Literature DB >> 20147498

Evaluation of indirect enzyme-linked immunosorbent assays and IgG avidity assays using a protein A-peroxidase conjugate for serological distinction between Brucella abortus S19-vaccinated and -infected cows.

Ana C A M Pajuaba1, Deise A O Silva, José R Mineo.   

Abstract

This study aimed to evaluate the use of protein A-peroxidase (horseradish peroxidase [HRPO]) in indirect enzyme-linked immunosorbent assays (iELISAs) and IgG avidity assays for serological distinction between Brucella abortus S19-vaccinated and -infected cows. Four groups were analyzed: GI, 41 nonvaccinated seropositive cows; GII, 79 S19-vaccinated heifers analyzed at 3 months postvaccination; GIII, 105 S19-vaccinated cows analyzed after 24 months of age; and GIV, 278 nonvaccinated seronegative cows. IgG levels and avidity to B. abortus smooth lipopolysaccharide (S-LPS) were determined using anti-bovine IgG-HRPO or protein A-HRPO conjugates. Similar levels of IgG anti-S-LPS were found with GI using both conjugates. Lower IgG levels were detected with GII, GIII, and GIV using protein A-HRPO. Both conjugates showed high performance in discriminating GI from GIII, with high sensitivity (Se; 97.6%) and specificity (Sp; 97.1%). Protein A-HRPO was better in distinguishing GI from GIV (Se, 97.6%; Sp, 94.6%) and GI from GII (Se, 80.5%; Sp, 94.9%). Protein A-HRPO excluded a higher number of positive samples with GII and GIV. IgG avidity showed that protein A-HRPO, but not anti-IgG-HRPO, was able to distinguish nonvaccinated from vaccinated cattle, showing a higher avidity index (AI) with GI than with GII, with 78% of serum samples in GII showing an AI of <50%. Therefore, the iELISA using B. abortus S-LPS antigen and protein A-HRPO conjugate for preferential detection of the IgG2 subclass was shown to be suitable for serological distinction between S19-vaccinated and -infected cows. Also, antibodies generated after vaccination showed lower avidity, suggesting a role for the IgG2 subclass as an antibody of higher-affinity maturation after infection, constituting an additional tool for differentiating vaccinated from infected cattle.

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Year:  2010        PMID: 20147498      PMCID: PMC2849348          DOI: 10.1128/CVI.00444-09

Source DB:  PubMed          Journal:  Clin Vaccine Immunol        ISSN: 1556-679X


  31 in total

1.  Enzyme immunoassay for the diagnosis of brucellosis: chimeric Protein A-Protein G as a common enzyme labeled detection reagent for sera for different animal species.

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Journal:  Vet Microbiol       Date:  2004-06-21       Impact factor: 3.293

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Journal:  Vet Rec       Date:  1996-02-10       Impact factor: 2.695

4.  Production of Brucella abortus-specific protein A-reactive antibodies (IgG2) in infected and vaccinated cattle.

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Journal:  Vet Microbiol       Date:  1986-06       Impact factor: 3.293

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6.  Evaluation of three Brucella soluble antigens used in an indirect Elisa to discriminate S19 vaccinated from naturally infected cattle.

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Journal:  Lancet       Date:  2004-06-12       Impact factor: 79.321

8.  Influence of brucellosis history on serological diagnosis and evolution of patients with acute brucellosis.

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Journal:  J Infect       Date:  2008-10-02       Impact factor: 6.072

9.  [The value of the immunoglobulin G avidity test for the serologic diagnosis of brucellosis].

Authors:  Selda Sayin Kutlu; Aysel Celikbaş; Onder Ergönül; Murat Kutlu; Sebahat Aksaray; Engin Güvener; Başak Dokuzoğuz
Journal:  Mikrobiyol Bul       Date:  2003-10       Impact factor: 0.622

10.  A modified ROC analysis for the selection of cut-off values and the definition of intermediate results of serodiagnostic tests.

Authors:  M Greiner; D Sohr; P Göbel
Journal:  J Immunol Methods       Date:  1995-09-11       Impact factor: 2.303

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2.  Enhancement of protective efficacy through adenoviral vectored vaccine priming and protein boosting strategy encoding triosephosphate isomerase (SjTPI) against Schistosoma japonicum in mice.

Authors:  Yang Dai; Xiaoting Wang; Jianxia Tang; Song Zhao; Yuntian Xing; Jianrong Dai; Xiaolin Jin; Yinchang Zhu
Journal:  PLoS One       Date:  2015-03-20       Impact factor: 3.240

3.  Evaluation of protective efficacy induced by different heterologous prime-boost strategies encoding triosephosphate isomerase against Schistosoma japonicum in mice.

Authors:  Yang Dai; Song Zhao; Jianxia Tang; Yuntian Xing; Guoli Qu; Jianrong Dai; Xiaolin Jin; Xiaoting Wang
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4.  Evaluation of two rapid immunochromatographic tests for diagnosis of brucellosis infection in cattle.

Authors:  Anitza Fragas Quintero; Dervel Felipe Díaz Herrera; Dayamí Martín Alfonso; Yanelis Cruz Santana; Raisa Betancourt Torres; Lucy Montano Tamayo
Journal:  Open Vet J       Date:  2018-07-07
  4 in total

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