Volume 9 Supplement 2

Parasite to Prevention: Advances in the understanding of malaria

Open Access

Intra-host dynamics of mixed species malaria parasite infections in mice and mosquitoes

  • Jianxia Tang1,
  • Megumi Inoue1,
  • Toshihiko Sunahara2,
  • Moe Kanda1,
  • Osamu Kaneko1 and
  • Richard Culleton1
Contributed equally
Malaria Journal20109(Suppl 2):O31

https://doi.org/10.1186/1475-2875-9-S2-O31

Published: 20 October 2010

Background

The distributions of human malaria parasite species overlap in most regions of the world where malaria is present, and co-infections involving two or more malaria parasites are common. Currently, very little is known about the consequences of any interactions that may occur between species during co-infection for disease severity and parasite transmission success. However, current anti-malarial interventions such as vector control and drug interventions and the future application of vaccines will and do have disproportionate effects on some species compared to others; with the ultimate consequence of reducing the number of species in circulation in any one area. We believe that such a situation warrants a clearer understanding of how the interactions between species affect malaria disease and transmission dynamics.

Methods

As controlled competition experiments using human malaria parasites are currently practically impossible, we assessed the consequences of mixed-species infections on parasite fitness, disease severity and transmission success using the rodent malaria parasite species Plasmodium chabaudi (strains AS and CB), P. yoelii yoelii (CU) and P. vinckei lentum (DS). We compared the fitness of individual species within co-infections and in single species infections in mice. We also assessed the disease severity of single versus mixed infections in mice by measuring mortality rates, anaemia and weight loss. Finally, we compared the transmission success of parasites in single or mixed species infections by quantifying oocyst development in Anopheles stephensi mosquitoes.

Results

We found that co-infections of P. yoelii with either P. vinckei or P. chabaudi led to a dramatic increase in infection virulence, with 100% mortality observed in mixed species infections, compared to no mortality for P. yoelii and P. vinckei single infections, and 40% mortality for P. chabaudi single infections. The increased mortality in the mixed infections was associated with an inability to clear parasitaemia (Figure 1a), with the non-P. yoelii parasite species persisting at higher parasite densities than in single infections (Figure 1b). P. yoelii growth was suppressed in all mixed infections compared to single infections. Transmissibility of P. vinckei and P. chabaudi to mosquitoes was also dramatically reduced in the presence of P. yoelii in co-infections compared to single infections (Figure 1c).
Figure 1

(a) Parasitaemia of mixed and single infections of P.yoelii and P. vinckei, in the mixed infection group, all mice died by day 12 post-inoculation. (b) Parasite density of P. vinckei in a mixed infection with P.yoelii, and in a single infection. (c) mean oocyst production per mosquito of P.vinckei and P. chabaudi in mixed infections with P. yoelii, and in a single infections. Data are means of five mice per group; error bars represent one standard error above and below the mean. Pv = P. vinckei, Pc = P. chabaudi, Py = P.yoelii. † = death.

Discussion

The increased virulence of co-infections containing P. yoelii (reticulocyte restricted) and P. chabaudi or P. vinckei (predominantly normocyte restricted) may be consequences of parasite cell tropism and/or immune modulation of the host. We explain the reduction in transmission success of species in co-infections in terms of inter-species gamete incompatibility.

Notes

Authors’ Affiliations

(1)
Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University
(2)
Department of International Health, Institute of Tropical Medicine (NEKKEN)

Copyright

© Culleton et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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