5–7 Oct 2026
Harnack-Haus
Europe/Berlin timezone

Functional dissection of the Bacillus subtilis SPβ prophage lysogeny-lysis system

5 Oct 2026, 16:55
20m
Goethe-Saal (Harnack-Haus)

Goethe-Saal

Harnack-Haus

Short-talk only Cellular organisation and regulation of the viral infection cycle Organisation and regulation of the viral infection cycle

Speakers

Fabian M. Commichau (Institute for Biology, FG Molecular Microbiology, University of Hohenheim, Stuttgart, Germany) Katharina Kohm

Description

SPβ-like phages possess a unique lysogeny control system [1]. Our recent work identified the master repressor of SPβ and an essential activator of the lytic cycle [2]; however, the regulatory network governing the lysis-lysogeny decision requires further elucidation [1]. Furthermore, fundamental mechanisms such as virion assembly or the adsorption of SPβ to its bacterial hosts remain poorly understood [3].

We are using time-resolved quantitative proteomics to gain a better understanding of the regulatory dynamics of SPβ. This involves studying (1) MrpR-dependent induction and (2) infection. Analyses of a non-inducible lysogen and an inducible lysogen revealed different dynamics of phage protein accumulation following induction. Time-resolved proteomics suggests that the absence of yosL affects the temporal organization and/or progression of the lytic phage program. Moreover, the study is investigating which temporal changes in the bacterial proteome are associated with successful lytic induction. During phage infection a rapid and sequential accumulation of phage proteins occurs. Most phage proteins were first detected during the early phase of infection, whilst other proteins accumulated at a later stage. This suggests a staggered expression program during infection.

In addition, we investigated the mechanisms underlying phage–host recognition. Isolation and whole-genome sequencing of B. subtilis strains resistant to SPβ infection confirmed the involvement of the minor teichoic acid biosynthesis genes ggaA and ggaB in phage resistance [4]. To identify a potential secondary receptor involved in SPβ adsorption or entry, transposon mutagenesis is currently being employed.

Reference #2

[2] Kohm K, Jalomo-Kharyova E, Krüger A, Basu S, Steinchen W, Bange G, Frunzke J, Hertel R, Commichau FM, Czech L (2023b) Structural and functional characterization of MrpR, the master repressor of the Bacillus subtilis prophage SPβ. Nucleic Acids Res. 51: 9452-9474.

Reference #1

[1] Kohm K, v. Clanner A, Hertel R, Commichau FM (2025) Closely related and yet special - how SPβ phages control lysis-lysogeny decisions. Trends Microbiol. 33: 387-396.

Reference #3

[3] Kohm K Hertel R (2021) The life cycle of SPβ and related phages. Arch Virol 166: 2119-2130.
[4] Estrela AI, De Lencastre H, Archer LJ (1986) Resistance of a Bacillus subtilis mutant to a group of temperate bacteriophages. Microbiology 132:411–415.

Author

Katharina Kohm

Co-authors

Robert Warneke (Institute for Biotechnology, FG Bioanalytic, TU Berlin, Germany) Najiba Azemi (Institute for Biotechnology, FG Bioanalytic, TU Berlin, Germany) Juri Rappsilber (Institute for Biotechnology, FG Bioanalytic, TU Berlin, Germany) Fabian M. Commichau (Institute for Biology, FG Molecular Microbiology, University of Hohenheim, Stuttgart, Germany)

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