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Similarities and Differences Between Staphylococcal and Streptococcal Toxic Shock Syndromes in Children: Results From
Etienne Javouhey1,2, Pierre-Adrien Bolze3, Claire Jamen1
1Pediatric Emergency and Critical Care Unit, Hospices Civils de Lyon, Hôpital Femme Mère Enfant, Bron, France.
Insights
Comparing staphylococcal and streptococcal toxic shock syndromes (TSS) in children reveals distinct clinical signs and origins. Streptococcal TSS showed more severe organ dysfunction and higher mortality risk, highlighting the need for early diagnosis and specific treatments.
Area of Science:
- Pediatric Infectious Diseases
- Toxicology
- Immunology
Background:
- Toxic shock syndromes (TSS) are severe, life-threatening conditions caused by staphylococcal or streptococcal infections.
- Early recognition and specific treatments are critical for improving outcomes in pediatric TSS cases.
- Understanding differences between staphylococcal and streptococcal TSS can aid in developing diagnostic criteria.
Purpose of the Study:
- To compare the clinical characteristics and outcomes of staphylococcal and streptococcal TSS in children.
- To identify potential early clinical diagnostic criteria for differentiating between the two types of TSS.
- To analyze toxin gene profiles and the utility of Vβ T-cell signatures for diagnosis.
Main Methods:
- Multicenter retrospective evaluation of clinical data, biological results, and treatment outcomes.
- Inclusion of children with confirmed or probable staphylococcal or streptococcal TSS admitted to pediatric intensive care units.
- Analysis of toxin gene profiles of isolated strains and Vβ T-cell signatures.
Main Results:
- Streptococcal TSS cases exhibited significantly higher organ dysfunction scores and required more frequent respiratory support compared to staphylococcal TSS.
- Lack of antitoxin therapy was associated with a higher case-fatality rate in pediatric TSS.
- Specific toxin gene profiles (CC30 for *Staphylococcus aureus*, emm1 for *Streptococcus pyogenes*) suggest clonal etiologies for both TSS types.
Conclusions:
- Staphylococcal and streptococcal TSS present with distinct clinical signs, infection origins, and prognoses, despite similar toxin mechanisms.
- Vβ T-cell signature detection proved useful for confirming TSS diagnoses and identifying involved toxins.
- Findings support the need for tailored diagnostic and therapeutic strategies based on the causative pathogen.
Abstract:
Introduction: Toxic shock syndromes (TSS) are severe shocks due to staphylococcal or streptococcal infection that require specific treatments. The early recognition of these shocks is crucial to improve their outcomes. Objectives: The primary objective of this study was to compare characteristics and outcomes of staphylococcal and streptococcal TSS in children, in order to identify putative early clinical diagnostic criteria. Secondary objectives were to determine the toxin gene profiles of associated isolated strains and the relevance of measuring Vβ T-cell signatures to confirm the diagnosis. Study design: We performed a multicenter retrospective evaluation of clinical data, biological results, and treatment outcomes of children with a confirmed or probable case of staphylococcal or streptococcal TSS. Children were consecutively included if they were admitted to the pediatric intensive care units of Lyon (France), between January 2005 and July 2011. Results: Among the 30 analyzed children, 15 presented staphylococcal TSS and 15 streptococcal TSS. The most frequent origin of staphylococcal and streptococcal TSS was the lower respiratory tract (53%) and the genital tract (47%) respectively. Non-menstrual TSS syndrome cases presented more frequently with neurological alterations, and digestive signs were predominant in menstrual forms. Compared to Staphylococcal TSS, Streptococcal TSS presented with higher organ dysfunction scores (median Pediatric Index of Mortality 2 score 20.9 (4.1-100) vs. 1.7 (1.3-2.3), p = 0.001), required respiratory support more frequently (80 vs. 33%, p = 0.02), were intubated for a longer time (3 days (0.75-5) vs. 1 day (0-1.5), p = 0.006) and had a non-significant trend of higher, case-fatality rate (20 vs. 7%, p = 0.60). The lack of antitoxin therapy was associated with higher case-fatality rate (50 vs. 4%, p = 0.04). The Vβ repertoire measurements exhibited toxin dependent-alterations in accordance with the toxin gene profiles of isolated strains in both types of toxic shock syndromes. Regarding toxin gene profiles of isolated strains, 10/15 Staphylococcus aureus belonged to clonal complex (CC) 30 and 6/12 Streptococcus pyogenes were emm1 type suggesting clonal etiologies for both staphylococcal and streptococcal TSS. Conclusion: Despite the involvement of functionally similar toxins, staphylococcal and streptococcal TSS differed by their clinical signs, origin of infection and prognosis. The detection of Vβ profiles was useful to confirm the diagnosis of staphylococcal and streptococcal TSS and for the identification of involved toxins.
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