Understanding the host inflammatory response to wound infection: An in vivo study of K lebsiella pneumoniae in a rabbit ear wound model

作者:Seth Akhil K; Geringer Matthew R; Gurjala Anandev N; Abercrombie Johnathan A; Chen Ping; You Tao; Hong Seok J; Galiano Robert D; Mustoe Thomas A; Leung Kai P*
来源:Wound Repair and Regeneration, 2012, 20(2): 214-225.
DOI:10.1111/j.1524-475X.2012.00764.x

摘要

Wound infection development is critically dependent on the complex interactions between bacteria and host. Klebsiella pneumoniae has become an increasingly common wound pathogen, but its natural history within wounds has never been studied. Using a validated, in vivo rabbit ear model, wounds were inoculated with K.?pneumoniae at different concentrations (102107 colony-forming units) with measurement of viable and nonviable bacterial counts, histological wound-healing parameters, and host inflammatory gene expression at multiple time points postinoculation (48, 96, and 240 hours). Bacteria and wound morphologies were evaluated with scanning electron microscopy. Comparable experiments were performed in ischemic ears to model immune response impairment. All wounds, despite different inoculants, equilibrated to similar bacterial concentrations by 96 hours. With a 106 colony-forming units inoculant, wounds at 240 hours showed decreased bacterial counts (p?<?0.01), with a corresponding improvement in healing (p?<?0.01) and a decrease in inflammatory response (p?<?0.05). In contrast, ischemic wounds revealed impaired inflammatory gene expression (p?<?0.05) resulting in higher steady-state bacterial concentrations (p?<?0.01), impaired healing (p?<?0.05), and biofilm formation on scanning electron microscopy. We conclude that a normal inflammatory response can effectively stabilize and overcome a K.?pneumoniae wound infection. An impaired host cannot control this bacterial burden, preventing adequate healing while allowing bacteria to establish a chronic presence. Our novel study quantitatively validates the host immune response as integral to wound infection dynamics.