Nontypeable pneumococci can be divided into multiple cps types, including one type expressing the novel gene pspK
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Updated: May 22, 2026

Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
In Ho Park1, Kyung-Hyo Kim, Ana Lucia Andrade
1Department of Pathology, School of Medicine, University of Alabama at Birmingham, AL, USA.
Abstract:
Although virulence of Streptococcus pneumoniae is associated with its capsule, some pathogenic S. pneumoniae isolates lack capsules and are serologically nontypeable (NT). We obtained 64 isolates that were identified as NT "pneumococci" (i.e., bacteria satisfying the conventional definition but without the multilocus sequence typing [MLST]-based definition of S. pneumoniae) by the traditional criteria. All 64 were optochin sensitive and had lytA, and 63 had ply. Twelve isolates had cpsA, suggesting the presence of a conventional but defective capsular polysaccharide synthesis (cps) locus. The 52 cpsA-negative isolates could be divided into three null capsule clades (NCC) based on aliC (aliB-like ORF1), aliD (aliB-like ORF2), and our newly discovered gene, pspK, in their cps loci. pspK encodes a protein with a long alpha-helical region containing an LPxTG motif and a YPT motif known to bind human pIgR. There were nine isolates in NCC1 (pspK(+) but negative for aliC and aliD), 32 isolates in NCC2 (aliC(+) aliD(+) but negative for pspK), and 11 in NCC3 (aliD(+) but negative for aliC and pspK). Among 52 cpsA-negative isolates, 41 were identified as S. pneumoniae by MLST analysis. All NCC1 and most NCC2 isolates were S. pneumoniae, whereas all nine NCC3 and two NCC2 isolates were not S. pneumoniae. Several NCC1 and NCC2 isolates from multiple individuals had identical MLST and cps regions, showing that unencapsulated S. pneumoniae can be infectious among humans. Furthermore, NCC1 and NCC2 S. pneumoniae isolates could colonize mice as well as encapsulated S. pneumoniae, although S. pneumoniae with an artificially disrupted cps locus did not. Moreover, an NCC1 isolate with pspK deletion did not colonize mice, suggesting that pspK is critical for colonization. Thus, PspK may provide pneumococci a means of surviving in the nasopharynx without capsule. IMPORTANCE The presence of a capsule is critical for many pathogenic bacteria, including pneumococci. Reflecting the pathogenic importance of the pneumococcal capsule, pneumococcal vaccines are designed to elicit anticapsule antibodies. Additional evidence for the pathogenic importance of the pneumococcal capsule is the fact that in pneumococci all the genes necessary for capsule production are together in one genetic locus, which is called the cps locus. However, there are occasional pathogenic pneumococci without capsules, and how they survive in the host without the capsule is unknown. Here, we show that in these acapsular pneumococci, the cps loci have been replaced with various novel genes and they can colonize mouse nasopharynges as well as capsulated pneumococci. Since the genes that replace the cps loci are likely to be important in host survival, they may show new and/or alternative capsule-independent survival mechanisms used by pneumococci.
Insights
Some Streptococcus pneumoniae strains lack capsules but can still cause infection. These unencapsulated strains, particularly those with the pspK gene, can colonize hosts, suggesting novel survival mechanisms beyond capsule production.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Genetics
Background:
- The capsule of Streptococcus pneumoniae is crucial for virulence, and vaccines target it.
- Some pathogenic S. pneumoniae isolates are nontypeable (NT) and lack capsules.
- Mechanisms of survival for acapsular S. pneumoniae in hosts remain largely unknown.
Purpose of the Study:
- To investigate the genetic makeup and survival strategies of NT S. pneumoniae isolates.
- To identify novel genes within the capsular polysaccharide synthesis (cps) locus of acapsular strains.
- To determine the role of identified genes, such as pspK, in host colonization.
Main Methods:
- Characterization of 64 NT pneumococcal isolates using traditional criteria, optochin sensitivity, lytA, ply, and cpsA gene detection.
- Division of cpsA-negative isolates into null capsule clades (NCC) based on aliC, aliD, and pspK gene presence.
- Multilocus sequence typing (MLST) to confirm S. pneumoniae identity and analyze genetic relatedness; mouse colonization experiments.
Main Results:
- Fifty-two of 64 isolates were cpsA-negative, categorized into NCC1 (pspK+), NCC2 (aliC+ aliD+), and NCC3 (aliD+).
- Forty-one cpsA-negative isolates were confirmed as S. pneumoniae by MLST; NCC1 and most NCC2 isolates were S. pneumoniae.
- NCC1 and NCC2 S. pneumoniae colonized mice similarly to encapsulated strains; pspK was critical for colonization in NCC1.
Conclusions:
- Acapsular S. pneumoniae can possess alternative genes in their cps loci, such as pspK, enabling host survival.
- The pspK gene appears essential for nasopharyngeal colonization in some unencapsulated S. pneumoniae strains.
- These findings reveal capsule-independent survival mechanisms in S. pneumoniae, potentially offering new therapeutic targets.
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