#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Involvement of the Cellular Phosphatase DUSP1 in Vaccinia Virus Infection


Poxviruses encode a large variety of proteins that mimic, block or enhance host cell signaling pathways on their own benefit. It has been reported that mitogen-activated protein kinases (MAPKs) are specifically upregulated during vaccinia virus (VACV) infection. Here, we have evaluated the role of the MAPK negative regulator dual specificity phosphatase 1 (DUSP1) in the infection of VACV. We demonstrated that DUSP1 expression is enhanced upon infection with the replicative WR virus and with the attenuated VACV viruses MVA and NYVAC. This upregulation is dependent on early viral gene expression. In the absence of DUSP1 in cultured cells, there is an increased activation of its molecular targets JNK and ERK and an enhanced WR replication. Moreover, DUSP1 knock-out (KO) mice are more susceptible to WR infection as a result of enhanced virus replication in the lungs. Significantly, MVA, which is known to produce non-permissive infections in most mammalian cell lines, is able to grow in DUSP1 KO immortalized murine embryo fibroblasts (MEFs). By confocal and electron microscopy assays, we showed that in the absence of DUSP1 MVA morphogenesis is similar as in permissive cell lines and demonstrated that DUSP1 is involved at the stage of transition between IVN and MV in VACV morphogenesis. In addition, we have observed that the secretion of pro-inflammatory cytokines at early times post-infection in KO mice infected with MVA and NYVAC is increased and that the adaptive immune response is enhanced in comparison with WT-infected mice. Altogether, these findings reveal that DUSP1 is involved in the replication and host range of VACV and in the regulation of host immune responses through the modulation of MAPKs. Thus, in this study we demonstrate that DUSP1 is actively involved in the antiviral host defense mechanism against a poxvirus infection.


Vyšlo v časopise: Involvement of the Cellular Phosphatase DUSP1 in Vaccinia Virus Infection. PLoS Pathog 9(11): e32767. doi:10.1371/journal.ppat.1003719
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003719

Souhrn

Poxviruses encode a large variety of proteins that mimic, block or enhance host cell signaling pathways on their own benefit. It has been reported that mitogen-activated protein kinases (MAPKs) are specifically upregulated during vaccinia virus (VACV) infection. Here, we have evaluated the role of the MAPK negative regulator dual specificity phosphatase 1 (DUSP1) in the infection of VACV. We demonstrated that DUSP1 expression is enhanced upon infection with the replicative WR virus and with the attenuated VACV viruses MVA and NYVAC. This upregulation is dependent on early viral gene expression. In the absence of DUSP1 in cultured cells, there is an increased activation of its molecular targets JNK and ERK and an enhanced WR replication. Moreover, DUSP1 knock-out (KO) mice are more susceptible to WR infection as a result of enhanced virus replication in the lungs. Significantly, MVA, which is known to produce non-permissive infections in most mammalian cell lines, is able to grow in DUSP1 KO immortalized murine embryo fibroblasts (MEFs). By confocal and electron microscopy assays, we showed that in the absence of DUSP1 MVA morphogenesis is similar as in permissive cell lines and demonstrated that DUSP1 is involved at the stage of transition between IVN and MV in VACV morphogenesis. In addition, we have observed that the secretion of pro-inflammatory cytokines at early times post-infection in KO mice infected with MVA and NYVAC is increased and that the adaptive immune response is enhanced in comparison with WT-infected mice. Altogether, these findings reveal that DUSP1 is involved in the replication and host range of VACV and in the regulation of host immune responses through the modulation of MAPKs. Thus, in this study we demonstrate that DUSP1 is actively involved in the antiviral host defense mechanism against a poxvirus infection.


Zdroje

1. TaylorJM, QuiltyD, BanadygaL, BarryM (2006) The vaccinia virus protein F1L interacts with Bim and inhibits activation of the pro-apoptotic protein Bax. J Biol Chem 281: 39728–39739.

2. HouW, GibbsJS, LuX, BrookeCB, RoyD, et al. (2012) Viral infection triggers rapid differentiation of human blood monocytes into dendritic cells. Blood 119: 3128–3131.

3. SutterG, Ramsey-EwingA, RosalesR, MossB (1994) Stable expression of the vaccinia virus K1L gene in rabbit cells complements the host range defect of a vaccinia virus mutant. J Virol 68: 4109–4116.

4. BeattieE, KauffmanEB, MartinezH, PerkusME, JacobsBL, et al. (1996) Host-range restriction of vaccinia virus E3L-specific deletion mutants. Virus Genes 12: 89–94.

5. Garcia-ArriazaJ, NajeraJL, GomezCE, TewabeN, SorzanoCO, et al. (2011) A candidate HIV/AIDS vaccine (MVA-B) lacking vaccinia virus gene C6L enhances memory HIV-1-specific T-cell responses. PLoS One 6: e24244.

6. NajeraJL, GomezCE, Domingo-GilE, GherardiMM, EstebanM (2006) Cellular and biochemical differences between two attenuated poxvirus vaccine candidates (MVA and NYVAC) and role of the C7L gene. J Virol 80: 6033–6047.

7. SchwenekerM, LukassenS, SpathM, WolferstatterM, BabelE, et al. (2012) The vaccinia virus O1 protein is required for sustained activation of extracellular signal-regulated kinase 1/2 and promotes viral virulence. J Virol 86: 2323–2336.

8. GuanKL (1994) The mitogen activated protein kinase signal transduction pathway: from the cell surface to the nucleus. Cell Signal 6: 581–589.

9. RenukaradhyaGJ, KhanMA, ShajiD, BrutkiewiczRR (2008) Vesicular stomatitis virus matrix protein impairs CD1d-mediated antigen presentation through activation of the p38 MAPK pathway. J Virol 82: 12535–12542.

10. MeddersKE, SejbukNE, MaungR, DesaiMK, KaulM (2010) Activation of p38 MAPK is required in monocytic and neuronal cells for HIV glycoprotein 120-induced neurotoxicity. J Immunol 185: 4883–4895.

11. HuangWR, WangYC, ChiPI, WangL, WangCY, et al. (2011) Cell entry of avian reovirus follows a caveolin-1-mediated and dynamin-2-dependent endocytic pathway that requires activation of p38 MAPK and Src signaling pathways as well as microtubules and small GTPase Rab5. J Biol Chem 286 (35) 30780–94.

12. PerdigueroB, EstebanM (2009) The interferon system and vaccinia virus evasion mechanisms. J Interferon Cytokine Res 29: 581–598.

13. SoaresJA, LeiteFG, AndradeLG, TorresAA, De SousaLP, et al. (2009) Activation of the PI3K/Akt pathway early during vaccinia and cowpox virus infections is required for both host survival and viral replication. J Virol 83: 6883–6899.

14. LinS, ChenW, BroylesSS (1992) The vaccinia virus B1R gene product is a serine/threonine protein kinase. J Virol 66: 2717–2723.

15. PunjabiA, TraktmanP (2005) Cell biological and functional characterization of the vaccinia virus F10 kinase: implications for the mechanism of virion morphogenesis. J Virol 79: 2171–2190.

16. LiuK, LemonB, TraktmanP (1995) The dual-specificity phosphatase encoded by vaccinia virus, VH1, is essential for viral transcription in vivo and in vitro. J Virol 69: 7823–7834.

17. AndradeAA, SilvaPN, PereiraAC, De SousaLP, FerreiraPC, et al. (2004) The vaccinia virus-stimulated mitogen-activated protein kinase (MAPK) pathway is required for virus multiplication. Biochem J 381: 437–446.

18. ChambardJC, LeflochR, PouyssegurJ, LenormandP (2007) ERK implication in cell cycle regulation. Biochim Biophys Acta 1773: 1299–1310.

19. LiuJ, LinA (2005) Role of JNK activation in apoptosis: a double-edged sword. Cell Res 15: 36–42.

20. CuendaA, RousseauS (2007) p38 MAP-kinases pathway regulation, function and role in human diseases. Biochim Biophys Acta 1773: 1358–1375.

21. MurphyLO, BlenisJ (2006) MAPK signal specificity: the right place at the right time. Trends Biochem Sci 31: 268–275.

22. CargnelloM, RouxPP (2011) Activation and function of the MAPKs and their substrates, the MAPK-activated protein kinases. Microbiol Mol Biol Rev 75: 50–83.

23. CauntCJ, KeyseSM (2012) Dual-specificity MAP kinase phosphatases (MKPs): shaping the outcome of MAP kinase signalling. FEBS J 280 (2) 489–504.

24. LauLF, NathansD (1985) Identification of a set of genes expressed during the G0/G1 transition of cultured mouse cells. EMBO J 4: 3145–3151.

25. DorfmanK, CarrascoD, GrudaM, RyanC, LiraSA, et al. (1996) Disruption of the erp/mkp-1 gene does not affect mouse development: normal MAP kinase activity in ERP/MKP-1-deficient fibroblasts. Oncogene 13: 925–931.

26. SlackDN, SeternesOM, GabrielsenM, KeyseSM (2001) Distinct binding determinants for ERK2/p38alpha and JNK map kinases mediate catalytic activation and substrate selectivity of map kinase phosphatase-1. J Biol Chem 276: 16491–16500.

27. OwensDM, KeyseSM (2007) Differential regulation of MAP kinase signalling by dual-specificity protein phosphatases. Oncogene 26: 3203–3213.

28. LiuYX, WangJ, GuoJ, WuJ, LiebermanHB, et al. (2008) DUSP1 is controlled by p53 during the cellular response to oxidative stress. Mol Cancer Res 6: 624–633.

29. ShieldsKM, PanzhinskiyE, BurnsN, ZawadaWM, DasM (2011) Mitogen-activated protein kinase phosphatase-1 is a key regulator of hypoxia-induced vascular endothelial growth factor expression and vessel density in lung. Am J Pathol 178: 98–109.

30. LasaM, Gil-AraujoB, PalafoxM, ArandaA (2010) Thyroid hormone antagonizes tumor necrosis factor-alpha signaling in pituitary cells through the induction of dual specificity phosphatase 1. Mol Endocrinol 24: 412–422.

31. LeeKH, LeeCT, KimYW, HanSK, ShimYS, et al. (2005) Preheating accelerates mitogen-activated protein (MAP) kinase inactivation post-heat shock via a heat shock protein 70-mediated increase in phosphorylated MAP kinase phosphatase-1. J Biol Chem 280: 13179–13186.

32. FranklinCC, SrikanthS, KraftAS (1998) Conditional expression of mitogen-activated protein kinase phosphatase-1, MKP-1, is cytoprotective against UV-induced apoptosis. Proc Natl Acad Sci U S A 95: 3014–3019.

33. BrondelloJM, PouyssegurJ, McKenzieFR (1999) Reduced MAP kinase phosphatase-1 degradation after p42/p44MAPK-dependent phosphorylation. Science 286: 2514–2517.

34. CaoW, BaoC, PadalkoE, LowensteinCJ (2008) Acetylation of mitogen-activated protein kinase phosphatase-1 inhibits Toll-like receptor signaling. J Exp Med 205: 1491–1503.

35. ChiH, FlavellRA (2008) Acetylation of MKP-1 and the control of inflammation. Sci Signal 1: pe44.

36. RothRJ, LeAM, ZhangL, KahnM, SamuelVT, et al. (2009) MAPK phosphatase-1 facilitates the loss of oxidative myofibers associated with obesity in mice. J Clin Invest 119: 3817–3829.

37. BoutrosT, NantelA, EmadaliA, TzimasG, ConzenS, et al. (2008) The MAP kinase phosphatase-1 MKP-1/DUSP1 is a regulator of human liver response to transplantation. Am J Transplant 8: 2558–2568.

38. Moncho-AmorV, Ibanez de CaceresI, BandresE, Martinez-PovedaB, OrgazJL, et al. (2011) DUSP1/MKP1 promotes angiogenesis, invasion and metastasis in non-small-cell lung cancer. Oncogene 30: 668–678.

39. DuricV, BanasrM, LicznerskiP, SchmidtHD, StockmeierCA, et al. (2010) A negative regulator of MAP kinase causes depressive behavior. Nat Med 16: 1328–1332.

40. ChiH, BarrySP, RothRJ, WuJJ, JonesEA, et al. (2006) Dynamic regulation of pro- and anti-inflammatory cytokines by MAPK phosphatase 1 (MKP-1) in innate immune responses. Proc Natl Acad Sci U S A 103: 2274–2279.

41. GuerraS, Lopez-FernandezLA, Pascual-MontanoA, MunozM, HarshmanK, et al. (2003) Cellular gene expression survey of vaccinia virus infection of human HeLa cells. J Virol 77: 6493–6506.

42. Domingo-GilE, GonzalezJM, EstebanM (2010) Identification of cellular genes induced in human cells after activation of the OAS/RNaseL pathway by vaccinia virus recombinants expressing these antiviral enzymes. J Interferon Cytokine Res 30: 171–188.

43. LudwigH, MagesJ, StaibC, LehmannMH, LangR, et al. (2005) Role of viral factor E3L in modified vaccinia virus ankara infection of human HeLa Cells: regulation of the virus life cycle and identification of differentially expressed host genes. J Virol 79: 2584–2596.

44. LanglandJO, KashJC, CarterV, ThomasMJ, KatzeMG, et al. (2006) Suppression of proinflammatory signal transduction and gene expression by the dual nucleic acid binding domains of the vaccinia virus E3L proteins. J Virol 80: 10083–10095.

45. KlotzC, ZieglerT, FigueiredoAS, RauschS, HepworthMR, et al. (2011) A helminth immunomodulator exploits host signaling events to regulate cytokine production in macrophages. PLoS Pathog 7: e1001248.

46. RodriguezN, DietrichH, MossbruggerI, WeintzG, SchellerJ, et al. (2010) Increased inflammation and impaired resistance to Chlamydophila pneumoniae infection in Dusp1(−/−) mice: critical role of IL-6. J Leukoc Biol 88: 579–587.

47. HammerM, EchtenachterB, WeighardtH, JozefowskiK, Rose-JohnS, et al. (2010) Increased inflammation and lethality of Dusp1−/− mice in polymicrobial peritonitis models. Immunology 131: 395–404.

48. RamirezJC, GherardiMM, EstebanM (2000) Biology of attenuated modified vaccinia virus Ankara recombinant vector in mice: virus fate and activation of B- and T-cell immune responses in comparison with the Western Reserve strain and advantages as a vaccine. J Virol 74: 923–933.

49. BablanianR, CoppolaG, ScribaniS, EstebanM (1981) Inhibition of viral protein synthesis: III. The effect of ultraviolet-irradiated virus on the inhibition of protein synthesis. Virology 112 (1) 1–12.

50. RodriguezJF, RodriguezD, RodriguezJR, McGowanEB, EstebanM (1988) Expression of the firefly luciferase gene in vaccinia virus: a highly sensitive gene marker to follow virus dissemination in tissues of infected animals. Proc Natl Acad Sci U S A 85: 1667–1671.

51. GomezCE, NajeraJL, Domingo-GilE, Ochoa-CallejeroL, Gonzalez-AseguinolazaG, et al. (2007) Virus distribution of the attenuated MVA and NYVAC poxvirus strains in mice. J Gen Virol 88: 2473–2478.

52. Garcia-ArriazaJ, NajeraJL, GomezCE, SorzanoCO, EstebanM (2010) Immunogenic profiling in mice of a HIV/AIDS vaccine candidate (MVA-B) expressing four HIV-1 antigens and potentiation by specific gene deletions. PLoS One 5: e12395.

53. NajeraJL, GomezCE, Garcia-ArriazaJ, SorzanoCO, EstebanM (2010) Insertion of vaccinia virus C7L host range gene into NYVAC-B genome potentiates immune responses against HIV-1 antigens. PLoS One 5: e11406.

54. FrazierWJ, WangX, WancketLM, LiXA, MengX, et al. (2009) Increased inflammation, impaired bacterial clearance, and metabolic disruption after gram-negative sepsis in Mkp-1-deficient mice. J Immunol 183: 7411–7419.

55. RodriguezD, EstebanM, RodriguezJR (1995) Vaccinia virus A17L gene product is essential for an early step in virion morphogenesis. J Virol 69: 4640–4648.

56. UngerB, MercerJ, BoyleKA, TraktmanP (2012) Biogenesis of the Vaccinia Virus Membrane: Genetic and Ultrastructural Analysis of the Contributions of the A14 and A17 Proteins. J Virol 87 (2) 1083–97.

57. Gallego-GomezJC, RiscoC, RodriguezD, CabezasP, GuerraS, et al. (2003) Differences in virus-induced cell morphology and in virus maturation between MVA and other strains (WR, Ankara, and NYCBH) of vaccinia virus in infected human cells. J Virol 77: 10606–10622.

58. SilvaPN, SoaresJA, BrasilBS, NogueiraSV, AndradeAA, et al. (2006) Differential role played by the MEK/ERK/EGR-1 pathway in orthopoxviruses vaccinia and cowpox biology. Biochem J 398: 83–95.

59. SantosCR, BlancoS, SevillaA, LazoPA (2006) Vaccinia virus B1R kinase interacts with JIP1 and modulates c-Jun-dependent signaling. J Virol 80: 7667–7675.

60. MyskiwC, ArsenioJ, van BruggenR, DeschambaultY, CaoJ (2009) Vaccinia virus E3 suppresses expression of diverse cytokines through inhibition of the PKR, NF-kappaB, and IRF3 pathways. J Virol 83: 6757–6768.

61. PereiraAC, Soares-MartinsJA, LeiteFG, Da CruzAF, TorresAA, et al. (2012) SP600125 inhibits Orthopoxviruses replication in a JNK1/2 -independent manner: Implication as a potential antipoxviral. Antiviral Res 93: 69–77.

62. SalojinKV, OwusuIB, MillerchipKA, PotterM, PlattKA, et al. (2006) Essential role of MAPK phosphatase-1 in the negative control of innate immune responses. J Immunol 176: 1899–1907.

63. LiY, YuanS, MoyerRW (1998) The non-permissive infection of insect (gypsy moth) LD-652 cells by Vaccinia virus. Virology 248: 74–82.

64. McFaddenG (2005) Poxvirus tropism. Nat Rev Microbiol 3: 201–213.

65. JanRH, LinYL, ChenCJ, LinTY, HsuYC, et al. (2012) Hepatitis B virus surface antigen can activate human monocyte-derived dendritic cells by NF-kB and p38 mitogen-activated protein kinase mediated signaling. Microbiol Immunol 56 (10) 719–27.

66. BretanaNA, LuCT, ChiangCY, SuMG, HuangKY, et al. (2012) Identifying protein phosphorylation sites with kinase substrate specificity on human viruses. PLoS One 7: e40694.

67. ConditRC, MoussatcheN, TraktmanP (2006) In a nutshell: structure and assembly of the vaccinia virion. Adv Virus Res 66: 31–124.

68. WangS, ShumanS (1995) Vaccinia virus morphogenesis is blocked by temperature-sensitive mutations in the F10 gene, which encodes protein kinase 2. J Virol 69: 6376–6388.

69. MercerJ, TraktmanP (2003) Investigation of structural and functional motifs within the vaccinia virus A14 phosphoprotein, an essential component of the virion membrane. J Virol 77: 8857–8871.

70. DerrienM, PunjabiA, KhannaM, GrubishaO, TraktmanP (1999) Tyrosine phosphorylation of A17 during vaccinia virus infection: involvement of the H1 phosphatase and the F10 kinase. J Virol 73: 7287–7296.

71. ReschW, WeisbergAS, MossB (2005) Vaccinia virus nonstructural protein encoded by the A11R gene is required for formation of the virion membrane. J Virol 79: 6598–6609.

72. BeaudG, BeaudR, LeaderDP (1995) Vaccinia virus gene H5R encodes a protein that is phosphorylated by the multisubstrate vaccinia virus B1R protein kinase. J Virol 69: 1819–1826.

73. SanchoMC, SchleichS, GriffithsG, Krijnse-LockerJ (2002) The block in assembly of modified vaccinia virus Ankara in HeLa cells reveals new insights into vaccinia virus morphogenesis. J Virol 76: 8318–8334.

74. JeffreyKL, CampsM, RommelC, MackayCR (2007) Targeting dual-specificity phosphatases: manipulating MAP kinase signalling and immune responses. Nat Rev Drug Discov 6: 391–403.

75. LiuY, ShepherdEG, NelinLD (2007) MAPK phosphatases–regulating the immune response. Nat Rev Immunol 7: 202–212.

76. HammerM, MagesJ, DietrichH, ServatiusA, HowellsN, et al. (2006) Dual specificity phosphatase 1 (DUSP1) regulates a subset of LPS-induced genes and protects mice from lethal endotoxin shock. J Exp Med 203: 15–20.

77. Cortes-SempereM, ChattopadhyayS, RoviraA, Rodriguez-FanjulV, Belda-IniestaC, et al. (2009) MKP1 repression is required for the chemosensitizing effects of NF-kappaB and PI3K inhibitors to cisplatin in non-small cell lung cancer. Cancer Lett 286: 206–216.

78. RinconM, DavisRJ (2009) Regulation of the immune response by stress-activated protein kinases. Immunol Rev 228: 212–224.

79. GomezCE, NajeraJL, JimenezEP, JimenezV, WagnerR, et al. (2007) Head-to-head comparison on the immunogenicity of two HIV/AIDS vaccine candidates based on the attenuated poxvirus strains MVA and NYVAC co-expressing in a single locus the HIV-1BX08 gp120 and HIV-1(IIIB) Gag-Pol-Nef proteins of clade B. Vaccine 25: 2863–2885.

80. IwasakiA, MedzhitovR (2010) Regulation of adaptive immunity by the innate immune system. Science 327: 291–295.

81. IborraS, IzquierdoHM, Martinez-LopezM, Blanco-MenendezN, Reis e SousaC, et al. (2012) The DC receptor DNGR-1 mediates cross-priming of CTLs during vaccinia virus infection in mice. J Clin Invest 122: 1628–1643.

82. HuangG, WangY, ShiLZ, KannegantiTD, ChiH (2011) Signaling by the phosphatase MKP-1 in dendritic cells imprints distinct effector and regulatory T cell fates. Immunity 35: 45–58.

Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

Článok vyšiel v časopise

PLOS Pathogens


2013 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#