Why antibiotic-resistant cells persist
University of Houston biomolecular engineer receives NSF CAREER award to explore cells that defy efforts to kill them
University of Houston
The CAREER award will provide Orman with $500,000 to study so-called persister cells - those that go dormant and then become tolerant to extraordinary levels of antibiotics.
Antibiotic tolerance is one of the most critical global public health threats of the 21st century.
"Nearly all bacterial cultures contain a small population of persister cells," said Orman. "Persisters are thought to be responsible for recurring chronic infections such as those of the urinary tract and for creating drug-resistant mutants." Biofilms, a slimy buildup of bacteria (like dental plaque) cause most bacterial infections, and persister cells, produced in biofilms, might cause biofilms to be multidrug tolerant, too.
Orman's goal is to figure out just what makes these persister cells tick, to identify common mechanisms they exhibit from a variety of bacterial strains. Interestingly, persister cells go in and out of their state of hibernation, and Orman will take a close look at that.
"Persister cell survival is marked by growth inhibition during antibiotic treatment and resumption of growth upon removal of antibiotics. Persisters are generally assumed to be dormant cells with a depressed metabolism," said Orman. In contrast, his hypothesis driving this project is that persisters have active but unique metabolic mechanisms that regulate the reversible switching and maintenance of these cells. As part of the project, Orman will also develop outreach programs and materials to reach underrepresented youth in fourth through eighth grades.
For Orman, the name of the cell fits well with his resolute persistence in studying them. Previously he developed the first methods to directly measure the metabolism of persister cells. He also developed cell sorting strategies to segregate persisters from highly heterogeneous bacterial cell populations. He will be using his methods in the NSF research project.
"The results will challenge paradigms regarding persister cell dormancy and metabolism, shed light on persister cell resuscitation mechanisms, provide platforms for studying the metabolic heterogeneity of persister cell subpopulations during and after antibiotic treatment, and integrate multiple lines of evidence to enhance our understanding of the eco-evolutionary aspects of bacterial persistence," said Orman.
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