Author

B. Krismer

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Microbiology· 5

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 5 Organism:human· 5 Research Focus:host-pathogen & immune response· 4 Research Focus:cell type annotation· 2 Assay:proteomics· 2 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:drug response / drug discovery· 1 Research Focus:ecology & biodiversity· 1

Frequent Co-Authors

A. Peschel· 4 shared S. Heilbronner· 3 shared D. Gerlach· 2 shared R. Rosenstein· 2 shared A. Bitzer· 1 shared A. Elsherbini· 1 shared A. Geyer· 1 shared A. Kraus· 1 shared

Activity by Year

2020-2024 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

4 shared papersMicrobiology

A. Peschel

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

Probiotic Lactobacilli activate Formyl-Peptide Receptor 2

D. Kretschmer, R. Rosenstein, A. Elsherbini, B. Krismer, P. OToole, D. Gerlach, A. Peschel

This study identifies peptides from probiotic lactobacilli that activate FPR2, promoting immune responses and potentially treating inflammatory gut diseases.

bioRxiv · May 7, 2024 · PreprintMicrobiology

Siderophore piracy enables the nasal commensal Staphylococcus lugdunensis to antagonize the pathogen Staphylococcus aureus

R. Rosenstein, B. O. T. Salazar, C. Sauer, S. Heilbronner, B. Krismer, A. Peschel

This study shows that Staphylococcus lugdunensis reduces S. aureus colonization by producing lugdunin, and that mutualistic interactions with other commensals enhance its growth through siderophore piracy.

bioRxiv · Feb 29, 2024 · PreprintMicrobiology

Nasal commensals reduce Staphylococcus aureus proliferation by restricting siderophore availability

Y. Zhao, A. Bitzer, J. J. Power, D. Belikova, B. Torres-Salazar, L. A. Adolf, D. Gerlach, B. Krismer, S. Heilbronner

The paper shows nasal commensals reduce S. aureus growth by consuming its siderophores, revealing inter-species competition and potential for probiotic strategies.

bioRxiv · Feb 20, 2024 · PreprintMicrobiology

Horizontal transfer of bacteriocin biosynthesis genes requires metabolic adaptation to improve compound production and cellular fitness

S. Krauss, T. A. Harbig, J. Rapp, T. Schäfle, M. Franz-Wachtel, L. Reetz, A. M. A. Elsherbini, B. Macek, S. Grond, H. Link, K. Nieselt, B. Krismer, A. Peschel, S. Heilbronner

This study shows that transferring bacteriocin biosynthesis genes between Staphylococcus aureus strains requires metabolic adaptation to enhance compound production and cellular fitness.

bioRxiv · Jul 28, 2022Microbiology

Sensitizing Staphylococcus aureus to antibacterial host defense by decoding and blocking the lipid flippase MprF

C. J. Slavetinsky, J. N. Hauser, C. Gekeler, J. Slavetinsky, A. Geyer, A. Kraus, D. Heilingbrunner, S. Wagner, M. Tesar, B. Krismer, S. Kuhn, C. M. Ernst, A. Peschel

This study develops MprF-targeting monoclonal antibodies that block the lipid flippase MprF, increasing MRSA susceptibility to antimicrobial peptides and antibiotics.

bioRxiv · Nov 12, 2020Microbiology