Background The global development of innovative antimicrobial drugs and drug design techniques has been necessitated by the persistent increase of multidrug resistant infections. Regardless of advances in technology for detecting pathogenic bacteria and their resistance genes (DNA-based assays), most bacteriological studies of infections still use conventional cultural techniques and susceptibility testing as reference standards. Commonly used conventional assays such as the disc diffusion test and broth micro-dilution have been effective in defining pathogen susceptibility and determining the minimum inhibitory concentration of antimicrobial agents. However, they are still prone to error and time consuming, hence, not sufficient in the face of the urgent need for answers to sporadic worldwide disease maladies. Main body In this review, we describe a developing but promising method for gauging/measuring the amount of energy released when a cell is actively metabolizing, which may then be used to calculate the bacterial cell's growth rate. The isothermal microcalorimetry (IMC) calscreener translate heat production of cellular metabolism which is pertinent to the operation of all biological life in demonstrating a more advanced technique for drug design and discovery, especially in the area of pathogen-specific chemotherapy. Conclusion The IMC calscreener technology is sacrosanct in establishing the heat levels in microwatt to read the metabolic kinematics of biological specimens with emphasis on medically-relevant bacteria within a closed scheme. The application of this technology also looks promising in antimicrobial chemotherapy and metal recovery.
Introduction: Andrographis paniculata (Burm. f.) is a significant pharmacological plant and regularly used in different parts of the world. The antibacterial activity of the methanol leaf extract of A. paniculata against bacterial consortia from blood of diabetic patients was evaluated in this study. Methods: The enumeration of bacteria from blood samples of diabetic patients and their antibiotic sensitivity pattern were done using standard techniques. The phytochemical analysis of A. paniculata methanol extract and antibacterial assay of the extract were also done using standard methods. Results: Staphylococcus aureus had the highest occurring rate of 19.56 % while Klebsiella pneumoniae had the lowest occurring rate of 0.40 %. The isolates exhibited different sensitivity patterns to conventional antibiotics. There were variations in the zones of inhibition of A. paniculata methanol extract against the bacterial isolates as extract showed concentration was dependent on antibacterial activity with all the bacterial isolates susceptible to the extract. The minimum inhibitory concentration (mg/ml) of the A. paniculata methanol extract ranged from 5 mg/ml to 10 mg/ml while the minimum bactericidal concentration (mg/ml) of the bacteria isolated from diabetic patients ranged from 10 mg/ml to 20 mg/ml. Conclusion: Findings revealed that the methanol leaf extract of A. paniculata very strong antibacterial activity for a wide range of bacteria from blood samples of diabetic patients and more reliable than commercially available antibiotics hence suggesting that leaves of A. paniculata can be used to develop novel antibacterial drugs.
Abstract. Babayemi OO, Oke EA, Bayode MT. 2021. Antibacterial activity of Jatropha tanjorensis leaf extracts against bacteria associated with wound infections from the clinical setting. Nusantara Bioscience 13: 260-267. The use of microbial agents to treat infectious wounds based on ethnobotanical knowledge is still minimal. Antibacterial activity of Jatropha tanjorensis J.L.Ellis & Saroja leaf crude extracts and commercial antibiotics were evaluated against bacterial isolates associated with wound samples using agar well diffusion and disc diffusion techniques, respectively. Phytochemical analysis of the sections was carried out using standard methods. Saponin (58 mg/g) was the highest phytochemical in the methanol extract while flavonoid (0.1 mg/g) was the lowest percentage in the coldwater extract. Methanol extract had had the highest Zone of Inhibition (ZOI) of 33 mm against Staphylococcus aureus coagulase-positive, while the lowest ZOI (5 mm) against S. aureus coagulase-positive was obtained from cold water extract. Methanol extract resulted in the highest ZOI ranging from 16 mm to 17 mm against Escherichia coli while the lowest ZOI was obtained from coldwater extract (3-4 mm). The highest Minimum Inhibitory Concentration (MIC) value of all extracts (100 mg/mL) was obtained against P. aeruginosa while the lowest MIC value was obtained against coagulase-positive S. aureus (12.5 mg/mL). All extracts contain Octadecanoic acid, n-hexadecanoic acid, and phytol. The study's outcome revealed that methanol extract had the highest inhibitory activity against bacteria isolated from wound samples compared to other crude extracts and ciprofloxacin. Jatropha tanjorensis could be used as a potent herbal remedy to reduce the adverse effects of wound infection.
Background: Hospital wastewaters contain blends of inorganic, natural constituents and contaminants that carry significant health risk when released directly into the environment. The aim of this study is to investigate the correlation between faecal indicator bacteria in diarrheagenic stools and wastewaters generated in University of Medical Sciences Teaching Hospital complex, Akure, Nigeria.Methodology: Quantification of faecal indicator bacteria was carried out on diarrheagenic faecal samples collected from 55 hospitalized patients and 68 wastewater samples from the medical laboratory science and laundry units of the hospital over of period of 12 weeks. Standard membrane filtration technique was performed using membrane intestinal enterococcus (m-ENT), membrane faecal coliform (m-FC), membrane lauryl sulphate (MLSA), eosin methylene blue (EMB) and Salmonella-Shigella (SS) agar plates, which were incubated at 37ºC for 24 hours (MLSA, EMB and SSA), 44ºC for 24 hours (m-FC); and 37ºC for 48 hours (m-ENT). Bacterial colonies on agar plates were counted and expressed as colony forming units (CFU) per 100ml of diarrheagenic stool and wastewater. Pearson’scorrelation analysis was used to determine the relationship between the level of faecal indicator bacteria in diarrheagenic stools and wastewaters at p<0.05 level of significance (and 95% confidence interval).Results: The faecal coliform counts (log 10 CFU/100ml) ranged from 1.18 to 1.54 in diarrheagenic stools, 1.32 to1.64 in laboratory wastewater and 1.08 to 2.19 in laundry wastewater. Escherichia coli count (log 10 CFU/100ml) ranged from 1.08 to 1.40 in diarrheagenic stools, 1.20 to 1.86 in laboratory wastewater and 0.30 to 1.81 in laundry wastewater. Intestinal enterococci count (log 10 CFU/100ml) ranged from 0 to 0.30 in diarrheagenic stools, 0.78 to 0.90 in laboratory wastewaters and 0.48 to 1.11 in laundry wastewaters. Pearson’s correlation co-efficient showed that all the faecal indicator bacteria count in diarrheagenic faecal samples exhibited positive correlation with those in laboratory wastewaters, but not with those from laundry wastewaters.Conclusion: The findings suggest that diarrheagenic stools should be properly disinfected after the performance of laboratory tests to prevent transmission of potential pathogens, and wastewater generated from hospitals should be treated prior to discharge into the environment, to prevent possible infections in the community. Keywords: Correlation, faecal indicator bacteria, public health, transmission, wastewater
Background The continuous increase in the resistance of pathogenic bacteria to antimicrobial agents elicits a source of concern for public health. Developing a method that allows for swift evaluation of the antibiotic sensitivity profile of bacteria is a major leap in antimicrobial research and could be one of the deciding factors in providing a lasting solution to antimicrobial resistance. The gradual and continuous reduction in the cost and turnaround time of whole-genome sequencing (WGS) has enabled scientists to develop WGS-based antimicrobial susceptibility testing using computational methods. The genes present on the ResFinder database were blasted against the WGS of the bacterial isolates obtained from NCBI database, and the best-matching genes were automatically generated by the system. Results Antimicrobial resistance genes were detected from the strains tested though not innate, thereby suggesting that they must have been acquired through horizontal gene transfer. Additionally, it was revealed that specific genes confer resistance to specific group of antibiotics. Conclusion The in silico method of antimicrobial resistance research provides for easy interpretation and reproducibility of results thereby reducing the cost and time utilized.
Aim: To investigate the antimicrobial susceptibility profile of Pseudomonas aeruginosa enumerated from wound swabs and urine samples from the University of Medical Sciences Teaching Hospital, Akure, Nigeria. Place of Study: University of Medical Sciences Teaching Hospital, Akure, Ondo State, Nigeria, between January and May, 2019. Methodology: Wound swabs and urine samples were collected from patients of University of Medical Sciences Teaching Hospital, Akure. Enumeration and identification of P. aeruginosa isolates was employed. Antibiotic sensitivity test was conducted on the enumerated P. aeruginosa strains from both clinical specimens via standard disc diffusion protocol. The susceptibility and resistance pattern of P. aeruginosa isolates was established utilizing clinical laboratory standard institute (CLSI) standard. Results: Ciprofloxacin was observed to display the highest zone of inhibition (ZOI) of 17.00±1.00 mm for P. aeruginosa isolate 1 and likewise the highest ZOI of 24.50±1.50 mm for P. aeruginosa strain 3. Fourteen strains of Pseudomonas aeruginosa exhibited highest resistance to septrin and augmentin for wound swabs as all 19 of the bacterial strains also exhibited the highest resistance to septrin, chloramphenicol, augmentin and streptomycin for urine specimens. Ten (10) of P. aeruginosa strains from wound swabs exhibited the highest intermediate susceptibility to perfloxacin. Eleven (11) strains of P. aeruginosa from urine specimens exhibited the highest intermediate susceptibility on sparfloxacin. All 19 strains of P. aeruginosa from urine specimens were susceptible to amoxicillin and gentamicin as completely minimal susceptibility was recorded for P. aeruginosa associated with wound swabs. Conclusion: This study demonstrated the high resistance pattern of P. aeruginosa associated with wound swabs and urine samples and emphasizes the need for the regimentation of over-the-counter remedy and antibiotic susceptibility appraisal of anti-pseudomonal drugs.
Aim: The prevalence, sensitivity profile and resistance of Gram-positive bacteria in wounds to commercial antibiotics were ascertained in this study. Place and duration of study: University of Medical Sciences Teaching Hospital, Akure, Nigeria, between January and June 2019. Methodology: Wound swabs sample collection, isolation of bacteria, identification of Gram-positive bacteria isolates and antibiotics sensitivity testing of isolated bacteria were determined employing standard protocols. Result: Three Gram-positive bacteria were isolated and presumptively identified to be S. aureus, S. epidermidis and S. pyogenes. S. aureus had the highest prevalence of 53% followed by S. epidermidis with 42% and S. pyogenes accounting for the least occurrence of 5%. Ninety percent (90%) of ten S. aureus strains were resistant to ciprofloxacin while only 10% had intermediate activity. The least resistance of S. aureus strains was against pefloxacin (40%), while to streptomycin, 87.5% of eight S. epidermidis strains were resistant and 12.5% had intermediate sensitivity. Susceptibility was observed in S. epidermidis against pefloxacin (12.5%) while 50% had intermediate sensitivity and 37.5% were resistant. The highest zone of inhibition of S. epidermidis was observed in strain 7 against pefloxacin (16.00±1.00 mm) and in S. aureus by strain 5 against pefloxacin (16.50±2.50 mm). Conclusion: Pefloxacin-sensitive Staphylococcus and Streptococcus species from wound swabs could become resistant overtime and this calls for incessant vigilance on Gram-positive wound bacteria antibiotic-susceptibility appraisal particularly in an antibiotics-abuse setting.
In this study, the effects of different steeping methods on the microbial quality of ‘ogi’ produced from Sorghum bicolor (Linn.) grains were carried out. The sorghum grains were divided into four parts; the first part (Sample A) was steeped with cold water at 30+ 2oC for 72 h and washed with water before milling, the second part (Sample B) was steeped with cold water at 30+2oC for 72 h but was not washed before milling, the third part (Sample C) was steeped with hot water at 30+2oC for 24 h and washed before milling, while the fourth part (Sample D) was steeped with hot water at 30+2oC for 24 h and was not washed before milling. The processed raw ‘ogi’ samples were subjected to standard microbiological techniques to enumerate the microorganisms present. The highest bacterial count of 3.5 x 103cfu/ml was observed in sample B, the highest fungal count of 2.5 x 104 sfu/ml was observed in sample B, while sample C yields the lowest bacterial count of 8.0 x 102 cfu/ml and fungal count of 4.0 x102 sfu/ml. Good hygienic conditions during the processing of the ‘ogi’ must also be employed to reduce the chances of microbial contamination.
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