Table 1 Primers and annealing temperatures for PCR amplification of each gene studied.

5'-GGACCACTGCATGGAATGTTAA-3'

5'-TGAGTGACTGCCGAAACATCTC-3'

60.6°C

5'-AGC CCC TCA AGT GCA CAG TG-3'

5'-TGCCAATGTGTTTTCCCTGA-3'

60.0°C

5'-GCGGACGCAGTCTGGG-3'

5'-ATGAGCTGGAGCATGTCTTCAAA-3'

67.3°C

5'-CACTTTAGCTCCAAGGATGA-3'

5'-TGGTTCAGTAGGCCATTCCT-3'

62.0°C

5'-AGAGGAGACAGATGAGGAGGAAG -3'

5'-AGATGGTGTTCTGCAGAGTCTTC -3'

63.9°C

5'- CAGCTGGGCCTAACTTTGAG -3'

5'- CCTCTCTGCAATCACACGAA -3'

61.5°C

5'-ATTCTGGCCCACCAACTTCGG -3'

5'-TGGAAGCCTGATGCTTTATCCCCA -3'

64.5°C

5'-ACGAGGCCCAGAGCAAGAG-3'

5'-GGTGTGGTGCCAGATCTTCTC-3'

60.0°C