Role of the Mycoplasma pneumoniae/Interleukin-8/Neutrophil Axis in the Pathogenesis of Pneumonia

PLoS One. 2016 Jan 11;11(1):e0146377. doi: 10.1371/journal.pone.0146377. eCollection 2016.

Abstract

Neutrophil infiltration is the characteristic pathological feature of M. pneumoniae pneumonia (MPP). This study aimed to explore the associations among neutrophil activity, clinical presentation, and role of the M. pneumoniae/interleukin-8 (IL-8)/neutrophil axis in the pathogenesis of MPP. A total of 42 patients with MPP were prospectively enrolled in the study. Neutrophil activity, including matrix metalloproteinase-9 (MMP-9), myeloperoxidase (MPO), and neutrophil elastase (NE), were measured. Clinical information was collected for all patients and control group. In vitro, IL-8 production was measured at different time points after M. pneumoniae infection of bronchial epithelial cells, and neutrophil activity was analyzed after IL-8 stimulation. The percentage of neutrophil in the bronchoalveolar lavage fluid was higher in the group of patients with high levels of M. pneumoniae DNA than in those with low levels of M. pneumoniae DNA (P < 0.05). IL-8, MMP-9, and NE in patients with MPP significantly increased compared with controls and decreased after treatment (P < 0.05). MPO and MMP-9 were associated with duration of fever (r = 0.332, P < 0.05) and length of stay (r = 0.342, P < 0.05), respectively. In vitro, M. pneumoniae induced IL-8 production by bronchial epithelial cells in a time dependent manner. MPO, MMP-9 and NE production by neutrophils significantly increased compared with medium controls after IL-8 stimulation. In summary, the M. pneumoniae/IL-8/neutrophil axis likely plays a vital role in the pathogenesis of MPP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Child, Preschool
  • Female
  • Humans
  • Interleukin-8 / genetics
  • Interleukin-8 / metabolism*
  • Leukocyte Elastase / genetics
  • Leukocyte Elastase / metabolism
  • Male
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • Mycoplasma pneumoniae / pathogenicity*
  • Neutrophil Infiltration / genetics
  • Neutrophil Infiltration / physiology
  • Peroxidase / genetics
  • Peroxidase / metabolism
  • Pneumonia, Mycoplasma / metabolism
  • Pneumonia, Mycoplasma / microbiology*
  • Prospective Studies

Substances

  • CXCL8 protein, human
  • Interleukin-8
  • Peroxidase
  • Leukocyte Elastase
  • Matrix Metalloproteinase 9

Grants and funding

This work was supported by the National Natural Science Foundation of China (Zhengrong Chen, grant number 81401296; Wei Ji, grant number 81570016), Science and Technology Projects for the youth of Suzhou (Zhengrong Chen, grant number KJXW2012019), and Suzhou Science and Technology Projects (Zhengrong Chen, grant number SYS201350; Yongdong Yan, grant number SYS201435), Science and Technology Projects of Suzhou sanitary bureau (Yongdong Yan, grant number lczx201409). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.