Abstract
The distribution of sex pheromone induced aggregation substance was studied on the cell surface of various Enterococcus faecalis strains. In the accompanying paper we have shown that the aggregation substance appears as a layer of hairlike structures. Using direct and indirect immunogold technique, transmission electron microscopy and high resolution scanning electron microscopy we investigated the appearance and distribution of the aggregation substance. The “hairs” increase in number with increasing exposure to sex pheromones (maximum density: 1300/μm2). We show that these structures are unequally distributed over the cell surface, even if the cells were induced by sex pheromones for a long period of time. Statistical analysis of the unequal distribution indicates that aggregation substance is incorporated into pre-existing “old” cell-walls and that this incorporation shows a saturation ca. 40 min after addition of sex pheromones.
Similar content being viewed by others
Abbreviations
- cAD1:
-
sex pheromone specific for plasmid pAD1
- cPD1:
-
sex pheromone specific for plasmid pPD1
- FESEM:
-
field emission scanning electron microscope
- pAD1:
-
conjugative plasmid specifically transferred in the presence of cAD1
- pPD1:
-
conjugative plasmid specifically transferred in the presence of cPD1
- TEM:
-
transmission electron microscope
References
Crewe AV, Wall J (1970) A scanning microscope with 5 Å resolution. J Mol Biol 48:375–393
Hermann R, Pawley J, Nagatani T, Müller M (1988) Double-axis rotary shadowing for high resolution scanning electron microscopy. Scanning Microscopy 2:1215–1230
Higgins ML, Shockman GD (1970) Model for cell wall growth of Streptococcus faecalis. J Bacteriol 101:643–648
Higgins ML, Shockman DG (1976) Study of a cycle of cell wall assembly in Streptococcus faecalis by three-dimensional reconstructions of thin sections of cells. J Bacteriol 127:1346–1358
Hodges GM, Southgate J, Toulson EC (1987) Colloidal gold — a powerful tool in scanning electron microscope immunocytochemistry: an overview of bioapplications. Scanning Microscopy 1:301–318
Ike Y, Clewell DB (1984) Genetic analysis of the pAD1 pheromone response in Streptococcus faecalis, using transposon Tn917 as an insertional mutagen. J Bacteriol 158:777–783
Kessler RE, Yagi Y (1983) Identification and partial characterization of a pheromone-induced adhesive surface antigen of Streptococcus faecalis. J Bacteriol 155:714–721
Sieber-Blum M, Sieber F, Yamada KM (1981) Cellular fibronectin promotes adrenergic differentiation of quail neural crest cells in vitro. Exp Cell Res 133:285–295
Spurr AR (1969) A low viscosity epoxy resin embedding medium for electron microscopy. J Ultrastr Res 26:31–43
Trejdosiewicz LK, Smolira MA, Hodges GM, Goodman SJ, Livingston DC (1981) Cell surface distribution of fibronectin in cultures of fibroblasts and bladder derived epithelium: SEM-immunogold localization compared to immunoperoxidase and immunofluorescence. J Microsc 123:227–236
Walther P, Müller M (1986) Detection of small (5–15 nm) gold labelled surface antigens using backscattered electrons. In: O'Hare AMF (ed) The science of biological specimen preparation. SEM Inc, Chicago, pp 195–201
Walther P, Ariano BH, Kriz S, Müller M (1983) High resolution SEM detection of protein-A gold (15 nm) marked surface antigens using backscattered electrons. Beitr Elektronenmikroskop Direktabb Oberfl 16:539–545
Yagi Y, Kessler RE, Shaw JH, Lopatin DE, An F, Clewell DB (1983) Plasmid content of Streptococcus faecalis strain 39-5 and identification of a pheromone (cPD1)-induced surface antigen. J Gen Microbiol 129:1207–1215
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Wanner, G., Formanek, H., Galli, D. et al. Localization of aggregation substances of Enterococcus faecalis after induction by sex pheromones. Arch. Microbiol. 151, 491–497 (1989). https://doi.org/10.1007/BF00454864
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00454864