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一种抗禽肺病毒活疫苗的实验与现场评估

Experimental and field evaluation of a live vaccine against avian pneumovirus.

作者信息

Patnayak Devi P, Sheikh Anwar M, Gulati Baldev R, Goyal Sagar M

机构信息

Department of Veterinary Diagnostic Medicine, College of Veterinary Medicine, University of Minnesota, St Paul, MN 55108, USA.

出版信息

Avian Pathol. 2002 Aug;31(4):377-82. doi: 10.1080/0307945022041651.

Abstract

The attenuation of an avian pneumovirus (APV) isolate (APV/MN/turkey/1-a/97) by 63 serial passages in cell culture (seven in chicken embryo fibroblasts and 56 in Vero cells) and its evaluation as a live attenuated vaccine in turkey poults is described. The birds were vaccinated with two different doses of attenuated virus (10(4.5) median tissue culture infectious dose (TCID(50))/ml and 10(2.5) TCID(50) /ml) at 2 weeks of age, and were challenged 2 weeks later with virulent APV. No clinical signs were seen in vaccinated, challenged birds, whereas severe clinical signs were observed in the mock-vaccinated, challenged group. Vaccinated birds developed anti-APV antibodies, which increased in titre following challenge with virulent virus. On challenge, none of the vaccinates was found to shed viral nucleic acid as detected by reverse transcriptase-polymerase chain reaction, but non-vaccinated, challenged birds did. The vaccine virus was also evaluated under field conditions in two farms. At one farm, the 'seeder bird approach' was used and two birds per 1,000 birds were vaccinated by the oculo-nasal route. In the second farm, the virus was given to all birds simultaneously in the drinking water. The birds vaccinated by the drinking water route seroconverted earlier and continued to shed virus for longer as compared with birds inoculated by the seeder bird approach. The overall results of this study indicate that the 63rd passage of APV was sufficiently attenuated and offered protection against challenge with virulent virus.

摘要

本文描述了禽肺病毒(APV)分离株(APV/MN/火鸡/1-a/97)在细胞培养中经63次连续传代(在鸡胚成纤维细胞上传代7次,在Vero细胞上传代56次)致弱,并作为火鸡弱毒活疫苗进行评估的过程。雏火鸡在2周龄时用两种不同剂量的致弱病毒(10(4.5)半数组织培养感染剂量(TCID(50))/ml和10(2.5) TCID(50)/ml)进行免疫接种,2周后用强毒APV进行攻毒。接种并攻毒的雏火鸡未出现临床症状,而 mock 免疫接种并攻毒的组则观察到严重的临床症状。接种疫苗的雏火鸡产生了抗APV抗体,在用强毒病毒攻毒后抗体滴度升高。攻毒时,通过逆转录聚合酶链反应检测发现,接种疫苗的雏火鸡均未排出病毒核酸,而未接种疫苗并攻毒的雏火鸡排出了病毒核酸。还在两个养殖场的田间条件下对疫苗病毒进行了评估。在一个养殖场,采用“带毒传播法”,每1000只鸡中有2只通过眼鼻途径接种疫苗。在第二个养殖场,将病毒同时加入饮水中给所有鸡饮用。与通过带毒传播法接种的鸡相比,通过饮水途径接种疫苗的鸡血清转化更早,且排出病毒的时间更长。本研究的总体结果表明,APV第63代传代病毒已充分致弱,并能提供针对强毒病毒攻毒的保护。

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