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Effect of the vaccination against Shiga toxin 2e in a farm with history of oedema disease, caused by atypical Escherichia coli producing Shiga toxin (STEC)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F22%3AN0000163" target="_blank" >RIV/00027162:_____/22:N0000163 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14310/22:00128669 RIV/62157124:16170/22:43880387

  • Result on the web

    <a href="https://www.agriculturejournals.cz/web/vetmed.htm?type=article&id=36_2022-VETMED" target="_blank" >https://www.agriculturejournals.cz/web/vetmed.htm?type=article&id=36_2022-VETMED</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.17221/36/2022-VETMED" target="_blank" >10.17221/36/2022-VETMED</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Effect of the vaccination against Shiga toxin 2e in a farm with history of oedema disease, caused by atypical Escherichia coli producing Shiga toxin (STEC)

  • Original language description

    Oedema disease (OD) is a disorder occurring in weaned piglets, caused by shigatoxigenic Escherichia coli strains (STEC). These strains typically harbour the stx2e gene and are equipped with fimbrial adhesins F18. Vaccination can be applied as a useful preventive measure but little is known about its efficacy in pigs, in which non-typical E. coli strains have been identified as an ethiological agent causing the OD. Therefore, aim of this study was to assess the effect of a commercially available vaccine application on oedema disease onset and on productive indicators on a farm, with a confirmed history of this disease caused by non-typical STEC. Piglets were separated in two groups. Group A (51 piglets) was vaccinated with Ecoporc Shiga® (Ceva Sante Animale, Libourne, France), group B (62 piglets) was used as control. During the study, weight gain, mortality, individual antibiotic treatment and average daily gain were monitored in all piglets. Fecal samples of the group B were examined for STEC. Isolated strains harbouring stx2e gene and determined by serogroupe were characterized using whole genome sequencing and their effect on Vero cells was assessed. Analysis of the productive indicators revealed significant increase of the body weight of the group A, lower morbidity and mortality of piglets compared to group B. In total, 12 (16.2%) of fecal samples were STEC positive. In isolated strains, serogroups O9 (1) and O100 (1) were confirmed. In two strains serogroup was not specified. No strains harboured genes for typical fimbrial adhesins but genes iha, orfA and orfB associated also with adherence were confirmed. Vero cell assay showed differences in the effect of tested strains on cell proliferation from no effect to high effect in dilution 1:8000. Positive effect of vaccination on monitored productive indicators was confirmed in the study. Furthermore, detail analysis of isolated strains suggests the possible involvement of different types of adhesins than typical F18 fimbriae in pathogenesis of oedema disease.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10606 - Microbiology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Veterinární medicína

  • ISSN

    0375-8427

  • e-ISSN

    1805-9392

  • Volume of the periodical

    67

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    9

  • Pages from-to

    510-518

  • UT code for WoS article

    000852197700001

  • EID of the result in the Scopus database

    2-s2.0-85140217879