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应急口蹄疫疫苗马来西亚97株和伊拉克64株对亚洲/G-IX/SEA-97谱系A型变异血清型病毒的异源攻击提供良好保护。

Emergency Foot-and-Mouth Disease Vaccines A Malaysia 97 and A Iraq 64 Offer Good Protection against Heterologous Challenge with A Variant Serotype A ASIA/G-IX/SEA-97 Lineage Virus.

作者信息

B Nagendrakumar, Dekker Aldo, Eblé Phaedra L, van Hemert-Kluitenberg Froukje, Weerdmeester Klaas, Horsington Jacquelyn, Vosloo W Wilna

机构信息

Australian Animal Health Laboratory, CSIRO-Health & Biosecurity, Geelong 3220, Australia.

Wageningen Bioveterinary Research (WBVR), Department of Virology, Laboratory Vesicular Diseases, Houtribweg 39, 8221 RA Lelystad, The Netherlands.

出版信息

Vaccines (Basel). 2020 Feb 10;8(1):80. doi: 10.3390/vaccines8010080.

Abstract

The continuous emergence of foot-and-mouth disease virus (FMDV) serotype A variants in South East Asia is of concern for international FMDV antigen banks, especially when in vitro tests predict a low antigenic match. A vaccination-challenge study was performed by using two emergency FMDV vaccines with A Iraq 64 (A22 IRQ) and A Malaysia 97 (A MAY 97) strains, against challenge with a variant strain of FMDV A/Asia/G-IX/SEA-97 lineage at 7- and 21-day post-vaccination (dpv). At 7 dpv, three of five female calves vaccinated with A MAY 97 and four of five vaccinated with A22 IRQ did not show lesions on the feet and were considered protected, while at 21 dpv all five calves were protected with each vaccine, indicating equal efficacy of both vaccine strains. Calves were protected despite relatively low heterologous neutralizing antibody titers to the challenge virus at the time of challenge. All the calves developed antibodies to the non-structural proteins, most likely due to the direct intradermolingual (IDL) inoculation. Only one calf from the A MAY 97-7 group had infectious virus in the serum 1-3-day post-challenge (dpc), while no virus could be isolated from the serum of cattle challenged on 21 dpv. The virus could be isolated from the oral swabs of all calves, 1-7 dpc with viral RNA detected 1-10 dpc. Nasal swabs were positive for virus 1-6 dpc in a small number of calves. The time between vaccination and infection did not have an impact on the number of animals with persistent infection, with almost all the animals showing viral RNA in their oro-pharyngeal fluid (probang) samples up to 35 dpc. Despite the poor matching data and field reports of vaccine failures, this study suggests that these vaccine strains should be effective against this new A/Asia/G/SEA-97 variant, provided they are formulated with a high antigen dose.

摘要

东南亚口蹄疫病毒(FMDV)A型变种的不断出现,令国际FMDV抗原库担忧,尤其是当体外试验预测抗原匹配度较低时。通过使用两种含有伊拉克64型(A22 IRQ)和马来西亚97型(A MAY 97)毒株的紧急FMDV疫苗,进行了一项疫苗接种-攻毒研究,以对抗在接种疫苗后7天和21天用FMDV A/亚洲/G-IX/SEA-97谱系的变异毒株进行攻毒。在接种疫苗后7天,接种A MAY 97的5头雌性犊牛中有3头以及接种A22 IRQ的5头中有4头在足部未出现病变,被认为受到保护,而在接种疫苗后21天,所有5头犊牛用每种疫苗均受到保护,表明两种疫苗毒株的效力相同。尽管在攻毒时针对攻毒病毒的异源中和抗体滴度相对较低,但犊牛仍受到了保护。所有犊牛均产生了针对非结构蛋白的抗体,很可能是由于直接皮内舌内(IDL)接种所致。A MAY 97 - 7组中只有1头犊牛在攻毒后1 - 3天血清中有传染性病毒,而在接种疫苗后21天攻毒的牛血清中未分离到病毒。在攻毒后1 - 7天,所有犊牛的口腔拭子中均可分离到病毒,在攻毒后1 - 10天可检测到病毒RNA。少数犊牛的鼻拭子在攻毒后1 - 6天呈病毒阳性。接种疫苗与感染之间的时间间隔对持续感染动物的数量没有影响,几乎所有动物在攻毒后35天内其口咽液(探咽)样本中均显示有病毒RNA。尽管匹配数据不佳且有疫苗失效的现场报告,但本研究表明,只要这些疫苗毒株以高抗原剂量配制,就应对这种新的A/亚洲/G/SEA - 97变种有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/667e/7157217/2546c13d21fe/vaccines-08-00080-g001.jpg

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