Exploring the Biocontrol Capability of Non-Mycotoxigenic Strains of Penicillium expansum .
Belén LlobregatLuis González-CandelasAna Rosa BallesterPublished in: Toxins (2024)
Penicillium expansum is one the major postharvest pathogens of pome fruit during postharvest handling and storage. This fungus also produces patulin, which is a highly toxic mycotoxin that can contaminate infected fruits and their derived products and whose levels are regulated in many countries. In this study, we investigated the biocontrol potential of non-mycotoxigenic strains of Penicillium expansum against a mycotoxigenic strain. We analyzed the competitive behavior of two knockout mutants that were unable to produce patulin. The first mutant (∆ patK ) involved the deletion of the patK gene, which is the initial gene in patulin biosynthesis. The second mutant (∆ veA ) involved the deletion of veA , which is a global regulator of primary and secondary metabolism. At the phenotypic level, the ∆ patK mutant exhibited similar phenotypic characteristics to the wild-type strain. In contrast, the ∆ veA mutant displayed altered growth characteristics compared with the wild type, including reduced conidiation and abnormal conidiophores. Neither mutant produced patulin under the tested conditions. Under various stress conditions, the ∆ veA mutants exhibited reduced growth and conidiation when exposed to stressors, including cell membrane stress, oxidative stress, osmotic stress, and different pH values. However, no significant changes were observed in the ∆ patK mutant. In competitive growth experiments, the presence of non-mycotoxigenic strains reduced the population of the wild-type strain during in vitro growth. Furthermore, the addition of either of the non-mycotoxigenic strains resulted in a significant decrease in patulin levels. Overall, our results suggest the potential use of non-mycotoxigenic mutants, particularly ∆ patK mutants, as biocontrol agents to reduce patulin contamination in food and feed.
Keyphrases
- wild type
- escherichia coli
- oxidative stress
- human health
- transcription factor
- magnetic resonance
- risk assessment
- stress induced
- copy number
- dna damage
- gene expression
- multidrug resistant
- computed tomography
- ischemia reperfusion injury
- gram negative
- induced apoptosis
- climate change
- diabetic rats
- genome wide identification