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. 2024 Jan 26;86(3):349–353. doi: 10.1292/jvms.23-0198

Table 2. Results of PCR amplification and sequencing of 18S rRNA genes in nutria feces using previously reported primers.

Primers
Samples
Forward Reverse Expected size (bp) A
B
C
Expected*1 amplicon Sequences*2 Nonspecific*3 bands Expected*1 amplicon Sequences*2 Nonspecific*3 bands Expected*1 amplicon Sequences*2 Nonspecific*3 bands
Nem18SF 18SPCR 1,500 - / +++ - / ++ + - +++
18SP2F 18SPCR 950 + - +++ + - +++ + - +++
SSU24HF 18SPCR 750 + Sm +++ - / +++ + Sm +++
18SP4F 18SPCR 710 + Sm +++ + - +++ + Sm +++
SSU23F 18SPCR 320 + - +++ + - ++ + - +++

Nem18SF 18SP8R 1,000 + Sm ++ - / + + Sm ++
18SP2F 18SP8R 550 + Sm ++ + - ++ + N.D.*4 ++
SSU24HF 18SP8R 250 + - - + - ++ + - +
18SP4F 18SP8R 210 + - - + - - + - +

*1 Expected amplicon. + and -: a band of the expected size was or was not present, respectively. *2 Sequences. /: not done, Sm: identical to those of S. myopotami; -: not determined due to multiple sequence signals or high homology with other microorganisms. *3 Nonspecific bands. -: 0 bands; +: 1 band; ++: 2 to 5 bands; +++: more than 6 bands. *4 N.D.: not determined due to the presence of 2 to 5 nonspecific bands around the expected amplicon.