Biology subjects

Gjennestad, R. S.

Publications and source records attributed to Gjennestad, R. S..

3 recordsLinked to original sources

bioRxiv2026

Cyclic di-AMP signalling affects cell division and penicillin susceptibility in Streptococcus pneumoniae.

Resistance to {beta}-lactam antibiotics in the human pathogen Streptococcus pneumoniae is mainly attributed to the acquisition of mutated versions of pbp2x, pbp2b and pbp1a, encoding functional penicillin binding proteins with reduced affinity to {beta}-lactams. This enables the bacterium to synthesise peptidoglycan required for cell division in the presence of higher {beta}-lactam concentrations. In addition, it has recently been shown that increased levels of the second messenger molecule cyclic di-AMP, resulting from mutations that compromise the cyclic di-AMP degrading phosphodiesterase Pde1, contribute to decreased {beta}-lactam susceptibility in this species. A link between cyclic di-AMP levels and beta-lactam resistance has also been reported in several other Gram-positive bacteria. Here, we further investigated this link in S. pneumoniae and present evidence supporting that cyclic di-AMP could be involved in regulation of cell division. We confirm that elevated cyclic di-AMP levels decreased penicillin susceptibility and cell size in pde1 mutants. Next, we show that low cyclic di-AMP levels had the opposite effects in which cells became more susceptible to penicillin and displayed an elongated morphology with multiple incomplete septa. Using fluorescence microscopy and bacterial two-hybrid assays, we found that proteins involved in cyclic di-AMP synthesis (CdaA, CdaR) and degradation (Pde1) were enriched around the division site and that they most probably interact with each other. Finally, we identified changes to the cell wall stem peptide composition of {Delta}pde1 cells. Together our findings indicate that cyclic di-AMP could function as a regulator of the division machinery.

microbiology↗

bioRxiv2025

The effect of MurM and a branched cell wall structure on penicillin resistance in Streptococcus pneumoniae

The aminoacyltransferase MurM is an important penicillin resistance determinant in Streptococcus pneumoniae. This enzyme attaches a serine or alanine to the dipeptide side chain of lipid II, resulting in branched muropeptides that can be crosslinked to stem peptides in the peptidoglycan layer by penicillin binding proteins (PBPs). Deletion of murM results in only linear muropeptides, and more importantly a significant reduction in resistance. Highly penicillin resistant pneumococci are known to express low-affinity PBPs, an altered MurM protein, and possess a highly branched cell wall structure. It has therefore been hypothesized that MurM, and thus branched muropeptides, are essential for resistance because they are better substrates for low-affinity PBPs. In this study, we found that neither the version of murM nor elevated levels of cell wall branching affected the resistance level. To further support this, we investigated whether branched muropeptide substrates compete better than linear versions with penicillin at the active site of low-affinity PBPs and quantified changes to the stem peptide composition of the resistant Pen6 strain in response to subinhibitory concentrations of penicillin. We found that the level of cell wall branching decreased during penicillin exposure. Together our results do not support the idea that elevated levels of branched muropeptides (more active MurM) are important for either the function of low-affinity PBPs or the cells response to penicillin. Nevertheless, since a functional MurM enzyme is important for resistance, we speculate that it might indirectly influence other functions related to cell wall synthesis and remodelling needed for a resistant phenotype. ImportanceA fundamental understanding of the mechanisms behind antibiotic resistance is needed to find strategies to extend the clinical relevance of existing drugs. This study explores the relationship between cell wall composition and penicillin resistance in Streptococcus pneumoniae. Here we confirm that branched peptide crosslinks in the cell wall are crucial for resistance but found no correlation between elevated branching levels and resistance. Our data suggest that the function of low-affinity penicillin binding proteins is not influenced by the lack of branched cell wall precursors. Instead, a branched cell wall might contribute to resistance via other cell wall biosynthesis and remodelling mechanisms. These insights could offer new perspectives on why a branched cell wall is important for penicillin resistance in pneumococci.

microbiology↗

bioRxiv2022

PAMP-Induced secreted Peptide-Like 6 (PIPL6) functions as an amplifier of plant immune response through RLK7 and WRKY33 module

Plant peptide hormones are engaged in the regulation of plant developmental programs and immunity. PAMP-Induced Peptide (PIP) hormones are new class of signaling peptide with diverse functional roles in the regulation of plant development and stress responses. In this study, we have investigated the function of PAMP-Induced secreted Peptide-Like 6 (PIPL6) as an amplifier of plant immunity against necrotrophic fungal pathogens in Arabidopsis thaliana. We have applied an integrated omics approach to unveil the function and downstream signaling pathways initiated by PIPL6. PIPL6 is highly and transiently induced by treatment with different elicitors. Exogenous application of synthetic peptide designed from the C-terminal conserved domain of PIPL6 resulted in strong transcriptional induction of many genes involved in the regulation of plant immunity. Further gene expression analysis revealed that induction of marker genes by PIPL6 peptide requires the receptor-like kinase 7 (RLK7). Immunoblotting and gene expression analysis demonstrated that exogenous applications of PIPL6 peptide activates MAPK6, MAPK3, and WRKY33 module in an RLK7-dependent manner. The levels of salicylic acid, jasmonic acid, camalexin, and glucosinolates were differentially regulated in PIPL6 knock-down and overexpression lines challenged by necrotrophic pathogen Botrytis cinerea. Bioassays using the necrotrophic fungal pathogens Botrytis cinerea and Alternaria brassicae showed that pipl6 knock-down lines were more susceptible to these pathogens while PIPL6 overexpression lines exhibited enhanced resistance. Altogether, these results indicate that the PIPL6 peptide functions as a new damage-associated molecular pattern (DAMP) and acts as an amplifier of Arabidopsis immunity.

plant biology↗