Abstract
Guinea pig polymorphonuclear leukocytes (PMN) were parasitized in vitro with yeast cells of Histoplasma capsulatum. Preparations stained after 3 h at 37 C with May Greenwald-Giemsa revealed that 87% of the yeasts were tinctorially altered. Such alterations corresponded to those displayed by fungus cells intentionally killed by heat or other means and thus the altered yeast were presumed to be dead. A combination of 10−5 M H2O2, 10−5 M KI, and horseradish peroxidase killed H. capsulatum. Death was assessed by the eosin-y dye exclusion test. All of the listed components were required for death of the fungus. A granule lysate preparation derived from guinea pig PMN leukocytes could replace the horseradish peroxidase in the fungicidal system. The granule lysates behaved in keeping with the attributes of a myeloperoxidase. Thus, PMN leukocytes and certain extracellular peroxidase systems kill the yeast cell phase of the dimorphic fungus H. capsulatum.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brune K., Leffell M. S., Spitznagel J. K. Microbicidal activity of peroxidaseless chicken heterophile leukocytes. Infect Immun. 1972 Mar;5(3):283–287. doi: 10.1128/iai.5.3.283-287.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DZAWACHISZWILI N., LANDAU J. W., NEWCOMER V. D., PLUNKETT O. A. THE EFFECT OF SEA WATER AND SODIUM CHLORIDE ON THE GROWTH OF FUNGI PATHOGENIC TO MAN. J Invest Dermatol. 1964 Aug;43:103–109. [PubMed] [Google Scholar]
- Diamond R. D., Root R. K., Bennett J. E. Factors influencing killing of Cryptococcus neoformans by human leukocytes in vitro. J Infect Dis. 1972 Apr;125(4):367–376. doi: 10.1093/infdis/125.4.367. [DOI] [PubMed] [Google Scholar]
- Gilbert B. E., Howard D. H. Uptake of Cystine by the Yeast Phase of Histoplasma capsulatum. Infect Immun. 1970 Aug;2(2):139–144. doi: 10.1128/iai.2.2.139-144.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HIRSCH J. G. Phagocytin: a bactericidal substance from polymorphonuclear leucocytes. J Exp Med. 1956 May 1;103(5):589–611. doi: 10.1084/jem.103.5.589. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HOWARD D. H. INTRACELLULAR BEHAVIOR OF HISTOPLASMA CAPSULATUM. J Bacteriol. 1964 Jan;87:33–38. doi: 10.1128/jb.87.1.33-38.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HOWARD D. H. INTRACELLULAR GROWTH OF HISTOPLASMA CAPSULATUM. J Bacteriol. 1965 Feb;89:518–523. doi: 10.1128/jb.89.2.518-523.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Howard D. H., Otto V., Gupta R. K. Lymphocyte-mediated cellular immunity in histoplasmosis. Infect Immun. 1971 Nov;4(5):605–610. doi: 10.1128/iai.4.5.605-610.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Howard D. H., Otto V. Protein synthesis by phagocytized yeast cells of Histoplasma capsulatum. Sabouraudia. 1969 Oct;7(3):186–194. [PubMed] [Google Scholar]
- Klebanoff S. J., Hamon C. B. Role of myeloperoxidase-mediated antimicrobial systems in intact leukocytes. J Reticuloendothel Soc. 1972 Aug;12(2):170–196. [PubMed] [Google Scholar]
- Lehrer R. I. Antifungal effects of peroxidase systems. J Bacteriol. 1969 Aug;99(2):361–365. doi: 10.1128/jb.99.2.361-365.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lehrer R. I., Cline M. J. Interaction of Candida albicans with human leukocytes and serum. J Bacteriol. 1969 Jun;98(3):996–1004. doi: 10.1128/jb.98.3.996-1004.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lehrer R. I., Jan R. G. Interaction of Aspergillus fumigatus Spores with Human Leukocytes and Serum. Infect Immun. 1970 Apr;1(4):345–350. doi: 10.1128/iai.1.4.345-350.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lehrer R. I. Measurement of candidacidal activity of specific leukocyte types in mixed cell populations I. Normal, myeloperoxidase-deficient, and chronic granulomatous disease neutrophils. Infect Immun. 1970 Jul;2(1):42–47. doi: 10.1128/iai.2.1.42-47.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McRipley R. J., Sbarra A. J. Role of the phagocyte in host-parasite interactions. XII. Hydrogen peroxide-myeloperoxidase bactericidal system in the phagocyte. J Bacteriol. 1967 Nov;94(5):1425–1430. doi: 10.1128/jb.94.5.1425-1430.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROWLEY D. A., HUBER M. Pathogenesis of experimental histoplasmosis in mice. I. Measurement of infecting dosages of the yeast phase of Histoplasma capsulatum. J Infect Dis. 1955 Mar-Apr;96(2):174–183. doi: 10.1093/infdis/96.2.174. [DOI] [PubMed] [Google Scholar]
- ROWLEY D. A., PINE L. Some nutritional factors influencing growth of yeast cells of Histoplasma capsulatum to mycelial colonies. J Bacteriol. 1955 Jun;69(6):695–700. doi: 10.1128/jb.69.6.695-700.1955. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sbarra A. J., Paul B. B., Jacobs A. A., Strauss R. R., Mitchell G. W., Jr Role of the phagocyte in host-parasite interactions. 38. Metabolic activities of the phagocyte as related to antimicrobial action. J Reticuloendothel Soc. 1972 Aug;12(2):109–126. [PubMed] [Google Scholar]
- Tacker J. R., Farhi F., Bulmer G. S. Intracellular fate of Cryptococcus neoformans. Infect Immun. 1972 Aug;6(2):162–167. doi: 10.1128/iai.6.2.162-167.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WILLIAMSON D. H., SCOPES A. W. The behaviour of nucleic acids in synchronously dividing cultures of Saccharomyces cerevisiae. Exp Cell Res. 1960 Aug;20:338–349. doi: 10.1016/0014-4827(60)90162-2. [DOI] [PubMed] [Google Scholar]
- Yen C. M., Howard D. H. Germination of blastospores of Histoplasma capslatum. Sabouraudia. 1970 Nov;8(3):242–252. [PubMed] [Google Scholar]
- Zeya H. I., Spitznagel J. K. Cationic proteins of polymorphonuclear leukocyte lysosomes. II. Composition, properties, and mechanism of antibacterial action. J Bacteriol. 1966 Feb;91(2):755–762. doi: 10.1128/jb.91.2.755-762.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Furth R., Hirsch J. G., Fedorko M. E. Morphology and peroxidase cytochemistry of mouse promonocytes, monocytes, and macrophages. J Exp Med. 1970 Oct 1;132(4):794–812. doi: 10.1084/jem.132.4.794. [DOI] [PMC free article] [PubMed] [Google Scholar]