W. Michael McShan, Ph.D.
Phone (405) 271-6593 x47256
Fax (405) 271-7505
Office CPB 307
My research interests focus on the genetics and genomics of group A streptococci (Streptococcus pyogenes), one of the most common bacterial pathogens of humans. Group A streptococcal infections are a leading cause of morbidity worldwide and are responsible for over $3 billion in annual treatment costs in the USA alone.
One project involves the novel control of DNA mismatch repair in S. pyogenes by a temperate bacteriophage (bacterial virus). This mechanism of control has never been observed before in any species and may represent an important system for the rapid acquisition of favorable mutations to allow the organism to escape host defenses or antimicrobial therapy. Genome analysis reveals that other streptococcal genes may be under bacteriophage control, and thus these studies may lead to an increased understanding of the control of many genes that may influence the ability of this bacterium to initiate infections and avoid host defenses.
A second line of investigation looks at the influence of a novel membrane protein on the expression of the extracellular bacterial toxins in S. pyogenes. Much of the damage that results from group A streptococcal infections is caused by the release of these toxin, and understanding the mechanisms controlling their production could lead to improved patient management.
Publications & Presentations
- 1. Luckett-Chastain L R, King C J, McShan M, Gipson J R, Gillaspy A F, Gallucci R. Loss of Interleukin-6 Influences Transcriptional Immune Signatures and Alters Bacterial Colonization in the Skin. Frontiers in Microbiology. 2021; 6
2. Rahman M, Nguyen S V, McCullor K A, King C J, Jorgensen J H, McShan M. Comparative Genome Analysis of the Daptomycin Resistant Streptococcus anginosus strain J4206 associated with Breakthrough Bacteremia. Genome Biol Evol. 2016
3. Bao Y J, Liang Z, Mayfield J A, McShan M, Lee S W, Ploplis V A, Castellino F J. Novel genomic rearrangements mediated by multiple genetic elements in Streptococcus pyogenes M23ND confer potential for evolutionary persistence. Microbiology. 2016; 162 : 1346-59
4. Hendrickson C, Euler C W, Nguyen S V, Rahman M, McCullor K A, King C J, Fischetti V A, McShan M. Elimination of chromosomal island SpyCIM1 from Streptococcus pyogenes strain SF370 reverses the mutator phenotype and alters global transcription. PLoS One. 2015; 10 : 23
5. Rahman M, Nguyen S V, McCullor K A, King C J, Jorgensen J H, McShan M. Complete Genome Sequence of Streptococcus anginosus J4211, a Clinical Isolate. Genome announcements. 2015; 3
- 1. Oklahoma Center for Respiratory and Infectious Diseases. NIH. Start Date: 2016. End Date: 2018.
2. Chromosomal Island SanCI and Streptococcus anginosus Global Transcription. Misc Non-Federal. Start Date: 2015. End Date: 2016.
3. Bacteriophage Control of DNA Repair in Streptococcus pyogenes. NIH. Start Date: 2013. End Date: 2016.
4. Mobile Element SpyCIM1 Enhances Survival in S. pyogenes. State Agency. Start Date: 2011. End Date: 2014.
Awards and Honors