This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rosey, E. L.
Right arrow Articles by Yancey, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rosey, E. L.
Right arrow Articles by Yancey, R. J., Jr

 Previous Article  |  Next Article 

J. Bacteriol., 10 1995, 5959-5970, Vol 177, No. 20
Copyright © 1995, American Society for Microbiology

Inactivation of Serpulina hyodysenteriae flaA1 and flaB1 periplasmic flagellar genes by electroporation-mediated allelic exchange

EL Rosey, MJ Kennedy, DK Petrella, RG Ulrich and RJ Yancey Jr
Upjohn Company, Kalamazoo, Michigan 49001, USA.

Serpulina hyodysenteriae, the etiologic agent of swine dysentery, contains complex periplasmic flagella which are composed of multiple class A and class B polypeptides. To examine the role these proteins play in flagellar synthesis, structure, and function and to develop strains which may provide insight into the importance of motility in the etiology of this pathogen, we constructed specific periplasmic flagellar mutations in S. hyodysenteriae B204. The cloned flaA1 and flaB1 genes were disrupted by replacement of internal fragments with chloramphenicol and/or kanamycin gene cassettes. Following delivery of these suicide plasmids into S. hyodysenteriae, homologous recombination and allelic exchange at the targeted chromosomal flaA1 and flaB1 genes was verified by PCR, sequence, and Southern analysis. The utility of a chloramphenicol resistance gene cassette for targeted gene disruption was demonstrated and found more amenable than kanamycin as a selective marker in S. hyodysenteriae. Immunoblots of cell lysates of the flagellar mutants with antiserum raised against purified FlaA or FlaB confirmed the absence of the corresponding sheath or core protein. Both mutations selectively abolished expression of the targeted gene without affecting synthesis of the other flagellar polypeptide. flaA1 and flaB1 mutant strains exhibited altered motility in vitro and were less efficient in movement through a liquid medium. Paradoxically, isogenic strains containing specifically disrupted flaA1 or flaB1 alleles were capable of assembling periplasmic flagella that were morphologically normal as evidenced by electron microscopy. This is the first report of specific inactivation of a motility-associated gene in spirochetes.


This article has been cited by other articles:

  • Yang, Y., Stewart, P. E., Shi, X., Li, C. (2008). Development of a Transposon Mutagenesis System in the Oral Spirochete Treponema denticola. Appl. Environ. Microbiol. 74: 6461-6464 [Abstract] [Full Text]  
  • Li, C., Wolgemuth, C. W., Marko, M., Morgan, D. G., Charon, N. W. (2008). Genetic Analysis of Spirochete Flagellin Proteins and Their Involvement in Motility, Filament Assembly, and Flagellar Morphology. J. Bacteriol. 190: 5607-5615 [Abstract] [Full Text]  
  • Stanton, T. B., Humphrey, S. B., Sharma, V. K., Zuerner, R. L. (2008). Collateral Effects of Antibiotics: Carbadox and Metronidazole Induce VSH-1 and Facilitate Gene Transfer among Brachyspira hyodysenteriae Strains. Appl. Environ. Microbiol. 74: 2950-2956 [Abstract] [Full Text]  
  • Motaleb, M. A., Sal, M. S., Charon, N. W. (2004). The Decrease in FlaA Observed in a flaB Mutant of Borrelia burgdorferi Occurs Posttranscriptionally. J. Bacteriol. 186: 3703-3711 [Abstract] [Full Text]  
  • Schultheiss, D., Kube, M., Schuler, D. (2004). Inactivation of the Flagellin Gene flaA in Magnetospirillum gryphiswaldense Results in Nonmagnetotactic Mutants Lacking Flagellar Filaments. Appl. Environ. Microbiol. 70: 3624-3631 [Abstract] [Full Text]  
  • Li, C., Corum, L., Morgan, D., Rosey, E. L., Stanton, T. B., Charon, N. W. (2000). The Spirochete FlaA Periplasmic Flagellar Sheath Protein Impacts Flagellar Helicity. J. Bacteriol. 182: 6698-6706 [Abstract] [Full Text]  
  • Haake, D. A. (2000). Spirochaetal lipoproteins and pathogenesis. Microbiology 146: 1491-1504 [Full Text]  
  • Haake, S. K., Yoder, S. C., Attarian, G., Podkaminer, K. (2000). Native Plasmids of Fusobacterium nucleatum: Characterization and Use in Development of Genetic Systems. J. Bacteriol. 182: 1176-1180 [Abstract] [Full Text]  
  • Dugourd, D., Martin, C., Rioux, C. R., Jacques, M., Harel, J. (1999). Characterization of a Periplasmic ATP-Binding Cassette Iron Import System of Brachyspira (Serpulina) hyodysenteriae. J. Bacteriol. 181: 6948-6957 [Abstract] [Full Text]  
  • Stanton, T. B., Rosey, E. L., Kennedy, M. J., Jensen, N. S., Bosworth, B. T. (1999). Isolation, Oxygen Sensitivity, and Virulence of NADH Oxidase Mutants of the Anaerobic Spirochete Brachyspira (Serpulina) hyodysenteriae, Etiologic Agent of Swine Dysentery. Appl. Environ. Microbiol. 65: 5028-5034 [Abstract] [Full Text]  
  • Sohaskey, C. D., Barbour, A. G. (1999). Esterases in Serum-Containing Growth Media Counteract Chloramphenicol Acetyltransferase Activity In Vitro. Antimicrob. Agents Chemother. 43: 655-660 [Abstract] [Full Text]  
  • Ge, Y., Li, C., Corum, L., Slaughter, C. A., Charon, N. W. (1998). Structure and Expression of the FlaA Periplasmic Flagellar Protein of Borrelia burgdorferi. J. Bacteriol. 180: 2418-2425 [Abstract] [Full Text]  
  • Gabe, J. D., Dragon, E., Chang, R.-J., McCaman, M. T. (1998). Identification of a Linked Set of Genes in Serpulina hyodysenteriae (B204) Predicted To Encode Closely Related 39-Kilodalton Extracytoplasmic Proteins. J. Bacteriol. 180: 444-448 [Abstract] [Full Text]