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. 2013 Jan 14;8(1):e52391. doi: 10.1371/journal.pone.0052391

Table 2. PCR and sequencing results (L1 region).

Sample ID WTP site Nested PCR PaVE prototype strains Nt identity Hemi-nested PCR PaVE prototype strains Nt identity
1528 Torino + HPV120 98.9%
1530 Torino + HPV11 96.6% + HPV11 99.7%
1530a Torino + HPV11 99.1
1535 Bari + HPV120 100%
1539 Palermo + HPV6 100% + HPV6 99.2%
1542 Palermo + HPV11 98.3% + HPV11 99.7%
1543 Cagliari + HPV16 100%
1545 Cagliari + HPV6 98.3% + HPV6 100%
1545a Cagliari + HPV6 100%
1546 Cagliari + HPV120 99.7%
1547 Cagliari + HPV6 98.3% + HPV6 99.5%
1549 Genova + HPV11 98.3% + HPV11 99.7%
1550 Genova + HPV6 97.4% + HPV6 99.2%
1552 Roma + HPV107 82.1%
1556 Genova + HPV16 100%
1565 Venezia + HPV6 98.3%
1568 Roma + HPV25 99.1% + HPV120 88.3%,
1570 Roma + HPV120 88%

PCR was performed by Method A (L1 consensus region), using MY11/MY09 for the first cycle and either GP5+/GP6+ primers (nested reaction), or GP5+/My09 (hemi-nested reaction) for the second run. The samples positive at least to one assay are included in the table. It shows in columns from the left: the sample ID numbers and WTP sites (white panel), the nested PCR results (grey panel), the hemi-nested PCR results (dark grey panel). The table also reports the HPV genotypes more closely related to the query sequences, and the percentages of nucleotide (nt) identity toward these prototypes obtained by BLAST analysis. The letter (a) indicates the sequences obtained after cloning.