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在与QX样传染性支气管炎病毒共感染攻毒模型中评估鸡毒支原体疫苗效力

Assessment of Mycoplasma gallisepticum vaccine efficacy in a co-infection challenge model with QX-like infectious bronchitis virus.

作者信息

Bwala Dauda G, Solomon Ponman, Duncan Neil, Wandrag Daniel B R, Abolnik Celia

机构信息

a Poultry Section, Department of Production Animal Studies, Faculty of Veterinary Science , University of Pretoria , Onderstepoort , South Africa.

b National Veterinary Research Institute , Vom , Nigeria.

出版信息

Avian Pathol. 2018 Jun;47(3):261-270. doi: 10.1080/03079457.2018.1440064. Epub 2018 Mar 14.

Abstract

Mycoplasma gallisepticum (MG) is the primary cause of chronic respiratory disease in poultry. We investigated the protective efficacy of the live-attenuated ts-11 and 6/85 MG vaccines against a local MG strain and, in order to enhance signs and mimic a typical field situation, we co-infected birds with a virulent strain of QX-like infectious bronchitis virus (IBV). Both vaccines showed similar ability to protect infected chickens from clinical signs, although ts-11 performed slightly better. Despite the lower protection against clinical disease, 6/85-vaccinated birds had significantly (P ≤ 0.05) lower tracheal lesion scores and mucosal thickness at day 28 post-vaccination (7 days post-challenge [dpc] with MG, 2 dpc IBV) and day 31 post-vaccination (10 dpc MG challenge, 5 dpc IBV) compared to ts-11 vaccinated birds, but these difference was not significant at day 33 (12 dpc MG, 7 dpc IBV). Pathogen infection and replication was assessed by qPCR, and the 6/85 vaccine produced a more significant (P ≤ 0.05) reduction in MG replication in the lungs, kidneys and livers but enhanced late replication in bursae and caecal tonsils. In contrast, the ts-11 vaccine had a more pronounced reductive effect on replication in tracheas, air sacs, bursae and heart at days 28 and 31, yet increased replication in lungs. Interestingly, both vaccines provided non-specific protection against IBV challenge. The co-challenge model provided useful data on vaccine efficacy, especially on days 31 and 33, and tracheas, lungs, air sacs, kidneys, liver and caecal tonsils were the best organs to assess.

摘要

鸡毒支原体(MG)是家禽慢性呼吸道疾病的主要病因。我们研究了减毒活疫苗ts - 11和6/85 MG疫苗对本地MG毒株的保护效力,并且为了增强症状并模拟典型的田间情况,我们用一种强毒株QX样传染性支气管炎病毒(IBV)对鸡进行了共同感染。两种疫苗在保护感染鸡免受临床症状影响方面表现出相似的能力,尽管ts - 11的表现略好。尽管对临床疾病的保护作用较低,但在接种疫苗后第28天(用MG攻毒后7天,IBV攻毒后2天)和接种疫苗后第31天(MG攻毒后10天,IBV攻毒后5天),与接种ts - 11疫苗的鸡相比,接种6/85疫苗的鸡气管病变评分和黏膜厚度显著更低(P≤0.05),但在第33天(MG攻毒后12天,IBV攻毒后7天)这些差异不显著。通过qPCR评估病原体感染和复制情况,6/85疫苗在肺、肾和肝脏中对MG复制的减少更为显著(P≤0.05),但增强了法氏囊和盲肠扁桃体中的后期复制。相比之下,ts - 11疫苗在第28天和第31天对气管、气囊、法氏囊和心脏中的复制有更明显的抑制作用,但增加了肺中的复制。有趣的是,两种疫苗都对IBV攻毒提供了非特异性保护。共同攻毒模型提供了关于疫苗效力的有用数据,特别是在第31天和第33天,气管、肺、气囊、肾、肝和盲肠扁桃体是评估的最佳器官。

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