| Literature DB >> 32937658 |
Justin S Bae1, Fei Da1, Ryan Liu1, Lei He2, Huiying Lv2, Emilie L Fisher1, Govindarajan Rajagopalan3, Min Li2, Gordon Y C Cheung1, Michael Otto1.
Abstract
Staphylococcal enterotoxin B (SEB), which is produced by the major human pathogen, Staphylococcus aureus, represents a powerful superantigenic toxin and is considered a bioweapon. However, the contribution of SEB to S. aureus pathogenesis has never been directly demonstrated with genetically defined mutants in clinically relevant strains. Many isolates of the predominant Asian community-associated methicillin-resistant S. aureus lineage sequence type (ST) 59 harbor seb, implying a significant role of SEB in the observed hypervirulence of this lineage. We created an isogenic seb mutant in a representative ST59 isolate and assessed its virulence potential in mouse infection models. We detected a significant contribution of seb to systemic ST59 infection that was associated with a cytokine storm. Our results directly demonstrate that seb contributes to S. aureus pathogenesis, suggesting the value of including SEB as a target in multipronged antistaphylococcal drug development strategies. Furthermore, they indicate that seb contributes to fatal exacerbation of community-associated methicillin-resistant S. aureus infection. Published by Oxford University Press for the Infectious Diseases Society of America 2020.Entities:
Keywords: zzm321990 Staphylococcus aureuszzm321990 ; CA-MRSA; ST59; cytokine storm; sepsis; staphylococcal enterotoxin B; superantigen
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Year: 2021 PMID: 32937658 PMCID: PMC8161638 DOI: 10.1093/infdis/jiaa584
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226