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Enhancement of pyocyanin production by subinhibitory concentration of royal jelly in Pseudomonas aeruginosa [version 2; peer review: 2 approved, 1 approved with reservations]

Authors :
Dina Auliya Amly
Puspita Hajardhini
Alma Linggar Jonarta
Heribertus Dedy Kusuma Yulianto
Heni Susilowati
Author Affiliations :
<relatesTo>1</relatesTo>Master of Dental Sciences Program, Faculty of Dentistry, Universitas Gadjah Mada, Sleman, Yogyakarta, 55281, Indonesia<br /><relatesTo>2</relatesTo>Department of Oral Biology, Faculty of Dentistry, Universitas Gadjah Mada, Sleman, Yogyakarta, 55281, Indonesia<br /><relatesTo>3</relatesTo>Department of Dental Biomedical Sciences, Faculty of Dentistry, Universitas Gadjah Mada, Sleman, Yogyakarta, 55281, Indonesia
Source :
F1000Research. 10:14
Publication Year :
2021
Publisher :
London, UK: F1000 Research Limited, 2021.

Abstract

Background: Pseudomonas aeruginosa, a multidrug-resistant Gram-negative bacterium, produces pyocyanin, a virulence factor associated with antibiotic tolerance. High concentrations of royal jelly have an antibacterial effect, which may potentially overcome antibacterial resistance. However, in some cases, antibiotic tolerance can occur due to prolonged stress of low-dose antibacterial agents. This study aimed to investigate the effect of subinhibitory concentrations of royal jelly on bacterial growth, pyocyanin production, and biofilm formation of P. aeruginosa. Methods: Pseudomonas aeruginosa ATCC 10145 and clinical isolates were cultured in a royal jelly-containing medium to test the antibacterial activity. Pyocyanin production was observed by measuring the absorbance at 690 nm after 36 h culture and determined using extinction coefficient 4310 M-1 cm-1. Static microtiter plate biofilm assay performed to detect the biofilm formation, followed by scanning electron microscopy. Results: Royal jelly effectively inhibited the viability of both strains from a concentration of 25%. The highest production of pyocyanin was observed in the subinhibitory concentration group 6.25%, which gradually decreased along with the decrease of royal jelly concentration. Results of one-way ANOVA tests differed significantly in pyocyanin production of the two strains between the royal jelly groups. Tukey HSD test showed concentrations of 12.5%, 6.25%, and 3.125% significantly increased pyocyanin production of ATCC 10145, and the concentrations of 12.5% and 6.25% significantly increased production of the clinical isolates. Concentrations of 12.5% and 6.125% significantly induced biofilm formation of P. aeruginosa ATCC 10145, in line with the results of the SEM analysis. Conclusions: Royal jelly concentrations of 25% or higher can inhibit bacterial growth; however, subinhibitory concentrations could increase pyocyanin production and biofilm formation in P. aeruginosa. It is advisable to determine the appropriate concentration of royal jelly to obtain beneficial virulence inhibiting activity.

Details

ISSN :
20461402
Volume :
10
Database :
F1000Research
Journal :
F1000Research
Notes :
Revised Amendments from Version 1 The new version of the manuscript contains revisions and additional research data on biofilms, including a quantitative and descriptive analysis of the effect of royal jelly on Pseudomonas aeruginosa biofilms. These changes include: 1. An explanation of the origin of the royal jelly used in this study. The revision is written in lines 2-6 of paragraph 2 of the Methods section. 2. Explanation of the method of identification of clinical isolate bacteria. The explanation is written in line 5 of paragraph 3 in the Methods section. 3. Explanation of the number of replications of research subjects for bacterial sensitivity studies, pyocyanin assay, and biofilm assay. The revision is in the last line of related paragraphs in the Methods section. 4. Adding new methods and data from the results of quantitative biofilm studies. Related changes were in the Abstract, paragraph 6 of the Methods, paragraph 5 of Results, Figure 4, and line 5 of paragraph 6 on the Discussion section in the manuscript. 5. Addition of new methods and data for descriptive analysis of biofilm using Scanning Electron Microscopy. Methods, results, discussion, and related references have been added to the Abstract, paragraph 7 of the Methods section, paragraph 6-7 of the Results section, Figure 5, and line 5 in paragraph 6 of the Discussion section. 6. An explanation of the royal jelly extraction method. Explanation to paragraph 2 of the Discussion section. Additional sources of literature have been written in the reference list numbers 37, 38, and 39. 7. Revision of the MIC value of royal jelly. Revision on the first sentence in Methods of Abstract and two last sentences in the Results section. 8. Explanation about the selected pyocyanin assay method has been communicated to the reviewer as a direct response in the journal system., , [version 2; peer review: 2 approved, 1 approved with reservations]
Publication Type :
Academic Journal
Accession number :
edsfor.10.12688.f1000research.27915.2
Document Type :
research-article
Full Text :
https://doi.org/10.12688/f1000research.27915.2