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Table 1 Primers used in Real Time qPCR

From: Impact of agr dysfunction on virulence profiles and infections associated with a novel methicillin-resistant Staphylococcus aureus (MRSA) variant of the lineage ST1-SCCmec IV

Target gene

Primer sequencea

Amplicon length (bp)

Reference

rnaIII

F: AATTTGTTCACTGTGTCGATAAT

135

This study

R:TGGAAAATAGTTGATGAGTTGTT

sarA

F: TTCTTTCTCTTTGTTTTCGCTG

115

This study

R: GTTATCAATGGTCACTTATGCT

spa

F: TGGTTTGCTGGTTGCTTCTTA

116

This study

R: GCAAAAGCAAACGGCACTAC

hla

F: TTTGTCATTTCTTCTTTTTCCCA

169

This study

R: AAGCATCCAAACAACAAACAAAT

psmα

F:TATCAAAAGCTTAATCGAACAATTC

176

53

R: CCCCTTCAAATAAGATGTTCATATC

sasG

F:GGTTTTCAGGTCCTTTTGGAT

192

This study

R:CTGGTGAAGAGCGAGTGAAA

fnbpA

F: ACTTGATTTTGTGTAGCCTTTTT

185

This study

R:GAAGAAGCACCAAAAGCAGTA

fnbpB

F:CGTTATTTGTAGTTGTTTGTGTT

118

This study

R:TGGAATGGGACAAGAAAAAGAA

rrna 16S

F: AGAGATAGAGCCTTCCCCTT

84

This study

R:TTAACCCAACATCTCACGACA

mecA

F:TCCAGATTACAACTTCACCAGG

162

54

 

R:CCACTTCATATCTTGTAACG

  
  1. aF and R: forward and reverse primers, respectively, in 5´→ 3´orientation. The cycling conditions for all primers were as follows: One cycle of 48°C/30min and 95°C/10 min, followed by 35 cycles of 95°C/30s, 55°C/45s and 72°C/45 s. Each run included a nontemplate and a gene-negative RNA controls.