Phytochemical Screening and in-vitro Evaluation of Antibacterial Activities of Echinops amplexicaulis, Ruta chalepensis and Salix subserrata Against Selected Pathogenic Bacterial Strains in West Shewa Zone, Ethiopia.

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.

Introduction

Ethnomedicine is a holistic study of indigenous knowledge of traditional medicine, socio-cultural experience, and the environment as it relates to health care and animal husbandry.1 Ethnomedicinal practice has been developed through trial and error, which later on is supported by actual experimentation.2 Also, ethnoveterinary medicine is often undertaken as part of a community-based approach that serves to improve animal health and provide basic veterinary services, most commonly in rural areas.3 Since plants are rich in phytochemicals (secondary metabolites), they are naturally occurring substances and provide health benefits. Alkaloids, flavonoids, tannins, phenols, saponin, steroids, glycosides, and terpenes are some of the plant’s major secondary metabolites4 that have antioxidant, anti-inflammatory, anti-cancer, and anti-microbial properties.5 According to the WHO reports, at least 80% of people in developing countries depend largely on indigenous practices for the control and treatment of various diseases affecting both humans and animals.6 In most developing countries where there is a shortage of animal health facilities and veterinarians, ethnoveterinary medicine provides alternative treatments for animal diseases that are locally available and usually cheaper than the standard treatments because livestock holders can prepare and use homemade remedies with least cost.7,8

Echinops amplexicaulis (“Kosorruu Harree” in Afan Oromo) belongs to the family Asteraceae and its species are found in Eastern and Southern Europe, Tropical North and East Africa, and Asia.9 Traditional medicine practitioners in Uganda used the entire root of this plant to treat HIV/AIDS and related conditions.10 This plant is also used to treat ulcerative lymphangitis and hepatitis.9 The frequently described application is to treat symptoms like inflammation, pain, and fever, and ailments related to the respiratory tract, including cough and sore throat.11 Members of the genus have been used as an aphrodisiac,12 facilitation of expulsion of retained placenta and delivery,13,14 as an abortifacient,15 treatment of uterus tumor,16 and leucorrhoea.17 E. bannaticus Rochel ex Schrad, E. cornigerus D.C., and E. polyceras Boiss are the species of Echinops that have been used in the management of kidney stones.18–20

Ruta chalepensis belongs to the Rutaceae family, which is distributed in temperate and tropical countries.21 The decoction of R. chalepensis is used as a medicinal remedy against the evil eye and for “spiritual cleansings”, whereas the infusions of its fresh leaves are widely used as a treatment for gastric disorders, headache, and rheumatism. It is also reported for its diuretic, anti-inflammatory, and anti-spasmodic properties.21 This plant has also been used as a mosquito repellent, an antidote to snake and scorpion venom poisoning, and as a poultice for bites and stings.22

Salix subserrata (Alaltuu in Afan Oromo) is a deciduous bush or small tree 2–10 m tall that grows along streams throughout Africa. The leaf furnishes a laxative for human and veterinary medicine. Roots are used in medicines that help cure stomach pains, fever, and headaches. Crushed leaves of S. subserrata are also reported to be used in treating patients with rabies after mixing with milk.23

Escherichia coli is a Gram-negative bacillus found in the large intestine and excreted naturally through the feces and urinary tracts. It is one of the most frequent causes of many common bacterial diseases including cholecystitis, bacteremia, cholangitis, urinary tract infections and travelers’ diarrhea, and other clinical infections, such as neonatal meningitis and pneumonia.24

Pseudomonas aeruginosa is also a gram-negative, rod-shaped, and mono flagellated microorganism. It has a pearlescent manifestation and a grape or tortilla. This organism grows well at 25–37°C and its ability to grow at 42°C distinguishes it from other Pseudomonas species.25

Staphylococcus aureus is a gram-positive coccus that colonizes the nasal mucosa and skin of healthy individuals. The organism can cause a wide range of diseases ranging from skin or soft tissue infections to systemic and fatal diseases.26 S. aureus possesses a specific virulence factor called coagulase, which plays a significant role in biofilm formation during S. aureus infection. Coagulase binds to host prothrombin and forms active staphylothrombin complexes that convert soluble monomeric fibrinogen into self-polymerizing insoluble fibrin and activates a coagulation cascade.26

Streptococcus pneumoniae is a gram-positive facultative anaerobe, currently one of the most considerable pathogens worldwide. It is a major cause of bacterial pneumonia, meningitis, and sepsis.27 It is also the principal cause of potentially life-threatening community-acquired disease and is associated with a predictable global mortality rate which is of the same order of magnitude as that of tuberculosis, and subsequent investigation has identified a unique mechanism of penicillin resistance in this bacterium.28

Antimicrobial resistance is spreading at an alarming rate, making treating bacterial infections in animals and humans more difficult. Even modern medicines have failed to treat those resistant bacteria since they are developing resistant behavior.29 Therefore, it is logical to search for alternative methods to manage infectious diseases. Ethnomedicinal practices are believed to be one of the potential bases for the development of safe and effective treatments. Ethiopia has a long history of a traditional health care system, but studies on traditional medicinal plants (TMP) have been limited in comparison to the country’s multiethnic, cultural, and flora diversity.30 Also, the use of medicinal plants to treat infections is an old practice in large parts of Ethiopia to solve health problems for livestock and humans.31–36 However, most of these experiences are not documented and supported by scientific experiments. Among medicinal plants, leaves of S. subserrata, fruits of R. chalepensis, and roots of E. amplexicaulis were frequently used for the treatments of disease-causing bacterial strains like S. aureus, E. coli, S. pneumoniae, and P. aeruginosa. Therefore, the objective of the current study was to evaluate the in-vitro antibacterial activities and to screen major phytochemical constituents of selected medicinal plants against reference bacterial strains.

Materials and Methods

Description of Plant Collection Areas

Plants were collected from the Ejere, Toke Kutaye, and Dendi districts of West Shewa, Oromia Regional State, Ethiopia from December 2019 to January 2020. Ejere woreda is in the central part of Ethiopia with longitude and latitude of 9.03° N 38.40° E and 9°2ʹN 38°24ʹ with an elevation of about 2360 MASL (meters above sea level). While Toke Kutaye district is located 162 km west of the capital city, Addis Ababa and the area lies within central Ethiopia with altitudes ranging from 1580 to 3194 MASL. It receives an annual rainfall of 800–100 mm and has an annual temperature range of 10–29 °C. Dendi is located 79 km west of Addis Ababa, and 35 km east of Ambo. The area lies within the central country with altitudes ranging from 2000 to 3288 MASL. It receives an annual rainfall of 750–1170 mm and has an annual temperature range of 9.3°C-23.8°C. The traditional knowledge and practice of ethnomedicine areas are well known. Moreover, the area is rich in different natural resources. For instance, “Chilimo” forest is the main source of the medicinal plant for local practitioners.37 All the study areas’ soil types ranged from loam to clay, and the subsurface horizons were clayey, with low percentage base saturation, soil pH, and exchangeable cations.38

Study Design

The phytochemical screening test and in-vitro antibacterial evaluation were done through a randomized experimental design. All experimental tests were done with triplicates alongside the positive and negative controls.

Plant Collection and Preparation

Fresh and healthy leaves of S. subserrata, roots of E. amplexicaulis, and fruits of R. chalepensis were collected after being identified by a botanist from the department of plant science at Ambo University. The collected plant parts were authenticated (herbarium) in the Plant Science Laboratory of Ambo University Guder Mamo Mezemir Campus, cleaned using sterilized distilled water, cut into smaller sizes of about 1–2 cm long, and dried under shade at room temperature for 15 (fifteen) days. Then, it was ground by using a conventional wooden-made pestle and mortar, pounded using an electric grinder into a fine powder, and finally kept in a refrigerator (4 °C) until used.36,39

Plant Extraction

Although a standardized extraction protocol has not been developed for herbal extracts, 20–95% of the solvents (polar or/and non-polar) substances are frequently used by the herbal medicine industry to prepare plant crude extracts.40 All three medicinal plants: E. amplexicaulis, R. chalepensis, and S. subserrata were extracted with methanol (99.8%) and petroleum ether (99.5%) based on the information from the traditional claim and previous studies. Two hundred grams of air-dried powdered plant materials were placed in a flat-bottom flask filled with 1000 mL of extracting solvents and macerated for 24 hrs over a rotary shaker at 121 rpm. The suspension was filtered with Whatman №. 1 paper. The resulting filtrate was then concentrated under reduced pressure in a rotary evaporator. The gummy residue was further dried, followed by a water bath and oven at 45 °C and 42 °C, respectively, until the solvent was removed. After the solvent was evaporated, the remaining crude extracts were diluted with 10 mL of sterile distilled water and kept in an airtight bottle in the refrigerator until the experiment was carried out.36

Preliminary Phytochemical Test

According to the concept of Pandey and Tripathi,41 each crude extract was tested for the presence of secondary metabolites that might be playing a significant role in the antibacterial activities of medicinal plants. Accordingly, each plant was tested for the presence of alkaloids, saponins, phenols, tannins, flavonoids, and phytosterols.

Test for alkaloids: 0.25 gm of the crude extract was added to five drops of HCl and then it was filtered and finally the filtrate was mixed with Wagner’s reagents to form a Brown or precipitate which indicates the presence of an alkaloid.

Test for saponin: 0.25 gm of crude plant extract was mixed with 20 mL distilled water and shaken in a graduate cylinder for 15 minutes to form a foam with a 1 cm layer indicating the presence of saponin.

Test for phenol: 0.25 gm of the crude extract was added to 4 drops of FeCl3 for the formation of a blue-black color which indicates the presence of phenols and this test is considered as a ferric chloride test.

Test for tannin: 0.25 gm of the crude extract was added to 1% gelatin solution containing NaCl for the formation of a precipitate, which in turn indicates the presence of tannin in the crude extract.

Test for flavonoid: Using an alkaline reagent test, a few drops of NaOH solution were added to the crude extract for the formation of an intense yellow color that becomes colorless and the addition of 10 drops of 1% hydrochloric acid showed the presence of flavonoids.

Test for phytosterol: The Szarkowski test was conducted by adding a few drops of chloroform to 0.25gm of crude extract and then filtered. The filtrate was then mixed with a few drops of concentrated H2SO4, shacked, and left to stand for a few minutes to obtain a golden yellow color, indicating the presence of phytosterols in the crude extract.

Source of Bacterial Strains

Reference bacterial strains, namely S. aureus (ATCC 25923), S. pneumoniae (ATCC 49619), E. coli (ATCC 25922), and P. aeruginosa (ATCC 27853) were utilized to evaluate antibacterial activities of crude plant extracts. These four American-type cell cultures (ATCC) were aseptically collected from the Ethiopian Public Health Institute (EPHI), Addis Ababa, and transported under the cold chain.

In-vitro Antibacterial Activity Test

The bacterial strains were cultured on blood agar plates at 37 °C for 18–24; then, pure colonies were transferred to the nutrient agar plate. Four to five bacteria colonies were inoculated into the nutrient broth and incubated for 2–6 hrs. Each cultured isolate was compared with 0.5 McFarland turbidity standards. Sterile physiological saline solution was used to standardize the turbidity of the isolates.

Agar-Well Diffusion Method

After inoculation of the bacteria with sterile swabs on the surface of Mueller Hinton agar plates, it was left to dry at room temperature. Four holes were made on the surface of the Mueller Hinton agar plate at equal distances from each other using a 6 mm diameter cork borer. The holes were then filled with the test sample (crude plant extracts) at a concentration of 100, 50, and 25 mg/mL, and negative control (5% DMSO). An antibiotic disk, ciprofloxacin (5 μg), was placed on the surface of the agar plate as a positive control.42 The experiment was repeated three times (3x). The plates were then left at room temperature for about an hour to favor diffusion and incubated at 37°c for 24 hrs. After 24 hrs. of incubation, the antibacterial activity was evaluated by measuring the diameter of the zone of inhibition including the hole.43

Minimum Inhibitory Concentration (MIC): Agar Dilution Method

The minimum inhibitory concentration (MIC) of all crude extracts was evaluated against S. aureus, P. aeruginosa, E. coli, and S. pneumoniae. A 5% Dimethyl sulfoxide (DMSO) was used to dilute crude plant extracts. Then, after serial dilution, the crude extract (2 mL) was mixed with molten Mueller Hinton agar (18 mL) and poured on sterilized Petri dishes. The plate was inoculated with the standardized (0.5 McFarland standard) bacterial inoculum and incubated at 37°C for 24 hrs. The result of bacterial inhibition was judged by comparison with growth in positive and negative controls.44

Data Analysis

Data were entered into Microsoft Excel and exported to STATA version 14 (1985–2015 Stata Corp) for statistical analysis. One-way ANOVA was performed to compare group means. The results for zones of inhibition of antibacterial activities and MIC were summarized in the form of means ± standard deviation. If secondary metabolites were present, slightly present, and absent, the phytochemical screening result was classified as “++”, “+”, and “-”, respectively.

Results

Phytochemical Screening of Crude Plant Extracts

The results of phytochemical screening of both methanol and petroleum ether plant extracts (E. amplexicaulis, R. chalepensis, and S. subserrata) were summarized (Table 1). The methanol extracts of R. chalepensis consisted of all tested secondary metabolites. Saponins and alkaloids were the most abundant secondary metabolites found in all crude extracts, while phytosterol was the least abundant.

Table 1

Results of Preliminary Phytochemical Screening of Selected Medicinal Plants

Plant Name (Part)	Solvents	Secondary Metabolites
		Saponins	Alkaloids	Flavonoids	Phytosterols	Phenols	Tannins
Echinops amplexicaulis (Root)	Methanol	++	++	+	–	–	+
	Petroleum ether	+	++	–	–	–	+
Ruta chalepensis (Fruit)	Methanol	++	++	++	+	++	++
	Petroleum ether	+	+	+	–	+	+
Salix subserrata (Leaf)	Methanol	++	++	–	+	+	–
	Petroleum ether	++	++	–	–	+	+

Notes: ++Present; +Slightly present; −Absence.

Antibacterial Activities of the Crude Extracts: Agar-Well Diffusion Method

The results of a zone of inhibition (mm, diameter) created by antibacterial activities of crude methanol and petroleum ether extracts of S. subserrata (Leaf), R. chalepensis (Fruit), and E. amplexicaulis plants were measured and summarized in Table 2. The concentration of these crude extracts was classified into 100, 50, and 25 mg/mL in three replicates and subjected to S. aureus, P. aeruginosa, E. coli, and S. pneumoniae. The methanol and petroleum ether plant extracts had shown a zone of inhibition against the selected bacterial strains and had a statistical significance difference between and within-group replicates at p <0.05. However, petroleum ether extract of S. subserrata against S. aureus and P. aeruginosa and methanol extracts of R. chalepensis against S. aureus were not statistically significant. All crude methanol plant extracts had better antibacterial activity when compared with petroleum ether extracts.

Table 2

The Antibacterial Activity of Methanol and Petroleum Ether Extracts of Three Medicinal Plants (Mean of Zone Inhibition of Three Replicates (Diameter in mm) ± Standard Deviation)

Medicinal Plants (Part)	Solvents	Concentrations (mg/mL)	Mean of Zone Inhibition (Diameter (mm) ± Standard Deviation
			P. aeruginosa	p-value	S. pneumoniae	p-value	S. aureus	p-value	E. coli	p-value
S. subserrata(Leaf)	Methanol	100	16.66±1.15	0.02	15± 0.00	0.00	16 ± 1.73	0.00	16 ± 0.00	0.00
		50	16.33± 1.15		13± 1.00		14.66±1.15		14.66± 0.57
		25	12.66±1.52		10±1.00		11±1.00		11±2.00
	Petroleum ether	100	16.33 ±1.52	0.14	15±0.00	0.04	16 ± 1.73	0.08	16±0.00	0.01
		50	14.66± 2.08		12.67 ± 1.53		13.67±3.05		13.67 ± 1.52
		25	12.66± 2.08		10.33±2.52		10.67 ± 2.08		11.33±1.52
R. chalepensis(Fruit)	Methanol	100	21.67 ± 0.58	0.00	19.33±0.58	0.01	15±0.00	0.14	20±0.00	0.00
		50	19±1.00		16.67 ± 1.52		13.33±0.57		18±1.00
		25	16±1.00		14.67 ± 1.53		11.33±3.21		16±1.00
	Petroleum ether	100	21.67 ± 0.57	0.00	19.33 ± 0.57	0.00	15±0.00	0.00	20±0.00	0.00
		50	18.33 ± 0.57		17.33 ± 0.57		12±1.00		17.67±0.57
		25	16.33 ± 0.57		16±0.00		10±1.00		16.33±1.15
E. amplexicaulis(Root)	Methanol	100	21±0.00	0.00	17±0.00	0.00	15±0.00	0.00	19±0.00	0.00
		50	18±1.00		14±1.00		12.33 ± 0.57		16±1.00
		25	15.33 ± 1.15		12±1.00		10.67 ± 0.57		12.33±0.57
	Petroleum ether	100	20±0.00	0.00	17±0.00	0.00	15±0.00	0.02	19±0.00	0.00
		50	19±0.00		15.33 ± 0.57		13±1.00		16.67± 0.57
		25	17±1.00		12.67± 1.52		11.33 ± 1.52		15.33±0.57
Negative control	Dimethyl Sulfoxide	5%	6±0.00		6±0.00		6±0.00		6±0.00
Positive control	Ciprofloxacin	5 μg	38±0.00		39±0.00		37±0.00		36±0.00

Note: p < 0.05 indicate a statistically significant between and within-group of replicates.

The MIC test was done using a serial dilution of crude plant extract using 5% DMSO. For extracts showing a diameter greater than or equal to 6 mm of the growth inhibition zone at 25 mg/mL, MIC was calculated. The methanol and petroleum ether crude extracts were applied to all reference bacterial strains with concentrations ranging from 1.5625 mg/mL to 12.5 mg/mL and the results are shown in Table 3. Compared to the remaining bacterial strains, P. aeruginosa had better antibacterial activities at a lower concentration. P. aeruginosa and E. coli were inhibited at 1.5625 mg/mL concentration by both crude plant extracts.

Table 3

Minimum Inhibitory Concentrations of Crude Extracts of Selected Medicinal Plants Against Selected Bacterial Strains (mg/ml)

Medicinal Plants (Part)	Solvents	The MIC of the Crude Extracts (mg/mL)
		P. aeruginosa	S. pneumoniae	S. aureus	E. coli
Salix subserrata(Leaf)	Methanol	1.5625	6.25	6.25	6.25
	Petroleum ether	3.125	6.25	6.25	6.25
Ruta chalepensis(Fruit)	Methanol	1.5625	6.25	3.125	1.5625
	Petroleum ether	1.5625	6.25	6.25	1.5625
Echinops amplexicaulis(Root)	Methanol	3.125	1.5625	3.125	3.125
	Petroleum ether	3.125	6.25	6.25	6.25

Discussion

The current study revealed that alkaloids, tannins, saponins, flavonoids, and phytosterols were the secondary metabolites found in the crude extract of E. amplexicaulis, R. chalepensis, and S. subserrata. The methanol extracts of E. amplexicaulis and S. subserrata contain most of the secondary metabolites. This is in line with a previous study by Najem et al,45 who reported saponins, alkaloids, tannins, and flavonoids found in methanol extracts of E. amplexicaulis, but phytosterols and phenols were absent. Kevin et al9 found small amounts of tannins and saponins in E. amplexicaulis crude extract but no flavonoids, in contrast to the current study. The difference might be due to soil content, geographical area, seasons of plant collection, plant parts, and growth stage of the plants. According to Copp,46 secondary metabolites of the terpenoids’ family had antibacterial activities, which may be related to their lipophilic nature and thus able to penetrate the bacterial cell wall. In general, the antibacterial activities of plant extracts may be associated with the presence of important secondary metabolites, which play a significant role in the treatment and control of various bacterial diseases, and thus these medicinal plants are used as alternative medicines.

A study by Emam et al47 indicated that the ethanol extract (80%) of the R. chalepensis leaves had alkaloids that are suggested to exhibit antifungal activity against the three phytopathogenic fungi R. solani, S. rolfsii, and F. solani when tested with the disk diffusion technique. Also, the secondary metabolites, namely alkaloids, flavonoids, and tannin of R. chalepensis leaves crude ethanolic extract, had anti-acetylcholinesterase inhibition and antioxidant activities in the gastrointestinal tract.48,49

The current experimental study showed that all three medicinal plants had remarkable antibacterial activities against all tested bacteria. This finding supports the traditional use in the treatment of bacterial infections in both humans and livestock. In the current study, petroleum ether and methanol extracts of R. chalepensis had a considerable antibacterial activity against the use of gram-positive and gram-negative bacterial species. Similarly, Amdouni et al50 used gas chromatography to identify the chemical composition of R. chalepensis leaves, stems, and roots grown under salt stress, and the extract of these plants had antibacterial activity against eight bacteria (Salmonella All, Salmonella K, Escherichia coli 45AG, Escherichia coli 45AI, Staphylococcus aureus 9402, Staphylococcus aureus 02B145, Listeria 477 and Pseudomonas aeruginosa ATCC 10145).

The methanol and petroleum ether extracts of R. chalepensis in the current study showed a higher zone of inhibition (21.67 ± 0.5) at 100 mg/mL concentration, which is contrary to the report of Seid and Ayisha51 that states the leaf extract of R. chalepensis showed the least zone of inhibition (2.49 mm). This is because a higher amount of secondary metabolites is found in the fruit than in the leaf of the indicated plant Krayni et al;52 in this study, the fruit part was used but in the previous study it was the leaf.

The antibacterial evaluation of the three plants results in various sizes of inhibition zones with both solvents against both the Gram-positive and Gram-negative bacteria. In particular, methanol extracts relatively showed a greater zone of inhibition (antibacterial activities) compared to the petroleum ether extracts. Seid and Ayisha51 were also reported the same finding in Ethiopia. This is associated with the extracting efficiency of methanol to liberate most of the biologically active phytochemical compounds like flavonoids, tannins, and carotenoids, which agrees with the ideas of Bakari et al53 and Felhi et al.54 On the other hand, in this study, Gram-positive bacterial strains were relatively less sensitive to both the petroleum ether and methanol extracts, which is in agreement with the results of Fentahun et al.30

The MIC determination test revealed that a different minimum concentration of the crude extract was gained in three of the plants that could inhibit the growth of the reference bacteria. The least MIC value was recorded for methanol extract of R. chalepensis against P. aeruginosa and E. coli. On the contrary, the higher concentration of crude extracts was inhibiting the growth of G-positive bacteria, S. pneumoniae. The MIC value is in line with the antibacterial activities of this plant on the same bacteria. This could be logically explained that R. chalepensis has a better antibacterial activity on G-negative bacteria than G-positives, at least those which are tested in this study. On the other hand, the MIC values of both the methanol and petroleum ether extracts of S. subserrata were 6.25 mg/mL against all the tested organisms except for P. aeruginosa in which the MIC value was 1.5625 mg/mL and 3.125 mg/mL for methanol and petroleum ether extracts, respectively. This also indicates that most of the potential phytochemicals are better extracted with methanol than petroleum ether. Overall, P. aeruginosa is highly susceptible to plant crude extracts even with a small dose.

Despite the important finding, in-vivo evaluation of antibacterial activities of the selected plants, toxicity studies, and quantification of secondary metabolites were not conducted in the current study due to a lack of laboratory animals and facilities.

Conclusion

The current study revealed that all tested plants had important active phytochemical constituents and antibacterial activities against reference bacterial strains. Methanol extracts of S. subserrata (leaves), R. chalepensis (fruits), and E. amplexicaulis (roots) 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 when compared to the remaining bacterial strains. Saponins and alkaloids were the abundant phytochemicals found in methanol and petroleum ether extracts of S. subserrata (Leaf), R. chalepensis (Fruit), and E. amplexicaulis (Roots), while phytosterol was meager. In addition to the current finding, more research on in-vivo antibacterial activity evaluation, toxicity studies, and quantitative analysis of secondary metabolites of crude extracts using advanced techniques is encouraged.