bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.07.14.664712

A chemically defined medium to support the growth of food-relevant Bacillus species

Abstract

The Bacillus genus contains many members with food significance, including the food-grade Bacillus subtilis clade often used in fermentations and the pathogenic Bacillus cereus clade. Chemically defined media for Bacillus species are crucial tools to allow detailed investigations of the influence of specific nutrients on growth and also improve reproducibility and consistency of experiments. Previous studies have focused on the development of defined media for single species, while the aim of this study was to develop a chemically defined medium that supports the growth of multiple food relevant Bacillus species. The new medium, Pafoba, was tested using two pathogenic strains of the Bacillus cereus clade and eleven strains of the Bacillus subtilis clade representing seven different clade members. All thirteen Bacillus strains were able to grow on Pafoba, of which ten displayed a similar or higher maximum OD600 on Pafoba medium compared to rich medium (Brain Heart Infusion broth). Detailed analysis revealed a biotin requirement for Bacillus subtilis strain PRO64, and the necessity of including essential amino acids for Bacillus weihenstephanensis and Bacillus cereus strains. In conclusion, the chemically defined Pafoba medium provides a controlled and reproducible growth environment for fundamental studies and is suitable for detection and enumeration of a broad range of Bacillus spp. related to food processing and safety. ImportanceBacillus species are important in both food fermentation and food safety. While members of the Bacillus subtilis clade are used in the production of fermented foods, those in the Bacillus cereus group are associated with foodborne illness. This study presents a chemically defined medium that supports the growth of multiple food-relevant Bacillus species, enabling precise control over nutrient composition. Knowledge of Bacillus cereus metabolism under defined conditions is essential to support efforts in food safety, risk assessment, and the development of targeted intervention strategies. Likewise, an understanding of Bacillus subtilis metabolism under defined conditions is essential to optimize fermentation processes, improve product consistency, and enhance functional food development. By providing a standardized and reproducible growth environment, the medium developed in this study will facilitate research that advances both microbial food safety and the controlled use of beneficial Bacillus strains in food production.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Canoy, T. S., Wiedenbein, E. S., McPhillips, C., Jespersen, L., Roder, H. L., Nielsen, D. S.. 2025-07-15. A chemically defined medium to support the growth of food-relevant Bacillus species. https://doi.org/10.1101/2025.07.14.664712

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

pTRIP, a novel integration plasmid for Listeria monocytogenes

In the past decades, several tools to genetically modify the human pathogen Listeria monocytogenes were developed. Here, we constructed a new integrative plasmid system for L. monocytogenes named pTRIP, for treB insertion plasmid. pTRIP is a vector which stably integrates into the treB locus of the wild type EGD-e. This locus encodes the sole trehalose-specific EIIB and EIIC component of a phosphotransferase system. Successful integration leads to the disruption of treB and thus, to an inability of the resulting L. monocytogenes strains to grow on trehalose as sole carbon source. Due to integration through double homologous recombination, it is the first integrative system which does not require antibiotic selection pressure. To assess functionality of the pTRIP system, prfA and its native promoter region were integrated into the treB locus of a {Delta}prfA strain. Complementation was confirmed in 78% of the isolated clones, indicating successful integration of prfA into the treB locus. We further constructed derivatives of pTRIP harboring the constitutive Pp60 (pTRIP1) and the inducible Prha (pTRIP2) promoter to further expand application possibilities. Microscopic analyses confirmed the functionality of both promoter constructs and showed dose-dependent induction for Prha. pTRIP is an efficient tool for stable gene expression as well as functional studies and expands genetic modification possibilities for L. monocytogenes.

microbiology↗

A rational design strategy and validation for protease-resistant fusion-inhibitor antiviral peptides

Peptide-based fusion inhibitors are promising pharmaceuticals in the fight against enveloped viruses relying on membrane fusion for host infection. However, peptide therapeutic applications have long been hindered by their poor stability in vivo. Here, we discovered that peptide inhibitors with the wildtype sequence of the heptad repeat 2 (HR2) domain of the SARS-CoV-2 spike protein are efficiently cleaved by Transmembrane Protease, Serine 2 (TMPRSS2), a key protease involved in the SARS-CoV-2 virus-cell fusion pathway. We then identified the corresponding cleavage sites and designed three protease-resistant peptides using ranking based on deep mutational scanning and natural occurrence. The three candidates all exhibit inhibitory activity in a cell-cell fusion assay. A high-resolution cryo-EM structure of the top candidate, HR2-NHN, bound to its HR1 target reveals the molecular basis for its potent activity. The top candidate of the cell-based screening assay significantly improved efficacy relative to the wildtype peptide when administered 12 h before infection in both an authentic virus-cell infection assay and a mouse assay. More broadly, our results suggest that the design strategies for protease-resistant peptides could be applied to a broad spectrum of other enveloped viruses and pave the way for the development of safe, prophylactic antivirals that can be administered before exposure.

microbiology↗

Host soluble inositol phosphate signaling promotes coronavirus replication

Coronaviruses rely extensively on host pathways for replication, making host-directed therapies an attractive strategy for broad-spectrum antivirals with reduced risk of viral resistance. Here we identify the host soluble inositol phosphate pathway as a previously unrecognized dependency for coronavirus infection. Genetic or pharmacologic inhibition of several kinases in this pathway markedly suppresses replication of both alpha- and betacoronaviruses, while increasing pathway activity promotes viral replication. We developed UNC7844, a potent multi-target inhibitor of these kinases, which reduces coronavirus replication by more than four orders of magnitude in cultured cells and suppresses coronavirus infection in mice. Mechanistically, UNC7844 suppresses inositol (pyro)phosphates production, disrupts phosphoinositide homeostasis, and impairs late endosomal dynamics, blocking early post-entry steps required for viral genome release and replication. Together, our findings establish the soluble inositol (pyro)phosphate pathway as an important regulator of coronavirus infection and highlight its inhibition as a promising host-directed antiviral strategy.

microbiology↗