Skip to main content
. 2016 Nov 21;12:259. doi: 10.1186/s12917-016-0888-0

Table 2.

Sensitivity (%) of PRRSV Ab ELISAs at each sampling point (95% confidence interval)

Study day 0 3 7 10 14
Group V
 IDEXX 0 (0–30) 0 (0–30) 0 (0–30) 80 (44–98) 100 (69–100)
 INgezim 90 (60–98) 70 (35–93) 100 (69–100) 100 (69–100) 100 (69–100)
 HIPRA A/S 20 (3–56) 20 (3–56) 10 (0–45) 50 (19–81) 50 (19–81)
 HIPRA E/S 0 (0–30) 0 (0–30) 0 (0–30) 20 (3–56) 20 (3–56)
 QIAGEN 0 (0–30) 0 (0–30) 0 (0–30) 80 (44–98) 100 (69–100)
 AJ 0 (0–30) 0 (0–30) 20 (3–56) 70 (35–93) 80 (44–98)
Group N
 IDEXX n.d. 0 (0–30) 0 (0–30) 70 (35–93) 90 (60–98)
 INgezim n.d. 0 (0–30) 0 (0–30) 100 (69–100) 100 (69–100)
 HIPRA A/S n.d. 0 (0–30) 0 (0–30) 0 (0–0) 30 (7–65)
 HIPRA E/S n.d. 0 (0–30) 0 (0–30) 0 (0–0) 0 (0–0)
 QIAGEN n.d. 0 (0–30) 0 (0–30) 40 (12–74) 90 (60–98)
 AJ n.d. 0 (0–30) 0 (0–30) 10 (0–45) 60 (26–88)

Group V: vaccination with an inactivated PRRSV type 1 vaccine on days -33 and -19

Groups V and N: intradermal application of an HP PRRSV field strain on day 0

n.d. not done