首页> 外文OA文献 >Efficacy of a high potency O1 Manisa monovalent vaccine against heterologous challenge with a FMDV O Mya98 lineage virus in pigs 4 and 7 days post vaccination
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Efficacy of a high potency O1 Manisa monovalent vaccine against heterologous challenge with a FMDV O Mya98 lineage virus in pigs 4 and 7 days post vaccination

机译:疫苗接种后4天和7天高效O1 manisa单价疫苗对FmDV O mya98谱系病毒进行异源攻击的效力

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摘要

Early protection with a high potency (>6PD50) foot-and-mouth disease (FMD) O1Manisa (Middle-EastSouth Asia lineage) vaccine against challenge with O/VIT/2010 (O Mya98 lineage) was tested in pigs. Onlytwo pigs that were vaccinated seven days prior to challenge had any demonstrable antibodies as a resultof vaccination at the time of challenge. However, 80% and 60% of pigs that were vaccinated seven andfour days prior to coronary band challenge were protected. Vaccination significantly reduced the amountof virus excreted in nasal swabs, saliva and faeces compared to unvaccinated and infected controls. Virusand viral RNA could be detected in some pigs until termination of the experiment 14 days after challenge.Antibodies to the non-structural proteins (NSP) were detected in only one pig that was challenged fourdays post vaccination (dpv) and transiently in two pigs that were challenged seven dpv at only one timepoint. For each vaccine and control group, a group of unvaccinated pigs were kept in the same room butwith no direct contact with the infected pigs to determine whether vaccination prevented transmission.Despite the presence of live virus and viral RNA in these indirect contact pigs, the groups in contact withthe vaccinated and infected pigs did not develop clinical signs nor did they sero-convert. Contact pigs inthe same room as unvaccinated challenged controls did show signs of disease and virus infection thatresulted in sero-conversion to the NSP. A breach of the wall that separated the two groups at nine dayspost challenge might have contributed to this finding. This study showed that high potency vaccine canprovide protection to pigs soon after vaccination and that aerosol transmission within rooms is a rareevent.
机译:在猪中测试了用高效力(> 6PD50)口蹄疫(FMD)O1Manisa(东南亚-中东血统)疫苗对O / VIT / 2010(O Mya98血统)攻击的早期保护。在攻击前7天接种疫苗的两只猪在攻击时由于接种疫苗而具有任何可证明的抗体。但是,有80%和60%的猪在冠状动脉带攻击前7天和4天进行了疫苗接种。与未接种疫苗和感染的对照相比,接种疫苗可大大减少鼻拭子,唾液和粪便中排出的病毒数量。在攻击后14天实验结束之前,在某些猪中可检测到病毒和病毒RNA。仅在接种后四天(dpv)攻击的一头猪中检测到非结构蛋白(NSP)抗体,在两只猪中短暂检测到非结构蛋白(NSP)抗体在一个时间点被挑战了7 dpv。对于每个疫苗和对照组,将一组未接种疫苗的猪关在同一房间内,但不与受感染的猪直接接触以确定疫苗接种是否阻止了传播。尽管这些间接接触的猪中存在活病毒和病毒RNA与接种和感染的猪接触后,没有出现临床体征,也没有血清转换。与未接种疫苗的对照对照组在同一房间内接触的猪确实显示出疾病和病毒感染的迹象,导致血清转化为NSP。在挑战发生后的九天,突破了分隔两组的墙,可能是这一发现的原因。这项研究表明,高效疫苗可以在接种疫苗后立即为猪提供保护,而在室内传播气溶胶是罕见的。

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