Literature DB >> 21434805

Development of vaccines toward the global control and eradication of foot-and-mouth disease.

Luis L Rodriguez1, Cyril G Gay.   

Abstract

Foot-and-mouth disease (FMD) is one of the most economically and socially devastating diseases affecting animal agriculture throughout the world. Although mortality is usually low in adult animals, millions of animals have been killed in efforts to rapidly control and eradicate FMD. The causing virus, FMD virus (FMDV), is a highly variable RNA virus occurring in seven serotypes (A, O, C, Asia 1, Sat 1, Sat 2 and Sat 3) and a large number of subtypes. FMDV is one of the most infectious agents known, affecting cloven-hoofed animals with significant variations in infectivity and virus transmission. Although inactivated FMD vaccines have been available for decades, there is little or no cross-protection across serotypes and subtypes, requiring vaccines that are matched to circulating field strains. Current inactivated vaccines require growth of virulent virus, posing a threat of escape from manufacturing sites, have limited shelf life and require re-vaccination every 4-12 months. These vaccines have aided in the eradication of FMD from Europe and the control of clinical disease in many parts of the world, albeit at a very high cost. However, FMDV persists in endemic regions impacting millions of people dependent on livestock for food and their livelihood. Usually associated with developing countries that lack the resources to control it, FMD is a global problem and the World Organization for Animal Health and the United Nations' Food Agriculture Organization have called for its global control and eradication. One of the main limitations to FMDV eradication is the lack of vaccines designed for this purpose, vaccines that not only protect against clinical signs but that can actually prevent infection and effectively interrupt the natural transmission cycle. These vaccines should be safely and inexpensively produced, be easy to deliver, and also be capable of inducing lifelong immunity against multiple serotypes and subtypes. Furthermore, there is a need for better integrated strategies that fit the specific needs of endemic regions. Availability of these critical components will greatly enhance the chances for the global control and eradication of FMDV.

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Year:  2011        PMID: 21434805     DOI: 10.1586/erv.11.4

Source DB:  PubMed          Journal:  Expert Rev Vaccines        ISSN: 1476-0584            Impact factor:   5.217


  41 in total

1.  Expression and purification of virus like particles (VLPs) of foot-and-mouth disease virus in Eri silkworm (Samia cynthia ricini) larvae.

Authors:  Manoj Kumar; P Saravanan; S K Jalali
Journal:  Virusdisease       Date:  2015-11-24

2.  An increase in acid resistance of foot-and-mouth disease virus capsid is mediated by a tyrosine replacement of the VP2 histidine previously associated with VP0 cleavage.

Authors:  Angela Vázquez-Calvo; Flavia Caridi; Francisco Sobrino; Miguel A Martín-Acebes
Journal:  J Virol       Date:  2013-12-18       Impact factor: 5.103

3.  Implication of Broadly Neutralizing Bovine Monoclonal Antibodies in the Development of an Enzyme-Linked Immunosorbent Assay for Detecting Neutralizing Antibodies against Foot-and-Mouth Disease Virus Serotype O.

Authors:  Yimei Cao; Kun Li; Sheng Wang; Yuanfang Fu; Pu Sun; Pinghua Li; Xingwen Bai; Jing Zhang; Xueqing Ma; Xiangchuan Xing; Shasha Zhou; Huifang Bao; Dong Li; Yingli Chen; Zhiyong Li; Zengjun Lu; Zaixin Liu
Journal:  J Clin Microbiol       Date:  2019-11-22       Impact factor: 5.948

4.  Molecular investigation of foot-and-mouth disease virus in domestic bovids from Gharbia, Egypt.

Authors:  Mahmoud Mohey Elhaig; Mohamed Nagi Elsheery
Journal:  Trop Anim Health Prod       Date:  2014-09-04       Impact factor: 1.559

5.  Evaluation of foot and mouth vaccination for yak (Bos grunniens) in Pakistan.

Authors:  J A Mortenson; E H Haq Khan; I Ali; S Manzoor; A Jamil; M Abubakar; M Afzal; M Hussain
Journal:  Trop Anim Health Prod       Date:  2017-02-28       Impact factor: 1.559

6.  Constitutively Active IRF7/IRF3 Fusion Protein Completely Protects Swine against Foot-and-Mouth Disease.

Authors:  Lisbeth Ramírez-Carvajal; Fayna Diaz-San Segundo; Elizabeth Ramirez-Medina; Luis L Rodríguez; Teresa de Los Santos
Journal:  J Virol       Date:  2016-09-12       Impact factor: 5.103

7.  Expression of porcine fusion protein IRF7/3(5D) efficiently controls foot-and-mouth disease virus replication.

Authors:  Lisbeth Ramírez-Carvajal; Fayna Díaz-San Segundo; Danielle Hickman; Charles R Long; James Zhu; Luis L Rodríguez; Teresa de los Santos
Journal:  J Virol       Date:  2014-07-16       Impact factor: 5.103

8.  Inhibition of EHMT2 Induces a Robust Antiviral Response Against Foot-and-Mouth Disease and Vesicular Stomatitis Virus Infections in Bovine Cells.

Authors:  Neetu Singh; Lisbeth Ramĩrez-Carvajal; Teresa de Los Santos; Michael C Golding; Charles R Long
Journal:  J Interferon Cytokine Res       Date:  2015-09-29       Impact factor: 2.607

9.  Evaluation of a Fiber-Modified Adenovirus Vector Vaccine against Foot-and-Mouth Disease in Cattle.

Authors:  Gisselle N Medina; Nestor Montiel; Fayna Diaz-San Segundo; Diego Sturza; Elizabeth Ramirez-Medina; Marvin J Grubman; Teresa de los Santos
Journal:  Clin Vaccine Immunol       Date:  2015-11-25

10.  A continuous bovine kidney cell line constitutively expressing bovine αvβ6 integrin has increased susceptibility to foot-and-mouth disease virus.

Authors:  Michael LaRocco; Peter W Krug; Ed Kramer; Zaheer Ahmed; Juan M Pacheco; Hernando Duque; Barry Baxt; Luis L Rodriguez
Journal:  J Clin Microbiol       Date:  2013-03-20       Impact factor: 5.948

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