For more than a decade, biologist Mariam Barlow has been working on the theory that administering antibiotics on a rotating basis could be a solution to antibiotic resistance. After years of research, Barlow had lots of data, but she needed a more precise way to make sense of it all — something that was so specific it could easily be used to treat patients. So, she joined forces with a team of mathematicians. And the amazing results could help solve an enormous, worldwide problem.
In a nutshell, the team of biologists and mathematicians developed a software program that generates a road map to reverse the evolution of antibiotic resistance in bacteria. In a study published earlier this month in the journal PLOS ONE, they unveiled a mathematical model that pinpoints optimal antibiotic cycling patterns with the highest probability of turning back the evolutionary clock of antibiotic resistance. Barlow, an evolutionary biologist and associate professor at the University of California-Merced School of Natural Sciences, told me that she and fellow researchers found cycles of antibiotics that could reverse resistance and drive bacteria back to a state observed in the 1960s — a state the researchers call the “wild type state.” So it’s not surprising that the software that makes it all possible was aptly named “Time Machine.”
“It makes sense that we would look for answers (to antibiotic resistance) in evolutionary biology,” Barlow told me. “Bacteria are so good at evolving — and they’ll probably find new ways we don’t even know about yet — but based on what we’ve seen, this is something we can deal with. Antibiotic resistance is something we can handle.”
The research comes at a time of widespread concern that without a coordinated, well-funded response to growing antibiotic resistance, medicine could lose some of its most effective, life-saving tools. Every year, according to the Centers for Disease Control and Prevention, about 2 million people become infected with antibiotic-resistant bacteria and at least 23,000 people die as a result of such infection. For example, last year, CDC described the development of antibiotic-resistant gonorrhea as an “urgent public health threat,” warning that we may run out of options for treating the sexually transmitted disease. Also at the federal level, the White House recently released its first “National Action Plan for Combating Antibiotic-Resistant Bacteria” and in his fiscal year 2016 budget proposal, President Obama recommended doubling federal funds to find solutions to antibiotic resistance to $1.2 billion (of course, that recommendation has to get through Congress). Everyone agrees that antibiotic resistance is a huge problem with fatal consequences.
Thankfully, Barlow and her colleagues may have found an answer that not only tackles resistance, but helps preserve the effectiveness of existing antibiotics. And here’s how they did it. Researchers created bacteria in the lab, exposed it to 15 different antibiotics and measured their growth rates. Using those measurements, the team of biologists and mathematicians computed the probability of mutations required to return the bacteria back to its harmless state. They tested up to six antibiotics in rotation at a time and computed thousands of measurements to find the most likely cycling strategies for reversing the development of antibiotic resistance.
Researchers eventually concluded that the Time Machine software and its mathematical foundations proved to be a promising way to quickly and more precisely generate an optimal antibiotic cycling plan most likely to reverse resistance. Simply put, the software is a matchmaker — it computes which antibiotic goes with which mutation at which point in time to best manage the evolution of resistance and ultimately, cure the patient.
And Barlow reminded me that this type of precision is not necessarily the norm in medicine. Even though incorrect antibiotic prescribing is a main driver of antibiotic resistance, the current dearth in rapid antibiotic-resistant diagnostics means physicians are often left with little choice but to start treating an ill patient before seeing any lab results. However, antibiotic cycling can help guide that process to make a better, more ordered treatment plan — “it’s an approach that can be accessible to any hospital and can help empiric therapy be more reliable,” Barlow said.
In the PLOS ONE study, authors Barlow, Kristina Crona, Portia Mira, Devin Greene, Juan Meza and Bernd Sturmfels write:
Efforts to remove resistance genes from clinical environments by either discontinuing or reducing the use of specific antibiotics for some period of time, either through general reduction of antibiotic consumption or periodic rotations of antibiotics (cycling) have not worked in any reliable or reproducible manner; indeed it would have been surprising if they had worked.
Since antibiotic resistance is unavoidable, it only makes sense to accept its inevitability and develop methods for mitigating the consequences. One reasonable approach is to rotate the use of antibiotics. This has been implemented in many ways and there are recent studies to model the optimal duration, mixing versus cycling, and how relaxed antibiotic cycles may be and still function as planned. However, none of those models have focused on developing a method for designing an optimal succession of antibiotics.
Which is exactly what the Time Machine software attempts to do. As the study mentioned, antibiotic cycling has been studied before, but it was the marriage of evolutionary biology and mathematics that made the difference, Barlow said.
“We took the theory of adaptive landscapes and used it as a foundation for organizing our data and with that style of organized data, a team of mathematicians was able to develop a model,” Barlow said. “It’s just one of those wonderful things that just falls into place.”
Study co-author Kristina Crona, an assistant professor in the Department of Mathematics and Statistics at American University, noted that the antibiotic cycling problem perfectly illustrates the role of mathematics in biology. Unfortunately, she told me, the two fields don’t have a strong tradition of working together.
“How can we use antibiotics as well as possible? What sequence of drugs would be best? How do we find the best treatment plan?” Crona asked. “These are all very quantitative problems. If we can move medicine and biology closer to mathematics, I think it would produce all kinds of advantages.”
Of course, the ultimate goal is to create a cycling protocol that physicians and health care providers can easily use in a clinical setting, Barlow said. To begin that translation process, Barlow and colleagues are collaborating with a hospital in Merced to collect resistant isolates and analyze the relationship between the development of antibiotic resistance and the antibiotics being prescribed by staff.
“I’ve gotten so many great responses (to the study), it’s almost overwhelming,” Barlow told me. “This idea that we’ve been working on for so long — to see it progress to a level that people can understand and get excited about is so rewarding.”
Kim Krisberg is a freelance public health writer living in Austin, Texas, and has been writing about public health for more than a decade.
“…she and fellow researchers found cycles of antibiotics that could reverse resistance and drive the bacteria back to the state it had been in the 1960s — a state the researchers call the “wild type state” … the team of biologists and mathematicians computed the probability of mutations required to return the bacteria back to its harmless state.”
Back to the 60s, to the “wild type state”, to the (peace and love) “harmless state”. Kind of goes together.
But I’m not sure it goes together for bacteria. Bacteria “evolved” resistance to antibiotics long before antibiotics were ever invented. Example:
Still pushing your lies and misrepresentations sn? Isn't there a commandment about that?
Antibiotic resistance is the evolutionary response to the strong selective pressure that results from exposure to these compounds. The horizontal dissemination of resistance genes into bacterial species and genera that are not themselves intrinsically resistant, as well as the maintenance of resistance mutations vertically through populations is likely to be the result of contemporary use of these drugs in the clinic and on the farm. Support for this hypothesis is the infrequency of antibiotic resistance in collections of pathogenic bacteria that pre-date the antibiotic era.
Bacteria recovered underneath undisturbed 30,000 year old permafrost contain genes encoding resistance to modern antibiotics like vancomycin, tetracycline, and beta lactams.
See Noevo, what are you going on about? Wild-type is simply the most common allele of a gene out in the wild (as opposed to in labs), and I don't think anyone has argued that antibiotic-resistant bacteria of any species is more common than their non-resistant counterparts.
This certainly sounds like good news. Too bad it's attracted some nonsense in the comments.
Next step should be to actually try this in-vitro and then try it on a mouse model. I'll be keeping my ears open for more on this subject.