The Type III-Dependent Hrp Pilus Is Required for Productive Interaction of Xanthomonas campestris pv. vesicatoria with Pepper Host Plants

• DOI: 10.1128/jb.187.7.2458-2468.2005
• Publication Date: 2005-03-17T21:41:33Z
• Authors: Ernst Weber; Tuula Ojanen-Reuhs; Elisabeth Huguet; Gerd Hause; Martin Romantschuk; Timo K. Korhonen; Ulla Bonas; Ralf Koebnik
• Keywords: 0303 health sciences; Base Sequence; Protein Conformation; Molecular Sequence Data; Xanthomonas campestris; [SDV] Life Sciences [q-bio]; Plant Leaves; 03 medical and health sciences; Bacterial Proteins; Fimbriae, Bacterial; Multigene Family; Consensus Sequence; Mutation; Amino Acid Sequence; Capsicum; Sequence Alignment; Plant Diseases

ABSTRACT

The plant pathogenic bacterium Xanthomonas campestris pv. vesicatoria expresses a type III secretion system that is necessary for both pathogenicity in susceptible hosts and the induction of the hypersensitive response in resistant plants. This specialized protein transport system is encoded by a 23-kb hrp (hypersensitive response and pathogenicity) gene cluster. Here we show that X. campestris pv. vesicatoria produces filamentous structures, the Hrp pili, at the cell surface under hrp -inducing conditions. Analysis of purified Hrp pili and immunoelectron microscopy revealed that the major component of the Hrp pilus is the HrpE protein which is encoded in the hrp gene cluster. Sequence homologues of hrpE are only found in other xanthomonads. However, hrpE is syntenic to the hrpY gene from another plant pathogen, Ralstonia solanacearum . Bioinformatic analyses suggest that all major Hrp pilus subunits from gram-negative plant pathogens may share the same structural organization, i.e., a predominant alpha-helical structure. Analysis of nonpolar mutants in hrpE demonstrated that the Hrp pilus is essential for the productive interaction of X. campestris pv. vesicatoria with pepper host plants. Furthermore, a functional Hrp pilus is required for type III-dependent protein secretion. Immunoelectron microscopy revealed that type III-secreted proteins, such as HrpF and AvrBs3, are in close contact with the Hrp pilus during and/or after their secretion. By systematic analysis of nonpolar hrp / hrc ( hrp conserved) and hpa ( hrp associated) mutants, we found that Hpa proteins as well as the translocon protein HrpF are dispensable for pilus assembly, while all other Hrp and Hrc proteins are required. Hence, there are no other conserved Hrp or Hrc proteins that act downstream of HrpE during type III-dependent protein translocation.