Aeromonas hydrophila, a Gram-negative bacterium widely found in freshwater environments, acts as a common conditional pathogen affecting humans, livestock, and aquatic animals. In this study, the impact of oridonin, an ent-kaurane diterpenoid compound derived from Rabdosia rubescens, on the virulence factors of A. hydrophila AS 1.1801 and its antibacterial mechanism was elucidated. The minimum inhibitory concentration (MIC) of oridonin against A. hydrophila AS 1.1801 was 100 μg/mL. Oridonin at inhibitory concentrations could significantly increase the electrical conductivity in the supernatant and escalate nucleic acid leakage (p < 0.01). This effect was concomitant with observed distortions in bacterial cells, the formation of cytoplasmic cavities, cellular damage, and pronounced inhibition of protein and nucleic acid synthesis. Additionally, oridonin at inhibitory levels exhibited a noteworthy suppressive impact on A. hydrophila AS 1.1801 across biofilm formation, motility, hemolytic activity, lipase activity, and protease activity (p < 0.05), demonstrating a dose-dependent enhancement. qRT-PCR analysis showed that the gene expression of luxR, qseB and omp were significantly downregulated after oridonin treatment in A. hydrophila AS 1.1801 (p < 0.05). Our results indicated that oridonin possessed significant antibacterial and anti-virulence effects on A. hydrophila AS 1.1801.

The regulation of plant biomass degradation by fungi is critical to the carbon cycle, and applications in bioproducts and biocontrol. Trichoderma harzianum is an important plant biomass degrader, enzyme producer, and biocontrol agent, but few putative major transcriptional regulators have been deleted in this species. The T. harzianum ortholog of the transcriptional activator XYR1/XlnR/XLR-1 was deleted, and the mutant strains were analyzed through growth profiling, enzymatic activities, and transcriptomics on cellulose. From plate cultures, the Δxyr1 mutant had reduced growth on D-xylose, xylan, and cellulose, and from shake-flask cultures with cellulose, the Δxyr1 mutant had ~90% lower β-glucosidase activity, and no detectable β-xylosidase or cellulase activity. The comparison of the transcriptomes from 18 h shake-flask cultures on D-fructose, without a carbon source, and cellulose, showed major effects of XYR1 deletion whereby the Δxyr1 mutant on cellulose was transcriptionally most similar to the cultures without a carbon source. The cellulose induced 43 plant biomass-degrading CAZymes including xylanases as well as cellulases, and most of these had massively lower expression in the Δxyr1 mutant. The expression of a subset of carbon catabolic enzymes, other transcription factors, and sugar transporters was also lower in the Δxyr1 mutant on cellulose. In summary, T. harzianum XYR1 is the master regulator of cellulases and xylanases, as well as regulating carbon catabolic enzymes.

The Bemisia tabaci species complex threatens worldwide agriculture. While host-plant resistance is sustainable and effective, it is a relatively unexplored strategy for whitefly control. Three alfalfa (Medicago sativa L.) populations were developed and used in high-throughput B. tabaci MEAM1 nymph-mortality screens. The phenotypic resistance/susceptibility spectrum in these populations indicated that whitefly resistance to MEAM1 is multigenic. Alfalfa lines highly resistant (R1, R2, and R3) and susceptible (S1) to B. tabaci MEAM1 were identified and further characterized. When life history parameters for three B. tabaci species (MEAM1, MED and NW1) were assessed on the four lines, whitefly species-specific responses to R1, R2 and R3 plants were revealed. While nymph mortality was high for MEAM1 and NW1 on resistant alfalfa, MED nymph development was surprisingly unimpaired. In addition, significant differences in oviposition, host-choice and longevity were observed amongst the three B. tabaci species. Collectively, these data indicated that R1, R2 and R3 plants each express a unique set of antibiotic/antixenotic resistance traits providing a potent multigenic and multi-faceted resistance to whiteflies with each B. tabaci species displaying distinct behaviors on the resistant lines. Our nymph-mortality simulation models indicate that deployment of the nymph mortality-mediated resistance of R1 and R3 alfalfa could substantially suppress whitefly population expansion in the field.

Microbial spoilage significantly limits meat shelf life, necessitating degradable packaging with strong antibacterial properties. Oridonin (ORI), effective against foodborne pathogens, was incorporated into a polyvinyl alcohol (PVA)/chitosan (CS) matrix. This study examined ORI’s effects on the physical properties and antibacterial activity of the films and evaluated their preservation efficacy on chilled chicken breasts. Structural analysis suggested good compatibility of the composite films, likely ascribed to the H-bonding between ORI and the PVA/CS matrix. Increasing ORI content enhanced mechanical performance, reduced surface wettability, and improved light barrier properties, while also significantly improving antibacterial capacity. The composite film containing 75 μg/mL ORI exhibited optimal overall performance and potent antibacterial activity against Staphylococcus aureus, Listeria monocytogenes, and Escherichia coli, as evidenced by inhibition zone diameters of 19.51, 18.64, and 16.36 mm, respectively. Preservation experiments showed that film and coating containing 75 μg/mL ORI significantly inhibited the rise in TVB-N concentration, pH, total bacterial count, and juice loss rate of chilled chicken breast during storage. The coating generally showed slightly better preservation performance than the pre-formed film and extended the shelf life of chilled chicken breast by 4 days. This study provided a foundation for PVA/CS@ORI films and coatings as antimicrobial packaging for chilled chicken breast.