Article

Epidemiological situation of foot-and-mouth disease in 2014–2015 and the beginning of 2016

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Abstract

This article presents key information about foot-and-mouth disease (FMD) outbreaks around the world, based on data from Office International des Epizooties (OIE), World Reference Laboratory for Foot-and-Mouth Disease (WRL FMD) and the European Laboratory for Foot and Mouth Disease (EURL) at the Pirbright Institute. In the years 2014–2015 and early 2016, FMD caused by immunologically diverse serotypes O, A, Asia 1, SAT 1, SAT 2, SAT 3 occurred in areas of Asia and Africa, but there were no new outbreaks of the disease in South America. Within this period of time the dominating serotype was serotype O. For many years there were no reports about outbreaks caused by serotype C, the last of them occurring in 2004 (Brazil, Kenya). Significant epidemiological events were related to spreading of the virus serotype O (ME-SA/Ind-2001) and A (ASIA/G-VII(G-18)) from the Indian subcontinent to new regions. Serotype O (ME-SA/Ind-2001) spread in the years 2013 – 2015 in the Middle East (United Arab Emirates, Saudi Arabia, Bahrain) and North Africa (Libya, Tunisia, Algeria, Morocco); it was also detected in 2015 in Southeast Asia (Laos). In turn, the serotype A (ASIA/G-VII(G-18)) was recorded in 2010 in Myanmar, and in 2015 appeared in the Middle East (Saudi Arabia, Iran, Armenia, Turkey). Those events constituted a threat to neighbouring countries and increased the risk of intrusion FMD to Europe. A reason for concern was also given by the numerous outbreaks of foot-and-mouth disease in South Korea, caused by serotype O (SEA/Mya-98). In European countries there have been no outbreaks since 2011 (Bulgaria). For the record, the last outbreak in Poland was identified 45 years ago, in 1971.

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... The serotype O, A, and C viruses have had the widest distribution and have been responsible for outbreaks in Europe, America, Asia, and Africa. The FMDV particle is roughly spherical in shape, and, about 25-30 nm in diameter (20,25). It consists of the RNA genome surrounded by a protein shell or capsid (15,23). ...
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The aim of the study was to evaluate the cytotoxicity of tulathromycin (macrolide antibiotic) on BHK-21 An30 cells and to determine the effect on FMD (Serotypes; A/TUR/11, O/TUR/07, Asia-1/TUR/15) virus propagation in vitro. In the result of MTT tests and cell culture studies, the non-toxic upper concentration of the tulathromycin limit for BHK-21 An30 cell culture was determined as 30 µg/ml in terms of cell morphologies and numbers. The mean FMD 146S virus particle values produced in BHK-21 An30 cell cultures containing 30 µg/ml of tulathromycin were found to be 0.47, 0.57 and 0.25 µg/ml; the mean infective titer determined as 107.03, 106.23 and 107.40 pfu/ml for A/TUR/11, O/TUR/07 and Asia-1/TUR/15, respectively. In the FMD virus cultures produced with medium containing penicillin-streptomycin, the mean values of 146S virus particles were determined to be A/TUR/11, O/TUR/07 and the Asia-1/TUR/15 serotypes were 0.50, 0.55, and 0.32 µg/ml, respectively, while the mean infective titers were 107.46, 106.62 and 107.73 pfu/ml, respectively. As a result, it was concluded that tulathromycin can be used as an antibiotic up to 30 µg/ml in a BHK-21 An30 cell culture and in the production media of the FMD virus A, O, and Asia-1 serotypes.
Article
Foot-and-mouth disease (FMD) is the most economically important veterinary pathogen due to its highly infectious nature, ability to cause persistent infections and long term effects on the condition and productivity of the many animal species it affects. Countries which have the disease have many trade restrictions placed upon them. In the last 15 years there have been significant advances in the understanding of FMD epidemiology. These have largely been due to the application of the molecular biological techniques of polymerase chain-reaction amplification and nucleotide sequencing. In the World Reference Laboratory for FMD (Pirbright, UK), a large sequence database has been built up. This database has been used to aid in the global tracing of virus movements. It has been possible to genetically group many FMDV's based on their geographic origin and this has led to their being referred to as topotypes. The implications of this are that inter-regional spread of viruses can often be easily recognised and any evolutionary changes which subsequently occur can be monitored. Using these techniques, for the first time, we have been able to unequivocally show the recent pandemic spread of a FMDV type O strain through the whole of Asia and into Africa and Europe. This type of surveillance will become increasingly important as further globalisation of markets occurs. An increased understanding of how FMDV strains move between geographic regions will play a pivotal role in the development of future disease control strategies.
Ochrona zdrowia świń. Polskie Wydawnictwo Rolnicze
  • Z Pejsak
Pejsak Z.: Ochrona zdrowia świń. Polskie Wydawnictwo Rolnicze, Poznań 2007, s. 162.