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Infection and Immunity, December 2003, p. 6995-7001, Vol. 71, No. 12
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.12.6995-7001.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Monoclonal Antibody MG96 Completely Blocks Plasmodium yoelii Development in Anopheles stephensi

Rhoel R. Dinglasan,1* Iesha Fields,2 Mohammed Shahabuddin,2 Abdu F. Azad,1 and John B. Sacci Jr.1

Department of Microbiology and Immunology, School of Medicine, University of Maryland, Baltimore, Maryland 21201,1 Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 208922

Received 13 June 2003/ Returned for modification 11 August 2003/ Accepted 3 September 2003

In spite of research efforts to develop vaccines against the causative agent of human malaria, Plasmodium falciparum, effective control remains elusive. The predominant vaccine strategy focuses on targeting parasite blood stages in the vertebrate host. An alternative approach has been the development of transmission-blocking vaccines (TBVs). TBVs target antigens on parasite sexual stages that persist within the insect vector, anopheline mosquitoes, or target mosquito midgut proteins that are presumed to mediate parasite development. By blocking parasite development within the insect vector, TBVs effectively disrupt transmission and the resultant cascade of secondary infections. Using a mosquito midgut-specific mouse monoclonal antibody (MG96), we have partially characterized membrane-bound midgut glycoproteins in Anopheles gambiae and Anopheles stephensi. These proteins are present on the microvilli of midgut epithelial cells in both blood-fed and unfed mosquitoes, suggesting that the expression of the protein is not induced as a result of blood feeding. MG96 exhibits a dose-dependent blocking effect against Plasmodium yoelii development in An. stephensi. We achieved 100% blocking of parasite development in the mosquito midgut. Preliminary deglycosylation assays indicate that the epitope recognized by MG96 is a complex oligosaccharide. Future investigation of the carbohydrate epitope as well as gene identification should provide valuable insight into the possible mechanisms of ookinete attachment and invasion of mosquito midgut epithelial cells.

* Corresponding author. Mailing address: Department of Microbiology and Immunology, School of Medicine, University of Maryland, 655 West Baltimore St., Baltimore, MD 21201. Phone: (410) 706-7066. Fax: (410) 706-0282. E-mail: rding001{at}umaryland.edu.

Editor: B. B. Finlay

Infection and Immunity, December 2003, p. 6995-7001, Vol. 71, No. 12
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.12.6995-7001.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

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