Table 2.
Primary infectiona | % homology to GenBank | Secondary infectiona | % homology to GenBank | n (%) |
---|---|---|---|---|
S. jamaicensis | 97.0–99.7 | 13 (15.8) | ||
S. jamaicensis | 97.1 | S. jamaicensis | 96.7 | 1 (1.2) |
S. jamaicensis | 97.7 | S. jamaicensis or S. (Frenkelia) microtib | 98.7 | 1 (1.2) |
S. jamaicensis or S. (Frenkelia) microtib | 99.7 | S. jamaicensis or S. (Frenkelia) microtib | 99.3 | 1 (1.2) |
S. jamaicensis or S. (Frenkelia) microtib | 99.3 | 4 (4.7) | ||
S. jamaicensis or S. (Frenkelia) microtib | 99.3–99.7 | S. jamaicensis | 97.7 | 2 (2.4) |
S. calchasi | 100 | 5 (5.9) | ||
S. turdusi | 98.7–99.7 | 4 (4.7) | ||
S. turdusi | 98.4 | S. columbae | 99.0 | 1 (1.2) |
S. columbae | 99.7 | 3 (3.5) | ||
S. columbae | 99.7 | S. turdusi | 98.7 | 1 (1.2) |
S. columbae | 99.7 | S. halieti | 100.0 | 1 (1.2) |
S. columbae | 99.7 | S. jamaicensis | 99.0 | 1 (1.2) |
S. halieti | 100 | 3 (3.5) | ||
Eumonospora henryae | 95.7 | 1 (1.2) | ||
Negative | 28 (32.9) | |||
Bad quality DNA | 11 (12.9) | |||
Unreadable sequencesc | 4 (4.7) |
Nine of 85 raptors presented mixed infections, i.e., chromatograms showed clear double peaks in only a few nucleotides. In these cases, two sequences were analyzed separately by combining only the high and low peak nucleotides. The closest BLASTn match for each sequence was considered the primary and secondary infection, respectively.
Eight of 85 raptors had sequences with identical homology percentage to two different sequences by BLASTn for S. jamaicensis and S. (Frenkelia) microti. In these cases, either of these parasites could be considered as the cause of infection.
Sequence considered unreadable when its respective chromatograph presented high background noise or mixed peaks that rendered it impossible to discern between nucleotides.