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Written informed consent was obtained from the patient. Throughout the study, all hospital and research staff adhered to the Good Clinical Practice guidelines of the 2013 Declaration of Helsinki and the general guidelines 86\/609\/EEC and 2000\/54\/EC for the protection of the European Community due to the handling of potentially infectious materials.","order":1,"name":"Ethics","label":"Ethics approval","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"All animal experiments were performed in accordance with the Czech Animal Protection Act (No. 246\/1992) and were approved by the Czech Ministry of Education, Youth, and Sports (MSMT-9487\/2019-5) and the Animal Welfare Committee of the Faculty of Medicine and Dentistry, Palack\u00fd University in Olomouc.","order":2,"name":"Ethics","label":"Animal welfare","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"Rat lung and urine samples were obtained from the LEWIS rat pulmonary mucormycosis model described in this study. The human BAL specimen was obtained from a patient with pulmonary mucormycosis under the approval of the Ethical Panel of University Hospital Innsbruck.","order":3,"name":"Ethics","label":"Source of biological material","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The authors declare no competing interests.","order":4,"name":"Ethics","label":"Competing interests","group":{"name":"EthicsHeading","label":"Declarations"}}]}}