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Presence Current · Arkansas
Last published 2026
Sources Institutional record
Refreshed 2026-10-09
Mark S. Smeltzer profile photo

Mark S. Smeltzer

Sourced from institutional research profiles (UAMS TRI or ARA).

◆ ARA Academy Federal Grant PI High Impact

Infectious Disease Research - UAMS Center for Microbial Pathogenesis and Host Inflammatory Responses

Also affiliated: Arkansas Children's Hospital (2005); Kansas State University (1992–1994); University of Arkansas Medical Center (2019–2021); United States Army Medical Research and Development Command (2015); Zimmer Biomet (United States) (2016); University of Memphis (2016–2017)

Microbiology & Immunology, College of Medicine

56 h-index 169 pubs 11,340 cited

  • Staphylococcus aureus
  • Biofilms
  • Humans
  • Staphylococcal Infections
  • Animals
  • Bacterial Proteins
  • Gene Expression Regulation, Bacterial
  • Mice
  • Anti-Bacterial Agents
  • Osteomyelitis
  • Mutation
  • Trans-Activators
  • Disease Models, Animal
  • Virulence
  • Microbial Sensitivity Tests

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Biography and Research Information

OverviewAI-generated summary

Mark S. Smeltzer investigates the pathogenesis of Staphylococcus aureus, with a particular focus on its ability to form biofilms and cause infections like osteomyelitis. His research explores the genetic and regulatory mechanisms that govern bacterial behavior, including gene expression and the release of extracellular DNA, which are crucial for biofilm development.

Smeltzer has secured significant federal funding for his work, including multiple awards from the National Institutes of Health (NIH) totaling over $2 million. These grants support his investigations into cellular metabolism, microbial pathogenesis, and the role of bacterial proteases in disease progression. He has also contributed to educational programs within the NIH framework.

His scholarly output includes over 160 publications, with an h-index of 56 and more than 11,000 citations, indicating a substantial impact in his field. Smeltzer leads a research group at the University of Arkansas for Medical Sciences and collaborates with several colleagues within the institution, including Karen E. Beenken and Mara J. Campbell, on numerous shared publications.

Metrics

  • h-index: 56
  • Publications: 169
  • Citations: 11,340

Positions

  • Professor 2003–present
    University of Arkansas for Medical Sciences Orthopaedic Surgery ORCID
  • Infectious Disease Research - UAMS Center for Microbial Pathogenesis and Host Inflammatory Responses publications 1995–2026
    University of Arkansas for Medical Sciences Microbiology & Immunology, College of Medicine Institutional directory
  • Associate Professor 2001–2003
    University of Arkansas for Medical Sciences Orthopaedic Surgery ORCID
  • Assistant Professor 1999–2001
    University of Arkansas for Medical Sciences Orthopaedic Surgery ORCID

Selected Publications

  • Osteomyelitis (2026)
    Nature Reviews Disease Primers 6 citations DOI OpenAlex
  • A transcriptomic-driven segmentation and cell simulation framework for high-resolution spatial transcriptomics and cell-cell communication (2026)
    bioRxiv (Cold Spring Harbor Laboratory) DOI OpenAlex
  • Mechanistic insights into the pathogenesis and therapeutic recalcitrance of Staphylococcus aureus osteomyelitis (2026)
    Clinical Microbiology Reviews 5 citations DOI OpenAlex
  • Lipolysis of host triacylglyceride-rich lipoproteins creates a toxic microenvironment for Staphylococcus aureus (2026)
    bioRxiv (Cold Spring Harbor Laboratory) DOI OpenAlex
  • Staphylococcus aureus Biofilm-Associated Infections: Have We Found a Clinically Relevant Target? (2025)
    Microorganisms 19 citations DOI OpenAlex
  • Staphylococcus aureus Proteins Implicated in the Reduced Virulence of sarA and sarA/agr Mutants in Osteomyelitis (2025)
    Microorganisms 6 citations DOI OpenAlex
  • The ability of sarA to limit protease production plays a key role in the pathogenesis of Staphylococcus aureus osteomyelitis irrespective of the functional status of agr (2024)
    Infection and Immunity 15 citations DOI OpenAlex
  • RANKL-mediated osteoclast formation is required for bone loss in a murine model of Staphylococcus aureus osteomyelitis (2024)
    Bone 22 citations DOI OpenAlex
  • Increased production of aureolysin and staphopain A is a primary determinant of the reduced virulence of Staphylococcus aureus sarA mutants in osteomyelitis (2024)
    mBio 13 citations DOI OpenAlex
  • Comparative evaluation of small molecules reported to be inhibitors of Staphylococcus aureus biofilm formation (2023)
    Microbiology Spectrum 7 citations DOI OpenAlex
  • Cartilage-inspired surface textures for improved tribological performance of orthopedic implants (2022)
    Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials 6 citations DOI OpenAlex
  • The major role of sarA in limiting Staphylococcus aureus extracellular protease production is correlated with decreased virulence in diverse clinical isolates in osteomyelitis (2022)
    bioRxiv (Cold Spring Harbor Laboratory) DOI OpenAlex
  • Pyroptosis and pyroptosis-inducing cancer drugs (2022)
    Acta Pharmacologica Sinica 161 citations DOI OpenAlex
  • Is amplification bias consequential in transposon sequencing (TnSeq) assays? A case study with a Staphylococcus aureus TnSeq library subjected to PCR-based and amplification-free enrichment methods (2021)
    Microbial Genomics 2 citations DOI OpenAlex
  • Evaluation of a bone filler scaffold for local antibiotic delivery to prevent Staphylococcus aureus infection in a contaminated bone defect (2021)
    Scientific Reports 26 citations DOI OpenAlex

View all publications on OpenAlex →

ARA Academy 2017 ARA Fellow

Dr. Smeltzer dedicates his research to combating Staphylococcus aureus, a bacterial pathogen responsible for approximately 20,000 American deaths annually. He focuses on bone infections and those involving indwelling orthopaedic devices. He also serves as Program Director of a COBRE promoting infectious disease research capacity at UAMS and central Arkansas.

Policy Impact

Leads a COBRE center promoting infectious disease research capacity in central Arkansas, generating NIH institutional funding and training biomedical researchers.

Growth Areas

['Population Health Innovations & Clinical Research']

Federal Grants 4 $2,046,459 total

NIH Co-PI Jul 2026 - Jun 2031

Clinician Research Education and Scientific Training (CREST) Program

National Institute of General Medical Sciences $269,148 T32
NIH Contact PI May 2022 - Apr 2027

Center for Microbial Pathogenesis and Host Inflammatory Responses

National Institute of General Medical Sciences $1,140,000 P30
NIH Contact PI Jun 2015 - Aug 2027

Defining the role of post-translational regulation by extracellular proteases in the pathogenesis of Staphylococcus aureus osteomyelitis

National Institute of Allergy and Infectious Diseases $451,739 R01
NIH Contact PI Aug 2012 - Apr 2023

Shared Resource to Investigate Cellular Metabolism

National Institute of General Medical Sciences $185,572 P20

Research Interests

Staphylococcus aureus, Staphylococcal infection, Osteomyelitis, Biofilm, Regulation

Grants & Funding

As listed on this researcher's institutional profile. Federal awards with verified records are shown above.

  • sarA as a Target for the Treatment and Prevention of Staphylococcal Biofilm-Associated Infection US Department of the Army Principal Investigator
  • sar-mediated regulation in Staphylococcus aureus NIH Principal Investigator
  • Capsule regulatory network in S. aureus pathogenesis NIH Co-Investigator
  • Biofilm Dissemination in Staphylococcus aureus NIH/Nat. Inst. of Allergy & Infectious Diseases via University of Southern Mississippi Principal Investigator
  • Investigating a Flexible, Degradable Local Antimicrobial Delivery System - Continuation - Continuation DHHS - Biomedical Advanced Research and Development Authority via University of Memphis Principal Investigator
  • Chitosan films for prevention of wound infections US Department of the Army Principal Investigator
  • Identification of Novel Regulatory Elements Contributing to Virulence in Staphylococcal Endocarditis American Heart Association Principal Investigator
  • Controlled Delivery of Cis-2-decenoic Acid for the Prevention of Infection by Bacterial Biofilms US Department of Defense Principal Investigator

Collaboration Network

374 Collaborators 124 Institutions 16 Countries

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