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. 2014 May 12;2014:420149. doi: 10.1155/2014/420149

Table 1.

Species specific primers used in our study.

Name of bacteria Forward primer (5′-3′) Reverse primer (5′-3′) T a**  (°C) Amplicon size (bp)
Pg TGTAGATGACTGATGGTGAAAACC ACGTCATCCCCACCTTCCTC 60 197
Tf GCGTATGTAACCTGCCCGCA TGCTTCAGTGTCAGTTATACCT 60 641
Pi TTTGTTGGGGAGTAAAGCGGG TCAACATCTCTGTATCCTGCGT 55 575
Pn ATGAAACAAAGGTTTTCCGGTAAG CCCACGTCTCTGTGGGCTGCGA 55 804
Cr TTTCGGAGCGTAAACTCCTTTTC TTTCTGCAAGCAGACACTCTT 60 598
Ec CTAATACCGCATACGTCCTAAG CTACTAAGCAATCAAGTTGCCC 60 688
Aa AGAGTTTGATCCTGGCTCAG CACTTAAAGGTCCGCCTACGTGCC 60* 593
Co AGAGTTTGATCCTGGCTCAG GATGCCGTCCCTATATACGGGG 55 185
Cs AGAGTTTGATCCTGGCTCAG GATGCCGCTCCTATATACCATTAGG 55* 185
Td AAGGCGGTAGAGCCGCTCA AGCCGCTGTCGAAAAGCCCA 55 311

*Confirmation was done using a separate run of PCR to differentiate from other bacteria in the same batch of PCR producing similar size of amplicons.

**T a: Annealing temperature.