Development of duck hepatitis A virus type 3 vaccine and its use to protect ducklings against infections

被引:45
作者
Kim, Min-Chul [1 ]
Kim, Min-Jeong [1 ]
Kwon, Yong-Kuk [1 ]
Lindberg, A. Michael [2 ]
Joh, Seong-Joon [1 ]
Kwon, Hyuk-Man [1 ]
Lee, Youn-Jeong [1 ]
Kwon, Jun-Hun [1 ]
机构
[1] Natl Vet Res & Quarantine Serv, Anyang 420824, South Korea
[2] Univ Kalmar, Sch Pure & Appl Nat Sci, SE-391826 Kalmar, Sweden
关键词
DHAV; duck hepatitis A virus; DHAV-3; duck hepatitis A virus-3; SPF; attenuated virus; Vaccine; MOLECULAR ANALYSIS; SERIAL PASSAGE; SEROTYPE;
D O I
10.1016/j.vaccine.2009.08.092
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A variant type of duck hepatitis A virus (DHAV), DHAV-3 was recently discovered in South Korea and China. Sequence analyses verified that the variant is genetically or serologically different from the DHAV-1 and DHAV-2 types. Duck hepatitis had been reported in South Korea since 1985 and an attenuated DHAV-1 vaccine had efficiently prevented epidemics of DHAV-1 until 2002. Despite the DHAV-1 based vaccine in use the novel DHAV-3 circulating in South Korea remains to be a threat to duckling farming. To develop a live attenuated vaccine against DHAV-3, a representative isolate, AP-04203, was therefore attenuated by repeated passages in SPF chicken embryos 100 times. The 100th passaged virus, AP-04203P100, did not cause clinical sign and mortality in 1-day-old ducklings as well as reversion of virulence capacity. The ducklings vaccinated with AP-04203P100 virus (10(3.0) ELD50/0.2 ml) on 1-day-old age via the intramuscular injection were well protected from 2 days after challenge with pathogenic AP04203P1 virus via the intramuscular route. In addition, the vaccine candidate also exhibited complete protection against currently circulating pathogenic DHAV-3 isolates. In conclusion, we demonstrate that the live attenuated virus, AP-04203P100, is a promising vaccine candidate facilitating the prevention of duck hepatitis caused by DHAV-3 around East Asia including South Korea. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6688 / 6694
页数:7
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