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Saudi Punica granatum L Peel Extract Achievement in Eradicating Zoonotic Pathogens

Research Article | DOI: https://doi.org/10.31579/2835-835X/126

Saudi Punica granatum L Peel Extract Achievement in Eradicating Zoonotic Pathogens

  • Sherifa Mostafa M. Sabra

S. Const., Prof., Dr. Microbiology

*Corresponding Author: Sherifa Mostafa M. Sabra S. Const., Prof., Dr. Microbiology.

Citation: Sherifa Mostafa M. Sabra, (2026), Saudi Punica granatum L Peel Extract Achievement in Eradicating Zoonotic Pathogens, Clinical Trials and Case Studies, 5(1); DOI:10.31579/2835-835X/126

Copyright: © 2026, Sherifa Mostafa M. Sabra. This is an open-access artic le distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Received: 02 February 2026 | Accepted: 11 February 2026 | Published: 18 February 2026

Keywords: punica granatum peel extract; escherichia coli; listeria monocytogenes; candida albicans; staphylococcus aureus; bacillus cereus; clostridium sp; campylobacter sp; shigella sp; brucella sp; salmonella sp

Abstract

Punica granatum peel extract is anti-zoonotic pathogens and energetic role in the zoonotic health field. It contains anti-zoonotic pathogens as phenolic acid, flavonoids, and Tannins. The aim was to conduct a laboratory experiment to test Saudi Punica granatum peel extract against zoonotic pathogens in order to demonstrate the extract's role in zoonotic health. The methodology was for an experiment exposing zoonotic pathogens to Saudi Punica granatum peel extract. The results of group A was included Escherichia coli, Listeria monocytogenes, and Candida albicans, after 12 hours eradications were (72.0%, 72.5% and 70.2%), and after 24 hours were (96.3%, 95.0%, and 95.2%), in range (95%-100%). Group B was included Staphylococcus aureus, and Bacillus cereus, after 12 hours were (60.5%, and 61.2%), and after 24 hours were (90.7%, and 91.8%), in range (90%-95%). Group C was included Clostridium sp., Campylobacter sp., and Shigella sp., after 12 hours were (56.3%, 57.6%, and 57.0%), and after 24 hours were (86.2%, 87.1%, and 86.0%), in range (85%-90%). Group D was included Brucella sp., and. Salmonella sp, after 12 hours were (61.4%, and 58.8%), and after 24 hours were (80.7% and 82.4%), in range (80%-85%). It was concluded that Saudi Punica granatum peel extract was capable to eradicate zoonotic pathogens pose a human's health risk, can be transmitted to humans and cause zoonotic diseases. It also protected animals and animal products, thus possessing cross-health protection properties for both humans and animals. It was recommended that Saudi Punica granatum peel extract using of in appropriate medicinal quantities to maintain zoonotic health.

Introduction

Punica granatum L is under "Subfamily Punicoideae", Punica granatum peel has a good position in the zoonotic health. Punica granatum peel extract is using as anti-zoonotic pathogens and plays an energetic role in the zoonotic health field. Punica granatum peel extract contains anti-zoonotic pathogens as phenolic acid, flavonoids, Tannins etc., that have been found very effective in the zoonotic health field. Due to the presence of anti-zoonotic pathogens action is authoritative for the zoonotic health improvement. The anti-zoonotic function is acting against various zoonotic pathogens [1].

Punica granatum peel extract contains compounds 5-hydroxy-methyl-furfural (36.6%), D-sucrose (23.2%), sorbitol (6.7%), palmitic acid β-mono-glyceride (5.6%), 2-furan-carboxal-dehyde (3.5%) and β-D-gluco-pyranose (3.3%) [2]. Punica granatum peel extract contains substantial quantities of poly-phenols as ellagic tannins, gallic acid, and ellagic acid [3]. 

Punica granatum peel extract contains active compounds control zoonotic pathogens activities [4]. Punica granatum peel extract contains active mixtures demonstrated as anti-zoonotic pathogens activity [5]. Punica granatum peel extracts due to content of high levels of phenolics and exhibited as antibacterial activity against zoonotic bacteria [6].

Punica granatum peel extract was very effective to control various zoonotic pathogens Staphylococcus sp. [7]. Punica granatum peel extract was effective against zoonotic bacteria Salmonella sp., Escherichia coli, and Staphylococcus aureus, control the production of enterotoxin [8]. Punica granatum peel extract had anti-zoonotic properties against Shigella sp. [7]. Punica granatum peel extract was highly susceptible to zoonotic bacteria Shigella sp. [9]. Punica granatum peel extract had anti-zoonotic pathogens activities Staphylococcus aureus NCTC 6571 [10]. Punica granatum peel extract was preventing zoonotic bacteria Escherichia coli, and Staphylococcus aureus [8]. Punica granatum peel extract had anti-zoonotic bacteria on Escherichia coli, and Listeria monocytogenes [11]. Punica granatum peel extracts had anti-zoonotic activity against Bacillus sp., Staphylococcus aureus, Escherichia coli, and Salmonella sp. Gram-positive bacteria were more sensitive to the extracts than Gram-negative [12]. Punica granatum peel extract used as anti-zoonotic microbial activity against enteropathogenic zoonotic bacteria Escherichia coli, Salmonella sp., and Shigella sp. [13]. 

Punica granatum peel extract had yeast anti-zoonotic on Candida albicans infection [14]. Punica granatum peel extract had positive anti-zoonotic on Candida albicans from family Saccharomycetaceae [15]. Punica granatum peel extract had preventing various zoonotic pathogens Candida albicans [16].

The importance it was for an aim of the research was to conduct a laboratory experiment to test Saudi Punica granatum peel extract against zoonotic pathogens in order to demonstrate the extract's role in zoonotic health.

Methodology:

Peel Extract:

Saudi Punica granatum sample was bought from the town market, the peel was manually peeled, was washed by distilled water, and 70% ethanol. The Saudi Punica granatum peel was extracted by "Hydro-Distillation" used "Clevenger-Type-Device". The dried peel was crushed by "Sterile-Mixer", was additional 30 g ground powder + 600 mL distilled water in 1000 mL bottle covering 600 mL, the mixture was boiling for 5 hours. Saudi Punica granatum peel extract was available as mL/100 g dry matter, then anhydrous Na2SO4 was dehydrated and dark glass container kept at 4◦C [17].

Zoonotic Pathogens:

The zoonotic pathogens isolates were collected from "Isolated-Lab.", were included Staphylococcus aureus, Clostridium sp., Bacillus cereus, Brucella sp., Salmonella sp., Escherichia coli, Campylobacter sp., Shigella sp., Listeria monocytogenes, and Candida albicans. They were cultured in "Muller-Hinton-Broth", were incubated at 37°C for 18 hours, then were subculture for pure colony on "Muller-Hinton-Agar" at 37°C for 18 hours. Then pure isolates were made in "Muller-Hinton-Broth", (1-2×108 CFU/mL) [18].

Laboratory Test:

An equal quantity of Saudi Punica granatum peel extract and pure isolates suspension were placed in each hole of "Micro-Titration-Plate", and were made three holes for each isolate. The plate was mixed by "Electric-Vibrator." The plate was incubated at (35-37) °C, then was checked at (12 and 24) hours. A mixture loopful was taken from each hole for culture on "Molar-Hinton-Agar" was incubated for 24 hours at (35-37) °C, the colony count was made [11].

Statistical Analyses

The results were made in triple trials, were existed as mean with standard errors. These final results were calculated by "Microsoft Excel Software" [19].

Results and Discussions:

Zoonotic pathogen

Item

Time

Group

Zero hours

12 hours

24 hours

Escherichia coli

Colony count

82±3

23±2   

3±2

A

lived percent

100%

28.0%

3.7%

Eradicated percent

00.0%

72.0%

96.3%

Listeria monocytogenes

Colony count

80±3

22±2   

4±2

lived percent

100%

27.5%

5.0%

Eradicated percent

00.0%

72.5%

95.0%

Candida albicans

Colony count

84±3

25±2   

4±2

lived percent

100%

29.8%

4.8%

Eradicated percent

00.0%

70.2%

95.2%

Staphylococcus aureus

Colony count

86±3

34±2   

8±2

B

lived percent

100%

39.5%

9.3%

Eradicated percent

00.0%

60.5%

90.7%

Bacillus cereus

Colony count

85±3

33±2   

7±2

lived percent

100%

38.8%

8.2%

Eradicated percent

00.0%

61.2%

91.8%

Clostridium sp.

Colony count

87±3

38±2   

12±2

C

lived percent

100%

43.7%

13.8%

Eradicated percent

00.0%

56.3%

86.2%

Campylobacter sp.

Colony count

85±3

36±2   

11±2

lived percent

100%

42.4%

12.9%

Eradicated percent

00.0%

57.6%

87.1%

Shigella sp.

Colony count

86±3

37±2   

12±2

lived percent

100%

43.0%

14.0%

Eradicated percent

00.0%

57.0%

86.0%

Brucella sp.

Colony count

83±3

32±2 

16±2

D

lived percent

100%

38.6%

19.3%

Eradicated percent

00.0%

61.4%

80.7%

Salmonella sp.

Colony count

85±3

35±2 

15±2

lived percent

100%

41.2%

17.6%

Eradicated percent

00.0%

58.8%

82.4%

Table 1: An estimated percentage of zoonotic pathogens after contact to Saudi Punica granatum peel extract

Figure 1: An estimated percentage of zoonotic pathogens after contact to Saudi Punica granatum peel extract

Table (1), and Figure (1) were showed an estimated percentage of zoonotic pathogens after contact to Saudi Punica granatum peel extract. Because Saudi Punica granatum peel extract contains active compounds that eradicated zoonotic pathogens [1-6].

Group A were contained zoonotic pathogens included Escherichia coli, Listeria monocytogenes, and Candida albicans. The results after twelve hours were showed the eradicated percent were (72.0%, 72.5% and 70.2%), and the results after twenty-four hours were showed the eradicated percent were (96.3%, 95.0%, and 95.2%). The results indicated that Saudi Punica granatum peel extract was eradicated group A in a range of (95%-100%) for zoonotic pathogens [8, 11-16].

Table (1), and Figure (1) were showed group B were contained zoonotic pathogens included Staphylococcus aureus, and Bacillus cereus. The results after twelve hours were showed the eradicated percent were (60.5%, and 61.2%), and the results after twenty-four hours were showed the eradicated percent were (90.7%, and 91.8%). The results indicated that Saudi Punica granatum peel extract was eradicated group B in a range of (90%-95%) for zoonotic pathogens [7-8, 10-12].

Table (1), and Figure (1) were showed group C were contained zoonotic pathogens included Clostridium sp., Campylobacter sp., and Shigella sp. The results after twelve hours were showed the eradicated percent were (56.3%, 57.6%, and 57.0%), and the results after twenty-four hours were showed the eradicated percent were (86.2%, 87.1%, and 86.0%). The results indicated that Saudi Punica granatum peel extract was eradicated group C in a range of (85%-90%) for tested zoonotic pathogens [9, 11, 13].

Table (1), and Figure (1) were showed group D were contained zoonotic pathogens included Brucella sp., and. Salmonella sp. The results after twelve hours were showed the eradicated percent were (61.4%, and 58.8%), and the results after twenty-four hours were showed the eradicated percent were (80.7% and 82.4%). The results indicated that Saudi Punica granatum peel extract was eradicated group D in a range of (80%-85%) for zoonotic pathogens [11-13].

The results were showed the main components effects in Saudi Punica granatum peel extract had the property of zoonotic pathogens eradication that are present in the animal environment and can be transmit to humans. These affecting the shared environment and causing zoonotic humans' diseases, especially farmers who are in close proximity to animals or workers handle animal products [1-6].

Conclusions:

It was concluded that, the research had shown that Saudi Punica granatum peel extract was capable of eradicate zoonotic pathogens pose a human's health risk, as these zoonotic pathogens can be transmitted to humans and cause zoonotic diseases. It also protected animals and animal products, thus possessing cross-health protection properties for both humans and animals.

Recommendations:

It was recommended that the using of Saudi Punica granatum peel extract in appropriate medicinal quantities to maintain zoonotic health.

Acknowledgments:

Thanks, were sent to all researchers who contributed to this research.

References

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