Evolutionary theory predicts that pairs of chromosomes within asexual organisms will evolve independently of each other and become increasingly different over time in a phenomenon called the 'Meselson effect'.
While this event was first predicted almost twenty years ago, evidence for it has proved elusive.
Now, researchers from the University of Glasgow have demonstrated the Meselson effect for the first time in any organism at a genome-wide level, studying a parasite called Trypanosoma brucei gambiense (T.b. gambiense). Their findings are to be published in the journal eLife. The research was conducted at the Wellcome Trust Centre for Molecular Parasitology in the University's Institute of Biodiversity Animal Health and Comparative Medicine.
T.b. gambiense is responsible for causing African sleeping sickness in humans, leading to severe symptoms including fever, headaches, extreme fatigue, and aching muscles and joints, which do not occur until weeks or sometimes even months after infection.
These symptoms extend to neurologic problems, such as progressive confusion and personality changes, when the infection invades the central nervous system.
In order to demonstrate the Meselson effect in T.b. gambiense, the research team, led by Dr. Annette Macleod, sequenced the genomes of 85 isolates of the parasite, including multiple samples from disease focus points within Guinea, Cote d'Ivoire and Cameroon, collected over fifty years from 1952 to 2004.
The similarity of the genomes studied from these different locations, together with a lack of recombination in the evolution of the parasite, suggests that this sub-species emerged from a single individual within the last 10,000 years.
"It was around this time that livestock farming was developing in West Africa, allowing the parasite, which was originally an animal organism, to 'jump' from one species to the other via the Tsetse fly," says lead author Dr. Willie Weir.
"Since then, mutations have built up and the lack of sexual recombination in T.b. gambiense means that the two chromosomes in each pair have evolved independently of each other, demonstrating the Meselson effect."
Dr. Weir adds that the parasites' inability to recombine with each other prevents genes from being exchanged between strains. This could subsequently hamper the ability of the organism to develop resistance to multiple drugs.
The team also uncovered evidence that the parasite uses gene conversion to compensate for its lack of sex.
This mechanism essentially repairs the inferior, or mutated, copy of a gene on a chromosome by 'copying and pasting' the superior copy from the chromosome's partner. The future challenge will be to investigate the effectiveness of this mechanism in the long term, as evolutionary theory suggests that asexual organisms should eventually face extinction. If T.b. gambiense shares this fate, the major cause of African sleeping sickness will be eliminated - although it is impossible to predict when this might happen.
The paper 'Population genomics reveals the origin and asexual evolution of human infective trypanosomes' can be freely accessed online at http://dx.doi.org/10.7554/eLife.11473. Contents, including text, figures, and data, are free to reuse under a CC BY 4.0 license.
eLife is a unique collaboration between the funders and practitioners of research to improve the way important research is selected, presented, and shared. eLife publishes outstanding works across the life sciences and biomedicine -- from basic biological research to applied, translational, and clinical studies. All papers are selected by active scientists in the research community. Decisions and responses are agreed by the reviewers and consolidated by the Reviewing Editor into a single, clear set of instructions for authors, removing the need for laborious cycles of revision and allowing authors to publish their findings quickly. eLife is supported by the Howard Hughes Medical Institute, the Max Planck Society, and the Wellcome Trust. Learn more at elifesciences.org.