First Report of Fusarium fujikuroi Causing Postharvest Rot of Kiwifruit (Actinidia chinensis) in Jiangxi Province, China.

Kiwifruits (Actinidia chinensis) are among the most widely planted fruit in Jiangxi Province, China. Infected kiwifruits of the cultivars 'Hongyang' and 'Jinyan' were obtained from a commercial orchard in Fengxin county, Jiangxi Province (28°67' N; 115°42' E) from September to November 2022. The 1200 kiwifruits were collected from cold storage (cold stored for 3 months at 2°C), and moved to room temperatures (15 to 20°C), approximately 20% had symptoms of postharvest soft rot 7 days later. The infected fruits had brown or dark gray spots on the peel. Most were round or oval, with a diameter of approximately 1~3 cm. The pulp was milky white, and there was a waterlogged ring at the junction of decay. The pathogen was isolated by removing several small pieces (3×3 mm) of infected tissue from the diseased kiwifruits, which were sterilized with 75% ethanol for 30 s, dipped in 1% NaClO for 1 min, and rinsed three times with sterile distilled water. These pieces were transferred onto potato dextrose agar (PDA) and incubated for 5 days at 28°C, 75% relative humidity (RH), separated, and repurified. Eight unidentified isolates with similar morphology were obtained on PDA (D3-1 to D3-8). These isolates had abundant aerial fluffy mycelia. The colonies were white during the early stage of culture and turned light purple in the later stage. The mycelia grew 5.8 mm day-1 (n=5) on average and produced abundant conidia 10 days later. The microconidia were solitary, transparent, ovoid, with 0 to 1 septa, and 3.6 to 11.2 × 1.6 to 3.5 µm (average 6.5 × 2.9 µm, n = 50). The macroconidia were sickle-shaped, slender and slightly curved, with 3 to 5 septa, and 22.3 to 53.9 × 2.6 to 5.4 µm (average 39.5 × 4.3 µm, n = 50). Chlamydospores were absent. The morphological characteristics enabled the identification of the pathogen as Fusarium spp. (Leslie and Summerell, 2006). Isolate D3-2 was further confirmed, and the primers ITS1/ITS4 (White et al. 1990), 5F2/7CR and EF1/EF2 (O'Donnell et al. 2022) were used to amplify the internal transcribed spacer (ITS) region, RNA polymerase II largest subunit (RPB2) gene and translation elongation factor-1 alpha regions (TEF-1α). The ITS (accession no. PP077075), RPB2 (PP566653) and TEF-1α (PP566654) sequences shared 99.62 to 100% identities with ITS (ON564593.1), RPB2 (ON734380.1) and TEF-1α (ON697186.1) of F. fujikuroi from NCBI, respectively. Thus, the pathogen was identified as F. fujikuroi based on morphological and molecular characteristics. Each of the three isolates was inoculated on surface-disinfected (75% ethanol, 5 min) disease-free kiwifruits of cv. 'Jinyan' and 'Hongyang'. The six kiwifruits were pierced by a sterile inoculation needle and inoculated with 20 µl spore suspension (1×106 spores/ml), and six kiwifruits were treated with spore suspension without any wounds, four control fruits were inoculated with sterile distilled water. All the fruits were sealed in a storage box, kept at an RH of 90%-95%, and incubated at a constant temperature of 28°C for 5 days. After 3 days, the fruit rotted at the inoculation site, and after 5 days, the lesions gradually increased, and the symptoms were the same as those of the original sample. The control fruits remained disease-free. The pathogenicity tests were repeated three times. Koch's postulates were completed by reisolating the fungus from infected kiwifruits, which was identified as F. fujikuroi by sequencing. Although F. solani (Yang et al. 2018) and F. acuminatum (Wang et al. 2015) have been previously reported to rot kiwifruits in China, this is the first report of F. fujikuroi causing postharvest rot on kiwifruits in China. This discovery can alert agronomists to prevent and control this pathogen.

Encapsulation on rhodochrosite stabilizes toxic CdS nanoparticles in aqueous oxidation systems.

Manganese (Mn) redox cycling and phase variation reactions play a crucial role in natural water settings. Rhodochrosite (MnCO3), a mineral commonly found in oxygen-deprived environments, develops a surface oxide film upon exposure to oxygen. This Mn oxide film significantly influences the fate of nanoparticles within its proximity. Employing atomic force microscopy (AFM), this study examined the growth of the Mn oxide film on MnCO3 and the encapsulation of cadmium sulfide nanoparticles (CdS-NPs). Results revealed the gradual development of a nanometer-thick oxide film on MnCO3 over time in aerobic conditions, with the rate of film formation correlated to the solution's ionic strength. The oxide film on MnCO3 encapsulated pre-adsorbed CdS-NPs, either through embedding or covering. Intriguingly, CdS-NPs were found to enhance the growth of the Mn oxide film, contributing to the fixation of CdS-NPs. Furthermore, an ultrasonic desorption protocol verified the stability of CdS-NPs encapsulated by the Mn oxide film on MnCO3. This study elucidates a novel mechanism for immobilizing CdS-NPs in aqueous oxidizing conditions, providing valuable insights into the behavior and distribution of toxic nanoparticles in environmental contexts. ENVIRONMENTAL IMPLICATION: This study classifies cadmium sulfide nanoparticles (CdS-NPs) as "hazardous material" due to the inherent toxicity of cadmium, posing risks to both ecological and human health. The research addresses environmental concerns by exploring the interaction between CdS-NPs and manganese (Mn) redox cycling. The formation of a Mn oxide film, encapsulating CdS-NPs, suggests a mechanism for limiting the dispersion of these hazardous nanoparticles in oxidizing water. This provides valuable insights for managing the environmental impact of CdS-NPs, offering a proactive strategy to mitigate their adverse effects in natural systems.

Evolutionary and phylogenetic analyses of 11 Cerasus species based on the complete chloroplast genome.

The subgenus Cerasus, one of the most important groups in the genus Prunus sensu lato, comprises over 100 species; however, the taxonomic classification and phylogenetic relationships of Cerasus remain controversial. Therefore, it is necessary to reconstruct the phylogenetic tree for known Cerasus species. Here, we report the chloroplast (cp) genome sequences of 11 Cerasus species to provide insight into evolution of the plastome. The cp genomes of the 11 Cerasus species (157,571-158,830 bp) displayed a typical quadripartite circular structure. The plastomes contain 115 unique genes, including 80 protein-coding genes, four ribosomal RNAs, and 31 transfer RNAs. Twenty genes were found to be duplicated in inverted repeats as well as at the boundary. The conserved non-coding sequences showed significant divergence compared with the coding regions. We found 12 genes and 14 intergenic regions with higher nucleotide diversity and more polymorphic sites, including matK, rps16, rbcL, rps16-trnQ, petN-psbM, and trnL-trnF. During cp plastome evolution, the codon profile has been strongly biased toward the use of A/T at the third base, and leucine and isoleucine codons appear the most frequently. We identified strong purifying selection on the rpoA, cemA, atpA, and petB genes; whereas ccsA, rps19, matK, rpoC2, ycf2 and ndhI showed a signature of possible positive selection during the course of Cerasus evolution. In addition, we further analyzed the phylogenetic relationships of these species with 57 other congenic related species.Through reconstructing the Cerasus phylogeny tree, we found that true cherry is similar to the flora of China forming a distinct group, from which P. mahaleb was separated as an independent subclade. Microcerasus was genetically closer to Amygdalus, Armeniaca, and Prunus (sensu stricto) than to members of true cherry, whereas P. japonica and P. tomentosa were most closely related to P. triloba and P. pedunculata. However, P. tianshanica formed a clade with P. cerasus, P. fruticosa, P. cerasus × P. canescens 'Gisela 6', and P. avium as a true cherry group. These results provide new insights into the plastome evolution of Cerasus, along with potential molecular markers and candidate DNA barcodes for further phylogenetic and phylogeographic analyses of Cerasus species.

Comparative transcriptome and metabolome analyses of cherry leaves spot disease caused by Alternaria alternata.

Alternaria alternata is a necrotrophic fungal pathogen with a broad host range that causes widespread and devastating disease in sweet cherry (Prunus avium). We selected a resistant cultivar (RC) and a susceptible cultivar (SC) of cherry and used a combined physiological, transcriptomic, and metabolomic approach to investigate the molecular mechanisms underlying the plant's resistance to A. alternata, of which little is known. We found that A. alternata infection stimulated the outbreak of reactive oxygen species (ROS) in cherry. The responses of the antioxidant enzymes and chitinase to disease were observed earlier in the RC than in the SC. Moreover, cell wall defense ability was stronger in the RC. Differential genes and metabolites involved in defense responses and secondary metabolism were primarily enriched in the biosynthesis of phenylpropanoids, tropane, piperidine and pyridine alkaloids, flavonoids, amino acids, and α-linolenic acid. Reprogramming the phenylpropanoid pathway and the α-linolenic acid metabolic pathway led to lignin accumulation and early induction of jasmonic acid signaling, respectively, in the RC, which consequently enhanced antifungal and ROS scavenging activity. The RC contained a high level of coumarin, and in vitro tests showed that coumarin significantly inhibited A. alternata growth and development and had antifungal effect on cherry leaves. In addition, differentially expressed genes encoding transcription factors from the MYB, NAC, WRKY, ERF, and bHLH families were highly expressed, they could be the key responsive factor in the response of cherry to infection by A. alternata. Overall, this study provides molecular clues and a multifaceted understanding of the specific response of cherry to A. alternata.

Influence of microplastics on the transport of antibiotics in sand filtration investigated by AFM force spectroscopy.

Microplastics and antibiotics were frequently detected in the effluent of sand filtration, while the presence of microplastics may change the interactions between the antibiotics and the quartz sands. However, the influence of microplastics on the transport of antibiotics in sand filtration has not been revealed. In this study, ciprofloxacin (CIP) and sulfamethoxazole (SMX) were respectively grafted on AFM probes to determine the adhesion forces to the representative microplastics (PS and PE) and the quartz sand. CIP and SMX exhibited low and high mobilities in the quartz sands, respectively. Compositional analysis of the adhesion forces indicated that the lower mobility of CIP in sand filtration columns could be attributed to the electrostatic attraction between the quartz sand and CIP compared with repulsion for SMX. Moreover, the significant hydrophobic interaction between the microplastics and the antibiotics could be responsible for the competitive adsorption of the antibiotics to the microplastics from the quartz sands; meanwhile, the π-π interaction further enhanced the adsorption of PS to the antibiotics. As a result of the high mobility of microplastics in the quartz sands, the carrying effect of microplastics enhanced the transport of antibiotics in the sand filtration columns regardless of their original mobilities. This study provided insights into the mechanism of the microplastics on enhancing the transport of antibiotics in sand filtration systems from the perspective of the molecular interaction.

Visualization the fixation of cadmium on manganese dioxide in sulfur reduction environments.

Manganese oxides as common soil components were considered as an important sink for the cadmium pollution, which, however, would be affected by the reductive sulfide introduced during the flooding period of paddy soil. In this study, the phase transitions caused by the reactions among S2-, MnO2 and Cd2+ were visualized by atomic force microscopy (AFM). The dissolution of MnO2 was in-situ studied by AFM in the S2-containing environments. Moreover, in the ternary system (S2-, MnO2 and Cd2+), the pre-adsorption of Cd2+ by the MnO2 nanosheets would promote the subsequent precipitation of CdS on the surface of MnO2, while the pre-formed CdS nanoparticles in the aquatic phase would tend to suspense rather than precipitating on MnO2. The kinetic study results indicated that the CdS crystallite generation rate was faster than the MnO2 dissolution rate in the aquatic environments with different sulfide contents. In the macroscopic Cd2+ fixation test, the introduction of S2- dramatically improved the fixation of the pre-adsorbed Cd2+ on the MnO2 nanosheets by forming the CdS precipitate. This study provided a fundamental understanding of the interactions among the S2-, MnO2 and Cd2+ ternary system and shed light on the development of Cd pollution remediation methods for paddy soils.

Metabolomics and Transcriptomics Analyses of Two Contrasting Cherry Rootstocks in Response to Drought Stress.

Drought is one of the main factors affecting sweet cherry yields, and cherry rootstocks can provide a range of tree vigor levels to better match sweet cherries with the characteristics of the soil. To investigate the molecular events of the cherry to water deficiency, we performed transcriptomic and metabolomic analyses of Prunus mahaleb CDR-1 (drought-tolerant cherry rootstock (DT)) and P. cerasus × P. canescens Gisela 5 (drought-susceptible cherry rootstock (DS)), respectively. The results revealed 253 common drought-responsive genes in leaves and roots in DT and 17 in DS; 59 upregulated metabolites were explored in leaves in DT and 19 were explored in DS. Differentially expressed metabolites related to the cyanoamino acid metabolism pathway and phenylpropanoid biosynthesis pathway may be key factors in the difference in drought resistance in the two rootstocks. Moreover, six central metabolites-3-cyanoalanine, phenylalanine, quinic acid, asparagine, p-benzoquinone, and phytosphingosine-were identified as potential biological markers of drought response in cherries and may be key factors in the difference in drought resistance, along with caffeic acid and chlorogenic acid. We also selected 17 differentially expressed genes as core candidate genes and the mechanism of DT in response to drought is summarized.

Fe(II) catalyzing sodium percarbonate facilitates the dewaterability of waste activated sludge: Performance, mechanism, and implication.

In this work, Fe(II) catalyzing sodium percarbonate (Fe(II)/SPC) was managed to facilitate waste activated sludge (WAS) dewatering for the first time. The results showed that after WAS was treated by 20 mg/g total suspended solids (TSS) Fe(II) and 50 mg/g TSS SPC, the water content of sludge cake (WCSC) by press filtration and capillary suction time (CST) dropped from 90.8% ± 1.6% and 96.1 ± 4.0 s (the control) to 55.6% ± 1.4% and 30.1 ± 2.5 s, respectively. The mechanism investigations indicated that four intermediates or products (i.e., •OH, H2O2, Fe(II), and Fe(III)) generated in the Fe(II)/SPC process were responsible for the improved WAS dewaterability, and •OH and Fe(III) were the two major contributors. It was found that •OH collapsed and fragmented extracellular polymeric substances, damaged cell wall and permeabilized cytoplasmic membrane, and transformed conformation of the extracellular proteins secondary structure via both affecting the hydrogen bond maintaining α-helix and cracking disulfide bond in cysteine residues while Fe(III), the oxidization product of Fe(II), decreased the surface electronegativity and water-affinity surface areas of WAS flocs. As a result, the bound water release, flocculability, surface hydrophobicity, drain capability, and flowability of WAS flocs were strengthened whereas the compact surface structure, colloidal forces, network strength, gel-like structure, and apparent viscosity of WAS flocs were weakened. In addition, Fe(II)/SPC process also reduced the recalcitrant organics and fecal coliforms in sludge, which facilitated land application of dewatered sludge. The findings acquired in this work not only deepens our understanding of Fe(II)/SPC-involved WAS treatment process but also may guide engineers to develop both effective and promising strategies to better condition WAS for dewatering in the future.

Effect of exogenous methyl jasmonate treatment on disease resistance of postharvest kiwifruit.

Kiwifruit (Actinidia deliciosa cv. Jinkui) were treated with 0.1 mmol/L methyl jasmonate (MeJA) to investigate the effects on disease resistance to soft rot caused by Botryosphaeria dothidea. The results showed that MeJA treatment significantly reduced the diameter of lesions after inoculation with B. dothidea. This treatment significantly enhanced the activities of related antioxidant protective enzymes, defence-related enzymes including catalase (CAT), peroxidase (POD), superoxide dismutase (SOD), polyphenol oxidase (PPO), chitinase (CHI), ß-1,3 glucanase (GLU) and increased the accumulation of total phenolic content, while the degree of membrane lipid peroxidation was reduced. MeJA treatment effectively enhanced gene expression of AcPOD, AcSOD, AcCHI and AcGLU. The results from this research suggest that MeJA treatment is a promising and safe strategy for controlling postharvest rot soft of kiwifruit.

How does zero valent iron activating peroxydisulfate improve the dewatering of anaerobically digested sludge?

Zero valent iron (ZVI) activating peroxydisulfate (PDS) was demonstrated to be effective in improving the dewaterability of anaerobically digested sludge (ADS). However, details of how ZVI/PDS enhances the dewaterability remain largely unknown. This work therefore aims to reveal the facts of what happen in ZVI/PDS involved ADS systems. Experimental results showed that ZVI/PDS treatment remarkably improved the dewaterability of ADS, with the minimal normalized capillary suction time of 8.6 ±â€¯0.5 s L/g·VSS being obtained at the dosages of 2 g/g TSS ZVI and 0.5 g/g TSS PDS, which was 42.5% of that in the control. In this case, 71.2% ±â€¯1.8% of water content (press filtration) was measured, which was 16.9% lower than that determined in the control. The mechanism investigations showed that ZVI activating PDS produced substantially reactive species, i.e., SO4•- and •OH, and these strong oxidative radicals decreased surface negative charges of ADS flocs, caused disruption of extracellular polymeric substances (EPS) and release of intracellular substances, and changed the secondary structure of proteins. Additionally, the products of ZVI oxidation, i.e., Fe2+ and Fe3+, were effective flocculants, thus their generation benefited the coagulation of ADS flocs through compressing double electric layers and neutralizing negative charges of sludge colloidal particles. As a result, the flocculability, hydrophobicity, and flowability of ADS were enhanced, but the bound water content, fractal dimension, and viscosity of ADS were decreased, which were responsible for the improvement of dewaterability. Further analyses exhibited that the contributions of these major contributors were different, and their contributions to the dewaterability improvement were in the order of SO4·- > ·OH > Fe2+/Fe3+. It was also found that ZVI/PDS treatment enhanced the degradation of recalcitrant organics, inactivation of the fecal coliforms, and mitigation of the toxicity of heavy metals in the dewatered sludge, which were beneficial to its land application.

Selective hydrodeoxygenation of p-cresol as a model for coal tar distillate on Ni-M/SiO2 (M = Ce, Co, Sn, Fe) bimetallic catalysts.

Ni-M/SiO2 with different binary metals M (M = Ce, Co, Sn, Fe) prepared by an incipient impregnation method was used in the hydrodeoxygenation (HDO) of low-temperature coal tar distillate, which is rich in phenolic compounds. p-Cresol, as a model compound of the distillate, was used to evaluate the activity and selectivity of BTX products on the series of reduced Ni-M/SiO2 catalysts in a fixed bed reactor. The properties of the catalysts were characterized by N2 adsorption-desorption, ICP-AES, XRD, H2-TPR, and XPS. Benzene and toluene as the direct deoxygenation (DDO) products and cyclohexane and methylcyclohexane as the hydrogenolysis (HYD) products were detected to evaluate the selectivity of the path in the deoxygenation process. In this series of catalysts, the order of reactivity was Ni-Ce > Ni-Sn > Ni-Co > Ni-Fe > monometallic Ni. Meanwhile, the addition of Ce and Co loaded in the Lewis acid sites of the catalyst affected the electron distribution of nickel atom and its atomic arrangement on the surface of the carrier. Compared to monometallic Ni, the DDO path become dominant on Ni-Ce and Ni-Co and the selectivity for BTX products increased from 58.8% to 77.4% and 71.1%, respectively. The binary metal Sn, unlike the former two metals, formed a Ni3Sn crystal form with Ni, which resulted in significant enhancement of the HYD path while obviously increasing the reactivity.