Luttrell, M. P. & Fischer, J. R. Mycoplasmosis. In Infectious Diseases of Wild Birds (eds Thomas, N. J. et al.) 317–331 (Blackwell Publishing Ltd, 2007).
Google Scholar
Luttrell, M. P., Kleven, S. H. & Mahnke, G. M. Mycoplasma synoviae in a released pen-raised wild turkey. Avian Dis. 36, 169–171 (1992).
Google Scholar
Forrester, C. A. et al. Mycoplasma gallisepticum in pheasants and the efficacy of tylvalosin to treat the disease. Avian Pathol. 40, 581–587 (2011).
Google Scholar
Welchman, D. D. E. B., Bradbury, J. M., Cavanagh, D. & Aebischer, N. J. Infectious agents associated with respiratory disease in pheasants. Vet. Rec. 150, 658–664 (2002).
Google Scholar
de Welchman, D. B. et al. Demonstration of Ornithobacterium rhinotracheale in pheasants (Phasianus colchicus) with pneumonia and airsacculitis. Avian Pathol. 42, 171–178 (2013).
Google Scholar
Cookson, K. C. & Shivaprasad, H. L. Mycoplasma gallisepticum infection in chukar partridges, pheasants, and peafowl. Avian Dis. 38, 914–921 (2016).
Google Scholar
Bencina, D., Mrzel, O., Rois Zorman, O., Bidovec, A. & Dovc, A. Characterisation of Mycoplasma gallisepticum strains involved in respiratory disease in pheasants and peafowl. Vet. Rec. 152, 230–234 (2003).
Google Scholar
Bradbury, J. M., Yavari, C. A. & Dare, C. M. Mycoplasmas and respiratory disease in pheasants and partridges. Avian Pathol. 30, 391–396 (2001).
Google Scholar
Bradbury, J. M., Yavari, C. A. & Dare, C. M. Detection of Mycoplasma synoviae in clinically normal pheasants. Vet. Rec. 148, 72–74 (2001).
Google Scholar
Wrobel, E. R., Wilcoxen, T. E., Nuzzo, J. T. & Seitz, J. Seroprevalence of avian pox and Mycoplasma gallisepticum in raptors in central Illinois. J. Raptor Res. 50, 289–294 (2016).
Google Scholar
Sawicka, A., Durkalec, M., Tomczyk, G. & Kursa, O. Occurrence of Mycoplasma gallisepticum in wild birds: A systematic review and meta-analysis. PLoS ONE 15, e0231545 (2020).
Google Scholar
Hartup, B. K., Kollias, G. V. & Ley, D. H. Mycoplasmal conjunctivitis in songbirds from New York. J. Wildl. Dis. 36, 257–264 (2000).
Google Scholar
Ley, D. H., Berkhoff, J. E. & Mclaren, J. M. Mycoplasma gallisepticum isolated from house finches (Carpodacus mexicanus) with conjunctivitis. Avian Dis. 40, 480–483 (1996).
Google Scholar
Fischer, J. R., Stallknecht, D. E., Luttrell, M. P., Dhondt, A. A. & Converse, K. A. Mycoplasmal conjunctivitis in wild songbirds: The spread of a new contagious disease in a mobile host population. Emerg. Infect. Dis. 3, 69–72 (1997).
Google Scholar
Farmer, K. L., Hill, G. E. & Roberts, S. R. Susceptibility of wild songbirds to the house finch strain of Mycoplasma gallisepticum. J. Wildl. Dis. 41, 317–325 (2005).
Google Scholar
Dhondt, A. A., Dhondt, K. V., Hochachka, W. M. & Schat, K. A. Can American goldfinches function as reservoirs for Mycoplasma gallisepticum? J. Wildl. Dis. 49, 49–54 (2013).
Google Scholar
Fry, M. A. Effects of Mycoplasma gallisepticum on experimentally infected Eastern bluebirds (Sialia sialis). Honors Theses 1116 (2019). https://egrove.olemiss.edu/hon_thesis/1116. (Accessed 10 November 2020).
Balenger, S. L. Costs associated with Mycoplasma gallisepticum infection of Eastern bluebirds (Sialia sialis). Integr. Comp. Biol. 59, e1–e260 (2019).
Google Scholar
Forsyth, M. H. et al. Mycoplasma sturni sp. nov., from the conjunctiva of a European starling (Sturnus vulgaris). Int. J. Syst. Bacteriol. 46, 716–719 (1996).
Google Scholar
Ley, D. H., Geary, S. J., Edward Berkhoff, J., McLaren, J. M. & Levisohn, S. Mycoplasma sturni from blue jays and northern mockingbirds with conjunctivitis in Florida. J. Wildl. Dis. 34, 403–406 (1998).
Google Scholar
Ley, D. H., Anderson, N., Dhondt, K. V. & Dhondt, A. A. Mycoplasma sturni from a California house finch with conjunctivitis did not cause disease in experimentally infected house finches. J. Wildl. Dis. 46, 994–999 (2010).
Google Scholar
Ley, D. H., Moresco, A. & Frasca, S. Conjunctivitis, rhinitis, and sinusitis in cliff swallows (Petrochelidon pyrrhonota) found in association with Mycoplasma sturni infection and cryptosporidiosis. Avian Pathol. 41, 395–401 (2012).
Google Scholar
Wellehan, J. F. X. et al. Mycoplasmosis in captive crows and robins from Minnesota. J. Wildl. Dis. 37, 547–555 (2001).
Google Scholar
Poveda, J. B., Giebel, J., Flossdorf, J., Meier, J. & Kirchhoff, H. Mycoplasma buteonis sp. nov., Mycoplasma falconis sp. nov., and Mycoplasma gypis sp. nov., three species from birds of prey. Int. J. Syst. Bacteriol. 44, 94–98 (1994).
Google Scholar
Ruder, M. G., Feldman, S. H., Wünschmann, A. & Mcruer, L. Association of Mycoplasma corogypsi and polyarthritis in a black vulture (Coragyps atratus) in Virginia. J. Wildl. Dis. 45, 808–816 (2009).
Google Scholar
Van Wettere, A. J., Ley, D. H., Scott, D. E., Buckanoff, H. D. & Degernes, L. A. Mycoplasma corogypsi associated polyarthritis and tenosynovitis in black vultures (Coragyps atratus). Vet. Pathol. 50, 291–298 (2013).
Google Scholar
Erdélyi, K., Tenk, M. & Dán, Á. Mycoplasmosis associated perosis type skeletal deformity in a saker falcon nestling in Hungary. J. Wildl. Dis. 35, 586–590 (1999).
Google Scholar
Fischer, L. et al. Description, occurrence and significance of Mycoplasma seminis sp. nov. isolated from semen of a gyrfalcon (Falco rusticolus). Vet. Microbiol. 247, 108789 (2020).
Google Scholar
Ziegler, L. et al. Mycoplasma hafezii sp. nov., isolated from the trachea of a peregrine falcon (Falco peregrinus). Int. J. Syst. Evol. Microbiol. 69, 773–777 (2019).
Google Scholar
Lecis, R. et al. Identification and characterization of novel Mycoplasma spp. belonging to the hominis group from griffon vultures. Res. Vet. Sci. 89, 58–64 (2010).
Google Scholar
Lierz, M., Hagen, N., Hernadez-Divers, S. J. & Hafez, H. M. Occurrence of mycoplasmas in freeranging birds of prey in Germany. J. Wildl. Dis. 44, 845–850 (2008).
Google Scholar
Volokhov, D. V. et al. Mycoplasma anserisalpingitidis sp. nov., isolated from European domestic geese (Anser anser domesticus) with reproductive pathology. Int. J. Syst. Evol. Microbiol. 70, 2369–2381 (2020).
Google Scholar
Dobos-Kovács, M., Varga, Z., Czifra, G. & Stipkovits, L. Salpingitis in geese associated with Mycoplasma sp. strain 1220. Avian Pathol. 38, 239–243 (2009).
Google Scholar
Gyuranecz, M. et al. Isolation of Mycoplasma anserisalpingitidis from swan goose (Anser cygnoides) in China. BMC Vet. Res. 16, 1–7 (2020).
Google Scholar
Kovács, Á. B. et al. The core genome multi-locus sequence typing of Mycoplasma anserisalpingitidis. BMC Genomics 21, 403 (2020).
Google Scholar
Carnaccini, S. et al. A novel Mycoplasma sp. associated with phallus disease in goose breeders: Pathological and bacteriological findings. Avian Dis. 60, 437–443 (2016).
Google Scholar
Landman, W. J. M. Is Mycoplasma synoviae outrunning Mycoplasma gallisepticum? A viewpoint from the Netherlands. Avian Pathol. 43, 2–8 (2014).
Google Scholar
Kursa, O., Tomczyk, G. & Sawicka, A. Prevalence and phylogenetic analysis of Mycoplasma synoviae strains isolated from Polish chicken layer flocks. J. Vet. Res. 63, 41–49 (2019).
Google Scholar
Catania, S. et al. Two strains of Mycoplasma synoviae from chicken flocks on the same layer farm differ in their ability to produce eggshell apex abnormality. Vet. Microbiol. 193, 60–66 (2016).
Google Scholar
Kang, M. S., Gazdzinski, P. & Kleven, S. H. Virulence of recent isolates of Mycoplasma synoviae in turkeys. Avian Dis. 46, 102–110 (2002).
Google Scholar
Lin, M. Y. & Kleven, S. H. Pathogenicity of two strains of Mycoplasma gallisepticum in turkeys. Avian Dis. 26, 360–364 (1982).
Google Scholar
Kleven, S. H. Mycoplasmas in the etiology of multifactorial respiratory disease. Poult. Sci. 77, 1146–1149 (1998).
Google Scholar
Stallknecht, D. E., Johnson, D. C., Emory, W. H. & Kleven, S. H. Wildlife surveillance during a Mycoplasma gallisepticum epornitic in domestic turkeys. Avian Dis. 26, 883–890 (1982).
Google Scholar
Gharaibeh, S. & Hailat, A. Mycoplasma gallisepticum experimental infection and tissue distribution in chickens, sparrows and pigeons. Avian Pathol. 40, 349–354 (2011).
Google Scholar
Benčina, D., Dorrer, D. & Tadina, T. Mycoplasma species isolated from six avian species. Avian Pathol. 16, 653–664 (1987).
Google Scholar
Tsai, H. J. & Lee, C. Y. Serological survey of racing pigeons for selected pathogens in Taiwan. Acta Vet. Hung. 54, 179–189 (2006).
Google Scholar
Michiels, T. et al. Prevalence of Mycoplasma gallisepticum and Mycoplasma synoviae in commercial poultry, racing pigeons and wild birds in Belgium. Avian Pathol. 45, 244–252 (2016).
Google Scholar
May, M., Balish, M. & Blanchard, A. The Order Mycoplasmatales. In The Prokaryotes (eds Rosenberg, E. et al.) 515–550 (Springer, 2004).
Lierz, M., Obon, E., Schink, B., Carbonell, F. & Hafez, H. M. The role of Mycoplasmas in a conservation project of the lesser kestrel (Falco naumanni). Avian Dis. 52, 641–645 (2008).
Google Scholar
Bolske, G. & Morner, T. Isolation of a Mycoplasma sp. from three buzzards (Buteo spp.). Avian Dis. 26, 406–411 (1982).
Google Scholar
Kempf, I., Chastel, C., Ferris, S., Gesbert, F. & Blanchard, A. Isolation and characterisation of a mycoplasma from a kittiwake (Rissa tridactyla). Vet. Rec. https://doi.org/10.1136/vr.146.6.168 (2000).
Google Scholar
Cockerham, S. et al. Microbial ecology of the western gull (Larus occidentalis). Microb. Ecol. 78, 665–676 (2019).
Google Scholar
Liao, F. et al. Characteristics of microbial communities and intestinal pathogenic bacteria for migrated Larus ridibundus in southwest China. Microbiology https://doi.org/10.1002/mbo3.693 (2019).
Google Scholar
Shimizu, T., Ern, H. & Nagatomo, H. Isolation and characterization of Mycoplasma columbinum and Mycoplasma columborale, two new species from pigeons. Int. J. Syst. Bacteriol. 28, 538–546 (1978).
Google Scholar
Nagatomo, H., Kato, H., Shimizu, T. & Katayama, B. Isolation of mycoplasmas from fantail pigeons. J. Vet. Med. Sci. 59, 461–462 (1997).
Google Scholar
Sawicka, A., Tomczyk, G., Kursa, O. & Stenzel, T. Occurrence and relevance of Mycoplasma spp. in racing and ornamental pigeons in Poland. Avian Dis. 63, 468 (2019).
Google Scholar
Möller Palau-Ribes, F. et al. Description and prevalence of Mycoplasma ciconiae sp. nov. isolated from white stork nestlings (Ciconia ciconia). Int. J. Syst. Evol. Microbiol. 66, 3477–3484 (2016).
Google Scholar
Goldberg, D. R. et al. The occurrence of mycoplasmas in selected wild North American waterfowl. J. Wildl. Dis. 31, 364–371 (1995).
Google Scholar
Bradbury, J. M. et al. Isolation of mycoplasma cloacale from a number of different avian hosts in great Britain and France. Avian Pathol. 16, 183–186 (1987).
Google Scholar
Poveda, J. B. et al. An epizootiological study of avian mycoplasmas in Southern Spain. Avian Pathol. 19, 627–633 (1990).
Google Scholar
Brown, D. R., Whitcomb, R. F. & Bradbury, J. M. Revised minimal standards for description of new species of the class Mollicutes (division Tenericutes). Int. J. Syst. Evol. Microbiol. 57, 2703–2719 (2007).
Google Scholar
Volokhov, D. V., Simonyan, V., Davidson, M. K. & Chizhikov, V. E. RNA polymerase beta subunit (rpoB) gene and the 16S–23S rRNA intergenic transcribed spacer region (ITS) as complementary molecular markers in addition to the 16S rRNA gene for phylogenetic analysis and identification of the species of the family Mycoplasmataceae. Mol. Phylogenet. Evol. 62, 515–528 (2012).
Google Scholar
Hartup, B. K. & Kollias, G. V. Field investigation of Mycoplasma gallisepticum infections in house finch (Carpodacus mexicanus) eggs and nestlings. Avian Dis. 43, 572 (1999).
Google Scholar
Paessler, M. et al. Disseminated Mycoplasma orale infection in a patient with common variable immunodeficiency syndrome. Diagn. Microbiol. Infect. Dis. 44, 201–204 (2002).
Google Scholar
Nikfarjam, L. & Farzaneh, P. Prevention and detection of Mycoplasma contamination in cell culture. Cell J. 13, 203–212 (2012).
Google Scholar
Trinh, P., Zaneveld, J. R., Safranek, S. & Rabinowitz, P. M. One health relationships between human, animal, and environmental microbiomes: A mini-review. Front. Public Health 6, 1–9 (2018).
Google Scholar
Baron, S. A., Diene, S. M. & Rolain, J. Human microbiomes and antibiotic resistance. Hum. Microbiome J. 10, 43–52 (2018).
Google Scholar
Diaz-torres, M. L. et al. Determining the antibiotic resistance potential of the indigenous oral microbiota of humans using a metagenomic approach. FEMS Microbiol. Lett. 258, 257–262 (2006).
Google Scholar
Sommer, M. O. A., Dantas, G. & Church, G. M. Functional characterization of the antibiotic resistance reservoir in the human microflora. Science 325, 1128–1131 (2009).
Google Scholar
Atterby, C. et al. Increased prevalence of antibiotic-resistant E. coli in gulls sampled in Southcentral Alaska is associated with urban environments. Infect. Ecol. Epidemiol. 6, 32334 (2016).
Google Scholar
Allen, H. K., Donato, J., Wang, H. H. & Cloud-hansen, K. A. Call of the wild: Antibiotic resistance genes in natural environments. Nat. Rev. Microbiol. 8, 251–259 (2010).
Google Scholar
Wang, J. et al. The role of wildlife (wild birds) in the global transmission of antimicrobial resistance genes. Zool. Res. 38, 55–80 (2017).
Google Scholar
Brittingham, M. C., Temple, S. A. & Duncan, R. M. A survey of the prevalence of selected bacteria in wild birds. J. Wildl. Dis. 24, 299–307 (1988).
Google Scholar
Škaraban, J., Matjašič, T., Janžekovič, F., Wilharm, G. & Trček, J. Cultivable bacterial microbiota from choanae of free-living birds captured in Slovenia. Folia Biol. Geol. 58, 105 (2017).
Google Scholar
Stenkat, J., Krautwald-Junghanns, E., Schmitz Ornes, A., Eilers, A. & Schmidt, V. Aerobic cloacal and pharyngeal bacterial flora in six species of free-living birds. J. Appl. Microbiol. https://doi.org/10.1111/jam.12636 (2014).
Google Scholar
Ferguson-Noel, N., Armour, N. K., Noormohammadi, A. H., El-Gazzar, M. & Bradbury, J. M. Mycoplasmosis. In Diseases of Poultry (ed. Swayne, D. E.) (Wiley, 2020).
Ely, C. R. et al. Circumpolar variation in morphological characteristics of greater white-fronted geese Anser albifrons. Bird Study 52, 104–119 (2005).
Google Scholar
Deng, X. et al. Spring migration duration exceeds that of autumn migration in far east asian greater white-fronted geese (Anser albifrons). Avian Res. 10, 1–11 (2019).
Google Scholar
Kölzsch, A. et al. Towards a new understanding of migration timing : slower spring than autumn migration in geese refl ects different decision rules for stopover use and departure. Oikos https://doi.org/10.1111/oik.03121 (2016).
Google Scholar
Gonzalez, L. M. Origin and formation of the Spanish imperial eagle (Aquila adalberti). J. Ornithol. 149, 151–159 (2008).
Google Scholar
Shamoun-Baranes, J. et al. The effect of wind, season and latitude on the migration speed of white storks Ciconia ciconia, along the eastern migration route. J. Avian Biol. 34, 97–104 (2003).
Google Scholar
Birds of the World. Cornell Laboratory of Ornithology (2020). https://birdsoftheworld.org/bow/home. (Accessed 17 August 2020).
Lierz, M. et al. Prevalence of mycoplasmas in eggs from birds of prey using culture and a genus-specific mycoplasma polymerase chain reaction. Avian Pathol. 36, 145–150 (2007).
Google Scholar
Raviv, Z. & Kleven, S. H. The development of diagnostic real-time Taqman PCRs for the four pathogenic avian mycoplasmas. Avian Dis. 53, 103–107 (2009).
Google Scholar
Kumar, S., Stecher, G., Li, M., Knyaz, C. & Tamura, K. MEGA X: Molecular evolutionary genetics analysis across computing platforms. Mol. Biol. Evol. 35, 1547–1549 (2018).
Google Scholar
Mangiafico, S. rcompanion: Functions to support extension education program evaluation. R package version 2.3.26. (2020).
Wickham, H., Romain, F., Lionel, H. & Müller, K. dplyr: A grammar of data manipulation. R package version 0.8.1. (2019).
Wickham, H. ggplot2 Vol. 35 (Springer, 2016).
Google Scholar
R Core Team. R: A Language and Environment for Statistical Computing. Version 4.0.4. (Foundation for Statistical Computing, 2021). https://www.r-project.org/. (Accessed 20 October 2020).
Fair, J. M. et al. (eds) Guidelines to the Use of Wild Birds in Research 3rd edn. (The Ornithological Council, 2010).
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