Table 1.
Primers used in this study
Gene | Primer | Sequence (5′-3′) | Reference |
---|---|---|---|
lytA | Forward | ACGCAATCTAGCAGATGAAGCA | [22] |
Reverse | TCGTGCGTTTTAATTCCAGCT | ||
Probe | FAM-GCCGAAAACGCTTGATACAGGGAG-BHQ1 | ||
plyNCRa | Forward | [GCAGTCGAACATGTAGCTGACTCAGGTCAC]AAAGGCTGCACGGACATTG | [12] |
Reverse | [TGGATCACTTGTGCAAGCATCACATCGTAG]CCGATTTGCCACTAGTGCGTAAGC | ||
cpsA | Forward | GCAGTACAGCAGTTTGTTGGACTGACC | [24] |
Reverse | GAATATTTTCATTATCAGTCCCAGTC |
aPacbio Universal Sequence overhang in []. Primers were HPLC purified and blocked at the 5′ site with an amino group