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The New Species Brucella microti Replicates in Macrophages and Causes Death in Murine Models of Infection

Identifieur interne : 001573 ( Istex/Corpus ); précédent : 001572; suivant : 001574

The New Species Brucella microti Replicates in Macrophages and Causes Death in Murine Models of Infection

Auteurs : María P. Jiménez De Bagüés ; Safia Ouahrani-Bettache ; Juan F. Quintana ; Olga Mitjana ; Nabil Hanna ; Stéphanie Bessoles ; Françoise Sanchez ; Holger C. Scholz ; Virginie Lafont ; Stephan Köhler ; Alessandra Occhialini

Source :

RBID : ISTEX:8799C525C2DF2F14574A7157E7EB70FB20F7AE8D

Abstract

Background. The recent isolation of Brucella microti from the common vole, the red fox, and the soil raises the possibility of an eventual reemergence of brucellosis in Europe. In this work, the pathogenic potential of this new Brucella species in both in vitro and in vivo models of infection was analyzed. Methods. The ability of B. microti (as compared to that of the closely related species Brucella suis) to replicate in human macrophages and in human and murine macrophage-like cells was determined. The behavior of B. microti and B. suis was evaluated in vivo in murine models of infection with Balb/c, CD1, and C57BL/6 mice. Results. B. microti showed an enhanced capacity for intramacrophagic replication compared with that of B. suis. Surprisingly, and in contrast to other species of Brucella, 105 colony-forming units of B. microti killed 82% of Balb/c mice within 7 days. Infection of spleen and liver with B. microti peaked at day 3, compared with B. suis infection, which peaked at day 7. Sublethal doses of B. microti induced good protection against a subsequent challenge with lethal doses. Conclusions. In experimental cellular and murine infections, B. microti exhibited a high pathogenic potential, compared with other Brucella species.

Url:
DOI: 10.1086/653084

Links to Exploration step

ISTEX:8799C525C2DF2F14574A7157E7EB70FB20F7AE8D

Le document en format XML

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<div type="abstract">Background. The recent isolation of Brucella microti from the common vole, the red fox, and the soil raises the possibility of an eventual reemergence of brucellosis in Europe. In this work, the pathogenic potential of this new Brucella species in both in vitro and in vivo models of infection was analyzed. Methods. The ability of B. microti (as compared to that of the closely related species Brucella suis) to replicate in human macrophages and in human and murine macrophage-like cells was determined. The behavior of B. microti and B. suis was evaluated in vivo in murine models of infection with Balb/c, CD1, and C57BL/6 mice. Results. B. microti showed an enhanced capacity for intramacrophagic replication compared with that of B. suis. Surprisingly, and in contrast to other species of Brucella, 105 colony-forming units of B. microti killed 82% of Balb/c mice within 7 days. Infection of spleen and liver with B. microti peaked at day 3, compared with B. suis infection, which peaked at day 7. Sublethal doses of B. microti induced good protection against a subsequent challenge with lethal doses. Conclusions. In experimental cellular and murine infections, B. microti exhibited a high pathogenic potential, compared with other Brucella species.</div>
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<abstract>Background. The recent isolation of Brucella microti from the common vole, the red fox, and the soil raises the possibility of an eventual reemergence of brucellosis in Europe. In this work, the pathogenic potential of this new Brucella species in both in vitro and in vivo models of infection was analyzed. Methods. The ability of B. microti (as compared to that of the closely related species Brucella suis) to replicate in human macrophages and in human and murine macrophage-like cells was determined. The behavior of B. microti and B. suis was evaluated in vivo in murine models of infection with Balb/c, CD1, and C57BL/6 mice. Results. B. microti showed an enhanced capacity for intramacrophagic replication compared with that of B. suis. Surprisingly, and in contrast to other species of Brucella, 105 colony-forming units of B. microti killed 82% of Balb/c mice within 7 days. Infection of spleen and liver with B. microti peaked at day 3, compared with B. suis infection, which peaked at day 7. Sublethal doses of B. microti induced good protection against a subsequent challenge with lethal doses. Conclusions. In experimental cellular and murine infections, B. microti exhibited a high pathogenic potential, compared with other Brucella species.</abstract>
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<article-title>The New Species
<italic>Brucella microti</italic>
Replicates in Macrophages and Causes Death in Murine Models of Infection</article-title>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Jiménez de Bagüés</surname>
<given-names>María P.</given-names>
</name>
<xref rid="aff1" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ouahrani-Bettache</surname>
<given-names>Safia</given-names>
</name>
<xref rid="aff2" ref-type="aff">2</xref>
<xref rid="aff3" ref-type="aff">3</xref>
<xref rid="aff4" ref-type="aff">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Quintana</surname>
<given-names>Juan F.</given-names>
</name>
<xref rid="aff1" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mitjana</surname>
<given-names>Olga</given-names>
</name>
<xref rid="aff1" ref-type="aff">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hanna</surname>
<given-names>Nabil</given-names>
</name>
<xref rid="aff2" ref-type="aff">2</xref>
<xref rid="aff3" ref-type="aff">3</xref>
<xref rid="aff4" ref-type="aff">4</xref>
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<name>
<surname>Bessoles</surname>
<given-names>Stéphanie</given-names>
</name>
<xref rid="aff2" ref-type="aff">2</xref>
<xref rid="aff3" ref-type="aff">3</xref>
<xref rid="aff4" ref-type="aff">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sanchez</surname>
<given-names>Françoise</given-names>
</name>
<xref rid="aff2" ref-type="aff">2</xref>
<xref rid="aff3" ref-type="aff">3</xref>
<xref rid="aff4" ref-type="aff">4</xref>
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<contrib contrib-type="author">
<name>
<surname>Scholz</surname>
<given-names>Holger C.</given-names>
</name>
<xref rid="aff5" ref-type="aff">5</xref>
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<contrib contrib-type="author">
<name>
<surname>Lafont</surname>
<given-names>Virginie</given-names>
</name>
<xref rid="aff2" ref-type="aff">2</xref>
<xref rid="aff3" ref-type="aff">3</xref>
<xref rid="aff4" ref-type="aff">4</xref>
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<name>
<surname>Köhler</surname>
<given-names>Stephan</given-names>
</name>
<xref rid="aff2" ref-type="aff">2</xref>
<xref rid="aff3" ref-type="aff">3</xref>
<xref rid="aff4" ref-type="aff">4</xref>
<xref rid="fn1" ref-type="fn">a</xref>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Occhialini</surname>
<given-names>Alessandra</given-names>
</name>
<xref rid="cor1" ref-type="corresp"></xref>
<xref rid="aff2" ref-type="aff">2</xref>
<xref rid="aff3" ref-type="aff">3</xref>
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<label>1</label>
<institution>Unidad de Sanidad Animal, Centro de Investigación y Tecnología Agroalimentaria, Gobierno de Aragón</institution>
,
<addr-line>Zaragoza, Spain</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<institution>Centre National de la Recherche Scientifique, Unité Mixte de Recherche (UMR) 5236, Centre d'Études d'Agents Pathogènes et Biotechnologies pour la Santé (CPBS)</institution>
,
<addr-line>Montpellier, France</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<institution>UMR 5236, CPBS, Université Montpellier I</institution>
,
<addr-line>Montpellier, France</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<institution>Université Montpellier II</institution>
,
<addr-line>Montpellier, France</addr-line>
</aff>
<aff id="aff5">
<label>5</label>
<institution>Department of Bacteriology, Bundeswehr Institute of Microbiology</institution>
,
<addr-line>Germany</addr-line>
</aff>
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<author-notes>
<corresp id="cor1">Reprints or correspondence: Dr Alessandra Occhialini, CBPS, UMR 5236, Université Montpellier II, cc 100, Pl. E. Bataillon, 34095 Montpellier cedex 05, France (
<email>aocchial@univ-montp2.fr</email>
).</corresp>
</author-notes>
<pub-date pub-type="ppub">
<day>1</day>
<month>7</month>
<year>2010</year>
</pub-date>
<volume>202</volume>
<issue>1</issue>
<fpage>3</fpage>
<lpage>10</lpage>
<history>
<date date-type="received">
<day>19</day>
<month>8</month>
<year>2009</year>
</date>
<date date-type="accepted">
<day>22</day>
<month>10</month>
<year>2009</year>
</date>
</history>
<copyright-statement>© 2010 by the Infectious Diseases Society of America</copyright-statement>
<copyright-year>2010</copyright-year>
<abstract>
<p>
<bold>
<italic>Background.</italic>
</bold>
The recent isolation of
<italic>Brucella microti</italic>
from the common vole, the red fox, and the soil raises the possibility of an eventual reemergence of brucellosis in Europe. In this work, the pathogenic potential of this new
<italic>Brucella</italic>
species in both in vitro and in vivo models of infection was analyzed.</p>
<p>
<bold>
<italic>Methods.</italic>
</bold>
The ability of
<italic>B. microti</italic>
(as compared to that of the closely related species
<italic>Brucella suis</italic>
) to replicate in human macrophages and in human and murine macrophage-like cells was determined. The behavior of
<italic>B. microti</italic>
and
<italic>B. suis</italic>
was evaluated in vivo in murine models of infection with Balb/c, CD1, and C57BL/6 mice.</p>
<p>
<bold>
<italic>Results.</italic>
</bold>
<italic>B. microti</italic>
showed an enhanced capacity for intramacrophagic replication compared with that of
<italic>B. suis.</italic>
Surprisingly, and in contrast to other species of
<italic>Brucella</italic>
, 10
<sup>5</sup>
colony-forming units of
<italic>B. microti</italic>
killed 82% of Balb/c mice within 7 days. Infection of spleen and liver with
<italic>B. microti</italic>
peaked at day 3, compared with
<italic>B. suis</italic>
infection, which peaked at day 7. Sublethal doses of
<italic>B. microti</italic>
induced good protection against a subsequent challenge with lethal doses.</p>
<p>
<bold>
<italic>Conclusions.</italic>
</bold>
In experimental cellular and murine infections,
<italic>B. microti</italic>
exhibited a high pathogenic potential, compared with other
<italic>Brucella</italic>
species.</p>
</abstract>
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<affiliation>Centre National de la Recherche Scientifique, Unité Mixte de Recherche (UMR) 5236, Centre d'Études d'Agents Pathogènes et Biotechnologies pour la Santé (CPBS), Montpellier, France</affiliation>
<affiliation>UMR 5236, CPBS, Université Montpellier I, Montpellier, France</affiliation>
<affiliation>Université Montpellier II, Montpellier, France</affiliation>
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<namePart type="given">Alessandra</namePart>
<namePart type="family">Occhialini</namePart>
<affiliation>Centre National de la Recherche Scientifique, Unité Mixte de Recherche (UMR) 5236, Centre d'Études d'Agents Pathogènes et Biotechnologies pour la Santé (CPBS), Montpellier, France</affiliation>
<affiliation>UMR 5236, CPBS, Université Montpellier I, Montpellier, France</affiliation>
<affiliation>Université Montpellier II, Montpellier, France</affiliation>
<affiliation>E-mail: aocchial@univ-montp2.fr</affiliation>
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<abstract>Background. The recent isolation of Brucella microti from the common vole, the red fox, and the soil raises the possibility of an eventual reemergence of brucellosis in Europe. In this work, the pathogenic potential of this new Brucella species in both in vitro and in vivo models of infection was analyzed. Methods. The ability of B. microti (as compared to that of the closely related species Brucella suis) to replicate in human macrophages and in human and murine macrophage-like cells was determined. The behavior of B. microti and B. suis was evaluated in vivo in murine models of infection with Balb/c, CD1, and C57BL/6 mice. Results. B. microti showed an enhanced capacity for intramacrophagic replication compared with that of B. suis. Surprisingly, and in contrast to other species of Brucella, 105 colony-forming units of B. microti killed 82% of Balb/c mice within 7 days. Infection of spleen and liver with B. microti peaked at day 3, compared with B. suis infection, which peaked at day 7. Sublethal doses of B. microti induced good protection against a subsequent challenge with lethal doses. Conclusions. In experimental cellular and murine infections, B. microti exhibited a high pathogenic potential, compared with other Brucella species.</abstract>
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<title>The Journal of Infectious Diseases</title>
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<title>The Journal of Infectious Diseases</title>
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<genre type="journal">journal</genre>
<identifier type="ISSN">0022-1899</identifier>
<identifier type="eISSN">1537-6613</identifier>
<identifier type="PublisherID">jid</identifier>
<identifier type="PublisherID-hwp">jinfdis</identifier>
<part>
<date>2010</date>
<detail type="volume">
<caption>vol.</caption>
<number>202</number>
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<caption>no.</caption>
<number>1</number>
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<start>3</start>
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<identifier type="DOI">10.1086/653084</identifier>
<accessCondition type="use and reproduction" contentType="copyright">© 2010 by the Infectious Diseases Society of America</accessCondition>
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