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Infection and Immunity, July 2002, p. 3330-3335, Vol. 70, No. 7
0019-9567/02/$04.00+0     DOI: 10.1128/IAI.70.7.3330-3335.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Localization within a Proline-Rich Antigen (Ag2/PRA) of Protective Antigenicity against Infection with Coccidioides immitis in Mice

Tao Peng,1,2 Lisa Shubitz,1,2 Julie Simons,1,2 Robert Perrill,1,2 Kris I. Orsborn,1,2,3 and John N. Galgiani1,3,4*

Valley Fever Center for Excellence,1 Medicine and Subspecialties Program,3 Research Program, Southern Arizona Veterans Affairs Health Care System,2 Department of Medicine, University of Arizona College of Medicine, Tucson, Arizona4

Received 16 January 2002/ Returned for modification 19 February 2002/ Accepted 2 April 2002

Subunits of a proline-rich coccidioidal antigen (Ag2/PRA) of Coccidioides immitis were analyzed by comparison as vaccines in mice. The optimal dose of plasmid vaccine encoding full-length Ag2/PRA was determined to be between 10 and 100 µg. Mice vaccinated with plasmids encoding amino acids (aa) 1 to 106 were as protective as full-length Ag2/PRA (aa 1 to 194). The subunit from aa 27 to 106 was significantly but less protective. Plasmids encoding aa 90 to 151 or aa 90 to 194 were not protective. Analogous results were obtained with recombinant vaccines of the same amino acid sequences. In addition, mixtures of aa 90 to 194 with either aa 1 to 106 or aa 27 to 106 did not enhance protection compared to the active single-recombinant subunits alone. Humoral response of total immunoglobulin G (IgG) and subclasses IgG1 and IgG2a were detectable in subunit vaccinations but at significantly (100-fold) lower concentrations than after vaccination with plasmids encoding full-length Ag2/PRA. Since virtually all protection by vaccination with full-length Ag2/PRA can be accounted for in the first half of the protein (aa 1 to 106), this subunit could make a multicomponent vaccine more feasible by reducing the quantity of protein per dose and the possibility of an untoward reactions to a foreign protein.


* Corresponding author. Mailing address: Valley Fever Center for Excellence, 3601 South Sixth Ave., Tucson, AZ 85723. Phone: (520) 629-4777. Fax: (520) 629-4738. E-mail: spherule{at}u.arizona.edu.

Editor: T. R. Kozel


Infection and Immunity, July 2002, p. 3330-3335, Vol. 70, No. 7
0019-9567/02/$04.00+0     DOI: 10.1128/IAI.70.7.3330-3335.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




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