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Transbound Emerg Dis. 2011 Apr;58(2):166-72. doi: 10.1111/j.1865-1682.2010.01186.x. Epub 2010 Dec 15.
2
Genetic basis of antigenic variation in foot-and-mouth disease serotype A viruses from the Middle East.中东地区 A 型口蹄疫病毒抗原变异的遗传基础。
Vaccine. 2014 Jan 23;32(5):631-8. doi: 10.1016/j.vaccine.2013.08.102. Epub 2013 Sep 10.
3
Evaluation and use of in-silico structure-based epitope prediction with foot-and-mouth disease virus.口蹄疫病毒基于结构的表位预测的评估与应用。
PLoS One. 2013 May 7;8(5):e61122. doi: 10.1371/journal.pone.0061122. Print 2013.
4
Southeast Asian foot-and-mouth disease viruses in Eastern Asia.东亚的东南亚口蹄疫病毒。
Emerg Infect Dis. 2012 Mar;18(3):499-501. doi: 10.3201/eid1803.110908.
5
Antigenic and genetic evolution of equine influenza A (H3N8) virus from 1968 to 2007.马流感 A(H3N8)病毒 1968 年至 2007 年的抗原和遗传进化。
J Virol. 2011 Dec;85(23):12742-9. doi: 10.1128/JVI.05319-11. Epub 2011 Sep 21.
6
Predicting antigenic sites on the foot-and-mouth disease virus capsid of the South African Territories types using virus neutralization data.利用病毒中和数据预测南非领土型口蹄疫病毒衣壳上的抗原位点。
J Gen Virol. 2011 Oct;92(Pt 10):2297-2309. doi: 10.1099/vir.0.032839-0. Epub 2011 Jun 22.
7
MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods.MEGA5:用于最大似然法、进化距离法和最大简约法的分子进化遗传学分析。
Mol Biol Evol. 2011 Oct;28(10):2731-9. doi: 10.1093/molbev/msr121. Epub 2011 May 4.
8
Genetic and antigenic characterization of H1 influenza viruses from United States swine from 2008.2008 年美国猪源 H1 流感病毒的遗传和抗原特征。
J Gen Virol. 2011 Apr;92(Pt 4):919-30. doi: 10.1099/vir.0.027557-0. Epub 2010 Dec 22.
9
Sequence-based prediction for vaccine strain selection and identification of antigenic variability in foot-and-mouth disease virus.基于序列的口蹄疫疫苗株选择预测和抗原变异性分析。
PLoS Comput Biol. 2010 Dec 9;6(12):e1001027. doi: 10.1371/journal.pcbi.1001027.
10
Characterisation and epitope mapping of neutralising monoclonal antibodies to A24 Cruzeiro strain of FMDV.鉴定和表位作图分析抗口蹄疫病毒 A24 Cruzeiro 株的中和性单克隆抗体。
Vet Microbiol. 2011 Apr 21;149(1-2):242-7. doi: 10.1016/j.vetmic.2010.11.003. Epub 2010 Nov 9.

口蹄疫病毒血清型 A 的抗原变异。

Antigenic variation of foot-and-mouth disease virus serotype A.

机构信息

Disease Dynamics Unit, Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge CB3 0ES, UK.

The Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.

出版信息

J Gen Virol. 2014 Feb;95(Pt 2):384-392. doi: 10.1099/vir.0.057521-0. Epub 2013 Nov 1.

DOI:10.1099/vir.0.057521-0
PMID:24187014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7346513/
Abstract

The current measures to control foot-and-mouth disease (FMD) include vaccination, movement control and slaughter of infected or susceptible animals. One of the difficulties in controlling FMD by vaccination arises due to the substantial diversity found among the seven serotypes of FMD virus (FMDV) and the strains within these serotypes. Therefore, vaccination using a single vaccine strain may not fully cross-protect against all strains within that serotype, and therefore selection of appropriate vaccines requires serological comparison of the field virus and potential vaccine viruses using relationship coefficients (r1 values). Limitations of this approach are that antigenic relationships among field viruses are not addressed, as comparisons are only with potential vaccine virus. Furthermore, inherent variation among vaccine sera may impair reproducibility of one-way relationship scores. Here, we used antigenic cartography to quantify and visualize the antigenic relationships among FMD serotype A viruses, aiming to improve the understanding of FMDV antigenic evolution and the scope and reliability of vaccine matching. Our results suggest that predicting antigenic difference using genetic sequence alone or by geographical location is not currently reliable. We found co-circulating lineages in one region that were genetically similar but antigenically distinct. Nevertheless, by comparing antigenic distances measured from the antigenic maps with the full capsid (P1) sequence, we identified a specific amino acid substitution associated with an antigenic mismatch among field viruses and a commonly used prototype vaccine strain, A22/IRQ/24/64.

摘要

目前控制口蹄疫(FMD)的措施包括接种疫苗、控制动物流动和扑杀感染或易感动物。通过接种疫苗控制 FMD 的困难之一是由于 FMD 病毒(FMDV)的七个血清型和这些血清型内的毒株之间存在大量的多样性。因此,使用单一疫苗株进行接种可能无法完全针对该血清型内的所有毒株提供交叉保护,因此选择合适的疫苗需要使用关系系数(r1 值)对田间病毒和潜在疫苗病毒进行血清学比较。这种方法的局限性在于,田间病毒之间的抗原关系没有得到解决,因为仅与潜在的疫苗病毒进行比较。此外,疫苗血清之间的固有差异可能会影响单向关系评分的重现性。在这里,我们使用抗原制图来量化和可视化 FMD 血清型 A 病毒之间的抗原关系,旨在提高对口蹄疫病毒抗原进化以及疫苗匹配的范围和可靠性的理解。我们的结果表明,仅使用遗传序列或地理位置预测抗原差异目前并不可靠。我们在一个地区发现了遗传上相似但抗原上不同的共同循环谱系。然而,通过比较抗原图谱测量的抗原距离与完整衣壳(P1)序列,我们确定了与田间病毒和常用原型疫苗株 A22/IRQ/24/64 之间的抗原不匹配相关的特定氨基酸取代。