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Svahn, I.

Publications and source records attributed to Svahn, I..

2 recordsLinked to original sources

Investigating the intraspecific diversity of Vitis vinifera responses to esca with a physiopathology approach

Woody plant dieback involves complex interactions between pathogens, plant functional traits and environmental conditions. The role of intraspecific variation in functional strategies in shaping susceptibility to dieback remains unclear, despite its importance for understanding plant adaptation to changing environments. We used a common garden containing 46 Vitis vinifera (grapevine) cultivars to test the hypothesis that differences in grapevine susceptibility to esca, a complex vascular disease leading to dieback, result from intraspecific syndromes of leaf gas exchange, wood anatomical and metabolic traits, and microbiome. Cultivars with conservative water use strategies tended to be less susceptible to esca whereas xylem anatomy did not affect esca susceptibility. Across cultivars, symptomatic plants displayed decreases in leaf gas exchange, stem starch storage and theoretical hydraulic conductivity in response to esca. Symptomatic stems accumulated more secondary metabolites (mostly glycosylated flavonoids and terpenes) in highly susceptible than in weakly susceptible genotypes, whereas stem microbial communities were unaffected. This suggests that disease expression is linked to cultivar-specific metabolic responses. Intraspecific variation in physiological strategies contributes to differences in susceptibility to a complex vascular disease. Integrative studies unravelling plant-microorganism-environment interactions are crucial to improve our understanding of complex plant diseases.

plant biology↗

Neutrophils degranulate GAG-containing proteoglycofili, which block Shigella growth and degrade virulence factors

Summary paragraphNeutrophil degranulation plays a central role in their ability to kill pathogens but also to stimulate other immune cells1-3. Here we show that neutrophil degranulation, induced in hypoxia or upon Shigella infection in vitro and in vivo, leads to the release of polymers called neutrophil Proteoglycofili (PGF). PGF are mainly composed of granular proteins (myeloperoxidase, elastase, lactoferrin, cathelicidin, albumin) pre-stored in various types of granules, and chondroitin sulfate. PGF individual fibers have a diameter of 43.9 {+/-} 20.3 nm and. They secreted by viable neutrophils and do not contain DNA, as opposed to NETs which contains also granular proteins, chondroitin sulfate in addition to chromatin, released upon neutrophil disintegration and cell death. We demonstrated that PGF block the growth of Shigella and other bacteria and degrade Shigella virulence factors. The degradation of the chondroitin sulfate polymers with testes hyaluronidases destabilizes PGF ultrastructure and abolishes its antimicrobial activity. Our results provide novel insights in the neutrophil degranulation process and open new doors for the investigation of PGF contribution to cytokines concentration gradient formation and adaptive immune cells activation. Further investigations are required to better appreciate the importance of this "sterile blaster" in infectious or inflammatory diseases.

immunology↗