Ronald C. Montelaro, PhD

Ronald Montelaro Professor Emeritus
Microbiology & Molecular Genetics
417 Bridgeside Point II
450 Technology Drive
Pittsburgh, Pennsylvania 15219

  FRIP Database
  PubMed Publications

Phone: (412) 648-8869
Fax: (412) 624-4440


      The primary focus of the Montelaro lab is to elucidate the intricate interactions between viral pathogens and host immune responses to determine the mechanisms by with host immunity contributes to protection and disease and to serve as a basis for the development of effective vaccines. A particular interest of the lab is to develop effective strategies to overcome the challenge of natural viral antigenic variation that has evolved as a common complication to the development of effective vaccines to important viral diseases, including those related to biodefense and emerging infectious diseases. Systems currently under investigation include HIV-1 and related animal lentiviruses (SHIV, SIV, and EIAV). Studies in these systems include investigation of the nature and role of antigenic variation during infection, the development of novel assays to characterize virus-specific innate, humoral, and cellular immune responses, and the design of engineered immunogens for effective vaccination against variant strains of a particular virus. In addition to these vaccine related studies, the lab also maintains a research program to develop novel de novo antimicrobial peptides (engineered cationic amphipathic peptides, or eCAPs) that can be used to inactivate a diverse spectrum of bacteria or enveloped viruses in a prophylactic or therapeutic treatment modalities.

Selected Publications

  • Deslouches, B., Steckbeck, J., Craigo, J., Doi, Y., Burns, J., and Montelaro, R. (2015) Engineered cationic antimicrobial peptides (eCAPs) to overcome multidrug resistance by ESKAPE pathogens. Antimicrobial. Agents & Chemotherapy 59: 1329-1333.

  • Craigo, J., Ezzelarab, C., Cook, S., Liu, C., Horohov, D., Issel, C., and Montelaro, R. (2015) Protective efficacy of centralized and polyvalent envelope immunogens in an attenuated equine lentivirus vaccine. PLoS Pathogens 11:e1004610. Doi:10.1371/journal.ppat.1004610. PMC4287611.

  • Steckbeck, J., Kuhlmann, AS, and Montelaro, R. (2014) Structural and functional comparisons of retroviral envelope protein C-terminal domain: still much to learn. Viruses 6: 284-300. PMC3917443

  • Yang, Y. Kulka, K., Montelaro, R., Reinhart, T., Sisson, J., Aderem, A., and Ojha, A. (2014) A hydrolase of trehalose dimycolate induces nutrient influx and stress sensitivity to balance intracellular growth of Mycobacterium tuberculosis. Cell Host & Microbe 15: 153-163.

  • Kuhlmann, A., Steckbeck, J., Sturgeon, T., Craigo, J., and Montelaro, R. (2014) Unique functional properties of conserved arginine residues in the lentivirus lytic peptide domains of the C-terminal tail of HIV-1 gp41. J. Biol. Chem. 289: 7630-7640.

  • Steckbeck, J., Deslouches, B., and Montelaro, R. (2014) Antimicrobial peptides: New drugs for bad bugs. Exp. Opinion Biol. Therap. 14: 10.1517/14712598.2013.844227.

  • Craigo, J. and Montelaro, R. (2013) Lessons in AIDS vaccine development learned from studies of equine infectious anemia virus infection and disease. Viruses 5: 2963-2976.

Ronald Montelaro
Ronald C. Montelaro, PhD
Affiliate, CVR
Professor Emeritus
Microbiology & Molecular Genetics
417 Bridgeside Point II
(412) 648-8869
Timothy Sturgeon
Timothy J. Sturgeon
Research, CVR
Process Research Manager
Center for Vaccine Research (CVR)
9028 BST3
(412) 383-5333


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Last Modified: Wednesday, February 25, 2009 at 12:15:22 AM
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