The Pseudomonas aeruginosa lectin LecB modulates intracellular reactive oxygen species production in human neutrophils
Artikel i vetenskaplig tidskrift, 2024

Pseudomonas aeruginosa is a Gram-negative bacterium and an opportunistic pathogen ubiquitously present throughout nature. LecB, a fucose-, and mannose-binding lectin, is a prominent virulence factor of P. aeruginosa, which can be expressed on the bacterial surface but also be secreted. However, the LecB interaction with human immune cells remains to be characterized. Neutrophils comprise the first line of defense against infections and their production of reactive oxygen species (ROS) and release of extracellular traps (NETs) are critical antimicrobial mechanisms. When profiling the neutrophil glycome we found several glycoconjugates on granule and plasma membranes that could potentially act as LecB receptors. In line with this, we here show that soluble LecB can activate primed neutrophils to produce high levels of intracellular ROS (icROS), an effect that was inhibited by methyl fucoside. On the other hand, soluble LecB inhibits P. aeruginosa-induced icROS production. In support of that, during phagocytosis of wild-type and LecB-deficient P. aeruginosa, bacteria with LecB induced less icROS production as compared with bacteria lacking the lectin. Hence, LecB can either induce or inhibit icROS production in neutrophils depending on the circumstances, demonstrating a novel and potential role for LecB as an immunomodulator of neutrophil functional responses.

host-pathogen interaction

NETs

glycan-binding proteins

immunomodulation

phagocytes

Författare

Felix Sanchez Klose

Chalmers, Life sciences, Kemisk biologi

Agnes Dahlstrand Rudin

Göteborgs universitet

Linda Bergqvist

Göteborgs universitet

Julia M. Scheffler

Göteborgs universitet

Katarina Jönsson

Göteborgs universitet

Ulrika Islander

Göteborgs universitet

Anna Karlsson-Bengtsson

Chalmers, Life sciences

Göteborgs universitet

Johan Bylund

Göteborgs universitet

Vignesh Venkatakrishnan

Chalmers, Life sciences, Kemisk biologi

European Journal of Immunology

0014-2980 (ISSN) 1521-4141 (eISSN)

Vol. 54 2 2350623

Glykosylering i humana neutrofiler vid sepsis och systemisk inflammation

Vetenskapsrådet (VR) (2018-03077), 2019-01-01 -- 2024-12-31.

Ämneskategorier

Mikrobiologi inom det medicinska området

DOI

10.1002/eji.202350623

PubMed

37972111

Mer information

Senast uppdaterat

2024-03-07