Microbicides have been one of the most successful weapons against infectious diseases, and are of particular importance in situations where the state-of-the-art treatment of the given infectious disease is difficult or ineffective. Most viral pathogenic agents causing severe diseases belong to this category . In the applicant's pilot experiments, he has defined peptidic molecules with anti-HIV-1 activities in vitro. Here he proposes studies that will provide guidance in the further development of these and other antiviral peptides that may be used as agents inhibiting sexual transmission of HIV. Both in vitro and in viva methods assessing their antiviral capacity will be employed. The focus of the first Specific Aim is to test antiviral effects using several HIV /SIV /SHIV- permissive cell lines as well as primary human and simian PBMC. Assays assessing, infectivity , cell fusion and potential virucidal effects of the peptides will be utilized together with several different isolates of HIV-1, SIV, and SHIV. These experiments may improve our understanding of the mechanism of their antiviral action. In addition, potential toxicities of the compounds will be analyzed in vitro. The main objective of the second Specific Aim is to investigate the hypothesis that a simple formulation containing an antiviral peptide (or several of them) applied to a mucosal surface is able to block the infection caused by the exposure of the mucosal surface to immunodeficiency viruses. This will be tested in the applicant's system of mucosal SIV/SHIV infection of rhesus macaques (Macaca mulatta). Successful outcomes of these experiments may result in designing novel anti-HIV chemoprophylactic agents.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI052049-01
Application #
6552852
Study Section
Special Emphasis Panel (ZHD1)
Project Start
2001-09-30
Project End
2005-08-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Brandt, Curtis R (2014) Peptide therapeutics for treating ocular surface infections. J Ocul Pharmacol Ther 30:691-9
Altmann, Sharon E; Brandt, Curtis R; Jahrling, Peter B et al. (2012) Antiviral activity of the EB peptide against zoonotic poxviruses. Virol J 9:6
Bultmann, Hermann; Girdaukas, Gary; Kwon, Glen S et al. (2010) The virucidal EB peptide protects host cells from herpes simplex virus type 1 infection in the presence of serum albumin and aggregates proteins in a detergent-like manner. Antimicrob Agents Chemother 54:4275-89
Altmann, S E; Jones, J C; Schultz-Cherry, S et al. (2009) Inhibition of Vaccinia virus entry by a broad spectrum antiviral peptide. Virology 388:248-59
Akkarawongsa, Radeekorn; Pocaro, Nina E; Case, Gary et al. (2009) Multiple peptides homologous to herpes simplex virus type 1 glycoprotein B inhibit viral infection. Antimicrob Agents Chemother 53:987-96
Akkarawongsa, Radeekorn; Potocky, Terra B; English, Emily P et al. (2008) Inhibition of herpes simplex virus type 1 infection by cationic beta-peptides. Antimicrob Agents Chemother 52:2120-9
Teuton, Jeremy R; Brandt, Curtis R (2007) Sialic acid on herpes simplex virus type 1 envelope glycoproteins is required for efficient infection of cells. J Virol 81:3731-9
Brandt, Curtis R; Akkarawongsa, Radeekorn; Altmann, Sharon et al. (2007) Evaluation of a theta-defensin in a Murine model of herpes simplex virus type 1 keratitis. Invest Ophthalmol Vis Sci 48:5118-24
Bultmann, Hermann; Teuton, Jeremy; Brandt, Curtis R (2007) Addition of a C-terminal cysteine improves the anti-herpes simplex virus activity of a peptide containing the human immunodeficiency virus type 1 TAT protein transduction domain. Antimicrob Agents Chemother 51:1596-607
Jones, Jeremy C; Turpin, Elizabeth A; Bultmann, Hermann et al. (2006) Inhibition of influenza virus infection by a novel antiviral peptide that targets viral attachment to cells. J Virol 80:11960-7

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