Circulating mitochondrial N-formyl peptides contribute to secondary nosocomial infection in patients with septic

Woon Yong Kwon1,2, Gil Joon Suh3,2, Yoon Sun Jung2

  • 1Department of Emergency Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; kwy711@hanmail.net.

Insights

High levels of circulating mitochondrial N-formyl peptides (mtFPs), specifically nicotinamide adenine dinucleotide dehydrogenase subunit-6 (ND6), are linked to secondary infections and mortality in septic shock patients. ND6 suppresses neutrophil migration, increasing infection risk.

Area of Science:

  • Immunology
  • Critical Care Medicine
  • Molecular Biology

Background:

  • Secondary infections significantly worsen outcomes for patients recovering from septic shock.
  • Neutrophil (polymorphonuclear leukocytes, PMNs) migration is crucial in preventing the progression from local bacterial inoculation to systemic secondary infection.
  • Mitochondrial N-formyl peptides (mtFPs) binding to formyl peptide receptor-1 (FPR1) can suppress PMN chemotaxis.

Purpose of the Study:

  • To investigate the association between circulating mtFPs and the development of secondary infections in septic shock patients.
  • To analyze the impact of circulating nicotinamide adenine dinucleotide dehydrogenase subunit-6 (ND6) on clinical outcomes and PMN chemotaxis.

Main Methods:

  • Clinical data and plasma samples were collected from 97 intensive care unit patients with septic shock (ICU stay > 72 hours).
  • Circulating ND6 levels were measured at admission.
  • Ex vivo experiments using isolated human PMNs assessed ND6's role in chemotaxis.

Main Results:

  • Elevated circulating ND6 levels at admission were independently associated with a higher risk of secondary infection (OR=30.317, P=0.004) and increased 90-day mortality (OR=1.572, P=0.049).
  • ND6 pretreatment suppressed FPR1-mediated PMN chemotaxis to bacterial peptides in vitro, despite increasing random PMN movement.
  • These findings suggest ND6 impairs directed neutrophil migration.

Conclusions:

  • Circulating mtFPs, particularly ND6, contribute to secondary infection development and mortality in septic shock survivors.
  • Suppression of FPR1-mediated PMN chemotaxis by ND6 likely underlies increased susceptibility to secondary infections.
  • Targeting mtFP-FPR1 interactions may offer therapeutic strategies to mitigate secondary infections in septic shock.