#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Fluorescence Lifetime Imaging Unravels Metabolism and Its Crosstalk with the Host Cell


Chlamydia trachomatis is an obligate intracellular bacterium that alternates between two metabolically different developmental forms. We performed fluorescence lifetime imaging (FLIM) of the metabolic coenzymes, reduced nicotinamide adenine dinucleotides [NAD(P)H], by two-photon microscopy for separate analysis of host and pathogen metabolism during intracellular chlamydial infections. NAD(P)H autofluorescence was detected inside the chlamydial inclusion and showed enhanced signal intensity on the inclusion membrane as demonstrated by the co-localization with the 14-3-3β host cell protein. An increase of the fluorescence lifetime of protein-bound NAD(P)H [τ2-NAD(P)H] inside the chlamydial inclusion strongly correlated with enhanced metabolic activity of chlamydial reticulate bodies during the mid-phase of infection. Inhibition of host cell metabolism that resulted in aberrant intracellular chlamydial inclusion morphology completely abrogated the τ2-NAD(P)H increase inside the chlamydial inclusion. τ2-NAD(P)H also decreased inside chlamydial inclusions when the cells were treated with IFNγ reflecting the reduced metabolism of persistent chlamydiae. Furthermore, a significant increase in τ2-NAD(P)H and a decrease in the relative amount of free NAD(P)H inside the host cell nucleus indicated cellular starvation during intracellular chlamydial infection. Using FLIM analysis by two-photon microscopy we could visualize for the first time metabolic pathogen-host interactions during intracellular Chlamydia trachomatis infections with high spatial and temporal resolution in living cells. Our findings suggest that intracellular chlamydial metabolism is directly linked to cellular NAD(P)H signaling pathways that are involved in host cell survival and longevity.


Vyšlo v časopise: Fluorescence Lifetime Imaging Unravels Metabolism and Its Crosstalk with the Host Cell. PLoS Pathog 7(7): e32767. doi:10.1371/journal.ppat.1002108
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1002108

Souhrn

Chlamydia trachomatis is an obligate intracellular bacterium that alternates between two metabolically different developmental forms. We performed fluorescence lifetime imaging (FLIM) of the metabolic coenzymes, reduced nicotinamide adenine dinucleotides [NAD(P)H], by two-photon microscopy for separate analysis of host and pathogen metabolism during intracellular chlamydial infections. NAD(P)H autofluorescence was detected inside the chlamydial inclusion and showed enhanced signal intensity on the inclusion membrane as demonstrated by the co-localization with the 14-3-3β host cell protein. An increase of the fluorescence lifetime of protein-bound NAD(P)H [τ2-NAD(P)H] inside the chlamydial inclusion strongly correlated with enhanced metabolic activity of chlamydial reticulate bodies during the mid-phase of infection. Inhibition of host cell metabolism that resulted in aberrant intracellular chlamydial inclusion morphology completely abrogated the τ2-NAD(P)H increase inside the chlamydial inclusion. τ2-NAD(P)H also decreased inside chlamydial inclusions when the cells were treated with IFNγ reflecting the reduced metabolism of persistent chlamydiae. Furthermore, a significant increase in τ2-NAD(P)H and a decrease in the relative amount of free NAD(P)H inside the host cell nucleus indicated cellular starvation during intracellular chlamydial infection. Using FLIM analysis by two-photon microscopy we could visualize for the first time metabolic pathogen-host interactions during intracellular Chlamydia trachomatis infections with high spatial and temporal resolution in living cells. Our findings suggest that intracellular chlamydial metabolism is directly linked to cellular NAD(P)H signaling pathways that are involved in host cell survival and longevity.


Zdroje

1. ShawEIDooleyCAFischerERScidmoreMAFieldsKA 2000 Three temporal classes of gene expression during the Chlamydia trachomatis developmental cycle. Mol Microbiol 37 913 925

2. HatchTPAl-HossainyESilvermanJA 1982 Adenine nucleotide and lysine transport in Chlamydia psittaci. J Bacteriol 150 662 670

3. TrentmannOHornMvan ScheltingaACNeuhausHEHaferkampI 2007 Enlightening energy parasitism by analysis of an ATP/ADP transporter from chlamydiae. PLoS Biol 5 e231

4. StephensRSKalmanSLammelCFanJMaratheR 1998 Genome sequence of an obligate intracellular pathogen of humans: Chlamydia trachomatis. Science 282 754 759

5. Iliffe-LeeERMcClartyG 1999 Glucose metabolism in Chlamydia trachomatis: the ‘energy parasite’ hypothesis revisited. Mol Microbiol 33 177 187

6. BellandRJZhongGCraneDDHoganDSturdevantD 2003 Genomic transcriptional profiling of the developmental cycle of Chlamydia trachomatis. Proc Natl Acad Sci U S A 100 8478 8483

7. HaferkampISchmitz-EsserSLinkaNUrbanyCCollingroA 2004 A candidate NAD+ transporter in an intracellular bacterial symbiont related to Chlamydiae. Nature 432 622 625

8. HarperAPogsonCIPearceJH 2000 Amino acid transport into cultured McCoy cells infected with Chlamydia trachomatis. Infect Immun 68 5439 5442

9. HarperAPogsonCIJonesMLPearceJH 2000 Chlamydial development is adversely affected by minor changes in amino acid supply, blood plasma amino acid levels, and glucose deprivation. Infect Immun 68 1457 1464

10. GerardHCFreiseJWangZRobertsGRudyD 2002 Chlamydia trachomatis genes whose products are related to energy metabolism are expressed differentially in active vs. persistent infection. Microbes Infect 4 13 22

11. HaiderSWagnerMSchmidMCSixtBSChristianJG 2010 Raman microspectroscopy reveals long-term extracellular activity of chlamydiae. Mol Microbiol 77 687 700

12. OjciusDMDeganiHMispelterJDautry-VarsatA 1998 Enhancement of ATP levels and glucose metabolism during an infection by Chlamydia. NMR studies of living cells. J Biol Chem 273 7052 7058

13. YaraeiKCampbellLAZhuXLilesWCKuoCC 2005 Effect of Chlamydia pneumoniae on cellular ATP content in mouse macrophages: role of Toll-like receptor 2. Infect Immun 73 4323 4326

14. BirdDKYanLVrotsosKMEliceiriKWVaughanEM 2005 Metabolic mapping of MCF10A human breast cells via multiphoton fluorescence lifetime imaging of the coenzyme NADH. Cancer Res 65 8766 8773

15. SkalaMCRichingKMBirdDKGendron-FitzpatrickAEickhoffJ 2007 In vivo multiphoton fluorescence lifetime imaging of protein-bound and free nicotinamide adenine dinucleotide in normal and precancerous epithelia. J Biomed Opt 12 024014

16. SkalaMCRichingKMGendron-FitzpatrickAEickhoffJEliceiriKW 2007 In vivo multiphoton microscopy of NADH and FAD redox states, fluorescence lifetimes, and cellular morphology in precancerous epithelia. Proc Natl Acad Sci U S A 104 19494 19499

17. ChiaTHWilliamsonASpencerDDLeveneMJ 2008 Multiphoton fluorescence lifetime imaging of intrinsic fluorescence in human and rat brain tissue reveals spatially distinct NADH binding. Opt Express 16 4237 4249

18. HuangSHeikalAAWebbWW 2002 Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein. Biophys J 82 2811 2825

19. LiDZhengWQuJY 2008 Time-resolved spectroscopic imaging reveals the fundamentals of cellular NADH fluorescence. Opt Lett 33 2365 2367

20. LakowiczJRSzmacinskiHNowaczykKJohnsonML 1992 Fluorescence lifetime imaging of free and protein-bound NADH. Proc Natl Acad Sci U S A 89 1271 1275

21. PollakNDolleCZieglerM 2007 The power to reduce: pyridine nucleotides--small molecules with a multitude of functions. Biochem J 402 205 218

22. NiesnerRNarangPSpieckerHAndresenVGerickeKH 2008 Selective detection of NADPH oxidase in polymorphonuclear cells by means of NAD(P)H-based fluorescence lifetime imaging. J Biophys 2008 602639

23. ZhangQPistonDWGoodmanRH 2002 Regulation of corepressor function by nuclear NADH. Science 295 1895 1897

24. ZhangQWangSYFleurielCLeprinceDRocheleauJV 2007 Metabolic regulation of SIRT1 transcription via a HIC1:CtBP corepressor complex. Proc Natl Acad Sci U S A 104 829 833

25. LiDZhengWQuJY 2009 Two-photon autofluorescence microscopy of multicolor excitation. Opt Lett 34 202 204

26. ScidmoreMAHackstadtT 2001 Mammalian 14-3-3beta associates with the Chlamydia trachomatis inclusion membrane via its interaction with IncG. Mol Microbiol 39 1638 1650

27. BeattyWLByrneGIMorrisonRP 1993 Morphologic and antigenic characterization of interferon gamma-mediated persistent Chlamydia trachomatis infection in vitro. Proc Natl Acad Sci U S A 90 3998 4002

28. MatsumotoABesshoHUehiraKSudaT 1991 Morphological studies of the association of mitochondria with chlamydial inclusions and the fusion of chlamydial inclusions. J Electron Microsc (Tokyo) 40 356 363

29. HeinzenRAHackstadtT 1997 The Chlamydia trachomatis parasitophorous vacuolar membrane is not passively permeable to low-molecular-weight compounds. Infect Immun 65 1088 1094

30. WilsonDPWhittum-HudsonJATimmsPBavoilPM 2009 Kinematics of intracellular chlamydiae provide evidence for contact-dependent development. J Bacteriol 191 5734 5742

31. WilsonDPTimmsPMcElwainDLBavoilPM 2006 Type III secretion, contact-dependent model for the intracellular development of chlamydia. Bull Math Biol 68 161 178

32. WilsonDPethicaRZhouYTalbotCVogelC 2009 SUPERFAMILY--sophisticated comparative genomics, data mining, visualization and phylogeny. Nucleic Acids Res 37 D380 D386

33. RaoSTRossmannMG 1973 Comparison of super-secondary structures in proteins. J Mol Biol 76 241 256

34. RothAKonigPvanZGKlingerMHellwig-BurgelT 2010 Hypoxia abrogates antichlamydial properties of IFN-gamma in human fallopian tube cells in vitro and ex vivo. Proc Natl Acad Sci U S A 107 19502 19507

35. TaylorMWFengGS 1991 Relationship between interferon-gamma, indoleamine 2,3-dioxygenase, and tryptophan catabolism. FASEB J 5 2516 2522

36. BlinovaKCarrollSBoseSSmirnovAVHarveyJJ 2005 Distribution of mitochondrial NADH fluorescence lifetimes: steady-state kinetics of matrix NADH interactions. Biochemistry 44 2585 2594

37. GuarenteLPicardF 2005 Calorie restriction--the SIR2 connection. Cell 120 473 482

38. MichanSSinclairD 2007 Sirtuins in mammals: insights into their biological function. Biochem J 404 1 13

39. FjeldCCBirdsongWTGoodmanRH 2003 Differential binding of NAD+ and NADH allows the transcriptional corepressor carboxyl-terminal binding protein to serve as a metabolic sensor. Proc Natl Acad Sci U S A 100 9202 9207

40. YuQHeikalAA 2009 Two-photon autofluorescence dynamics imaging reveals sensitivity of intracellular NADH concentration and conformation to cell physiology at the single-cell level. J Photochem Photobiol B 95 46 57

41. VishwasraoHDHeikalAAKasischkeKAWebbWW 2005 Conformational dependence of intracellular NADH on metabolic state revealed by associated fluorescence anisotropy. J Biol Chem 280 25119 25126

42. EvansNDGnudiLRolinskiOJBirchDJPickupJC 2005 Glucose-dependent changes in NAD(P)H-related fluorescence lifetime of adipocytes and fibroblasts in vitro: potential for non-invasive glucose sensing in diabetes mellitus. J Photochem Photobiol B 80 122 129

43. WagnieresGAStarWMWilsonBC 1998 In vivo fluorescence spectroscopy and imaging for oncological applications. Photochem Photobiol 68 603 632

44. BrunnerEDomhofSLangerF 2002 Nonparametric analysis of longitudinal data in factorial experiments. New York Wiley

Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

Článok vyšiel v časopise

PLOS Pathogens


2011 Číslo 7
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Aktuální možnosti diagnostiky a léčby litiáz
nový kurz
Autori: MUDr. Tomáš Ürge, PhD.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#