Pretreatment of epithelial cells with live Streptococcus pneumoniae has no detectable effect on influenza A virus

Kang Ouyang1, Shireen A Woodiga2, Varun Dwivedi3

  • 1College of Animal Science and Technology, Guangxi University, Nanning, China; Food Animal Health Research Program (FAHRP), OARDC, Department of Veterinary Preventive Medicine, The Ohio State University, Wooster, Ohio, United States of America.

Plos One
|March 6, 2014
PubMed

Insights

Streptococcus pneumoniae (pneumococcus) did not directly affect influenza A virus (IAV) replication in epithelial cells in vitro at lower concentrations. Higher pneumococcal concentrations led to cell death, obscuring potential effects on IAV.

Area of Science:

  • Microbiology
  • Virology
  • Immunology

Background:

  • Influenza A virus (IAV) and Streptococcus pneumoniae (pneumococcus) are key upper respiratory tract pathogens.
  • Coinfection with these pathogens often leads to exacerbated disease.
  • The direct impact of S. pneumoniae on IAV replication in vitro remains largely unknown.

Purpose of the Study:

  • To investigate the direct effect of S. pneumoniae on IAV replication in epithelial cells.
  • To determine if S. pneumoniae influences IAV replication in vitro.

Main Methods:

  • Utilized four IAV-permissive epithelial cell lines, including human-derived ones.
  • Employed 12 pneumococcal strains and six IAV strains.
  • Assessed IAV replication using a standard immunofluorescence assay (IFA).

Main Results:

  • Pretreatment of MDCK cells with high concentrations (7.5×10^6 CFUs) of live S. pneumoniae caused time-dependent cell death.
  • Lower concentrations (≤7.5×10^5 CFUs) of S. pneumoniae showed no detectable effect on cell morphology or IAV replication.
  • The study did not observe a direct effect of S. pneumoniae on IAV replication in vitro.

Conclusions:

  • S. pneumoniae did not directly enhance or inhibit IAV replication in epithelial cell lines at tested concentrations.
  • High bacterial loads of S. pneumoniae induce cell death, complicating the assessment of direct viral effects.
  • In vivo coinfections may differ due to host factors influencing pathogen interactions.

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