EVALUATION OF ANTIBACTERIAL ACTIVITY OF ETHANOL LEAF EXTRACTS OF PSIDIUM GUAJAVA LINN. AGAINST CLINICAL ISOLATES FROM WOUND INFECTIONS

Author(s):  
Ananthan Anuswedha
2017 ◽  
Vol 1 (2) ◽  
pp. 013-019 ◽  
Author(s):  
Kenneth Ekeleme ◽  
Paul Tsaku ◽  
Istifanus Nkene ◽  
Uba Ufomadu ◽  
Rejoice Abimiku ◽  
...  

2020 ◽  
Vol 36 (1) ◽  
pp. 11-18
Author(s):  
Philip A. Idowu ◽  
Tajudeen A. Adegbenle

Increasing resistance of typhoidal Salmonella enterica to conventional antibiotics has caused more cases of typhoid, therapeutic failure, morbidity and mortality; creating the need to search for new and effective antimicrobial agents from medicinal plants. The present study aimed to detect antisalmonella activity and cytotoxicity (safety) status of the stem bark and leaves of two Nigerian medicinal plants, Trichilia megalantha and Trichilia welwitschii. Nine clinical isolates of Salmonella paratyphi, whose antibiogram were determined by Kirby-Bauer disc diffusion method were used. Antibacterial activity, minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of the extracts on the clinical isolates were done by agar cup diffusion and agar dilution methods, respectively. Acute toxicity of the extracts was determined using brine shrimp lethality assay (BSLA). All the nine isolates of Salmonella paratyphi were resistant to β-lactam antibiotics (augmentin, cefuroxime, ceftazidime and ampicillin) but susceptible to fluoroquinolones (ciprofloxacin, ofloxacin), nitrofurantoin and gentamicin. The crude extracts of the two plants elicited activity against the nine clinical isolates with the bark extracts being more active than the leaf extracts. T. welwitschii was slightly less active than T. megalantha. The MIC and MBC ranged 1.25 - 5.0 mg/ ml and 2.5 - 10 mg/ml, respectively for the plants. The antisalmonella activity of methanolic extracts of both plants were found to be less than that of ciprofloxacin and ofloxacin. With modal cytotoxicity values of 400 - 500 μg/ml, the plant parts were considered nontoxic. Therefore, T. megalantha and T. welwitschii could provide a potential source of antibacterial agent(s) for the treatment of Salmonella paratyphoid infections. Keywords: Trichilia megalantha; Trichilia welwitschii, antisalmonella; cytotoxicity; Salmonella paratyphi 


Author(s):  
Mutiat Adetayo Omotayo ◽  
Mary Oluwatoyin Avungbeto ◽  
Oluwole Olusoji Eleyowo

Aim: This study evaluates the antioxidant and antibacterial activity of Anacardium occidentale and Psidium guajava methanolic leaf extracts. Place and Duration of Study: The study was carried out in the Biochemistry and Microbiology Laboratory, Department of Science Laboratory Technology, School of Pure and Applied Science, Lagos State Polytechnic, Ikorodu, Lagos- Nigeria for the period of three months between August and October 2015. Methodology: Lycophene and β-carotene was assessed using the method of Nagata and Yamashita while total phenolic and total flavonoid content was assessed by the Folin-Ciocalteau assay and aluminum chloride colorimetric assay respectively. The antioxidant activity was evaluated using the DPPH radical scavenging activity. Antimicrobial activity was assessed by the agar well diffusion technique and mode of action was evaluated by studying the leakage of UV260 and UV280 absorbing materials spectrophotometrically. Results: A. occidentale and P. guajava methanolic leaf extracts evaluated in this study possessed significant amount of antioxidant compounds lycophene, β-carotene, total phenol and flavonoids. The extracts exhibited antioxidant activity by scavenging DPPH radicals in a dose dependent pattern with IC50 of 47.45, 43.49, 41.46 and 27.21 μg/mL for A. occidentale, P. guajava, vitamin C and Gallic acid respectively. Also, the plant extracts exhibited antimicrobial activity against E. coli, S. aureus, P. auraginosa and C. albicans and disrupted microbial membrane evident in the increase in absorbance values of UV260 and UV280 absorbing materials with time. Conclusion: A. occidentale and P. guajava methanolic leaf extracts possess antioxidant and antimicrobial activity and serve as potential source of drugs.


Planta Medica ◽  
2015 ◽  
Vol 81 (16) ◽  
Author(s):  
BF Navarro ◽  
M del Carmen Ortiz García ◽  
BN Marin ◽  
ML Rodríguez ◽  
AV Hernández

2019 ◽  
Vol 20 (4) ◽  
pp. 317-326 ◽  
Author(s):  
Manaf AlMatar ◽  
Işıl Var ◽  
Begüm Kayar ◽  
Emel Eker ◽  
Ebru Kafkas ◽  
...  

Background: The global rise of multi-drug resistant M. tuberculosis demands unconventional treatment to enhance the efficiency of current drugs. Punica granatum, which is known as pomegranate, is considered as a member of the Punicaceae family. Pomegranate, which is broadly documented for its activity against a wide spectrum of bacterial pathogens, deserves further scrutiny in this respect. Methods: Within this scope, this study investigated the effect of fresh pomegranate juice (FPJ) on the antibacterial activity of anti-tuberculosis drugs (Rifampin (R) and Isoniazid (INH)) against MDR-TB clinical isolates. The drug resistance profiles in M. tuberculosis clinical isolates were determined by susceptibility test using BACTEC MGIT 960 system. Four concentrations of fresh pomegranate juice (FPJ) (5%, 10%, 15%, and 20%) were evaluated in combination with R and INH at a dose range of (1.0 µg/ml) and (0.1 µg/ml), respectively against the MDR-TB isolates by the BACTEC MGIT 960 system. Moreover, this study scrutinized individual phenolic compounds of FPJ by using highperformance liquid chromatography (HPLC). The total polyphenols (TP), total flavonoid (TF), total anthocyanins content (TAC), and the antioxidant capacity were also assessed in FPJ. Results: Synergistic effects were observed between R and INH with FPJ against all tested strains. However, combination therapy of rifampin was more effective than isoniazid one. Therefore, the combination of R and FPJ has been used against (27) MDR-TB clinical isolates. 5% of FPJ plus R (1.0 µg/ml) were found to suppress the growth of one isolates for first group (INH and R resistant). However, 5% of FPJ demonstrated no synergistic impact with R for second (SM, R and INH resistant) and third group (INH, EMB, R and SM resistant). Moreover, 10% of FPJ and R (1.0 μg/ml) inhibited the bacterial growth of three isolates of first group and two isolates and one isolate for second and third group, respectively. Remarkably, 15% of FPJ plus R (1.0 µg/ml) appeared to inhibit the growth of MDR-TB isolates for all tested groups indicating a strong synergistic effect. Regarding H37RV, the complete inhibition of the bacterial growth was found to occur at 15% and 20% concentrations of FPJ only. Minimum inhibitory concentration (MIC) of FPJ ranged from (4% to13%) for first group and from (10% to15%) for second and third group. Thus, FPJ at 15% inhibited 100% of bacteria for all tested isolates (MIC100% =15%). Phenolic compounds identified in FPJ were gallic acid, benzoic acid, syringic, folic acid, pelargonidin, naringin+ellagic acid, naringenin, chlorogenic acid, caffeic acid, catechin, myricetin, kaempferol, quercetin, cyanidin-3-glycoside, p-cummaric acid, ferulic acid, and rutin. Total phenolic (TP), total flavonoid (TF), and total anthocyanin (TA) content were 841.5 mg/L, 638.73 mg RE/L, and 47.43 mg/L, accordingly. Conclusion: Overall, FPJ displayed synergistic effect with R against MDR-TB clinical isolates due to its high content of polyphenol and antioxidant capability.


2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Resmi Mustarichie ◽  
Sulistiyaningsih Sulistyaningsih ◽  
Dudi Runadi

This study is aimed at determining antibacterial activity from ethanol extracts and the most active fraction of cassava leaves against clinical isolates of Staphylococcus epidermidis and Propionibacterium acnes. Research carried out by the experimental method involved determination of plants, extraction with maceration method, fractionation with liquid-liquid extraction, antibacterial activity testing of extracts and fractions by agar diffusion method, determination of most active fraction from the extract, and minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) testing of most active fraction by microdilution method. The results showed that ethanol extracts of cassava leaves had antibacterial activity against both bacteria with the most active fraction indicated by ethyl acetate. MIC values of ethyl acetate fraction against S. epidermidis were in the concentration range of 2.5%–5.0% (w/v) and against P. acnes were in the concentration range of 1.25%–2.5% (w/v). The MBC value of ethyl acetate fraction against S. epidermidis was at a concentration of 5% (w/v), while P. acnes was at a concentration of 2.5% (w/v). From the results of this study, it can be concluded that the ethanol extract of cassava leaves (Manihot esculenta Crantz) has antibacterial activity against clinical isolates of Staphylococcus epidermidis as well as on Propionibacterium acnes. The fraction with the best activity from the ethanol extract of cassava leaves to the two test bacteria was shown by ethyl acetate fraction. It is suggested that cassava leaves are possible to be developed into standardized antiacne herbal.


2020 ◽  
Vol 7 (Supplement_1) ◽  
pp. S662-S662
Author(s):  
Alita Miller ◽  
Sarah McLeod ◽  
Samir Moussa ◽  
Meredith Hackel

Abstract Background The incidence of infections caused by multidrug-resistant (MDR) Acinetobacter baumannii (Ab) is increasing at an alarming rate in certain regions of the world, including the Middle East. Sulbactam (SUL) has intrinsic antibacterial activity against Ab; however, the prevalence of β-lactamases in Ab has limited its therapeutic utility. Durlobactam (DUR, formerly ETX2514) is a diazabicyclooctenone β-lactamase inhibitor with broad-spectrum activity against Ambler class A, C and D β-lactamases that restores SUL activity in vitro against MDR Ab. SUL-DUR is an antibiotic designed to treat serious infections caused by Acinetobacter, including multidrug-resistant strains, that is currently in Phase 3 clinical development. In global surveillance studies of >3600 isolates from 2012-2017, the MIC90 of SUL-DUR was 2 mg/L. Although surveillance systems to monitor MDR infections in the Middle East are currently being established, quantitative, prevalence-based data are not yet available. Therefore, the potency of SUL-DUR was determined against 190 recent, diverse Ab clinical isolates from this region. Methods 190 Ab isolates were collected between 2016 - 2018 from medical centers located in Israel (N = 47), Jordan (N = 36), Qatar (N = 13), Kuwait (N = 42), Lebanon (N = 8), Saudi Arabia (N = 24) and United Arab Emirates (N = 20). Seventy-five percent and 20.5% of these isolates were from respiratory and blood stream infections, respectively. Susceptibility to SUL-DUR and comparator agents was performed according to CLSI guidelines, and data analysis was performed using CLSI and EUCAST breakpoint criteria where available. Results This collection of isolates was 86% carbapenem-resistant and 90% sulbactam-resistant (based on a breakpoint of 4 mg/L). The addition of SUL-DUR (fixed at 4 mg/L) decreased the sulbactam MIC90 from 64 mg/L to 4 mg/L. Only 3 isolates (1.6%) had SUL-DUR MIC values of > 4 mg/L. This potency was consistent across countries, sources of infection and subsets of resistance phenotypes. Conclusion SUL-DUR demonstrated potent antibacterial activity against recent clinical isolates of Ab from the Middle East, including MDR isolates. These data support the global development of SUL-DUR for the treatment of MDR Ab infections. Disclosures Alita Miller, PhD, Entasis Therapeutics (Employee) Sarah McLeod, PhD, Entasis Therapeutics (Employee) Samir Moussa, PhD, Entasis Therapeutics (Employee)


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