Search

Antimicrobial resistance to commercially available medications has become a global issue, yet there is still the possibility of developing new drugs from medicinal plants. As a result, the aims of the present study were to screen secondary metabolites and to evaluate in vitro antifungal activities of

Antimicrobial resistance to commercially available medications has become a global issue, yet there is still the possibility of developing new drugs from medicinal plants. As a result, the aims of the present study were to screen secondary metabolites and to evaluate in vitro antifungal activities of Brucea antidysenterica, Aloe vera, and Justicia schimperiana. After the plants were identified, their leaves were collected, washed, dried under the shade, pulverized, and extracted with methanol (99.8%) using the maceration technique. The presence of secondary metabolites in plant extracts was screened using various laboratory protocols. The antifungal activities of the plant extract against reference fungal strains of Candida albicans and Aspergillus niger at concentrations of 200, 100, and 50 mg/mL were assessed using the agar-well diffusion method. Ketoconazole (15 μg) was used as a positive control, while 5% dimethyl sulfoxide and/or 5% Tween 80 were used as negative controls. All tests were conducted in triplicate. Alkaloids, flavonoids, and phenols were secondary metabolites found in all plant extracts. The extract of leaves of B. antidysenterica and J. schimperiana formed a mean zone of inhibition of 15.5 ± 0.5 mm and 15.3 ± 0.58 mm, respectively, against Candida albicans at a concentration of 200 mg/mL, whereas extracts of A. vera leaves formed a 12.3 ± 0.58 mm inhibition zone only against Aspergillus niger at 200 mg/mL. In conclusion, the current study found that B. antidysenterica, A. vera, and J. schimperiana had antifungal activity. In addition, all these plants had a variety of secondary metabolites that possibly have antifungal activities. Studies on in vivo investigations and isolation of specific antifungal compounds from these medicinal plants are suggested.

Askale Gizaw,1 Petros Admasu,2 Achalu Nagasa,3 Solomon Shiferaw,1 Morka Dandecha Bayu,1 Adem Abdella3 1Department of Veterinary Laboratory Technology, Ambo University, Ambo, Oromia, Ethiopia; 2Department of Veterinary Science, Ambo University, Ambo, Oromia, Ethiopia; 3Department of Veterinary Medicine, Haramaya University, Harar, Oromia, EthiopiaCorrespondence: Askale Gizaw, Department of Veterinary Laboratory Technology, Ambo University, P.O. Box 19, Ambo, Oromia, Ethiopia, Tel +251-940047577, Email askalegizaw21@gmail.comBackground: Ovine oestrosis is an economically important and widely distributed parasitic disease of sheep that is caused by Oestrus ovis larvae across the world. Despite the fact that Oestrus ovis is a common parasite in Ethiopia and that there are many sheep in the study area, there is no information on the prevalence, larval burden, predilection sites, and risk factors associated with Oestrus ovis infestation in sheep in the Dendi district of West Shewa Zone, Ethiopia.Methods: A cross-sectional study was conducted from November 2017 to April 2018, to estimate the prevalence, risk factors, and larval burden, and identify common predilection sites for Oestrus ovis larvae. A total of 180 sheep heads were randomly selected from five purposely selected restaurants in Ginchi town, Dendi district, transported to the laboratory, opened with a hand saw, and visually examined for infestations. The larvae were collected from positive sheep heads and counted. The sites where the larvae were obtained were recorded. The data were analyzed using SPSS version 20 software.Results: Of the total of 180 examined sheep heads, 104 (57.8%) were infested with larvae of Oestrus ovis. In the study, a statistically significant difference (p > 0.05) was not observed in the prevalence of Oestrus ovis in relation to all considered risk factors such as sex, age, and origin of sheep. From 104 infested sheep, a total of 664 larvae were detected in different parts of sheep heads. The mean larval intensity per infected animal with Oestrus ovis was 6.38. In this study, the minimum and maximum numbers of larvae recovered were 1 and 26, respectively. The nasal cavity, nasal sinus and frontal sinus were the predilection sites of Oestrus ovis larvae identified in this study.Conclusion: Oestrosis is an important and common parasitic disease of sheep in the study area.Keywords: Dendi, Ethiopia, Oestrus ovis, ovine, prevalence, risk factors

Lencho Megersa Marami,1 Getachew Mulatu Dilba,1 Dagmawit Atalel Babele,1 Edilu Jorga Sarba,2 Askale Gizaw,1 Wakuma Mitiku Bune,1 Morka Dandecha Bayu,1 Petros Admasu,2 Abraham Mekbeb,2 Miressa Tadesse,3 Kebede Abdisa,2 Dejene Bayisa4 1Ambo University, College of Agriculture and Veterinary Science, Department of Veterinary Laboratory Technology, Ambo, Oromia, Ethiopia; 2Ambo University, College of Agriculture and Veterinary Science, Department of Veterinary Science, Ambo, Oromia, Ethiopia; 3Ambo University, College of Computational and Natural Science, Department of Chemistry, Ambo, Oromia, Ethiopia; 4Jeldu Woreda, Livestock and Fishery Development Office, Gojo, Oromia, EthiopiaCorrespondence: Getachew Mulatu DilbaAmbo University, College of Agriculture and Veterinary Science, Department of Veterinary Laboratory Technology, P.O. Box 19, Ambo, Oromia, EthiopiaTel +251-912717217Email getachew.mulatu@ambou.edu.etBackground: Although traditional healers in Ethiopia have a long history of using medicinal plants to treat diseases in animals and humans, studies on the antibacterial activities and potential bioactive ingredients of most medicinal plants have been insufficient. Therefore, this study aimed to evaluate the in-vitro antibacterial activities and to screen phytochemical constituents of selected medicinal plants against reference bacterial strains.Methods: The fresh and healthy roots of Echinops amplexicaulis, fruits of Ruta chalepensis, and leaves of Salix subserrata were collected from West Shewa Zone, Ethiopia. Agar well diffusion and agar dilution methods were used to evaluate antibacterial activities and minimum inhibitory concentrations (MIC). All the crude plant extracts were tested against Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli and Pseudomonas aeruginosa at concentrations of 100, 50, and 25 mg/mL in each triplet (3x). MIC of crude extracts ranging from 1.5625 to 12.50 mg/mL was applied to all bacterial strains. The positive control was ciprofloxacin disk (5 μg) and the negative control was 5% dimethyl sulfoxide. The presence of secondary metabolites of each crude extract was screened. The group means comparisons were done using one-way ANOVA and results were presented as mean ± standard deviation.Results: Although all selected plant extracts had shown antibacterial activities, methanol extracts had a greater zone of inhibition against all reference bacterial strains when compared to petroleum ether extracts. The growth of P. aeruginosa was inhibited at a minimum concentration of both methanol and petroleum extracts (1.5625 mg/mL) when compared to the remaining bacterial strains. Phytochemical screening showed that saponins and alkaloids were found in all crude plant extracts, while phytosterol was meager.Conclusion: This study revealed that all tested plants had significant secondary metabolites and antibacterial activities against reference bacterial strains.Keywords: antibacterial activity, crude plant extract, ethnomedicine, methanol, petroleum ether

Background Although traditional healers in Ethiopia have a long history of using medicinal plants to treat diseases in animals and humans, studies on the antibacterial activities and potential bioactive ingredients of most medicinal plants have been insufficient. Therefore, this study aimed to evaluate the in-vitro antibacterial activities and to screen phytochemical constituents of selected medicinal plants against reference bacterial strains. Methods The fresh and healthy roots of Echinops amplexicaulis, fruits of Ruta chalepensis, and leaves of Salix subserrata were collected from West Shewa Zone, Ethiopia. Agar well diffusion and agar dilution methods were used to evaluate antibacterial activities and minimum inhibitory concentrations (MIC). All the crude plant extracts were tested against Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli and Pseudomonas aeruginosa at concentrations of 100, 50, and 25 mg/mL in each triplet (3x). MIC of crude extracts ranging from 1.5625 to 12.50 mg/mL was applied to all bacterial strains. The positive control was ciprofloxacin disk (5 μg) and the negative control was 5% dimethyl sulfoxide. The presence of secondary metabolites of each crude extract was screened. The group means comparisons were done using one-way ANOVA and results were presented as mean ± standard deviation. Results Although all selected plant extracts had shown antibacterial activities, methanol extracts had a greater zone of inhibition against all reference bacterial strains when compared to petroleum ether extracts. The growth of P. aeruginosa was inhibited at a minimum concentration of both methanol and petroleum extracts (1.5625 mg/mL) when compared to the remaining bacterial strains. Phytochemical screening showed that saponins and alkaloids were found in all crude plant extracts, while phytosterol was meager. Conclusion This study revealed that all tested plants had significant secondary metabolites and antibacterial activities against reference bacterial strains.