Adaptive mutation mechanism may explain some forms of antibiotic resistance

Scientists at Winship Cancer Institute, Emory University have observed that an apparent "back channel" for genetic information called retromutagenesis can encourage adaptive mutation to take place in bacteria.

The results are scheduled for publication in PLOS Genetics on Tuesday, August 25.

"This mechanism may explain how bacteria develop resistance to some types of antibiotics under selective pressure, as well as how mutations in cancer cells enable their growth or resistance to chemotherapy drugs," says senior author Paul Doetsch, PhD.

Doetsch is professor of biochemistry, radiation oncology and hematology and medical oncology at Emory University School of Medicine and associate director of basic research at Winship Cancer Institute. The first author of the paper is recently graduated Genetics and Molecular Biology graduate student Jordan Morreal, PhD.

Retromutagenesis resolves the puzzle: if cells aren't growing because they're under stress, which means their DNA isn't being copied, how do the new mutants appear?

The answer: a mutation appears in the RNA first.

The mutation in the RNA results in a protein with augmented function that helps the cells grow, giving them a chance to replicate their DNA and for subsequent DNA mutations to exert their effects.

In the PLOS Genetics paper, scientists led by Doetsch and colleague Bernard Weiss, MD, provide evidence that retromutagenesis is occurring in E. coli bacteria forced to grow on the sugar lactose as their only source of energy.

The bacterial strain tested had a disabling mutation in a gene that, if functional, would allow the cells to use lactose. When exposed to high levels of nitrous acid, a DNA-damaging agent, mutations appeared in the bacteria and some of the bacteria could grow. By analyzing where exactly on the DNA the mutations occurred, the scientists concluded that retromutagenesis was contributing to bacterial growth.

"Most of the previous experiments on adaptive mutation have attempted to rule out growth of the parent cells during selection, which is almost impossible to do with the necessary rigor... Instead of measuring overall DNA replication via cellular growth in the parental population during selection as in previously published experiments, we are able to gauge DNA replication specifically in the revertants via NTS [non-transcribed strand] mutations. Low frequency of NTS mutations found after direct selection indicates there was little DNA synthesis before gene expression and strongly supports the model of retromutagenesis," the authors write.

The authors note that retromutagenesis may explain previous observations of bacteria developing resistance to the antibiotic ciprofloxacin, as well as mutations in the human p53 Ras oncogene, seen in many forms of cancer.

The research was supported by the National Institute of Environmental Health Sciences (P01ES011163).