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Biology subjects

Walker, H. A.

Publications and source records attributed to Walker, H. A..

2 recordsLinked to original sources

Tissue osmotic surveillance shapes susceptibility of zebrafish to wound infections

Wounds represent compromised tissues that are susceptible to opportunistic infections. Tissue factors predisposing to wound infection include edema, poor vascularity, tissue hypoxia, necrosis, and wound size. However, it is unclear whether factors external to the tissue play a role. Detection of osmolarity imbalances between internal and external environment has been shown to alter epithelial wound closure and immune cell recruitment at injury sites. However, it remains unclear whether these osmotic surveillance pathways affect susceptibility to pathogenic wound infections. Here, we use live imaging and disease monitoring in zebrafish larvae to understand susceptibility of wound infection towards Pseudomonas aeruginosa. We show that exposure of wounds to isotonic solution results in enhanced susceptibility and pathogen burden. Furthermore, we demonstrate that this higher propensity for infection depends on osmolarity-mediated changes in wound sealing and neutrophil recruitment during the early stages of the wound response. These findings inform the design of experimental wound infection models as well as the clinical management of wounds.

cell biology↗

In form for a swarm: programmable neutrophil swarming impacts infection outcome

Many migrating cells pattern signalling molecules to support their accumulation in target tissues. During inflammation, neutrophils achieve rapid swarming at sites of injury or infection by generating spatiotemporal gradients of chemoattractants. Whether these self-generated behaviours can be re-programmed to change disease course is unclear. Here, we show that neutrophil chemoattractant patterning machinery is subject to transcriptional reprogramming after microbial experience, leading to enhanced swarming and control of infection at subsequent wound sites in zebrafish. Through in vitro assays, we demonstrate that "trained swarming phenotypes" are cell-intrinsic and independent of the nature of the microbial target. Furthermore, genetic enhancement of 5-lipoxygenase in neutrophils is sufficient to improve neutrophil swarming and resistance to wound infection. Through mathematical modelling, we demonstrate that neutrophil-intrinsic alterations in chemoattractant release are sufficient to recapitulate trained swarming in infection-experienced animals. Together, these data suggest new routes for reprogramming cell migration in disease settings, via manipulating their ability to shape chemoattractant landscapes.

immunology↗