NO-stressed Y. pseudotuberculosis have decreased cell division rates in the mouse spleen

Abstract

Fluorescence dilution approaches can detect bacterial cell division events, and can detect if there are differential rates of cell division across individual cells within a population. This approach typically involves inducing expression of a fluorescent protein, and then tracking partitioning of fluorescence into daughter cells. However, fluorescence can be diluted very quickly within a rapidly replicating population, such as pathogenic bacterial populations replicating within host tissues. To overcome this limitation, we have generated a revTetR reporter construct, where mCherry is constitutively expressed, and repressed by addition of tetracyclines, resulting in fluorescence dilution within defined timeframes. We show that mCherry signal is diluted in replicating populations, and that mCherry signal accumulates in growth-inhibited populations, including during exposure to inhibitory concentrations of antibiotics and during nitric oxide exposure. Furthermore, we show that tetracyclines can be delivered to the mouse spleen during Yersinia pseudotuberculosis infection. We defined a drug concentration that results in even exposure of cells to tetracyclines, and used this system to visualize cell division within defined timeframes post-inoculation. revTetR mCherry signal did not appear enriched in a particular spatial location within replicating centers of bacteria. However, the addition of a NO-sensing reporter (Phmp::gfp) showed that heightened NO exposure correlated with heightened mCherry signal, suggesting decreased cell division within this subpopulation. This revTetR reporter will provide a critical tool for future studies to identify and isolate slowly replicating bacterial subpopulations from host tissues.