Abstract
The ability to sense and respond to the signals deriving from either the environment or other living organisms, is one of most important features of life. Pathogenic bacteria, like all living organisms, have developed efficient systems to scout the surroundings and adapt their life according to the signals that they can sense. The signals sensed by bacteria can be divided into three main categories: those deriving from the environment, those deriving from other organisms and those deriving from other bacteria (population signals). The signals perceived from the environment can be of physical or chemical nature, such as temperature, osmolarity, pH, light, CO2, ammonia, oxygen, metals, nutrients, etc. The signals deriving from other living organisms may be either diffusable molecules such as chemoattractants, or signals that derive from direct contact with the organism. The signals deriving from other bacteria are usually diffusable molecules produced by the bacteria themselves which accumulate in the medium and increase in concentration with the bacterial cell density. This book contains nine chapters describing the regulatory systems of bacterial virulence that have been best characterized at the molecular level. The chapters go from the ironmediated regulation of diphtheria toxin production that is the oldest report of environmental regulation of virulence, described by Pappenheimer and Johnson in 1936,1 to the most recent reports on autocrine regulation of virulence expression in Staphylococcus aureus and Pseudomonas aeruginosa. In the following pages, we would like to give a general overview of the different systems, in an attempt to point out the mechanisms that are common to most bacteria. A summary of signals perceived by bacteria is shown in Figure I.1.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Pappenheimer AM, Johnson SJ. Studies on diphtheria toxin production. I: the effect of iron and copper. Br J Exp Pathol 1936; 17: 335–341.
Miller JF, Mekalanos JJ, Falkow S. Coordinate regulation and sensory transduction in the control of bacterial virulence. Science 1989; 243: 916–922.
Ronson CW, Nixon BT, Ausubel FM. Conserved domains in bacterial regulatory proteins that respond to environmental stimuli. Cell 1987; 49: 579–581.
Gross R, Aricb B, Rappuoli R. Families of bacterial signal-transducing proteins. Mol Microbiol 1989; 3: 1661–1667.
Alex LA, Simon MI. Protein histidine kinases and signal transduction in prokaryotes and eukaryotes. TIG 1994; 10: 133.
Chang C, Kwok SF, Bleecker AB et al. Arabidopsis ethylene-response gene ETR1: Similarity of product to two-component regulators. Science 1993; 262: 539–544.
Ota IM, Varshaysky A. A yeast protein similar to bacterial two-component regulators. Science 1993; 262: 566–569.
Maeda T, Wurgler-Murphy SM, Saito H. A two-component system that regulates an osmosensing MAP kinase cascade in yeast. Nature 1994; 369: 242–244.
Winans SC. Two-way chemical signaling in Agrobacterium-plant interactions. Microbiology Rev 1992; 56: 12–31.
Wick MJ, Madara JL, Fields BN et al. Molecular cross talk between epithelial cells and pathogenic microorganisms. Cell 1991; 67: 651–659.
Bliska JB, Galan JE, Falkow S. Signal transduction in the mammalian cell during bacterial attachment and entry. Cell 1993; 73: 903–920.
Forsberg A, Rosqvist R, Wolf-Watz H. Regulation and polarized transfer of the Yersinia outer proteins (Yops) involved in antiphagecytosis. Trends in Microbiology. 1994; 2: 14–19.
Rosqvist R, Magnusson KE, Wolf-Watz H. Target cell contact triggers expression and polarized transfer of Yersinia YopE cytotoxin into mammalian cells. EMBO J 1994; 13: 964–972.
Vuopio-Varkila J, Schoolnik GK. Localized adherence by enteropathogenic Escherichia coli as an inducible phenotype associated with the expression of new outer membrane proteins. J Exp Med 1991; 174: 1167–1177.
Giron JA, Suk Yue Ho A, Schoolnik GK. An inducible bundle-forming pilus of enteropathogenic Escherichia coli. Science 1991; 254: 710–713.
Menard R, Sansonetti P, Parsot C. The secretion of the Shigella flexneri Ipa invasins is activated by epithelial cells and controlled by Ipa B and Ipa D. EMBO J 1994; 13: 5293–5302.
Galan JE. Salmonella entry into mammalian cells: Different yet converging signal transduction pathways? Trends in Cell Biol 1994; 4: 196–199.
Huisman GW, Kolter R. Sensing starvation: A homoserine lactone-dependent signaling pathway in Escherichia coli. Science 1994; 265: 537.
Claiborne Fuqua W, Winans SC, Greenberg EP. Quorom sensing in bacteria: the LuxR-LuxI family of cell density-responsive transcriptional regulators. J Bacteriol 1994; 176: 269–275.
Passador L, Cook JM, Gambello MJ et al. Expression of Psuedomonas aeruginosa virulence genes requires cell-to-cell communication. Science 1993; 260: 1127.
Magnuson R, Solomon J, Grossman AD. Biochemical and genetic characterization of a competence pheromone from B. subtilis. Cell 1994; 77: 207–216.
Balaban N, Novick RP. Autocrine regulation of toxin synthesis by Staphylococcus aureus. Proc Natl Acad Sci USA 1995; 92: 1619–1693.
Swift S, Bainton NJ, Winson MK. Gram-negative bacterial communication by N-acyl homoserine lactones: a universal language.? Trends Microbiol 1994; 2: 193–198.
Rights and permissions
Copyright information
© 1995 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Rappuoli, R., Scarlato, V., Aricò, B., Balaban, N. (1995). Introduction. In: Signal Transduction and Bacterial Virulence. Medical Intelligence Unit. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-22406-9_1
Download citation
DOI: https://doi.org/10.1007/978-3-662-22406-9_1
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-662-22408-3
Online ISBN: 978-3-662-22406-9
eBook Packages: Springer Book Archive