Jun;154(3):1104–1109. doi: 10.1128/jb.154.3.1104-1109.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas C. E., Sparling P. F. Identification and cloning of a fur homologue from Neisseria meningitidis. Mol Microbiol. 1994 Feb;11(4):725–737. doi: 10.1111/j.1365-2958.1994.tb00350.x. [DOI] [PubMed] [Google Scholar]
- Tully M., Williams A., Fitzgeorge R. B. Transposon mutagenesis in Legionella pneumophila. II.--Mutants exhibiting impaired intracellular growth within cultured macrophages and reduced virulence in vivo. Res Microbiol. 1992 Jun;143(5):481–488. doi: 10.1016/0923-2508(92)90094-5. [DOI] [PubMed] [Google Scholar]
- Wadowsky R. M., Butler L. J., Cook M. K., Verma S. M., Paul M. A., Fields B. S., Keleti G., Sykora J. L., Yee R. B. Growth-supporting activity for Legionella pneumophila in tap water cultures and implication of hartmannellid amoebae as growth factors. Appl Environ Microbiol. 1988 Nov;54(11):2677–2682. doi: 10.1128/aem.54.11.2677-2682.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weinberg E. D. Iron and infection. Microbiol Rev. 1978 Mar;42(1):45–66. doi: 10.1128/mr.42.1.45-66.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weinberg E. D. Iron and susceptibility to infectious disease. Science. 1974 May 31;184(4140):952–956. doi: 10.1126/science.184.4140.952. [DOI] [PubMed] [Google Scholar]