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Anna-Maria Dietl, PhD

Anna-Maria_DietlEMail: anna-maria.dietl@i-med.ac.at

Phone: +43/(0)512/9003-70217

Fax: +43/(0)512-9003-73100

 

Short curriculum

2008-2011 Bachelor studies in Biology at the Leopold-Franzens-University, Innsbruck
2011-2014

Master studies in Microbiology at the Leopold-Franzens-University, Innsbruck
Thesis: "The proteinogenic and non proteinogenic function of histidine in Aspergillus funigatus"

2014-2018 PhD studies at the Division of Molecular Biology, Biocenter, Innsbruck Medical University
Thesis: "Biosynthetic pathways of histidine, arginine, siroheme and B vitamins as antifungal drug targets in Aspergillus fumigatus". Program: HOROS
since 2019 Postdoc at the Division of Molecular Biology, Biocenter, Innsbruck Medical University

 

Research fields

Molecular microbiology

 

Publications

  1. Dietl A-M, Binder U, Shadkchan Y, Osherov N, Haas H (2018). Siroheme is essential for assimilation of nitrate and sulfate as well as detoxification of nitric oxide but dispensable for virulence of Aspergillus fumigatus. Front Microbiol, doi: 10.3389/fmicb.2018.02615.

  2. Dietl A-M, Meir Z, Shadkchan Y, Osherov N, Haas H (2018). Riboflavin and Pantothenic acid biosynthesis are crucial for iron homeostasis and virulence in the pathogenic mold Aspergillus fumigatus. Virulence, doi: 10.1080/21505594.2018.1482181.

  3. Jahreis S, Böttcher S, Hartung S, Rachow T, Rummler S, DietlA-M, Haas H, Walther G, Hochhaus A, von Lilienfeld-Toal M(2018). Human MAIT cells are rapidly activated by clinically relevant Aspergillusssp. in an antigen presenting cell-dependent manner. Eur J Immunol, doi: 10.1002/eji.201747312.

  4. Kurucz V, Krüger T, Antal K, Dietl A-M, Haas H, Pócsi I, Kniemeyer O, Tamas E(2018). Additional oxidative stress reroutes the global response of Aspergillus fumigatusto iron depletion. BMC Genomics, 19:357. doi: 10.1186/s12864-018-4730-x.

  5.  Sass G, Nazik H, Penner J, Shah H, Ansari SR, Clemons KV, Groleau M-C, Dietl A-M, Visca P, Haas H, Déziel E, Stevens DA (2018).Aspergillus-Pseudomonasinteraction, relative to competition.Med Mycol, doi: 10.1093/mmy/myy087.

  6. Sass G, Nazik H, Penner J, Shah H, Ansari SR, Clemons KV, Groleau M-C, Dietl A-M, Visca P, Haas H, Déziel E, Stevens DA (2017). Studies of Pseudomonas aeruginosa mutants indicate pyoverdine as the central factor in inhibition of Aspergillus fumigatusbiofilm. J Bacteriol 1:345-17, doi: 10.1128/JB.00345-17.

  7. Dietl A-M, Amich J, Leal S, Beckmann N, Binder U, Beilhack A, Pearlman E, Haas H (2016). Histidine biosynthesis plays a crucial role in metal homeostasis and virulence of Aspergillus fumigatus. Virulence 6:1-12., doi:10.1080/21505594.2016.1146848.

  8. Kaltdorf M, Srivastava M, Gupta SK, Liang C, Binder J, Dietl A-M, Meir Z, Haas H, Osherov N, Krappmann S, Dandekar T (2016). Systematic identification of anti-fungal drug targets by a metabolic network approach. Front Mol Biosci 3:22, doi: 10.3389/fmolb.2016.00022.

  9. Ben Yaakov D, Rivkin A, Mircus G, Albert N, Dietl AM, Kovalerchick D, Carmeli S, Haas H, Kontoyiannis DP, Osherov N (2016). Identification and characterization of haemofungin, a novel antifungal compound that inhibits the final step of haem biosynthesis. J Antimicrob Chemother. 71(4):946-52. doi: 10.1093/jac/dkv446. 

Institut für Molekularbiologie