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. 2012 Jan 24;7(1):e30648. doi: 10.1371/journal.pone.0030648

Table 1. Primers used in this study.

Gene and direction Sequence
IS900, L1 ± CCCGTGACAAGGCCGAAGA
IS900, L9 ± CGGCCCTGGCGTTCCTATG
IS900, 900 R ŧ ACGCTGTCTACCACCCCGCA
spoIVA, F AAATCGGCACACGAAAAGTC
spoIVA, R TGCCAATACCGGGATATCAT
Clostridium 16SrDNA, F Ψ AAAGATGGCATCATCATTCAAC
Clostridium 16SrDNA, R Ψ TACCGTCATTATCTTCCCCAAA
Universal 16SrRNA, F AGAGTTTGATCCTGGCTCAG
Universal 16SrRNA, R GGGTGGATCCTCCTT
MAP1002c, F CGGGTGTGGAACTACGACTT
MAP1002c, R TCTTCTTCCTCAGGTACGAGATGT
MAP0475, F GACAAGGTATTCCAGGTGCTG
MAP0475, R CTCGGCGACCTTGTTGAC
MAP0987, F GCACGACGGCATCGTTAT
MAP0987, R GTCAAGTCCGTCCGTCTCGGTGA
±

Motiwala, A.S., et al. Molecular epidemiology of Mycobacterium avium subsp. paratuberculosis: evidence for limited strain diversity, strain sharing, and identification of unique targets for diagnosis. J Clin Micobiol, 2003. 41(5):2015–26.

ŧ

Bull, T.J., et al. Characterization of IS900 loci in Mycobacterium avium subsp. paratuberculosis and development of multiplex PCR typing. Microbiology, 2000. 146:3285.

Ψ

Wang, R.F., et al. A 16S rDNA-based PCR method for rapid and specific detection of Clostridium perferingens in food. Mol Cell Probes,m1994. 8(2): 131–7.