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EVALUATION OF NEW COMMERCIAL KITS
      FOR ANTI-NSP FMDV ANTIBODIES
  Giovanna DHO1, Santina GRAZIOLI1, Wim SCHIELEN2, Emiliana BROCCHI1
1 Istituto   Zooprofilattico Sperimentale della Lombardia e dell’Emilia Romagna
                                      (IZSLER)
                                   Brescia, ITALY
             2 Prionics   Lelystad B.V., 8211 AR Lelystad, The Netherlands

                     Jerez de la Frontera 29-31 october 2012



                                                                             IZSLER
OBJECTIVE: provide information on the diagnostic performance of new NSP-assays available
on the market or coming soon but not officially validated.

COMMERCIAL KITS FOR NSP ANTIBODY DETECTION EVALUATED




 LF - BioNote (Korea)      LF - UBIO (India)     3ABC competitive ELISA   3D competitive ELISA
                                                    BioNote (Korea)             Prionics

INTERNATIONAL REFERENCE PANELS OF NSP SERA USED FOR KITS EVALUATION
 WRL panel, composed of 36 sera derived from experimental cattle;
 Panaftosa panel, composed of 34 sera focused on field samples.

                                                                                       IZSLER
RESULTS
                   PRIONICS    IZSLER   PRIONICS PRIONICS BIONOTE
                                                                       UBIO    BioNote
                   NS ELISA     ELISA      (B)      (A)     ELISA
                                                                       LFD       LFD
                     3ABC       3ABC       3D       3D      3ABC

                       6          4         5        14        20        27        43
     MISSED          (10%)      (7%)     (8,5%)    (24%)     (34%)     (46%)     (73%)

                       53        55         54       45        39        32        16
     DETECTED        (90%)     (93%)     (91.5%)   (76%)     (66%)     (54%)     (27%)

3D-ELISA-conjugate B showed performance similar to that of the two reference tests;
3D-ELISA-conjugate A resulted less sensitive;
The two 3D-ELISAs compensate each other, not missing the same sera;
BioNote ELISA presented a lower detection rate, but mainly evidenced by the WRL reference sera;
LFDs showed the lowest sensitivity.

 CONCLUSION: Only the 3D-ELISA (with conjugate B alone, or both tests with conjugate B and A
 run in parallel) has shown sufficient requisites and an extended validation is recommended.

                                                                                          IZSLER

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Commercial NSP Tests Evaluated for FMDV Antibody Detection

  • 1. EVALUATION OF NEW COMMERCIAL KITS FOR ANTI-NSP FMDV ANTIBODIES Giovanna DHO1, Santina GRAZIOLI1, Wim SCHIELEN2, Emiliana BROCCHI1 1 Istituto Zooprofilattico Sperimentale della Lombardia e dell’Emilia Romagna (IZSLER) Brescia, ITALY 2 Prionics Lelystad B.V., 8211 AR Lelystad, The Netherlands Jerez de la Frontera 29-31 october 2012 IZSLER
  • 2. OBJECTIVE: provide information on the diagnostic performance of new NSP-assays available on the market or coming soon but not officially validated. COMMERCIAL KITS FOR NSP ANTIBODY DETECTION EVALUATED LF - BioNote (Korea) LF - UBIO (India) 3ABC competitive ELISA 3D competitive ELISA BioNote (Korea) Prionics INTERNATIONAL REFERENCE PANELS OF NSP SERA USED FOR KITS EVALUATION  WRL panel, composed of 36 sera derived from experimental cattle;  Panaftosa panel, composed of 34 sera focused on field samples. IZSLER
  • 3. RESULTS PRIONICS IZSLER PRIONICS PRIONICS BIONOTE UBIO BioNote NS ELISA ELISA (B) (A) ELISA LFD LFD 3ABC 3ABC 3D 3D 3ABC 6 4 5 14 20 27 43 MISSED (10%) (7%) (8,5%) (24%) (34%) (46%) (73%) 53 55 54 45 39 32 16 DETECTED (90%) (93%) (91.5%) (76%) (66%) (54%) (27%) 3D-ELISA-conjugate B showed performance similar to that of the two reference tests; 3D-ELISA-conjugate A resulted less sensitive; The two 3D-ELISAs compensate each other, not missing the same sera; BioNote ELISA presented a lower detection rate, but mainly evidenced by the WRL reference sera; LFDs showed the lowest sensitivity. CONCLUSION: Only the 3D-ELISA (with conjugate B alone, or both tests with conjugate B and A run in parallel) has shown sufficient requisites and an extended validation is recommended. IZSLER