Hemotropic mycoplasmas in little brown bats (Myotis lucifugus)

• Published in: Parasites & vectors 2014-03, Vol.7 (1), p.117-117, Article 117
• Main Authors: Mascarelli, Patricia E, Keel, Michael K, Yabsley, Michael, Last, Lisa A, Breitschwerdt, Edward B, Maggi, Ricardo G
• Format: Article
• Language: English
• Subjects: anemia; Animals; Appalachian Region - epidemiology; Ascomycota - isolation & purification; bacteria; Base Sequence; Bat; Bats; Chiroptera - microbiology; Deoxyribonucleic acid; Disease; Disease Reservoirs; DNA; DNA, Bacterial - chemistry; DNA, Bacterial - genetics; DNA, Ribosomal - chemistry; DNA, Ribosomal - genetics; genes; Geomyces; Haemoplasma; Hemotropic mycoplasma; host specificity; Infections; Mammals; Molecular Sequence Data; Mortality; Mycoplasma; Mycoplasma - classification; Mycoplasma - genetics; Mycoplasma - isolation & purification; Mycoplasma haemomuris; Mycoplasma Infections - epidemiology; Mycoplasma Infections - microbiology; Mycoplasma Infections - mortality; Mycoplasma Infections - veterinary; Mycplasma; Myotis; Myotis lucifugus; nose; Nose - pathology; nucleotide sequences; pathogens; Phylogenetics; Phylogeny; polymerase chain reaction; Polymerase Chain Reaction - veterinary; Prevalence; Pseudogymnoascus; ribosomal DNA; ribosomal RNA; RNA, Ribosomal, 16S - genetics; Sequence Analysis, DNA - veterinary; sequence homology; Spleen - pathology; Studies; Trees; Veterinary colleges; Veterinary medicine; wildlife; WNS
• ISSN: 1756-3305; 1756-3305
• DOI: 10.1186/1756-3305-7-117

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.