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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1111/1462-2920.15051</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">118278</subfield>
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    <subfield code="a">ART-2020-118278</subfield>
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  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Wrobel, A.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">The inverse autotransporters of Yersinia ruckeri, YrInv and YrIlm, contribute to biofilm formation and virulence</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2020</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Yersinia ruckeri causes enteric redmouth disease (ERM) that mainly affects salmonid fishes and leads to significant economic losses in the aquaculture industry. An increasing number of outbreaks and the lack of effective vaccines against some serotypes necessitates novel measures to control ERM. Importantly, Y. ruckeri survives in the environment for long periods, presumably by forming biofilms. How the pathogen forms biofilms and which molecular factors are involved in this process, remains unclear. Yersinia ruckeri produces two surface-exposed adhesins, belonging to the inverse autotransporters (IATs), called Y. ruckeri invasin (YrInv) and Y. ruckeri invasin-like molecule (YrIlm). Here, we investigated whether YrInv and YrIlm play a role in biofilm formation and virulence. Functional assays revealed that YrInv and YrIlm promote biofilm formation on different abiotic substrates. Confocal microscopy revealed that they are involved in microcolony interaction and formation, respectively. The effect of both IATs on biofilm formation correlated with the presence of different biopolymers in the biofilm matrix, including extracellular DNA, RNA and proteins. Moreover, YrInv and YrIlm contributed to virulence in the Galleria mellonella infection model. Taken together, we propose that both IATs are possible targets for the development of novel diagnostic and preventative strategies to control ERM.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/704903/EU/Bacterial Adhesion Control through Surface TArgeted Regulation/BAC-STAR</subfield>
    <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 704903-BAC-STAR</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">by</subfield>
    <subfield code="u">http://creativecommons.org/licenses/by/3.0/es/</subfield>
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    <subfield code="a">5.491</subfield>
    <subfield code="b">2020</subfield>
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    <subfield code="a">MICROBIOLOGY</subfield>
    <subfield code="b">30 / 136 = 0.221</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
    <subfield code="e">T1</subfield>
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  <datafield tag="592" ind1=" " ind2=" ">
    <subfield code="a">1.954</subfield>
    <subfield code="b">2020</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Microbiology</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Ecology, Evolution, Behavior and Systematics</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Saragliadis, A.</subfield>
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    <subfield code="a">Pérez-Ortega, J.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sittman, C.</subfield>
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    <subfield code="a">Göttig, S.</subfield>
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    <subfield code="a">Liskiewicz, K.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Spence, M.H.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Schneider, K.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Leo, J.C.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Arenas, J.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-8134-0693</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Linke, D.</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1009</subfield>
    <subfield code="2">773</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Patología Animal</subfield>
    <subfield code="c">Área Sanidad Animal</subfield>
  </datafield>
  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">22, 7 (2020), 2939-2955</subfield>
    <subfield code="p">Environ. microbiol.</subfield>
    <subfield code="t">Environmental Microbiology</subfield>
    <subfield code="x">1462-2912</subfield>
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    <subfield code="u">http://zaguan.unizar.es/record/89811/files/texto_completo.jpg?subformat=icon</subfield>
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    <subfield code="a">2022-04-26-08:53:28</subfield>
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