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Updated: May 12, 2026

Constructing Mutants in Serotype 1 Streptococcus pneumoniae strain 519/43
Published on: September 11, 2020
Acquisition of the Sda1-encoding bacteriophage does not enhance virulence of the serotype M1 Streptococcus pyogenes
Carola Venturini1, Cheryl-Lynn Y Ong, Christine M Gillen
1School of Chemistry and Molecular Bioscience and Australian Infectious Diseases Research Centre, The University of Queensland, St. Lucia, QLD, Australia.
Abstract:
The resurgence of invasive disease caused by Streptococcus pyogenes (group A Streptococcus [GAS]) in the past 30 years has paralleled the emergence and global dissemination of the highly virulent M1T1 clone. The GAS M1T1 clone has diverged from the ancestral M1 serotype by horizontal acquisition of two unique bacteriophages, encoding the potent DNase Sda1/SdaD2 and the superantigen SpeA, respectively. The phage-encoded DNase promotes escape from neutrophil extracellular traps and is linked to enhanced virulence of the M1T1 clone. In this study, we successfully used in vitro lysogenic conversion to transfer the Sda1-encoding phage from the M1T1 clonal strain 5448 to the nonclonal M1 isolate SF370 and determined the impact of this horizontal gene transfer event on virulence. Although Sda1 was expressed in SF370 lysogens, no capacity of the phage-converted strain to survive human neutrophil killing, switch to a hyperinvasive covRS mutant form, or cause invasive lethal infection in a humanized plasminogen mouse model was observed. This work suggests that the hypervirulence of the M1T1 clone is due to the unique synergic effect of the M1T1 clone bacteriophage-specific virulence factor Sda1 acting in concert with the M1T1 clone-specific genetic scaffold.
Insights
The highly virulent Streptococcus pyogenes M1T1 clone
Area of Science:
- Microbiology
- Genetics
- Infectious Diseases
Background:
- The invasive Streptococcus pyogenes (group A Streptococcus [GAS]) M1T1 clone has emerged globally.
- This clone acquired bacteriophages encoding DNase Sda1 and superantigen SpeA, enhancing virulence.
Purpose of the Study:
- To investigate the role of the Sda1-encoding phage in GAS virulence.
- To determine if horizontal gene transfer of Sda1 alone confers hypervirulence.
Main Methods:
- Lysogenic conversion used to transfer Sda1-encoding phage from M1T1 strain 5448 to M1 strain SF370.
- Assessed virulence factors including neutrophil evasion, covRS mutation, and lethality in a humanized mouse model.
Main Results:
- Sda1 was expressed in the phage-converted SF370 strain.
- No enhanced neutrophil survival, hyperinvasive covRS mutant formation, or increased lethality was observed.
Conclusions:
- The Sda1-encoding phage alone does not confer hypervirulence to the M1T1 clone.
- Hypervirulence of the M1T1 clone likely results from Sda1 acting synergistically with the M1T1 genetic background.
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