Oxidized Fatty Acids as Inter-Kingdom Signaling Molecules

Oxylipins or oxidized fatty acids are a group of molecules found to play a role in signaling in many different cell types. These fatty acid derivatives have ancient evolutionary origins as signaling molecules and are ideal candidates for inter-kingdom communication. This review discusses examples of the ability of organisms from different kingdoms to “listen” and respond to oxylipin signals during interactions. The interactions that will be looked at are signaling between animals and plants; between animals and fungi; between animals and bacteria and between plants and fungi. This will aid in understanding these interactions, which often have implications in ecology, agriculture as well as human and animal health.

[1]  T. Kotsimbos,et al.  Loss of fat-free mass over four years in adult cystic fibrosis is associated with high serum interleukin-6 levels but not tumour necrosis factor-alpha. , 2014, Clinical nutrition.

[2]  A. Edefonti,et al.  Effects of treatment in the levels of circulating cytokines and growth factors in cystic fibrosis and dialyzed patients by multi-analytical determination with a biochip array platform. , 2013, Cytokine.

[3]  J. Mainz,et al.  Soluble inflammation markers in nasal lavage from CF patients and healthy controls. , 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

[4]  N. Høiby,et al.  Respiratory bacterial infections in cystic fibrosis , 2013, Current opinion in pulmonary medicine.

[5]  C. Hertweck,et al.  Biosynthesis of Archetypal Plant Self‐Defensive Oxylipins by an Endophytic Fungus Residing in Mangrove Embryos , 2012, Chembiochem : a European journal of chemical biology.

[6]  J. Ocampo,et al.  Plant 9-lox oxylipin metabolism in response to arbuscular mycorrhiza , 2012, Plant signaling & behavior.

[7]  E. Esquivel-Naranjo,et al.  An injury-response mechanism conserved across kingdoms determines entry of the fungus Trichoderma atroviride into development , 2012, Proceedings of the National Academy of Sciences.

[8]  J. Albertyn,et al.  Arachidonic acid metabolites in pathogenic yeasts , 2012, Lipids in Health and Disease.

[9]  B. Morrissey,et al.  Metabolomic profiling of regulatory lipid mediators in sputum from adult cystic fibrosis patients. , 2012, Free radical biology & medicine.

[10]  B. Morrissey,et al.  Omics approaches in cystic fibrosis research: a focus on oxylipin profiling in airway secretions , 2012, Annals of the New York Academy of Sciences.

[11]  David S Domozych,et al.  The Charophycean green algae as model systems to study plant cell walls and other evolutionary adaptations that gave rise to land plants , 2012, Plant signaling & behavior.

[12]  G. Geginat,et al.  Production of prostaglandins, isoprostanes and thromboxane by Aspergillus fumigatus: identification by gas chromatography-tandem mass spectrometry and quantification by enzyme immunoassay. , 2012, Molecular immunology.

[13]  N. Yoshinaga,et al.  Function and evolutionary diversity of fatty acid amino acid conjugates in insects , 2011 .

[14]  Michael V Kolomiets,et al.  The lipid language of plant-fungal interactions. , 2011, Fungal genetics and biology : FG & B.

[15]  I. Buttino,et al.  Impact of the diatom oxylipin 15S-HEPE on the reproductive success of the copepod Temora stylifera , 2011, Hydrobiologia.

[16]  J. Albertyn,et al.  Effect of inhibitors of arachidonic acid metabolism on prostaglandin E2 production by Candida albicans and Candida dubliniensis biofilms , 2011, Medical Microbiology and Immunology.

[17]  Kosaku Takahashi,et al.  Biosynthesis of jasmonic acid in a plant pathogenic fungus, Lasiodiplodia theobromae. , 2010, Phytochemistry.

[18]  K. Dehesh,et al.  Arachidonic Acid: An Evolutionarily Conserved Signaling Molecule Modulates Plant Stress Signaling Networks[C][W] , 2010, Plant Cell.

[19]  L. A. Dias-Melicio,et al.  Paracoccidioides brasiliensis Uses Endogenous and Exogenous Arachidonic Acid for PGEx Production , 2010, Mycopathologia.

[20]  A. Ianora,et al.  Toxigenic effects of diatoms on grazers, phytoplankton and other microbes: a review , 2010, Ecotoxicology.

[21]  Martin J. Mueller,et al.  Pollen allergens do not come alone: pollen associated lipid mediators (PALMS) shift the human immue systems towards a TH2-dominated response , 2009, Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology.

[22]  M. Kolomiets,et al.  Host-derived lipids and oxylipins are crucial signals in modulating mycotoxin production by fungi , 2009 .

[23]  Martin J. Mueller,et al.  Pollen-Derived E1-Phytoprostanes Signal via PPAR-γ and NF-κB-Dependent Mechanisms1 , 2009, The Journal of Immunology.

[24]  A. Lüscher,et al.  Plant enemy-derived elicitors increase the foliar tannin concentration of Onobrychis viciifolia without a trade-off to growth. , 2008, Annals of botany.

[25]  S. Ikeda,et al.  Candida albicans abrogates the expression of interferon-gamma-inducible protein-10 in human keratinocytes. , 2008, FEMS immunology and medical microbiology.

[26]  I. Feussner,et al.  Reciprocal oxylipin‐mediated cross‐talk in the Aspergillus–seed pathosystem , 2007, Molecular microbiology.

[27]  Yan Lu,et al.  Candida albicans Modulates Host Defense by Biosynthesizing the Pro-Resolving Mediator Resolvin E1 , 2007, PloS one.

[28]  A. Fontana,et al.  LOX‐Induced Lipid Peroxidation Mechanism Responsible for the Detrimental Effect of Marine Diatoms on Zooplankton Grazers , 2007, Chembiochem : a European journal of chemical biology.

[29]  L. A. Dias-Melicio,et al.  Prostaglandin E2 inhibits Paracoccidioides brasiliensis killing by human monocytes. , 2007, Microbes and infection.

[30]  N. Keller,et al.  Oxylipins as developmental and host-fungal communication signals. , 2007, Trends in microbiology.

[31]  V. O’Donnell,et al.  Inflammation and immune regulation by 12/15-lipoxygenases. , 2006, Progress in lipid research.

[32]  A. M. Saliba,et al.  Eicosanoid‐mediated proinflammatory activity of Pseudomonas aeruginosa ExoU , 2005, Cellular microbiology.

[33]  Q. Myrvik,et al.  Splenic PGE2‐releasing macrophages regulate Th1 and Th2 immune responses in mice treated with heat‐killed BCG , 2005, Journal of leukocyte biology.

[34]  S. Sahi,et al.  Oxygenation by COX-2 (cyclo-oxygenase-2) of 3-HETE (3-hydroxyeicosatetraenoic acid), a fungal mimetic of arachidonic acid, produces a cascade of novel bioactive 3-hydroxyeicosanoids. , 2005, The Biochemical journal.

[35]  J. Frisvad,et al.  Aspergillus Cyclooxygenase-Like Enzymes Are Associated with Prostaglandin Production and Virulence , 2005, Infection and Immunity.

[36]  Martin J. Mueller,et al.  Abbreviations used: Bet.-APE, , 2022 .

[37]  G. Huffnagle,et al.  Regulation of Candida albicans Morphogenesis by Fatty Acid Metabolites , 2004, Infection and Immunity.

[38]  Charles N. Serhan,et al.  Resolvins, docosatrienes, and neuroprotectins, novel omega-3-derived mediators, and their endogenous aspirin-triggered epimers , 2004, Lipids.

[39]  J. Mekalanos,et al.  The opportunistic pathogen Pseudomonas aeruginosa carries a secretable arachidonate 15-lipoxygenase , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[40]  Jack C. Schultz,et al.  CROSS‐KINGDOM CROSS‐TALK: HORMONES SHARED BY PLANTS AND THEIR INSECT HERBIVORES , 2004 .

[41]  Makoto Murakami,et al.  Recent advances in molecular biology and physiology of the prostaglandin E2-biosynthetic pathway. , 2004, Progress in lipid research.

[42]  John H. Loughrin,et al.  Volicitin, An Elicitor of Maize Volatiles in Oral Secretion of Spodoptera Exigua: Isolation and Bioactivity , 2004, Journal of Chemical Ecology.

[43]  J. Erb-Downward,et al.  Production of Eicosanoids and Other Oxylipins by Pathogenic Eukaryotic Microbes , 2003, Clinical Microbiology Reviews.

[44]  May R. Berenbaum,et al.  Jasmonate and salicylate induce expression of herbivore cytochrome P450 genes , 2002, Nature.

[45]  H. Kuhn,et al.  Mammalian arachidonate 15-lipoxygenases structure, function, and biological implications. , 2002, Prostaglandins & other lipid mediators.

[46]  J. Schultz Shared Signals and the Potential for Phylogenetic Espionage Between Plants and Animals1 , 2002, Integrative and comparative biology.

[47]  Y. Sugimoto,et al.  Prostaglandin receptors: advances in the study of EP3 receptor signaling. , 2002, Journal of biochemistry.

[48]  H. Weber Fatty acid-derived signals in plants. , 2002, Trends in plant science.

[49]  J. Ring,et al.  Lipid mediators from pollen act as chemoattractants and activators of polymorphonuclear granulocytes. , 2002, The Journal of allergy and clinical immunology.

[50]  D. Harmsen,et al.  Selective (R)-3-hydroxylation of FA by Stenotrophomonas maltophilia , 2002, Lipids.

[51]  G. Toews,et al.  Production of Prostaglandins and Leukotrienes by Pathogenic Fungi , 2002, Infection and Immunity.

[52]  C. Funk,et al.  Prostaglandins and leukotrienes: advances in eicosanoid biology. , 2001, Science.

[53]  D. Zeldin Epoxygenase Pathways of Arachidonic Acid Metabolism* , 2001, The Journal of Biological Chemistry.

[54]  P. Markaki,et al.  Methyl jasmonate stimulates aflatoxin B1 biosynthesis by Aspergillus parasiticus. , 2001, Journal of agricultural and food chemistry.

[55]  G. Toews,et al.  Pathogenic Yeasts Cryptococcus neoformans and Candida albicans Produce Immunomodulatory Prostaglandins , 2001, Infection and Immunity.

[56]  M. T. Peraçoli,et al.  Modulatory effect of prostaglandins on human monocyte activation for killing of high‐ and low‐virulence strains of Paracoccidioides brasiliensis , 2001, Immunology.

[57]  M. Carroll,et al.  A new class of lipid mediators: cytochrome P450 arachidonate metabolites , 2000, Thorax.

[58]  Martin J. Mueller,et al.  Formation of isoprostane F(2)-like compounds (phytoprostanes F(1)) from alpha-linolenic acid in plants. , 2000, Free radical biology & medicine.

[59]  A. M. Calvo,et al.  Sporogenic Effect of Polyunsaturated Fatty Acids on Development of Aspergillus spp , 1999, Applied and Environmental Microbiology.

[60]  S. Parchmann,et al.  Evidence for the Formation of Dinor Isoprostanes E1from α-Linolenic Acid in Plants* , 1998, The Journal of Biological Chemistry.

[61]  Ted C. J. Turlings,et al.  An Elicitor of Plant Volatiles from Beet Armyworm Oral Secretion , 1997 .

[62]  T. C. Nesbitt,et al.  Seed lipoxygenase products modulate Aspergillus mycotoxin biosynthesis , 1997 .

[63]  M. Goodrich-Tanrikulu,et al.  The plant growth regulator methyl jasmonate inhibits aflatoxin production by Aspergillus flavus. , 1995, Microbiology.

[64]  W. Henderson The Role of Leukotrienes in Inflammation , 1994, Annals of Internal Medicine.

[65]  M. Betz,et al.  Prostaglandin E2 inhibits production of Th1 lymphokines but not of Th2 lymphokines. , 1991, Journal of immunology.

[66]  S. Witkin,et al.  Prostaglandin E2 enhances and gamma interferon inhibits germ tube formation in Candida albicans , 1990, Infection and immunity.

[67]  W. Smith,et al.  The eicosanoids and their biochemical mechanisms of action. , 1989, The Biochemical journal.