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Modified live infectious bursal disease virus (IBDV) vaccine delays infection of neonatal broiler chickens with variant IBDV compared to turkey herpesvirus (HVT)-IBDV vectored vaccine
被引:22
作者:
Kurukulasuriya, Shanika
[1
]
Ahmed, Khawaja Ashfaque
[1
]
Ojkic, Davor
[2
]
Gunawardana, Thushari
[1
]
Goonewardene, Kalhari
[1
]
Gupta, Ashish
[1
]
Chow-Lockerbie, Betty
[1
]
Popowich, Shelly
[1
]
Willson, Philip
[3
]
Tikoo, Suresh K.
[4
,5
]
Gomis, Susantha
[1
]
机构:
[1] Univ Saskatchewan, Dept Vet Pathol, Western Coll Vet Med, 52 Campus Dr, Saskatoon, SK S7N 5B4, Canada
[2] Univ Guelph, Hlth Anim Lab, POB 3612, Guelph, ON N1H 6R8, Canada
[3] Univ Saskatchewan, Canadian Ctr Hlth & Safety Agr, Saskatoon, SK S7N 5E5, Canada
[4] Univ Saskatchewan, Sch Publ Hlth, Vaccinol & Immunotherapeut Program, Saskatoon, SK S7N 5E3, Canada
[5] Univ Saskatchewan, Vaccine & Infect Dis Org, 120 Vet Rd, Saskatoon, SK S7N 5E3, Canada
来源:
基金:
加拿大自然科学与工程研究理事会;
关键词:
Infectious bursal disease (IBD);
VP2 hyper-variable domain;
Bursal atrophy;
Immunosuppression;
Maternal antibodies;
T-cell response;
OVO VACCINATION;
VIRULENT IBDV;
STRAINS;
EFFICACY;
ANTIBODY;
PROTECTION;
CHALLENGE;
HVT;
INTERMEDIATE;
POULTRY;
D O I:
10.1016/j.vaccine.2017.01.005
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Chickens are commonly processed around 35-45 days of age in broiler chicken industry hence; diseases that occur at a young age are of paramount economic importance. Early age infection with infectious bur sal disease virus (IBDV) results in long-lasting immunosuppression and profound economic losses. To our knowledge, this is the first study comparing the protection efficacy of modified live (MdLV) IBDV and herpesvirus turkey (HVT)-IBDV vaccines against early age variant IBDV (varIBDV) infection in chicks. Experiments were carried out in IBDV maternal antibody (MtAb) positive chicks (n = 330), divided into 6 groups (n = 50-60/group), namely Group 1 (saline), Group 2 (saline + varIBDV), Group 3 (HVT-IBDV), Group 4 (HVT-IBDV + varIBDV), Group 5 (MdLV) and Group 6 (MdLV + varIBDV). HVT-IBDV vaccination was given via the in ovo route to 18-day-old embryonated eggs. MdLV was administered via the subcutaneous route in day-old broilers. Group 2, Group 4 and Group 6 were orally challenged with varIBDV (SK-09, 3 x 10(3) EID50) at day 6 post-hatch. IBDV seroconversion, bursal weight to body weight ratio (BBW) and bursal histopathology were assessed at 19 and 35 days of age. Histopathological examination at day 19 revealed that varIBDV-SK09 challenge caused severe bursal atrophy and lower BBW in HVT-IBDV but not in MdLV vaccinated chicks. However by day 35, all challenged groups showed bursal atrophy and seroconversion. Interestingly, RT-qPCR analysis after varIBDV-SK09 challenge demonstrated an early (9 days of age) and significantly high viral load (similar to 5744 folds) in HVT-IBDV vaccinated group vs unvaccinated challenged group (similar to 2.25 folds). Furthermore, flow cytometry analysis revealed inhibition of cytotoxic CD8(+) T-cell response (CD44-downregulation) and decreased splenic lymphocytes counts in chicks after HVT-IBDV vaccination. Overall, our data suggest that MdLV delays varIBDV pathogenesis, whereas, HVT-IBDV vaccine is potentially immunosuppressive, which may increase the risk of early age varIBDV infection in broilers. (C) 2017 Elsevier Ltd. All rights reserved.
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页码:882 / 888
页数:7
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