Previous Article | Next Article 
Microbiology and Molecular Biology Reviews, September 1999, p. 621-641, Vol. 63, No. 3
1092-2172/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Gliding Motility in Bacteria: Insights from Studies of
Myxococcus xanthus
Alfred M.
Spormann*
Departments of Civil and Environmental
Engineering and of Biological Sciences, Stanford University,
Stanford, California 94305
Gliding motility is observed in a large variety of phylogenetically unrelated bacteria. Gliding provides a means for microbes to travel in environments with a low water content, such as might be found in biofilms, microbial mats, and soil. Gliding is defined as the movement of a cell on a surface in the direction of the long axis of the cell. Because this definition is operational and not mechanistic, the underlying molecular motor(s) may be quite different in diverse microbes. In fact, studies on the gliding bacterium Myxococcus xanthus suggest that two independent gliding machineries, encoded by two multigene systems, operate in this microorganism. One machinery, which allows individual cells to glide on a surface, independent of whether the cells are moving alone or in groups, requires the function of the genes of the A-motility system. More than 37 A-motility genes are known to be required for this form of movement. Depending on an additional phenotype, these genes are divided into two subclasses, the agl and cgl genes. Videomicroscopic studies on gliding movement, as well as ultrastructural observations of two myxobacteria, suggest that the A-system motor may consist of multiple single motor elements that are arrayed along the entire cell body. Each motor element is proposed to be localized to the periplasmic space and to be anchored to the peptidoglycan layer. The force to glide which may be generated here is coupled to adhesion sites that move freely in the outer membrane. These adhesion sites provide a specific contact with the substratum. Based on single-cell observations, similar models have been proposed to operate in the unrelated gliding bacteria Flavobacterium johnsoniae (formerly Cytophaga johnsonae), Cytophaga strain U67, and Flexibacter polymorphus (a filamentous glider). Although this model has not been verified experimentally, M. xanthus seems to be the ideal organism with which to test it, given the genetic tools available. The second gliding motor in M. xanthus controls cell movement in groups (S-motility system). It is dependent on functional type IV pili and is operative only when cells are in close proximity to each other. Type IV pili are known to be involved in another mode of bacterial surface translocation, called twitching motility. S-motility may well represent a variation of twitching motility in M. xanthus. However, twitching differs from gliding since it involves cell movements that are jerky and abrupt and that lack the organization and smoothness observed in gliding. Components of this motor are encoded by genes of the S-system, which appear to be homologs of genes involved in the biosynthesis, assembly, and function of type IV pili in Pseudomonas aeruginosa and Neisseria gonorrhoeae. How type IV pili generate force in S-motility is currently unknown, but it is to be expected that ongoing physiological, genetic, and biochemical studies in M. xanthus, in conjunction with studies on twitching in P. aeruginosa and N. gonorrhoeae, will provide important insights into this microbial motor. The two motility systems of M. xanthus are affected to different degrees by the MglA protein, which shows similarity to a small GTPase. Bacterial chemotaxis-like sensory transduction systems control gliding motility in M. xanthus. The frz genes appear to regulate gliding movement of individual cells and movement by the S-motility system, suggesting that the two motors found in this bacterium can be regulated to result in coordinated multicellular movements. In contrast, the dif genes affect only S-system-dependent swarming.
*
Mailing address: Departments of Civil and Environmental
Engineering and of Biological Sciences, Stanford University, Stanford, CA 94305. Phone: (650) 723-3668. Fax: (650) 725-3164. E-mail: spormann{at}stanford.edu.
Microbiology and Molecular Biology Reviews, September 1999, p. 621-641, Vol. 63, No. 3
1092-2172/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Clausen, M., Jakovljevic, V., Sogaard-Andersen, L., Maier, B.
(2009). High-Force Generation Is a Conserved Property of Type IV Pilus Systems. J. Bacteriol.
191: 4633-4638
[Abstract]
[Full Text]
-
Murray, T. S., Kazmierczak, B. I.
(2008). Pseudomonas aeruginosa Exhibits Sliding Motility in the Absence of Type IV Pili and Flagella. J. Bacteriol.
190: 2700-2708
[Abstract]
[Full Text]
-
Mignot, T., Shaevitz, J. W., Hartzell, P. L., Zusman, D. R.
(2007). Evidence That Focal Adhesion Complexes Power Bacterial Gliding Motility. Science
315: 853-856
[Abstract]
[Full Text]
-
Sliusarenko, O., Zusman, D. R., Oster, G.
(2007). Aggregation during Fruiting Body Formation in Myxococcus xanthus Is Driven by Reducing Cell Movement. J. Bacteriol.
189: 611-619
[Abstract]
[Full Text]
-
Karlin, S., Brocchieri, L., Mrazek, J., Kaiser, D.
(2006). Distinguishing features of {delta}-proteobacterial genomes. Proc. Natl. Acad. Sci. USA
103: 11352-11357
[Abstract]
[Full Text]
-
Ueki, T., Xu, C.-Y., Inouye, S.
(2005). SigF, a New Sigma Factor Required for a Motility System of Myxococcus xanthus. J. Bacteriol.
187: 8537-8541
[Abstract]
[Full Text]
-
Pham, V. D., Shebelut, C. W., Mukherjee, B., Singer, M.
(2005). RasA Is Required for Myxococcus xanthus Development and Social Motility. J. Bacteriol.
187: 6845-6848
[Abstract]
[Full Text]
-
Hasselbring, B. M., Jordan, J. L., Krause, D. C.
(2005). Mutant Analysis Reveals a Specific Requirement for Protein P30 in Mycoplasma pneumoniae Gliding Motility. J. Bacteriol.
187: 6281-6289
[Abstract]
[Full Text]
-
Islam, Md. T., Hashidoko, Y., Deora, A., Ito, T., Tahara, S.
(2005). Suppression of Damping-Off Disease in Host Plants by the Rhizoplane Bacterium Lysobacter sp. Strain SB-K88 Is Linked to Plant Colonization and Antibiosis against Soilborne Peronosporomycetes. Appl. Environ. Microbiol.
71: 3786-3796
[Abstract]
[Full Text]
-
Pham, V. D., Shebelut, C. W., Diodati, M. E., Bull, C. T., Singer, M.
(2005). Mutations affecting predation ability of the soil bacterium Myxococcus xanthus. Microbiology
151: 1865-1874
[Abstract]
[Full Text]
-
Pelling, A. E., Li, Y., Shi, W., Gimzewski, J. K.
(2005). Nanoscale visualization and characterization of Myxococcus xanthus cells with atomic force microscopy. Proc. Natl. Acad. Sci. USA
102: 6484-6489
[Abstract]
[Full Text]
-
Lancero, H., Caberoy, N. B., Castaneda, S., Li, Y., Lu, A., Dutton, D., Duan, X.-y., Kaplan, H. B., Shi, W., Garza, A. G.
(2004). Characterization of a Myxococcus xanthus mutant that is defective for adventurous motility and social motility. Microbiology
150: 4085-4093
[Abstract]
[Full Text]
-
Nielsen, M., Rasmussen, A. Aa., Ellehauge, E., Treuner-Lange, A., Sogaard-Andersen, L.
(2004). HthA, a putative DNA-binding protein, and HthB are important for fruiting body morphogenesis in Myxococcus xanthus. Microbiology
150: 2171-2183
[Abstract]
[Full Text]
-
Kimura, Y., Ishida, S., Matoba, H., Okahisa, N.
(2004). RppA, a transducer homologue, and MmrA, a multidrug transporter homologue, are involved in the biogenesis and/or assembly of polysaccharide in Myxococcus xanthus. Microbiology
150: 631-639
[Abstract]
[Full Text]
-
Rasmussen, A. A., Sogaard-Andersen, L.
(2003). TodK, a Putative Histidine Protein Kinase, Regulates Timing of Fruiting Body Morphogenesis in Myxococcus xanthus. J. Bacteriol.
185: 5452-5464
[Abstract]
[Full Text]
-
Li, Y., Sun, H., Ma, X., Lu, A., Lux, R., Zusman, D., Shi, W.
(2003). Extracellular polysaccharides mediate pilus retraction during social motility of Myxococcusxanthus. Proc. Natl. Acad. Sci. USA
100: 5443-5448
[Abstract]
[Full Text]
-
Heulin, T., Barakat, M., Christen, R., Lesourd, M., Sutra, L., De Luca, G., Achouak, W.
(2003). Ramlibacter tataouinensis gen. nov., sp. nov., and Ramlibacter henchirensis sp. nov., cyst-producing bacteria isolated from subdesert soil in Tunisia. Int. J. Syst. Evol. Microbiol.
53: 589-594
[Abstract]
[Full Text]
-
Ng, W.-O., Grossman, A. R., Bhaya, D.
(2003). Multiple Light Inputs Control Phototaxis in Synechocystis sp. Strain PCC6803. J. Bacteriol.
185: 1599-1607
[Abstract]
[Full Text]
-
Bardy, S. L., Ng, S. Y. M., Jarrell, K. F.
(2003). Prokaryotic motility structures. Microbiology
149: 295-304
[Abstract]
[Full Text]
-
Velicer, G. J., Lenski, R. E., Kroos, L.
(2002). Rescue of Social Motility Lost during Evolution of Myxococcus xanthus in an Asocial Environment. J. Bacteriol.
184: 2719-2727
[Abstract]
[Full Text]
-
Yoshihara, S., Geng, X., Ikeuchi, M.
(2002). pilG Gene Cluster and Split pilL Genes Involved in Pilus Biogenesis, Motility and Genetic Transformation in the Cyanobacterium Synechocystis sp. PCC 6803. Plant Cell Physiol
43: 513-521
[Abstract]
[Full Text]
-
Hunnicutt, D. W., Kempf, M. J., McBride, M. J.
(2002). Mutations in Flavobacterium johnsoniae gldF and gldG Disrupt Gliding Motility and Interfere with Membrane Localization of GldA. J. Bacteriol.
184: 2370-2378
[Abstract]
[Full Text]
-
Yoshimura, H., Yoshihara, S., Okamoto, S., Ikeuchi, M., Ohmori, M.
(2002). A cAMP Receptor Protein, SYCRP1, is Responsible for the Cell Motility of Synechocystis sp. PCC 6803. Plant Cell Physiol
43: 460-463
[Abstract]
[Full Text]
-
Lancero, H., Brofft, J. E., Downard, J., Birren, B. W., Nusbaum, C., Naylor, J., Shi, W., Shimkets, L. J.
(2002). Mapping of Myxococcus xanthus Social Motility dsp Mutations to the dif Genes. J. Bacteriol.
184: 1462-1465
[Abstract]
[Full Text]
-
Bourret, R. B., Charon, N. W., Stock, A. M., West, A. H.
(2002). Bright Lights, Abundant Operons--Fluorescence and Genomic Technologies Advance Studies of Bacterial Locomotion and Signal Transduction: Review of the BLAST Meeting, Cuernavaca, Mexico, 14 to 19 January 2001. J. Bacteriol.
184: 1-17
[Full Text]
-
McCarter, L. L.
(2001). Polar Flagellar Motility of the Vibrionaceae. Microbiol. Mol. Biol. Rev.
65: 445-462
[Abstract]
[Full Text]
-
Hunnicutt, D. W., McBride, M. J.
(2001). Cloning and Characterization of the Flavobacterium johnsoniae Gliding Motility Genes gldD and gldE. J. Bacteriol.
183: 4167-4175
[Abstract]
[Full Text]
-
Bhaya, D., Takahashi, A., Grossman, A. R.
(2001). Light regulation of type IV pilus-dependent motility by chemosensor-like elements in Synechocystis PCC6803. Proc. Natl. Acad. Sci. USA
10.1073/pnas.131201098v1
[Abstract]
[Full Text]
-
Skerker, J. M., Berg, H. C.
(2001). Direct observation of extension and retraction of type IV pili. Proc. Natl. Acad. Sci. USA
10.1073/pnas.121171698v1
[Abstract]
[Full Text]
-
Lünsdorf, H., Schairer, H. U.
(2001). Frozen motion of gliding bacteria outlines inherent features of the motility apparatus. Microbiology
147: 939-947
[Abstract]
[Full Text]
-
D'Argenio, D. A., Gallagher, L. A., Berg, C. A., Manoil, C.
(2001). Drosophila as a Model Host for Pseudomonas aeruginosa Infection. J. Bacteriol.
183: 1466-1471
[Abstract]
[Full Text]
-
Yoshihara, S., Geng, X. X., Okamoto, S., Yura, K., Murata, T., Go, M., Ohmori, M., Ikeuchi, M.
(2001). Mutational Analysis of Genes Involved in Pilus Structure, Motility and Transformation Competency in the Unicellular Motile CyanobacteriumSynechocystis sp. PCC 6803. Plant Cell Physiol
42: 63-73
[Abstract]
[Full Text]
-
Yang, Z., Ma, X., Tong, L., Kaplan, H. B., Shimkets, L. J., Shi, W.
(2000). Myxococcus xanthus dif Genes Are Required for Biogenesis of Cell Surface Fibrils Essential for Social Gliding Motility. J. Bacteriol.
182: 5793-5798
[Abstract]
[Full Text]
-
Kempf, M. J., McBride, M. J.
(2000). Transposon Insertions in the Flavobacterium johnsoniae ftsX Gene Disrupt Gliding Motility and Cell Division. J. Bacteriol.
182: 1671-1679
[Abstract]
[Full Text]
-
Hunnicutt, D. W., McBride, M. J.
(2000). Cloning and Characterization of the Flavobacterium johnsoniae Gliding-Motility Genes gldB and gldC. J. Bacteriol.
182: 911-918
[Abstract]
[Full Text]
-
Sun, H., Yang, Z., Shi, W.
(1999). Effect of cellular filamentation on adventurous and social gliding motility of Myxococcus xanthus. Proc. Natl. Acad. Sci. USA
96: 15178-15183
[Abstract]
[Full Text]
-
Jelsbak, L., Sogaard-Andersen, L.
(2002). Pattern formation by a cell surface-associated morphogen in Myxococcus xanthus. Proc. Natl. Acad. Sci. USA
99: 2032-2037
[Abstract]
[Full Text]
-
Skerker, J. M., Berg, H. C.
(2001). Direct observation of extension and retraction of type IV pili. Proc. Natl. Acad. Sci. USA
98: 6901-6904
[Abstract]
[Full Text]
-
Bhaya, D., Takahashi, A., Grossman, A. R.
(2001). Light regulation of type IV pilus-dependent motility by chemosensor-like elements in Synechocystis PCC6803. Proc. Natl. Acad. Sci. USA
98: 7540-7545
[Abstract]
[Full Text]