Exposure of a bacterial culture to an antibiotic or other lethal stress typically results in the generation of sub-populations of live cells ("persisters") and dead cells, and, in some cases, viable but non-culturable cells. Studies aimed at understanding the mechanisms of antibiotic killing and bacterial persistence will require the purification and analysis of each of these sub-populations in isolation. This paper reports a method based on continuous-flow dielectrophoresis to separate live and dead cells from antibiotic-treated bacterial cultures. Our experiments were carried out on Mycobacterium smegmatis, a model organism that is closely related to the etiological agent of human tuberculosis.
Sandor Kasas, María Inés Villalba, Allan Bonvallat, Eugenia Rossetti
Camille Véronique Bernadette Goemans, Florian Huber
César Pulgarin, Stefanos Giannakis, Truong-Thien Melvin Le, Jérémie Decker