Comparison of two serological diagnosis tests for bovine paratuberculosis.

Mycobacterium avium subsp. paratuberculosis Bovine paratuberculosis ELISA Sonicated antigen

Journal

Veterinary research communications
ISSN: 1573-7446
Titre abrégé: Vet Res Commun
Pays: Switzerland
ID NLM: 8100520

Informations de publication

Date de publication:
05 Apr 2024
Historique:
received: 25 01 2024
accepted: 25 03 2024
medline: 5 4 2024
pubmed: 5 4 2024
entrez: 4 4 2024
Statut: aheadofprint

Résumé

Mycobacterium avium subsp. paratuberculosis (MAP) is the causal agent of paratuberculosis (PTBC), a chronic infectious granulomatous enteritis of ruminants. The PTBC diagnosis with commercial ELISA has limitations in sensitivity and specificity, and its results depend on the state of progress of the disease. This research aimed to evaluate two different ELISAs: (a) an "in-house" ELISA with a sonicated antigen obtained from a MAP I47 strain, and (b) a commercial ELISA. In total, the evaluated sample consisted of 394 bovine serum samples from 12 farms in Argentina with high (5-9%) and low (≤ 0.05%) prevalence of PTBC. The evaluation of the new antigen (2.5 µg/mL) was against a 1:50 dilution of the M. phlei faced sera. The cut-off point, sensitivity, and specificity determinations of both techniques were by ROC curve analysis. The area under the curve for the I47 ELISA was 0.9 (CI 95%, 0.93-0.97). With a cut-off point of 8.8%, the sensitivity was 84.3% and the specificity 96.6%. The agreement between both techniques was 0.7 (CI 95%, 0.6-0.8). These results indicate a high discriminative capacity to differentiate positive and negative bovine sera of MAP infection with the I47 ELISA. This result would represent an advantage to dispense with the imported kit.

Identifiants

pubmed: 38575801
doi: 10.1007/s11259-024-10363-7
pii: 10.1007/s11259-024-10363-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature B.V.

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Auteurs

S Tieri (S)

Laboratorio de Bacteriología, Producción Animal, Instituto Nacional de Tecnología Agropecuaria INTA, Balcarce, Buenos Aires, CC 276, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas CONICET, Buenos Aires, Argentina.

C Morsella (C)

Laboratorio de Bacteriología, Producción Animal, Instituto Nacional de Tecnología Agropecuaria INTA, Balcarce, Buenos Aires, CC 276, Argentina.

L Méndez (L)

Laboratorio de Bacteriología, Producción Animal, Instituto Nacional de Tecnología Agropecuaria INTA, Balcarce, Buenos Aires, CC 276, Argentina.

B Vasini (B)

University of North Texas Health Science Center, Fort Worth, TX, 76107, USA.

C Garro (C)

Instituto de Patobiología, INTA Castelar, CICVyA, Buenos Aires, Argentina.

Fernando Paolicchi (F)

Laboratorio de Bacteriología, Producción Animal, Instituto Nacional de Tecnología Agropecuaria INTA, Balcarce, Buenos Aires, CC 276, Argentina. paolicchi.fernando@inta.gob.ar.
Facultad de Ciencias Agrarias, Universidad Nacional de Mar del Plata, Balcarce, Buenos Aires, Argentina. paolicchi.fernando@inta.gob.ar.

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