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Characterization of Inflammatory Responses During Intranasal Colonization with Streptococcus pneumoniae
Published on: January 17, 2014
Virulence in mice of pneumococcal clonal types with known invasive disease potential in humans
Andreas Sandgren1, Barbara Albiger, Carlos J Orihuela
1Swedish Institute for Infectious Disease Control, Solna, Sweden.
Abstract:
Streptococcus pneumoniae isolates of serotypes 1, 4, 6B, 7F, 14, and 19F belonging to clonal types with known invasive disease potential in humans were used to infect C57BL/6 and BALB/c mice. Most isolates were able to colonize the nasopharynx for 7 days. One serotype 19F isolate of the clonal type ST162 had higher bacterial numbers than other isolates and clonal types of the same serotype. Serotype 4 clones caused the most-severe invasive disease, whereas serotype 1 clones caused low-level bacteremia without disease symptoms. BALB/c mice were more likely than C57BL/6 mice to develop meningitis. Disease kinetics varied significantly between clonal types. Although most induced a robust tumor necrosis factor response, some isolates of serotype 1 and 7F did not, suggesting that invasive disease caused by different clonal types may result in different degrees of host response. Capsular serotype, other clonal properties, and host factors are important for the development of pneumococcal disease.
Insights
Different Streptococcus pneumoniae clones cause varying disease severity and host responses in mice. Serotype 4 clones caused severe invasive disease, while serotype 1 clones caused mild bacteremia, highlighting the importance of clonal type and host factors.
Area of Science:
- Microbiology
- Immunology
- Infectious Diseases
Background:
- Streptococcus pneumoniae causes significant human disease.
- Specific serotypes and clonal types are associated with invasive potential.
- Host factors influence disease development.
Purpose of the Study:
- To investigate the impact of different Streptococcus pneumoniae clonal types on disease development in mice.
- To compare disease severity and host responses between various serotypes and clonal types.
- To explore the role of host genetics in pneumococcal meningitis susceptibility.
Main Methods:
- Infection of C57BL/6 and BALB/c mice with S. pneumoniae isolates of serotypes 1, 4, 6B, 7F, 14, and 19F.
- Assessment of nasopharyngeal colonization, bacterial load, and disease severity.
- Monitoring of host immune responses, including tumor necrosis factor (TNF) production.
- Comparison of disease kinetics and outcomes between different clonal types and mouse strains.
Main Results:
- Most S. pneumoniae isolates colonized the nasopharynx; ST162 (serotype 19F) showed higher bacterial numbers.
- Serotype 4 clones induced the most severe invasive disease, while serotype 1 clones caused minimal bacteremia.
- BALB/c mice exhibited higher susceptibility to meningitis compared to C57BL/6 mice.
- Disease kinetics and TNF responses varied significantly among clonal types, with some serotype 1 and 7F isolates eliciting weak responses.
Conclusions:
- Capsular serotype, clonal properties, and host factors are critical determinants of pneumococcal disease development and severity.
- Distinct clonal types of S. pneumoniae can elicit differential host immune responses.
- Mouse models reveal strain-specific variations in colonization, invasion, and host response to pneumococcal infections.
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