Resistance To Antibiotics İs Ancient, McMaster Study Finds
Scientists were surprised at how fast bacteria developed resistance to the miracle antibiotic drugs when they were developed less than a century ago. Now scientists at McMaster University have found that resistance has been around for at least 30,000 years. Research findings published August 31 in the science journal Nature show antibiotic resistance is a natural phenomenon that predates the modern clinical antibiotic use. Principal investigators for the study are Gerry Wright, scientific director of the Michael G. DeGroote Institute for Infectious Disease Research and Hendrik Poinar, McMaster evolutionary geneticist.
"Antibiotic resistance is seen as a current problem and the fact that antibiotics are becoming less effective because of resistance spreading in hospitals is a known fact," said Wright. "The big question is where does all of this resistance come from?"
After years of studying bacterial DNA extracted from soil frozen in 30,000-year-old permafrost from the Yukon Territories, the researchers were able to develop methods to isolate DNA within McMaster's Ancient DNA Centre. Using state-of-the-art molecular biological techniques, methods were developed to tease out small stretches of ancient DNA.
Researchers discovered antibiotic resistant genes existed beside genes that encoded DNA for ancient life, such as mammoths, horse and bison as well as plants only found in that locality during the last interglacial period in the Pleistocene era, at least 30,000 years ago. They focused on a specific area of antibiotic resistance to the drug vancomycin, a significant clinical problem that emerged in 1980s and continues to be associated with outbreaks of hospital-acquired infections worldwide.
"We identified that these genes were present in the permafrost at depths consistent with the age of the other DNAs, such as the mammoth. Brian Golding of McMaster's Department of Biology showed that these were not contemporary, but formed part of the same family tree. We then recreated the gene product in the lab, purified its protein and showed that it had the same activity and structure then as it does now."
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