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Brief Reports

Novel fluconazole-resistant zoonotic yeast isolated from mastitis

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References

  • Chakrabarti A, Rudramurthy SM, Kale P, et al. Epidemiological study of a large cluster of fungaemia cases due to Kodamaea ohmeri in an Indian tertiary care centre. Clin Microbiol Infect. 2014;20(2):O83–O89.
  • Borelli BM, Ferreira EG, Lacerda ICA, Franco GR, Rosa CA. Yeast populations associated with the artisanal cheese produced in the region of Serra da Canastra. World J Microbiol Biotechnol. 2006;22(11):1115–1119.
  • Diallo K, Lefevre B, Cadelis G, et al. A case report of fungemia due to Kodamaea ohmeri. BMC Infect Dis. 2019;19(1):570.
  • González-Avila M, Gómez-Gómez JV, Texis APE, Imbert-Palafox JL, Becerril-Flores MA, Blasco JL. Uncommon fungi isolated from diabetic patients toenails with or without visible onychomycoses. Mycopathologia. 2011;172(3):207–213.
  • Al-Sweih N, Khan ZU, Ahmad S, et al. Kodamaea ohmeri as an emerging pathogen: a case report and review of the literature. Med Mycol. 2011;49(7):766–770.
  • Chiu CH, Wang YC, Shang ST, Chang FY. Kodamaea ohmeri fungaemia successfully treated with caspofungin. Int J Antimicrob Agents. 2010;35(1):98–99.
  • Menon T, Herrera M, Periasamy S, Palanivelu V, Sikhamani R, Wickes B. Oral candidiasis caused by Kodamaea ohmeri in a HIV patient in Chennai, India. Mycoses. 2010;53(5):458–459.
  • Sundaram PS, Bijulal S, Tharakan JA, Antony M. Kodamaea ohmeri tricuspid valve endocarditis with right ventricular inflow obstruction in a neonate with structurally normal heart. Ann Pediatr Cardiol. 2011;4(1):77–80.
  • García-Tapia A, García-Agudo R, Marín P, Conejo JL, García-Martos P. Kodamaea ohmeri fungemia associated with surgery. Rev Iberoam Micol. 2007;24(2):155–156.
  • Han XY, Tarrand JJ, Escudero E. Infections by the yeast Kodomaea (Pichia) ohmeri: two cases and literature review. Eur J Clin Microbiol Infect Dis. 2004;23(2):127–130.
  • Manzano-Gayosso P, Hernández-Hernández F, Méndez-Tovar LJ, et al. Onychomycosis incidence in type 2 diabetes mellitus patients. Mycopathologia. 2008;166(1):41–45.
  • Puerto JL, García-Martos P, Saldarreaga A, Ruiz-Aragón J, García-Agudo R, Aoufi S. First report of urinary tract infection due to Pichia ohmeri. Eur J Clin Microbiol Infect Dis. 2002;21(8):630–631.
  • Yang BH, Peng MY, Hou SJ, Sun JR, Lee SY, Lu JJ. Fluconazole-resistant Kodamaea ohmeri fungemia associated with cellulitis: case report and review of the literature. Int J Infect Dis. 2009;13(6):e493–e497.
  • Gaudie CM, Wragg PN, Barber AM. Outbreak of disease due to Candida krusei in a small dairy herd in the UK. Vet Rec. 2009;165(18):535–537.
  • Spanamberg A, Wünder EA, Brayer Pereira DI, et al. Diversity of yeast from bovine mastitis in Southern Brazil. Rev Iberoam Micol. 2008;25(3):154–156.
  • Tarfarosh MA, Purohit SK. Isolation of Candida spp. from mastitic cows and milkers. Acta Vet Scand. 2008;3:14.
  • Pengov A. Prevalence of mycotic mastitis in cows. Acta Vet. 2002;52(2–3):133–136.
  • Capoor MR, Nair D, Deb M, Verma PK, Srivastava L, Aggarwal P. Emergence of non-albicans Candida species and antifungal resistance in a tertiary care hospital. Jpn J Infect Dis. 2005;58(6):344–348.
  • Vaezi A, Fakhim H, Khodavaisy S, et al. Epidemiological and mycological characteristics of candidemia in Iran: a systematic review and meta-analysis. J Mycol Med. 2017;27(2):146–152.
  • Vlek A, Kolecka A, Khayhan K, Theelen B, Groenewald M, Boel E, et al. Interlaboratory comparison of sample preparation methods, database expansions, and cutoff values for identification of yeasts by matrix-assisted laser desorption ionization-time of flight mass spectrometry using a yeast test panel. J Clin Microbiol. 2014;52(8):3023–3029.
  • Quindos G, Vargas RA, Helou S. Evaluación micolo ’gica de un nuevo medio de cultivo cromógeno (Candida ID_) para el aislamiento e identificación presuntiva de Candida albicans. Rev Iberoam Micol. 2001;18:23.
  • Aslani N, Janbabaei G, Abastabar M, et al. Identification of uncommon oral yeasts from cancer patients by MALDI-TOF mass spectrometry. BMC Infect Dis. 2018;18(1):24.
  • Clinical and Laboratory Standards Institute. 2017. Summary Minutes. Subcommittee on Antifungal Susceptibility Tests. Tampa, FL: Clinical and Laboratory Standards Institute.
  • Clinical and Laboratory Standards Institute. 2020. Epidemiological Cutoff Values for Antifungal Susceptibility Testing. Tampa, FL: Clinical and Laboratory Standards Institute.
  • El-Sharoud WM, Belloch C, Peris D, Querol A. Molecular identification of yeasts associated with traditional Egyptian dairy products. J Food Sci. 2009;74(7):M341–M346.
  • White TJ, Bruns T, Lee S, Taylor J. Amplification and direct sequence of fungal ribosomal RNA genes for phylogenetics. In: Innes MA, Gelfan DH, Sninsky JJ, White TJ, eds. PCR Protocols: A Guide to Methods and Applications. San Diego, CA: Academic Press Incorporation; 1990:115–122.
  • Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33(7):1870–1874.
  • Bangar YC, Verma MR, Dohare AK, Mukherjee R. Meta-analysis of prevalence of clinical mastitis in crossbred cows in India (1995-2014). J Anim Res. 2016; 6(6):933–938.
  • Tarazona-Manrique LE, Villate-Hernández JR, Andrade-Becerra RJ. Bacterial and fungal infectious etiology causing mastitis in dairy cows in the highlands of Boyacá (Colombia). Rev Med Vet Zoot. 2019;66(3):208–218.
  • Pote ST, Sonawane MS, Rahi P, Shah SR, et al. Distribution of pathogenic yeasts in different clinical samples: their identification, antifungal susceptibility pattern, and cell invasion assays. Infect Drug Resist. 2020;13:1133–1145.
  • Santos RC, Marin JM. Isolation of Candida spp. from mastitic bovine milk in Brazil. Mycopathologia. 2005;159(2):251–253.
  • Krukowski H, Tietze M, Majewski T, Rózanski P. Survey of yeast mastitis in dairy herds of small-type farms in the Lublin region, Poland. Mycopathologia. 2001;150(1):5–7.
  • Lee JS, Shin JH, Kim M-N, et al. Kodamaea ohmeri isolates from patients in a university hospital: identification, antifungal susceptibility, and pulsed-field gel electrophoresis analysis. J Clin Microbiol. 2007;45(3):1005–1010.
  • Seng P, Rolain JM, Fournier PE, La Scola B, Drancourt M, Raoult D. MALDI-TOF-mass spectrometry applications in clinical microbiology. Future Microbiol. 2010;5(11):1733–1754.
  • Posteraro B, De Carolis E, Vella A, Sanguinetti M. MALDI-TOF mass spectrometry in the clinical mycology laboratory: identification of fungi and beyond. Expert Rev Proteomics. 2013;10 (2):151–164.
  • Cobo F. Application of MALDI-TOF mass spectrometry in clinical virology: a review. Open Virol J. 2013;7:84–90.
  • Singhal N, Kumar M, Kanaujia PK, Virdi JS. MALDI-TOF mass spectrometry: an emerging technology for microbial identification and diagnosis. Front Microbiol. 2015;6:791.
  • Calderaro A, Piergianni M, Montecchini S, et al. MALDI-TOF mass spectrometry as a potential tool for Trichomonas vaginalis identification. BMC Infect Dis. 2016;16:261.
  • Tsuchida S, Umemura H, Nakayama T. Current Status of Matrix-assisted laser desorption/ionization–time-of-flight mass spectrometry (MALDI-TOF MS) in clinical diagnostic microbiology. Molecules. 2020;25:4775.
  • Leaw SN, Chang HC, Sun HF, Barton R, Bouchara JP, Chang TC. Identification of medically important yeast species by sequence analysis of the internal transcribed spacer regions. J Clin Microbiol. 2006;44(3):693–699.
  • Martins HPR, da Silva MC, Paiva LCF, Svidzinski TIE, Consolaro MEL. Efficacy of fluconazole and nystatin in the treatment of vaginal Candida species. Acta Derm Venereol. 2012;92(1):78–82.
  • Seker E. Identification of Candida species isolated from Bovine mastitic milk and their in vitro hemolytic activity in Western Turkey. Mycopathologia. 2010;169:303.
  • Hogeveen H, Steeneveld W, Wolf CA. Production diseases reduce the efficiency of dairy production: a review of the results, methods, and approaches regarding the economics of mastitis. Annu Rev Resour Econ. 2019;11(1):289–312.
  • Romero J, Benavides E, Meza C. Assessing financial impacts of subclinical mastitis on Colombian dairy farms. Front Vet Sci. 2018;5:273.
  • Kivaria FM, Noordhuizen JPTM. A retrospective study of the aetiology and temporal distribution of bovine clinical mastitis in smallholder herds in the Dar es Salaam region of Tanzania. Vet. J. 2007;173(3):617–622.
  • Krukowski H, Lisowski A, Rózański P, Skórka A. Yeasts and algae isolated from cows with mastitis in the south-eastern part of Poland. Pol J Vet Sci. 2006;9(3):181–184.

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