Multi-drug resistance to antibiotics represents a growing challenge in treating infectious diseases. Outside the hospital, bacteria with the multi-drug resistance (MDR) phenotype have an increased prevalence in anthropized environments, thus implying that chemical stresses, such as metals, hydrocarbons, organic compounds, etc., are the source of such resistance. There is a developing hypothesis regarding the role of metal contamination in terrestrial and aquatic environments as a selective agent in the proliferation of antibiotic resistance caused by the co-selection of antibiotic and metal resistance genes carried by transmissible plasmids and/or associated with transposons. Efflux pumps are also known to be involved in either antibiotic or metal resistance. In order to deal with these situations, microorganisms use an effective strategy that includes a range of expressions based on biochemical and genetic mechanisms. The data from numerous studies suggest that heavy metal contamination could affect the dissemination of antibiotic-resistant genes. Environmental pollution caused by anthropogenic activities could lead to mutagenesis based on the synergy between antibiotic efficacy and the acquired resistance mechanism under stressors. Moreover, the acquired resistance includes plasmid-encoded specific efflux pumps. Soil microbiomes have been reported as reservoirs of resistance genes that are available for exchange with pathogenic bacteria. Importantly, metal-contaminated soil is a selective agent that proliferates antibiotic resistance through efflux pumps. Thus, the use of multi-drug efflux pump inhibitors (EPIs) originating from natural plants or synthetic compounds is a promising approach for restoring the efficacy of existing antibiotics, even though they face a lot of challenges.

During the process of adapting to metal contamination, plants produce secondary metabolites that have the potential to modulate multidrug-resistant (MDR) phenotypes; this is achieved by inhibiting the activity of efflux pumps to reduce the minimum inhibitory concentrations (MICs) of antimicrobial substrates. Our study evaluated the effect of secondary metabolites of belowground parts of Pteris vittata L. and Fallopia japonica, two metal-tolerant plants from northern Vietnam, on six antibiotic-resistant Stenotrophomonas maltophilia strains possessing efflux pump resistance mechanisms that were isolated from soil and clinical samples. The chemical composition of aqueous and dichloromethane (DCM) fractions extracted from P. vittata and F. japonica was determined using UHPLC-DAD-ESI/QTOF analysis. The antibacterial and efflux pump inhibitory activities of the four fractions were evaluated for the six strains (K279a, 0366, BurA1, BurE1, PierC1, and 502) using a microdilution assay at fraction concentrations of 62.5, 125, and 250 μg/mL. The DCM fraction of F. japonica exhibited remarkable antibacterial activity against strain 0366, with a MIC of 31.25 μg/mL. Furthermore, this fraction also significantly decreased gentamicin MIC: four-fold and eight-fold reductions for BurA1 and BurE1 strains, respectively (when tested at 250 μg/mL), and two-fold and eight-fold reductions for K279a and BurE1 strains, respectively (when tested at 125 μg/mL). Pure emodin, the main component identified in the DCM fraction of F. japonica, and sennidine A&B only reduced by half the MIC of gentamicin (when tested at 30 μg/mL). Our results suggest that the DCM fraction components of F. japonica underground parts may be potential candidates for new bacterial efflux pump inhibitors (EPIs).

Reducing chemical fertilizer while remaining high crop yield has become a trend of agricultural practice. The purpose of this study was to investigate the effects of nitrogen (N) input on the structure of the fungal community and mycorrhizal inoculum potential in rhizosphere of Curcuma longa, aiming to minimize the use of chemicals and optimize the effect of biofertilizer for sustainable turmeric farming. For this, a field study was conducted in two successive years 2015 and 2016 with applications of varrying N fertilizer rates N0 (0 kgN ha⁻¹ y⁻¹), N150 (150 kgN ha⁻¹ y⁻¹), N350 (350 kgN ha⁻¹ y⁻¹), and N500 (500 kgN ha⁻¹ y⁻¹) in combination with mycorrhizal biofertilizer on turmeric plants in Hung-Yen. Rhizosphere soils were then analyzed for the abundance of predominant fungal taxon based on amplicon sequencing of rDNA internal transcribed spacer regions. Metagenomic results indicated significant effects of N inputs on rhizosphere fungal communities composition, with dominance of ascomyceteous fungi under optimized N levels, whereas basidiomycetous fungi were more abundant under higher N input. Operational taxonomic units relating to the predominantly abundant genus Glomus were found apparently in higher proportion under optimized N inputs (N150). The results demonstrate an enhanced productivity and icreased mycorrhizal inoculating potential by appropriated N fertilizer application in turmeric rhizosphere.

Laccase (EC 1.10.3.2) is a multi-copper oxidase that utilizes molecular oxygen to oxidize phenolic rings to phenyloxy radicals. Due to its capability to use a wide variety of phenolic and non-phenolic substrates, this oxidative enzyme has potential applications in the food, pharmaceutical, and environmental industries. In the present study, a laccase (PleuLac) from the white-rot fungus Pleurotus pulmonarius VAST02.42 that was newly isolated from Muong Phang special-use forest, was purified and studied on physical-chemical properties. After ultrafiltration (10, 30 kDa cut-off), laccase was successfully purified to apparent homogeneity (specific activity of 28 U.mg-1) by using the anion-exchange chromatography (e.g., DEAE-Cellulose, HiTrapTM Q XL columns) and size-exclusion chromatography (Superdex G-100). After the final purification step, a total activity of 532 U was acquired with a recovery of 8.3 % and purity of 9.6-fold. The molecular weight (Mw) of PleuLac was determined to be 35 kDa by SDS-PAGE electrophoresis. This enzyme exhibited an optimal activity at 40 ºC and pH of 5.5; it is stable at 25 ºC after incubation of 120 min and pH of 5.0. This purified and characterized PleuLac will serve for further application study on catalyzing the oxidation of essential oils to value-added products in combination with peroxidase.