AI Article Synopsis

  • Pseudomonas aeruginosa, a common cause of hospital infections, often shows resistance to many antibiotics, complicating treatment.
  • A study found that administering 3-methyladenine (3-MA) intravenously before infection improves survival in a mouse model by reducing bacterial load and inflammation, without relying on neutrophil recruitment.
  • The protective effects of 3-MA are linked to enhanced neutrophil killing ability, highlighting its potential for new therapeutic strategies against P. aeruginosa-induced pneumonia.

Article Abstract

Pseudomonas aeruginosa is one of the leading causes of nosocomial infections worldwide. Clinical isolates that are resistant to multiple antimicrobials make it intractable. The interactions between P. aeruginosa and host cell death have multiple effects on bacterial clearance and inflammation; however, the potential intervention effects remain to be defined. Herein, we demonstrated that intravenous administration of 3-methyladenine before, but not after, P. aeruginosa infection enhanced autophagy-independent survival, which was accompanied by a decrease in the bacterial load, alleviation of pathology and reduction in inflammatory cytokines, in an acute pneumonia mouse model. Interestingly, these beneficial effects were not dependent on neutrophil recruitment or phagocytosis, but on the enhanced killing capacity induced by inhibiting the cell death of 3-MA pretreated neutrophils. These findings demonstrate a novel protective role of 3-MA pretreatment in P. aeruginosa-induced acute pneumonia.

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Source
http://dx.doi.org/10.1016/j.ijmm.2023.151574DOI Listing

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