Research Areas
- Evolutionary Physiology
- Eco-Immunology
Doctoral Thesis
The molecular underpinnings of phenotypic plasticity in Tribolium castaneum immune responses
- Supervisors
- Doctoral Subject
- Biologie
- Doctoral Degree
- Dr. rer. nat.
- Awarded by
- Department 13 – Biology
CV
Education
Positions
Projects
in process
- The influence of parasite diversity on the evolution and function of the immune system of the Mexcian Cavefish, Astyanax mexicanus (since )
Own resources project - CRC TRR 212 B06 - Genetic and phenotypic characterisation of immunological niche conformance in cavefish ( – )
Subproject in DFG-joint project hosted outside WWU: DFG - Collaborative Research Centre | Project Number: TRR 212/2
finished
- SPP 1399 - Work package: Coevulution between Tribolium castaneum and Bacillus thuringiensis: On the evolutionary significance of genetic specificity and specific immunity. ( – )
Subproject in DFG-joint project hosted at WWU: DFG - Priority Programme | Project Number: KU 1929/4-1:1
- The influence of parasite diversity on the evolution and function of the immune system of the Mexcian Cavefish, Astyanax mexicanus (since )
Publications
- . . ‘Metabolic reprogramming underlies cavefish muscular endurance despite loss of muscle mass and contractility.’ Proceedings of the National Academy of Sciences of the United States of America (PNAS) 120, No. 5. doi: 10.1073/pnas.2204427120.
- . . ‘Paternal knockdown of tRNA (cytosine-5-)-methyltransferase (Dnmt2 ) increases offspring susceptibility to infection in red flour beetles.’ Insect Molecular Biology 2022. doi: 10.1111/imb.12798.
- . . ‘Liver-derived cell lines from cavefish Astyanax mexicanus as an in vitro model for studying metabolic adaptation.’ Scientific Reports 12, No. 10115. doi: 10.1038/s41598-022-14507-0.
- . . ‘The metabolome of Mexican cavefish shows a convergent signature highlighting sugar, antioxidant, and Ageing-Related metabolites.’ eLife 11, No. e74539. doi: 10.7554/eLife.74539.
- . . ‘Genome-wide analysis of cis-regulatory changes underlying metabolic adaptation of cavefish.’ Nature Genetics 54: 684–693. doi: 10.1038/s41588-022-01049-4.
- . . ‘Enhanced lipogenesis through Pparγ helps cavefish adapt to food scarcity.’ Current biology . doi: 10.1016/j.cub.2022.03.038.
- . . ‘Image3C, a multimodal image-based and label-independent integrative method for single-cell analysis.’ eLife 10: e65372C1 - eLife 2021;10:e65372DO - 10.7554/eLife.65372. doi: 10.7554/eLife.65372.
- . . ‘A chromosome-level genome of Astyanax mexicanus surface fish for comparing population-specific genetic differences contributing to trait evolution.’ Nature Communications 12, No. 1: 1447. doi: 10.1038/s41467-021-21733-zDO-10.1038/s41467-021-21733-z.
- . . ‘Adaptation to low parasite abundance affects immune investment and immunopathological responses of cavefish.’ Nature Ecology and Evolution 2020. doi: 10.1038/s41559-020-1234-2.
- . . ‘Comparative transcriptome analysis of wild and lab populations of Astyanax mexicanus uncovers differential effects of environment and morphotype on gene expression.’ Journal of Experimental Zoology Part B: Molecular and Developmental Evolution 1-10. doi: 10.1002/jez.b.22933.
- . . ‘Experimental evolution of immunological specificity.’ Proceedings of the National Academy of Sciences 116. doi: 10.1073/pnas.1904828116.
- . . ‘An Adult Brain Atlas Reveals Broad Neuroanatomical Changes in Independently Evolved Populations of Mexican Cavefish .’ Frontiers in Neuroanatomy 13: 88. doi: 10.3389/fnana.2019.00088.
- . . ‘Gamete Collection and In Vitro Fertilization of Astyanax mexicanus.’ Journal of Visualized Experiments 2019, No. 147: e59334.
- . . ‘Stable transgenesis in Astyanax mexicanus using the Tol2 transposase system.’ Developmental Dynamics 248, No. 8: 679–687. doi: 10.1002/dvdy.32.
- . . ‘Early adipogenesis contributes to excess fat accumulation in cave populations of Astyanax mexicanus.’ Developmental Biology 441, No. 2: 297–304. doi: 10.1016/j.ydbio.2018.06.003.
- . . ‘Insulin resistance in cavefish as an adaptation to a nutrient-limited environment.’ Nature 555, No. 7698: 647–651. doi: 10.1038/nature26136.
- . . ‘Oral immune priming with Bacillus thuringiensis induces a shift in the gene expression of Tribolium castaneum larvae.’ BMC Genomics 18, No. 1: 329.
- . . ‘Immune priming in arthropods: an update focusing on the red flour beetle.’ Zoology 119. doi: 10.1016/j.zool.2016.03.006.
- . . ‘Down syndrome cell adhesion molecule 1: testing for a role in insect immunity, behaviour and reproduction.’ Royal Society Open Science 3, No. 4: 160138.
- . . ‘Downregulation of the evolutionary capacitor Hsp90 is mediated by social cues.’ Proceedings of the Royal Society of London B 282. doi: 10.1098/rspb.2015.2041.
- . . ‘Dscam and pancrustacean immune memory - A review of the evidence.’ Developmental and Comparative Immunology 48. doi: 10.1016/j.dci.2014.03.004.
- . . ‘Infection routes matter in population-specific responses of the red flour beetle to the entomopathogen Bacillus thuringiensis.’ BMC Genomics 16, No. 1: 445.
- . . ‘The red flour beetle as a model for bacterial oral infections.’ PloS one 8. doi: 10.1371/journal.pone.0064638.
Dr. Robert Peuß
