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用B亚型禽偏肺病毒减毒活疫苗对雏鸡进行免疫接种:对攻毒的保护作用和免疫反应可能与疫苗剂量无关。

Vaccination of chicks with live attenuated subtype B avian metapneumovirus vaccines: protection against challenge and immune responses can be unrelated to vaccine dose.

作者信息

Ganapathy Kannan, Jones Richard Charles

机构信息

Department of Veterinary Pathology, University of Liverpool, Leahurst, Neston, South Wirral CH64 7TE, UK.

出版信息

Avian Dis. 2007 Sep;51(3):733-7. doi: 10.1637/0005-2086(2007)51[733:VOCWLA]2.0.CO;2.

Abstract

Live attenuated subtype B avian metapneumovirus (aMPV) vaccines from two different commercial sources (Vac 1 and Vac 2) were used to vaccinate two groups of day-old specific-pathogen-free chicks. The chicks were challenged at 21 or 49 days of age with a virulent subtype B virus. Parameters compared were persistence of vaccine viruses, their ability to induce humoral antibody responses, and the protection they offered against virulent challenge. Vac 1 virus was detectable for at least 14 days after vaccination, and Vac 2 virus was detectable for at least 7 days after vaccination. The serologic response after Vac 1 by using a subtype B-based enzyme-linked immunosorbent assay was significantly higher than that induced by Vac 2, even though the titer of the recommended dose had a higher titer than Vac 1. After challenge at 21 or 49 days of age, both vaccines gave 100% protection against clinical disease. For the recovery of challenge virus, one of 10 chicks given the Vac 2 was positive by virus isolation or reverse transcriptase-polymerase chain reaction (RT-PCR) on each occasion except on day 10 after challenge at 49 days. With groups vaccinated with Vac 1, no challenge virus was detected except on day 5 after challenge at 49 days, when one of 10 chickens was positive only by RT-PCR. This study has shown that commercial aMPV vaccines from different sources can provide identical protection in terms of clinical disease after virulent challenge and in their ability to induce humoral antibodies, even though the titer of their recommended doses is widely different.

摘要

来自两种不同商业来源(疫苗1和疫苗2)的减毒活B亚型禽偏肺病毒(aMPV)疫苗被用于给两组1日龄无特定病原体雏鸡接种。这些雏鸡在21日龄或49日龄时用强毒B亚型病毒进行攻毒。比较的参数包括疫苗病毒的持续性、诱导体液抗体反应的能力以及它们对强毒攻毒提供的保护。疫苗1病毒在接种后至少可检测到14天,疫苗2病毒在接种后至少可检测到7天。使用基于B亚型的酶联免疫吸附测定法检测,疫苗1接种后的血清学反应显著高于疫苗2诱导的反应,尽管推荐剂量的疫苗2滴度高于疫苗1。在21日龄或49日龄攻毒后,两种疫苗对临床疾病均提供100%的保护。对于攻毒病毒的回收,除了在49日龄攻毒后第10天外,每次接种疫苗2的10只雏鸡中有1只通过病毒分离或逆转录聚合酶链反应(RT-PCR)呈阳性。对于接种疫苗1的组,除了在49日龄攻毒后第5天,10只鸡中有1只仅通过RT-PCR呈阳性外,未检测到攻毒病毒。这项研究表明,来自不同来源的商业aMPV疫苗在强毒攻毒后的临床疾病方面以及诱导体液抗体的能力方面可以提供相同的保护,尽管它们推荐剂量的滴度差异很大。

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