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Journal of Bacteriology, April 2008, p. 2841-2850, Vol. 190, No. 8
0021-9193/08/$08.00+0     doi:10.1128/JB.01775-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Secretome Analysis Uncovers an Hcp-Family Protein Secreted via a Type VI Secretion System in Agrobacterium tumefaciens{triangledown} ,{dagger}

Hung-Yi Wu, Pei-Che Chung, Hsiao-Wei Shih, Sy-Ray Wen, and Erh-Min Lai*

Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan

Received 9 November 2007/ Accepted 29 January 2008

Agrobacterium tumefaciens is a plant-pathogenic bacterium capable of secreting several virulence factors into extracellular space or the host cell. In this study, we used shotgun proteomics analysis to investigate the secretome of A. tumefaciens, which resulted in identification of 12 proteins, including 1 known secretory protein (VirB1*) and 11 potential secretory proteins. Interestingly, one unknown protein, which we designated hemolysin-coregulated protein (Hcp), is a predicted soluble protein without a recognizable N-terminal signal peptide. Western blot analysis revealed that A. tumefaciens Hcp is expressed and secreted when cells are grown in both minimal and rich media. Further biochemical and immunoelectron microscopy analysis demonstrated that intracellular Hcp is localized mainly in the cytosol, with a small portion in the membrane system. To investigate the mechanism of secretion of Hcp in A. tumefaciens, we generated mutants with deletions of a conserved gene, icmF, or the entire putative operon encoding a recently identified type VI secretion system (T6SS). Western blot analysis indicated that Hcp was expressed but not secreted into the culture medium in mutants with deletions of icmF or the t6ss operon. The secretion deficiency of Hcp in the icmF mutant was complemented by heterologous trans expression of icmF, suggesting that icmF is required for Hcp secretion. In tumor assays with potato tuber disks, deletion of hcp resulted in approximately 20 to 30% reductions in tumorigenesis efficiency, while no consistent difference was observed when icmF or the t6ss operon was deleted. These results increase our understanding of the conserved T6SS used by both plant- and animal-pathogenic bacteria.

* Corresponding author. Mailing address: 128, Sec. 2, Academia Road, Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan 11529. Phone: 886-2-2789-2981. Fax: 886-2-2782-7954. E-mail: emlai{at}gate.sinica.edu.tw

{triangledown} Published ahead of print on 8 February 2008.

{dagger} Supplemental material for this article may be found at http://jb.asm.org/.

Journal of Bacteriology, April 2008, p. 2841-2850, Vol. 190, No. 8
0021-9193/08/$08.00+0     doi:10.1128/JB.01775-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



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