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Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)

BACKGROUND: Hemotropic mycoplasmas are epicellular erythrocytic bacteria that can cause infectious anemia in some mammalian species. Worldwide, hemotropic mycoplasmas are emerging or re-emerging zoonotic pathogens potentially causing serious and significant health problems in wildlife. The objective...

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Autores principales: Mascarelli, Patricia E, Keel, Michael K, Yabsley, Michael, Last, Lisa A, Breitschwerdt, Edward B, Maggi, Ricardo G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994326/
https://www.ncbi.nlm.nih.gov/pubmed/24655520
http://dx.doi.org/10.1186/1756-3305-7-117
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author Mascarelli, Patricia E
Keel, Michael K
Yabsley, Michael
Last, Lisa A
Breitschwerdt, Edward B
Maggi, Ricardo G
author_facet Mascarelli, Patricia E
Keel, Michael K
Yabsley, Michael
Last, Lisa A
Breitschwerdt, Edward B
Maggi, Ricardo G
author_sort Mascarelli, Patricia E
collection PubMed
description BACKGROUND: Hemotropic mycoplasmas are epicellular erythrocytic bacteria that can cause infectious anemia in some mammalian species. Worldwide, hemotropic mycoplasmas are emerging or re-emerging zoonotic pathogens potentially causing serious and significant health problems in wildlife. The objective of this study was to determine the molecular prevalence of hemotropic Mycoplasma species in little brown bats (Myotis lucifugus) with and without Pseudogymnoascus (Geomyces) destrucans, the causative agent of white nose syndrome (WNS) that causes significant mortality events in bats. METHODS: In order to establish the prevalence of hemotropic Mycoplasma species in a population of 68 little brown bats (Myotis lucifugus) with (n = 53) and without (n = 15) white-nose syndrome (WNS), PCR was performed targeting the 16S rRNA gene. RESULTS: The overall prevalence of hemotropic Mycoplasmas in bats was 47%, with similar (p = 0.5725) prevalence between bats with WNS (49%) and without WNS (40%). 16S rDNA sequence analysis (~1,200 bp) supports the presence of a novel hemotropic Mycoplasma species with 91.75% sequence homology with Mycoplasma haemomuris. No differences were found in gene sequences generated from WNS and non-WNS animals. CONCLUSIONS: Gene sequences generated from WNS and non-WNS animals suggest that little brown bats could serve as a natural reservoir for this potentially novel Mycoplasma species. Currently, there is minimal information about the prevalence, host-specificity, or the route of transmission of hemotropic Mycoplasma spp. among bats. Finally, the potential role of hemotropic Mycoplasma spp. as co-factors in the development of disease manifestations in bats, including WNS in Myotis lucifugus, remains to be elucidated.
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spelling pubmed-39943262014-04-23 Hemotropic mycoplasmas in little brown bats (Myotis lucifugus) Mascarelli, Patricia E Keel, Michael K Yabsley, Michael Last, Lisa A Breitschwerdt, Edward B Maggi, Ricardo G Parasit Vectors Research BACKGROUND: Hemotropic mycoplasmas are epicellular erythrocytic bacteria that can cause infectious anemia in some mammalian species. Worldwide, hemotropic mycoplasmas are emerging or re-emerging zoonotic pathogens potentially causing serious and significant health problems in wildlife. The objective of this study was to determine the molecular prevalence of hemotropic Mycoplasma species in little brown bats (Myotis lucifugus) with and without Pseudogymnoascus (Geomyces) destrucans, the causative agent of white nose syndrome (WNS) that causes significant mortality events in bats. METHODS: In order to establish the prevalence of hemotropic Mycoplasma species in a population of 68 little brown bats (Myotis lucifugus) with (n = 53) and without (n = 15) white-nose syndrome (WNS), PCR was performed targeting the 16S rRNA gene. RESULTS: The overall prevalence of hemotropic Mycoplasmas in bats was 47%, with similar (p = 0.5725) prevalence between bats with WNS (49%) and without WNS (40%). 16S rDNA sequence analysis (~1,200 bp) supports the presence of a novel hemotropic Mycoplasma species with 91.75% sequence homology with Mycoplasma haemomuris. No differences were found in gene sequences generated from WNS and non-WNS animals. CONCLUSIONS: Gene sequences generated from WNS and non-WNS animals suggest that little brown bats could serve as a natural reservoir for this potentially novel Mycoplasma species. Currently, there is minimal information about the prevalence, host-specificity, or the route of transmission of hemotropic Mycoplasma spp. among bats. Finally, the potential role of hemotropic Mycoplasma spp. as co-factors in the development of disease manifestations in bats, including WNS in Myotis lucifugus, remains to be elucidated. BioMed Central 2014-03-24 /pmc/articles/PMC3994326/ /pubmed/24655520 http://dx.doi.org/10.1186/1756-3305-7-117 Text en Copyright © 2014 Mascarelli 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mascarelli, Patricia E
Keel, Michael K
Yabsley, Michael
Last, Lisa A
Breitschwerdt, Edward B
Maggi, Ricardo G
Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)
title Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)
title_full Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)
title_fullStr Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)
title_full_unstemmed Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)
title_short Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)
title_sort hemotropic mycoplasmas in little brown bats (myotis lucifugus)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994326/
https://www.ncbi.nlm.nih.gov/pubmed/24655520
http://dx.doi.org/10.1186/1756-3305-7-117
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