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  1. Article ; Online: Development of a Multiplex Bead Assay to Detect Serological Responses to Brucella Species in Domestic Pigs and Wild Boar with the Potential to Overcome Cross-Reactivity with Yersinia enterocolitica O:9

    Antonia Touloudi / John McGiven / Shaun Cawthraw / George Valiakos / Polychronis Kostoulas / Lucy Duncombe / Christian Gortázar / Mariana Boadella / Marina Sofia / Zoi Athanasakopoulou / Dimitris C. Chatzopoulos / Vassiliki Spyrou / Liljana Petrovska / Charalambos Billinis

    Microorganisms, Vol 10, Iss 7, p

    2022  Volume 1362

    Abstract: The aim of this study was to develop a multiplex bead assay using a Brucella rLPS antigen, a Brucella suis smooth antigen, and a Yersinia enterocolitica O:9 antigen that not only discriminates Brucella -infected from Brucella -uninfected pigs and wild ... ...

    Abstract The aim of this study was to develop a multiplex bead assay using a Brucella rLPS antigen, a Brucella suis smooth antigen, and a Yersinia enterocolitica O:9 antigen that not only discriminates Brucella -infected from Brucella -uninfected pigs and wild boar, but also overcomes the cross reactivity with Y. enterocolitica O:9. Sera from 126 domestic pigs were tested: 29 pigs were Brucella infected, 80 were non-infected and 17 were confirmed to be false positive serological reactors (FPSR). Sera from 49 wild boar were tested: 18 were positive and 31 were negative. Using the rLPS antigen, 26/29 Brucella -infected domestic pigs and 15/18 seropositive wild boar were positive, while 75/80 non- Brucella infected domestic pigs, all FPSR, and all seronegative wild boar were negative. Using the smooth B. suis 1330 antigen, all Brucella -infected domestic pigs, 9/17 FPSR and all seropositive wild boar were positive, while all non-infected pigs and 30/31 seronegative wild boar were negative. The ratio of the readouts from the smooth B. suis antigen and Y. enterocolitica O:9 antigen enabled discriminating all Brucella infected individuals from the FPSR domestic pigs. These results demonstrate the potential of this assay for use in the surveillance of brucellosis, overcoming the cross-reactivity with Y. enterocolitica .
    Keywords multiplex bead assay ; Brucella suis ; wild boar ; domestic pigs ; cross-reactivity ; rLPS antigen ; Biology (General) ; QH301-705.5
    Subject code 630
    Language English
    Publishing date 2022-07-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: The Tip of Brucella O-Polysaccharide Is a Potent Epitope in Response to Brucellosis Infection and Enables Short Synthetic Antigens to Be Superior Diagnostic Reagents

    Lucy Duncombe / Laurence Howells / Anna Haughey / Andrew V. Taylor / Daryan Kaveh / Sevil Erdenliğ Gϋrbilek / Anne Dell / Paul G. Hitchen / Stuart M. Haslam / Satadru Sekhar Mandal / N. Vijaya Ganesh / David R. Bundle / John McGiven

    Microorganisms, Vol 10, Iss 708, p

    2022  Volume 708

    Abstract: Brucellosis is a global disease and the world’s most prevalent zoonosis. All cases in livestock and most cases in humans are caused by members of the genus Brucella that possess a surface O-polysaccharide (OPS) comprised of a rare monosaccharide 4-deoxy- ... ...

    Abstract Brucellosis is a global disease and the world’s most prevalent zoonosis. All cases in livestock and most cases in humans are caused by members of the genus Brucella that possess a surface O-polysaccharide (OPS) comprised of a rare monosaccharide 4-deoxy-4-formamido-D-mannopyranose assembled with α1,2 and α1,3 linkages. The OPS of the bacterium is the basis for serodiagnostic tests for brucellosis. Bacteria that also contain the same rare monosaccharide can induce antibodies that cross-react in serological tests. In previous work we established that synthetic oligosaccharides, representing elements of the Brucella A and M polysaccharide structures, were excellent antigens to explore the antibody response in the context of infection, immunisation and cross reaction. These studies suggested the existence of antibodies that are specific to the tip of the Brucella OPS. Sera from naturally and experimentally Brucella abortus -infected cattle as well as from cattle experimentally infected with the cross-reactive bacterium Yersinia enterocolitica O:9 and field sera that cross react in conventional serological assays were studied here with an expanded panel of synthetic antigens. The addition of chemical features to synthetic antigens that block antibody binding to the tip of the OPS dramatically reduced their polyclonal antibody binding capability providing conclusive evidence that the OPS tip (non-reducing end) is a potent epitope. Selected short oligosaccharides, including those that were exclusively α1,2 linked, also demonstrated superior specificity when evaluated with cross reactive sera compared to native smooth lipopolysaccharide (sLPS) antigen and capped native OPS. This surprising discovery suggests that the OPS tip epitope, even though common to both Brucella and Y. enterocolitica O:9, has more specific diagnostic properties than the linear portion of the native antigens. This finding opens the way to the development of improved serological tests for brucellosis.
    Keywords Brucella ; O-polysaccharide ; epitope ; Biology (General) ; QH301-705.5
    Subject code 540
    Language English
    Publishing date 2022-03-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Novel Solutions for Vaccines and Diagnostics To Combat Brucellosis

    Satadru Sekhar Mandal / Lucy Duncombe / N. Vijaya Ganesh / Susmita Sarkar / Laurence Howells / Philip J. Hogarth / David R. Bundle / John McGiven

    ACS Central Science, Vol 3, Iss 3, Pp 224-

    2017  Volume 231

    Keywords Chemistry ; QD1-999
    Language English
    Publishing date 2017-03-01T00:00:00Z
    Publisher American Chemical Society
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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