AccScience Publishing / EJMO / Volume 2 / Issue 2 / DOI: 10.14744/ejmo.2017.18189
RESEARCH ARTICLE

Efficacy of Calendula Officinalis as an Antibacterial Agent for In Vitro Pseudomonas Aeruginosa

Mbuso Mabuza1
Show Less
1 Department of Medical Microbiology, University of KwaZulu-Natal, Nelson R. Mandela Faculty of Medicine, Durban, South Africa
Submitted: 19 July 2017 | Accepted: 25 December 2017 | Published: 5 February 2018
© 2018 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC-by the license) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

Objectives: The aim of this in vitro microbial study was to evaluate the efficacy of Calendula officinalis tincture 60% (v/v) ethanol as an antibacterial agent for in vitro Pseudomonas aeruginosa.

Methods: The standardized disk diffusion method was employed. Seven pairs of Mueller–Hinton agar plates were used; one plate was the experiment and one a control. P. aeruginosa broth cultures were grown for 24 hours. A sterile cotton swab was soaked in P. aeruginosa broth culture and then streaked evenly in 3 directions over the entire surface of the agar plates to obtain a uniform inoculum. Sterile filter paper disks (0.45-µm pore size; 5-mm diameter) were impregnated with standardized amounts of C. officinalis tincture 60% (v/v) ethanol. The first set of disks was impregnated with undiluted C. officinalis tincture 60% (v/v) ethanol, and the subsequent sets of disks we re impregnated with a series of 2-fold dilutions of C. officinalis tincture 60% (v/v) ethanol. One disk from each set was aseptically placed on the inoculated agar surface of each plate. The plates were inverted and incubated at 37°C in ambient air for 24 hours, after which any presence of clear zones of inhibition were observed against a light background and the diameter of these zones was measured. The whole procedure was performed in triplicate. The mean activity of the 2 treatment groups was 6.88 and 6.69 mm, respectively.

Results: The antibacterial activity of C. officinalis tincture 60% (v/v) ethanol and the 60% ethanol control groups showed a similar pattern on in vitro P. aeruginosa. There was no statistically significant difference between the experimental and control groups (p>0.05; t-test). 

Conclusion: There was no evidence to prove the efficacy of C. officinalis tincture 60% (v/v) ethanol as an antibacterial agent for in vitro P. aeruginosa.

Keywords
Antibacterial
antibiotic resistance
Calendula officinalis
efficacy
in vitro
Pseudomonas aeruginosa
Conflict of interest
The author declares that he has no competing interests.
References

1. Cox SD, Mann CM, Markham JL, Bell HC, Gustafson JE, Warmington JR, et al. The mode of antimicrobial action of the essential oil of Melaleuca alternifolia (tea tree oil). J Appl Microbiol 2000;88:170–5. [CrossRef]
2. Hancock RE, Speert DP. Antibiotic resistance in Pseudomonas aeruginosa: mechanisms and impact on treatment. Drug Resist Updat 2000;3:247–55. [CrossRef]
3. Gordon SM, Schmitt SK, Jacobs M, Smedira NM, Goormastic M, Banbury MK, et al. Nosocomial bloodstream infections in patients with implantable left ventricular assist devices. Ann Thorac Surg 2001;72:725–30. [CrossRef]
4. Halabi M, Wiesholzer-Pittl M, Schöberl J, Mittermayer H. Nontouch fittings in hospitals: a possible source of Pseudomonas aeruginosa and Legionella spp. J Hosp Infect 2001;49:117–21.
5. Kosorok MR, Zeng L, West SE, Rock MJ, Splaingard ML, Laxova A, et al. Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition. Pediatr Pulmonol 2001;32:277–87. [CrossRef]
6. Pennington H. Millennium bugs. Biologist (London) 2000;47:93–5.
7. Davies J. Unanswered questions concerning antibiotic resistance. Clin Microbiol Infect 1998;4:2–3. [CrossRef]
8. Petry JJ, Hadley SK. Medicinal herbs: answers and advice, part 1. Hosp Pract (1995) 2001;36:57–60. [CrossRef]
9. Abu-Ghazaleh BM. Effect of sodium chloride and citric acid on growth and toxin production by A. caviae and A. sobria at moderate and low temperatures. New Microbiol 2000;23:433–40.
10. Iatsyno AI, Belova LF, Lipkina GS, Sokolov SI, Trutneva EA. Pharmacology of calenduloside B, a new triterpene glycoside from the roots of Calendula officinalis. Farmakol Toksikol 1978;41:556–60.
11. Nichols WW, Evans MJ, Slack MP, Walmsley HL. The penetration of antibiotics into aggregates of mucoid and non-mucoid Pseudomonas aeruginosa. J Gen Microbiol 1989;135:1291–303.
12. Palenic B, Block JC, Burns RG, Characklis WG, Christensen BE, Ghiorse WC, et al. Biofilms: properties and processes. In: Characklis WG, Wilderer PA, editors. Structure and Function of Biofilms. Chichester: John Wiley and Sons; 1989.
13. Wyatt TD. The control of biofilm in recreational waters. In: Denyer SP, Gorman SP, Sussman M, editors. Microbial Biofilms: Formations and Control. London: Blackwell Scientific Publications; 1993.
14. Jones RN; College of American Pathologists Microbiology Resource Committe. Method preferences and test accuracy of antimicrobial susceptibility testing: updates from the College of Amercian Pathologists Microbiology Surveys Program. Arch Pathol Lab Med 2001;125:1285–9.
15. Sechi LA, Lezcano I, Nunez N, Espim M, Duprè I, Pinna A, et al. Antibacterial activity of ozonized sunflower oil (Oleozon). J Appl Microbiol 2001;90:279–84. [CrossRef]

Share
Back to top
Eurasian Journal of Medicine and Oncology, Electronic ISSN: 2587-196X Print ISSN: 2587-2400, Published by AccScience Publishing