Abstract
We studied the immune responses of guinea pigs and humans to two Legionella pneumophila antigens. Guinea pigs surviving a lethal intraperitoneal challenge dose of virulent L. pneumophila exhibited strong cutaneous delayed-type hypersensitivity (DTH) reactions to purified OmpS (28-kDa major outer membrane protein) and Hsp60 (heat shock protein or common antigen), while weak DTH reactions were noted for extracellular protease (major secretory protein [MSP] [ProA]) and no reaction was observed with an ovalbumin (OA) control. Lymphocyte proliferation responses (LPRs) were measured for peripheral blood and spleen lymphocytes from guinea pigs surviving sublethal and lethal challenge doses of L. pneumophila. Lymphocytes from uninfected animals showed no proliferation to Hsp60 or OmpS, while lymphocytes from sublethally and lethally challenged animals exhibited strong proliferative responses to Hsp60 and OmpS. Guinea pigs vaccinated with purified OmpS exhibited low antibody titers and strong DTH and LPRs to OmpS, whereas lymphocytes from animals vaccinated with Hsp60 exhibited weak DTH responses and high antibody titers to Hsp60. All guinea pigs immunized with OmpS survived experimental challenge with L. pneumophila (two of two in a pilot study and seven of seven in trial 2) versus zero of seven OA-immunized controls (P = 0.006 by Fisher's exact test). In three vaccine trials in which animals were vaccinated with Hsp60, only 1 guinea pig of 15 survived lethal challenge. Peripheral blood lymphocytes (PBLs) from humans with legionellosis showed stronger LPRs to OmpS than PBLs from humans with no history of legionellosis (P = 0.0002 by Mann-Whitney test). PBLs of humans surviving legionellosis exhibited a lower but highly significant proliferative response to Hsp60 (P < 0.0001 compared with controls by Mann-Whitney test). These studies indicate that OmpS and Hsp60 are important antigens associated with the development of protective cellular immunity. However, as determined in vaccine trial studies in the guinea pig model for legionellosis, the species-specific antigen OmpS proved much more effective than the genus-common Hsp60 antigen.
Full text
PDF








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]
- Bellinger-Kawahara C., Horwitz M. A. Complement component C3 fixes selectively to the major outer membrane protein (MOMP) of Legionella pneumophila and mediates phagocytosis of liposome-MOMP complexes by human monocytes. J Exp Med. 1990 Oct 1;172(4):1201–1210. doi: 10.1084/jem.172.4.1201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bhardwaj N., Nash T. W., Horwitz M. A. Interferon-gamma-activated human monocytes inhibit the intracellular multiplication of Legionella pneumophila. J Immunol. 1986 Oct 15;137(8):2662–2669. [PubMed] [Google Scholar]
- Blanchard D. K., Friedman H., Stewart W. E., 2nd, Klein T. W., Djeu J. Y. Role of gamma interferon in induction of natural killer activity by Legionella pneumophila in vitro and in an experimental murine infection model. Infect Immun. 1988 May;56(5):1187–1193. doi: 10.1128/iai.56.5.1187-1193.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blanchard D. K., Stewart W. E., 2nd, Klein T. W., Friedman H., Djeu J. Y. Cytolytic activity of human peripheral blood leukocytes against Legionella pneumophila-infected monocytes: characterization of the effector cell and augmentation by interleukin 2. J Immunol. 1987 Jul 15;139(2):551–556. [PubMed] [Google Scholar]
- Blander S. J., Breiman R. F., Horwitz M. A. A live avirulent mutant Legionella pneumophila vaccine induces protective immunity against lethal aerosol challenge. J Clin Invest. 1989 Mar;83(3):810–815. doi: 10.1172/JCI113962. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blander S. J., Horwitz M. A. Major cytoplasmic membrane protein of Legionella pneumophila, a genus common antigen and member of the hsp 60 family of heat shock proteins, induces protective immunity in a guinea pig model of Legionnaires' disease. J Clin Invest. 1993 Feb;91(2):717–723. doi: 10.1172/JCI116253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blander S. J., Horwitz M. A. Vaccination with Legionella pneumophila membranes induces cell-mediated and protective immunity in a guinea pig model of Legionnaires' disease. Protective immunity independent of the major secretory protein of Legionella pneumophila. J Clin Invest. 1991 Mar;87(3):1054–1059. doi: 10.1172/JCI115065. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blander S. J., Horwitz M. A. Vaccination with the major secretory protein of Legionella induces humoral and cell-mediated immune responses and protective immunity across different serogroups of Legionella pneumophila and different species of Legionella. J Immunol. 1991 Jul 1;147(1):285–291. [PubMed] [Google Scholar]
- Blander S. J., Horwitz M. A. Vaccination with the major secretory protein of Legionella pneumophila induces cell-mediated and protective immunity in a guinea pig model of Legionnaires' disease. J Exp Med. 1989 Mar 1;169(3):691–705. doi: 10.1084/jem.169.3.691. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blander S. J., Szeto L., Shuman H. A., Horwitz M. A. An immunoprotective molecule, the major secretory protein of Legionella pneumophila, is not a virulence factor in a guinea pig model of Legionnaires' disease. J Clin Invest. 1990 Sep;86(3):817–824. doi: 10.1172/JCI114779. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Breiman R. F., Horwitz M. A. Guinea pigs sublethally infected with aerosolized Legionella pneumophila develop humoral and cell-mediated immune responses and are protected against lethal aerosol challenge. A model for studying host defense against lung infections caused by intracellular pathogens. J Exp Med. 1987 Mar 1;165(3):799–811. doi: 10.1084/jem.165.3.799. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Butler C. A., Hoffman P. S. Characterization of a major 31-kilodalton peptidoglycan-bound protein of Legionella pneumophila. J Bacteriol. 1990 May;172(5):2401–2407. doi: 10.1128/jb.172.5.2401-2407.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Butler C. A., Street E. D., Hatch T. P., Hoffman P. S. Disulfide-bonded outer membrane proteins in the genus Legionella. Infect Immun. 1985 Apr;48(1):14–18. doi: 10.1128/iai.48.1.14-18.1985. [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]
- 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., Calarco K., Yasui V. K. Antimicrobial therapy of experimentally induced Legionnaires' disease in guinea pigs. Am Rev Respir Dis. 1984 Nov;130(5):849–856. doi: 10.1164/arrd.1984.130.5.849. [DOI] [PubMed] [Google Scholar]
- Engleberg N. C., Carter C., Weber D. R., Cianciotto N. P., Eisenstein B. I. DNA sequence of mip, a Legionella pneumophila gene associated with macrophage infectivity. Infect Immun. 1989 Apr;57(4):1263–1270. doi: 10.1128/iai.57.4.1263-1270.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Engleberg N. C., Howe D. C., Rogers J. E., Arroyo J., Eisenstein B. I. Characterization of a Legionella pneumophila gene encoding a lipoprotein antigen. Mol Microbiol. 1991 Aug;5(8):2021–2029. doi: 10.1111/j.1365-2958.1991.tb00824.x. [DOI] [PubMed] [Google Scholar]
- Gabay J. E., Horwitz M. A. Isolation and characterization of the cytoplasmic and outer membranes of the Legionnaires' disease bacterium (Legionella pneumophila). J Exp Med. 1985 Feb 1;161(2):409–422. doi: 10.1084/jem.161.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hindahl M. S., Iglewski B. H. Isolation and characterization of the Legionella pneumophila outer membrane. J Bacteriol. 1984 Jul;159(1):107–113. doi: 10.1128/jb.159.1.107-113.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoffman P. S., Butler C. A., Quinn F. D. Cloning and temperature-dependent expression in Escherichia coli of a Legionella pneumophila gene coding for a genus-common 60-kilodalton antigen. Infect Immun. 1989 Jun;57(6):1731–1739. doi: 10.1128/iai.57.6.1731-1739.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoffman P. S., Houston L., Butler C. A. Legionella pneumophila htpAB heat shock operon: nucleotide sequence and expression of the 60-kilodalton antigen in L. pneumophila-infected HeLa cells. Infect Immun. 1990 Oct;58(10):3380–3387. doi: 10.1128/iai.58.10.3380-3387.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoffman P. S., Ripley M., Weeratna R. Cloning and nucleotide sequence of a gene (ompS) encoding the major outer membrane protein of Legionella pneumophila. J Bacteriol. 1992 Feb;174(3):914–920. doi: 10.1128/jb.174.3.914-920.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoffman P. S., Seyer J. H., Butler C. A. Molecular characterization of the 28- and 31-kilodalton subunits of the Legionella pneumophila major outer membrane protein. J Bacteriol. 1992 Feb;174(3):908–913. doi: 10.1128/jb.174.3.908-913.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Horwitz M. A. Cell-mediated immunity in Legionnaires' disease. J Clin Invest. 1983 Jun;71(6):1686–1697. doi: 10.1172/JCI110923. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Horwitz M. A., Silverstein S. C. Intracellular multiplication of Legionnaires' disease bacteria (Legionella pneumophila) in human monocytes is reversibly inhibited by erythromycin and rifampin. J Clin Invest. 1983 Jan;71(1):15–26. doi: 10.1172/JCI110744. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Husmann L. K., Johnson W. Adherence of Legionella pneumophila to guinea pig peritoneal macrophages, J774 mouse macrophages, and undifferentiated U937 human monocytes: role of Fc and complement receptors. Infect Immun. 1992 Dec;60(12):5212–5218. doi: 10.1128/iai.60.12.5212-5218.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kaufmann S. H. Heat shock proteins and the immune response. Immunol Today. 1990 Apr;11(4):129–136. doi: 10.1016/0167-5699(90)90050-j. [DOI] [PubMed] [Google Scholar]
- Keen M. G., Hoffman P. S. Characterization of a Legionella pneumophila extracellular protease exhibiting hemolytic and cytotoxic activities. Infect Immun. 1989 Mar;57(3):732–738. doi: 10.1128/iai.57.3.732-738.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klein T. W., Friedman H., Widen R. Relative potency of virulent versus avirulent Legionella pneumophila for induction of cell-mediated immunity. Infect Immun. 1984 Jun;44(3):753–755. doi: 10.1128/iai.44.3.753-755.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koga T., Wand-Württenberger A., DeBruyn J., Munk M. E., Schoel B., Kaufmann S. H. T cells against a bacterial heat shock protein recognize stressed macrophages. Science. 1989 Sep 8;245(4922):1112–1115. doi: 10.1126/science.2788923. [DOI] [PubMed] [Google Scholar]
- Lecker S., Lill R., Ziegelhoffer T., Georgopoulos C., Bassford P. J., Jr, Kumamoto C. A., Wickner W. Three pure chaperone proteins of Escherichia coli--SecB, trigger factor and GroEL--form soluble complexes with precursor proteins in vitro. EMBO J. 1989 Sep;8(9):2703–2709. doi: 10.1002/j.1460-2075.1989.tb08411.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ludwig B., Schmid A., Marre R., Hacker J. Cloning, genetic analysis, and nucleotide sequence of a determinant coding for a 19-kilodalton peptidoglycan-associated protein (Ppl) of Legionella pneumophila. Infect Immun. 1991 Aug;59(8):2515–2521. doi: 10.1128/iai.59.8.2515-2521.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mustafa A. S., Lundin K. E., Oftung F. Human T cells recognize mycobacterial heat shock proteins in the context of multiple HLA-DR molecules: studies with healthy subjects vaccinated with Mycobacterium bovis BCG and Mycobacterium leprae. Infect Immun. 1993 Dec;61(12):5294–5301. doi: 10.1128/iai.61.12.5294-5301.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nurminen M., Butcher S., Idänpän-Heikkilä I., Wahlström E., Muttilainen S., Runeberg-Nyman K., Sarvas M., Mäkelä P. H. The class 1 outer membrane protein of Neisseria meningitidis produced in Bacillus subtilis can give rise to protective immunity. Mol Microbiol. 1992 Sep;6(17):2499–2506. doi: 10.1111/j.1365-2958.1992.tb01426.x. [DOI] [PubMed] [Google Scholar]
- Orme I. M., Andersen P., Boom W. H. T cell response to Mycobacterium tuberculosis. J Infect Dis. 1993 Jun;167(6):1481–1497. doi: 10.1093/infdis/167.6.1481. [DOI] [PubMed] [Google Scholar]
- Orme I. M., Miller E. S., Roberts A. D., Furney S. K., Griffin J. P., Dobos K. M., Chi D., Rivoire B., Brennan P. J. T lymphocytes mediating protection and cellular cytolysis during the course of Mycobacterium tuberculosis infection. Evidence for different kinetics and recognition of a wide spectrum of protein antigens. J Immunol. 1992 Jan 1;148(1):189–196. [PubMed] [Google Scholar]
- Ott M., Messner P., Heesemann J., Marre R., Hacker J. Temperature-dependent expression of flagella in Legionella. J Gen Microbiol. 1991 Aug;137(8):1955–1961. doi: 10.1099/00221287-137-8-1955. [DOI] [PubMed] [Google Scholar]
- Sampson J. S., Plikaytis B. B., Wilkinson H. W. Immunologic response of patients with legionellosis against major protein-containing antigens of Legionella pneumophila serogroup 1 as shown by immunoblot analysis. J Clin Microbiol. 1986 Jan;23(1):92–99. doi: 10.1128/jcm.23.1.92-99.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shinnick T. M. The 65-kilodalton antigen of Mycobacterium tuberculosis. J Bacteriol. 1987 Mar;169(3):1080–1088. doi: 10.1128/jb.169.3.1080-1088.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tartakovskii I. S., Zubashev I. K., Koniukhov V. F., Petrosov V. V., Eruslanov B. V., Nebozhina L. V., Rodionov A. V., Dmitriev B. A., Suchkov Iu G., Pronin A. V. Izuchenie protektivnykh svoistv razlichnykh antigenov legionell pri éksperimental'noi legionelleznoi infektsii. Zh Mikrobiol Epidemiol Immunobiol. 1990 May;(5):81–85. [PubMed] [Google Scholar]
- Weeratna R., Marrie T. J., Logan S. M., Hoskin D., Hoffman P. S., Yates L., Burbridge S., Haldane D., Bezanson G. Legionnaires' disease in cardiac transplant patients: a cell-mediated immune response develops despite cyclosporine therapy. J Infect Dis. 1993 Aug;168(2):521–522. doi: 10.1093/infdis/168.2.521. [DOI] [PubMed] [Google Scholar]
- Wilkinson H. W., Cruce D. D., Broome C. V. Validation of Legionella pneumophila indirect immunofluorescence assay with epidemic sera. J Clin Microbiol. 1981 Jan;13(1):139–146. doi: 10.1128/jcm.13.1.139-146.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Young D., Lathigra R., Hendrix R., Sweetser D., Young R. A. Stress proteins are immune targets in leprosy and tuberculosis. Proc Natl Acad Sci U S A. 1988 Jun;85(12):4267–4270. doi: 10.1073/pnas.85.12.4267. [DOI] [PMC free article] [PubMed] [Google Scholar]