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Table 1 Transcriptome profiling and validation techniques used for Mtb sputum transcriptomics

From: Lipid droplets and the transcriptome of Mycobacterium tuberculosis from direct sputa: a literature review

Comparative transcriptomics of SMtb

RNA profiling method

Validation

#Transcript

Reference

SMtb vs culture with 7H10 agar /7H9 broth/Dubos a

Microarray

qRT-PCR

516

[29]

SMtb vs culture

Microarray

qRT-PCR

557

[89]

SMtb vs MAF/Mtb

qRT-PCR

 

2179

[90]

SMtb vs Exponential phase of liquid culture

Dual RNA seq

Nano String

198

[91]

SMtb vs Stationary phase of liquid culture

Dual RNA seq

Nano String

392

[91]

Sputum vs MGIT 460 culture

Microarray

qRT-PCR

1083

[92]

SMtb at Day 3 vs SMtb at day0 treatment

Microarray

qRT-PCR

109

[92]

SMtb at Day7/14 vs day 0 treatment

Microarray

qRT-PCR

39

[92]

Lipid rich Dubos brothb vs Dextrose rich Dubos brothb

RNA seq

qRT-PCR

–

[60]

SMtb/ BAL-Mtb vs 7H9/ DTAc culture

qRT-PCR

 

–

[93]

SMtb before Rx vs SMtb after Rx

qRT-PCR

qRT-PCR

2411

[94]

Sputum Mtb vS culture H37Rv

Microarray

qRT-PCR

–

[95]

  1. a7H10 agar with oleic acid-albumin-dextrose-catalase supplement or in 7H9 broth with albumin-dextrose-catalase supplement, 0.2% glycerol and 0.05% Tween-80. Hypoxic (non-replicating persistence) cultures M. tuberculosis strains H37Rv and CH were grown in Dubos Tween albumin broth. bDubos broth (Difco), without glycerol, containing 0.5% albumin, supplemented with either 0.2% dextrose or a lipid mixture (oleic acid, palmitic acid, stearic acid, at final concentration of 0.001% each, plus 0.01% cholesterol). c7H9 media (0.05% Tween 80, 0.2% glycerol, 10% ADC supplement)/ DTA: Dubos Tween albumin; for the NRP-2 model was grown in 100 mL Dubos Tween albumin (DTA). SMtb sputum-derived M. tuberculosis, Mtb Mycobacterium tuberculosis, vs versus, Rx treatment, MAF Mycobacterium africanum, L4 Lineage 4, qRT-PCR Real-Time Quantitative Reverse Transcription PCR, RNA seq RNA-sequencing, DTA Dubos Tween, BAL Broncho alveolar lavage