Literature DB >> 15939741

Evaluation of five antibody detection tests for diagnosis of bovine paratuberculosis.

Michael T Collins1, Scott J Wells, Kristine R Petrini, James E Collins, Ronald D Schultz, Robert H Whitlock.   

Abstract

Five diagnostic tests based on enzyme-linked immunosorbent assay (ELISA) technology for bovine paratuberculosis were evaluated by using individual serum or milk samples from 359 dairy cattle in seven paratuberculosis-free herds and 2,094 dairy cattle in seven Mycobacterium paratuberculosis-infected dairy herds. Three independent laboratories using three different culture procedures completed fecal cultures for M. paratuberculosis on these cattle and found 417 cows to be shedding M. paratuberculosis in their feces. An animal that was fecal culture positive for M. paratuberculosis by any of the three laboratories was considered a confirmed case of infection. The specificity of three ELISAs (two on serum and one on milk) was > or =99.8%. The specificity of the remaining two ELISAs, both done on serum, was 94.9 and 84.7%. Four of the five ELISAs evaluated produced similar sensitivity in detecting fecal culture-positive cattle (27.8 to 28.9%). Serum ELISA "D" had the lowest specificity (84.7%) and the highest sensitivity (44.5%), but if the cutoff value defining a positive test was changed from 125 to 250% (of the positive control) the sensitivity and specificity, 31.8 and 97.5%, respectively, were comparable to those of the other four assays. If the case definition for M. paratuberculosis infection was based on the culture results of a single laboratory instead of the combined results of three laboratories, ELISA sensitivity estimates were 45.7 to 50.0%. With the exception of ELISA D, assay agreement was high (kappa 0.66 to 0.85) for categorical assay interpretations (positive or negative), but linear regression of quantitative results showed low correlation coefficients (r(2) = 0.40 to 0.68) due to the fact that ELISA results for some cows were high in one assay but low in another assay. Likelihood ratio analysis showed a direct relationship between the magnitude of ELISA result and the odds of a cow shedding M. paratuberculosis in its feces. If used judiciously and interpreted quantitatively, these ELISAs are useful tools in support of paratuberculosis control programs in dairy herds.

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Year:  2005        PMID: 15939741      PMCID: PMC1151972          DOI: 10.1128/CDLI.12.6.685-692.2005

Source DB:  PubMed          Journal:  Clin Diagn Lab Immunol        ISSN: 1071-412X


  29 in total

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Authors:  M B Jakobsen; L Alban; S S Nielsen
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Journal:  J Am Vet Med Assoc       Date:  2001-04-01       Impact factor: 1.936

5.  ELISA and fecal culture for paratuberculosis (Johne's disease): sensitivity and specificity of each method.

Authors:  R H Whitlock; S J Wells; R W Sweeney; J Van Tiem
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6.  Herd testing to control bovine Johne's disease.

Authors:  T Jubb; J Galvin
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7.  Use of a PCR method on fecal samples for diagnosis of sheep paratuberculosis.

Authors:  J M Garrido; N Cortabarria; J A Oguiza; G Aduriz; R A Juste
Journal:  Vet Microbiol       Date:  2000-12-20       Impact factor: 3.293

8.  Evaluation of enzyme-linked immunosorbent assays performed on milk and serum samples for detection of paratuberculosis in lactating dairy cows.

Authors:  Steven H Hendrick; Todd E Duffield; David E Kelton; Ken E Leslie; Kerry D Lissemore; Marie Archambault
Journal:  J Am Vet Med Assoc       Date:  2005-02-01       Impact factor: 1.936

Review 9.  Control of Mycobacterium avium subsp. paratuberculosis infection in agricultural species.

Authors:  D J Kennedy; G Benedictus
Journal:  Rev Sci Tech       Date:  2001-04       Impact factor: 1.181

Review 10.  Mycobacterium avium subsp. paratuberculosis: pathogen, pathogenesis and diagnosis.

Authors:  E J Manning; M T Collins
Journal:  Rev Sci Tech       Date:  2001-04       Impact factor: 1.181

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  59 in total

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Authors:  Robert E Click; Craig L Van Kampen
Journal:  Virulence       Date:  2010 May-Jun       Impact factor: 5.882

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Journal:  Clin Diagn Lab Immunol       Date:  2005-12

4.  Proper estimation of sensitivity and specificity.

Authors:  Michael T Collins
Journal:  Clin Vaccine Immunol       Date:  2006-12

5.  Testing the interaction between NOD-2 status and serological response to Mycobacterium paratuberculosis in cases of inflammatory bowel disease.

Authors:  Charles N Bernstein; Ming-Hsi Wang; Michael Sargent; Steven R Brant; Michael T Collins
Journal:  J Clin Microbiol       Date:  2007-01-24       Impact factor: 5.948

6.  Receiver operating characteristic-based assessment of a serological test used to detect Johne's disease in Israeli dairy herds.

Authors:  Marcelo Chaffer; Ariel L Rivas; Daniel Elad; Ori Koren; Shlomo Garazi; Gerardo Chowell; Steven J Schwager
Journal:  Can J Vet Res       Date:  2008-01       Impact factor: 1.310

7.  High prevalence of subclinical paratuberculosis in buffaloes (Bubalus bubalis) in Maranhão, Brazil.

Authors:  Helder de Moraes Pereira; Hamilton Pereira Santos; Emerson Antônio Araújo de Oliveira; Thais Bastos Rocha; Ítala Mayara Silva Araújo; Diego Moraes Soares; Felício Garino Junior; Pedro Paulo Feitosa de Albuquerque; Rinaldo Aparecido Mota
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8.  Rapid expression of Mycobacterium avium subsp. paratuberculosis recombinant proteins for antigen discovery.

Authors:  Lingling Li; Shirin Munir; John P Bannantine; Srinand Sreevatsan; Sagarika Kanjilal; Vivek Kapur
Journal:  Clin Vaccine Immunol       Date:  2006-11-01

9.  A Novel Real-Time PCR-Based Screening Test with Pooled Fecal Samples for Bovine Johne's Disease.

Authors:  Satoko Kawaji; Reiko Nagata; Yasutaka Minegishi; Yumi Saruyama; Akiko Mita; Shingo Kishizuka; Masahiro Saito; Yasuyuki Mori
Journal:  J Clin Microbiol       Date:  2020-11-18       Impact factor: 5.948

10.  Risk factors for herds to test positive for Mycobacterium avium ssp. paratuberculosis-antibodies with a commercial milk enzyme-linked immunosorbent assay (ELISA) in Ontario and western Canada.

Authors:  Ulrike S Sorge; Kerry Lissemore; Ann Godkin; Jocelyn Jansen; Steven Hendrick; Scott Wells; David F Kelton
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