Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 18 February 1994:
Vol. 263. no. 5149, pp. 961 - 963
DOI: 10.1126/science.8310293

Articles

Science, Vol 263, Issue 5149, 961-963
Copyright © 1994 by American Association for the Advancement of Science


articles

Antigenic diversity and the transmission dynamics of Plasmodium falciparum

S Gupta, K Trenholme, RM Anderson, and KP Day

Department of Zoology, Oxford University, United Kingdom.

The average age of humans at their first infection with Plasmodium falciparum is typically less than 1 year in most endemic areas. This has been interpreted as evidence of the high transmissibility of the parasite, with the implication that control of malaria will require high levels of coverage with a potential vaccine. This interpretation is challenged by mathematical models that demonstrate that the long period required to develop immunity to malaria permits a high risk (or low average age) of infection even when parasite transmissibility is low. Patterns of seroconversion to five antigenically distinct isolates of P. falciparum in a highly malarious area of Papua New Guinea indicate that each is only mildly transmissible and that malaria, as a construct of several such independently transmitted strains, has a basic reproductive rate (or transmissibility) that is an order of magnitude lower than other estimates.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Pneumococcal Carriage in United Kingdom Families: Estimating Serotype-specific Transmission Parameters from Longitudinal Data.
A. Melegaro, Y. Choi, R. Pebody, and N. Gay (2007)
Am. J. Epidemiol. 166, 228-235
   Abstract »    Full Text »    PDF »
Serotype cycles in cholera dynamics.
K. Koelle, M. Pascual, and M. Yunus (2006)
Proc R Soc B 273, 2879-2886
   Abstract »    Full Text »    PDF »
AN EPIDEMIOLOGIC MODEL OF THE INCIDENCE OF ACUTE ILLNESS IN PLASMODIUM FALCIPARUM MALARIA..
T. SMITH, A. ROSS, N. MAIRE, C. ROGIER, J.-F. TRAPE, and L. MOLINEAUX (2006)
Am J Trop Med Hyg 75, 56-62
   Abstract »    Full Text »    PDF »
The effects of host contact network structure on pathogen diversity and strain structure.
C. OF. Buckee, K. Koelle, M. J. Mustard, and S. Gupta (2004)
PNAS 101, 10839-10844
   Abstract »    Full Text »    PDF »
Dynamics and selection of many-strain pathogens.
J. R. Gog and B. T. Grenfell (2002)
PNAS 99, 17209-17214
   Abstract »    Full Text »    PDF »
Entamoeba histolytica Lectins Contain Unique 6-Cys or 8-Cys Chitin-Binding Domains.
K. Van Dellen, S. K. Ghosh, P. W. Robbins, B. Loftus, and J. Samuelson (2002)
Infect. Immun. 70, 3259-3263
   Abstract »    Full Text »    PDF »
Antigenic Diversity in Eimeria maxima and the Influence of Host Genetics and Immunization Schedule on Cross-Protective Immunity.
A. L. Smith, P. Hesketh, A. Archer, and M. W. Shirley (2002)
Infect. Immun. 70, 2472-2479
   Abstract »    Full Text »    PDF »
Plasmodium falciparum Genotypes, Low Complexity of Infection, and Resistance to Subsequent Malaria in Participants in the Asembo Bay Cohort Project.
O. H. Branch, S. Takala, S. Kariuki, B. L. Nahlen, M. Kolczak, W. Hawley, and A. A. Lal (2001)
Infect. Immun. 69, 7783-7792
   Abstract »    Full Text »    PDF »
The Epidemic Behavior of the Hepatitis C Virus.
O. G. Pybus, M. A. Charleston, S. Gupta, A. Rambaut, E. C. Holmes, and P. H. Harvey (2001)
Science 292, 2323-2325
   Abstract »    Full Text »    PDF »
Bayesian Analysis of an Epidemiologic Model of Plasmodium falciparum Malaria Infection in Ndiop, Senegal.
N. Cancre, A. Tall, C. Rogier, J. Faye, O. Sarr, J.-F. Trape, A. Spiegel, and F. Bois (2000)
Am. J. Epidemiol. 152, 760-770
   Abstract »    Full Text »    PDF »
Molecular Epidemiology of Entamoeba spp.: Evidence of a Bottleneck (Demographic Sweep) and Transcontinental Spread of Diploid Parasites.
S. Ghosh, M. Frisardi, L. Ramirez-Avila, S. Descoteaux, K. Sturm-Ramirez, O. A. Newton-Sanchez, J. I. Santos-Preciado, C. Ganguly, A. Lohia, S. Reed, et al. (2000)
J. Clin. Microbiol. 38, 3815-3821
   Abstract »    Full Text »
Etiology of interepidemic periods of mosquito-borne disease.
S. I. Hay, M. F. Myers, D. S. Burke, D. W. Vaughn, T. Endy, N. Ananda, G. D. Shanks, R. W. Snow, and D. J. Rogers (2000)
PNAS 97, 9335-9339
   Abstract »    Full Text »    PDF »
Malaria Transmission and Naturally Acquired Immunity to PfEMP-1.
K. P. Piper, R. E. Hayward, M. J. Cox, and K. P. Day (1999)
Infect. Immun. 67, 6369-6374
   Abstract »    Full Text »    PDF »
Allelic Diversity and Antibody Recognition of Plasmodium falciparum Merozoite Surface Protein 1 during Hypoendemic Malaria Transmission in the Brazilian Amazon Region.
L. A. Da Silveira, M. L. Dorta, E. A. S. Kimura, A. M. Katzin, F. Kawamoto, K. Tanabe, and M. U. Ferreira (1999)
Infect. Immun. 67, 5906-5916
   Abstract »    Full Text »    PDF »
Discrete-Event Models of Mixed-Phenotype Plasmodium falciparum Malaria..
F. E. McKenzie, R. C. Wong, and W. H. Bossert (1999)
SIMULATION 73, 213-217
   Abstract »    PDF »
Chaos, Persistence, and Evolution of Strain Structure in Antigenically Diverse Infectious Agents.
S. Gupta, N. Ferguson, and R. Anderson (1998)
Science 280, 912-915
   Abstract »    Full Text »
Association of Malaria Parasite Population Structure, HLA, and Immunological Antagonism.
S. C. Gilbert, M. Plebanski, S. Gupta, J. Morris, M. Cox, M. Aidoo, D. Kwiatkowski, B. M. Greenwood, H. C. Whittle, and A. V. Hill (1998)
Science 279, 1173-1177
   Abstract »    Full Text »
Population Structure of the Relapsing Fever Spirochete Borrelia hermsii as Indicated by Polymorphism of Two Multigene Families That Encode Immunogenic Outer Surface Lipoproteins.
B. J. Hinnebusch, A. G. Barbour, B. I. Restrepo, and T. G. Schwan (1998)
Infect. Immun. 66, 432-440
   Abstract »    Full Text »    PDF »
A New Gene Family (ariel) Encodes Asparagine-Rich Entamoeba histolytica Antigens, Which Resemble the Amebic Vaccine Candidate Serine-Rich E. histolytica Protein.
Z. Mai and J. Samuelson (1998)
Infect. Immun. 66, 353-355
   Abstract »    Full Text »    PDF »
Mathematical studies of parasitic infection and immunity.
R. Anderson (1994)
Science 264, 1884-1886
   Abstract »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)