Pseudomonas aeruginosa produces aspirin insensitive eicosanoids and contributes to the eicosanoid profile of polymicrobial biofilms with Candida albicans

被引:17
作者
Fourie, Ruan [1 ]
Ells, Ruan [1 ,2 ]
Kemp, Gabre [1 ]
Sebolai, Olihile M. [1 ]
Albertyn, Jacobus [1 ]
Pohl, Carolina H. [1 ]
机构
[1] Univ Free State, Dept Microbial, Biochem & Food Biotechnol, Bloemfontein, South Africa
[2] Univ Free State, Natl Control Lab Biol Prod, Bloemfontein, South Africa
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2017年 / 117卷
基金
新加坡国家研究基金会;
关键词
Acetylsalicylic acid; Biofilm; Candida albicans; Eicosanoid; Nordihydroguaiaretic acid; Pseudomonas aeruginosa; PROSTAGLANDIN E-2 PRODUCTION; ARACHIDONIC-ACID; CYSTIC-FIBROSIS; VIRULENCE; INHIBITOR; PYOCYANIN; GROWTH; CYCLOOXYGENASE-2; INFLAMMATION; INFECTIONS;
D O I
10.1016/j.plefa.2017.01.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interaction of clinically relevant microorganisms is the focus of various studies, e.g. the interaction between the pathogenic yeast, Candida albicans, and the bacterium, Pseudomonas aeruginosa. During infection both release arachidonic acid, which they can transform into eicosanoids. This study evaluated the production of prostaglandin E-2, prostaglandin F-2 alpha and 15-hydroxyeicosatetraenoic acid by biofilms of P. aeruginosa and C. albicans. The influence of co-incubation, acetylsalicylic acid and nordihydroguaiaretic acid on biofilm formation and eicosanoid production was evaluated. Acetylsalicylic acid decreased colony forming units of P. aeruginosa, but increased metabolic activity and eicosanoid production of the cells. In contrast to prostaglandin E2, prostaglandin F-2a production by C. albicans was insensitive to acetylsalicylic acid, indicating that different enzymes are responsible for their production in this yeast. Nordihydroguaiaretic acid inhibited biofilm formation by P. aeruginosa, however co-incubation provided protection against this inhibitor. Production of these eicosanoids could affect pathogen-clearance and infection dynamics and this previously uncharacterized facet of interaction could facilitate novel therapeutic intervention against polymicrobial infection.
引用
收藏
页码:36 / 46
页数:11
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