scholarly journals Diagnosis Based on 1D Gene Analysis of the Foot-And-Mouth Disease Virus

2020 ◽  
pp. 227-234
Author(s):  
Choe SunIl ◽  
Jin MyongIl ◽  
Hwang GwangJo ◽  
Choe KyongHo ◽  
IM MyongDok ◽  
...  
Keyword(s):  
Nucleotide Sequence ◽  
Disease Virus ◽  
Foot And Mouth Disease ◽  
Viral Disease ◽  
Mouth Disease ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Relationship Of ◽  
Fmdv Type ◽  
Mutation Region

A foot and mouth disease (FMD) is an acute, febrile and high contagious viral disease in many cloven hoofed domestic animals and more than 70 wild ones, resulting in severe finantial loss throughout the world. Choosing the correct seeds for foot-and-mouth disease (FMD) is an important issue in protecting this disease, and it is urgently necessary to establish a plan for vaccination in areas affected by FMD and to protect new foot-and-mouth disease. The genetic diversity and antigenic diversity of foot-and-mouth disease virus (FMDV) make eradication through vaccination difficult. Variable antigenic types exist in different geographic areas, and research projects on existing antigenic types are necessary to select vaccine in such an environment. From this, in this paper, oligonucleotide primers for detection and Selecting Serotype of FMDV were newly designed and synthesized. In addition, the nucleotide sequence of the 1D gene was aligned, the mutation region was determined, and the homology and phylogenetic relationship of the nucleotide sequence were analyzed. The antigenicity of the FMDV type O strains in the Democratic People's Republic of Korea and the correspondence between them were examined. The neutralization reaction was used to examine antigenicity between FMDV to select waxy seeds. To prevent FMD through this primer design and experimental method, the nucleic acid of FMDV was amplified by RT-PCR. Then, the nucleotide sequence of the 1D gene corresponding to the virus VP1 protein was analyzed and compared to select a seed vaccine strain.

Development of Protective Immunity against Inactivated Iranian Isolate of Foot-and-Mouth Disease Virus Type O/IRN/2007 Using Gamma Ray-Irradiated Vaccine on BALB/c Mice and Guinea Pigs

Intervirology ◽  
2015 ◽  
Vol 58 (3) ◽  
pp. 190-196 ◽  
Author(s):  
Farahnaz Motamedi-Sedeh ◽  
Hoorieh Soleimanjahi ◽  
Amir Reza Jalilian ◽  
Homayoon Mahravani ◽  
Kamalodin Shafaee ◽  
...  
Keyword(s):  
Immune Responses ◽  
Disease Virus ◽  
Guinea Pigs ◽  
Gamma Ray ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Economic Losses ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Fmdv Type

Objectives: Foot-and-mouth disease virus (FMDV) causes a highly contagious disease in cloven-hoofed animals and is the most damaging disease of livestock worldwide, leading to great economic losses. The aim of this research was the inactivation of FMDV type O/IRN/1/2007 to produce a gamma ray-irradiated (GRI) vaccine in order to immunize mice and guinea pigs. Methods: In this research, the Iranian isolated FMDV type O/IRN/1/2007 was irradiated by gamma ray to prepare an inactivated whole virus antigen and formulated as a GRI vaccine with unaltered antigenic characteristics. Immune responses against this vaccine were evaluated on mice and guinea pigs. Results: The comparison of the immune responses between the GRI vaccine and conventional vaccine did not show any significant difference in neutralizing antibody titer, memory spleen T lymphocytes or IFN-γ, IL-4, IL-2 and IL-10 concentrations (p > 0.05). In contrast, there were significant differences in all of the evaluated immune factors between the two vaccinated groups of mice and negative control mice (p < 0.05). The protective dose 50 for the conventional and GRI vaccines obtained were 6.28 and 7.07, respectively, which indicated the high potency of both vaccines. Conclusion: GRI vaccine is suitable for both routine vaccination and control of FMDV in emergency outbreaks.

scholarly journals Myocarditis Associated with Foot-and-Mouth Disease Virus Type O in Lambs

2007 ◽  
Vol 44 (5) ◽  
pp. 589-599 ◽  
Author(s):  
M. Y. Gulbahar ◽  
W. C. Davis ◽  
T. Guvenc ◽  
M. Yarim ◽  
U. Parlak ◽  
...  
Keyword(s):  
Cardiac Myocytes ◽  
Disease Virus ◽  
Mononuclear Cells ◽  
Foot And Mouth Disease ◽  
Inflammatory Cells ◽  
Interstitial Cells ◽  
Mouth Disease ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Fmdv Type

The present study describes the pathogenetic mechanisms of myocarditis in 9 lambs that died in a foot-and-mouth disease outbreak in Samsun, Turkey. In all the heart samples tested, ELISA and sequencing for phylogenetic analyses showed that the virus, namely O/TUR/Samsun/05, was associated with the PanAsia pandemic strain of foot-and-mouth disease virus (FMDV) type O. The lambs had myocardial lesions but no typical vesicular lesions. In situ reverse transcription showed that many cardiomyocytes and some interstitial cells were positive for FMDV type O. Inflammatory infiltration, hyaline degeneration, and necrosis of sheets of myocytes were observed. The cellular infiltrates were mononuclear cells, including many lymphocytes, macrophages, a few plasma cells, and neutrophils. Major histocompatibility complex Class II+ dendritic and mononuclear cells, γδ T cells, CD172A+ and CD14+ macrophages and monocytes, and IgM+ B cells were detected mainly in the infected hearts. Inducible nitric oxide synthetase (iNOS) was seen mostly in areas of inflammation infiltrated by large numbers of cells. Of the 2 α-subunits of integrin known to be used as receptors by FMDV in epithelial tissues, CD49e (integrin α5) was detected in the membranes of cardiac myocytes with intercalated discs, but CD51 (integrin αV) was not detected in cardiac myocytes from infected or normal lambs. Interstitial and inflammatory cells were positive for both integrin subunits. The terminal deoxynucleotidyl transferase mediated dUTP nick-end labeling (TUNEL)-positive signal was detected in the nuclei of both cardiac myocytes and interstitial cells from infected lambs. These findings suggest that the iNOS expressed by inflammatory cells in lesions may have a deleterious effect on cardiac myocytes in these lesions.

The nucleotide sequence of cDNA coding for the structural proteins of foot-and-mouth disease virus

Gene ◽  
1982 ◽  
Vol 17 (2) ◽  
pp. 153-161 ◽  
Author(s):  
J.C. Boothroyd ◽  
T.J.R. Harris ◽  
D.J. Rowlands ◽  
P.A. Lowe
Keyword(s):  
Nucleotide Sequence ◽  
Disease Virus ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Structural Proteins ◽  
Mouth Disease Virus ◽  
Foot And Mouth

The nucleotide sequence of foot-and-mouth disease virus O/FRA/1/2001 and comparison with its British parental strain O/UKG/35/2001

2005 ◽  
Vol 108 (1-2) ◽  
pp. 225-229 ◽  
Author(s):  
Isabelle Nobiron ◽  
Michelle Rémond ◽  
Claude Kaiser ◽  
Françoise Lebreton ◽  
Stéphan Zientara ◽  
...  
Keyword(s):  
Nucleotide Sequence ◽  
Disease Virus ◽  
Parental Strain ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Mouth Disease Virus ◽  
Foot And Mouth

scholarly journals Insertion of type O-conserved neutralizing epitope into the foot-and-mouth disease virus type Asia1 VP1 G-H loop: effect on viral replication and neutralization phenotype

2012 ◽  
Vol 93 (7) ◽  
pp. 1442-1448 ◽  
Author(s):  
Haiwei Wang ◽  
Mei Xue ◽  
Decheng Yang ◽  
Guohui Zhou ◽  
Donglai Wu ◽  
...  
Keyword(s):  
Disease Virus ◽  
Neutralizing Antibodies ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Neutralizing Epitope ◽  
Fmdv Serotypes ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Fmdv Type ◽  
Neutralizing Epitopes

Previously, we finely mapped the neutralizing epitopes recognized by foot-and-mouth disease virus (FMDV) type Asia1-specific mAb 3E11 and FMDV type O-specific mAb 8E8. In this study, we engineered recombinant FMDVs of the serotype Asia1 (rFMDVs) displaying the type O-neutralizing epitope recognized by the mAb 8E8. These epitope-inserted viruses were genetically stable and exhibited growth properties that were similar to those of their parental virus. Importantly, the recombinant virus rFMDV-C showed neutralization sensitivity to both FMDV type Asia1 and type O mAbs, as well as to polyclonal antibodies. These results indicated that this epitope-inserted virus has the potential to induce neutralizing antibodies against both FMDV type Asia1 and type O. Our results demonstrated that the G-H loop of FMDV type Asia1 effectively displays the protective neutralizing epitopes of other FMDV serotypes, making this an attractive approach for the design of novel FMDV vaccines.

Differences in the susceptibility of dromedary and Bactrian camels to foot-and-mouth disease virus

2008 ◽  
Vol 137 (4) ◽  
pp. 549-554 ◽  
Author(s):  
M. LARSKA ◽  
U. WERNERY ◽  
J. KINNE ◽  
R. SCHUSTER ◽  
G. ALEXANDERSEN ◽  
...  
Keyword(s):  
Disease Virus ◽  
Clinical Signs ◽  
Foot And Mouth Disease ◽  
Type A ◽  
Mouth Disease ◽  
Dromedary Camels ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Bactrian Camels ◽  
Fmdv Type

SUMMARYIn this study, two sheep, eight dromedary camels and two Bactrian camels were inoculated with foot-and-mouth disease virus (FMDV) type A SAU 22/92. Five naive dromedary camels and four sheep were kept in direct or indirect contact with the inoculated camels. The inoculated sheep, which served as positive controls, displayed typical moderate clinical signs of FMD and developed viraemia and high antibody titres. The presence of the virus was also detected in probang and mouth-swab samples for several days after inoculation. In contrast, the inoculated dromedary camels were not susceptible to FMDV type A infection. None of them showed clinical signs of FMD or developed viraemia or specific anti-FMDV antibodies despite the high dose of virus inoculated. All the contact sheep and contact dromedaries that were kept together with the inoculated camels remained virus-negative and did not seroconvert when tested up to 28 days post-inoculation (p.i.). In comparison with the non-susceptible dromedaries, the two inoculated Bactrian camels showed moderate to severe clinical signs of FMD; however, the clinical signs of FMD appeared rather late, between 8 and 14 days p.i., compared to the inoculated sheep. Characteristic FMD lesions in the Bactrian camels, accompanied with severe lameness, were only observed on the hind feet. The presence of the virus in the serum samples of both Bactrian camels was detected by real-time RT–PCR in one of the animals on days 3 and 7 p.i. and in the second animal from days 1 to 3 p.i. and subsequently again on day 21 p.i. The Bactrian camels developed high titres of antibodies to the inoculated FMDV which appeared at 7–10 days p.i. and lasted up to 130 days p.i. Only low and transient amounts of FMDV were detected in the mouth-swab and probang samples collected from both Bactrian camels.

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