dc.contributor.advisor | Reece, Sarah | en |
dc.contributor.advisor | Obbard, Darren | en |
dc.contributor.advisor | West, Stuart | en |
dc.contributor.author | Ramiro, Ricardo S. | en |
dc.date.accessioned | 2013-07-12T10:30:40Z | |
dc.date.available | 2013-07-12T10:30:40Z | |
dc.date.issued | 2012-11-30 | |
dc.identifier.uri | http://hdl.handle.net/1842/7542 | |
dc.description.abstract | Despite over a century of research, malaria parasites (Plasmodium) still remain a
major cause of mortality and morbidity worldwide. In recent years, the application of
theoretical principles from ecology and evolutionary biology to the study of these
parasites has started to provide insight into variety of fundamental subjects from the
evolution of virulence to the facultative strategies (i.e. phenotypic plasticity) that
parasites use to maximize their transmission. It is now becoming increasingly clear
that to understand and predict population level patterns of virulence and transmission,
the processes that occur at the between-host level must be studied in light of the
interactions that happen within hosts (between parasites and between parasites and
hosts). In this thesis I combine concepts from evolutionary biology and ecology with
tools from molecular and cellular biology and evolutionary genetics, which allow me
to study rodent malaria parasites at both evolutionary and ecological timescales. The
work I present in this thesis has the following four components:
1). Phylogenetics (chapter 2): I applied recently developed phylogenetic
methods to a large DNA sequence dataset that I generated, to provide a
better understanding of the phylogeny of rodent malaria parasites and
investigate how selection has shaped their genomes. I show that all rodent
malaria subspecies can be considered species, provide the first time line
for the evolution of this group of parasites and demonstrate that most loci
are under purifying selection.
2). Hybridization and reproductive isolation (chapter 3): I show that
hybridization between two rodent malaria parasites (P. berghei and P.
yoelii) can occur, but only occurs at high levels when one of two proteins
(P230 or P48/45) is absent from the surface of female gametes, which
indicates that these proteins are involved in gamete recognition. I find that
P230, P48/45 and P47 (a possible interaction partner) are evolving under
positive selection, a feature often observed in gamete recognition proteins
of other taxa. Finally, I show that the fertilization success of P. berghei is
reduced in the presence of P. yoelii, but not vice-versa, which indicates
asymmetric reproductive interference.
3). Sex allocation (chapter 4): I carry the first test of sex allocation’s
assumption that immunity impacts on the fertility of Plasmodium male
gametocytes/gametes more than on the fertility of females. I show that
while the fertility of both males and females is equally affected, males are
affected during gametogenesis and females are mostly affected through
gamete dysfunction (i.e. gametes can mate but zygotes fail to develop),
which is in agreement with the assumptions of theory. In collaboration, I
incorporate these effects into sex allocation theory and predict that malaria
parasites can minimize the effects of factors that kill gametocytes/gametes
by adjusting their sex ratios. On the other hand sex ratio adjustment cannot
compensate for gamete dysfunction or zygote death. These results have
applied implications for transmission-blocking vaccines.
4). Infection dynamics of mixed-species infections (chapter 5): I develop a
series of experiments to test how a focal parasite species (P. yoelii) is
affected by competition with heterospecifics (P. chabaudi) and how the
interaction between the two species is mediated by immunity and resource
availability. I show that P. chabaudi can boost P. yoelii above its single
species level (i.e. facilitation) and that this is mediated by resource
availability. On the other hand, P. yoelii’s performance can also be
hindered in mice that were exposed to a P. chabaudi infection. My results
also reveal that host mortality is exacerbated in mixed-species infections
of naïve mice, which may be due to an inability of the host to achieve the
right balance between the production and the destruction of red blood
cells, when dealing with a mixed-species infection.
The work I present here tackles fundamental questions concerning the transmission
biology and the within-host interactions of malaria parasites The results presented
demonstrate the importance of interactions between hosts and parasites and between
different parasite species (at the molecular and the whole organism levels) for
determining the outcome of transmission, virulence and within-host parasite
performance. | en |
dc.language.iso | en | |
dc.publisher | The University of Edinburgh | en |
dc.relation.hasversion | Ramiro, R. S., J. Alpedrinha, L. Carter, A. Gardner, and S. E. Reece. 2011. Sex and Death: The Effects of Innate Immune Factors on the Sexual Reproduction of Malaria Parasites. PLoS Pathog 7. | en |
dc.relation.hasversion | Reece, S. E., R. S. Ramiro, and D. H. Nussey. 2009. Plastic parasites: sophisticated strategies for survival and reproduction? . Evol Appl 2:11-23. | en |
dc.subject | malaria | en |
dc.subject | Plasmodium hybridisation | en |
dc.subject | mating | en |
dc.subject | mixed-species | en |
dc.title | Evolution and ecology of malaria parasites: from mating to mixed‐species infections | en |
dc.type | Thesis or Dissertation | en |
dc.type.qualificationlevel | Doctoral | en |
dc.type.qualificationname | PhD Doctor of Philosophy | en |