Table 2.
Viral isolation from nasal swabs taken from vaccinated and unvaccinated ponies after challenge with A/eq/Ohio/03 virus.
Group | N | Egga (No. ponies with positive results) b |
Duration of shedding d (egg) a |
EID50 (per mL)e |
PCRf | Duration of shedding d (PCR) |
---|---|---|---|---|---|---|
Monovalent NS | 4 | 1 | 2 | - | 3256 | 2.5 |
Monovalent NF | 4 | 1 | 0.67 | - | 2491 | 1.67 |
Trivalent NF | 3 | 0 | 0 | - | 2525 | 0.5 |
Control NF | 4 | 4c | 5 | + (0 – 1×104) | 3.07×106 | 5.25 |
virus growth in embryonated eggs. Nasal swab samples (0.1ml, undiluted) were injected into allantoic cavities of each of three 10-day-old eggs. Following incubation, allantoic fluids were harvested and tested for virus by hemagglutination assay. If any one egg tested positive, the swab sample was called virus-positive and the pony from which it originated was counted as shedding virus on that day.
results (positive or negative) are cumulative from days 2–5 post-challenge
on day 2 post-challenge, only 2 of the 4 ponies were positive by HA assay. On all other days, all 4 ponies were positive.
mean number of days of virus shedding
value on day 2 post-challenge
mean value on day 3 post-challenge (day of peak shedding in control group)
+ = influenza detected, − = influenza not detected