Caloric restriction restores the chronological life span of the goa1 null mutant of Candida albicans in spite of high cell levels of ROS

Fungal Genetics and Biology

Volumn 49, Issue 12, 2012, Pages 1023-1032

  Chen, Hui ^a,b   Calderone, Richard ^a   Sun, Nuo ^a   Wang, Yun ^a,c   Li, Dongmei ^a  

^a GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

^b HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^c SHANTOU UNIVERSITY MEDICAL COLLEGE   (China)

Author keywords

Caloric restriction; Candida; Chronological aging; Microarray; Mitochondria; ROS

Indexed keywords

ADENOSINE TRIPHOSPHATE; COPPER ZINC SUPEROXIDE DISMUTASE; GLUCOSE; GLUTATHIONE PEROXIDASE 1; REACTIVE OXYGEN METABOLITE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE;

ANTIOXIDANT ACTIVITY; ARTICLE; BIOGENESIS; CALORIC RESTRICTION; CANDIDA ALBICANS; CARBON UTILIZATION; CHRONOLOGY; CONTROLLED STUDY; DISORDERS OF PEROXISOMAL FUNCTIONS; ENZYME ACTIVITY; FATTY ACID OXIDATION; FUNGAL GENE; FUNGAL STRAIN; FUNGAL VIABILITY; FUNGUS GROWTH; GENE EXPRESSION PROFILING; GOA31 GENE; LIFESPAN; LIPID PEROXIDATION; MICROARRAY ANALYSIS; MITOCHONDRIAL MEMBRANE POTENTIAL; NONHUMAN; NUCLEIC ACID SYNTHESIS; PRIORITY JOURNAL; RADICAL REACTION; RESPIRATORY CHAIN; SACCHAROMYCES CEREVISIAE; TRANSCRIPTION REGULATION; TRANSLATION REGULATION; UPREGULATION;

CALORIC RESTRICTION; CANDIDA ALBICANS; CULTURE MEDIA; FUNGAL PROTEINS; GENE EXPRESSION PROFILING; GLUCOSE; LIPID PEROXIDATION; LONGEVITY; MICROARRAY ANALYSIS; MITOCHONDRIAL PROTEINS; REACTIVE OXYGEN SPECIES;

CANDIDA; CANDIDA ALBICANS;

EID: 84869886429     PISSN: 10871845     EISSN: 10960937     Source Type: Journal    
DOI: 10.1016/j.fgb.2012.09.007     Document Type: Article

References (43)

1. Alex D., Li D. Back to the future: Candida mitochondria and energetic. Candida and Candidiasis 2011, 331-341. ASM Press Inc., Washington, DC. R. Calderone, C. Clancy (Eds.).
2. Bambach A., Fernandes M.P., Ghosh A., Kruppa M., Alex D., Li D., Fonzi W.A., Chauhan N., Sun N., Agrellos O.A., Vercesi A.E., Rolfes R.J., Calderone R. Goa1p of Candida albicans localizes to the mitochondria during stress and is required for mitochondrial function and virulence. Eukaryot. Cell 2009, 8:1706-1720.
3. Barrientos A. In vivo and in organello assessment of OXPHOS activities. Methods 2002, 26:307-316.
4. Bhushan D., Pandey A., Choudhary M.K., Datta A., Chakraborty S., Chakraborty N. Comparative proteomics analysis of differentially expressed proteins in chickpea extracellular matrix during dehydration stress. Mol. Cell Proteom. 2007, 6:1868-1884.
5. Bruss M.D., Khambatta C.F., Ruby M.A., Aggarwal A., Hellerstein M.K. Calorie restriction increases fatty acid synthesis and whole body fat oxidation rates. Am. J. Physiol. Endocrinol. Metab. 2010, 298:E108-116.
6. Cavalheiro R.A., Fortes F., Borecky J., Faustinoni V.C., Schreiber A.Z., Vercesi A.E. Respiration, oxidative phosphorylation, and uncoupling protein in Candida albicans. Braz. J. Med. Biol. Res. 2004, 37:1455-1461.
7. Choi J.S., Choi K.M., Lee C.K. Caloric restriction improves efficiency and capacity of the mitochondrial electron transport chain in Saccharomyces cerevisiae. Biochem. Biophys. Res. Commun. 2011, 409:308-314.
8. del Rio L.A., Corpas F.J., Sandalio L.M., Palma J.M., Barroso J.B. Plant peroxisomes, reactive oxygen metabolism and nitric oxide. IUBMB Life 2003, 55:71-81.
9. Favre C., Aguilar P.S., Carrillo M.C. Oxidative stress and chronological aging in glycogen-phosphorylase-deleted yeast. Free Radic. Biol. Med. 2008, 45:1446-1456.
10. Fleury C., Mignotte B., Vayssiere J.L. Mitochondrial reactive oxygen species in cell death signaling. Biochimie 2002, 84:131-141.
11. Fu X.H., Meng F.L., Hu Y., Zhou J.Q. Candida albicans, a distinctive fungal model for cellular aging study. Aging Cell 2008, 7:746-757.
12. Gohil V.M., Sheth S.A., Nilsson R., Wojtovich A.P., Lee J.H., Perocchi F., Chen W., Clish C.B., Ayata C., Brookes P.S., Mootha V.K. Nutrient-sensitized screening for drugs that shift energy metabolism from mitochondrial respiration to glycolysis. Nat. Biotechnol. 2010, 28:249-255.
13. Goth L. A simple method for determination of serum catalase activity and revision of reference range. Clin. Chim. Acta. 1991, 196:143-151.
14. Ingavale S.S., Chang Y.C., Lee H., McClelland C.M., Leong M.L., Kwon-Chung K.J. Importance of mitochondria in survival of Cryptococcus neoformans under low oxygen conditions and tolerance to cobalt chloride. PLoS Pathog. 2008, 4:e1000155.
15. Jethwaney D., Hofer M., Khaware R.K., Prasad R. Functional reconstitution of a purified proline permease from Candida albicans: interaction with the antifungal cispentacin. Microbiology 1997, 143(Pt 2):397-404.
16. Jollow D.J., Mitchell J.R., Zampaglione N., Gillette J.R. Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacology 1974, 11:151-169.
17. Joseph-Horne T., Hollomon D.W., Wood P.M. Fungal respiration: a fusion of standard and alternative components. Biochim. Biophys. Acta 2001, 1504:179-195.
18. Khan A., Ahmad A., Akhtar F., Yousuf S., Xess I., Khan L.A., Manzoor N. Induction of oxidative stress as a possible mechanism of the antifungal action of three phenylpropanoids. FEMS Yeast Res. 2011, 11:114-122.
19. Lazarou M., Thorburn D.R., Ryan M.T., McKenzie M. Assembly of mitochondrial complex I and defects in disease. Biochim. Biophys. Acta 2009, 1793:78-88.
20. Li D., Chen H., Florentino A., Alex D., Sikorski P., Fonzi W.A., Calderone R. Enzymatic dysfunction of mitochondrial complex I of the Candida albicans goa1 mutant is associated with increased reactive oxidants and cell death. Eukaryot. Cell 2011, 10:672-682.
21. Lorenz M.C., Bender J.A., Fink G.R. Transcriptional response of Candida albicans upon internalization by macrophages. Eukaryot. Cell 2004, 3:1076-1087.
22. Ludovico P., Rodrigues F., Almeida A., Silva M.T., Barrientos A., Corte-Real M. Cytochrome c release and mitochondria involvement in programmed cell death induced by acetic acid in Saccharomyces cerevisiae. Mol. Biol. Cell 2002, 13:2598-2606.
23. Maeda I., Delessert S., Hasegawa S., Seto Y., Zuber S., Poirier Y. The peroxisomal Acyl-CoA thioesterase Pte1p from Saccharomyces cerevisiae is required for efficient degradation of short straight chain and branched chain fatty acids. J. Biol. Chem. 2006, 281:11729-11735.
24. Marklund S., Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur. J. Biochem. 1974, 47:469-474.
25. Martins Vde.P., Dinamarco T.M., Curti C., Uyemura S.A. Classical and alternative components of the mitochondrial respiratory chain in pathogenic fungi as potential therapeutic targets. J. Bioenerg. Biomembr. 2011, 43:81-88.
26. Moore C.M., Hoey E.M., Trudgett A., Timson D.J. Artemisinins act through at least two targets in a yeast model. FEMS Yeast Res. 2011, 11:233-237.
27. Moreira P.I., Oliveira C.R. Mitochondria as potential targets in antidiabetic therapy. Handbook Exp. Pharmacol. 2011, 203:331-356.
28. Nandita S.P.J. Catalase activity assays. In Current protocols in toxicology 2006, John Wiley & Sons Inc., pp. 7.7.1-7.7.16.
29. Okamoto K., Shaw J.M. Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes. Annu. Rev. Genet. 2005, 39:503-536.
30. Osiewacz H.D., Scheckhuber C.Q. Impact of ROS on ageing of two fungal model systems: Saccharomyces cerevisiae and Podospora anserina. Free Radic. Res. 2006, 40:1350-1358.
31. Osorio N.S., Carvalho A., Almeida A.J., Padilla-Lopez S., Leao C., Laranjinha J., Ludovico P., Pearce D.A., Rodrigues F. Nitric oxide signaling is disrupted in the yeast model for Batten disease. Mol. Biol. Cell. 2007, 18:2755-2767.
32. Pan Y. Mitochondria, reactive oxygen species, and chronological aging: a message from yeast. Exp. Gerontol. 2011, 46:847-852.
33. Ripcke J., Zarse K., Ristow M., Birringer M. Small-molecule targeting of the mitochondrial compartment with an endogenously cleaved reversible tag. Chembiochem 2009, 10:1689-1696.
34. Ryu J.H., Lee Y., Han S.K., Kim H.Y. The role of hydrogen peroxide produced by polychlorinated biphenyls in PMR1-deficient yeast cells. J. Biochem. 2003, 134:137-142.
35. Simon R., Lam A., Li M.C., Ngan M., Menenzes S., Zhao Y. Analysis of gene expression data using BRB-ArrayTools. Cancer Inform. 2007, 3:11-17.
36. Skinner C., Lin S.J. Effects of calorie restriction on life span of microorganisms. Appl. Microbiol. Biotechnol. 2010, 88:817-828.
37. Speijer D. Oxygen radicals shaping evolution: why fatty acid catabolism leads to peroxisomes while neurons do without it: FADH(2)/NADH flux ratios determining mitochondrial radical formation were crucial for the eukaryotic invention of peroxisomes and catabolic tissue differentiation. Bioessays 2011, 33:88-94.
38. Steels E.L., Learmonth R.P., Watson K. Stress tolerance and membrane lipid unsaturation in Saccharomyces cerevisiae grown aerobically or anaerobically. Microbiology 1994, 140(Pt 3):569-576.
39. Strijbis K., Distel B. Intracellular acetyl unit transport in fungal carbon metabolism. Eukaryot. Cell 2010, 9:1809-1815.
40. Trancikova A., Weisova P., Kissova I., Zeman I., Kolarov J. Production of reactive oxygen species and loss of viability in yeast mitochondrial mutants: protective effect of Bcl-xL. FEMS Yeast Res. 2004, 5:149-156.
41. Tusher V.G., Tibshirani R., Chu G. Significance analysis of microarrays applied to the ionizing radiation response. Proc. Natl. Acad. Sci. USA 2001, 98:5116-5121.
42. van Roermund C.W., Hettema E.H., Kal A.J., van den Berg M., Tabak H.F., Wanders R.J. Peroxisomal beta-oxidation of polyunsaturated fatty acids in Saccharomyces cerevisiae: isocitrate dehydrogenase provides NADPH for reduction of double bonds at even positions. EMBO J. 1998, 17:677-687.
43. Wright G.W., Simon R.M. A random variance model for detection of differential gene expression in small microarray experiments. Bioinformatics 2003, 19:2448-2455.