MIXED-GENOTYPE INFECTIONS OF MALARIA PARASITES - WITHIN-HOST DYNAMICSAND TRANSMISSION SUCCESS OF COMPETING CLONES

Citation
Lh. Taylor et al., MIXED-GENOTYPE INFECTIONS OF MALARIA PARASITES - WITHIN-HOST DYNAMICSAND TRANSMISSION SUCCESS OF COMPETING CLONES, Proceedings - Royal Society. Biological Sciences, 264(1383), 1997, pp. 927-935
Citations number
44
Categorie Soggetti
Biology
ISSN journal
09628452
Volume
264
Issue
1383
Year of publication
1997
Pages
927 - 935
Database
ISI
SICI code
0962-8452(1997)264:1383<927:MIOMP->2.0.ZU;2-O
Abstract
Mixed-genotype infections of microparasites are common, but almost not hing is known about how competitive interactions within hosts affect t he subsequent transmission success of individual genotypes. We investi gated changes in the composition of mixed-genotype infections of the r odent malaria Plasmodium chabaudi clones CR and ER by monoclonal antib ody analysis of the asexual infection in mice, and by PCR amplificatio n of clone-specific alleles in oocysts sampled from mosquitoes which h ad fed on these mice. Mixed-clone infections were initiated with a 9:1 ratio of the two clones, with ER as the minority in the first experim ent and CR as the minority in the second experiment. When beginning as the majority, clones achieved parasite densities in mice comparable t o those achieved in control (single-clone) infections. When they began as the minority, clones were suppressed to less than 10 % of control parasitaemias during the early part of the infections. However, in mos quitoes, the frequency of the initially rare clone was substantially g reater than it was in mice at the start of the infection or four days prior to the feed. In both experiments, the minority clone in the inoc ula produced as many, or more, oocysts than it did as a single-clone i nfection. These experiments show that asexual dominance during most of the infection is poorly correlated to transmission probability, and t herefore that the assumption that within-host population size correlat es to transmission probability may not be warranted. They also raise t he fundamental question of why transmission rates of individual genoty pes are often higher from mixed than single-clone infections.