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Chronic "Candidatus Mycoplasma turicensis" infection

"Candidatus Mycoplasma turicensis" infects felids. The pathogenesis of "Candidatus M. turicensis" chronic infection is poorly understood. The goals of the present study were to (1) induce reactivation of the infection in chronic carrier cats by attempted immunosuppression, (2) id...

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Autores principales: Novacco, Marilisa, Boretti, Felicitas S, Wolf-Jäckel, Godelind A, Riond, Barbara, Meli, Marina L, Willi, Barbara, Lutz, Hans, Hofmann-Lehmann, Regina
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090992/
https://www.ncbi.nlm.nih.gov/pubmed/21507220
http://dx.doi.org/10.1186/1297-9716-42-59
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author Novacco, Marilisa
Boretti, Felicitas S
Wolf-Jäckel, Godelind A
Riond, Barbara
Meli, Marina L
Willi, Barbara
Lutz, Hans
Hofmann-Lehmann, Regina
author_facet Novacco, Marilisa
Boretti, Felicitas S
Wolf-Jäckel, Godelind A
Riond, Barbara
Meli, Marina L
Willi, Barbara
Lutz, Hans
Hofmann-Lehmann, Regina
author_sort Novacco, Marilisa
collection PubMed
description "Candidatus Mycoplasma turicensis" infects felids. The pathogenesis of "Candidatus M. turicensis" chronic infection is poorly understood. The goals of the present study were to (1) induce reactivation of the infection in chronic carrier cats by attempted immunosuppression, (2) identify potential tissue sequestration using real-time TaqMan(® )PCR and (3) monitor the humoral immune response by DnaK enzyme-linked immunosorbent assay (ELISA). Ten specified pathogen-free cats that had ostensibly recovered from experimental "Candidatus M. turicensis" infection were used: five cats (group 1) received high dose methylprednisolone (attempted immunosuppression), while five cats served as untreated controls (group 2). Besides weekly blood samples, tissue samples were collected from bone marrow, kidney, liver and salivary glands at selected time points. The cats in group 1 had significantly lower lymphocyte counts and higher blood glucose levels after methylprednisolone administration than the controls. After methylprednisolone administration one blood and three tissue samples from cats in group 1 tested PCR-positive; before the administration, only one sample was positive. All other samples tested PCR-negative. All cats stayed seropositive; the antibody levels of the cats in group 1 showed a significant transient decrease after methylprednisolone administration. This is the first study to report the presence of "Candidatus M. turicensis" in tissues of chronically infected cats and the persistence of anti-feline hemoplasma antibodies in the absence of detectable bacteremia. Methylprednisolone administration did not lead to a significant reactivation of the infection. Our results enhance the knowledge of "Candidatus M. turicensis" infection pathogenesis and are clinically relevant to the prognosis of hemoplasma-infected cats.
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spelling pubmed-30909922011-05-11 Chronic "Candidatus Mycoplasma turicensis" infection Novacco, Marilisa Boretti, Felicitas S Wolf-Jäckel, Godelind A Riond, Barbara Meli, Marina L Willi, Barbara Lutz, Hans Hofmann-Lehmann, Regina Vet Res Research "Candidatus Mycoplasma turicensis" infects felids. The pathogenesis of "Candidatus M. turicensis" chronic infection is poorly understood. The goals of the present study were to (1) induce reactivation of the infection in chronic carrier cats by attempted immunosuppression, (2) identify potential tissue sequestration using real-time TaqMan(® )PCR and (3) monitor the humoral immune response by DnaK enzyme-linked immunosorbent assay (ELISA). Ten specified pathogen-free cats that had ostensibly recovered from experimental "Candidatus M. turicensis" infection were used: five cats (group 1) received high dose methylprednisolone (attempted immunosuppression), while five cats served as untreated controls (group 2). Besides weekly blood samples, tissue samples were collected from bone marrow, kidney, liver and salivary glands at selected time points. The cats in group 1 had significantly lower lymphocyte counts and higher blood glucose levels after methylprednisolone administration than the controls. After methylprednisolone administration one blood and three tissue samples from cats in group 1 tested PCR-positive; before the administration, only one sample was positive. All other samples tested PCR-negative. All cats stayed seropositive; the antibody levels of the cats in group 1 showed a significant transient decrease after methylprednisolone administration. This is the first study to report the presence of "Candidatus M. turicensis" in tissues of chronically infected cats and the persistence of anti-feline hemoplasma antibodies in the absence of detectable bacteremia. Methylprednisolone administration did not lead to a significant reactivation of the infection. Our results enhance the knowledge of "Candidatus M. turicensis" infection pathogenesis and are clinically relevant to the prognosis of hemoplasma-infected cats. BioMed Central 2011 2011-04-20 /pmc/articles/PMC3090992/ /pubmed/21507220 http://dx.doi.org/10.1186/1297-9716-42-59 Text en Copyright ©2011 Novacco et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Novacco, Marilisa
Boretti, Felicitas S
Wolf-Jäckel, Godelind A
Riond, Barbara
Meli, Marina L
Willi, Barbara
Lutz, Hans
Hofmann-Lehmann, Regina
Chronic "Candidatus Mycoplasma turicensis" infection
title Chronic "Candidatus Mycoplasma turicensis" infection
title_full Chronic "Candidatus Mycoplasma turicensis" infection
title_fullStr Chronic "Candidatus Mycoplasma turicensis" infection
title_full_unstemmed Chronic "Candidatus Mycoplasma turicensis" infection
title_short Chronic "Candidatus Mycoplasma turicensis" infection
title_sort chronic "candidatus mycoplasma turicensis" infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090992/
https://www.ncbi.nlm.nih.gov/pubmed/21507220
http://dx.doi.org/10.1186/1297-9716-42-59
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