Efficacy of an adenovirus-vectored foot-and-mouth disease virus serotype A subunit vaccine in cattle using a direct contact transmission model

被引:7
|
作者
Neilan, John G. [1 ]
Schutta, Christopher [1 ]
Barrera, Jose [2 ,3 ]
Pisano, Melia [3 ,4 ]
Zsak, Laszlo [1 ]
Hartwig, Ethan [5 ]
Rasmussen, Max V. [1 ]
Kamicker, Barbara J. [3 ]
Ettyreddy, Damodar [6 ]
Brough, Douglas E. [6 ]
Butman, Bryan T. [6 ]
Brake, David A. [7 ]
机构
[1] Plum Isl Anim Dis Ctr, US Dept Homeland Secur Sci & Technol Directorate, POB 848, Greenport, NY 11944 USA
[2] McConnell Grp Inc, Plum Isl Anim Dis Ctr, POB 848, Greenport, NY 11944 USA
[3] Leidos, Plum Isl Anim Dis Ctr, POB 848, Greenport, NY 11944 USA
[4] Oak Ridge Inst Sci & Educ, Plum Isl Anim Dis Ctr, Res Participat Program, Oak Ridge, TN USA
[5] ARS, USDA, Foreign Anim Dis Res Unit, Plum Isl Anim Dis Ctr, POB 848, Greenport, NY 11944 USA
[6] GenVec Inc, 910 Clopper Rd,Suite 220N, Gaithersburg, MD 20878 USA
[7] BioQuest Associates LLC, Plum Isl Anim Dis Ctr, POB 848, Greenport, NY 11944 USA
来源
BMC VETERINARY RESEARCH | 2018年 / 14卷
关键词
Foot-and-mouth disease virus; FMDV A24/Cruzeiro/BRA/55; Replication-deficient human adenovirus vectored vaccine; DIVA; Vaccine efficacy; EMERGENCY VACCINATION; IMMUNE-RESPONSES; CARRIER STATE; PROTECTION; CHALLENGE; INFECTION; POTENCY; SWINE; PIGS; FMDV;
D O I
10.1186/s12917-018-1582-1
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: A direct contact transmission challenge model was used to simulate natural foot-and-mouth disease virus (FMDV) spread from FMDV A24/Cruzeiro/BRA/55 infected 'seeder' steers to naive or vaccinated steers previously immunized with a replication-deficient human adenovirus-vectored FMDV A24/Cruzeiro/BRA/55 capsid-based subunit vaccine (AdtA24). In two independent vaccine efficacy trials, AdtA24 was administered once intramuscularly in the neck 7 days prior to contact with FMDV A24/Cruzeiro/BRA/55-infected seeder steers. Results: In Efficacy Study 1, we evaluated three doses of AdtA24 to estimate the 50%/90% bovine protective dose (BPD50/90) for prevention of clinical FMD. In vaccinated, contact-challenged steers, the BPD 51(50/90) was 3.1 x 10(10 )/ 55 x 10(10) AdtA24 particles formulated without adjuvant. In Efficacy Study 2, steers vaccinated with 5 x 10(10) AdtA24 particles, exposed to FMDV A24/Cruzeiro/BRA/55-infected seeder steers, did not develop clinical FMD or transmit FMDV to other vaccinated or naive, non-vaccinated steers. In contrast, naive, non-vaccinated steers that were subsequently exposed to FMDV A24/Cruzeiro/BRA/55-infected seeder steers developed clinical FMD and transmitted FMDV by contact to additional naive, non-vaccinated steers. The AdtA24 vaccine differentiated infected from vaccinated animals (DIVA) because no antibodies to FMDV nonstructural proteins were detected prior to FMDV exposure. Conclusions: A single dose of the AdtA24 non-adjuvanted vaccine conferred protection against clinical FMD at 7 days post-vaccination following direct contact transmission from FMDV-infected, naive, non-vaccinated steers. The AdtA24 vaccine was effective in preventing FMDV transmission from homologous challenged, contact-exposed, AdtA24-vaccinated, protected steers to co-mingled, susceptible steers, suggesting that the vaccine may be beneficial in reducing both the magnitude and duration of a FMDV outbreak in a commercial cattle production setting.
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页数:9
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