Scientists reveal the origins of sleeping sickness parasite
Published: 26 January 2016
A parasite which kills thousands of people each year in sub-Saharan Africa arose comparatively recently, and its unusual sex life may lead to its own extinction. Researchers in the Institute reveal that T.b. gambiense, the main cause of sleeping sickness, has existed for thousands of years without reproducing sexually. The team show that T.b. gambiense jumped into to humans in the past 10,000 with present day populations all descended from a single ancestor.
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A parasite which kills thousands of people each year in sub-Saharan Africa arose comparatively recently, and its unusual sex life may lead to its own extinction.
Researchers from the Institute and Wellcome Trust Centre for Molecular Parasitology have discovered that Trypanosoma brucei gambiense (T.b. gambiense), the main parasite that causes African Sleeping Sickness, has existed for thousands of years without reproducing sexually.
In a study, published today in the journal eLife, the researchers describe how sequencing the genomes of a large collection of T.b. gambiense has revealed that the parasite population today is made up entirely of asexual clones descended from a single ancestor.
Originally an animal parasite, T.b. gambiense ‘jumped’ into the human population within the last 10,000 years, at a time when livestock farming was developing in West Africa. The parasite is transmitted to humans bitten by tsetse flies, but once in the bloodstream, T.b. gambiense can lie dormant for months or years without causing symptoms. Infected people suffer increasing damage to their nervous system, until they eventually lapse into a coma—the symptom which gives sleeping sickness its name.
The team have been using whole genome sequencing of T.b. gambiense (the main cause of sleeping sickness in sub-Saharan Africa), to hunt for an elusive genetic phenomenon first proposed 20 years ago. This phenomenon—the Meselson effect—predicts that pairs of chromosomes within asexual organisms will evolve independently of each other and become increasingly different over time. But until this study, no-one has found conclusive evidence of the effect's existence. This report provides the first demonstration of the Meselson effect at a genome-wide level in any organism.
The study’s lead author Dr Willie Weir and member of the Institute, said:
“An organism’s genetic blueprint is encoded in DNA packaged within structures called chromosomes. Most organisms have two copies of each chromosome and, through sexual reproduction, the DNA within the chromosomes can recombine randomly, in effect shuffling the deck of DNA cards. This process generates genetic diversity and, through natural selection, undesirable combinations and mutations are eliminated from the population, promoting long-term survival of the species.
However, some organisms appear not to have sex at all. Evolutionary theory predicts that they should face extinction in the long-term and that a lack of sexual recombination should leave a characteristic genetic ‘signature’ in their DNA. While being theoretically predicted for almost twenty years, evidence for this signature has been elusive.”
The team’s research has shown that T.b. gambiense arose from a single individual parasite within the last ten millennia and, over time, mutations have accumulated on each chromosome copy. Because of a lack of sexual recombination, each copy has evolved independently of the other, demonstrating the predicted ‘Meselson effect’.
Dr Macleod, senior author on the paper, added: “We have detected the first conclusive evidence of this effect in any organism at the genome-wide level. Essentially, the parasite compensates for its lack of sex by overwriting mutations through ‘copying and pasting’ DNA from one chromosome to another. However, our study suggests that this can only go some way to compensating for a lack of sex. Theoretically, this parasite species cannot survive indefinitely without sex and the predicted consequence of this is that it will become extinct in the long-term.
In the near to medium term, though, identifying this weakness in the parasite could help researchers find ways to develop new forms of treatment for sleeping sickness which build on our findings. For example, the inability of individuals to share genetic information with each other could hamper the ability of the organism to develop resistance to multiple drugs.”
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. The research was funded by the Wellcome Trust.
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First published: 26 January 2016