This project will investigate a new hypothesis regarding how the mobile genetic element (SCCmec) that carries methicillin resistance spreads among S. aureus strains: We propose that it encodes previously unsuspected functionality for its own replication, which would enhance the efficiency of any horizontal gene transfer mechanism. MRSA (methicillin resistant S. aureus) is a serious and growing public health problem. The recombinases that integrate and excise the SCCmec element into and out of the host genome have been identified and are under study in our lab. However, nothing is known about the events between excision from one genome and appearance in another. While analyzing the conserved ORFs that flank recombinase genes, we realized that some of are likely to have functions in DNA replication. This proposal focuses on a large putative ATPase (Cch) that we discovered is related to the known replication initiation proteins encoded by S. aureus pathogenicity islands (SaPIs). Our preliminary structural and biochemical data suggest that the SCCmec protein in question (Cch) is a self-loading helicase whose closest homologs in the ATPase domain are, surprisingly, the eukaryotic and archaeal replicative MCM helicases. Thus we have determined the first structure of that type of helicase in the active ring form. This work will change how people think about SCCmec elements and how they spread methicillin resistance and will provide new model systems for understanding mechanisms of self-loading and MCM-like helicases.
Aim 1 : Structural understanding of Cch Aim 2: How structurally similar / different are the subtypes of SaPI / SCC replication initiator? Aim 3: What are the biochemical activities of Cch and SaPI3 rep?

Public Health Relevance

MRSA (methicillin resistant S. aureus) is a growing public health problem. This project will use crystallography and biochemistry to investigate a new hypothesis regarding how the mobile genetic element (SCCmec) that carries methicillin resistance spreads among S. aureus strains: We propose that it encodes functionality for its own replication, which would enhance the efficiency of horizontal gene transfer to new strains.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI117593-01
Application #
8873188
Study Section
Macromolecular Structure and Function B Study Section (MSFB)
Program Officer
Huntley, Clayton C
Project Start
2015-02-01
Project End
2017-01-31
Budget Start
2015-02-01
Budget End
2016-01-31
Support Year
1
Fiscal Year
2015
Total Cost
$237,000
Indirect Cost
$87,000
Name
University of Chicago
Department
Biochemistry
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Mir-Sanchis, Ignacio; Roman, Christina A; Misiura, Agnieszka et al. (2016) Staphylococcal SCCmec elements encode an active MCM-like helicase and thus may be replicative. Nat Struct Mol Biol 23:891-898
Arkhipova, Irina R; Rice, Phoebe A (2016) Mobile genetic elements: in silico, in vitro, in vivo. Mol Ecol 25:1027-31