Drug Res (Stuttg) 2019; 69(12): 658-664
DOI: 10.1055/a-0929-4380
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Pyocyanin, a Metabolite of Pseudomonas Aeruginosa, Exhibits Antifungal Drug Activity Through Inhibition of a Pleiotropic Drug Resistance Subfamily FgABC3

Bilal Houshaymi
1   Department of Microbiology, Faculty of Public Health, Lebanese University, Bekaa, Lebanon
,
Rana Awada
2   Department of Cell Biology, Faculty of Sciences, Lebanese University, Beirut, Lebanon
,
Mamdouh Kedees
3   Department of Cell Biology, State University of New York, New York, USA
,
Zeina Soayfane
2   Department of Cell Biology, Faculty of Sciences, Lebanese University, Beirut, Lebanon
› Author Affiliations
Acknowledgement This work was supported by the Lebanese University funds.
Further Information

Publication History

received 27 March 2019

accepted 14 May 2019

Publication Date:
28 June 2019 (online)

Abstract

The fungus Fusarium graminearum is the causative agent of economically significant plant diseases such as Fusarium Healed Blight (FHB) of cereals, its mycotoxins as deoxynivalenol (DON), Nivalenol (NIV) and Zearalenone (ZEN) contaminate wheat and other grains. The objectives of the present study were to determine the mechanism by which the bacterium Pseudomonas aeruginosa inhibits the growth of F. graminearum. Our results indicate that P. aeruginosa metabolites as pyocyanin has effective antifungal properties. Pyocyanin was produced by P. aeruginosa when cultured on mineral salt medium and reached a maximum concentration after 72 h. Pyocyanin significantly decreased mycotoxins of F. graminearum, a 25 mg/ml of pyocyanin for 72 h decreased DON by 68.7% and NIV by 57.7%.

Real-Time PCR analysis demonstrated that the antifungal effect is mediated by downregulation of the Pleiotropic Drug Resistance (PDR) subfamily FgABC3. 25 mg/ml of pyocyanin decreased FgABC3-mRNA by 60%, inhibited the fungal growth and decreased the area of mycelial growth at 12, 24, 36 and 72 h post incubation by 40–50%. Deletion of FgABC3 led to enhanced accumulation of DON and NIV by 40 and 60%, respectively.

The data presented in this report may have significance in understanding mechanism by which certain bacterial metabolites exert a beneficial effect and for developing antifungal drugs.

 
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