Prospection for more specific targets in mycobacterial genomes seems consequently necessary in order to improve current detection tools based on proteins and/or DNA. The new atpE real-time PCR method that we propose is just as specific, but more sensitive than the previously proposed rrs real-time PCR method which cannot detect some mycobacterial species [17]. The proposed strategy is aimed at comparing mycobacterial and non-mycobacterial genomic proteins to Crenolanib in vitro reference genomic DNA of M. tuberculosis H37Rv, sorting proteins according to similarity requests and listing candidate proteins (Figure 1). We chose

to perform protein-level comparisons in order to identify exclusively conserved proteins in Mycobacterium spp. because non-coding regions, as intergenic regions and insertion

click here sequences, are known to be less conserved than coding regions in M. tuberculosis genomes [30]. According to literature, our results selleck products emphasized that almost half of the M. tuberculosis H37Rv predicted proteins are potentially present in the genomes of CNM group members. More precisely, mycobacteria belong to Actinobacteria which may explain the presence of 48 to 73% shared genes among high G + C content microorganisms [31–34]. In addition, horizontal gene transfers from different bacteria widely present in soil or water, especially Rhodococcus sp., Nocardia sp. and Streptomyces sp. were previously considered to have happened in the Mycobacterium genus which may also explain the shared proteins with non-mycobacterial species [24, 27, 35]. These observations show that CNM group members must be taken into account in order to develop highly specific mycobacterial targets, considering Cobimetinib molecular weight that these bacteria are commonly found in aquatic and terrestrial environments [36, 37]. Our study

showed that 11 proteins exclusively conserved in the 16 mycobacterial genomes studied could be selected using our genome comparison strategy (i.e. proteins coded by atpE, atpB, cmaA1, lppM, PE5, PPE48, esxG, esxH and esxR genes, as well as an oxidoreductase and a small secreted protein). Only the aptE gene could be used to design primers and a probe for mycobacteria detection. Concerning the other genes, the sequence polymorphism among NTM species did not allow designing molecular targets for Mycobacterium spp. detection. However, these genes could be of immunological or pathogenic importance. Indeed, PE and PPE family proteins represent 0.9 to 4.2% of the genome coding capacity of several mycobacteria [22, 25, 26, 35], and are suspected to play a major antigenic role in immune response [38]. PE and PPE family proteins are often associated with mycobacterial esx gene clusters, which encode ATP dependent specific secretion system [24] and are required to export specific members of the 6-kDa early secreted antigenic target (ESAT-6) protein family [26].