tuberculosis clinical strains (KL463; KL1936) sensitive to RMP. The selected transformants were verified by PCR amplification as described above. The resultant clinical strains carrying mutated rpoB genes

were subjected to RMP resistance analysis by the proportional method. The results obtained were compared to the RMP-resistance of clinical strains click here carrying the same mutations and to the H37Ra recombinants described above (Table 4). The mutated rpoB genes generating high RMP-resistance level in M. tuberculosis H37Ra (H526D; D516V; S531L) were also responsible for high level of resistance of both clinical strains when introduced into their chromosomal DNA. On the other hand, mutation Q513L identified in an M. tuberculosis strain with resistance to a high level of RMP (MIC up to 50 μg/ml) which did not cause significant resistance of M. tuberculosis H37Ra (MIC up to 6.2 μg/ml), was responsible for RMP-resistance of KL463 and KL1936 strains at the level depending on the host (up to 12.5 and 50 μg/ml, respectively). The double mutation of rpoB in positions 510 (Q/H) and 516 (D/Y) identified in a highly resistant M. tuberculosis strain CB-839 research buy (MIC 25 μg/ml)

which did not reveal resistance in H37Ra (MIC 1.5 μg/ml) was responsible for low level of resistance of both clinical tubercle bacilli hosts (MIC 6.2 μg/ml). The overproduction of mutated RpoB does not cause high level of resistance to RMP We could not exclude that the different over resistance of M. tuberculosis hosts carrying identical mutations in rpoB depends on different expression of RpoB controlled by unknown regulatory proteins. For example, the raised expression of target molecule (InhA) due to accumulations of mutations in https://www.selleckchem.com/products/qnz-evp4593.html promoter region is one of the known mechanisms of resistance to INH. As questions arose as to whether expression of mutated rpoB genes under control of the heat shock promoter (P hsp60) resulted in increased resistance of M. tuberculosis to RMP, the wild type rpoB and its mutated copies were cloned under control of the heat shock promoter

as described in Methods. Although we did not have antibodies to test the level of expression for RpoB, the expression system is known to be very efficient [24, 25]. The self-replicating constructs (pMERP1-9, Fig. 1) appeared to be very unstable when introduced into M. tuberculosis host (data not shown). Therefore the vectors (pMHRP1-9), which are able to integrate into attB site of mycobacterial chromosomal DNA, carrying wild type and mutated rpoB under P hsp60 promoter were constructed and electroporated into M. tuberculosis H37Ra. The presence of the relevant DNA introduced into the attB site of chromosomal DNA was verified by PCR amplification. The resultant recombinant strains were subjected to RMP resistance analysis by the proportional method.