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Clonal basis for resurgence of serious Streptococcus pyogenes disease in the 1980s
P P Cleary1, E L Kaplan, J P Handley
1Department of Microbiology, UMHC, University of Minnesota, Minneapolis 55455.
Abstract:
During the 1980s there was a resurgence of serious Streptococcus pyogenes infections with complications, including rheumatic fever, sepsis, severe soft-tissue invasion, and toxic-shock-like syndrome (TSLS). We have investigated the suggested association between expression of a scarlet fever toxin, SPE A, and systemic toxicity, and the possibility that a new highly virulent clone of S pyogenes has emerged and spread world wide. We studied serotype M1 strains, the serotype most commonly associated with serious complications. 19 isolates from patients with sepsis, with or without TSLS, and 48 from patients with uncomplicated pharyngitis or superficial skin infection were subjected to restriction-enzyme digestion and electrophoresis; 56 isolates (19 serious, 37 uncomplicated disease) were then examined by hybridisation to an speA gene probe. 17 (90%) of the 19 serious-disease isolates had a characteristic ("invasive", I) restriction-fragment profile and were positive for the speA gene. Significantly lower proportions of the isolates from patients with uncomplicated disease had the I profile (21/48 [44%]; p = 0.0035) and speA (20/37 [54%]; p less than 0.001). These findings suggest that the strains from patients with serious disease are a unique clone, which became the predominant cause of severe streptococcal infections in the United States and elsewhere in the late 1980s.
Insights
A specific Streptococcus pyogenes clone, linked to scarlet fever toxin SPE A, emerged in the 1980s. This highly virulent strain caused severe infections like sepsis and toxic-shock-like syndrome (TSLS) globally.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- The 1980s saw a rise in severe Streptococcus pyogenes infections, including sepsis and toxic-shock-like syndrome (TSLS).
- A potential link between the scarlet fever toxin (SPE A) and increased systemic toxicity was investigated.
- The emergence and global spread of a new, highly virulent Streptococcus pyogenes clone were hypothesized.
Purpose of the Study:
- To investigate the association between SPE A toxin expression and systemic toxicity in Streptococcus pyogenes.
- To determine if a new, highly virulent clone of Streptococcus pyogenes emerged and spread worldwide.
- To analyze serotype M1 strains, commonly linked to severe Streptococcus pyogenes complications.
Main Methods:
- Restriction-enzyme digestion and electrophoresis were used to analyze 19 isolates from severe infections and 48 from uncomplicated cases.
- Hybridization with an speA gene probe was performed on 56 isolates (19 severe, 37 uncomplicated).
- Isolates were categorized based on a characteristic "invasive" (I) restriction-fragment profile.
Main Results:
- 17 out of 19 (90%) isolates from serious infections exhibited the "invasive" (I) profile and were speA positive.
- Significantly lower proportions of uncomplicated isolates showed the I profile (44%) and speA gene (54%).
- The "invasive" profile and speA gene presence were strongly associated with severe Streptococcus pyogenes disease (p < 0.001).
Conclusions:
- The findings suggest that severe Streptococcus pyogenes infections in the late 1980s were predominantly caused by a unique, highly virulent clone.
- This clone, characterized by the "invasive" profile and speA gene, became globally prevalent.
- The study highlights the role of specific genetic factors in the virulence of Streptococcus pyogenes.
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