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1
Options for control of foot-and-mouth disease: knowledge, capability and policy.口蹄疫防控的选择:知识、能力与政策
Philos Trans R Soc Lond B Biol Sci. 2009 Sep 27;364(1530):2657-67. doi: 10.1098/rstb.2009.0100.
2
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3
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Developing vaccines against foot-and-mouth disease and some other exotic viral diseases of livestock.研发口蹄疫和其他一些外来家畜病毒性疾病的疫苗。
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Developing Vaccines Against Foot-and-Mouth Disease: a Biotechnological Approach.开发针对口蹄疫的疫苗:一种生物技术方法。
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Rapid Engineering of Foot-and-Mouth Disease Vaccine and Challenge Viruses.口蹄疫疫苗及攻击病毒的快速工程制作
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Review of the status and control of foot and mouth disease in sub-Saharan Africa.撒哈拉以南非洲口蹄疫的现状与防控综述
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Validation of a high performance liquid chromatography method for quantitation of foot-and-mouth disease virus antigen in vaccines and vaccine manufacturing.验证一种高效液相色谱法,用于定量检测疫苗和疫苗生产中的口蹄疫病毒抗原。
Vaccine. 2019 Aug 23;37(36):5288-5296. doi: 10.1016/j.vaccine.2019.07.051. Epub 2019 Jul 25.

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An antigen panel to assess the regional relevance of foot and mouth disease vaccines.用于评估口蹄疫疫苗区域相关性的抗原组。
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Spatial and temporal patterns of foot and mouth disease outbreaks (2011-2022) in cattle export-sourcing areas of southeastern Ethiopia.埃塞俄比亚东南部牛只出口源地区口蹄疫疫情的时空模式(2011 - 2022年)
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Detection and genomic characterisation of foot-and-mouth disease virus serotypes circulating in Cameroon using environmental sampling.利用环境采样对喀麦隆流行的口蹄疫病毒血清型进行检测和基因组特征分析。
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本文引用的文献

1
Multiple origins of foot-and-mouth disease virus serotype Asia 1 outbreaks, 2003-2007.2003 - 2007年亚洲1型口蹄疫病毒疫情的多个起源地
Emerg Infect Dis. 2009 Jul;15(7):1046-51. doi: 10.3201/eid1507.081621.
2
Use of infrared thermography to detect thermographic changes in mule deer (Odocoileus hemionus) experimentally infected with foot-and-mouth disease.利用红外热成像技术检测实验感染口蹄疫的骡鹿(白尾鹿)的热成像变化。
J Zoo Wildl Med. 2009 Jun;40(2):296-301. doi: 10.1638/2008-0087.1.
3
Recent spread of a new strain (A-Iran-05) of foot-and-mouth disease virus type A in the Middle East.中东地区近期出现A型口蹄疫病毒新毒株(A-Iran-05)的传播。
Transbound Emerg Dis. 2009 Jun;56(5):157-69. doi: 10.1111/j.1865-1682.2009.01074.x.
4
Quantifying the risk of localised animal movement bans for foot-and-mouth disease.量化口蹄疫局部动物移动禁令的风险。
PLoS One. 2009;4(5):e5481. doi: 10.1371/journal.pone.0005481. Epub 2009 May 8.
5
Performance of real-time reverse transcription polymerase chain reaction for the detection of foot-and-mouth disease virus during field outbreaks in the United Kingdom in 2007.2007年英国口蹄疫疫情期间实时逆转录聚合酶链反应检测口蹄疫病毒的性能
J Vet Diagn Invest. 2009 May;21(3):321-30. doi: 10.1177/104063870902100303.
6
Foot-and-mouth disease virus can induce a specific and rapid CD4+ T-cell-independent neutralizing and isotype class-switched antibody response in naïve cattle.口蹄疫病毒可在未接触过该病毒的牛中诱导出一种特异性且快速的、不依赖CD4+ T细胞的中和及抗体类别转换抗体反应。
J Virol. 2009 Apr;83(8):3626-36. doi: 10.1128/JVI.02613-08. Epub 2009 Jan 28.
7
The tale of a modern animal plague: tracing the evolutionary history and determining the time-scale for foot and mouth disease virus.一场现代动物瘟疫的故事:追溯口蹄疫病毒的进化史并确定其时间尺度
Virology. 2008 Dec 20;382(2):250-6. doi: 10.1016/j.virol.2008.09.011. Epub 2008 Oct 21.
8
Foot-and-mouth disease virus persists in the light zone of germinal centres.口蹄疫病毒在生发中心的亮区持续存在。
PLoS One. 2008;3(10):e3434. doi: 10.1371/journal.pone.0003434. Epub 2008 Oct 20.
9
Development and laboratory validation of a lateral flow device for the detection of foot-and-mouth disease virus in clinical samples.用于检测临床样本中口蹄疫病毒的侧向流动装置的研发与实验室验证
J Virol Methods. 2009 Jan;155(1):10-7. doi: 10.1016/j.jviromet.2008.09.009. Epub 2008 Nov 5.
10
Therapeutic application of RNA interference against foot-and-mouth disease virus in vitro and in vivo.RNA干扰在体外和体内对口蹄疫病毒的治疗应用
Antiviral Res. 2008 Nov;80(2):178-84. doi: 10.1016/j.antiviral.2008.06.001. Epub 2008 Jul 2.

口蹄疫防控的选择:知识、能力与政策

Options for control of foot-and-mouth disease: knowledge, capability and policy.

作者信息

Paton David J, Sumption Keith J, Charleston Bryan

机构信息

Pirbright Laboratory, Institute for Animal Health, Woking, Surrey GU24 0NF, UK.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2009 Sep 27;364(1530):2657-67. doi: 10.1098/rstb.2009.0100.

DOI:10.1098/rstb.2009.0100
PMID:19687036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2865093/
Abstract

Foot-and-mouth disease can be controlled by zoo-sanitary measures and vaccination but this is difficult owing to the existence of multiple serotypes of the causative virus, multiple host species including wildlife and extreme contagiousness. Although intolerable to modern high-production livestock systems, the disease is not usually fatal and often not a priority for control in many developing countries, which remain reservoirs for viral dissemination. Phylogenetic analysis of the viruses circulating worldwide reveals seven principal reservoirs, each requiring a tailored regional control strategy. Considerable trade benefits accrue to countries that eradicate the disease but as well as requiring regional cooperation, achieving and maintaining this status using current tools takes a great deal of time, money and effort. Therefore, a progressive approach is needed that can provide interim benefits along the pathway to final eradication. Research is needed to understand and predict the patterns of viral persistence and emergence and to improve vaccine selection. Better diagnostic methods and especially better vaccines could significantly improve control in both the free and the affected parts of the world. In particular, vaccines with improved thermostability and a longer duration of immunity would facilitate control and make it less reliant on advanced veterinary infrastructures.

摘要

口蹄疫可通过动物卫生措施和疫苗接种加以控制,但由于致病病毒存在多种血清型、包括野生动物在内的多种宿主物种以及极强的传染性,控制工作颇具难度。尽管这种疾病对于现代高产畜牧系统而言是无法容忍的,但它通常并不致命,在许多发展中国家往往也并非控制重点,而这些国家仍是病毒传播的疫源地。对全球流行病毒进行的系统发育分析揭示了七个主要疫源地,每个疫源地都需要量身定制的区域控制策略。根除该疾病的国家可获得可观的贸易利益,但除了需要区域合作外,利用现有工具实现并维持这一状态需要大量的时间、资金和精力。因此,需要一种循序渐进的方法,以便在最终根除的道路上提供中期效益。需要开展研究,以了解和预测病毒持续存在和出现的模式,并改进疫苗选择。更好的诊断方法,尤其是更好的疫苗,可显著改善全球无疫地区和受影响地区的控制情况。特别是,具有更高热稳定性和更长免疫期的疫苗将有助于控制工作,并减少对先进兽医基础设施的依赖。