Disc Diffusion Method Research Articles

Physiochemical Analysis, Antioxidant Activity, Antimicrobial Activity and Phenolic Profile of Ipomoea eriocarpa R. Br. Leaves.

Many active substances found in plants are essential in the treatment of transmissible and non-transmissible ailments. To enhance their well-being and capabilities, most people around the globe use medicines from plants and herbal origin. The goal of the current study was an assessment of physiochemical properties as well as measuring the effect of various solvents (ethanol, chloroform, and water) on the phenolic profile and on free radical scavenging potential. The standard procedures were used for the preliminary phytochemical, physiochemical and fluorescence analysis. Folin-Ciocalteu and colorimetric methods were used to determine the quantitative phytochemical analysis, respectively. The free radical scavenging potential was determined through 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′′-casino-bis (3-ethylbenzothiazoline-6-sulphonic) acid (ABTS) assays. The antimicrobial activity was assessed using the disk diffusion method on a range of bacterial and fungal strains. The finding showed that ethanol was the best solvent for extracting polyphenols. The presence of alkaloids, carbohydrates, flavonoids, glycosides, phenolic compounds, and tannins was observed in the plant. Additionally, fluorescence characteristics and physiochemical parameters provided valuable data that can be used to establish standards for this plant. Results of quantitative phytochemical estimation revealed that the ethanol extract had a higher phenolic content (71.82 mg/g GAE) and flavonoid content (82.7 mg/g QE), while the aqueous extract had the lowest phenolic content (27.05 mg/g GAE) and flavonoid content (18.93 mg/g QE). The I. eriocarpa ethanolic extract had the maximum scavenging potential against DPPH (32.36 µg/mL) and ABTS (55.54 µg/mL). The results of the antimicrobial activity assessment also indicate that the ethanol extract exhibited a greater inhibition zone when tested against both bacterial strains. Results of thecurrent study suggested that the ethanolic extract has significant antioxidant potential and has the capability of being a notable source of organic antioxidants for the formulation of functional foods.

Protein‐Based Polymeric Metal–Nanocomposite Derived From Egg Albumin: A Highly Effective Antimicrobial Agent Against Bacteria

ABSTRACTThe synthesis of four distinct protein‐based metal nanocomposites has been fabricated by employing egg albumin and zinc metal through a simple, straightforward two‐step method. The Fourier transform infrared (FTIR), X‐ray diffraction (XRD), and scanning electron microscopy (SEM) analyses confirmed the successful incorporation of zinc nanoparticles into the protein matrix and revealed an irregular microporous structure with average crystallite sizes of less than 100 nm. Thermal stability was assessed via thermogravimetric (TG) and derivative thermal gravimetry (DTG) analysis, revealing a notable increase in thermal stability in a high‐temperature range (300°C°C–700°C), suggesting remarkable stability at elevated temperatures. Antimicrobial efficacy against both gram‐positive (B. cereus and Lactobacillus spp.) and gram‐negative bacteria (E. coli and K. pneumoniae) was evaluated using paper disk diffusion, pour plate, and minimum inhibitory concentration (MIC) methods. All samples exhibited antibacterial efficacy, with zone of inhibition (ZOI) diameters ranging from 12 to 35 mm, and demonstrated a bactericidal effect by eliminating 93 to 98% of bacteria within 8 to 20 h at their MICs. Notably, protein–ZnO–PANI exhibited potent antimicrobial activity against all four bacterial strains and among all the samples, demonstrated higher antimicrobial activity than the unpolymerized nanocomposites. The disk diffusion study confirmed that a concentration of 25 μg/mL of protein–ZnO–PANI resulted in ZOI measurements of 25 mm and 35 mm, whereas MIC values of 300 μg/mL and 200 μg/mL were observed against Bacillus cereus and E. coli, respectively, and killed 95% of B. cereus and 98% of E. coli within 24 h. Based on the obtained results, a plausible mechanism was also proposed.

Antimicrobial Susceptibility Patterns of Bacteria Associated with Upper Respiratory Tract Infections in North and South Waziristan, Pakistan

Background: Upper respiratory tract infections (URTIs) are a significant cause of outpatient visits globally, with antimicrobial resistance (AMR) presenting a growing challenge to effective treatment. In Pakistan's tribal regions, limited healthcare access exacerbates this issue.Objective: To determine the prevalence of bacterial pathogens causing URTIs and assess their antimicrobial susceptibility patterns in North and South Waziristan, Pakistan.Methods: This cross-sectional study involved 300 throat swabs collected from outpatients between January and June 2023. Samples were inoculated on Blood, MacConkey, and Chocolate agars, followed by incubation at 37°C for 24 hours. Standard biochemical tests were used for bacterial identification, and the Kirby-Bauer disc diffusion method assessed antimicrobial susceptibility. Statistical analysis was performed using SPSS version 25.0, with p-values ≤ 0.05 considered significant.Results: Pathogens were isolated in 93% of samples, with Staphylococcus aureus (40.2%), viridans group streptococci (35.7%), and Streptococcus pyogenes (17.1%) being the most common. Resistance was highest in viridans group streptococci (33.7% to tazobactam) and lowest in Streptococcus pyogenes (26.3%).Conclusion: The high rates of resistance, particularly in viridans group streptococci, highlight the need for targeted interventions to mitigate AMR in this region.

Physicochemical characteristics and antibiotic resistance patterns of enteric bacteria isolated from harvested rainwater (HRW) in Oraukwu, Anambra State, Nigeria

infections temperature, colour, turbidity, DO, TDS, TSS, alkalinity, hardness, chloride, and some heavy metals of the water samples were examined using APHA method. Bacteriological analyses were performed using the membrane filtration technique. Colonies formed were counted and expressed in CFU/100mL. Enteric bacteria were enumerated and characterized by their morphological characteristics and biochemical tests. Axenic cultures of the isolates were further subjected to antimicrobial susceptibility testing (AST) using the modified Kirby-Bauer disc diffusion method, based on the guidelines by CLSI. Results revealed that physicochemical parameters and some heavy metals were within acceptable limits, except for Fe (0.01-0.72 mg/L) and Pb (0.01-0.25 mg/L). Total bacterial counts ranged from 1.2×104 to 6.8×104 CFU/100mL, indicating high contamination. Morphological characteristics revealed twelve (12) isolates of enteric bacteria, comprising Escherichia coli (41.67%), Salmonella sp. (33.33%) and Shigella sp. (25%). All the isolates exhibited 100% resistant to augmentin and tetracycline, but showed varying degrees of susceptibilities; E. coli to levofloxacin (60%), Salmonella sp. to ertapenem, imipenem, levofloxacin and nalidixic acid (100%), and Shigella sp. to ceftriaxone and ertapenem (100%). ‘First flush’ diverters are recommended to be installed within the water collecting system, in order to divert runoff from the rooftop after a period of no rainfall. Antibiotics which the isolates were susceptible to are recommended for the treatment of infections caused by these pathogens.

Antimicrobial properties and biocompatibility of semi-synthetic carbohydrate-based ionic hydrogels.

Hydrogels have gained significant interest in the last decades, especially in the medical sector, due to their versatile properties. While hydrogels from naturally occurring polysaccharides (e.g. cellulose) are well-known, those produced from polymerizable carbohydrate-based monomers remain underexplored. However, these semi-synthetic hydrogels offer the great advantage of having adjustable properties for customization depending on their application. The objective of this study was to characterize semi-synthetic carbohydrate-based ionic hydrogels produced from GVIM-I (glucosyl vinyl imidazolium iodide). The antimicrobial activity was evaluated using the disk diffusion method, which demonstrated that all samples exhibit inhibitory effects on the growth of Candida auris. In vitro biocompatibility was determined by cell viability studies with L929 mouse fibroblasts, and a correlation was observed between eluate concentration and cell viability. In particular, the type of initiator system employed for polymerization was found to affect cell viability. The direct contact assessments showed that specific pre-treatments of the hydrogels resulted in higher cell viability than non-treated hydrogels. The results also revealed the impact of crosslinker concentration and type and identified poly(ethylene glycol)diacrylate (PEGDA) 575 as a promising crosslinker for future medical applications. LC-MS analysis of the wash medium identified unreacted GVIM-I as the leached material, which is presumed to be the cause of the observed cytotoxicity. Overall, the study provides valuable insights into the characteristics of GVIM-I based hydrogels and sheds light on the factors that influence their cytotoxicity and potential for medical application.

ISOLATION, IDENTIFICATION AND ANTIMICROBIAL RESISTANCE PROFILES OF BACTERIA FROM SPOILED FRUITS IN RAWALAKOT DISTRICT POONCH, AZAD JAMMU AND KASHMIR

Fruits play a vital role in human diet by providing essential growth factors such as vitamins and minerals in daily diet which help to live healthy life. Bacteria are important factor for spoilage of fruits. Bacterial degradation first causes softening of tissues as pectin are degraded and the whole fruit may eventually degenerate into a slimy mass. Spoilage refers to any change in fruit condition in which fruit become unacceptable or undesirable for human use. Therefore present study was conducted at Rawalakot, District Pooch AJK, to identify the bacteria (E. coli and Staphylococcus aureus) from spoiled fruit samples as well as to determine the antimicrobial resistance pattern of these isolated bacteria using antibiotic disc diffusion method. For this purpose a total of 100 spoiled fruit samples (50 samples of spoiled apple and 50 samples of spoiled banana) were randomly collected from different locations of Rawalakot including Kharick, Kasaigali, D. Chowk, Nala Bazar and Supply Bazar by random sampling technique. Results of the study showed that out of 50 samples of Banana 25(50%) samples were positive for Staphylococcus aureus and 25(50%) were positive for E. coli. While among 50 samples of Apple 25(50%) were positive for E. coli and 25(50%) were positive for Staphylococcus aureus respectively. For antimicrobial susceptibility test disc diffusion method was followed. S. aureus from apple samples the highest resistance was observed for Sulphamethox 25(100%) and Cefoxtin 25(100%) while for banana the highest %age was recorded for Amoxicillin 25(100%) and Sulphamethox 25(100%) respectively. E. coli from apple samples strains were highly resistant to Erythromycin 22(88%), while for banana the highest percentage was recorded for Amoxicillin 23(92%) and Erythromycin 20(80%).

Genetic and in-silico approaches for investigating the mechanisms of ciprofloxacin resistance in Salmonella typhi: Mutations, extrusion, and antimicrobial resistance

Salmonella enterica serovar Typhi spreads typhoid infection in humans through the consumption of contaminated food and water. Poor sanitation plays a pivotal role in its dissemination. Over time, the bacterium has acquired resistance to many promising antibiotics, posing a growing global health concern and hindering the achievement of sustainable development goals. This study aims to elucidate the molecular complexity of fluoroquinolone resistance, a first-line treatment for typhoid infection. To achieve this aim, 80 clinical isolates were collected from various diagnostic laboratories. These isolates were confirmed based on morphological characteristics and biochemical tests. Multidrug-resistant (MDR) and extensively drug-resistant (XDR) isolates were identified using the Kirby-Bauer disc diffusion method. The mechanism of ciprofloxacin resistance was investigated by sequencing the quinolone resistance-determining region (QRDR) genes and identifying the presence of the qnrS1 gene. As a result of this study, 60 % of isolates showed resistance to ciprofloxacin. At the same time, the qnrS1 gene was present in all the selected strains while mutation analysis identified significant mutation in QRDR of DNA gyrase subunit A (gyrA) and Topoisomerase IV (parC) gene. The combinatorial effect was further investigated by downloading 286 draft genomes. The Mutation analysis reveals significant mutations at gyrA S83F, gyrA D87N, gyrA S83Y, gyrB S464F, parC S80I, and parE L416F. Additionally, docking analysis indicates reduced binding affinity and altered solvent accessibility, which show the structural changes at mutation sites. This study provides crucial insights that mutation reduces the binding affinity while qnrS1 acts as a transport channel to extrude the ciprofloxacin. In the future, further validation through experimental mutagenesis is recommended, for targeted therapeutic interventions against the mounting threat of antibiotic-resistant S. Typhi.

Multicentre evaluation of in vitro activity of contezolid against drug-resistant Staphylococcus and Enterococcus.

To investigate susceptibility to contezolid, a novel oxazolidinone, multicentre surveillance was conducted involving 2449 strains of Staphylococcus and Enterococcus collected from 65 hospitals across China. The MICs of contezolid, linezolid and other clinically significant antibiotics were determined by the broth microdilution method. Consistency with the broth microdilution method for contezolid was assessed using agar dilution method, as well as disc diffusion and ETEST for linezolid, respectively. WGS was conducted on all 20 linezolid-resistant and 30 randomly non-resistant strains to analyse linezolid resistance genes (optrA, poxtA, cfr) and 23S rRNA mutation sites. All strains exhibited WT susceptibility to contezolid, while resistance proportions to daptomycin, vancomycin, teicoplanin, tigecycline and eravacycline ranged from 0% to 5.2% in Staphylococcus, and from 0% to 7.8% in Enterococcus. Linezolid resistance was higher in Enterococcus faecalis (4.4%) compared with Enterococcus faecium (0.2%). Contezolid showed a lower MIC50 (0.5 mg/L) than linezolid (2 mg/L) for methicillin-resistant Staphylococcus. Against Enterococcus, contezolid demonstrated a cumulative MIC percentage of 70% for VRE and 39.1% for E. faecalis (at MIC = 1 mg/L), whereas linezolid showed 0% and 1.1%, respectively. Among the 20 linezolid-resistant Enterococcus strains, all carried the optrA gene without 23S rRNA mutations. For contezolid, MICs were 4 mg/L for 19 strains and 2 mg/L for 1 strain. The ETEST, agar dilution and disc diffusion methods showed essential and categorical agreements of >90% for linezolid, with no major errors or very major errors. Contezolid demonstrated significant in vitro antibacterial activity against methicillin-resistant Staphylococcus, VRE and linezolid-resistant E. faecalis.

Antibiotic Susceptibility Pattern of Pseudomonas aeruginosa and Detection of Virulence Genes in a Tertiary Care Hospital, Kathmandu, Nepal

Pseudomonas aeruginosa is one of the most common causes of hospital-acquired infections. It threatens worldwide public health because of its intrinsic antibiotic resistance and virulence. In this context, this research aimed to determine the occurrence of P. aeruginosa in a clinical setting, examine its susceptibility to antibiotics, and detect the presence of virulence genes, viz. exoY, oprL and toxA in all isolates. It was a cross-sectional study carried out from June 2022 to December 2022. A total of 1356 clinical specimens were collected and processed in the laboratory for Gram staining, culture techniques, and biochemical tests. The Kirby-Bauer disk diffusion method was applied to examine the antibiotic susceptibility pattern and conventional PCR was used to detect the virulence genes in all confirmed P. aeruginosa isolates. 40.5% of specimens showed bacterial growth, of which only 3.02% were identified as P. aeruginosa. Among them, 61.0% were multidrug resistant and 29.2% were β-lactamase producers. Aztreonam (70.7%) was the most effective antibiotic. Among all P. aeruginosa isolates, 68.3% isolates were exoY positive, 61.0% were oprL positive and 56.1% were toxA positive. Strategic interventions are required to stop the emergence and spread of antimicrobial resistance as a result of the isolation of multidrug resistant (MDR) isolates carrying these virulence genes. This study can benefit the medical staff and the entire community in building a surveillance system and enhancing infection control procedures.

Uji Efektivitas Daya Hambat Ekstrak dan Perasan Lidah Buaya (Aloe barbadensis Miller) pada Bakteri Staphylococcus Aureus dengan Metode Difusi

Aloe vera is a plant that is rich in minerals, vitamins, and antibacterial properties. A study to analyze the antibacterial effectiveness of aloe vera in inhibiting the growth of Staphylococcus aureus bacteria isolated from acne pus. This study was an experimental laboratory study using the disc diffusion method, located at the Bacteriology Laboratory, Department of Medical Laboratory Technology, Poltekkes Kemenkes Surabaya, from February to May 2024. There were 6 sample treatments with 4 replications, 4 treatments of extract and juice concentration variations, namely concentrations of 70%, 80%, 90%, 100%, positive control using penicillin antibiotics, and negative control using clean distilled water. The results of this study show that at aloe vera extract concentrations of 70%, 80%, 90%, and 100%, the average diameter of the inhibition zone was 9 mm, 10 mm, 11 mm, and 12 mm, respectively, while in aloe vera juice, these concentrations did not form an inhibition zone. So it was concluded that aloe vera extract is more effective than aloe vera juice, the most successful test material to slow the growth of Staphylococcus aureus bacteria in this study was aloe vera extract with a concentration of 100%. This study also conducted qualitative phytochemical testing on aloe vera extract which has antibacterial compounds, namely saponins, tannins, flavonoids, and terpenoids. The results of the study on the effectiveness of the inhibitory power of aloe vera extract and juice against Staphylococcus aureus bacteria using the disc diffusion method were analyzed using quantitative descriptive and presented in tabulation form in the form of the diameter of the inhibition zone formed.

MODIFICATION OF GLASS IONOMER FILLING MATERIAL BY METAL NANOPARTICLES AND THEIR COMPOUNDS: EFFECT ON ANTI-MICROBIAL ACTIVITY

Background: Glass ionomer filling materials are widely used in stomatology, but do not have an antimicrobial effect that effectively prevents the development of secondary and recurrent dental caries. Researchers are attempting to modify these materials by introducing various biologically active additives into them. The aim of the study was to evaluate the antimicrobial properties of a dental ionomer filling material modified withadditives based on high–energy nanoparticles of silver, copper, titanium and their compounds. Material and methods: Colloidal aqueous and alcoholic solutions of metals and their oxides with stabilizers were obtained by the electroerosion method. Citric acid, cetylpyridinium chloride and Trilon B were used as stabilizers. The zeta potential and the distribution of particles of the dispersed phase in solutions were measured. Samples of dental glass ionomer cement "Cemion-Aqua" were impregnated with colloidal solutions of nanoparticles. The microbiological activity of glass ionomer fillings samples in relation to plaque was determined by disc diffusion and suspension methods. Results: The results showed that modification of glass ionomer cement samples with silver hydrosols in citric acid solutions with concentrations of 0.04% and 0.0025% increases the zone of radial lysis of microbial plaque colonies around the cement samples by 1.5 and 2.5 times compared with the control. By the suspension method, it was determined that silver hydrosols in a solution of citric acid and without it reduce the formation of colonies of microorganisms to several units up to 72 hours of exposure compared with the control. And copper hydrosols in solutions of cetylpyridinium chloride prevent an increase in the number of colonies of microorganisms after 24 hours of exposure compared with the control. Silver hydrosol in a solution of citric acid with a concentration of 0.0025% and silver alcohol sol reduce the number of colonies of microorganisms to several units after 3 hours of exposure.

Phytochemical Analysis and Nanoparticle Formulations of Extracts Myristica fragrans Houtt Leaves as Antibacterial

Myristica fragrans Houtt leaves contain secondary metabolites such as flavonoids, terpenoids and alkaloids, which have antibacterial properties. At the nanoscale, the particles have a bigger surface contact area, resulting in increased amounts and solubility of the active chemical. This leads to a stronger antibacterial activity. This study aims to examine the influence of several chitosan variations on particle size, antibacterial properties and the form of nanoparticles produced from Myristica fragrans leaves ethanol extract. Ethanol extract was analyzed using the UV-Vis spectrophotometric method to quantify total flavonoid content. Nanoparticles were synthesized using the ionic gelation technique with several ratios of chitosan and sodium tripolyphosphate, specifically 8:1, 10:1 and 12:1. Nanoparticles were analyzed with a Particle Size Analyzer (PSA) and Scanning Electron Microscopy (SEM). Agar diffusion test for bacteria germs using a paper backer. Myristica fragrans leaves ethanol extract was 50, 40 and 30 %, while nanoparticle extract was 5, 4 and 3 %. The overall flavonoid concentration in the QE/ethanol extract was 39.7252 ± 1.9596 mg. Antibacterial test results against Staphylococcus aureus and Escherichia coli bacteria and Myristica fragrans leaves extract limit inhibition area at 30 % (13.35 mm), 40 % (13.68 mm) and 50 % (13.93 mm) for Staphylococcus aureus and 30 (13.28), 40 (13.45) and 50 % (13.81 mm) for Escherichia coli. Myristica fragrans leaves extract chitosan nanoparticles included 3 (14.70), 4 (15.30) and 5 % (15.56 mm) for Staphylococcus aureus and 3 (14.60), 4 (14.65) and 5 % (15.05 mm) for Escherichia coli. Ionic gelation can create nanoparticles of Myristica fragrans leaves ethanol extract with chitosan and sodium tripolyphosphate. Myristica fragrans leaves nanoparticle ethanol extract exhibits better antibacterial activity than ethanol extract. Increasing chitosan concentration affects particle size. The ethanol extract of Myristica fragrans nanoparticle leaves showed slightly better antibacterial activity than the ethanol extract. HIGHLIGHTS Nanoparticles of extracts and extracts have proven excellent antibacterial activity against human pathogens through paper disc diffusion method. Antibacterial test results against Staphylococcus aureus and Escherichia coli bacteria and Myristica fragrans leaves extract limit inhibition area at 30 % (13.35 mm), 40 % (13.68 mm), and 50 % (13.93 mm) for Staphylococcus aureus and 30 % (13.28 mm), 40 % (13.45 mm), and 50 % (13.81 mm) for Escherichia coli. Myristica fragrans leaves extract chitosan nanoparticles included 3 % (14.70 mm), 4 % (15.30 mm), and 5 % (15.56 mm) for Staphylococcus aureus and 3 % (14.60 mm), 4 % (14.65 mm), and 5 % (15.05 mm) for Escherichia coli. The synthesized extract nanoparticles can be used against human pathogens acts as antibacterial drugs. GRAPHICAL ABSTRACT

Isolation and antimicrobial susceptibility profile of Salmonella species from slaughtered cattle carcasses and abattoir personnel at Dessie, municipality Abattoir, Northeast Ethiopia

BackgroundAntibiotic-resistant Salmonella is one of the main public health concerns in the world. Isolation of Salmonella in abattoirs has been considered the core source of infection in the community from meat. Still, there is limited information on the contamination rate of cattle carcasses.ObjectiveThis study aimed to document the occurrence and antimicrobial susceptibility profile of Salmonella species recovered from cattle carcass and abattoir personnel at Dessie, municipality abattoir, Northeast Ethiopia:MethodsA total of 336 carcass swabs of abdomen, neck, and hind limb from cattle carcasses and 24 stool samples were collected from abattoir personnel using a systematic sampling method from February to April 2019. The collected samples were transported using Cary-Blair transport media and cultivated on Selenite cysteine F-broth, Brilliant green agar, and Xylose-lysine deoxycholate agar plates to isolate Salmonella species. Gram stain, colony morphology, and biochemical tests were performed to identify the isolated bacteria. An antimicrobial susceptibility test for Salmonella was performed using the Kirby-Bauer Disc Diffusion method. Descriptive statistics; both bivariable and multivariable logistic regression analysis was performed using SPSS version 25 software. P-value < 0.05 at 95% CI was considered statistically significant.ResultsThe prevalence of salmonella species was 8%(27/336) from all samples.‘The prevalence of Salmonella isolates in cattle carcass and abattoir personnel was 8%(25/312) and 8.3%(2/24) respectively. The antimicrobial test showed that Salmonella species were 100% resistant to ampicillin, 59.3% to trimethoprim-sulfamethoxazole, 59.3% to tetracycline, and 55.6% to amoxicillin/clavulanate. From the total antimicrobial tested bacteria, 81.5%(22/27) were resistant to three and above classes of antibiotics (drug classes). Unwashed knives, carcasses, and hands of butchers during slaughtering were significantly associated (p < 0.05) with Salmonella found in carcasses.ConclusionsSalmonella isolation rates from cattle carcasses were high, with the bacteria showing notable resistance to most tested antibiotics. Poor hygiene practices, unsanitized equipment, and unhygienic beef processing were contributing factors.

ANTIBIOGRAM ASSAY OF E.COLI ISOLATES IN PATIENTS WITH URINARY TRACT INFECTION

Screening of prevalent bacterial pathogens for antibiotic susceptibility profiles in different regions is necessary. E. coli and other pathogens are so common in our environment that it is essential to monitor trends in antibiotic susceptibility regularly. Objective: The aim of the study was to find out the antibiotic susceptibility pattern of E.coli isolates in patients with urinary tract infection. Methods: This study was conducted at the Saidu Group of Teaching Hospital Swat after taking permission from the ethical committee of the institute. We collected a total of 900 urine samples from males and females of all ages for culture and sensitivity. The Kirby-Bauer disc diffusion method was used to assess the antibiogram on Mueller-Hinton agar. The plates were kept in incubator at 37°C for the 48 hours, and the inhibition zone was measured. The antibiogram was performed by Kirby-Bauer disc diffusion method applying various antibiotics. The bacterial strains were classified in to three majors groups on the basis of antibiotic susceptibility pattern resistant (R) sensitive (S), and intermediate (I). Data was statistically analyzed presented in the tables and figures. Results: For culture and sensitivity testing, a total of 900 urine samples from patients with suspected UTIs were obtained from the several departments' inpatient and outpatient to the microbiological lab. Substantial bacteriuria was noted in 250 (27.7%). The most prevalent bacteria isolated was E.coli (55%) and its antibiogram was carried out. Ampicillin had the highest proportion of resistance (96.1%), followed by Ceftriaxone (91%), Moxifloxacin (87.1%), and Ceftazidime (75.5%). Whereas it was sensitive to Fosfomycin (94.2%), followed by Sulzone ( 84.3%), Imepinem (84.3%) and Amikacin (78%). Conclusion: It was concluded from the current study that the most prevalent bacteria causing urinary tract infection was E.coli, and this bacteria showed remarkable resistance against Ampicillin Ceftriaxone, Moxifloxacin, and Ceftazidime. The most used bacterium antibiotics for therapy were Fosfomycin, Imepinem and Amikacin. Therefore, antibiotic susceptibility should be considered before therapy.

Antibiotic Resistance of Escherichia coli and Salmonella spp. Strains Isolated from Some Selected Poultry Farms in the Oforikrom Municipality Kumasi, Ghana

Antimicrobial resistance (AMR) is a serious worldwide issue that poses a significant risk to human and animal health. In this study, isolates of Salmonella spp. and Escherichia coli from poultry farms in the Kumasi Metropolis, Ghana, were evaluated for AMR prevalence and trends. Samples were gathered from different farms using cloacal swabs and surgical shoe covers. The resistance and susceptibility levels were assessed using the Kirby Bauer disk diffusion method. Twenty-four isolates of Salmonella spp. and E. coli were identified. The E. coli bacteria that were found were resistant to Ciprofloxacin, Tetracycline, Ampicillin, Cefotaxime, Co-trimoxazole, and Cefuroxime but susceptible to Gentamicin and Amikacin. The Salmonella strains that were identified were resistant to Cefuroxime, Tetracycline, Ampicillin, Ciprofloxacin, Cefotaxime, Co-Trimoxazole, and Gentamicin but susceptible to Amikacin, Ofloxacin, and Chloramphenicol. This study suggests broader research on antibiotic resistance in birds and educating poultry farmers about changing medication practices due to increasing pathogen resistance.

Green Synthesis of Chitosan-coated Tin Dioxide Nanoparticles Using Moringa oleifera Flower Extract Against Breast Cancer via the Caspase-dependent Apoptotic Pathway

Background and Purpose In the present work, chitosan is furnished with tin dioxide (CsSnO2) nanoparticles (NPs) synthesized using the green route using Moringa oleifera ( M. oleifera) flower extract. Methods These preparation methods are low-cost, easily reproducible, nontoxic, and eco-friendly. X-ray diffraction (XRD), dynamic light scattering (DLS), field emission scanning electron microscope (FESEM), energy dispersive X-ray, Fourier-transform infrared spectroscopy (FT-IR), and photoluminescence (PL) analysis were used to learn more about the CsSnO2 NPs. The antibacterial property of CsSnO2 NPs was assessed by the disc diffusion method against various pathogens. The MTT assay was done to assess the cytotoxicity of CsSnO2 NPs in MCF-7 cells. The expressions of the apoptotic proteins were examined using assay kits. Results XRD results demonstrated that the formulated CsSnO2 NPs exhibit a tetragonal structure. From the FT-IR spectra, the Sn–O stretching peak was observed at 579 cm–1. A FESEM image shows that the CsSnO2 NPs were formed into a spherical structure. Surface defects, such as tin and oxygen vacancies, are visible in the PL spectra, and the average particle size of CsSnO2 NPs is 32 nm. Thus, surface defects are essential parameters for biocidal properties. The antimicrobial property of CsSnO2 NPs and amoxicillin was investigated against bacteria and human fungal pathogens. CsSnO2 NPs exhibit similar antimicrobial properties as compared to amoxicillin. Also, the dosage of CsSnO2 NPs elevated their antimicrobial activity. The anticancer property of the green-synthesized CsSnO2 NPs against MCF-7 cells was further analyzed to study their ability to cytotoxicity and apoptosis induction, like caspase-3, -8, and -9 activation. Conclusion The study’s outcome revealed that the green synthesized CsSnO2 NPs are an outstanding candidate for cancer therapy.

Occurrence, Molecular Serogroups, Antimicrobial Susceptibility and Identification by MALDI-TOF MS of Listeria monocytogenes Isolated from RTE Meat Products in Southern Poland.

L. monocytogenes is considered one of the most dangerous foodborne pathogens. This study aimed to determine the occurrence of L. monocytogenes in RTE meat products from southern Poland, including serogroups and antimicrobial susceptibility, and to assess the usefulness of MALDI-TOF MS as a tool for identifying L. monocytogenes. A total of 848 production batches of RTE meat products were analyzed for L. monocytogenes. All L. monocytogenes isolates were serotyped using the multiplex PCR method, tested for antimicrobial susceptibility using the disk diffusion method and identified using the MALDI-TOF MS method. L. monocytogenes was detected in 52/848 batches of RTE meat products (6.13%). The isolates belonged to four serogroups: 17/52 (33%) isolates to IVb; 15/52 (29%) isolates to IIa; 10/52 (19%) isolates to IIc and 10/52 (19%) isolates to IIb. All isolates (52/52) showed susceptibility to the tested antimicrobials. Using MALDI-TOF MS, 10/52 isolates (19.2%) were identified at the level of secure genus identification, probable species identification; 37/52 isolates (71.2%) were identified at the level of probable genus identification; 3/52 isolates (5.8%) were incorrectly identified as L. innocua; and 2/52 isolates (3.8%) were not identified. The occurrence of L. monocytogenes in RTE meat products was low. Almost half of the analyzed isolates were L. monocytogenes of serogroups, which are most often associated with listeriosis in humans in Poland. All isolates showed susceptibility to five commonly used antimicrobials for treating listeriosis. The use of MALDI-TOF MS as a tool for the identification of L. monocytogenes indicated its limitations related to the insufficient representation of the pathogen in the reference database.

Antibiotic resistant Escherichia coli strains inhealthy pets from Tamaulipas, Mexico.

Antibiotic resistance constitutes a significant public health challenge, with diverse reservoirs of resistant bacteria playing pivotal roles in their dissemination. Among these reservoirs, pets are carrying antibiotic-resistant strains. The objective of this study was to assess the resistance profiles of Escherichia coli, and the prevalence of extended-spectrum β-lactamase (ESBL) producing E. coli strains in dogs and cats from Tamaulipas, Mexico. A total of 300 stool samples (150 dogs and 150 cats) from healthy pets were subjected to analysis. Antibiotic susceptibility testing and the identification of ESBLs were carried out by disc diffusion method. The presence of resistance genes, class 1, 2, and 3 integrons (intI1, intI2, and intI3) and phylogroups was determined by PCR analysis. The findings reveal that 42.6% (128/300) of the strains exhibited resistance to at least one of the eight antibiotics assessed, and 18.6% (56/300) demonstrated multidrug resistance (MDR), that distributed across 69 distinct resistance patterns. Altogether 2.6% of E. coli strains (8/300) were confirmed as TEM and CTX-M type ESBL producers. These outcomes underscore the roles of dogs and cats in Tamaulipas as reservoirs for the dissemination of MDR and/or ESBL strains. The results underscore the necessity for conducting prevalence studies on ESBL-producing E. coli, forming a foundation for comprehending the present scenario and formulating strategies for the control and mitigation of this issue.

Detection and characterization of multidrug resistant Escherichia coli carrying virulence gene isolated from broilers in Bangladesh.

The emergence and dissemination of multidrug resistant (MDR) bacteria pose a severe threat to public health by limiting clinical treatment and prophylactic options. This study investigates the prevalence of Escherichia coli in broilers, their phenotypic antimicrobial resistance (AMR) profiles and the presence of virulence-associated genes (VAGs) and antimicrobial resistance genes (ARGs) using polymerase chain reaction (PCR). A total of 216 pooled cloacal samples were collected from 1080 broilers across six districts of Bangladesh. Each pooled sample comprised randomly selected cloacal swabs from five birds per farm. E. coli isolates were identified using standard bacteriological approach, followed by biochemical assays and PCR. Antimicrobial susceptibility was assessed using the Kirby-Bauer disc diffusion method, and the presence of ARGs and VAGs was determined via PCR. Five selected isolates were partially sequenced for five VAGs using Sanger sequencing. A total of 177 E. coli isolates (81.94%, 95% confidence interval: 76.24%-86.53%) were identified. The isolates showed the highest resistance to ampicillin (93.79%), followed by tetracycline (91.53%), erythromycin (89.27%) and ciprofloxacin (87%). Conversely, ceftriaxone (80.79%) showed highest susceptibility, followed by gentamicin (37.29%) and neomycin (31.07%). All isolates were MDR, with a multiple antibiotic resistance indexes were <0.3. A significant percentage (16.38%) of E. coli isolates were MDR to five antimicrobial classes and harboured blaTEM, sul1, ere (A), tetA, tetB and tetC genes. The highest prevalent ARGs were blaTEM (88.14%) followed by ere (A) (83.62%) and sul 1 (72.32%). The prevalence of VAGs was astA (56.50%), iucD (31.07%), iss (21.47%), irp2 (15.82%) and cva/cvi (3.39%), respectively. This study highlights the presence of ARGs contributing to the development of MDR in E. coli carrying VAGs in broilers. Effective monitoring and surveillance of antimicrobial usage in poultry production systems are urgently required to prevent emergence and dissemination of AMR.

A comparative study of a rapid phenotypic antimicrobial susceptibility testing system directly from positive blood cultures to the disk diffusion and VITEK 2 methods

BackgroundSepsis is a life-threatening condition that impacts 49 million people annually and causes 11 million deaths worldwide. Surviving bloodstream infections (BSIs) depends on the rapid administration of effective antimicrobial treatment, underscoring a need for rapid antimicrobial susceptibility testing (AST). AimTo evaluate the performance of Quantamatrix's dRAST v2.5 system (Seoul, South Korea) for AST directly from positive blood cultures as compared to the Disk-Diffusion (DD) and VITEK 2 methods. MethodsThe study included 191 positive blood cultures from clinical samples and spiked blood culture bottles. Following Gram staining and species-level identification, AST was performed by VITEK 2 and standard DD methods using CLSI (2021) interpretation. ResultsdRAST demonstrated very good AST performance for a Gram-negative isolate, and good performance for Gram-positive isolates, meeting CLSI criteria for the acceptance of a new method. Antimicrobials that were not considered verified compared to VITEK 2 and DD were cefazolin, ceftazidime, meropenem, and trimethoprim/sulfamethoxazole for Gram-negatives and clindamycin, erythromycin, penicillin, and oxacillin for Gram-positives. dRAST ESBL detection results were strongly correlated with the ESBL phenotypes obtained with other methods. Additional resistance mechanisms were in concordance with traditional tests. ConclusionsdRAST demonstrated good AST performance, meeting CLSI criteria for most relevant antibiotics. dRAST was associated with a significant reduction in time-to-results, labor, and the subjectivity of result analyses, making it a valuable addition to efforts supporting the treatment of patients with bacteremia.AST (antimicrobial susceptibility test), blood culture, dRAST, rapid methods, sepsis, turnaround time (TAT).