#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Intracellular Vesicle Acidification Promotes Maturation of Infectious Poliovirus Particles


The autophagic pathway acts as part of the immune response against a variety of pathogens. However, several pathogens subvert autophagic signaling to promote their own replication. In many cases it has been demonstrated that these pathogens inhibit or delay the degradative aspect of autophagy. Here, using poliovirus as a model virus, we report for the first time bona fide autophagic degradation occurring during infection with a virus whose replication is promoted by autophagy. We found that this degradation is not required to promote poliovirus replication. However, vesicular acidification, which in the case of autophagy precedes delivery of cargo to lysosomes, is required for normal levels of virus production. We show that blocking autophagosome formation inhibits viral RNA synthesis and subsequent steps in the virus cycle, while inhibiting vesicle acidification only inhibits the final maturation cleavage of virus particles. We suggest that particle assembly, genome encapsidation, and virion maturation may occur in a cellular compartment, and we propose the acidic mature autophagosome as a candidate vesicle. We discuss the implications of our findings in understanding the late stages of poliovirus replication, including the formation and maturation of virions and egress of infectious virus from cells.


Vyšlo v časopise: Intracellular Vesicle Acidification Promotes Maturation of Infectious Poliovirus Particles. PLoS Pathog 8(11): e32767. doi:10.1371/journal.ppat.1003046
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003046

Souhrn

The autophagic pathway acts as part of the immune response against a variety of pathogens. However, several pathogens subvert autophagic signaling to promote their own replication. In many cases it has been demonstrated that these pathogens inhibit or delay the degradative aspect of autophagy. Here, using poliovirus as a model virus, we report for the first time bona fide autophagic degradation occurring during infection with a virus whose replication is promoted by autophagy. We found that this degradation is not required to promote poliovirus replication. However, vesicular acidification, which in the case of autophagy precedes delivery of cargo to lysosomes, is required for normal levels of virus production. We show that blocking autophagosome formation inhibits viral RNA synthesis and subsequent steps in the virus cycle, while inhibiting vesicle acidification only inhibits the final maturation cleavage of virus particles. We suggest that particle assembly, genome encapsidation, and virion maturation may occur in a cellular compartment, and we propose the acidic mature autophagosome as a candidate vesicle. We discuss the implications of our findings in understanding the late stages of poliovirus replication, including the formation and maturation of virions and egress of infectious virus from cells.


Zdroje

1. WhittonJL, CornellCT, FeuerR (2005) Host and virus determinants of picornavirus pathogenesis and tropism. Nat Rev Microbiol 3(10) 765–776.

2. DalesS, EggersHJ, TammI, PaladeGE (1965) Electron microscopic study of the formation of poliovirus. Virology 26: 379–389.

3. SchlegelA, GiddingsTHJr, LadinskyMS, KirkegaardK (1996) Cellular origin and ultrastructure of membranes induced during poliovirus infection. J Virol 70(10) 6576–6588.

4. TanidaI (2011) Autophagy basics. Microbiol Immunol 55(1) 1–11.

5. MizushimaN (2007) Autophagy: Process and function. Genes Dev 21(22) 2861–2873.

6. TanidaI (2011) Autophagosome formation and molecular mechanism of autophagy. Antioxid Redox Signal 14: 2201–14.

7. XieZ, KlionskyDJ (2007) Autophagosome formation: Core machinery and adaptations. Nat Cell Biol 9(10) 1102–1109.

8. MousaviSA, KjekenR, BergTO, SeglenPO, BergT, et al. (2001) Effects of inhibitors of the vacuolar proton pump on hepatic heterophagy and autophagy. Biochim Biophys Acta 1510 (1–2) 243–257.

9. EskelinenEL (2005) Maturation of autophagic vacuoles in mammalian cells. Autophagy 1(1) 1–10.

10. IshikawaT, FurunoK, KatoK (1983) Ultrastructural studies on autolysosomes in rat hepatocytes after leupeptin treatment. Exp Cell Res 144(1) 15–24.

11. DunnWAJr (1990) Studies on the mechanisms of autophagy: Formation of the autophagic vacuole. J Cell Biol 110(6) 1923–1933.

12. JacksonWT, GiddingsTHJr, TaylorMP, MulinyaweS, RabinovitchM, et al. (2005) Subversion of cellular autophagosomal machinery by RNA viruses. PLoS Biol 3(5) e156.

13. Taylor MP. (2007) Utilization of autophagy protein LC3 during poliovirus infection [PhD dissertation]. Palo Alto (California): Stanford University Medical Center, Stanford University.

14. NiemannA, BaltesJ, ElsasserHP (2001) Fluorescence properties and staining behavior of monodansylpentane, a structural homologue of the lysosomotropic agent monodansylcadaverine. Journal of Histochemistry & Cytochemistry 49(2) 177–185.

15. SuhyDA, GiddingsTHJr, KirkegaardK (2000) Remodeling the endoplasmic reticulum by poliovirus infection and by individual viral proteins: An autophagy-like origin for virus-induced vesicles. J Virol 74(19) 8953–8965.

16. YangZ, KlionskyDJ (2010) Mammalian autophagy: Core molecular machinery and signaling regulation. Curr Opin Cell Biol 22(2) 124–131.

17. RoteKV, RechsteinerM (1983) Degradation of microinjected proteins: Effects of lysosomotropic agents and inhibitors of autophagy. J Cell Physiol 116(1) 103–110.

18. KawaiA, UchiyamaH, TakanoS, NakamuraN, OhkumaS (2007) Autophagosome-lysosome fusion depends on the pH in acidic compartments in CHO cells. Autophagy 3(2) 154–157.

19. BergTO, FengsrudM, StromhaugPE, BergT, SeglenPO (1998) Isolation and characterization of rat liver amphisomes. evidence for fusion of autophagosomes with both early and late endosomes. J Biol Chem 273(34) 21883–21892.

20. KemballCC, HarkinsS, WhitmireJK, FlynnCT, FeuerR, et al. (2009) Coxsackievirus B3 inhibits antigen presentation in vivo, exerting a profound and selective effect on the MHC class I pathway. PLoS Pathog 5(10) e1000618.

21. WongJ, ZhangJ, SiX, GaoG, MaoI, et al. (2008) Autophagosome supports coxsackievirus B3 replication in host cells. J Virol 82(18) 9143–9153.

22. FortierA, de ChastellierC, BalorS, GrosP (2007) Birc1e/Naip5 rapidly antagonizes modulation of phagosome maturation by legionella pneumophila. Cell Microbiol 9(4) 910–923.

23. JoshiAD, SwansonMS (2011) Secrets of a successful pathogen: Legionella resistance to progression along the autophagic pathway. Front Microbiol 2: 138.

24. SwansonMS, Fernandez-MoreiraE (2002) A microbial strategy to multiply in macrophages: The pregnant pause. Traffic 3(3) 170–177.

25. WelschS, MillerS, Romero-BreyI, MerzA, BleckCK, et al. (2009) Composition and three-dimensional architecture of the dengue virus replication and assembly sites. Cell Host Microbe 5(4) 365–375.

26. HeatonNS, RandallG (2010) Dengue virus-induced autophagy regulates lipid metabolism. Cell Host Microbe 8(5) 422–432.

27. BayerN, SchoberD, PrchlaE, MurphyRF, BlaasD, et al. (1998) Effect of bafilomycin A1 and nocodazole on endocytic transport in HeLa cells: Implications for viral uncoating and infection. J Virol 72(12) 9645–9655.

28. HeleniusA, MarshM, WhiteJ (1982) Inhibition of semliki forest virus penetration by lysosomotropic weak bases. J Gen Virol 58 Pt 1: 47–61.

29. PerezL, CarrascoL (1993) Entry of poliovirus into cells does not require a low-pH step. J Virol 67(8) 4543–4548.

30. RacanielloVR, BaltimoreD (1981) Cloned poliovirus complementary DNA is infectious in mammalian cells. Science 214(4523) 916–919.

31. MaynellLA, KirkegaardK, KlymkowskyMW (1992) Inhibition of poliovirus RNA synthesis by brefeldin A. J Virol 66(4) 1985–1994.

32. TaylorMP, KirkegaardK (2007) Modification of cellular autophagy protein LC3 by poliovirus. J Virol 81(22) 12543–12553.

33. SwansonMS, IsbergRR (1996) Analysis of the intracellular fate of legionella pneumophila mutants. Ann N Y Acad Sci 797: 8–18.

34. KemballCC, AlirezaeiM, FlynnCT, WoodMR, HarkinsS, et al. (2010) Coxsackievirus infection induces autophagy-like vesicles and megaphagosomes in pancreatic acinar cells in vivo. J Virol 84(23) 12110–12124.

35. SantanaS, BullidoMJ, RecueroM, ValdiviesoF, AldudoJ (2012) Herpes simplex virus type I induces an incomplete autophagic response in human neuroblastoma cells. J Alzheimers Dis 30: 815–31.

36. PankivS, ClausenTH, LamarkT, BrechA, BruunJA, et al. (2007) p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy. J Biol Chem 282(33) 24131–24145.

37. BjorkoyG, LamarkT, BrechA, OutzenH, PeranderM, et al. (2005) p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death. J Cell Biol 171(4) 603–614.

38. TanidaI, Minematsu-IkeguchiN, UenoT, KominamiE (2005) Lysosomal turnover, but not a cellular level, of endogenous LC3 is a marker for autophagy. Autophagy 1(2) 84–91.

39. SeglenPO, GordonPB (1982) 3-methyladenine: Specific inhibitor of autophagic/lysosomal protein degradation in isolated rat hepatocytes. Proc Natl Acad Sci U S A 79(6) 1889–1892.

40. SchnellmannRG, WilliamsSW (1998) Proteases in renal cell death: Calpains mediate cell death produced by diverse toxicants. Ren Fail 20(5) 679–686.

41. KabeyaY, MizushimaN, UenoT, YamamotoA, KirisakoT, et al. (2000) LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing. EMBO J 19(21) 5720–5728.

42. KirisakoT, IchimuraY, OkadaH, KabeyaY, MizushimaN, et al. (2000) The reversible modification regulates the membrane-binding state of Apg8/Aut7 essential for autophagy and the cytoplasm to vacuole targeting pathway. J Cell Biol 151(2) 263–276.

43. TakeshigeK, BabaM, TsuboiS, NodaT, OhsumiY (1992) Autophagy in yeast demonstrated with proteinase-deficient mutants and conditions for its induction. J Cell Biol 119(2) 301–311.

44. BarrettAJ (1979) Cathepsin D: The lysosomal aspartic proteinase. Ciba Found Symp (75) 37–50.

45. OhkumaS, PooleB (1981) Cytoplasmic vacuolation of mouse peritoneal macrophages and the uptake into lysosomes of weakly basic substances. J Cell Biol 90(3) 656–664.

46. PooleB, OhkumaS (1981) Effect of weak bases on the intralysosomal pH in mouse peritoneal macrophages. J Cell Biol 90(3) 665–669.

47. BienzK, EggerD, RasserY, BossartW (1980) Kinetics and location of poliovirus macromolecular synthesis in correlation to virus-induced cytopathology. Virology 100(2) 390–399.

48. DroseS, AltendorfK (1997) Bafilomycins and concanamycins as inhibitors of V-ATPases and P-ATPases. J Exp Biol 200(Pt 1) 1–8.

49. RoseJK, TrachselH, LeongK, BaltimoreD (1978) Inhibition of translation by poliovirus: Inactivation of a specific initiation factor. Proc Natl Acad Sci U S A 75(6) 2732–2736.

50. GradiA, SvitkinYV, ImatakaH, SonenbergN (1998) Proteolysis of human eukaryotic translation initiation factor eIF4GII, but not eIF4GI, coincides with the shutoff of host protein synthesis after poliovirus infection. Proc Natl Acad Sci U S A 95(19) 11089–11094.

51. CaliguiriLA, TammI (1968) Action of guanidine on the replication of poliovirus RNA. Virology 35(3) 408–417.

52. PawankarR, LeeKH, NonakaM, TakizawaR (2007) Role of mast cells and basophils in chronic rhinosinusitis. Clin Allergy Immunol 20: 93–101.

53. PalmenbergAC (1982) In vitro synthesis and assembly of picornaviral capsid intermediate structures. J Virol 44(3) 900–906.

54. PfisterT, EggerD, BienzK (1995) Poliovirus subviral particles associated with progeny RNA in the replication complex. J Gen Virol 76 (Pt 1)(Pt 1) 63–71.

55. HindiyehM, LiQH, BasavappaR, HogleJM, ChowM (1999) Poliovirus mutants at histidine 195 of VP2 do not cleave VP0 into VP2 and VP4. J Virol 73(11) 9072–9079.

56. ComptonSR, NelsenB, KirkegaardK (1990) Temperature-sensitive poliovirus mutant fails to cleave VP0 and accumulates provirions. J Virol 64(9) 4067–4075.

57. NugentCI, KirkegaardK (1995) RNA binding properties of poliovirus subviral particles. J Virol 69(1) 13–22.

58. Fernandez-TomasCB, BaltimoreD (1973) Morphogenesis of poliovirus. II. demonstration of a new intermediate, the proviron. J Virol 12(5) 1122–1130.

59. GuttmanN, BaltimoreD (1977) Morphogenesis of poliovirus. IV. existence of particles sedimenting at 150S and having the properties of provirion. J Virol 23(2) 363–367.

60. AmerAO, SwansonMS (2005) Autophagy is an immediate macrophage response to legionella pneumophila. Cell Microbiol 7(6) 765–778.

61. BelovGA, Altan-BonnetN, KovtunovychG, JacksonCL, Lippincott-SchwartzJ, et al. (2007) Hijacking components of the cellular secretory pathway for replication of poliovirus RNA. J Virol 81(2) 558–567.

62. RustRC, LandmannL, GosertR, TangBL, HongW, et al. (2001) Cellular COPII proteins are involved in production of the vesicles that form the poliovirus replication complex. J Virol 75(20) 9808–9818.

63. HsuNY, IlnytskaO, BelovG, SantianaM, ChenYH, et al. (2010) Viral reorganization of the secretory pathway generates distinct organelles for RNA replication. Cell 141(5) 799–811.

64. BelovGA, NairV, HansenBT, HoytFH, FischerER, et al. (2012) Complex dynamic development of poliovirus membranous replication complexes. J Virol 86(1) 302–312.

65. GengJ, KlionskyDJ (2010) The golgi as a potential membrane source for autophagy. Autophagy 6(7) 950–951.

66. ReggioriF, WangCW, NairU, ShintaniT, AbeliovichH, et al. (2004) Early stages of the secretory pathway, but not endosomes, are required for cvt vesicle and autophagosome assembly in saccharomyces cerevisiae. Mol Biol Cell 15(5) 2189–2204.

67. HolseyC, NairCN (1993) Poliovirus-induced intracellular alkalinization involves a proton ATPase and protein phosphorylation. J Cell Physiol 155(3) 606–614.

68. SchwerdtCE, FoghJ (1957) The ratio of physical particles per infectious unit observed for poliomyelitis viruses. Virology 4(1) 41–52.

69. Racaniello VR. (2007) Picornaviridae; the viruses and their replication. In: Fields' Virology. Fields BN, Knipe DM, Howley PM, editors. Philadelphia: Lippincott Williams & Wilkins. pp. 795–838.

70. Krejbich-TrototP, GayB, Li-Pat-YuenG, HoarauJJ, Jaffar-BandjeeMC, et al. (2011) Chikungunya triggers an autophagic process which promotes viral replication. Virol J 8: 432.

71. DiazA, WangX, AhlquistP (2010) Membrane-shaping host reticulon proteins play crucial roles in viral RNA replication compartment formation and function. Proc Natl Acad Sci U S A 107(37) 16291–16296.

72. GuskeyLE, SmithPC, WolffDA (1970) Patterns of cytopathology and lysosomal enzyme release in poliovirus-infected HEp-2 cells treated with either 2-(alpha-hydroxybenzyl)-benzimidazole or guanidine HCl. J Gen Virol 6(1) 151–161.

73. BablanianR, EggersHJ, TammI (1965) Studies on the mechanism of poliovirus-induced cell damage. ii. the relation between poliovirus growth and virus-induced morphological changes in cells. Virology 26: 114–121.

74. FlanaganJF (1966) Hydrolytic enzymes in KB cells infected with poliovirus and herpes simplex virus. J Bacteriol 91(2) 789–797.

75. TaylorMP, BurgonTB, KirkegaardK, JacksonWT (2009) Role of microtubules in extracellular release of poliovirus. J Virol 83: 6599–6609.

76. EggerD, TeterinaN, EhrenfeldE, BienzK (2000) Formation of the poliovirus replication complex requires coupled viral translation, vesicle production, and viral RNA synthesis. J Virol 74(14) 6570–6580.

77. DuranJM, AnjardC, StefanC, LoomisWF, MalhotraV (2010) Unconventional secretion of Acb1 is mediated by autophagosomes. J Cell Biol 188(4) 527–536.

78. ManjithayaR, AnjardC, LoomisWF, SubramaniS (2010) Unconventional secretion of pichia pastoris Acb1 is dependent on GRASP protein, peroxisomal functions, and autophagosome formation. J Cell Biol 188(4) 537–546.

79. KirkegaardK, JacksonWT (2005) Topology of double-membraned vesicles and the opportunity for non-lytic release of cytoplasm. Autophagy 1(3) 182–184.

80. BrunsC, McCafferyJM, CurwinAJ, DuranJM, MalhotraV (2011) Biogenesis of a novel compartment for autophagosome-mediated unconventional protein secretion. J Cell Biol 195(6) 979–992.

Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

Článok vyšiel v časopise

PLOS Pathogens


2012 Číslo 11
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

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#