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Characterization of Inflammatory Responses During Intranasal Colonization with Streptococcus pneumoniae
Published on: January 17, 2014
Isolation site influences virulence phenotype of serotype 14 Streptococcus pneumoniae strains belonging to multilocus
Zarina Amin1, Richard M Harvey1, Hui Wang1
1Research Centre for Infectious Diseases, Department of Molecular and Cellular Biology, School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Abstract:
Streptococcus pneumoniae is a diverse species causing invasive as well as localized infections that result in massive global morbidity and mortality. Strains vary markedly in pathogenic potential, but the molecular basis is obscured by the diversity and plasticity of the pneumococcal genome. We have previously reported that S. pneumoniae serotype 3 isolates belonging to the same multilocus sequence type (MLST) differed markedly in in vitro and in vivo phenotypes, in accordance with the clinical site of isolation, suggesting stable niche adaptation within a clonal lineage. In the present study, we have extended our analysis to serotype 14 clinical isolates from cases of sepsis or otitis media that belong to the same MLST (ST15). In a murine intranasal challenge model, five ST15 isolates (three from blood and two from ears) colonized the nasopharynx to similar extents. However, blood and ear isolates exhibited significant differences in bacterial loads in other host niches (lungs, ear, and brain) at both 24 and 72 h postchallenge. In spite of these differences, blood and ear isolates were present in the lungs at similar levels at 6 h postchallenge, suggesting that early immune responses may underpin the distinct virulence phenotypes. Transcriptional analysis of lung tissue from mice infected for 6 h with blood isolates versus ear isolates revealed 8 differentially expressed genes. Two of these were exclusively expressed in response to infection with the ear isolate. These results suggest a link between the differential capacities to elicit early innate immune responses and the distinct virulence phenotypes of clonally related S. pneumoniae strains.
Insights
Clonally related Streptococcus pneumoniae strains, specifically serotype 14, show distinct virulence. Differences in early immune responses correlate with varied bacterial loads in host niches, impacting disease severity.
Area of Science:
- Microbiology
- Infectious Diseases
- Genomics
Background:
- Streptococcus pneumoniae causes significant global morbidity and mortality.
- Pneumococcal strain virulence varies due to genome diversity and plasticity.
- Previous studies indicated niche adaptation in clonal lineages of S. pneumoniae serotype 3.
Purpose of the Study:
- To investigate virulence differences in clonally related S. pneumoniae serotype 14 isolates.
- To explore the role of early host immune responses in differential pathogenesis.
- To identify potential molecular mechanisms underlying distinct virulence phenotypes.
Main Methods:
- Utilized a murine intranasal challenge model with S. pneumoniae serotype 14, multilocus sequence type (ST15) isolates from blood and ear infections.
- Quantified bacterial loads in nasopharynx, lungs, ear, and brain at 24 and 72 hours post-infection.
- Performed transcriptional analysis of mouse lung tissue at 6 hours post-infection to assess host gene expression.
Main Results:
- All ST15 isolates colonized the nasopharynx similarly, but blood and ear isolates showed differential bacterial loads in other host niches.
- Similar lung bacterial levels at 6 hours post-infection suggest early immune responses influence subsequent virulence.
- Transcriptional analysis revealed 8 differentially expressed genes, with 2 exclusively expressed in response to ear isolates.
Conclusions:
- Clonally related S. pneumoniae serotype 14 strains exhibit distinct virulence phenotypes.
- Differential early innate immune responses are linked to these distinct virulence capacities.
- Suggests a mechanism for niche adaptation and varied disease outcomes within a clonal lineage.
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