As one of the factors affecting the treatment outcomes, drug tolerance in mycobacteriosis has not been paid due attention. Genome-wide association studies on 607 Mycobacterium tuberculosis clinical isolates with phenotypic drug susceptibility test data revealed that a K114N mutation on the rv2820c gene was highly enriched in capreomycin-resistant isolates (32/213, 15.02%). However, the mutation was also observed in capreomycin-sensitive isolates (10/394, 2.53%). In most cases (31/42, 73.81%), the rv2820c K114N mutation occurred in isolates with the known capreomycin resistance conferring mutation rrs A1401G. In contrast, the general frequency of the rv2820c K114N mutation was low in 7061 genomes downloaded from the National Center for Biotechnology Information database. To determine the impact of this mutation on the antimycobacterial activity of capreomycin, the intact rv2820c gene and the rv2820c K114N mutant were over-expressed in Mycobacterium smegmatis (Ms), and the results of susceptibility tests showed that the rv2820c K114N mutation did not affect the minimum inhibition concentration (MIC) of capreomycin. Subsequently, the data of time-kill assays showed that, it took only 2 h of capreomycin treatment (40 μg/ml, 5 × MIC) to kill 99.9% bacterial cells of Ms MC 2 155 pMV261::rv2820c H37Rv , while it took 6 h to achieve that for Ms MC 2 155 pMV261::rv2820c K114N . Taken together, these data suggested that the rv2820c K114N mutation is related with capreomycin tolerance, which merits further investigation.
Keyphrases
- mycobacterium tuberculosis
- pulmonary tuberculosis
- multiple sclerosis
- mass spectrometry
- ms ms
- electronic health record
- emergency department
- magnetic resonance
- genome wide
- cell proliferation
- working memory
- oxidative stress
- copy number
- big data
- genetic diversity
- contrast enhanced
- health information
- drug induced
- data analysis
- machine learning
- cell cycle arrest
- pi k akt