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Table 2 Primers used for amplification and sequencing of M.tuberculosis clinical strains

From: Molecular characterization of amikacin, kanamycin and capreomycin resistance in M/XDR-TB strains isolated in Thailand

Gene

Primer name (position*)

Primer sequence (5′→3′)

Annealing temp (°C)

PCR product size (bp)

Purpose

Reference

rrs

F-rrs (-44)

5′-TTCTAAATACCTTTGGCTCCCT-3′

51

1,680

PCR/Seq

[42]

R-rrs (1,636)

5′-TGGCCAACTTTGTTGTCATGCA-3′

53

 

PCR/Seq

[42]

F-rrs1 (554)

5′-CTGGGCGTAAAGAGCTCGTA-3′

54

 

Seq

This study

F-rrs2 (1,114)

5′-GTTGCCAGCACGTAATGGTG-3′

54

 

Seq

This study

R-rrs1 (483)

5′-TCCACCTACCGTCAATCCGA-3′

54

 

Seq

This study

R-rrs2 (1,073)

5′-ATCTCACGACACGAGCTGAC-3′

54

 

Seq

This study

eis (Rv2416c)

F-Rv2417c (-316)

5′-GCGGTGCATCACGTCGCCGA-3′

60

1,661

PCR/Seq

This study

R-eis-Rv2415c (1,345)

5′-GCAACGCGATCCGCGAGTGC-3′

60

 

PCR/Seq

This study

F-eis1 (247)

5′-AGTTTCGTCGCGGTGGCGCC-3′

60

 

Seq

This study

F-eis2 (816)

5′-GGACCCGTTACCCCACCTGC-3′

60

 

Seq

This study

R-eis1 (240)

5′-GGCGGTCGGGAGCACCACTT-3′

60

 

Seq

This study

R-eis2 (769)

5′-TCAGGGCCCGCCACAACGCA-3′

60

 

Seq

This study

tap (Rv1258c)

F-Rv1259 (-496)

5′-CAGGCCGGCCCTATGCAGTG-3′

60

1,847

PCR/Seq

This study

R-Rv1257c (1,351)

5′-CGGTCTTGCCGGTAGCCGTC-3′

60

 

PCR/Seq

This study

F-tap1 (41)

5′-TCGCAACGCTGATGGCGGCC-3′

60

 

Seq

This study

F-tap2 (641)

5′-AGGGGCTGCGCTTCGTCTGG-3′

60

 

Seq

This study

R-tap1 (210)

5′-CCCGAAGTAGTCGACCGCGG-3′

60

 

Seq

This study

R-tap2 (862)

5′-GACGGGGAACGCGGATAGCC-3′

60

 

Seq

This study

whiB7 (Rv3197A)

F URT-whiB7 (-451)

5′-GCTGGTTCGCGGTCGGACCT-3′

60

550

PCR/Seq

This study

R whiB7 (99)

5′-CGGGGTATCGGCGAACCACA-3′

58

 

PCR/Seq

This study

tlyA (Rv1694)

F-tlyA (1)

5′-GTGGCACGACGTGCCCGCGT-3′

62

807

PCR/Seq

This study

R-tlyA (807)

5′-CTACGGGCCCTCGCTAATCG-3′

58

 

PCR/Seq

This study

  1. *The first 5′nucleotide position of each primer was counted from the translation start codon of each gene.