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. 2014 May 27;7:243. doi: 10.1186/1756-3305-7-243

Table 1.

Species-specific ITS rDNA primers

Species [GenBank Acc.Number] Annealing temperature Primer name Primer sequence 5’-3’ PCR product size (nt) Amplified region
C. labracis [JQ694148]
66.6°C
Caino_F
ACGTGCAGCTCATGACACGG
301
ITS1
 
 
Caino_R
TCAGTCAAGCCAGGGGAAGG
 
 
M. obovata [JQ694145]
 
Macv_F
CCCGAGGCACTCAAAGACTG
537
ITS1
 
 
Macv_R
TCAGTCGAGCCCAGGATAGG
 
 
M. novaezealandensis [KJ540203]
64°C
Maritr_F
TTGACATTCGGCCGGGGTGC
214
ITS2
 
Maritr_R
ACCGGCCTAAAGCGCACAGA
 
 
Philophthalmus sp. [KJ540204]
 
Philsp_F
CGTGAGAGATCACGCGAGG
352
ITS2
    Philsp_R TGTGCGCCTCACCAAGTGAG    

Species-specific ITS rDNA primers designed in this study for amplification of i) C. labracis and M. obovata, infecting G. adansonii snails from the Ebro Delta (Spain) and ii) M. novaezealandensis and Philophthalmus sp., infecting Z. subcarinatus snails from Otago Habour (New Zealand).