Single Amino Acid Replacements in RocA Disrupt Protein-Protein Interactions To Alter the Molecular Pathogenesis of Group A Streptococcus

Author:

Bernard Paul E.12ORCID,Duarte Amey1,Bogdanov Mikhail3,Musser James M.14,Olsen Randall J.124

Affiliation:

1. Center for Molecular and Translational Human Infectious Disease Research, Department of Pathology and Genomic Medicine, Houston Methodist Research Institute and Houston Methodist Hospital, Houston, Texas, USA

2. Texas A&M Health Science Center College of Medicine, Bryan, Texas, USA

3. Department of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, Texas, USA

4. Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA

Abstract

Group A Streptococcus (GAS) is a human-specific pathogen and major cause of disease worldwide. The molecular pathogenesis of GAS, like many pathogens, is dependent on the coordinated expression of genes encoding different virulence factors. The c ontrol o f v irulence r egulator/ s ensor (CovRS) two-component system is a major virulence regulator of GAS that has been extensively studied. More recent investigations have also involved r egulator o f C ov (RocA), a regulatory accessory protein to CovRS.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

American Heart Association

Fondren Foundation

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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