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Updated: May 25, 2026

Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
Characterization of nontypeable and atypical Streptococcus pneumoniae pediatric isolates from 1994 to 2010
Jessica Ing1, Edward O Mason, Sheldon L Kaplan
1Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Abstract:
Streptococcus pneumoniae is a major cause of bacteremia, meningitis, pneumonia, sinusitis, and acute otitis media in children. Although optochin susceptibility, bile solubility, and Quellung testing are the standards for identifying and differentiating pneumococci, there are several reports of nontypeable pneumococci that give inconsistent results with one or more of these tests. We characterized 52 isolates previously labeled as nontypeable pneumococci. Microbiological methods included repeating the Quellung reaction using a new and expanded group of antisera, optochin susceptibility and bile solubility tests, and automated Vitek 2 identification. Molecular methods included PCR detection of ply and psaA genes, multilocus sequence typing (MLST), 16S rRNA gene sequencing, and pyrosequencing. Of the 52 isolates, 38 (73%) were optochin susceptible, were psaA and ply positive, and could be serotyped by the Quellung reaction. The remaining 14 isolates, isolated from patients with otitis media (n = 6), bacteremia (n = 6), meningitis (n = 1), and pneumonia (n = 1), underwent further analysis. Three of these 14 isolates were nontypeable due to autoagglutination but were pneumococci by all tests and represented pneumococcal sequence types previously recognized by MLST. The 11 remaining isolates were optochin resistant, and 6 of these were bile soluble. Three of 11 were both psaA and ply positive and clustered with pneumococci by MLST (2 were bile soluble); 8 lacked psaA (5 ply positive, 4 bile soluble) and likely belonged to other Streptococcus species. In conclusion, few isolates were truly nontypeable by Quellung reaction, and MLST and the presence of psaA proved useful in distinguishing between atypical pneumococci and other streptococcal species.
Insights
Nontypeable Streptococcus pneumoniae isolates were re-evaluated. Most were confirmed pneumococci, with molecular methods like MLST proving crucial for accurate identification and differentiation from other Streptococcus species.
Area of Science:
- Microbiology
- Molecular Biology
- Clinical Diagnostics
Background:
- Streptococcus pneumoniae causes severe childhood infections.
- Traditional identification methods (optochin, bile solubility, Quellung) can be unreliable for some pneumococcal strains.
- Nontypeable pneumococci present diagnostic challenges.
Purpose of the Study:
- To re-characterize isolates previously labeled as nontypeable pneumococci.
- To determine the accuracy of standard identification methods versus molecular techniques.
- To differentiate true pneumococci from other Streptococcus species.
Main Methods:
- Re-testing with expanded Quellung antisera, optochin susceptibility, and bile solubility.
- Automated Vitek 2 identification.
- Molecular analyses including PCR for psaA and ply genes, multilocus sequence typing (MLST), 16S rRNA sequencing, and pyrosequencing.
Main Results:
- 73% of isolates were confirmed as typable pneumococci.
- Three isolates were nontypeable due to autoagglutination but confirmed as pneumococci by MLST.
- Eleven isolates were optochin resistant; molecular methods distinguished pneumococci from other Streptococcus species, with psaA and MLST being key differentiators.
Conclusions:
- Few isolates were truly nontypeable by Quellung reaction.
- MLST and psaA gene detection are valuable for distinguishing atypical pneumococci.
- Accurate identification is essential for understanding pneumococcal disease epidemiology and treatment.
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