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Updated: Jul 31, 2026

Capsular Serotyping of Streptococcus pneumoniae Using the Quellung Reaction
Published on: February 24, 2014
Comparative genomic and morphological analyses of capsular and capsular-deficient pneumococcal strains simultaneously
Noriko Takeuchi1, Misako Ohkusu1, Yoko Kusuya2
1Department of Infectious Diseases, Medical Mycology Research Center, Chiba University, Chiba, Japan.
Introduction:
To understand the in-vivo dynamics in pneumococci, investigation into the carriage in patients with invasive pneumococcal disease (IPD) is extremely important.
Methods:
To clarify genomic and morphological differences between pneumococcal strains simultaneously isolated from different sites in a patient with IPD, we conducted comparative analyses of two strains. A capsular strain isolated from the blood and a non-capsular strain isolated from the sputum of a patient with IPD were used.
Results:
The strain isolated from blood was serotype 24B with capsule. The strain isolated from sputum with capsular type 24 genes was non-encapsulated, and genomic analysis revealed an insertion region in the wcxK gene. Its biofilm-forming capacity was higher than that of the capsular strain, as was that of the pspK-positive true non-encapsulated strain. Furthermore, observing the microbe using transmission electron microscopy revealed that the strain isolated from sputum lacked a capsule, like the pspK-positive true non-encapsulated strain.
Conclusions:
Our analysis of the two strains isolated from the blood and sputum of a patient with IPD showed one possible in-vivo morphological change in Streptococcus pneumoniae.
Insights
Investigating pneumococcal strains from invasive pneumococcal disease (IPD) patients revealed a non-encapsulated strain from sputum with enhanced biofilm formation, suggesting in-vivo capsule loss in Streptococcus pneumoniae.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Understanding in-vivo dynamics of pneumococci is crucial for invasive pneumococcal disease (IPD) research.
- Investigating pneumococcal carriage in IPD patients provides insights into disease progression.
Purpose of the Study:
- To compare genomic and morphological differences between pneumococcal strains from different sites within an IPD patient.
- To investigate potential in-vivo morphological changes in Streptococcus pneumoniae.
Main Methods:
- Comparative genomic and morphological analysis of two pneumococcal strains (capsular from blood, non-capsular from sputum) from an IPD patient.
- Genomic analysis focused on the wcxK gene and insertion regions.
- Biofilm-forming capacity assessment.
- Transmission electron microscopy for capsule visualization.
Main Results:
- The blood isolate was a capsular serotype 24B strain.
- The sputum isolate was non-encapsulated, with genomic analysis revealing an insertion in the wcxK gene.
- The non-encapsulated strain exhibited higher biofilm-forming capacity compared to the capsular strain.
- Electron microscopy confirmed the absence of a capsule in the sputum isolate.
Conclusions:
- Comparative analysis of Streptococcus pneumoniae strains from blood and sputum of an IPD patient suggests a possible in-vivo morphological change involving capsule loss.
- The non-encapsulated strain's enhanced biofilm formation may play a role in IPD pathogenesis.
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