AJTMH ASTMH MEMBERSHIP INFORMATION: astmh@astmh.org
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 75(1), 2006, pp. 112-125
Copyright © 2006 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental figures
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by MCQUEEN, P. G.
Right arrow Articles by MCKENZIE, F. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by MCQUEEN, P. G.
Right arrow Articles by MCKENZIE, F. E.
Related Collections
Right arrow Modeling
Right arrow Malaria

COMPETITION FOR RED BLOOD CELLS CAN ENHANCE PLASMODIUM VIVAX PARASITEMIA IN MIXED-SPECIES MALARIA INFECTIONS

PHILIP G. MCQUEEN* AND F. ELLIS MCKENZIE
Center for Information Technology and Fogarty International Center, National Institutes of Health, Bethesda, Maryland

We assess the consequences of competition for red blood cells (RBCs) in co-infections with the two major agents of human malaria, Plasmodium vivax and Plasmodium falciparum, using differential equations to model the population dynamics of RBCs and parasites. P. vivax parasitizes only the youngest RBCs, but this can reduce the broader RBC population susceptible to P. falciparum. We found that competition for RBCs typically causes one species to suppress the other, depending on their relative reproduction rates and timing of inoculation. However, if the species’ reproduction rates are nearly equal, transient increases in RBC production stimulated by the presence of P. falciparum may boost P. vivax parasitemia above its single-species infection level. Conversely, P. falciparum parasitemia is rarely enhanced above its single-species level. Furthermore, transients in RBC production can induce coupled oscillations in the parasitemia of both species. These results are remarkably robust to changes in model parameters.


Received June 24, 2005. Accepted for publication February 22, 2006.

Acknowledgments: We thank David L. Smith, Wendy P. O’Meara, and three anonymous reviewers for helpful comments.

* Address correspondence to Philip G. McQueen, Mathematical & Statistical Computing Laboratory Division of Computational Bioscience, CIT/NIH, 12 South Drive, Bethesda, MD 20892-5620. E-mail: mcqueenp{at}mail.nih.gov

Authors’ addresses: Philip G. McQueen, Mathematical & Statistical Computing Laboratory Division of Computational Bioscience, CIT/NIH, 12 South Drive, Bethesda, MD 20892-5620, E-mail: mcqueenp{at}mail.nih.gov. F. Ellis McKenzie, Fogarty International Center, NIH Building 16, Bethesda, MD 20892, E-mail: mckenzel{at}mail.nih.gov.

Note: Additional supplemental figures appear online at www.ajtmh.org.




This article has been cited by other articles:


Home page
J. Immunol.Home page
M. Niikura, S. Kamiya, K. Kita, and F. Kobayashi
Coinfection with Nonlethal Murine Malaria Parasites Suppresses Pathogenesis Caused by Plasmodium berghei NK65
J. Immunol., May 15, 2008; 180(10): 6877 - 6884.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the American Society of Tropical Medicine and Hygiene.