Gelb J, Keeler C L, Nix W A, Rosenberger J K, Cloud S S
Delaware Agricultural Experiment Station, Department of Animal and Food Sciences, College of Agricultural Sciences, University of Delaware, Newark 19717-1303, USA.
Avian Dis. 1997 Jul-Sep;41(3):661-9.
A previously unrecognized infectious bronchitis virus (IBV) serotype, referred to hereafter as the Delaware variant (DE var), was isolated from commercial broiler chickens during a severe, widespread respiratory disease epornitic in the Delmarva peninsula region of the United States in January-March 1992. The DE var serotype was found to be antigenically unrelated by virus-neutralization (VN) test to nine reference IBV serotypes from North America. Additional VN tests indicated that the DE var isolates (DE/072/92, DE/121/ 92, DE/152/92, and DE/174/92) from broilers were fully or partially neutralized by monospecific antisera prepared against themselves and against two IBV field isolates (DE/492/90 and DE/903/90) recovered from a Delmarva commercial layer flock experiencing egg production losses in 1990. Antigenic relatedness values determined by VN indicated layer isolate DE/492/90 was more closely related to the broiler DE var isolates than was layer isolate DE/903/90. Cross-challenge tests performed in specific-pathogen-free chickens also demonstrated the antigenic similarity of the broiler (DE/072/92 and DE/174/92) and the layer isolates (DE/492/90 and DE/903/90), with heterologous strain protection values ranging from 55% to 100%. Protection values of DE var isolates vs. Massachusetts 41 and Arkansas DPI were considerably lower (0-60%). The S-1 gene of the US/DE/072/92 isolate of the DE var serotype was amplified by reverse transcription polymerase chain reaction, cloned, and sequenced. The DE var S-1 gene sequence was compared with the S-1 gene sequences of IBV serotypes from North America, Europe, and Australia. A dendrogram based on this analysis supported the conclusion that the DE var serotype is highly novel among IBV. A high degree of similarity (> 88%) was observed between the S-1 genes of the DE var broiler isolates (DE/072/92 and DE/174/92) and layer isolates (DE/492/90 and DE/903/90). These data, taken with the VN and cross-challenge results, establish a genetic as well as an antigenic link between the isolates from layers and broilers and indicate the DE var serotype was responsible for both infectious bronchitis outbreaks.
1992年1月至3月,在美国德尔马瓦半岛地区一场严重且广泛传播的呼吸道疾病 epizootic(动物流行病)期间,从商业肉鸡中分离出一种先前未被识别的传染性支气管炎病毒(IBV)血清型,此后称为特拉华变种(DE var)。通过病毒中和(VN)试验发现,DE var血清型与来自北美的9种参考IBV血清型在抗原上不相关。额外的VN试验表明,针对肉鸡的DE var分离株(DE/072/92、DE/121/92、DE/152/92和DE/174/92)制备的单特异性抗血清可完全或部分中和这些分离株,以及针对从1990年经历产蛋损失的德尔马瓦商业蛋鸡群中回收的两种IBV野外分离株(DE/492/90和DE/903/90)。通过VN确定的抗原相关性值表明,蛋鸡分离株DE/492/90比蛋鸡分离株DE/903/90与肉鸡DE var分离株的关系更密切。在无特定病原体的鸡中进行的交叉攻毒试验也证明了肉鸡(DE/072/92和DE/174/92)和蛋鸡分离株(DE/492/90和DE/903/90)的抗原相似性,异源菌株保护值范围为55%至100%。DE var分离株对马萨诸塞41型和阿肯色DPI型的保护值则低得多(0 - 60%)。通过逆转录聚合酶链反应扩增、克隆并测序了DE var血清型的美国/DE/072/92分离株的S-1基因。将DE var S-1基因序列与来自北美、欧洲和澳大利亚的IBV血清型的S-1基因序列进行了比较。基于此分析的系统发育树支持了DE var血清型在IBV中高度新颖的结论。在DE var肉鸡分离株(DE/072/92和DE/174/92)和蛋鸡分离株(DE/492/90和DE/903/90)的S-1基因之间观察到高度相似性(> 88%)。这些数据与VN和交叉攻毒结果一起,在蛋鸡和肉鸡的分离株之间建立了遗传以及抗原联系,并表明DE var血清型是这两次传染性支气管炎疫情的病因。