Literature DB >> 23611726

New route for fast detection of antibodies against zoonotic pathogens in sera of slaughtered pigs by means of flow-through chemiluminescence immunochips.

Klaus Wutz1, Verena Katharina Meyer, Silke Wacheck, Piotr Krol, Manfred Gareis, Christina Nölting, Friedhelm Struck, Erwin Soutschek, Oliver Böcher, Reinhard Niessner, Michael Seidel.   

Abstract

The research on fast screening methods for antibodies against zoonotic pathogens in slaughter animals is important for food safety in farming and meat-processing industries. As a proof-of-concept study, antibodies against the emerging zoonotic pathogen hepatitis E virus (HEV) and enteropathogenic Yersinia spp. were analyzed in parallel using immobilized recombinant antigens (rAgs) of HEV genotypes 1 and 3 and Yersinia outer protein D (YopD) on a flow-through chemiluminescence immunochip. These rAgs are usually part of commercially available line immunoassays (LIAs) used for human diagnostics. In this study, sera from slaughtered pigs were tested on the microarray analysis platform MCR 3 to detect anti-HEV and anti-Yersinia IgG. The new method was characterized regarding signal reproducibility and specificity. The analytical performance was compared with in-house enzyme-linked immunosorbent assay (ELISA) and a LIA based on recomLine HEV (Mikrogen) or the ELISA test kit pigtype Yersinia Ab (Qiagen), respectively. The immunochip revealed the highest analytical sensitivity and was processed in 9 min automatically on the MCR 3. A comparative screening of swine serum samples from Bavarian slaughterhouses regarding anti-HEV and anti-Yersinia IgG seroprevalence was conducted. By using the LIA, 78% of the sera were tested positive for HEV antibodies. The immunochip and the ELISA identified anti-HEV IgG in 96% and 93% of the tested samples using the O2C-gt1 and O2C-gt3 rAg, respectively. The screening for anti-Yersinia IgG resulted in 86% positive findings using the immunochip and 57% and 48% for the ELISA methods, respectively, indicating a higher detection capability of the new method. Serum samples of slaughtered pigs could be analyzed faster and in an automated way on the microarray analysis platform MCR 3 which shows the great potential of the new immunochip assay format for multiplexed serum screening purposes.

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Year:  2013        PMID: 23611726     DOI: 10.1021/ac400781t

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  4 in total

1.  Regeneration of recombinant antigen microarrays for the automated monitoring of antibodies against zoonotic pathogens in swine sera.

Authors:  Verena K Meyer; Catharina Kober; Reinhard Niessner; Michael Seidel
Journal:  Sensors (Basel)       Date:  2015-01-23       Impact factor: 3.576

2.  Genotyping and detection of common avian and human origin-influenza viruses using a portable chemiluminescence imaging microarray.

Authors:  Yingjie Zhang; Qiqi Liu; Dou Wang; Suhong Chen; Xiaobo Wang; Shengqi Wang
Journal:  Springerplus       Date:  2016-10-25

3.  Development of a miniaturized protein microarray as a new serological IgG screening test for zoonotic agents and production diseases in pigs.

Authors:  Katharina Loreck; Sylvia Mitrenga; Diana Meemken; Regina Heinze; Annett Reissig; Elke Mueller; Ralf Ehricht; Claudia Engemann; Matthias Greiner
Journal:  PLoS One       Date:  2019-05-22       Impact factor: 3.240

4.  Automated, flow-based chemiluminescence microarray immunoassay for the rapid multiplex detection of IgG antibodies to SARS-CoV-2 in human serum and plasma (CoVRapid CL-MIA).

Authors:  Julia Klüpfel; Rosa Carolina Koros; Kerstin Dehne; Martin Ungerer; Silvia Würstle; Josef Mautner; Martin Feuerherd; Ulrike Protzer; Oliver Hayden; Martin Elsner; Michael Seidel
Journal:  Anal Bioanal Chem       Date:  2021-05-13       Impact factor: 4.142

  4 in total

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