Mosquito transmission, growth phenotypes and the virulence of malaria parasites
© Pollitt et al.; licensee BioMed Central Ltd. 2013
Received: 17 October 2013
Accepted: 4 December 2013
Published: 6 December 2013
A series of elegant experiments was recently published which demonstrated that transmission of malaria parasites through mosquitoes elicited an attenuated growth phenotype, whereby infections grew more slowly and reached peak parasitaemia at least five-fold lower than parasites which had not been mosquito transmitted. To assess the implications of these results it is essential to understand whether the attenuated infection phenotype is a general phenomenon across parasites genotypes and conditions.
Using previously published data, the impact of mosquito transmission on parasite growth rates and virulence of six Plasmodium chabaudi lines was analysed.
The effect of mosquito transmission varied among strains, but did not lead to pronounced or consistent reductions in parasite growth rate.
Mosquito-induced attenuated growth phenotype is sensitive to experimental conditions.
Malaria infections vary hugely in the amount of harm caused to their hosts (virulence). This variation can, in part, be explained by host factors but parasites themselves also vary [1–4]. In a recent publication, Spence et al. demonstrated that the virulence of an infection may be mediated by the environment that parasites have experienced. Using a model rodent malaria system, they showed that malaria parasites are intrinsically modified during the process of developing within the vector and establishing a new infection in a vertebrate host. Parasites that had recently been transmitted through a mosquito displayed an attenuated growth phenotype, with infections growing more slowly and achieving a peak parasitaemia at least five-fold lower than that achieved by parasites that had not been mosquito transmitted (MT). Spence et al. demonstrated that this altered phenotype was correlated with the expression of a different set of antigenic proteins in the parasites eliciting a different immune response in the host, to which they attribute the enhanced control of parasite replication. The attenuated growth phenotype was associated with less severe virulence, including reduced anaemia and weight loss.
Full experimental design and parasite line histories are reported elsewhere  (see also Figure 1B). Briefly, six lines of Plasmodium chabaudi (CW-0, CW-A, CW-V, ER, AS, AJ) were either transmitted though mosquitoes or maintained via serial blood transfer. Three lines that shared an ancestral genotype had different passage histories (CW-O: recently derived from a wild isolate; CW-A, CW-V: multiple passages through mice). All infections were initiated via IP injection with 104-106 blood stage parasites and parasitaemia, mouse weight and erythrocyte density (anaemia) were monitored.
All analysis was performed using R (version 2.14.1). Day 8 parasitaemia (proportion of red cells infected with malaria parasites) was analysed using a general linear model with binomial errors. Day 8 parasite density (number of parasites per microlitre of blood) was log transformed to fit models assumptions before analysis with a general linear model. Model simplification was followed by sequentially dropping the least significant term and comparing the change in deviance, with and without the term.
Results and discussion
Two measures of virulence, anaemia and weight loss, were measured. In the experiments of Spence et al., the attenuated growth phenotype was associated with negligible weight loss, and a doubling of minimum red blood cell (RBC) densities compared to infections initiated with serial blood passage (SBP); in the experiments reported here, mosquito transmission, on average, reduced weight loss and anaemia during infection, but the effect was relatively minor and varied among strains ( and Figure 2C and D).
There are likely many small differences in the experimental set up in the two studies. For instance, the strain of the vector (although not the mice) varied between studies. Mouse diet also varied: the mice used here  were provided with para-aminobenzoic acid (PABA) which is known to increase parasite growth rates . Since the patterns of parasitaemia from SBP initiated infections presented here do not differ substantially from those in , whether or not PABA could have a differential affect on SBP and MT parasites remains an open question. More subtle, but potentially important, is a difference in the timing of infections in the two studies. The infection protocols are illustrated in Figure 1. In both cases, data for SBP initiated infections are generated by injecting parasitized RBCs into experimental hosts, after growing up parasites from cryopreserved stocks in donor mice, which can involve multiple passages in different donor mice before experimental infections. Spence et al. initiated MT infections directly from such SBP-infected mice, allowing them to compare infections initiated before and directly after the transmission event. Recently MT infections – those generated by injecting parasitized RBCs from MT infections into new hosts – also showed the attenuated phenotype.
This latter group of infections most closely resembles the mosquito-transmitted lines from Mackinnon et al., reported here. Blood from mosquito-transmitted infections was cryogenically preserved (so that SBP and MT infections could be compared contemporaneously). Parasites were subsequently grown up from these samples in donor mice and injected into experimental hosts. ‘Recently MT’ parasites were serially blood-passaged between two and five times (Figure 1 in ) compared to one round of SBP in Spence et al.’s recently MT parasites. Although Spence et al. did not explore the dynamics of infection with recently MT parasites that endured more rounds of SBP, they showed that the attenuation of day 7 parasitaemia generated from MT starts to degrade after five rounds (Supplementary Figure Five in ). From these data, it would be expected that the MT lines from Mackinnon et al. would still demonstrate an attenuated phenotype, particularly the ER and the three CW lines, which were passaged only twice. Whether freezing, which the MT lines analysed here experienced, fundamentally alters antigen expression and virulence is an important open question, of interest to all researchers using cryopreserved malaria parasite stocks.
Finally, differences in pre-mosquito passage history may be important. The AS line used by Spence et al. had undergone SBP 26–30 times since isolation from the natural host; the lines shown here been passaged a maximum of 11 time . The three CW lines reported here also share a common ancestor, but have different pre-transmission passage histories - the line with the greatest number of passages showed the smallest effect of mosquito transmission (CW-V; Figure 2) in this and another experiment .
Clearly, all of the above hypotheses can be tested empirically. The re-analysis of earlier experiments has been reported here to encourage such further work and so that those following up the important work of Spence et al. are aware that experimental details apparently matter considerably.
Spence et al. suggested that the growth rate attenuation they discovered is the result of differences in antigenic expression profiles, regulated by something in the mosquito transmission pathway, which elicit different host immune responses. Here it is shown that, in earlier experiments, mosquito passage did not consistently or substantially attenuate parasite growth phenotype. The experiments from which these data arose differ from the experiments of Spence et al. in a number of potentially important ways. This suggests that a comparison of host immune profiles generated by infections with a number of different lines may shed more light on the strain variation and qualitative differences in the effects of mosquito transmission. Whether such alteration of expression profiles is, for example, vector or parasite strain specific is unknown.
Authors are funded by the National Institutes of Health (LCP and AFR; R01 GM089932 and R01AI089819), and an NSERC Discovery Grant (NM). The original experiments were funded by The Leverhulme Trust. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank members of the Read-Thomas lab group, the Center for Infectious Disease Dynamics, and the Research and Policy in Infectious Disease Dynamics program of the Science and Technology Directorate, Department of Homeland Security, and the Fogarty International Center for discussion.
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