Suppr超能文献

在无特定病原体胚胎的卵内接种后,检测淋巴组织中的传染性法氏囊病疫苗病毒。

Detection of infectious bursal disease vaccine viruses in lymphoid tissues after in ovo vaccination of specific-pathogen-free embryos.

作者信息

Corley M M, Giambrone J J, Dormitorio T V

机构信息

Department of Poultry Science, Alabama Agricultural Experimental Station, Auburn University, 36849, USA.

出版信息

Avian Dis. 2001 Oct-Dec;45(4):897-905.

Abstract

Control of infectious bursal disease virus (IBDV) by vaccination is important for poultry production worldwide. Two vaccines, an IBDV immune complex (ICX) vaccine and an IBDV-2512 vaccine, were administered at 100 mean embryo infectious dose to specific-pathogen-free 18-day-old broiler embryos in ovo. At 3, 6, 9, 15, and 21 days post in ovo vaccination (PIOV), bursa, spleen, and thymus tissues were collected and analyzed for virus protein by antigen capture chemiluminescent enzyme-linked immunosorbent assay (ELISA). Chicks were bled and antibody titers were determined by the antibody ELISA. At 21 days PIOV, chickens were challenged with a 1:500 dilution of an antigenic standard IBDV strain. At 28 days PIOV, birds were euthanatized and bursa weight:body weight ratios were determined. Embryos vaccinated with either vaccine exhibited 92% hatchability; however, within 1 wk of hatch, birds vaccinated with IBDV-2512 showed 56% mortality, whereas those given IBDV-ICX had only 3.2% mortality. Both IBDV-ICX and IBDV-2512 vaccines were detected in bursa, spleen, and thymus at day 3 PIOV. A 5-day delay in virus replication was observed with IBDV-ICX vaccine. By day 15 PIOV, the IBDV-ICX was no longer detectable in the bursa and spleen but persisted in the thymus. The IBDV-2512 vaccine persisted in the spleen and thymus on day 15 PIOV. By day 21 PIOV, neither vaccine virus was detected in any lymphoid organ. This assay can be useful in the early detection of vaccine virus in the tissues of chickens vaccinated via the in ovo route. Both vaccines caused bursal atrophy at all times PIOV. The IBDV-2512 caused splenomegaly at day 6 PIOV, whereas splenomegaly was not seen in IBDV-ICX-vaccinated birds until day 9 PIOV. Thymus atrophy was observed in IBDV-2512-vaccinated chicks from day 3 PIOV, whereas this occurred on day 15 PIOV in IBDV-ICX-vaccinated birds. Bursa weight: body weight ratios in IBDV-ICX-vaccinated unchallenged and vaccinated challenged birds were not different (P < 0.05).

摘要

通过接种疫苗控制传染性法氏囊病病毒(IBDV)对全球家禽生产至关重要。两种疫苗,即IBDV免疫复合物(ICX)疫苗和IBDV - 2512疫苗,以100个平均胚胎感染剂量接种到特定病原体-free的18日龄肉仔鸡胚胎的卵内。在卵内接种疫苗(PIOV)后3、6、9、15和21天,收集法氏囊、脾脏和胸腺组织,并通过抗原捕获化学发光酶联免疫吸附测定(ELISA)分析病毒蛋白。对雏鸡采血并通过抗体ELISA测定抗体滴度。在PIOV 21天时,用抗原标准IBDV毒株1:500稀释液对鸡进行攻毒。在PIOV 28天时,对鸡实施安乐死并测定法氏囊重量与体重之比。用任何一种疫苗接种的胚胎孵化率均为92%;然而,在孵化后1周内,接种IBDV - 2512的鸡死亡率为56%,而接种IBDV - ICX的鸡死亡率仅为3.2%。在PIOV第3天时,在法氏囊、脾脏和胸腺中均检测到IBDV - ICX和IBDV - 2512疫苗。观察到IBDV - ICX疫苗的病毒复制延迟了5天。到PIOV第15天时,在法氏囊和脾脏中不再能检测到IBDV - ICX,但在胸腺中仍持续存在。在PIOV第15天时,IBDV - 2512疫苗仍存在于脾脏和胸腺中。到PIOV第21天时,在任何淋巴器官中均未检测到疫苗病毒。该检测方法可用于早期检测通过卵内途径接种疫苗的鸡组织中的疫苗病毒。两种疫苗在所有PIOV时间点均导致法氏囊萎缩。IBDV - 2512在PIOV第6天时导致脾肿大,而接种IBDV - ICX的鸡直到PIOV第9天才出现脾肿大。从PIOV第3天起,在接种IBDV - 2512的雏鸡中观察到胸腺萎缩,而在接种IBDV - ICX的鸡中,胸腺萎缩发生在PIOV第15天。接种IBDV - ICX且未攻毒和攻毒的鸡的法氏囊重量与体重之比无差异(P < 0.05)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验