Arachidonic Acid Stress Impacts Pneumococcal Fatty Acid Homeostasis

被引:33
作者
Eijkelkamp, Bart A. [1 ]
Begg, Stephanie L. [1 ]
Pederick, Victoria G. [1 ]
Trapetti, Claudia [1 ]
Gregory, Melissa K. [2 ]
Whittall, Jonathan J. [1 ]
Paton, James C. [1 ]
McDevitt, Christopher A. [1 ]
机构
[1] Univ Adelaide, Res Ctr Infect Dis, Sch Biol Sci, Adelaide, SA, Australia
[2] Univ Adelaide, Adelaide Med Sch, Adelaide, SA, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
host lipids; free fatty acids; membrane fluidity; macrophages; antibacterial fatty acids; FASII; STREPTOCOCCUS-PNEUMONIAE; ZINC HOMEOSTASIS; RESPONSE REGULATOR; IN-VITRO; VIRULENCE; BIOSYNTHESIS; EXPRESSION; GENES; IDENTIFICATION; REQUIREMENT;
D O I
10.3389/fmicb.2018.00813
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Free fatty acids hold dual roles during infection, serving to modulate the host immune response while also functioning directly as antimicrobials. Of particular importance are the long chain polyunsaturated fatty acids, which are not commonly found in bacterial organisms, that have been proposed to have antibacterial roles. Arachidonic acid (AA) is a highly abundant long chain polyunsaturated fatty acid and we examined its effect upon Streptococcus pneumoniae. Here, we observed that in a murine model of S. pneumoniae infection the concentration of AA significantly increases in the blood. The impact of AA stress upon the pathogen was then assessed by a combination of biochemical, biophysical and microbiological assays. In vitro bacterial growth and intra-macrophage survival assays revealed that AA has detrimental effects on pneumococcal fitness. Subsequent analyses demonstrated that M exerts antimicrobial activity via insertion into the pneumococcal membrane, although this did not increase the susceptibility of the bacterium to antibiotic, oxidative or metal ion stress. Transcriptomic profiling showed that AA treatment also resulted in a dramatic down-regulation of the genes involved in fatty acid biosynthesis, in addition to impacts on other metabolic processes, such as carbon-source utilization. Hence, these data reveal that M has two distinct mechanisms of perturbing the pneumococcal membrane composition. Collectively, this work provides a molecular basis for the antimicrobial contribution of M to combat pneumococcal infections.
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页数:12
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共 68 条
[1]   Unsaturated Fatty Acids Promote the Phagocytosis of P-aeruginosa and R-equi by RAW264.7 Macrophages [J].
Adolph, Stephanie ;
Fuhrmann, Herbert ;
Schumann, Julia .
CURRENT MICROBIOLOGY, 2012, 65 (06) :649-655
[2]  
ALBERT A., 1950, BIOCHEM JOUR, V47, pxxvii
[3]   Differential expression analysis for sequence count data [J].
Anders, Simon ;
Huber, Wolfgang .
GENOME BIOLOGY, 2010, 11 (10)
[4]   Selected lipids activate phagosome actin assembly and maturation resulting in killing of pathogenic mycobacteria [J].
Anes, E ;
Kühnel, MP ;
Bos, E ;
Moniz-Pereira, J ;
Habermann, A ;
Griffiths, G .
NATURE CELL BIOLOGY, 2003, 5 (09) :793-802
[5]   Riboflavin (vitamin B2) and oxidative stress: a review [J].
Ashoori, Marziyeh ;
Saedisomeolia, Ahmad .
BRITISH JOURNAL OF NUTRITION, 2014, 111 (11) :1985-1991
[6]   Essentiality of FASII pathway for Staphylococcus aureus [J].
Balemans, Wendy ;
Lounis, Nacer ;
Gilissen, Ron ;
Guillemont, Jerome ;
Simmen, Kenny ;
Andries, Koen ;
Koul, Anil .
NATURE, 2010, 463 (7279) :E3-E4
[7]   Efficacy and Safety of Arachidonic Acid for Treatment of School-Age Children in Schistosoma mansoni High-Endemicity Regions [J].
Barakat, Rashida ;
Abou El-Ela, Nadia E. ;
Sharaf, Soraya ;
El Sagheer, Ola ;
Selim, Sahar ;
Tallima, Hatem ;
Bruins, Maaike J. ;
Hadley, Kevin B. ;
El Ridi, Rashika .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2015, 92 (04) :797-804
[8]   Dysregulation of transition metal ion homeostasis is the molecular basis for cadmium toxicity in Streptococcus pneumoniae [J].
Begg, Stephanie L. ;
Eijkelkamp, Bart A. ;
Luo, Zhenyao ;
Counago, Rafael M. ;
Morey, Jacqueline R. ;
Maher, Megan J. ;
Ong, Cheryl-lynn Y. ;
McEwan, Alastair G. ;
Kobe, Bostjan ;
O'Mara, Megan L. ;
Paton, James C. ;
McDevitt, Christopher A. .
NATURE COMMUNICATIONS, 2015, 6
[9]   Cytosolic Phospholipase A2α Promotes Pulmonary Inflammation and Systemic Disease during Streptococcus pneumoniae Infection [J].
Bhowmick, Rudra ;
Clark, Stacie ;
Bonventre, Joseph V. ;
Leong, John M. ;
McCormick, Beth A. .
INFECTION AND IMMUNITY, 2017, 85 (11)
[10]   Systemic Disease during Streptococcus pneumoniae Acute Lung Infection Requires 12-Lipoxygenase-Dependent Inflammation [J].
Bhowmick, Rudra ;
Maung, Nang H. Tin ;
Hurley, Bryan P. ;
Ghanem, Elsa Bou ;
Gronert, Karsten ;
McCormick, Beth A. ;
Leong, John M. .
JOURNAL OF IMMUNOLOGY, 2013, 191 (10) :5115-5123