Search Results (30)

Aedes aegypti mosquitoes are established throughout Nouakchott, Mauritania, where its insecticide resistance status is unknown and dengue has become endemo-epidemic since 2014. Eggs were collected using ovitraps at 12 sites in five districts of Nouakchott, in August 2024. Adult females and larvae of the F1 generation were used for bioassays. Permethrin, deltamethrin, bendiocarb, and malathion were evaluated at discriminating concentrations. Larval assays were carried out at seven concentrations with Bacillus thuriengensis var israelensis (Bti) and temephos. The presence of knockdown resistance (kdr) mutations known to be associated with pyrethroid resistance was assessed by polymerase chain reaction and amplicons sequencing. Adults showed high levels of resistance to all insecticides tested. Larvae were susceptible to Bti (LD50 < 50 µg/L) and temephos (LD50% = 6.8 ± 0.7 µg/L). Only three kdr point mutations, S989P, V1016G, and F1534C, were found. The tri-locus genotypes SP/VG/FC were significantly associated with pyrethroid survival while only the tri-locus genotypes PP/GG/FF showed significant association with deltamethrin resistance. Given their level of insecticide resistance, there is an urgent need to control Ae. aegypti populations by several methods, including the use of biological larvicides, physical elimination of peridomestic breeding sites, water drainage, and public education to prevent arbovirus transmission. Full article

The cowpea is a vital crop for low-resource farmers in the Sahel, but post-harvest losses due to insect pests remain a major challenge. Callosobruchus maculatus (Fabricius, 1775), is the primary pest responsible for most of the damage to stored cowpeas. Recently, Trogoderma granarium (Everts, 1898) was found infesting cowpeas in large warehouses in Niger. This study evaluated hermetic storage bags to manage both common and emerging insect pests. Treatments included (i) the Purdue Improved Crop Storage (PICS) hermetic bag; (ii) a woven polypropylene (PP) bag with a polyethylene (PE) liner and Phostoxin; and (iii) a woven PP bag without Phostoxin (control). Naturally infested cowpea grains were obtained from the Office des Produits Vivriers du Niger (OPVN) warehouse in Maradi, Niger. Infestation levels were assessed using 12 samples of 500 g each, randomly collected from each treatment at the start and end of the trial. Major pests identified were C. maculatus, T. granarium, and Tribolium sp., with initial populations of 0.83, 0.44, and 0.83 adults per 500 g of cowpea, respectively. After six months of storage, pest densities in the control increased significantly: 232-fold for C. maculatus, 7.4-fold for T. granarium, and 2.7-fold for Tribolium sp.; resulting in a 38.5% weight loss. In contrast, both the Phostoxin and the PICS hermetic bags effectively suppressed pest populations, preventing weight loss. This study confirms the efficacy of hermetic storage, such as the PICS bag, in protecting cowpeas from both common and emerging pests. Full article

Salix psammophila, C. Wang & Chang Y. Yang, a desert-adapted shrub, is recognized for its exceptional drought tolerance and plays a vital role in ecosystem maintenance. However, research on S. psammophila has been limited due to the lack of an efficient and reliable genetic transformation method, including gene functional studies. The Agrobacterium-mediated transient overexpression assay is a rapid and powerful tool for analyzing gene function in plant vivo. In this study, tissue culture seedlings of S. psammophila were utilized as the recipient materials, and the plant expression vector pCAMBIA1301, containing the GUS reporter gene, was transferred into the seedlings via an Agrobacterium-mediated method. To enhance the efficiency of the system, the effects of secondary culture time, Agrobacterium concentration, infection time, and co-culture duration on the transient transformation efficiency of S. psammophila were explored. The optimal combination for the instantaneous transformation of S. psammophila tissue culture seedlings mediated by Agrobacterium was determined as follows: a secondary culture time of 30 d, a value of OD₆₀₀ of 0.8, an infection time of 3 h, and a co-culture duration of 48 h. Subsequently, the effectiveness of the transformation system was validated using the S. psammophila drought response gene SpPP2C80. To further confirm the accuracy of the system, SpPP2C80-overexpressing Arabidopsis was constructed and drought resistance analysis was performed. The results were consistent with the transient overexpression of SpPP2C80 in S. psammophila tissue culture seedlings, indicating that this system can be effectively employed for studying gene function in S. psammophila. These findings provide essential information for investigating gene function in non-model plants and pave the way for advancements in molecular biology research in S. psammophila. Full article

Euterpe oleracea Mart., also known for its fruit açaí, is a palm native to the Amazon region. The state of Pará, Brazil, accounts for over 90% of açaí production. Demand for the fruit in national and international markets is increasing; however, climate change and diseases such as anthracnose, caused by the fungus Colletotrichum sp., lead to decreased production. To meet demand, measures such as expanding cultivation in upland areas are often adopted, requiring substantial economic investments, particularly in irrigation. Therefore, the aim of this study was to evaluate the potential of açaí rhizobacteria in promoting plant growth (PGPR). Rhizospheric soil samples from floodplain and upland açaí plantations were collected during rainy and dry seasons. Bacterial strains were isolated using the serial dilution method, and subsequent assays evaluated their ability to promote plant growth. Soil analyses indicated that the sampling period influenced the physicochemical properties of both areas, with increases observed during winter for most soil components like organic matter and C/N ratio. A total of 177 bacterial strains were isolated from rhizospheres of açaí trees cultivated in floodplain and upland areas across dry and rainy seasons. Among these strains, 24% produced IAA, 18% synthesized ACC deaminase, 11% mineralized organic phosphate, and 9% solubilized inorganic phosphate, among other characteristics. Interestingly, 88% inhibited the growth of phytopathogenic fungi of the genera Curvularia and Colletotrichum. Analysis under simulated water stress using Polyethylene Glycol 6000 revealed that 23% of the strains exhibited tolerance. Two strains were identified as Bacillus proteolyticus (PP218346) and Priestia aryabhattai (PP218347). Inoculation with these strains increased the speed and percentage of açaí seed germination. When inoculated in consortium, 85% of seeds germinated under severe stress, compared to only 10% in the control treatment. Therefore, these bacteria show potential for use as biofertilizers, enhancing the initial development of açaí plants and contributing to sustainable agricultural practices. Full article

Butirosins are naturally occurring aminoglycoside (AG) antibiotics featuring a 4,5-disubstituted 2-deoxystreptamine (2-DOS) with a (2S)-4-amino-2-hydroxybutyrate (AHBA) side chain. This side chain has been shown to confer resistance against AG-modifying enzymes, leading to ongoing studies on the butirosin biosynthetic pathway and the corresponding enzymes. Butirosin is produced by Niallia (formerly Bacillus) circulans and Bacillus vitellinus, with most research focused on the first strain. To date, no whole-genome analysis has been performed on B. vitellinus. In this study, we sequenced the complete genome of B. vitellinus NBRC 13296 and performed a comparative analysis of different butirosin biosyntheric gene clusters (BGCs), including those from N. circulans. The complete genome of B. vitellinus NBRC 13296 comprises a 6,331,192-base circular chromosome with GC content of 52.68%. The annotation revealed the presence of 5605 CDSs, 70 tRNA genes, 30 rRNA genes, and 3 ncRNA genes in NBRC 13296. The highest dDDH and ANI values between NBRC 13296 and the most closely related type strain, Paenibacillus chitinolyticus KCCM 41,400, were 97.8% and 98.66%, respectively. Based on these genome-based comparative analyses, we propose reclassifying B. vitellinus NBRC 13296 as P. chitinolyticus. Genome mining revealed 18 gene clusters encoding the biosynthesis of diverse secondary metabolites in the genome of B. vitellinus NBRC 13296, indicating the enormous biosynthetic potential of this strain. The predicted structural diversity of the secondary metabolites includes aminoglycosides, PKS, NRPS, PKS–NRPS hybrids, metallophores, phosphonates, terpenes, β-lactones, and RiPP peptides. We then comparatively characterized the butirosin BGCs previously studied in several N. circulans strains. Additionally, the comparative genome analysis revealed complete butirosin BGCs identified from P. chitinolyticus KCCM 41,400, P. chitinolyticus NRRL B-23119, P. chitinolyticus NRRL B-23120, P. chitinolyticus B-14908, P. chitinolyticus YSY-3.1, P. chitinolyticus JMW06, Paenibacillus sp. GbtcB18, Paenibacillus sp. HGH0039, and Paenibacillus sp. MZ04-78.2. Finally, we identified the core region consisting of BtrS, BtrN, BtrM, BtrL, BtrA, BtrB, BtrC, BtrD, BtrD, BtrE, BtrF, BtrG, BtrH, BtrI, BtrI, BtrJ, BtrK, BtrO, BtrP, and BtrV, followed by an upstream region organizing BtrQ, BtrW, BtrX, BtrY, and BtrZ in the same transcriptional direction and sequential genetic arrangement, and a downstream region organizing various proteins based on BtrT, BtrR2, BtrU, and BtrR1. Our study provides insights into the reclassification of B. vitellinus NBRC 13296 to P. chitinolyticus and suggests the need for continued studies on butirosin biosynthesis from an enzymatic perspective. Full article

Qingye ramie is a multi-purpose crop, used as a feed ingredient in southern China, that is susceptible to drought. Qingye ramie was studied to investigate the effects of high temperatures and drought on its growthh. The results show that, after drought, ramie leaves turn yellow and that the height of the plant, the number of tillers, and its antioxidant activity decreased. To elucidate the molecular mechanism of drought tolerance, we performed RNA sequencing (RNA-seq) on drought-stressed samples and found that 3893 differentially expressed genes showed significant changes; 1497 genes were upregulated, and 2796 genes were downregulated. These genes were categorized into four metabolic pathways and were mainly enriched in plant hormone signal transcription, phenylpropanoid biosynthesis, amino sugar and nucleotide sugar metabolism, and starch and sucrose metabolism. Among these, we mapped the regulatory mechanism of Qingye ramie under drought and adversity. Of these, the expression of MAPK-related genes in the plant hormone pathway was the most significant. The expression of three MAPK serine/threonine protein kinase genes was upregulated by 2.62- to 3.45-fold and the expression of PP2C-related genes increased by 3.34- to 14.12-fold. The expression of PYR/PYL genes decreased significantly by 2.92–7.09-fold. Furthermore, in addition to NAC, ERF, MYB, bHLH, bZIP, C2H2, GeBP, and WRKY transcription factors that have been shown to regulate drought. Some other transcription factors, such as CCL, ASD, SAU, and SPS, were also up- or downregulated in Qingye ramie. Then, the samples were analyzed by qRT-PCR and the variations were consistent with the sequencing results. Consequently, we suggest that the changes after drought stress in green-leaf ramie may be regulated by these transcription factors. Further studies can be carried out in the future, which will provide valuable and important information on the plant’s drought resistance mechanism and deepen our understanding of the mechanisms of drought resistance in Qingye ramie. Full article

The cold-adapted Psychrobacter sp. strain DAB_AL62B, isolated from ornithogenic deposits on the Arctic island of Spitsbergen, harbors a 34.5 kb plasmid, pP62BP1, which carries a genetic SLF module predicted to enable the host bacterium to metabolize alkyl sulfates including sodium dodecyl sulfate (SDS), a common anionic surfactant. In this work, we experimentally confirmed that the pP62BP1-harboring strain is capable of SDS degradation. The slfCHSL genes were shown to form an operon whose main promoter, P_slfC, is negatively regulated by the product of the slfR gene in the absence of potential substrates. We showed that lauryl aldehyde acts as an inducer of the operon. The analysis of the draft genome sequence of the DAB_AL62B strain revealed that the crucial enzyme of the SDS degradation pathway—an alkyl sulfatase—is encoded only within the plasmid. The SLF module is flanked by two restriction–modification systems, which were shown to exhibit the same sequence specificity. We hypothesize that the maintenance of pP62BP1 may be dependent on this unique genetic organization. Full article

Several nucleotide analogues have been approved for use in treating hepatitis B virus (HBV) infection. Long-term exposure to therapy leads to the emergence of mutations within the HBV DNA polymerase gene, resulting in drug resistance, a major factor contributing to therapy failure. Chronic HBV patients from the Khyber Pakhtunkhwa province, Pakistan, who had completed 6 months of therapy participated in this study. Samples were collected from 60 patients. In this study, the entire reverse transcriptase domain of the HBV polymerase gene was amplified using nested polymerase chain reaction and sequenced. Drug-resistant mutations were detected in nine (22.5%) patients. All of these patients had lamivudine-resistant mutations (rtM204V + L180M), while seven individuals (17.5%) had both lamivudine- plus entecavir-resistant mutations (L180M + M204V + S202G). N236T, a mutation that gives rise to tenofovir and adefovir resistance, was observed in two (5%) patients. T184A, a partial drug-resistant mutation to entecavir, was found in five (12.5%) patients. Furthermore, other genotypic variants (100%) and vaccine escape mutations (5%) were additionally observed. Moreover, pN459Y (35%), pN131D (20%), pL231S (20%), pP130Q (17.5%), pS189Q (12.5%), pP161S (5%), pH160P (2.5%), pT322S (2.5%), and pA223S (2.5%) mutations in the polymerase gene, as well as sA166V (17.5%), sQ181K (12.5%), sV184R (7.5%), sA17E (5%), sP153S/K (5%), sW156C (5%), sC76Y (2.5%), and S132F (2.5%) mutations in the small surface gene, were identified for the first time in this study. Phylogenetic analysis showed that genotype D was predominant amongst the HBV carriers. Subtype D1 was found in most patients, while two patients were subtype D9. These novel findings may contribute to the body of knowledge and have clinical significance for treating and curing HBV infections in Pakistan. Full article

Nitrate-nitrogen (NO₃⁻–N) removal and garden waste disposal are critical concerns in urban environmental protection. In this study, biochars were produced by pyrolyzing various garden waste materials, including grass clippings (GC), Rosa chinensis Jacq. branches (RC), Prunus persica branches (PP), Armeniaca vulgaris Lam. branches (AV), Morus alba Linn. sp. branches (MA), Platycladus orientalis (L.) Franco branches (PO), Pinus tabuliformis Carrière branches (PT), and Sophorajaponica Linn. branches (SL) at three different temperatures (300 °C, 500 °C, and 700 °C). These biochars, labeled as GC300, GC500, GC700, and so on., were then used to adsorb NO₃⁻–N under various conditions, such as initial pH value, contact time, initial NO₃⁻–N concentration, and biochar dosage. Kinetic data were analyzed by pseudo-first-order and pseudo-second-order kinetic models. The equilibrium adsorption data were evaluated by Langmuir, Freundlich, Temkin and Dubinin–Radushkevich models. The results revealed that the biochar yields varied between 14.43% (PT700) and 47.09% (AV300) and were significantly influenced by the type of garden waste and decreased with increasing pyrolysis temperature, while the pH and ash content showed an opposite trend (p < 0.05). The efficiency of NO₃⁻–N removal was significantly influenced by the type of feedstock, preparation process, and adsorption conditions. Higher pH values had a negative influence on NO₃⁻–N adsorption, while longer contact time, higher initial concentration of NO₃⁻–N, and increased biochar dosage positively affected NO₃⁻–N adsorption. Most of the kinetic data were better fitted to the pseudo-second-order kinetic model (0.998 > R² > 0.927). Positive b values obtained from the Temkin model indicated an exothermic process of NO₃⁻–N adsorption. The Langmuir model provided better fits for more equilibrium adsorption data than the Freundlich model, with the maximum NO₃⁻–N removal efficiency (62.11%) and adsorption capacity (1.339 mg·g⁻¹) in PO700 under the conditions of pH = 2, biochar dosage = 50 mg·L⁻¹, and a reaction time of 24 h. The outcomes of this study contribute valuable insights into garden waste disposal and NO₃⁻–N removal from wastewater, providing a theoretical basis for sustainable environmental management practices. Full article

Anti-glycolipid antibodies have been reported to play pathogenic roles in peripheral inflammatory neuropathies, such as Guillain–Barré syndrome. On the other hand, the role in multiple sclerosis (MS), inflammatory demyelinating disease in the central nervous system (CNS), is largely unknown, although the presence of anti-glycolipid antibodies was reported to differ among MS patients with relapsing-remitting (RR), primary progressive (PP), and secondary progressive (SP) disease courses. We investigated whether the induction of anti-glycolipid antibodies could differ among experimental MS models with distinct clinical courses, depending on induction methods. Using three mouse strains, SJL/J, C57BL/6, and A.SW mice, we induced five distinct experimental autoimmune encephalomyelitis (EAE) models with myelin oligodendrocyte glycoprotein (MOG)_35–55, MOG_92–106, or myelin proteolipid protein (PLP)_139–151, with or without an additional adjuvant curdlan injection. We also induced a viral model of MS, using Theiler’s murine encephalomyelitis virus (TMEV). Each MS model had an RR, SP, PP, hyperacute, or chronic clinical course. Using the sera from the MS models, we quantified antibodies against 11 glycolipids: GM1, GM2, GM3, GM4, GD3, galactocerebroside, GD1a, GD1b, GT1b, GQ1b, and sulfatide. Among the MS models, we detected significant increases in four anti-glycolipid antibodies, GM1, GM3, GM4, and sulfatide, in PLP_139–151-induced EAE with an RR disease course. We also tested cellular immune responses to the glycolipids and found CD1d-independent lymphoproliferative responses only to sulfatide with decreased interleukin (IL)-10 production. Although these results implied that anti-glycolipid antibodies might play a role in remissions or relapses in RR-EAE, their functional roles need to be determined by mechanistic experiments, such as injections of monoclonal anti-glycolipid antibodies. Full article

Post-harvest loss continues to be a significant problem in the food industry. Different packaging materials, designed to reduce fruit damage, are anticipated for various applications in the supply chain. Recently, stamped paper (SP) and expandable polystyrene (EPS) trays have been introduced as tomato retail packaging. Although the combination of paper trays and clear plastic are still not 100% biodegradable packaging, they are promising alternatives to the heavy utilisation of petrochemical-based polymers. This study investigated the effects of different packaging materials and storage conditions on the ‘Nema-Netta’ tomatoes’ quality attributes. The treatments consisted of a stamped paper (SP) + polyvinyl chloride (PVC), expandable polystyrene (EPS) + polyvinyl chloride (PVC), stamped paper (SP)+ flow wrap, expandable polystyrene (EPS) + flow wrap, polypropylene (PP), and unpackaged tomatoes stored at cold and ambient conditions. Firmness, physiological weight loss (PWL), pH value, titratable acidity (TA) and total sugars were evaluated at seven-day intervals, over 28 days. Temperature and relative humidity at cold storage ranged between 8–12 °C, 78–80% RH and 22–26 °C, 68–72% RH at ambient storage conditions. The packaging and storage conditions significantly affected the PWL, firmness, pH, TA and total sugars. Samples in the EPS Tray combined with the PVC wrap at cold storage maintained the quality of the tomatoes better than the other packaging. The combination of packaging and cold storage created an ideal environment for maintaining the quality of tomatoes. The relative differences between EPS Tray + PVC (non-biodegradable) and SP Tray + PVC (biodegradable) were less than 5% in multiple tests. Full article

Aim: To assess changes in blood pressure (BP) and arterial stiffness among 84 rotating shift and 25 dayworkers (control subjects) at two industrial plants during a 4-year follow-up, and to assess changes in outcome variables among shift workers at the two plants after a reduction in the number of night shifts during the last year of follow-up in one of the plants. Methods: We collected demographic data using a questionnaire, examined systolic and diastolic blood pressure (sBP, dBP), central systolic and diastolic aorta pressure (cSP, cDP), augmentation pressure (AP), central pulse pressure (cPP), and pulse wave velocity (PWV). We registered sleep quality. The last 4–14 months of follow-up one plant implemented a 12-week shift plan reducing the total number of night shifts and consecutive night shifts from 16.8 to 14 and from 7.2 to 4. To assess differences in change of outcomes between study groups we applied linear mixed models. Results: The dayworkers were older, more hypertensive, reported less sleep disturbance, and smoked/snuffed less than the shift workers did. The adjusted annual increase in PWV was 0.34 m/s (95%CI, 0.22, 0.46) among shift workers and 0.09 m/s (95%CI, −0.05, 0.23) in dayworkers, yielding a significant difference of change of 0.25 m/s (95%CI, 0.06, 0.43). No significant differences were found between the two groups of shift workers in any cardiovascular disease (CVD) outcome during the last year of follow-up. Conclusions: Shift work in industry is associated with arterial stiffness, reflecting an increased risk of future CVD. No significant changes in arterial stiffness were identified as a consequence of a small reduction in the number of night shifts and consecutive night shifts. Full article

Salmonella enterica as common pathogens of humans and animals are good model organisms to conduct research on bacterial biology. Because these bacteria can multiply in both the external environments and in the living hosts, they prove their wide adaptability. It has been previously demonstrated that prolonged exposition of Salmonella serotype O48 cells to normal human serum led to an increase in resistance to sera in connection with the synthesis of very long O-antigen. In this work, we have studied the phenotype connected to virulence of Salmonella enterica strains that were subjected to consecutive passages in 50% human serum from platelet-poor plasma (SPPP). We found that eight passages in SPPP may not be enough for the bacteria to become serum-resistant (S. Typhimurium ATCC 14028, S. Senftenberg). Moreover, C1q and C3c complement components bound to Salmonellae (S. Typhimurium ATCC 14028, S. Hammonia) membrane proteins, which composition has been changed after passaging in sera. Interestingly, passages in SPPP generated genetic changes within gene fljB, which translated to cells’ motility (S. Typhimurium ATCC 14028, S. Erlangen). One strain, S. Hammonia exposed to a serum developed a multi-drug resistance (MDR) phenotype and two S. Isaszeg and S. Erlangen tolerance to disinfectants containing quaternary ammonium salts (QAS). Furthermore, colonial morphotypes of the serum adaptants were similar to those produced by starter cultures. These observations suggest that overcoming stressful conditions is manifested on many levels. Despite great phenotypic diversity occurring after prolonged exposition to SPPP, morphotypes of colonies remained unchanged in basic media. This work is an example in which stable morphotypes distinguished by altered virulence can be confusing during laboratory work with life-threatening strains. Full article

Cancers of the oral cavity can develop in the anatomic area extending from the lip, gum, tongue, mouth, and to the palate. Histologically, about 85–90% of oral cavity cancers are of the type squamous cells carcinomas (SCCs). The incidence of oral tongue SCC is higher in the tongue than any other anatomic area of the oral cavity. Here, we investigated the therapeutic effects and molecular mechanisms of docetaxel, which is a paclitaxel antitumor agent, on the cell growth of a human tongue SCC-derived SAS cell line. The results showed that docetaxel (10–300 nM) induced cytotoxicity and caspase-3 activity in SAS cells. Moreover, docetaxel (100 nM) promoted the expression of apoptosis-related signaling molecules, including the cleavages of caspase-3, caspase-7, and poly (ADP-ribose) polymerase (PARP). In mitochondria, docetaxel (100 nM) decreased the mitochondrial membrane potential (MMP) and Bcl-2 mRNA and protein expression and increased cytosolic cytochrome c protein expression and Bax mRNA and protein expression. In terms of mitogen-activated protein kinase (MAPK) and adenosine monophosphate-activated protein kinase (AMPK) signaling, docetaxel increased the expression of phosphorylated (p)-extracellular signal-regulated kinase (ERK), p-c-Jun N-terminal kinase (JNK), and p-AMPKα protein expression but not p-p38 protein expression. Moreover, the increase in caspase-3/-7 activity and Bax protein expression and decreased Bcl-2 protein expression and MMP depolarization observed in docetaxel-treated SAS cells could be reversed by treatment with either SP600125 (a JNK inhibitor), PD98059 (an MEK1/2 (mitogen-activated protein kinase kinase 1/2) inhibitor), or compound c (an AMPK inhibitor). The docetaxel-induced increases in p-JNK, p-ERK, and p-AMPKα protein expression could also be reversed by treatment with either SP600125, PD98059, or compound c. These results indicate that docetaxel induces human tongue SCC cell apoptosis via interdependent MAPK-JNK, MAPK-ERK1/2, and AMPKα signaling pathways. Our results show that docetaxel could possibly exert a potent pharmacological effect on human oral tongue SCC cell growth. Full article

In this work, compacts from mechanical mixtures of CaF₂ micron powder (MCP) with CaF₂ nanopowder (NP) additives were produced, with mass ratios of the mixture components ranging from 10:0.125 to 10:1, respectively, using magnetic pulse (MP) and static pressing (SP) methods. The effects of pressure (P_p) and pressing temperature (T_p), concentration and phase composition of the additive on the density and color of compacts were studied, taking into account the properties of the initial components of the mixtures. The evolution of pulsed cathodoluminescence (PCL) spectra and photoluminescence (PL) of compacts from pure powders and their mixtures depending on P_p, T_p and characteristics of initial CaF₂ NP was also studied. A new near-infrared (NIR) band associated with fluoride vacancies was discovered with a maximum at ~765 nm in PCL spectra of compacts produced by MP at a temperature of 425 °C. A blue band at 435 nm associated with impurity oxygen vacancies in the CaF₂ lattice was found in PL spectra compacts of pure NP and powder mixtures. The density of compacts of pure NP and MCP reached 89% of the theoretical density, and the density of compacts of mixtures did not exceed 78%. The defective structure and phase composition of the CaF₂ NP had a decisive effect on the luminescent properties of compacts from mixtures of micro- and nanopowders. Full article