The type III protein secretion system contributes to Xanthomonas citri subsp. citri biofilm formation
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Sgro, Germán G
Garofalo, Cecilia G
Ficarra, Florencia A
Gehring, Christoph A
KAUST DepartmentBiological and Environmental Sciences and Engineering (BESE) Division
Bioscience Core Lab
Molecular Signalling Group
Online Publication Date2014-04-18
Print Publication Date2014
Permanent link to this recordhttp://hdl.handle.net/10754/325248
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AbstractBackground: Several bacterial plant pathogens colonize their hosts through the secretion of effector proteins by a Type III protein secretion system (T3SS). The role of T3SS in bacterial pathogenesis is well established but whether this system is involved in multicellular processes, such as bacterial biofilm formation has not been elucidated. Here, the phytopathogen Xanthomonas citri subsp. citri (X. citri) was used as a model to gain further insights about the role of the T3SS in biofilm formation. Results: The capacity of biofilm formation of different X. citri T3SS mutants was compared to the wild type strain and it was observed that this secretion system was necessary for this process. Moreover, the T3SS mutants adhered proficiently to leaf surfaces but were impaired in leaf-associated growth. A proteomic study of biofilm cells showed that the lack of the T3SS causes changes in the expression of proteins involved in metabolic processes, energy generation, exopolysaccharide (EPS) production and bacterial motility as well as outer membrane proteins. Furthermore, EPS production and bacterial motility were also altered in the T3SS mutants. Conclusions: Our results indicate a novel role for T3SS in X. citri in the modulation of biofilm formation. Since this process increases X. citri virulence, this study reveals new functions of T3SS in pathogenesis. 2014 Zimaro et al.; licensee BioMed Central Ltd.
CitationZimaro T, Thomas L, Marondedze C, Sgro GG, Garofalo CG, et al. (2014) The type III protein secretion system contributes to Xanthomonas citri subsp. citri biofilm formation. BMC Microbiology 14: 96. doi:10.1186/1471-2180-14-96.
PubMed Central IDPMC4021560
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