Abstract
Xanthomonas axonopodis pv. citri, the phytopathogen responsible for citrus canker has a number of protein secretion systems and among them, at least one type V protein secretion system belonging to the two-partner secretion pathway. This system is mainly associated to the translocation of large proteins such as adhesins to the outer membrane of several pathogens. Xanthomonas axonopodis pv. citri possess a filamentous hemagglutinin-like protein in close vicinity to its putative transporter protein, XacFhaB and XacFhaC, respectively. Expression analysis indicated that XacFhaB was induced in planta during plant-pathogen interaction. By mutation analysis of XacFhaB and XacFhaC genes we determined that XacFhaB is involved in virulence both in epiphytic and wound inoculations, displaying more dispersed and fewer canker lesions. Unexpectedly, the XacFhaC mutant in the transporter protein produced an intermediate virulence phenotype resembling wild type infection, suggesting that XacFhaB could be secreted by another partner different from XacFhaC. Moreover, XacFhaB mutants showed a general lack of adhesion and were affected in leaf surface attachment and biofilm formation. In agreement with the in planta phenotype, adhesin lacking cells moved faster in swarming plates. Since no hyperflagellation phenotype was observed in this bacteria, the faster movement may be attributed to the lack of cell-to-cell aggregation. Moreover, XacFhaB mutants secreted more exopolysaccharide that in turn may facilitate its motility. Our results suggest that this hemagglutinin-like protein is required for tissue colonization being mainly involved in surface attachment and biofilm formation, and that plant tissue attachment and cell-to-cell aggregation are dependent on the coordinated action of adhesin molecules and exopolysaccharides.
Highlights
Protein secretion in gram-negative bacteria is accomplished by different pathways that are highly conserved in bacterial species
Pattern and profile searches revealed that the XacFhaB two-partner secretion (TPS) domain is followed by a number of conserved repeats predicted to form a repetitive b-strand structure, a feature shared with other TpsA proteins
In this study we analyzed the role of FhaB and FhaC, components of the two partner secretion system in the interaction between X. axonopodis pv. citri and orange, its host plant
Summary
Protein secretion in gram-negative bacteria is accomplished by different pathways that are highly conserved in bacterial species. The well studied filamentous hemagglutinin (FHA) protein of the whooping cough agent Bordetella pertussis is a 230-kDa adhesin, named FhaB, is secreted by the other TPS partner FhaC, standing for TpsA and TpsB, respectively [5]. The domain core is folded into a right-handed parallel b-helix of nine coils that comprises three helical b–sheets [4]. Sequence comparison of this domain from different animal and plant pathogens revealed two conserved regions (C) and two less conserved regions (LC) in an alternating organization LC1– C1–LC2–C2 [4]. The results suggested that the most likely model for the mature protein would be that of an elongated b-helix in which the b-helical fold continues beyond the TPS domain [6]
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