The creation of genetically modified and entirely synthetic organisms continues to generate excitement as well as worry.
Such organisms are already churning out insulin and other drug ingredients, helping produce biofuels, teaching scientists about human disease and improving fishing and agriculture. While the risks can be exaggerated to frightening effect, modified organisms do have the potential to upset natural ecosystems if they were to escape.
Physical containment isn't enough. Lab dishes and industrial vats can break; workers can go home with inadvertently contaminated clothes. And some organisms are meant for use in open environments, such as mosquitoes that can't spread malaria.
So attention turns to biocontainment: building in biological safeguards to prevent modified organisms from surviving where they're not meant to. To do so, geneticists and synthetic biologists find themselves taking a cue from safety engineers.
"If you make a chemical that's potentially explosive, you put stabilizers in it. If you build a car, you put in seat belts and airbags," said George Church, Robert Winthrop Professor of Genetics at Harvard Medical School and core faculty member at the Wyss Institute.
And if you've created the world's first genomically recoded organism, a strain of Escherichia coli with a radically changed genome, as Church's group announced in 2013, you make its life dependent on something only you can supply.
Church and colleagues report Jan. 21 in Nature that they further modified their 2013 E. coli to incorporate a synthetic amino acid in many places throughout their genomes. Without this amino acid, the bacteria can't perform the vital job of translating their RNA into properly folded proteins.
The E. coli can't make this unnatural amino acid themselves or find it anywhere in the wild; they have to eat it in specially cooked-up lab cultures.
A separate team reports in Nature that it was able to engineer the same strain of E. coli to become dependent on a synthetic amino acid using different methods. That group was led by a longtime collaborator of Church's, Farren Isaacs of Yale University.
The two studies are the first to use synthetic nutrient dependency as a biocontainment strategy, and suggest that it might be useful for making genetically modified organisms safer in an open environment.
In addition, "We now have the first example of genome-scale engineering rather than gene editing or genome copying," said Church. "This is the most radically altered genome to date in terms of genome function. We have not only a new code, but also a new amino acid, and the organism is totally dependent on it."
Church's team, led by first authors Dan Mandell and Marc Lajoie, HMS research fellows in genetics, also made the E. coli resistant to two viruses, with plans to expand that list.
The modifications offer theoretically safer E. coli strains that could be used in biotechnology applications with less fear that they will be contaminated by viruses, which can be financially disastrous, or cause ecological trouble if they spill. (E. coli is one of the main organisms used in industry.)
Hooked on amino acids
Scientists have been exploring two main biocontainment methods, but each has weaknesses. Church was determined to fix them.
One method involves turning normally self-sufficient organisms like E. coli into auxotrophs, which can't make certain nutrients they need for growth. Humans are auxotrophs, which is why we need to include vitamins and other "essential" nutrients in our diets.
Altering the genetics of E. coli so they can't make a naturally occurring nutrient doesn't always work, said Church, because some of them manage to scavenge the nutrient from their surroundings. He lowered that risk by making the E. coli dependent on a nutrient not found in nature.
Another pitfall of making auxotrophs is that some E. coli could evolve a way to synthesize the nutrient they need. Or they could acquire the ability while exchanging bits of DNA with other E. coli in a process called horizontal gene transfer.
Church believes his team protected against those possibilities because it had to make 49 genetic changes to the E. coli to make them dependent on the artificial nutrient. The chance one of the bacteria could randomly undo all of those changes without also acquiring a harmful mutation, he said, is incredibly slim.
Church's solution also took care of concerns he had with another biocontainment technique, in which genetic "kill switches" make bacteria vulnerable to a toxin so spills can be quickly neutralized. "All you have to do to kill a kill switch is turn it off," which can be done in any number of ways, Church said. Routing around the dependency on the artificial amino acid is much harder.
Church determined that another key to making a successful "synthetic auxotroph" was to ensure that the E. coli's lives depended on the artificial amino acid. Otherwise, escaped E. coli could keep rolling along even if they couldn't make or scavenge it. So his group targeted proteins that drive the essential functions of the cell.
"If you put it off on the periphery, like on the paint job of your car, the car will still run," he explained. "You have to embed the dependency smack in the middle of the engine, like the crank shaft, so it now has a particular part you can only get from, say, one manufacturer in Europe."
Building a safer bacterium
The need to choose a process essential to E. coli survival and a nutrient not found in nature "limited us to a small number of genes," Church said. His team used computational tools to design proteins that might cause the desired "irreversible, inescapable dependency." They took the best candidates, synthesized them and tested them in actual E. coli.
They ended up with three successful redesigned essential proteins and two dependent E. coli strains. "Using three proteins together is more powerful than using them separately," Church said. He envisions future E. coli modified to require even more synthetic amino acids to make escape virtually impossible.
As it was, the escape rate--the number of E. coli able to survive without being fed the synthetic amino acid--was "so low we couldn't detect it," Church said.
The group grew a total of 1 trillion E. coli cells from various experiments, and after two weeks none had escaped. "That's 10,000 times better than the National Institutes of Health's recommendation for escape rate for genetically modified organisms," said Church.
The weaknesses in Church's methods remain to be seen. For now, he is satisfied with the results his group has obtained by pushing the limits of available testing.
"As part of our dedication to safety engineering in biology, we're trying to get better at creating physically contained test systems to develop something that eventually will be so biologically contained that we won't need physical containment anymore," said Church.
In the meantime, he said, "we can use the physical containment to debug it and make sure it actually works."
This work was funded by the U.S. Department of Energy (grant DE-FG02-02ER63445).
Written by Stephanie Dutchen
Harvard Medical School (hms.harvard.edu) has more than 7,500 full-time faculty working in 11 academic departments located at the School's Boston campus or in one of 47 hospital-based clinical departments at 16 Harvard-affiliated teaching hospitals and research institutes. Those affiliates include Beth Israel Deaconess Medical Center, Brigham and Women's Hospital, Cambridge Health Alliance, Boston Children's Hospital, Dana-Farber Cancer Institute, Harvard Pilgrim Health Care, Hebrew Senior Life, Joslin Diabetes Center, Judge Baker Children's Center, Massachusetts Eye and Ear Infirmary, Massachusetts General Hospital, McLean Hospital, Mount Auburn Hospital, Schepens Eye Research Institute, Spaulding Rehabilitation Hospital and VA Boston Healthcare System.