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Staps, T.

Publications and source records attributed to Staps, T..

2 recordsLinked to original sources

Defining the Xanthomonas euvesicatoria type II-secreted effector arsenal: core nutritional functions and effector diversity

O_LIThe type II secretion (T2S) system is conserved across the Xanthomonas lineage, yet its contributions to pathogenicity and secreted protein repertoires are poorly defined. We demonstrate that T2S systems in Xanthomonas pathovars with divergent hosts and lifestyles are required for disease. C_LIO_LIIn planta quantification of cell wall compositional changes during infection by Xanthomonas euvesicatoria (Xe) revealed that T2S-dependent depletion of galacturonic acid occurs during host colonization, providing experimental evidence for T2 effector (T2E)-mediated cell wall remodeling. C_LIO_LIUsing an in planta label-free proteomics approach, we identified two known and 20 new Xe T2Es from tomato apoplast, many with annotated functions in polysaccharide and protein cleavage. Growth assays on plant cell wall extracts and purified substrates revealed T2S-mediated metabolization of plant cell wall polysaccharides and proteins not only by Xe, but also by Xanthomonas axonopodis pv. glycines (Xag) and Xanthomonas campestris pv. campestris (Xcc). Interestingly, comparative sequence analysis revealed that the T2E repertoires have diversified among these pathogens, with differences in protease repertoire being the most pronounced. C_LIO_LIOur methodology establishes a framework for T2E discovery, enabling future functional dissection of this understudied effector class and its crosstalk with other bacterial virulence factors. C_LI

plant biology↗

Mutualist-pathogen co-colonisation modulates phosphoinositide signatures at host intracellular interfaces

The host membrane that surrounds intracellular microbes forms a critical interface influencing whether interactions result in mutualism or pathogenesis. While phosphoinositide identities differ between pathogen and mutualist interface membranes, it is unclear if these are modulated during co-colonisation. To address this, we generated Nicotiana benthamiana plants expressing biosensors for PI4P and PI(4,5)P2 and imaged root colonisation by the pathogenic oomycete Phytophthora palmivora and the mutualistic fungus Funneliformis mosseae. Binary host-microbe interactions revealed distinct patterns: PI(4,5)P2 was tip-enriched at mutualist structures but evenly distributed around pathogen structures, while PI4P was absent from pathogen-associated membranes but present at mutualist interfaces. Strikingly, co-colonisation altered host membrane identity, triggering PI4P recruitment at pathogen haustoria, and enhanced resistance to P. palmivora. These findings reveal that phosphoinositide signatures distinguish pathogenic and mutualistic interfaces and are dynamically remodelled during co-colonisation, likely influencing interaction outcomes. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=105 SRC="FIGDIR/small/661106v1_ufig1.gif" ALT="Figure 1"> View larger version (27K): org.highwire.dtl.DTLVardef@9c0024org.highwire.dtl.DTLVardef@1cd5b98org.highwire.dtl.DTLVardef@138938dorg.highwire.dtl.DTLVardef@15f2633_HPS_FORMAT_FIGEXP M_FIG C_FIG

plant biology↗