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Real-Time PCR Detection and HRM Differentiation of Selected Brucella Species

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70565813%3A_____%2F18%3AN0000035" target="_blank" >RIV/70565813:_____/18:N0000035 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Real-Time PCR Detection and HRM Differentiation of Selected Brucella Species

  • Original language description

    Brucellosis still belongs to a significant cause of zoonosis in many countries in the world, e.g. Latin America or the Middle East. Pathogenic Brucella species still represent a considerable risk of human infection due to its natural reservoirs – farm animals, as well as insufficient vaccination. Moreover, these bacteria could be also misused as a bioterrorist weapon in the form of aerosol. Another factor according to that these agents are classified as highly risky is the low infectious dose of approximately ten to hundred bacteria. Here, we would like to present a new methodology for the detection and differentiation of main pathogenic Brucella species – B. abortus, melitensis and suis. This methodology is based on the real-time PCR followed by the high resolution melting analysis (HRM). The HRM analysis was chosen because of a high degree of genomic sequence similarity among Brucella species. The assay is consisted of four sets of primers separated into two reactions that are able to be run under the same cycling and melting conditions. The first reaction enables the detection of and separation between two groups of Brucella. B. abortus together with B. melitensis are found in group one, group two includes both B. suis and canis. According to the first reaction, target Brucella species are distinguished from other non-target Brucella. Only samples classified as the members of particular target group are further evaluated in the second reaction. The second reaction involves two additional sets of primers designed to differentiate inside both group one and two between B. abortus and melitensis or between B. suis and canis, respectively. Finally, all target Brucella are distinguished from each other on the basis of the HRM analysis. The assay is aimed to detect all B. abortus and melitensis biovars. In case of B. suis, the assay is designed to detect B. suis biovars 1-4. Biovar 5 of B. suis contains a higher portion of genomic sequence variability alike the rest of B. suis biovars. The whole methodology is validated in concert with the MIQE guidelines.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    10600 - Biological sciences

Result continuities

  • Project

    <a href="/en/project/VI20172019063" target="_blank" >VI20172019063: Development of New Methodologies for Detection of Biological Agents in Area of Observance of the Biological Weapons Convention</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů