Previous Article | Next Article 
Journal of Bacteriology, August 2002, p. 4500-4509, Vol. 184, No. 16
0021-9193/02/$04.00+0 DOI: 10.1128/JB.184.16.4500-4509.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Proteolytic Cleavage of the FlhB Homologue YscU of Yersinia pseudotuberculosis Is Essential for Bacterial Survival but Not for Type III Secretion
Moa Lavander,1 Lena Sundberg,1,2 Petra J. Edqvist,2 Scott A. Lloyd,2,
Hans Wolf-Watz,2 and Åke Forsberg1,2*
Department of Medical Countermeasures, Division of NBC-Defense, Swedish Defense Research Agency, S-901 82 Umeå,1
Department of Molecular Biology, Umeå University, S-901 87 Umeå, Sweden2
Received 13 March 2002/
Accepted 17 May 2002
Pathogenic Yersinia species employ a type III secretion system (TTSS) to target antihost factors, Yop proteins, into eukaryotic cells. The secretion machinery is constituted of ca. 20 Ysc proteins, nine of which show significant homology to components of the flagellar TTSS. A key event in flagellar assembly is the switch from secreting-assembling hook substrates to filament substrates, a switch regulated by FlhB and FliK. The focus of this study is the FlhB homologue YscU, a bacterial inner membrane protein with a large cytoplasmic C-terminal domain. Our results demonstrate that low levels of YscU were required for functional Yop secretion, whereas higher levels of YscU lowered both Yop secretion and expression. Like FlhB, YscU was cleaved into a 30-kDa N-terminal and a 10-kDa C-terminal part. Expression of the latter in a wild-type strain resulted in elevated Yop secretion. The site of cleavage was at a proline residue, within the strictly conserved amino acid sequence NPTH. A YscU protein with an in-frame deletion of NPTH was cleaved at a different position and was nonfunctional with respect to Yop secretion. Variants of YscU with single substitutions in the conserved NPTH sequencei.e., N263A, P264A, or T265Awere not cleaved but retained function in Yop secretion. Elevated expression of these YscU variants did, however, result in severe growth inhibition. From this we conclude that YscU cleavage is not a prerequisite for Yop secretion but is rather required to maintain a nontoxic fold.
* Corresponding author. Mailing address: Department of Medical Countermeasures, Division of NBC-Defense, Swedish Defense Research Agency, S-901 82 Umeå, Sweden. Phone: 46-90-10-66-60. Fax: 46-90-10-68-00. E-mail:
ake.forsberg{at}foi.se.
Present address: Department of Pediatrics, Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201.
Journal of Bacteriology, August 2002, p. 4500-4509, Vol. 184, No. 16
0021-9193/02/$04.00+0 DOI: 10.1128/JB.184.16.4500-4509.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Bjornfot, A.-C., Lavander, M., Forsberg, A., Wolf-Watz, H.
(2009). Autoproteolysis of YscU of Yersinia pseudotuberculosis Is Important for Regulation of Expression and Secretion of Yop Proteins. J. Bacteriol.
191: 4259-4267
[Abstract]
[Full Text]
-
Lorenz, C., Buttner, D.
(2009). Functional Characterization of the Type III Secretion ATPase HrcN from the Plant Pathogen Xanthomonas campestris pv. vesicatoria. J. Bacteriol.
191: 1414-1428
[Abstract]
[Full Text]
-
Riordan, K. E., Sorg, J. A., Berube, B. J., Schneewind, O.
(2008). Impassable YscP Substrates and Their Impact on the Yersinia enterocolitica Type III Secretion Pathway. J. Bacteriol.
190: 6204-6216
[Abstract]
[Full Text]
-
Wood, S. E., Jin, J., Lloyd, S. A.
(2008). YscP and YscU Switch the Substrate Specificity of the Yersinia Type III Secretion System by Regulating Export of the Inner Rod Protein YscI. J. Bacteriol.
190: 4252-4262
[Abstract]
[Full Text]
-
Carlsson, K. E., Liu, J., Edqvist, P. J., Francis, M. S.
(2007). Influence of the Cpx Extracytoplasmic-Stress-Responsive Pathway on Yersinia sp.-Eukaryotic Cell Contact. Infect. Immun.
75: 4386-4399
[Abstract]
[Full Text]
-
Zenk, S. F., Stabat, D., Hodgkinson, J. L., Veenendaal, A. K. J., Johnson, S., Blocker, A. J.
(2007). Identification of minor inner-membrane components of the Shigella type III secretion system 'needle complex'. Microbiology
153: 2405-2415
[Abstract]
[Full Text]
-
Carlsson, K. E., Liu, J., Edqvist, P. J., Francis, M. S.
(2007). Extracytoplasmic-Stress-Responsive Pathways Modulate Type III Secretion in Yersinia pseudotuberculosis. Infect. Immun.
75: 3913-3924
[Abstract]
[Full Text]
-
Wand, M. E., Sockett, R. E., Evans, K. J., Doherty, N., Sharp, P. M., Hardie, K. R., Winzer, K.
(2006). Helicobacter pylori FlhB Function: the FlhB C-Terminal Homologue HP1575 Acts as a "Spare Part" To Permit Flagellar Export When the HP0770 FlhBCC Domain Is Deleted.. J. Bacteriol.
188: 7531-7541
[Abstract]
[Full Text]
-
Ferris, H. U., Furukawa, Y., Minamino, T., Kroetz, M. B., Kihara, M., Namba, K., Macnab, R. M.
(2005). FlhB Regulates Ordered Export of Flagellar Components via Autocleavage Mechanism. J. Biol. Chem.
280: 41236-41242
[Abstract]
[Full Text]
-
Ghosh, P.
(2004). Process of Protein Transport by the Type III Secretion System. Microbiol. Mol. Biol. Rev.
68: 771-795
[Abstract]
[Full Text]
-
Alegria, M. C., Docena, C., Khater, L., Ramos, C. H. I., da Silva, A. C. R., Farah, C. S.
(2004). New Protein-Protein Interactions Identified for the Regulatory and Structural Components and Substrates of the Type III Secretion System of the Phytopathogen Xanthomonas axonopodis Pathovar citri. J. Bacteriol.
186: 6186-6197
[Abstract]
[Full Text]
-
Olsson, J., Edqvist, P. J., Broms, J. E., Forsberg, A., Wolf-Watz, H., Francis, M. S.
(2004). The YopD Translocator of Yersinia pseudotuberculosis Is a Multifunctional Protein Comprised of Discrete Domains. J. Bacteriol.
186: 4110-4123
[Abstract]
[Full Text]
-
Edqvist, P. J., Olsson, J., Lavander, M., Sundberg, L., Forsberg, A., Wolf-Watz, H., Lloyd, S. A.
(2003). YscP and YscU Regulate Substrate Specificity of the Yersinia Type III Secretion System. J. Bacteriol.
185: 2259-2266
[Abstract]
[Full Text]