2015
DOI: 10.1155/2015/964178
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Specific Proteins in Nontuberculous Mycobacteria: New Potential Tools

Abstract: Nontuberculous mycobacteria (NTM) have been isolated from water, soil, air, food, protozoa, plants, animals, and humans. Although most NTM are saprophytes, approximately one-third of NTM have been associated with human diseases. In this study, we did a comparative proteomic analysis among five NTM strains isolated from several sources. There were different numbers of protein spots from M. gordonae (1,264), M. nonchromogenicum type I (894), M. nonchromogenicum type II (935), M. peregrinum (806), and M. scrofula… Show more

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Cited by 4 publications
(5 citation statements)
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“…Therefore, our findings require further molecular analyses to support species identification. Nevertheless, the species of NTM reported here agree with those previously reported in Mexico in human lungs [ 25 , 26 , 27 , 28 ], water [ 29 , 30 ], and salad samples [ 31 ].…”
Section: Discussionsupporting
confidence: 91%
“…Therefore, our findings require further molecular analyses to support species identification. Nevertheless, the species of NTM reported here agree with those previously reported in Mexico in human lungs [ 25 , 26 , 27 , 28 ], water [ 29 , 30 ], and salad samples [ 31 ].…”
Section: Discussionsupporting
confidence: 91%
“…Healthcare providers should carefully assess causality association of the isolated NTM species with patient's symptoms and signs. Approximately, one-third of NTM species are potentially pathogenic for humans 128 . Some of the common pathogenic NTM species are listed in Table VII 2 3 10 129 .…”
Section: Diagnosismentioning
confidence: 99%
“…Acquired resistance for macrolide in MAC occurs due to point mutations in the 23S rRNA ( rrl ) gene and for amikacin due to mutations in 16S rRNA ( rrs ) gene (amikacin resistance is observed in MAC isolates cultured from sputum specimens of patients who were extensively exposed to the drug or related aminoglycosides) 18 . For MAC, DST against macrolides [clarithromycin is used as a class agent; minimum inhibitory concentration (MIC) cut-off: >32 μg/ml] and amikacin (MIC cut-off: >64 μg/ml for parenteral and >128 μg/ml for liposomal amikacin) and, for M. kansasii , DST against rifampicin (MIC >2 μg/ml) and clarithromycin are used (MIC ≥32 μg/ml) 128 . When M. kansasii is resistant against rifampicin, DST for amikacin, ciprofloxacin, doxycycline, linezolid, minocycline, moxifloxacin, rifabutin, and trimethoprim-sulfamethoxazole is recommended 18 .…”
Section: Diagnosismentioning
confidence: 99%
“…Sensitive diagnostic methods that are capable of segregating virulent NTMs from non‐virulent species, based on heterologous protein sequences, and the identification of NTMs responsible for the synthesis of lipids that regulate immune interactions are urgently necessary. 73 , 74 Overall, the microbiota metabolites appear to be the most influential and easily modifiable factor that may be used to alter susceptibility. An in‐depth study examining these contributions is of the uppermost priority.…”
Section: Pathogenesis Of Ntm Pulmonary Infectionmentioning
confidence: 99%