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Journal of Bacteriology, February 2005, p. 829-839, Vol. 187, No. 3
0021-9193/05/$08.00+0     doi:10.1128/JB.187.3.829-839.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Disparate Subcellular Localization Patterns of Pseudomonas aeruginosa Type IV Pilus ATPases Involved in Twitching Motility

Poney Chiang,1 Marc Habash,1 and Lori L. Burrows1*

Centre for Infection and Biomaterials Research, Hospital for Sick Children Research Institute, and Department of Surgery, University of Toronto, Toronto, Ontario, Canada1

Received 31 August 2004/ Accepted 19 October 2004

The opportunistic pathogen Pseudomonas aeruginosa expresses polar type IV pili (TFP), which are responsible for adhesion to various materials and twitching motility on surfaces. Twitching occurs by alternate extension and retraction of TFP, which arise from assembly and disassembly of pilin subunits at the base of the pilus. The ATPase PilB promotes pilin assembly, while the ATPase PilT or PilU or both promote pilin dissociation. Fluorescent fusions to two of the three ATPases (PilT and PilU) were functional, as shown by complementation of the corresponding mutants. PilB and PilT fusions localized to both poles, while PilU fusions localized only to the piliated pole. To identify the portion of the ATPases required for localization, sequential C-terminal deletions of PilT and PilU were generated. The conserved His and Walker B boxes were dispensable for polar localization but were required for twitching motility, showing that localization and function could be uncoupled. Truncated fusions that retained polar localization maintained their distinctive distribution patterns. To dissect the cellular factors involved in establishing polarity, fusion protein localization was monitored with a panel of TFP mutants. The localization of yellow fluorescent protein (YFP)-PilT and YFP-PilU was independent of the subunit PilA, other TFP ATPases, and TFP-associated proteins previously shown to be associated with the membrane or exhibiting polar localization. In contrast, YFP-PilB exhibited diffuse cytoplasmic localization in a pilC mutant, suggesting that PilC is required for polar localization of PilB. Finally, localization studies performed with fluorescent ATPase chimeras of PilT and PilU demonstrated that information responsible for the characteristic localization patterns of the ATPases likely resides in their N termini.

* Corresponding author. Mailing address: Centre for Infection and Biomaterials Research, 7142A Elm Wing, Hospital for Sick Children Research Institute, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8. Phone: (416) 813-6293. Fax: (416) 813-6240. E-mail: lori.burrows{at}sickkids.ca.

Journal of Bacteriology, February 2005, p. 829-839, Vol. 187, No. 3
0021-9193/05/$08.00+0     doi:10.1128/JB.187.3.829-839.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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