Comparison of three ELISA kits for the detection of antibodies against foot-and-mouth disease virus non-structural proteins

Three foot-and-mouth disease virus non-structural protein antibody kits: CHEKIT FMD-3ABC, Ceditest FMDVNS and 3ABC-ELISA were compared. These ELISAs were performed using panel of sera collected from negative (noninfected), vaccinated with trivalent foot and mouth disease vaccine, experimentally infected cattle as well as from animals that had been vaccinated and subsequently infected. Moreover, the panel of the FAO/OIE international reference sera for the purposes of Phase XVIII exercise was tested. The Ceditest kit had a better relative specificity (99.7% for naive and 98.8% for vaccinated cattle) than the CHEKIT and 3ABC-ELISA kits (97.2 – 98.8% and 98.1 – 99.2%, respectively). A relative sensitivity of all used kits exceeded 98%, however, the Ceditest FMDV-NS kit had the higher sensitivity (99.1%) than the CHEKIT and 3ABC-ELISA (98.2%). The weak 2 O SKR 1/2000 reference serum tested within Phase XVIII collaborative study was detected only in Ceditest kit. It can be concluded that all tested kits can be a useful tool for export/import serological examination, for foot and mouth disease control programmes and especially for eradication campaigns in situation where emergency vaccination was

[1]  A. Dekker,et al.  Comparable sensitivity and specificity in three commercially available ELISAs to differentiate between cattle infected with or vaccinated against foot-and-mouth disease virus. , 2004, Veterinary microbiology.

[2]  G. Belsham,et al.  Differentiating infection from vaccination in foot-and-mouth disease using a panel of recombinant, non-structural proteins in ELISA. , 1998, Vaccine.

[3]  R. Kitching A recent history of foot-and-mouth disease. , 1998, Journal of comparative pathology.

[4]  M. D. Diego,et al.  THE non-structural polyprotein 3ABC of foot-and-mouth disease virus as a diagnostic antigen in ELISA to differentiate infected from vaccinated cattle , 1997, Archives of Virology.

[5]  F. Brown,et al.  Absence of protein 2C from clarified foot-and-mouth disease virus vaccines provides the basis for distinguishing convalescent from vaccinated animals. , 1996, Vaccine.

[6]  V. O'Donnell,et al.  Detection of Antibodies against Foot-and-Mouth Disease Virus Using a Liquid-Phase Blocking Sandwich ELISA (LPBE) with a Bioengineered 3D Protein , 1996, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

[7]  E. Beck,et al.  Diagnosis of persistent aphthovirus infection and its differentiation from vaccination response in cattle by use of enzyme-linked immunoelectrotransfer blot analysis with bioengineered nonstructural viral antigens. , 1993, American journal of veterinary research.

[8]  E. Beck,et al.  Expression of the aphthovirus RNA polymerase gene in Escherichia coli and its use together with other bioengineered nonstructural antigens in detection of late persistent infections. , 1991, Virology.

[9]  M. Tesar,et al.  Identification of foot-and-mouth disease virus replication in vaccinated cattle by antibodies to non-structural virus proteins. , 1990, Vaccine.

[10]  M. Ackermann,et al.  Antibodies to foot-and-mouth disease virus infection associated (VIA) antigen: use of a bioengineered VIA protein as antigen in an ELISA. , 1989, Veterinary microbiology.

[11]  J. Dopazo,et al.  Immunogenicity of non-structural proteins of foot-and-mouth disease virus: differences between infected and vaccinated swine , 2005, Archives of Virology.

[12]  W. Niedbalski Comparison of different ELISA methods for the detection of antibodies against foot-and-mouth disease virus [FMDV] type O , 2004 .

[13]  P. Moonen,et al.  Comparison of commercial ELISAs for antibodies against FMDV non-structural proteins , 2004 .

[14]  W. Niedbalski Prevalence of seroreagents to FMDV in the cattle population in Poland: results of 9-year monitoring studies. , 2003, Polish journal of veterinary sciences.

[15]  B. Haas,et al.  Differentiation of infection from vaccination by detection of antibodies to the non-structural protein 3ABC of foot-and-mouth disease virus , 2003 .

[16]  K. Sorensen,et al.  Differentiation of infection from vaccination in foot-and-mouth disease by the detection of antibodies to the non-structural proteins 3D, 3AB and 3ABC in ELISA using antigens expressed in baculovirus , 1998, Archives of Virology.

[17]  E. Brocchi,et al.  Diagnostic potential of Mab-based ELISAs for antibodies to non-structural proteins of foot-and-mouth disease virus to differentiate infection from vaccination. , 1998, The Veterinary quarterly.

[18]  R. H. Jacobson Validation of serological assays for diagnosis of infectious diseases. , 1998, Revue scientifique et technique.

[19]  P. Moonen,et al.  The FMD-NS ELISA, the most sensitive test to detect FMDV infected animals in a vaccinated population , 1998 .

[20]  O. Taboga,et al.  Foot-and-mouth disease virus-infected but not vaccinated cattle develop antibodies against recombinant 3AB1 nonstructural protein , 1997, Archives of Virology.