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Infection and Immunity, March 2003, p. 1416-1426, Vol. 71, No. 3
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.3.1416-1426.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Geographical Structure of Diversity and Differences between Symptomatic and Asymptomatic Infections for Plasmodium falciparum Vaccine Candidate AMA1

Alfred Cortés,1* Mata Mellombo,1 Ivo Mueller,2 Ariadna Benet,1 John C. Reeder,2 and Robin F. Anders3

Papua New Guinea Institute of Medical Research, Madang, MP511,1 Papua New Guinea Institute of Medical Research, Goroka, EHP441, Papua New Guinea,2 The Cooperative Research Centre for Vaccine Technology, Department of Biochemistry, La Trobe University, Melbourne, Victoria 3086, Australia3

Received 26 July 2002/ Returned for modification 10 October 2002/ Accepted 21 November 2002

Plasmodium falciparum apical membrane antigen 1 (AMA1) is a prime malaria vaccine candidate. Antigenic diversity within parasite populations is one of the main factors potentially limiting the efficacy of any asexual-stage vaccine, including one based on AMA1. The DNA coding for the most variable region of this antigen, domain I, was sequenced in 168 samples from the Wosera region of Papua New Guinea, including samples from symptomatic and asymptomatic infections. Neutrality tests applied to these sequences provided strong evidence of selective pressure operating on the sequence of ama1 domain I, consistent with AMA1 being a target of protective immunity. Similarly, a peculiar pattern of geographical diversity and the particular substitutions found were suggestive of strong constraints acting on the evolution of AMA1 at the population level, probably as a result of immune pressure. In addition, a strong imbalance between symptomatic and asymptomatic infections was detected in the frequency of particular residues at certain polymorphic positions, pointing to AMA1 as being one of the determinants of the morbidity associated with a particular strain. The information yielded by this study has implications for the design and assessment of AMA1-based vaccines and provides additional data supporting the importance of AMA1 as a malaria vaccine candidate.

* Corresponding author. Mailing address: Papua New Guinea Institute of Medical Research, P.O. Box 378, Madang, MP511, Papua New Guinea. Phone: 675-8522909. Fax: 675-8523289. E-mail: acortes{at}pngimr.org.pg.

Editor: J. M. Mansfield

Infection and Immunity, March 2003, p. 1416-1426, Vol. 71, No. 3
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.3.1416-1426.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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