Table 1.
Embryo vaccination with recombinant IBVs, analysis of hatch, clinical signs, serological responses and protection from virulent challenge
| Virus | Hatch rate (%) | Mean ciliary activity posthatch (%) | Serological response (log2) ELISA | Protection (based on ciliary activity postchallenge) |
|
|---|---|---|---|---|---|
| Day 5 | Day 7 | ||||
| Beau-R | 73 | 71 | 6.30 | 0 | 30 |
| BeauR–M41(S) | 82 | 77 | 7.05 | 80 | 100 |
| CV1 | 18 | 5 | 10.5 | 100 | 100 |
| Placebo | 85 | 98 | ≤5.64 | 0 | 0 |
Fertile SFP eggs were inoculated with either a commercial vaccine (CV1; 104 EID50); the molecularly cloned Beaudette strain Beau-R (106 EID50); Beau-R in which the S protein gene had been replaced by that from the pathogenic M41 strain, to make BeauR–M41(S) (106 EID50); or a placebo. Hatch was assessed at 21.5 days of incubation. Ciliary activity was assessed in five birds at day 6 posthatch, serological responses by ELISA at 4 weeks posthatch. All birds were challenged with virulent M41 at 4 weeks posthatch and the ciliary activity determined at 5 and 7 days postchallenge by microscopic observation of tracheal rings. A high percentage of ciliary activity was indicative of protection.