
Trail following by gliding bacteria.
R P Burchard
Abstract
Slime trails, which are deposited on surfaces by gliding bacteria and which serve as preferential pathways for gliding motility, were tested for the species specificity of their support of movement. Among the pairs of bacteria tested, a variety of gliding bacteria and a flagellated bacterium moved along trails of unrelated species. Thus, the trails did not serve as pheromones. Rather, they may have guided gliding elasticotactically. Some biological implications of this finding are considered.
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- Burchard R. P. Gliding motility mutants of Myxococcus xanthus. J Bacteriol. 1970 Nov;104(2):940–947. doi: 10.1128/jb.104.2.940-947.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burchard R. P. Gliding motility of prokaryotes: ultrastructure, physiology, and genetics. Annu Rev Microbiol. 1981;35:497–529. doi: 10.1146/annurev.mi.35.100181.002433. [DOI] [PubMed] [Google Scholar]
- Burchard R. P. Myxospore induction in a nondispersed growing mutant of Myxococcus xanthus. J Bacteriol. 1975 Apr;122(1):302–306. doi: 10.1128/jb.122.1.302-306.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burton S. D., Lee J. D. Improved enrichment and isolation procedures for obtaining pure cultures of beggiatoa. Appl Environ Microbiol. 1978 Mar;35(3):614–617. doi: 10.1128/aem.35.3.614-617.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- COSTERTON J. W., MURRAY R. G., ROBINOW C. F. Observations on the motility and the structure of Vitreoscilla. Can J Microbiol. 1961 Jun;7:329–339. doi: 10.1139/m61-040. [DOI] [PubMed] [Google Scholar]
- Castenholz R. W. Thermophilic blue-green algae and the thermal environment. Bacteriol Rev. 1969 Dec;33(4):476–504. doi: 10.1128/br.33.4.476-504.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dunny G. M., Brown B. L., Clewell D. B. Induced cell aggregation and mating in Streptococcus faecalis: evidence for a bacterial sex pheromone. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3479–3483. doi: 10.1073/pnas.75.7.3479. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eberhard A. Inhibition and activation of bacterial luciferase synthesis. J Bacteriol. 1972 Mar;109(3):1101–1105. doi: 10.1128/jb.109.3.1101-1105.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fuscoe F. J. The role of extracellular slime secretion in the swarming of Proteus. Med Lab Technol. 1973 Oct;30(4):373–382. [PubMed] [Google Scholar]
- Gnosspelius G. Myxobacterial slime and proteolytic activity. Arch Microbiol. 1978 Jan 23;116(1):51–59. doi: 10.1007/BF00408733. [DOI] [PubMed] [Google Scholar]
- HESS E. H. Shadows and depth perception. Sci Am. 1961 Mar;204:138–148. doi: 10.1038/scientificamerican0361-138. [DOI] [PubMed] [Google Scholar]
- Henrichsen J. Bacterial surface translocation: a survey and a classification. Bacteriol Rev. 1972 Dec;36(4):478–503. doi: 10.1128/br.36.4.478-503.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hodgkin J., Kaiser D. Cell-to-cell stimulation of movement in nonmotile mutants of Myxococcus. Proc Natl Acad Sci U S A. 1977 Jul;74(7):2938–2942. doi: 10.1073/pnas.74.7.2938. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KARLSON P., LUSCHER M. Pheromones': a new term for a class of biologically active substances. Nature. 1959 Jan 3;183(4653):55–56. doi: 10.1038/183055a0. [DOI] [PubMed] [Google Scholar]
- Kaiser D., Manoil C., Dworkin M. Myxobacteria: cell interactions, genetics, and development. Annu Rev Microbiol. 1979;33:595–639. doi: 10.1146/annurev.mi.33.100179.003115. [DOI] [PubMed] [Google Scholar]
- Lamont H. C. Shear-oriented microfibrils in the mucilaginous investments of two motile oscillatoriacean blue-green algae. J Bacteriol. 1969 Jan;97(1):350–361. doi: 10.1128/jb.97.1.350-361.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NOREN B., RAPER K. B. Antibiotic activity of myxobacteria in relation to their bacteriolytic capacity. J Bacteriol. 1962 Jul;84:157–162. doi: 10.1128/jb.84.1.157-162.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pangborn J., Kuhn D. A., Woods J. R. Dorsal-ventral differentiation in Simonsiella and other aspects of its morphology and ultrastructure. Arch Microbiol. 1977 Jun 20;113(3):197–204. doi: 10.1007/BF00492025. [DOI] [PubMed] [Google Scholar]
- Parish J. H. Transfer of drug resistance to myxococcus from bacteria carrying drug-resistance factors. J Gen Microbiol. 1975 Apr;87(2):198–210. doi: 10.1099/00221287-87-2-198. [DOI] [PubMed] [Google Scholar]
- Pate J. L., Ordal E. J. The fine structure of Chondrococcus columnaris. I. Structure and formation of mesosomes. J Cell Biol. 1967 Oct;35(1):1–13. doi: 10.1083/jcb.35.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qualls G. T., Stephens K., White D. Morphogenetic movements and multicellular development in the fruiting Myxobacterium, Stigmatella aurantiaca. Dev Biol. 1978 Sep;66(1):270–274. doi: 10.1016/0012-1606(78)90291-9. [DOI] [PubMed] [Google Scholar]
- Reichenbach H. Nannocystis exedens gen. nov., spec. nov., a new myxobacterium of the family Sorangiaceae. Arch Mikrobiol. 1970;70(2):119–138. doi: 10.1007/BF00412203. [DOI] [PubMed] [Google Scholar]
- Reichenbach H. Taxonomy of the gliding bacteria. Annu Rev Microbiol. 1981;35:339–364. doi: 10.1146/annurev.mi.35.100181.002011. [DOI] [PubMed] [Google Scholar]
- Reichenbach H. Untersuchungen an Archangium violaceum. Ein Beitrag zur Kenntnis der Myxobakterien. Arch Mikrobiol. 1965 Dec 7;52(4):376–403. [PubMed] [Google Scholar]
- Rosenberg E., Keller K. H., Dworkin M. Cell density-dependent growth of Myxococcus xanthus on casein. J Bacteriol. 1977 Feb;129(2):770–777. doi: 10.1128/jb.129.2.770-777.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simon G. D., White D. Growth and morphological characteristics of a species of Flexibacter. Arch Mikrobiol. 1971;78(1):1–16. doi: 10.1007/BF00409084. [DOI] [PubMed] [Google Scholar]
- Stanier R. Y. A Note on Elasticotaxis in Myxobacteria. J Bacteriol. 1942 Oct;44(4):405–412. doi: 10.1128/jb.44.4.405-412.1942. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stephens K., Hegeman G. D., White D. Pheromone produced by the myxobacterium Stigmatella aurantiaca. J Bacteriol. 1982 Feb;149(2):739–747. doi: 10.1128/jb.149.2.739-747.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Strohl W. R., Larkin J. M. Enumeration, isolation, and characterization of beggiatoa from freshwater sediments. Appl Environ Microbiol. 1978 Nov;36(5):755–770. doi: 10.1128/aem.36.5.755-770.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sutherland I. W., Thomson S. Comparison of polysaccharides produced by Myxococcus strains. J Gen Microbiol. 1975 Jul;89(1):124–132. doi: 10.1099/00221287-89-1-124. [DOI] [PubMed] [Google Scholar]
- Wireman J. W., Dworkin M. Morphogenesis and developmental interactions in myxobacteria. Science. 1975 Aug 15;189(4202):516–523. doi: 10.1126/science.806967. [DOI] [PubMed] [Google Scholar]
- von Krüger W. M., Parish J. H. beta-Lactamase activity and resistance to penicillins in Myxococcus xanthus. Arch Microbiol. 1981 Oct;130(2):150–154. doi: 10.1007/BF00411069. [DOI] [PubMed] [Google Scholar]