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Lack of cross-protection against Mycoplasma haemofelis infection and signs of enhancement in “Candidatus Mycoplasma turicensis”-recovered cats

Identifieur interne : 000948 ( Main/Exploration ); précédent : 000947; suivant : 000949

Lack of cross-protection against Mycoplasma haemofelis infection and signs of enhancement in “Candidatus Mycoplasma turicensis”-recovered cats

Auteurs : Julia Baumann [Suisse] ; Marilisa Novacco [Suisse] ; Barbara Willi [Suisse] ; Barbara Riond [Suisse] ; Marina L. Meli [Suisse] ; Felicitas S. Boretti [Suisse] ; Regina Hofmann-Lehmann [Suisse]

Source :

RBID : PMC:4581119

Abstract

Mycoplasma haemofelis” and “Candidatus Mycoplasma turicensis” are feline hemoplasmas that induce hemolytic anemia. Protection from homologous re-challenge was recently demonstrated in cats recovered from primary infection. Here, we determined if cats recovered from “Cand. M. turicensis” infection were protected against infections with the more pathogenic M. haemofelis. Ten specified pathogen-free cats were exposed to M. haemofelis. Five of the ten cats had recovered from “Cand. M. turicensis” bacteremia (group A), and five cats were naïve controls (group B). No cross-protection was observed. By contrast, the “Cand. M. turicensis”-recovered cats displayed faster M. haemofelis infection onset (earlier PCR-positive and anemic) than the controls. No “Cand. M. turicensis” was detected in any cat. M. haemofelis shedding was observed in saliva, feces and urine. In both groups, evidence of a Th1 response was observed (high IFN-γ, low IL-4), but IL-10 levels were also high. In group A, total, CD4+ and CD8+ T cells increased within days after M. haemofelis exposure. At times of maximal bacteremia, macrocytic hypochromic anemia, neutropenia, monocytosis and a decrease in leukocyte, eosinophil, and lymphocyte counts and subsets thereof (B- and T-cells, CD4+, CD8+ and CD4+CD25+ cells) were particularly significant in group A. Moreover, an increase in protein concentrations, hypoalbuminemia and a polyclonal hypergammaglobulinemia were observed. Five of ten M. haemofelis-infected cats subsequently cleared bacteremia without antibiotic treatment. In conclusion, the study suggests that a previous hemoplasma infection, even when the cat has ostensibly recovered, may influence subsequent infections, lead to an enhancement phenomenon and other differences in infection kinetics.

Electronic supplementary material

The online version of this article (doi:10.1186/s13567-015-0240-x) contains supplementary material, which is available to authorized users.


Url:
DOI: 10.1186/s13567-015-0240-x
PubMed: 26403079
PubMed Central: 4581119


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<author>
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<name sortKey="Meli, Marina L" sort="Meli, Marina L" uniqKey="Meli M" first="Marina L" last="Meli">Marina L. Meli</name>
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<name sortKey="Boretti, Felicitas S" sort="Boretti, Felicitas S" uniqKey="Boretti F" first="Felicitas S" last="Boretti">Felicitas S. Boretti</name>
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<name sortKey="Hofmann Lehmann, Regina" sort="Hofmann Lehmann, Regina" uniqKey="Hofmann Lehmann R" first="Regina" last="Hofmann-Lehmann">Regina Hofmann-Lehmann</name>
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<title level="j">Veterinary Research</title>
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<date when="2015">2015</date>
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<div type="abstract" xml:lang="en">
<p>
<italic>Mycoplasma haemofelis</italic>
” and “
<italic>Candidatus</italic>
Mycoplasma turicensis” are feline hemoplasmas that induce hemolytic anemia. Protection from homologous re-challenge was recently demonstrated in cats recovered from primary infection. Here, we determined if cats recovered from “
<italic>Cand.</italic>
M. turicensis” infection were protected against infections with the more pathogenic
<italic>M. haemofelis</italic>
. Ten specified pathogen-free cats were exposed to
<italic>M. haemofelis</italic>
. Five of the ten cats had recovered from “
<italic>Cand.</italic>
M. turicensis” bacteremia (group A), and five cats were naïve controls (group B). No cross-protection was observed. By contrast, the “
<italic>Cand.</italic>
M. turicensis”-recovered cats displayed faster
<italic>M. haemofelis</italic>
infection onset (earlier PCR-positive and anemic) than the controls. No “
<italic>Cand.</italic>
M. turicensis” was detected in any cat.
<italic>M. haemofelis</italic>
shedding was observed in saliva, feces and urine. In both groups, evidence of a Th1 response was observed (high IFN-γ, low IL-4), but IL-10 levels were also high. In group A, total, CD4+ and CD8+ T cells increased within days after
<italic>M. haemofelis</italic>
exposure. At times of maximal bacteremia, macrocytic hypochromic anemia, neutropenia, monocytosis and a decrease in leukocyte, eosinophil, and lymphocyte counts and subsets thereof (B- and T-cells, CD4+, CD8+ and CD4+CD25+ cells) were particularly significant in group A. Moreover, an increase in protein concentrations, hypoalbuminemia and a polyclonal hypergammaglobulinemia were observed. Five of ten
<italic>M. haemofelis</italic>
-infected cats subsequently cleared bacteremia without antibiotic treatment. In conclusion, the study suggests that a previous hemoplasma infection, even when the cat has ostensibly recovered, may influence subsequent infections, lead to an enhancement phenomenon and other differences in infection kinetics.</p>
<sec>
<title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/s13567-015-0240-x) contains supplementary material, which is available to authorized users.</p>
</sec>
</div>
</front>
<back>
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<name sortKey="Holznagel, E" uniqKey="Holznagel E">E Holznagel</name>
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<name sortKey="Hofmann Lehmann, R" uniqKey="Hofmann Lehmann R">R Hofmann-Lehmann</name>
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<name sortKey="Allenspach, K" uniqKey="Allenspach K">K Allenspach</name>
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<name sortKey="Huettner, S" uniqKey="Huettner S">S Huettner</name>
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<name sortKey="Forster, U" uniqKey="Forster U">U Forster</name>
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<name sortKey="Niederer, E" uniqKey="Niederer E">E Niederer</name>
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<name sortKey="Joller, H" uniqKey="Joller H">H Joller</name>
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<author>
<name sortKey="Willett, Bj" uniqKey="Willett B">BJ Willett</name>
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<author>
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<name sortKey="Bae, D" uniqKey="Bae D">D Bae</name>
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</div1>
</back>
</TEI>
<affiliations>
<list>
<country>
<li>Suisse</li>
</country>
<region>
<li>Canton de Zurich</li>
</region>
<settlement>
<li>Zurich</li>
</settlement>
<orgName>
<li>Université de Zurich</li>
</orgName>
</list>
<tree>
<country name="Suisse">
<region name="Canton de Zurich">
<name sortKey="Baumann, Julia" sort="Baumann, Julia" uniqKey="Baumann J" first="Julia" last="Baumann">Julia Baumann</name>
</region>
<name sortKey="Baumann, Julia" sort="Baumann, Julia" uniqKey="Baumann J" first="Julia" last="Baumann">Julia Baumann</name>
<name sortKey="Boretti, Felicitas S" sort="Boretti, Felicitas S" uniqKey="Boretti F" first="Felicitas S" last="Boretti">Felicitas S. Boretti</name>
<name sortKey="Hofmann Lehmann, Regina" sort="Hofmann Lehmann, Regina" uniqKey="Hofmann Lehmann R" first="Regina" last="Hofmann-Lehmann">Regina Hofmann-Lehmann</name>
<name sortKey="Hofmann Lehmann, Regina" sort="Hofmann Lehmann, Regina" uniqKey="Hofmann Lehmann R" first="Regina" last="Hofmann-Lehmann">Regina Hofmann-Lehmann</name>
<name sortKey="Meli, Marina L" sort="Meli, Marina L" uniqKey="Meli M" first="Marina L" last="Meli">Marina L. Meli</name>
<name sortKey="Meli, Marina L" sort="Meli, Marina L" uniqKey="Meli M" first="Marina L" last="Meli">Marina L. Meli</name>
<name sortKey="Novacco, Marilisa" sort="Novacco, Marilisa" uniqKey="Novacco M" first="Marilisa" last="Novacco">Marilisa Novacco</name>
<name sortKey="Novacco, Marilisa" sort="Novacco, Marilisa" uniqKey="Novacco M" first="Marilisa" last="Novacco">Marilisa Novacco</name>
<name sortKey="Riond, Barbara" sort="Riond, Barbara" uniqKey="Riond B" first="Barbara" last="Riond">Barbara Riond</name>
<name sortKey="Willi, Barbara" sort="Willi, Barbara" uniqKey="Willi B" first="Barbara" last="Willi">Barbara Willi</name>
<name sortKey="Willi, Barbara" sort="Willi, Barbara" uniqKey="Willi B" first="Barbara" last="Willi">Barbara Willi</name>
</country>
</tree>
</affiliations>
</record>

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