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Table 3 Primers used to amplify the VNTR regions included in the study.

From: Multiple-locus, variable number of tandem repeat analysis (MLVA) of the fish-pathogen Francisella noatunensis

Primer-name

Sequence

Tm°C

Target

Optimized Tm°

Amplicon size

Fnn-VNTR1F

ATCTTGGAAATTAACTACTTTC

46.1

VNTR no 1

55

211

Fnn-VNTR1R

ACCTTTTTCTACACCAATAG

47.2

   

Fnn-VNTR2F

GTAAACGTAGTTTTTGGAAGTCCAT

53.7

VNTR no 2

54

217

Fnn-VNTR2R

GGATGGCAATCTTGTGTAAA

50.7

   

Fnn-VNTR3F

CAAACCTTCATCTCCACTAC

50.4

VNTR no 3

50

212

Fnn-VNTR3R

TGCTCTTTTCCCTCTATATA

47.2

   

Fnn-VNTR4F

AGTTTCATTTATCAGGTGAC

47.5

VNTR no4

54

311

Fnn-VNTR4R

AGACTAATAGCCTTCCAAAA

48.5

   

Fnn-VNTR5F

CTGGACATTAGTATCAGGAT

48.3

VNTR no 5

55

312

Fnn-VNTR5R

GCAGTGGTAACAATTTTAAG

47.2

   

Fnn-VNTR6F

GCTGTTGGAGATAGTAAATAATTGC

52.3

VNTR no 6

55

301

Fnn-VNTR6R

TTAGCTTCTTTAAGACCAAG

47.2

   

Fnn-VNTR7F

CTTCTTCTCAACCATACCAG

50.1

VNTR no 7

54

439

Fnn-VNTR7R

ACAAGCATATAGACTTATATTGA

46.9

   

Fnn-VNTR1-2F

AAATGTAGAGTTTCCATCCAAC

47.1

VNTR no 1

55

613

Fnn-VNTR1-2R

AGTCGTATTTCTGCTTCAATC

45.6

   

Fnn-VNTR2-2F

CATGGGCTACTTTTGGAATATATAC

47.7

VNTR no 2

55

559

Fnn-VNTR2-2R

TCGGTTTGACTGATGTCATG

44.6

   
  1. Flanking primers were designed based on preliminary data of the whole genome sequence of F. noatunensis ssp. noatunensis isolate GM2212. The attributes of the primers in the study; primer sequence, optimized annealing temperature (Tm°) and amplicon size of the GM2212 isolate.