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. 2017 Feb 28:8:294.
doi: 10.3389/fmicb.2017.00294. eCollection 2017.

Prevalence of M75 Streptococcus pyogenes Strains Harboring slaA Gene in Patients Affected by Pediatric Obstructive Sleep Apnea Syndrome in Central Italy

Elisa Viciani  1 , Francesca Montagnani  2 , Giacinta Tordini  3 , Antonio Romano  4 , Lorenzo Salerni  4 , Andrea De Luca  2 , Paolo Ruggiero  5 , Andrea G O Manetti  5
Affiliations

Prevalence of M75 Streptococcus pyogenes Strains Harboring slaA Gene in Patients Affected by Pediatric Obstructive Sleep Apnea Syndrome in Central Italy

Elisa Viciani et al. Front Microbiol. .

Abstract

Recently we reported an association between pediatric obstructive sleep apnea syndrome (OSAS) and Group A streptococcus (GAS) sub-acute chronic tonsil colonization. We showed that GAS may contribute to tonsil hyperplasia via a streptolysin O (SLO)-dependent cysteinyl leukotrienes (CysLTs) production, which can trigger T and B cell proliferation. In the present study, we characterized the GAS strains isolated from pediatric OSAS patients in comparison with a panel of age and sex matched GAS strains unrelated to OSAS, but isolated in the same area and during the same period ranging from 2009 to 2013. We found that slaA gene, previously reported to be associated to CysLTs production pathway, was significantly associated to GAS OSAS strains. Moreover, the most numerous group (32%) of the GAS OSAS strains belonged to M75 type, and 6 out of 7 of these strains harbored the slaA gene. Multilocus Sequence Typing (MLST) experiments demonstrated that the clone emm75/ST49/ smeZ, slaA was associated to OSAS cases. In conclusion, we found an association between slaA gene and the GAS OSAS strains, and we showed that the clone emm75/ST49 harboring genes smeZ and slaA was exclusively isolated from patients affected by OSAS, thus suggesting that this genotype might be associated to the pathogenesis of OSAS, although further studies are needed to elucidate the possible role of SlaA in tonsil hypertrophy development.

Keywords: Multilocus Sequence Typing (MLST); Streptococcus pyogenes; molecular epidemiology; obstructive sleep apnea syndrome (OSAS); slaA gene.

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Figures

Figure 1
Figure 1
In vitro expression analysis (real time qRT-PCR), of slaA in GAS OSAS isolates co-cultured with A549 human epithelial lung cells and collected at time 0 (t0) or after 1 h 30 min (t1). The quantity of cDNA for slaA gene was normalized to the quantity of gyrA cDNA in each RNA sample. The reported values, expressed as fold changes, are the means ± standard errors from three independently isolated RNA preparations analyzed in triplicate. *p < 0.05, **p < 0.01, Unpaired t-test.
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