Search Results (653)

Healthcare-associated infections (HAIs) remain a significant global challenge, affecting approximately 7% of patients in developed countries and over 10% in developing regions, according to the World Health Organization. Medical textiles, particularly hospital bed linens and pillowcases, play a critical role in the transmission of pathogenic microorganisms due to their porous structure and moisture-retaining properties, which support microbial survival and proliferation, including bacteria such as Staphylococcus aureus and Escherichia coli. Conventional disinfection methods, including laundering and thermal treatments, provide only temporary protection, leading to rapid recontamination during use. In recent years, various antimicrobial agents and functionalization techniques have been developed to impart long-lasting antiseptic properties to textile materials. However, these approaches differ significantly in terms of antimicrobial efficiency, durability, cost-effectiveness, and environmental impact, making the selection of optimal strategies challenging for practical healthcare applications. This review provides a comprehensive comparative analysis of antimicrobial agents used in healthcare textile functionalization, including metal-based nanoparticles, organic compounds, and bio-based materials. In addition, it evaluates key modification methods such as coating, padding, and in situ synthesis, with particular emphasis on their influence on antimicrobial performance, wash durability, and practical applicability. Furthermore, this review discusses major challenges associated with the use of antiseptic coatings, including toxicity, environmental concerns, and economic limitations. Based on the analysis, promising directions for the development of safer, cost-effective, and durable antimicrobial textile systems are highlighted, offering valuable insights for future research and real-world healthcare applications. Full article

This work presents an energy-efficient and simple method for producing luminescent, antibacterial sulfur quantum dots (SQDs). For the first time, polyethyleneimine (PEI)-coated SQDs were synthesized via a mechanochemical technique, utilizing either elemental sulfur or sodium thiosulfate as the sulfur source. The roles of hydrogen peroxide (H₂O₂) as an etching agent and of sodium hydroxide (NaOH) in the PEI-mediated SQD formation were investigated. The as-synthesized SQDs were characterized by UV-visible, Raman, infrared (IR), and photoluminescence (PL) spectroscopy, as well as by transmission electron microscopy (TEM) and atomic force microscopy (AFM). Both TEM and AFM analyses revealed similarly small SQD sizes (average diameter ~3 nm), independent of the sulfur source used. The influence of synthesis conditions on the optical properties, including the photoluminescence quantum yield (QY), was evaluated. SQDs derived from elemental sulfur, PEI, and NaOH exhibited the best water solubility and the strongest photoemission in the 400–550 nm range. Antibacterial activity was assessed against representative Gram-positive and Gram-negative strains, and minimum inhibitory concentration (MIC) values were determined. The PEI-coated SQDs demonstrated antibacterial activity against the Gram-positive bacteria Bacillus subtilis, Staphylococcus aureus, and Staphylococcus epidermidis, which is attributed primarily to the sulfur component. Full article

Neonatal infections remain a leading cause of morbidity and mortality worldwide, particularly among preterm and low-birth-weight infants and in low- and middle-income countries. This burden has intensified with the global increase in multidrug-resistant (MDR) bacteria, especially in neonatal intensive care units, where prolonged hospitalization, invasive interventions, and exposure to broad-spectrum antibiotics promote colonization, transmission, and invasive infection. In this narrative review, we explore the epidemiology and microbiological characteristics of MDR bacterial infections in newborns, alongside their associated risk factors, diagnostic challenges, treatment outcomes, and prevention strategies. Across different settings, Gram-negative pathogens, particularly Klebsiella pneumoniae, Escherichia coli, and Acinetobacter baumannii, account for a substantial proportion of severe neonatal infections, whereas methicillin-resistant Staphylococcus aureus remains important in selected units. The risk of MDR infection is driven by a complex interplay of factors, ranging from maternal and perinatal exposures to the inherent immunological vulnerability of newborns, hospital-based transmission, antibiotic selection pressure, and structural deficiencies in healthcare infrastructure. Diagnosis remains challenging because clinical presentations are nonspecific and culture-based methods are constrained by low blood volumes, prior antimicrobial exposure, and delayed turnaround times. Treatment is increasingly complicated due to resistance to standard empirical regimens, substantial regional variation in susceptibility profiles, and limited neonatal pharmacokinetic and safety data for reserve agents. Current evidence mainly supports surveillance-informed empirical therapy, susceptibility-guided treatment adjustment, antimicrobial stewardship, and strict infection prevention measures. Future progress will require neonatal-specific clinical trials, harmonized surveillance systems, stronger molecular epidemiology, and more equitable access to microbiological diagnostics and effective treatment. Full article

Methicillin-resistant Staphylococcus aureus (MRSA) is a major antimicrobial-resistant pathogen affecting both human and animal health. Although historically associated with healthcare settings, MRSA is now established in livestock production and throughout the production chain. Its detection in animals, food products, and processing environments reflects the complex ecology of antimicrobial resistance (AMR) in modern food systems. This narrative review synthesizes current evidence on the molecular basis of methicillin resistance and multidrug resistance determinants, as well as the epidemiology of MRSA in food-associated settings. Particular emphasis is placed on its occurrence in animal-derived foods and key reservoirs within farms, slaughterhouses, and processing environments. Livestock-associated populations are dominated by clonal complex CC398. In contrast, CC9 is prevalent in pig production systems in Asia, while CC5-related lineages occur at the human and animal interface. MRSA has been detected in retail meat and animal-derived foods at low but measurable prevalence, indicating contamination during slaughter and processing. Virulence determinants include staphylococcal enterotoxins linked to food poisoning and Panton–Valentine leukocidin associated with severe infections. Biofilm formation and adhesins further support persistence and colonization. Epidemiological and molecular evidence indicates that livestock, processing environments, and food-contact surfaces act as interconnected reservoirs sustaining MRSA circulation. Human exposure occurs primarily through occupational contact and environmental pathways, whereas foodborne transmission appears less common. Effective control requires integrated surveillance, responsible antimicrobial use in livestock production, and strict hygiene practices throughout the production chain within a One Health framework. Full article

Pathogen manipulation of host behavior is a widespread evolutionary strategy to enhance its transmission, yet whether different pathogens elicit distinct behavioral and molecular responses in the same host remains poorly understood. We performed parallel behavioral assays and comparative transcriptomic analyses on third-instar Lymantria dispar larvae infected with Lymantria dispar multiple nucleopolyhedrovirus (LdMNPV, virus), Staphylococcus aureus (bacterium) and Metarhizium anisopliae (fungus). Climbing height was recorded over 72 h post-infection, and gene expression pattern was profiled using RNA-seq at 72 h. Only LdMNPV infection induced significant, sustained upward climbing behavior among the three pathogen infection groups. All three pathogens activated Toll and IMD immune pathways, but LdMNPV triggered substantially broader transcriptomic reprogramming. Notably, the virus specifically upregulated multiple energy metabolism pathways (nicotinate/nicotinamide metabolism, pyruvate metabolism, TCA cycle and oxidative phosphorylation) and the neuroactive ligand-receptor interaction pathway—a pattern absent in bacterial and fungal infections. LdMNPV drove tree-top disease through a virus-specific, multi-system manipulation strategy that couples metabolic activation with neural signaling modulation. This comparative study reveals fundamental differences in behavioral manipulation across pathogen kingdoms and provides candidate pathways for functional validation. Full article

Bioactive glass (BAG) S53P4 is a clinically approved bone substitute with antibacterial, osteoconductive and osteostimulatory properties. Its antibacterial effect is associated with ion release, local pH elevation and osmolality, but the precise biochemical and biophysical mode-of-action is unclear. This study investigates the antibacterial mechanism of BAG S53P4 eluates. BAG eluates, collected at 2, 4, 8, and 24 h, eradicated Staphylococcus aureus. Elemental analysis revealed an early increase in concentrations of Si and Na, a later rise in Ca, depletion of P over time and rapid loss of Mg. Membrane disturbances occurred within 5 min, evident by permeability for SYTOX, aligning with time-kill kinetics for S. aureus and Bacillus subtilis. In B. subtilis, 2h-BAG-eluate induced rapid delocalization of marker proteins for cell division and DNA repair, signaling membrane potential collapse and nucleoid condensation. Transcriptomics revealed early transcription remodeling reflecting ionic and energetic imbalance, including disruption of central metabolism, redox homeostasis, and translational stability. Scanning electron microscopy revealed severe cell surface damage and particulate deposits on S. aureus. Transmission electron microscopy showed cell envelop disruptions and cytoplasmic leakage. Energy dispersive X-ray analysis identified Si on bacterial cell surface at 4 h and intracellular accumulation in punctured, empty cells at 24 h. Overall, BAG ionic dissolution products kill bacteria through a stepwise mechanism involving membrane damage, protein delocalization and metabolic impairment, accompanied by Si deposition on bacterial surfaces and loss of Mg. This finally leads to cell wall degradation, cytoplasmic content leakage and further Si deposition on the cells and inside cell ghosts. Full article

Background/Objectives: Carbon dots (CDs) are promising antimicrobial nanomaterials owing to their biocompatibility, environmental friendliness, and tunable surface chemistry. This study aimed to synthesize nitrogen-doped CDs (AS-CDs) and develop a light-responsive antibacterial system through conjugation with chlorin e6 (Ce6). Methods: AS-CDs were synthesized by a microwave-assisted method using L-ascorbic acid and spermidine, followed by conjugation with Ce6. The materials were characterized by transmission electron microscopy, zeta potential analysis, and spectroscopic methods, and their antibacterial activity was evaluated against Escherichia coli, Staphylococcus aureus, and methicillin-resistant S. aureus (MRSA) under both dark and visible-light conditions. Cytotoxicity was assessed using HaCaT cells. Results: The AS-CDs exhibited a uniform nanoscale morphology with an average diameter of 6.3 nm and a positive surface charge of +15.6 mV, together with intrinsic broad-spectrum antibacterial activity. Ce6 conjugation further enhanced antibacterial efficacy under light irradiation, with the CDs-Ce6 conjugate achieving complete eradication of S. aureus and MRSA and marked inhibition of E. coli at 2.5 μg/mL. Cytotoxicity studies demonstrated low toxicity in HaCaT cells within the effective antibacterial concentration range. Conclusions: These findings highlight the potential of microwave-synthesized, photosensitizer-conjugated CDs as next-generation antimicrobial agents. This platform offers a cost-effective, sustainable, eco-friendly, and efficient platform for combating bacterial infections, with broader potential in pharmaceutical and biomedical applications. Full article

Green synthesis is an eco-friendly, simple, and cost-effective process for the synthesis of metal nanoparticles from plant extracts that are rich in bioactive compounds. In the current study, the antioxidant potential and total soluble polyphenol content (TPC) of different parts of Ligusticum mutellina (L.) Crantz were evaluated using DPPH (2,2-diphenyl-1-picrylhydrazyl) and FRAP (ferric reducing antioxidant power) assays, and the results indicated that the seed extract was the most active plant part. HPLC analysis indicated the presence of phenolic compounds such as gallic acid, protocatechuic acid, and catechin, which may contribute to the reduction and stabilization of AgNPs. Silver nanoparticles (AgNPs) were synthesized from the aqueous seed extract of L. mutellina. The formation of nanoparticles was confirmed by UV–Vis spectroscopy, FT-IR analysis, powder X-ray diffraction (PXRD), and transmission electron microscopy (TEM). The UV–Vis spectrum indicated a surface plasmon resonance peak at around 411 nm, and PXRD analysis indicated an average crystallite size of around 13 nm. TEM analysis revealed predominantly spherical nanoparticles with an average size of 25.36 ± 10.76 nm. The synthesized AgNPs exhibited strong antibacterial activity against Gram-positive (Staphylococcus aureus and Bacillus subtilis) and Gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria. Overall, the results demonstrate that L. mutellina seed extract represents an effective natural source of reducing and stabilizing agents for green nanoparticle synthesis and highlight the potential of the obtained AgNPs as environmentally friendly antimicrobial materials. Full article

Chitosan-based active films containing microwave-extracted Terminalia catappa leaf extract (TE) and hydrothermally synthesised zinc oxide were developed and characterised. The selected extraction condition (440 W, 20 min, followed by freeze drying) gave 29.5% extract recovery and a total phenolic content of 639.5 mg GAE/g extract. Structural analyses showed that the original crystalline ZnO phase was no longer detectable after film formation under acidic casting conditions, whereas zinc remained present in the film matrix, indicating acid-mediated dissolution and/or structural transformation during casting. Zinc-containing films exhibited higher tensile strength (up to 36.0 MPa), increased glass transition temperature (up to 122.9 °C), and reduced moisture content and water vapour transmission. TE contributed antioxidant activity and light-shielding properties, with antioxidant capacity reaching 22.1 mg Trolox/g film. Films containing ≥0.2% initial ZnO also showed disc-diffusion antimicrobial activity against Escherichia coli (up to 22.7 mm) and Staphylococcus aureus (up to 20.7 mm). A preliminary 7-day banana-wrapping study further suggested that intermediate formulations containing 0.1–0.2% TE and 0.2–0.3% initial ZnO provided a useful balance among mechanical performance, optical properties, antimicrobial activity, and visual preservation. Overall, zinc–polyphenol–chitosan interactions played an important role in governing film structure and functionality. Full article

Objective: The objective of this study is to evaluate the ability of silver oxide nanoparticle (Ag₂ONP)-functionalized high-efficiency particulate air (HEPA) filters and colloidal Ag₂ONP suspensions to inhibit biofilm formation by major respiratory pathogens causing infections at operating rooms. Background: Respiratory infections caused by bacterial pathogens such as Streptococcus pneumoniae, Pseudomonas aeruginosa and Staphylococcus species are often associated with the formation of biofilms, which confer increased resistance to antibiotics and host immune responses. Effective strategies to prevent biofilm formation on biological surfaces and in air filtration systems are urgently needed in clinical settings. Methods: The biofilm-forming ability of each bacterial strain was assessed by crystal violet microplate assay, viable count or confocal microscopy after prior incubation of the culture medium with Ag₂ONP-coated HEPA filter material or colloidal Ag₂ONP suspension. Results: Both silver-functionalized filters and silver nanoparticle suspensions significantly inhibited biofilm formation by S. pneumoniae and P. aeruginosa, with near-complete suppression observed. In the case of S. aureus and S. epidermidis, the silver nanoparticle suspension showed partial inhibition of biofilm development. Conclusions: Ag₂ONP-functionalized HEPA filters and colloidal Ag₂ONP suspensions effectively prevent biofilm formation by major respiratory pathogens, for both Gram-negative and Gram-positive bacteria. These materials show promise for integration with air filtration and surface coating systems to reduce microbial load and transmission in healthcare environments such as operating room facilities. Full article

Background: Livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA) ST398 poses a significant zoonotic threat, largely due to its capacity to acquire and disseminate antimicrobial resistance through mobile genetic elements (MGEs). Ready-to-eat (RTE) foods may serve as critical interfaces for zoonotic spillover. However, genomic data on ST398-MRSA-Vc isolates from RTE foods remain scarce, leaving the characteristics of their MGEs largely unresolved. Methods: This study performed whole-genome sequencing and comparative genomic analysis of an ST398-MRSA-Vc isolate (NPREF115) from an RTE pork product in China. Using NPREF115 and 134 publicly available S. aureus genomes from diverse sources, we constructed a core genome phylogeny and conducted SNP and pangenome analyses, with a focus on MGEs. Results: Phylogenetic analysis revealed that our foodborne ST398-MRSA-Vc isolate clustered with human, Capra pyrenaica, bovine, and swine-derived ST398-MRSA-Vc isolates. SNP analysis indicated NPREF115 was most closely related to human clinical isolates (132 and 140 SNPs, respectively), consistent with shared ancestry rather than recent cross-host transmission. Genomic divergence was largely confined to MGEs, including SCCmec, prophages, genomic islands, and a chromosomally integrated Tn560 carrying the ant(9)-Ia-lsa(E)-lnu(B) multidrug resistance cluster. Notably, NPREF115 harbored a unique metabolic gene that may facilitate persistence in high-osmolarity food environments. Conclusions: The successful colonization of food by the ST398-MRSA-Vc isolate is likely associated with the acquisition of multiple MGEs harboring antimicrobial resistance genes. Transmission of ST398-MRSA-Vc between food, human, and livestock hosts was accompanied by changes in genes involved in metabolism. These findings underscore the importance of monitoring MGEs in genomic surveillance of foodborne MRSA. Full article

Cutaneous wound healing is a complex biological process often impaired by bacterial infections, especially by Staphylococcus aureus. To address this, alginate (ALG)/chitosan (CS) polyelectrolyte multilayer (PEM) films incorporating alginate-coated silver nanoparticles (ALG–AgNPs) were fabricated by layer-by-layer self-assembly. The films exhibited a porous, layered morphology with homogeneous distribution of ALG–AgNPs, hydrophilic surfaces (contact angle ≈ 55°), a high swelling degree (~175%), and a water vapor transmission rate of 1830 g m⁻²·day⁻¹. Thermal analyses showed similar degradation profiles up to 600 °C, with the ALG–AgNP film displaying lower moisture loss and higher dehydration temperature, consistent with enhanced ionic and coordination crosslinking (–NH₃⁺/–COO⁻ and Ag–O–C bonds). The release of Ag⁺ in PBS (pH 7.4) was ~3% after 24 h, following a Korsmeyer–Peppas mechanism (R² = 0.97, n < 0.5), and degradation, with ~40% mass loss in 6 days, indicated gradual matrix disintegration. Cytocompatibility studies revealed >80% viability for fibroblasts, keratinocytes, macrophages, and <2% hemolysis of red blood cells. Immune assays showed a tendency towards reduced TNF-α and IL-1β and regulated IL-6/IL-8 release. Antibacterial evaluations demonstrated a 5-log reduction in planktonic bacterial viability and >2-log reduction in adhesion, and an 11 ± 1 mm inhibition zone for S. aureus. These results demonstrate that ALG/CS–AgNP PEM films combine biocompatibility, antibacterial efficacy, controlled degradation, and structural stability, making them promising multifunctional scaffolds for the regeneration of infected skin wounds. Full article

PrFeTiO₃ perovskite composite was synthesized, and its structural, morphological, chemical, and optical properties were comprehensively characterized. X-ray diffraction (XRD) and a selected area electron diffraction (SAED) confirm the formation of an orthorhombic distorted perovskite phase with no secondary impurities. Transmission electron microscope (TEM) observations show aggregated nanocrystalline domains, while EDS mapping reveals homogeneous cation distribution (Pr, Fe, Ti, O), confirming successful incorporation of Fe and Ti into the perovskite lattice. X-ray photoelectron spectroscopy (XPS) analysis identifies Pr³⁺, Fe³⁺, and Ti⁴⁺ as the dominant oxidation states, supporting charge-compensated B-site substitution. Optical analysis reveals a bandgap of ~2.0 eV, significantly narrower than pristine titanates, indicating enhanced visible-light absorption. This multi-modal characterization verifies the successful formation of PrFeTiO₃ and highlights its potential as a visible-light-active photocatalyst. Although PrTiO₃ showed little reactivity to visible light, PrFeTiO₃ showed excellent efficiency in visible light photocatalytic reactions. PrFeTiO₃ showed more than 20 times better performance than PrTiO₃ in the photodegradation of methylene blue in the liquid phase and formaldehyde in the gas phase. Furthermore, PrFeTiO₃ showed more than 95% superior bactericidal activity against the pathogenic bacterium Staphylococcus aureus than PrTiO₃. Its high photocatalytic efficiency can be attributed to its strong photosensitivity to visible light and small band gap energy. Full article

The process of ensuring the safety of the food supply is dynamic. Both the possibility of contamination and the effectiveness of safety precautions are impacted by changes in the kinds of food consumed, the geographical origins of food products, and the methods by which these foods are processed. For instance, compared to earlier generations, consumers’ general understanding of safe food preparation and handling techniques has decreased due to a higher reliance on prepackaged convenience foods. Nowadays, consumers depend increasingly on other people to make sure the food they eat is safe. Growing consumption of minimally processed foods and growing imports of fresh products from other nations have resulted from changes in consumer tastes and food processing technologies. This review aims to critically synthesize existing knowledge on microbial risks in food, focusing on their sources, mechanisms of contamination, risk evaluation methodologies, and implementation of food safety measures. Major foodborne pathogens, including Salmonella, Escherichia coli, Listeria monocytogenes, and Norovirus, are discussed alongside factors influencing their survival and transmission. Today Clostridium botulinum, Staphylococcus aureus, and Salmonella spp. remain among the major foodborne pathogens, but during the last two decades food-borne diseases such as shigellosis, listeriosis, campylobacteriosis, and diseases caused by pathogenic strains of Escherichia coli have become increasingly salient. These new concerns necessitate continued investment in research and technology development to improve the safety of the food supply. The review highlights current approaches to microbiological risk assessment, regulatory frameworks, and control strategies, while also addressing emerging challenges such as antimicrobial resistance, biofilms, and ready-to-eat foods. By integrating risk evaluation with practical implementation strategies, this review provides valuable insights for researchers, regulators, and food industry stakeholders seeking to strengthen food safety systems and reduce the burden of foodborne diseases. Full article

A comparative cross-sectional study was undertaken in organized and unorganized dairy sectors to evaluate the prevalence of bovine mastitis and the antibiotic resistance in Staphylococcus spp. of dairy animals and their associated personnel. A total of 391 households (HH) consisting of 211 and 180 HHs from organized and unorganized sectors, respectively, were selected based on 30-cluster sampling methodology in southern and northeastern regions of India. From 391 HHs, a total of 1920 milking cows (organized dairy—533; unorganized dairy—1387) were screened for subclinical and clinical mastitis by the California Mastitis Test (CMT). Out of 1920 milk samples, 1002 milk samples, 362 associated personnel hand and nasal swabs, and 27 milking machine swabs were sourced. The samples were subjected to Staphylococcus spp. by isolation and identification by multiplex polymerase chain reactions (mPCRs) and antibiotic sensitivity testing (ABST) to determine antimicrobial resistance (AMR) profiles. CMT results showed high mastitis prevalence (54.65%) in unorganized farms compared to organized ones (45.78%), with a significant association of mastitis to dairy sectors (p = 0.0004). On speciation, S. aureus isolates were comparatively less than those of coagulase-negative staphylococci (CoNS) (3.5% and 7.7%, respectively) in the organized dairy sector, and the same was recorded for the unorganized dairy sector (0.85% and 13.19%, respectively). In both the dairy sectors, the highest antibiotic resistance for Staphylococcus spp. was observed against the β-lactams (penicillins and cephalosporins) group (71.36% and 76.59%) and the lowest for nitrofurans (3.5% and 3%), oxazolidines (0.7% and 5.1%), and rifamycin (0.7% and 5.1%), respectively. In both the sectors, human isolates had comparatively high mecA positives (15.70% and 15.96%) compared to the animal isolates (8.36% and 12.94%). Based on mPCR, a smaller number of methicillin-resistant S. aureus (MRSA) isolates (3.95%) than methicillin-resistant coagulase-negative Staphylococci (MRCoNS) was detected in milk samples (6.05%), and the same was observed for associated personnel samples (MRCoNS (14.63%) compared to MRSA (1.05%)). In four HHs, mecA positives were detected in both animal and human samples, and this highlights the transmission dynamics of mecA between animals and humans in households. The resistance of Staphylococcus spp. to β-lactams highlights the need for cautious antibiotic use to prevent AMR. Full article