Assessment of the potency and effectiveness of a heptavalent oil-adjuvanted (ISA 206) foot-and-mouth disease vaccine in Egypt
0301 basic medicine
Immunology
Cattle Diseases
Dynamics of Livestock Disease Transmission and Control
Antibodies, Viral
Biochemistry
Agricultural and Biological Sciences
Serotype
03 medical and health sciences
Adjuvants, Immunologic
In vitro
Virology
Health Sciences
Animals
Aetiology, Diagnosis, and Management of Myocarditis
Foot-and-mouth disease
Biology
Ecology, Evolution, Behavior and Systematics
Inactivated vaccine
Antibody
2. Zero hunger
Foot-and-mouth disease virus
Brief Report
FOS: Clinical medicine
Vaccination
Life Sciences
Viral Vaccines
Outbreak
Potency
Neutralizing antibody
Bluetongue Virus and Culicoides-Borne Diseases in Europe
3. Good health
Virus
Foot-and-Mouth Disease Virus
Seroconversion
Foot-and-Mouth Disease
Medicine
Cattle
Egypt
Cardiology and Cardiovascular Medicine
Titer
Agronomy and Crop Science
DOI:
10.1007/s00705-022-05624-2
Publication Date:
2023-01-12T10:03:15Z
AUTHORS (10)
ABSTRACT
AbstractFoot-and-mouth disease (FMD) is a serious highly contagious viral disease affecting all cloven-hoofed animals, and outbreaks can have a severe economic impact. An inactivated heptavalent oil-adjuvanted FMD vaccine (Aphtovac-7, MEVAC) was prepared from the foot-and-mouth disease virus (FMDV) strains A-Iran05, A-Africa-IV, O-PanAsia2, O-Manisa, O-EA3, SAT-2 Gharbia, and SAT-2 LIB-12. The vaccine potency and effectiveness were evaluated in three groups of 6- to 8-month-old calves and 200 adult dairy cattle under field conditions. All animals were vaccinated with the vaccine preparation, and the three groups of calves were challenged after 28 days by intradermolingual inoculation with 104 50% tissue culture infective dose (TCID50) of FMDV serotype A, O, or SAT-2. Mock-vaccinated calves (two per group) served as unvaccinated controls during the challenge test. Adult dairy cattle were tested for seroconversion using a virus neutralization test at 30, 60, and 120 days post-vaccination. All calves displayed complete protection against challenge with the different serotypes of FMDV when compared to the control groups. Serum samples collected after the primary and booster immunizations at 30 days post-vaccination contained high titers of protective antibodies (≥ 1/32; i.e. 1.5 log10). Antibodies persisted until the end of the study period (120 days), with a peak value around 60 days post-vaccination. The heptavalent FMD vaccine preparation was found to be potent and capable of providing a protective immune response under both experimental and field conditions.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (28)
CITATIONS (5)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....