Figure 3 Functional clustering of common regulated MAP genes under acid-nitrosative multi-stress and THP-1 infection. Expression ratios were log2-transformed, and displayed according to the color code at the top of the figure. Venn diagrams showing the number of overlapping and unique genes modulated more than 2.0-fold under the two experimental conditions are on the right of each colored macrocluster. The number of induced or repressed overlapping genes is indicated in the green ellipse or red ellipse, respectively. The down-regulation of pyrimidine synthesis is a common repressed metabolism between the acid-nitrosative selleck chemical stress
and the infection especially in the first where the synthesis is repressed by the pyrR regulator resulting in a down-regulation of pyr genes, perfectly JPH203 solubility dmso correlated with the same mechanism of genic regulation occurred in previous experiments inherent MTB’s response to inhibitors of translation [19] in which it was shown that the translational inhibition induced the bacterium to trigger a response that included both the repression of de novo nucleotides synthesis and the increase of the synthesis of ribosomes. Finally,
the situation appears very complex in the common metabolism of synthesis of vitamins and cofactors in which the click here up-regulation of folate synthesis occurs in both transcriptional
profiles with the same entry aminodeoxychorismate lyase protein (MAP1079) as well as the synthesis of vitamin B12 (cobT) and the synthesis of porphyrins 4��8C (hemE). In this case, the up-regulation of porphyrins synthesis may be due to the situation of starvation that requires MAP to shift its energy metabolism from an aerobic condition to an anaerobic state using enzymes that cooperate with ferredoxines in the transfer of electrons in redox reactions as like as a metabolism pattern already identified in previous studies with the induction of slow growth and hypoxic cultures of Mycobacterium smegmatis (MSMEG) [57]. Further evidences about the switch of energy metabolism from aerobic pathway to anaerobic conditions are represented by the common up-regulation of the synthesis of menaquinone in both experiments, respectively with menA and menB in acid-nitrosative stress and in the cellular infection, since it could be an essential factor for the survival of non-replicating mycobacteria [58], thus corroborating the decrease of cell multiplication given by the down-regulation of functional genes for cell division. The only homology in the down-regulation profile of metabolism of cofactors is the repression of coaA, probably in line with the down-regulation of lipid degradation.