{"title":"The History of Infectious Bursal Disease: The Second Period Between 1977 and 2005.","authors":"Silke Rautenschlein, K A Schat, Y M Saif","doi":"10.1637/aviandiseases-D-24-00095","DOIUrl":null,"url":null,"abstract":"<p><p>Major progress has been achieved since the first historical review of infectious bursal disease (H. N. Lasher and V. S. Davis, <i>Avian Diseases,</i> Vol. 41, pp. 11-19; 1997), much of it between 1977 and 2005. Significant findings in the 1980s were the presence of serotype 2 of infectious bursal disease virus (IBDV) and the diversity of antigenic and immunogenic types of IBDV. In the late 1980s, very virulent IBDV strains emerged and became widespread in many countries by the late 1990s. Soon after the discovery of the antigenic variants, specific commercial vaccines were developed and used successfully in the field. The structure of the virus was discovered, which led to the elucidation of virus genes being responsible for some of the virus' biological functions, including immunogenicity. A consequence of these findings was the development of a new class of recombinant vaccines, which were commercially licensed. Reverse genetics became another tool for virus characterization. The development of monoclonal antibodies allowed the identification of immunoglobulin M positive (IgM+) B cells as the major target cells for infection. A role of macrophages and T cells in IBDV pathogenesis and pathology of the bursa of Fabricius was suggested. New tools for serology and virus identification-ELISA and reverse transcriptase (RT) PCR, respectively-provided new insights in the epidemiology. The widespread use of ELISA kits facilitated the use of vaccines in the face of maternally derived antibodies against IBDV, allowing the determination of time of vaccine breakthrough and therefore vaccine administration.</p>","PeriodicalId":516846,"journal":{"name":"Avian diseases","volume":"69 2","pages":"134-145"},"PeriodicalIF":1.3000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Avian diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1637/aviandiseases-D-24-00095","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Major progress has been achieved since the first historical review of infectious bursal disease (H. N. Lasher and V. S. Davis, Avian Diseases, Vol. 41, pp. 11-19; 1997), much of it between 1977 and 2005. Significant findings in the 1980s were the presence of serotype 2 of infectious bursal disease virus (IBDV) and the diversity of antigenic and immunogenic types of IBDV. In the late 1980s, very virulent IBDV strains emerged and became widespread in many countries by the late 1990s. Soon after the discovery of the antigenic variants, specific commercial vaccines were developed and used successfully in the field. The structure of the virus was discovered, which led to the elucidation of virus genes being responsible for some of the virus' biological functions, including immunogenicity. A consequence of these findings was the development of a new class of recombinant vaccines, which were commercially licensed. Reverse genetics became another tool for virus characterization. The development of monoclonal antibodies allowed the identification of immunoglobulin M positive (IgM+) B cells as the major target cells for infection. A role of macrophages and T cells in IBDV pathogenesis and pathology of the bursa of Fabricius was suggested. New tools for serology and virus identification-ELISA and reverse transcriptase (RT) PCR, respectively-provided new insights in the epidemiology. The widespread use of ELISA kits facilitated the use of vaccines in the face of maternally derived antibodies against IBDV, allowing the determination of time of vaccine breakthrough and therefore vaccine administration.
自传染性法氏囊病的第一次历史回顾以来,取得了重大进展(H. N. Lasher和V. S. Davis,禽病,第41卷,第11-19页;1997年),其中大部分发生在1977年至2005年之间。20世纪80年代的重大发现是传染性法氏囊病病毒(IBDV)血清2型的存在以及IBDV抗原型和免疫原型的多样性。1980年代末,出现了毒性很强的IBDV毒株,并于1990年代末在许多国家广泛传播。在发现抗原性变异后不久,开发了特定的商业疫苗并在该领域成功使用。病毒的结构被发现,这导致了病毒基因的一些生物学功能,包括免疫原性负责的阐明。这些发现的一个结果是开发了一类新的重组疫苗,并获得了商业许可。反向遗传学成为病毒表征的另一种工具。单克隆抗体的发展使得免疫球蛋白M阳性(IgM+) B细胞被鉴定为感染的主要靶细胞。巨噬细胞和T细胞参与了IBDV在法氏囊的发病和病理过程。血清学和病毒鉴定的新工具——elisa和逆转录酶(RT) PCR分别为流行病学提供了新的见解。酶联免疫吸附试验试剂盒的广泛使用促进了疫苗在面对母源性IBDV抗体时的使用,从而可以确定疫苗突破的时间,从而确定疫苗的施用。