There is also evidence that tubercle bacilli suffer nutrient deprivation in lung lesions [7]. Vorinostat Conditions of nutrient limitation have been used to investigate the ability of M. tuberculosis to persist in a non-growing state for long periods of time [7–9]. Importantly, dormancy is a common behavior to both pathogenic and non-pathogenic mycobacteria, in vitro [4, 10, 11], allowing the study of pathogenic species by using non-pathogens as model. M. smegmatis is a fast growing non pathogenic mycobacterium frequently used as a model system to study its pathogenic counterpart M. tuberculosis. M.

smegmatis becomes dormant in low oxygen concentration conditions [5] and remains viable for over 650 days when it suffers carbon, nitrogen and phosphorous-starvation [12]. Based on www.selleckchem.com/products/crt0066101.html these observations, we decided to use low oxygen and limiting nutrient conditions to develop an in vitro system. Then, we used such system to screen a library of M. smegmatis generated by insertion

mutagenesis and look for mutants defective in dormancy [13]. This strategy allowed the isolation of two mutants with insertions mapping in the uvrA gene. The UvrA protein belongs to the nucleotide excision Z-DEVD-FMK cell line repair system (NER) and is highly conserved among mycobacteria. NER counteracts the deleterious effects of DNA lesions acting as an endonuclease enzyme complex including four Uvr proteins: UvrA, UvrB, UvrC, and UvrD. UvrA, togheter with UvrB, plays a key role in the recognition of DNA damaged sites [14]. UvrC, together with UvrB, perform a single strand incision at both sides of the damaged site and the DNA fragment is removed by the action of the UvrD helicase. Oxymatrine While this DNA-repair system has been largely analyzed in E. coli [14], it remains poorly characterized in mycobacteria. It has been recently reported that the M. smegmatis genome is predicted to encode two additional UvrA proteins, named UvrA2 and UvrA-like protein, whose function are still unknown [15]. Here we report that the M. smegmatis UvrA protein is

essential for the mycobacterial dormancy behavior and survival in hostile growth conditions, such as low oxygen and carbon content, also observed in the granuloma. Our results, together with recent analyses [16–19], suggest that the NER system plays a key role in M. smegmatis dormancy. Results M. smegmatis dormancy is induced under conditions of low oxygen and low carbon availability In order to develop a simple and reliable strategy to screen a M. smegmatis library for mutants unable to grow in conditions of hypoxia and low carbon concentration, we first compared the effects of these conditions on the dormancy behavior of M. smegmatis wt and ppk1- mutant cells [the latter were used as a control as they have been recently reported to be sensitive to hypoxic condition [20].