Inhibition of Fatty Acid Synthase (Fas2) Induces Mitochondrial Cell Death in Serum
We have recently observed that a fatty acid auxotrophic mutant (fatty acid synthase, Fas2Δ/Δ) of the emerging human pathogenic yeast Candida parapsilosis dies after incubation in various media including serum. In the present study we describe the mechanism for cell death induced by serum and glucose containing media. We show that Fas2Δ/Δ yeast cells are profoundly susceptible to glucose leading us to propose that yeast cells lacking fatty acids exhibit uncontrolled metabolism in response to glucose. We demonstrate that incubation of Fas2Δ/Δ yeast cells with serum leads to cell death, and this process can be prevented with inhibition of protein or DNA synthesis, indicating that newly synthesized cellular components are detrimental to the mutant cells. Furthermore, we have found that cell death is mediated by mitochondria. Suppression of electron transport enzymes using inhibitors such as cyanide or azide prevents ROS overproduction and Fas2Δ/Δ yeast cell death. Additionally, deletion of mitochondrial DNA, which encodes several subunits for enzymes of the electron transport chain, significantly reduces serum-induced Fas2Δ/Δ yeast cell death. Therefore, our results show that serum and glucose media induce Fas2Δ/Δ yeast cell death by triggering unbalanced metabolism, which is regulated by mitochondria. To our knowledge, this is the first study to critically define a link between cytosolic fatty acid synthesis and mitochondrial function in response to serum stress in C. parapsilosis.
Vyšlo v časopise:
Inhibition of Fatty Acid Synthase (Fas2) Induces Mitochondrial Cell Death in Serum. PLoS Pathog 8(8): e32767. doi:10.1371/journal.ppat.1002879
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1002879
Souhrn
We have recently observed that a fatty acid auxotrophic mutant (fatty acid synthase, Fas2Δ/Δ) of the emerging human pathogenic yeast Candida parapsilosis dies after incubation in various media including serum. In the present study we describe the mechanism for cell death induced by serum and glucose containing media. We show that Fas2Δ/Δ yeast cells are profoundly susceptible to glucose leading us to propose that yeast cells lacking fatty acids exhibit uncontrolled metabolism in response to glucose. We demonstrate that incubation of Fas2Δ/Δ yeast cells with serum leads to cell death, and this process can be prevented with inhibition of protein or DNA synthesis, indicating that newly synthesized cellular components are detrimental to the mutant cells. Furthermore, we have found that cell death is mediated by mitochondria. Suppression of electron transport enzymes using inhibitors such as cyanide or azide prevents ROS overproduction and Fas2Δ/Δ yeast cell death. Additionally, deletion of mitochondrial DNA, which encodes several subunits for enzymes of the electron transport chain, significantly reduces serum-induced Fas2Δ/Δ yeast cell death. Therefore, our results show that serum and glucose media induce Fas2Δ/Δ yeast cell death by triggering unbalanced metabolism, which is regulated by mitochondria. To our knowledge, this is the first study to critically define a link between cytosolic fatty acid synthesis and mitochondrial function in response to serum stress in C. parapsilosis.
Zdroje
1. SchullerHJ, FortschB, RautenstraussB, WolfDH, SchweizerE (1992) Differential proteolytic sensitivity of yeast fatty acid synthetase subunits alpha and beta contributing to a balanced ratio of both fatty acid synthetase components. Eur J Biochem 203: 607–614.
2. ZhaoXJ, McElhaney-FeserGE, BowenWH, ColeMF, BroedelSEJr, et al. (1996) Requirement for the Candida albicans FAS2 gene for infection in a rat model of oropharyngeal candidiasis. Microbiology 142 (Pt 9) 2509–2514.
3. NguyenLN, TrofaD, NosanchukJD (2009) Fatty acid synthase impacts the pathobiology of Candida parapsilosis in vitro and during mammalian infection. PloS one 4: e8421.
4. ParikhSL, XiaoG, TongePJ (2000) Inhibition of InhA, the enoyl reductase from Mycobacterium tuberculosis, by triclosan and isoniazid. Biochemistry 39: 7645–7650.
5. WrightHT, ReynoldsKA (2007) Antibacterial targets in fatty acid biosynthesis. Curr Opin Microbiol 10: 447–453.
6. WangJ, SoissonSM, YoungK, ShoopW, KodaliS, et al. (2006) Platensimycin is a selective FabF inhibitor with potent antibiotic properties. Nature 441: 358–361.
7. PriceAC, ChoiKH, HeathRJ, LiZ, WhiteSW, et al. (2001) Inhibition of beta-ketoacyl-acyl carrier protein synthases by thiolactomycin and cerulenin. Structure and mechanism. J Biol Chem 276: 6551–6559.
8. BrinsterS, LamberetG, StaelsB, Trieu-CuotP, GrussA, et al. (2009) Type II fatty acid synthesis is not a suitable antibiotic target for Gram-positive pathogens. Nature 458: 83–86.
9. BalemansW, LounisN, GilissenR, GuillemontJ, SimmenK, et al. (2010) Essentiality of FASII pathway for Staphylococcus aureus. Nature 463: E3; discussion E4.
10. BlankenshipJR, HeitmanJ (2005) Calcineurin is required for Candida albicans to survive calcium stress in serum. Infect Immun 73: 5767–5774.
11. KingsburyJM, McCuskerJH (2010) Fungal homoserine kinase (thr1Delta) mutants are attenuated in virulence and die rapidly upon threonine starvation and serum incubation. Eukaryot Cell 9: 729–737.
12. NikawaH, NishimuraH, MakihiraS, HamadaT, SadamoriS, et al. (2000) Effect of serum concentration on Candida biofilm formation on acrylic surfaces. Mycoses 43: 139–143.
13. PaderuP, Garcia-EffronG, BalashovS, DelmasG, ParkS, et al. (2007) Serum differentially alters the antifungal properties of echinocandin drugs. Antimicrob Agents Chemother 51: 2253–2256.
14. OdabasiZ, PaetznickV, RexJH, Ostrosky-ZeichnerL (2007) Effects of serum on in vitro susceptibility testing of echinocandins. Antimicrob Agents Chemother 51: 4214–4216.
15. MakiK, MatsumotoS, WatabeE, IguchiY, TomishimaM, et al. (2008) Use of a serum-based antifungal susceptibility assay to predict the in vivo efficacy of novel echinocandin compounds. Microbiol Immunol 52: 383–391.
16. TrofaD, GacserA, NosanchukJD (2008) Candida parapsilosis, an emerging fungal pathogen. Clin Microbiol Rev 21: 606–625.
17. van AsbeckEC, ClemonsKV, StevensDA (2009) Candida parapsilosis: a review of its epidemiology, pathogenesis, clinical aspects, typing and antimicrobial susceptibility. Crit Rev Microbiol 35: 283–309.
18. NguyenLN, GacserA, NosanchukJD (2011) The stearoyl-coenzyme A desaturase 1 is essential for virulence and membrane stress in Candida parapsilosis through unsaturated fatty acid production. Infect Immun 79: 136–145.
19. GacserA, TrofaD, SchaferW, NosanchukJD (2007) Targeted gene deletion in Candida parapsilosis demonstrates the role of secreted lipase in virulence. J Clin Invest 117: 3049–3058.
20. GoldringES, GrossmanLI, KrupnickD, CryerDR, MarmurJ (1970) The petite mutation in yeast. Loss of mitochondrial deoxyribonucleic acid during induction of petites with ethidium bromide. J Mol Biol 52: 323–335.
21. RockenfellerP, RingJ, MuschettV, BeranekA, BuettnerS, et al. (2010) Fatty acids trigger mitochondrion-dependent necrosis. Cell cycle 9: 2836–2842.
22. GeraghtyP, KavanaghK (2003) Disruption of mitochondrial function in Candida albicans leads to reduced cellular ergosterol levels and elevated growth in the presence of amphotericin B. Arch Microbiol 179: 295–300.
23. MadeoF, FrohlichE, LigrM, GreyM, SigristSJ, et al. (1999) Oxygen stress: a regulator of apoptosis in yeast. J Cell Biol 145: 757–767.
24. PhillipsAJ, SudberyI, RamsdaleM (2003) Apoptosis induced by environmental stresses and amphotericin B in Candida albicans. Proc Natl Acad Sci U S A 100: 14327–14332.
25. LottTJ, KuykendallRJ, WelbelSF, PramanikA, LaskerBA (1993) Genomic heterogeneity in the yeast Candida parapsilosis. Curr Genet 23: 463–467.
26. KingsburyJM, McCuskerJH (2010) Homoserine toxicity in Saccharomyces cerevisiae and Candida albicans homoserine kinase (thr1Delta) mutants. Eukaryot Cell 9: 717–728.
27. HenrySA (1973) Death resulting from fatty acid starvation in yeast. J Bacteriol 116: 1293–1303.
28. MillardPJ, RothBL, ThiHP, YueST, HauglandRP (1997) Development of the FUN-1 family of fluorescent probes for vacuole labeling and viability testing of yeasts. Appl Environ Microbiol 63: 2897–2905.
29. HenrySA, AtkinsonKD, KolatAI, CulbertsonMR (1977) Growth and metabolism of inositol-starved Saccharomyces cerevisiae. J Bacteriol 130: 472–484.
30. BoerVM, AminiS, BotsteinD (2008) Influence of genotype and nutrition on survival and metabolism of starving yeast. Proc Natl Acad Sci U S A 105: 6930–6935.
31. PettiAA, CrutchfieldCA, RabinowitzJD, BotsteinD (2011) Survival of starving yeast is correlated with oxidative stress response and nonrespiratory mitochondrial function. Proc Natl Acad Sci U S A 108: E1089–1098.
32. VandenabeeleP, GalluzziL, Vanden BergheT, KroemerG (2010) Molecular mechanisms of necroptosis: an ordered cellular explosion. Nat Rev Mol Cell Biol 11: 700–714.
33. NguyenLN, NosanchukJD (2011) Lipid droplet formation protects against gluco/lipotoxicity in Candida parapsilosis: An essential role of fatty acid desaturase Ole1. Cell cycle 10: 3159–67.
34. BandyopadhyayS, ZhanR, WangY, PaiSK, HirotaS, et al. (2006) Mechanism of apoptosis induced by the inhibition of fatty acid synthase in breast cancer cells. Cancer Res 66: 5934–5940.
35. KunauWH, HartigA (1992) Peroxisome biogenesis in Saccharomyces cerevisiae. Antonie Van Leeuwenhoek 62: 63–78.
36. KuratCF, WolinskiH, PetschniggJ, KaluarachchiS, AndrewsB, et al. (2009) Cdk1/Cdc28-dependent activation of the major triacylglycerol lipase Tgl4 in yeast links lipolysis to cell-cycle progression. Mol Cell 33: 53–63.
37. RuckenstuhlC, Carmona-GutierrezD, MadeoF (2010) The sweet taste of death: glucose triggers apoptosis during yeast chronological aging. Aging 2: 643–649.
38. GranotD, LevineA, Dor-HefetzE (2003) Sugar-induced apoptosis in yeast cells. FEMS Yeast Res 4: 7–13.
39. WeinbergerM, MesquitaA, CarollT, MarksL, YangH, et al. (2010) Growth signaling promotes chronological aging in budding yeast by inducing superoxide anions that inhibit quiescence. Aging 2: 709–726.
40. LiuY, FiskumG, SchubertD (2002) Generation of reactive oxygen species by the mitochondrial electron transport chain. J Neurochem 80: 780–787.
41. ChenY, McMillan-WardE, KongJ, IsraelsSJ, GibsonSB (2007) Mitochondrial electron-transport-chain inhibitors of complexes I and II induce autophagic cell death mediated by reactive oxygen species. J Cell Sci 120: 4155–4166.
42. ParsonsJB, FrankMW, SubramanianC, SaenkhamP, RockCO (2011) Metabolic basis for the differential susceptibility of Gram-positive pathogens to fatty acid synthesis inhibitors. Proc Natl Acad Sci U S A 108: 15378–15383.
43. XuJ, SaundersCW, HuP, GrantRA, BoekhoutT, et al. (2007) Dandruff-associated Malassezia genomes reveal convergent and divergent virulence traits shared with plant and human fungal pathogens. Proc Natl Acad Sci U S A 104: 18730–18735.
44. DeAngelisYM, SaundersCW, JohnstoneKR, ReederNL, ColemanCG, et al. (2007) Isolation and expression of a Malassezia globosa lipase gene, LIP1. J Invest Dermatol 127: 2138–2146.
45. NguyenLN, GacserA, NosanchukJD (2011) Secreted lipases supply fatty acids for yeast growth in the absence of de novo fatty acid synthesis. Virulence 2: 538–41.
Štítky
Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
PLOS Pathogens
2012 Číslo 8
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Koronavirus hýbe světem: Víte jak se chránit a jak postupovat v případě podezření?
Najčítanejšie v tomto čísle
- Invariant NKT Cells: Regulation and Function during Viral Infection
- Host Defense and Tolerance: Unique Challenges in the Placenta
- Nonhuman Primate Models for HIV Cure Research
- Exon Level Transcriptomic Profiling of HIV-1-Infected CD4 T Cells Reveals Virus-Induced Genes and Host Environment Favorable for Viral Replication