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Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones

Bovine respiratory disease (BRD) is common in calves in Algeria, but to date, Mycoplasma bovis has never been monitored as a potential etiological agent. Here, to assess the presence (direct detection) and circulation (indirect detection) of M. bovis, broncho-alveolar lavage fluids (BALF) and serum...

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Autores principales: Oucheriah, Yasmine, Heleili, Nouzha, Colin, Adélie, Mottet, Catherine, Tardy, Florence, Becker, Claire A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163989/
https://www.ncbi.nlm.nih.gov/pubmed/35669175
http://dx.doi.org/10.3389/fvets.2022.910799
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author Oucheriah, Yasmine
Heleili, Nouzha
Colin, Adélie
Mottet, Catherine
Tardy, Florence
Becker, Claire A. M.
author_facet Oucheriah, Yasmine
Heleili, Nouzha
Colin, Adélie
Mottet, Catherine
Tardy, Florence
Becker, Claire A. M.
author_sort Oucheriah, Yasmine
collection PubMed
description Bovine respiratory disease (BRD) is common in calves in Algeria, but to date, Mycoplasma bovis has never been monitored as a potential etiological agent. Here, to assess the presence (direct detection) and circulation (indirect detection) of M. bovis, broncho-alveolar lavage fluids (BALF) and serum samples were collected from 60 veal calf farms in Algeria. A commercial ELISA kit (ID Screen(®) ELISA) was used to screen for the presence of specific antibodies against M. bovis in 351 blood sera collected from both diseased and healthy calves, and 69% (241 sera) tested positive. BALFs from the 176 diseased calves were used to screen for M. bovis by real-time-PCR (rt-PCR), and 102 (58%) tested positive. A non-exhaustive set of 53 clones were isolated from 44 calves and further subtyped using polC gene sequencing. No predominant subtype was found, and two clones exhibited a new subtype. Fourteen clones were further characterized by multilocus sequence typing, and results showed a high degree of genetic diversity, with some clones having new alleles and subtypes. The minimum inhibitory concentrations (MICs) of 5 antimicrobials regularly used to treat BRD was determined on 45 clones. Susceptibility profiles showed very broad diversity, confirming the variety of clones actively circulating. We detected clones with high MICs, including increased MICs of enrofloxacin (n = 5). This is the first study to report the presence of M. bovis in Algeria in calves with BRD. This research also finds broad genetic and phenotypic diversity in the actively circulating isolates.
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spelling pubmed-91639892022-06-05 Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones Oucheriah, Yasmine Heleili, Nouzha Colin, Adélie Mottet, Catherine Tardy, Florence Becker, Claire A. M. Front Vet Sci Veterinary Science Bovine respiratory disease (BRD) is common in calves in Algeria, but to date, Mycoplasma bovis has never been monitored as a potential etiological agent. Here, to assess the presence (direct detection) and circulation (indirect detection) of M. bovis, broncho-alveolar lavage fluids (BALF) and serum samples were collected from 60 veal calf farms in Algeria. A commercial ELISA kit (ID Screen(®) ELISA) was used to screen for the presence of specific antibodies against M. bovis in 351 blood sera collected from both diseased and healthy calves, and 69% (241 sera) tested positive. BALFs from the 176 diseased calves were used to screen for M. bovis by real-time-PCR (rt-PCR), and 102 (58%) tested positive. A non-exhaustive set of 53 clones were isolated from 44 calves and further subtyped using polC gene sequencing. No predominant subtype was found, and two clones exhibited a new subtype. Fourteen clones were further characterized by multilocus sequence typing, and results showed a high degree of genetic diversity, with some clones having new alleles and subtypes. The minimum inhibitory concentrations (MICs) of 5 antimicrobials regularly used to treat BRD was determined on 45 clones. Susceptibility profiles showed very broad diversity, confirming the variety of clones actively circulating. We detected clones with high MICs, including increased MICs of enrofloxacin (n = 5). This is the first study to report the presence of M. bovis in Algeria in calves with BRD. This research also finds broad genetic and phenotypic diversity in the actively circulating isolates. Frontiers Media S.A. 2022-05-20 /pmc/articles/PMC9163989/ /pubmed/35669175 http://dx.doi.org/10.3389/fvets.2022.910799 Text en Copyright © 2022 Oucheriah, Heleili, Colin, Mottet, Tardy and Becker. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Oucheriah, Yasmine
Heleili, Nouzha
Colin, Adélie
Mottet, Catherine
Tardy, Florence
Becker, Claire A. M.
Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones
title Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones
title_full Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones
title_fullStr Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones
title_full_unstemmed Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones
title_short Prevalence of Mycoplasma bovis in Algeria and Characterisation of the Isolated Clones
title_sort prevalence of mycoplasma bovis in algeria and characterisation of the isolated clones
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163989/
https://www.ncbi.nlm.nih.gov/pubmed/35669175
http://dx.doi.org/10.3389/fvets.2022.910799
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