Molecular identification of non-tuberculous mycobacterial species isolated from extrapulmonary samples using real-time PCR and rpoB sequence analysis.
Mohammad HashemzadehAram Asarehzadegan DezfuliAzar Dokht KhosraviMaryam Moradi BandbalAtousa GhorbaniMahtab HamedSoolmaz Khandan DezfuliPublished in: AMB Express (2023)
Tuberculosis (TB) is one of the leading causes of mortality among infectious diseases and accounts for a serious health hazard wordwide. Apart from TB, the members of non-tuberculous mycobacteria (NTM), which includes around 170 species, may also cause different diseases in humans. Therefore this study aimed to investigate the distribution of NTM strains isolated from extrapulmonary (EP) samples by Real-Time PCR and PCR-sequencing methods in Southwest Iran. Three hundred and twenty-five suspected EP samples were collected from patients referred to the referral hospitals in Ahvaz, Iran. The isolates were initially screened by acid fast staining and identified by phenotypic culture and biochemical tests. The Real-Time PCR and rpoB- based PCR methods were performed followed by sequence analysis of rpoB gene. From 124 samples, 77 (62%) were positive for NTM by culture and rpoB sequence analysis. M. fortuitum was the most commonly isolated NTM in present study. In Real-Time PCR, only 69 (55.64%) isolates showed more homology with standard NTM isolates. In general, the growing trend of EPNTM infections in Iran needs specific programs and resources to get a better diagnosis. PCR sequencing is a reliable method, it can be used for definitive identification of positive cultures for identification of NTM species.
Keyphrases
- real time pcr
- mycobacterium tuberculosis
- genetic diversity
- infectious diseases
- public health
- end stage renal disease
- ejection fraction
- primary care
- escherichia coli
- newly diagnosed
- emergency department
- mental health
- squamous cell carcinoma
- hepatitis c virus
- dna methylation
- gene expression
- bioinformatics analysis
- pulmonary embolism
- social media
- patient reported
- copy number