Abstract
The interaction, between mycoplasma (PPLO) and human or rabbit leukocytes was examined in vitro. Upon incubation of M. hominis or M. arthritidis for 2 hr with rabbit peritoneal exudate granulocytes or leukocytes from human peripheral blood, no killing of mycoplasma was observed either in the presence or absence of type-specific antiserum. However, 14CO2 production from glucose-1-14C was stimulated up to 10-fold in the presence of live or heat-killed PPLO. The extent of stimulation depended upon the number of organisms and the presence of type-specific antiserum. The stimulation of 14CO2 production seems not because of tight adherence of PPLO to the leukocytes, since PPLO were quantitatively recovered in the medium after sedimenting the granulocytes. The enhanced conversion of medium lysolecithin to cellular lecithin that accompanies phagocytosis of polystyrene particles was significantly reduced when PPLO were also present. Mycoplasma alone elicited no stimulation of lecithin formation. Killing of E. coli, a microorganism readily engulfed and killed by leukocytes in vitro, was diminished when the leukocytes were preincubated with mycoplasma. These findings indicate that M. hominis and M. arthritidis are not ingested by granulocytes to any detectable extent, but that these organisms affect the leukocytes' metabolism and also impair phagocytosis of E. coli.
Full Text
The Full Text of this article is available as a PDF (732.7 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
- CLYDE W. A., Jr MYCOPLASMA SPECIES IDENTIFICATION BASED UPON GROWTH INHIBITION BY SPECIFIC ANTISERA. J Immunol. 1964 Jun;92:958–965. [PubMed] [Google Scholar]
- Chen T. A., Granados R. R. Plant-Pathogenic Mycoplasma-Like Organism: Maintenance in vitro and Transmission to Zea mays L. Science. 1970 Mar 20;167(3925):1633–1636. doi: 10.1126/science.167.3925.1633. [DOI] [PubMed] [Google Scholar]
- Dajani A. S., Ayoub E. M. Mycoplasmacidal effect of polymorphonuclear leukocyte extract. J Immunol. 1969 Mar;102(3):698–702. [PubMed] [Google Scholar]
- Denny F. W., Clyde W. A., Jr, Glezen W. P. Mycoplasma pneumoniae disease: clinical spectrum, pathophysiology, epidemiology, and control. J Infect Dis. 1971 Jan;123(1):74–92. doi: 10.1093/infdis/123.1.74. [DOI] [PubMed] [Google Scholar]
- ELSBACH P. COMPARISON OF UPTAKE OF PALMITIC, STEARIC, OLEIC AND LINOLEIC ACID BY POLYMORPHONUCLEAR LEUKOCYTES. Biochim Biophys Acta. 1964 Feb 24;84:8–17. doi: 10.1016/0926-6542(64)90095-2. [DOI] [PubMed] [Google Scholar]
- Elsbach P. Metabolism of lysophosphatidyl ethanolamine and lysophosphatidyl choline by homogenates of rabbit polymorphonuclear leukocytes and alveolar macrophages. J Lipid Res. 1967 Jul;8(4):359–365. [PubMed] [Google Scholar]
- Elsbach P. Phospholipid metabolism by phagocytic cells. I. A comparison of conversion of [32P]lysolecithin to lecithin and glycerylphosphorylcholine by homogenates of rabbit polymorphonuclear leukocytes and alveolar macrophages. Biochim Biophys Acta. 1966 Dec 7;125(3):510–524. [PubMed] [Google Scholar]
- Elsbach P., Zucker-Franklin D., Sansaricq C. Increased lecithin synthesis during phagocytosis by normal leukocytes and by leukocytes of a patient with chronic granulomatous disease. N Engl J Med. 1969 Jun 12;280(24):1319–1322. doi: 10.1056/NEJM196906122802403. [DOI] [PubMed] [Google Scholar]
- Elsbach P., van den Berg J. W., van den Bosch H., van Deenen L. L. Metabolism of phospholipids by polymorphonuclear leukocytes. Biochim Biophys Acta. 1965 Oct 4;106(2):338–347. doi: 10.1016/0005-2760(65)90042-1. [DOI] [PubMed] [Google Scholar]
- Graham R. C., Jr, Karnovsky M. J., Shafer A. W., Glass E. A., Karnovsky M. L. Metabolic and morphological observations on the effect of surface-active agents of leukocytes. J Cell Biol. 1967 Mar;32(3):629–647. doi: 10.1083/jcb.32.3.629. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones T. C., Hirsch J. G. The interaction in vitro of Mycoplasma pulmonis with mouse peritoneal macrophages and L-cells. J Exp Med. 1971 Feb 1;133(2):231–259. doi: 10.1084/jem.133.2.231. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rossi F., Zatti M., Patriarca P., Cramer R. Effect of specific antibodies on the metabolism of guinea pig polymorphonuclear leukocytes. J Reticuloendothel Soc. 1971 Jan;9(1):67–85. [PubMed] [Google Scholar]
- Thomas L. Mechanisms of pathogenesis in Mycoplasma infection. Harvey Lect. 1969;63:73–98. [PubMed] [Google Scholar]
- Thomas L. Mycoplasmas as infectious agents. Annu Rev Med. 1970;21:179–186. doi: 10.1146/annurev.me.21.020170.001143. [DOI] [PubMed] [Google Scholar]
- Wurster N., Elsbach P., Simon E. J., Pettis P., Lebow S. The effects of the morphine analogue levorphanol on leukocytes. Metabolic effects at rest and during phagocytosis. J Clin Invest. 1971 May;50(5):1091–1099. doi: 10.1172/JCI106580. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zucker-Franklin D., Davidson M., Thomas L. The interaction of mycoplasmas with mammalian cells. I. HeLa cells, neutrophils, and eosinophils. J Exp Med. 1966 Sep 1;124(3):521–532. doi: 10.1084/jem.124.3.521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zucker-Franklin D., Davidson M., Thomas L. The interaction of mycoplasmas with mammalian cells. II. Monocytes and lymphocytes. J Exp Med. 1966 Sep 1;124(3):533–542. doi: 10.1084/jem.124.3.533. [DOI] [PMC free article] [PubMed] [Google Scholar]