Pentamidine inhibition of streptopain attenuates Streptococcus pyogenes virulence
Keya Trivedi1, Christopher N LaRock2,3,4
1Department of Biology, Emory University, Atlanta, Georgia, USA.
Insights
Researchers found that pentamidine, an existing drug, inhibits streptopain, a key virulence factor in Group A Streptococcus infections. This inhibition makes the bacteria vulnerable to the immune system, offering a new strategy for treating severe GAS diseases.
Area of Science:
- Microbiology
- Infectious Diseases
- Drug Discovery
Background:
- * *Streptococcus pyogenes* (Group A Streptococcus, GAS) causes severe infections with high mortality, especially in resource-poor areas.
- * Conventional antibiotic monotherapy has a high failure rate, necessitating novel therapeutic approaches.
- * The GAS virulence factor streptopain (SpeB) promotes pathogenesis by inducing inflammation, tissue damage, and immune evasion.
Purpose of the Study:
- * To identify novel compounds, including repurposed drugs, that inhibit streptopain activity.
- * To evaluate the anti-virulence potential of identified inhibitors against GAS.
- * To explore new therapeutic strategies for invasive Group A Streptococcus infections.
Main Methods:
- * Screening of 400 diverse off-patent drugs and drug-like compounds for streptopain protease inhibitors.
- * In vitro testing of lead compounds for activity at low concentrations.
- * Assessment of anti-virulence effects during *in vitro* GAS infection models.
Main Results:
- * Pentamidine, an anti-protozoal drug, significantly inhibited streptopain proteolysis.
- * Inhibition of streptopain by pentamidine sensitized GAS to killing by human innate immune cells.
- * Identified inhibitors represent potential starting points for GAS drug discovery and repurposing.
Conclusions:
- * Targeting the GAS virulence factor streptopain is a viable strategy to enhance host immune response.
- * Pentamidine shows promise as an adjunctive therapy for *Streptococcus pyogenes* infections.
- * Repurposing existing drugs like pentamidine offers a novel approach to combat severe GAS diseases.
Abstract:
The obligate human pathogen Streptococcus pyogenes (also known as GAS; Group A Streptococcus) carries high morbidity and mortality, primarily in impoverished or resource-poor regions. The failure rate of monotherapy with conventional antibiotics is high, and invasive infections by this bacterium frequently require extensive supportive care and surgical intervention. Thus, it is important to find new compounds with adjunctive therapeutic benefits. The conserved secreted protease streptopain (Streptococcal pyogenic exotoxin B; SpeB) directly contributes to disease pathogenesis by inducing pathological inflammation, degrading tissue, and promoting the evasion of antimicrobial host defense proteins. This study screened 400 diverse off-patent drugs and drug-like compounds for inhibitors of streptopain proteolysis. Lead compounds were tested for activity at lower concentrations and anti-virulence activities during in vitro infection. Significant inhibition of streptopain was seen for pentamidine, an anti-protozoal drug approved for the treatment of Pneumocystis pneumonia, leishmaniasis, and trypanosomiasis. Streptopain inhibition rendered GAS susceptible to killing by human innate immune cells. These studies identify unexploited molecules as new starting points for drug discovery and a potential for repurposing existing drugs for the treatment of infections by GAS.IMPORTANCEStreptococcus pyogenes is a common cause of severe invasive infections. Repeated infections can trigger autoimmune diseases such as acute rheumatic fever and rheumatic heart disease. This study examines how targeting a specific, highly conserved virulence factor of the secreted cysteine protease streptopain can sensitize a serious pathogen to killing by the immune system. Manipulating the host-pathogen interaction, rather than attempting to directly kill a microbe, is a promising therapeutic strategy. Notably, its benefits include limiting off-target effects on the microbiota. Streptopain inhibitors, including the antifungal and antiparasitic drug pentamidine as identified in this work, may therefore be useful in the treatment of S. pyogenes infection.
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