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Updated: May 2, 2026

Investigating the Effects of Probiotics on Pneumococcal Colonization Using an In Vitro Adherence Assay
Published on: April 28, 2014
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.
Abstract:
Influenza A virus (IAV) and Streptococcus pneumoniae (pneumococcus) are two major upper respiratory tract pathogens responsible for exacerbated disease in coinfected individuals. Despite several studies showing increased susceptibility to secondary bacterial infections following IAV infection, information on the direct effect of S. pneumoniae on IAV in vitro is unknown. This is an important area of investigation as S. pneumoniae is a common commensal of the human upper respiratory tract, present as an important coinfecting pathogen with IAV infection. A recent study showed that S. pneumoniae enhances human metapneumovirus infection in polarized bronchial epithelial cells in vitro. The aim of the current study was to determine whether treatment of epithelial cells with S. pneumoniae affects IAV replication using a standard immunofluorescence assay (IFA). For this study we used four IAV permissive epithelial cell lines including two human-derived cell lines, 12 pneumococcal strains including recent human clinical isolates which represent different genetic backgrounds and serotypes, and six IAV strains of varying genetic nature and pathogenic potential including the pandemic 2009 H1N1 virus. Our results suggested that pretreatment of MDCK cells with 7.5×10(6) colony-forming units (CFUs) of live S. pneumoniae resulted in gradual cell-death in a time-dependent manner (0.5 to 4 hr). But, pretreatment of cell lines with 7.5×10(5) and lower CFUs of S. pneumoniae had no detectable effect on either the morphology of cells or on the IAV replication. However, unlike in epithelial cell lines, due to influence of secreted host factors the effect of pneumococci on IAV replication may be different during coinfections in vivo in the human upper respiratory tract, and in vitro with primary human polarized bronchial epithelial cells.
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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