-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
Inactivation of the Host Lipin Gene Accelerates RNA Virus Replication through Viral Exploitation of the Expanded Endoplasmic Reticulum Membrane
RNA viruses take advantage of cellular resources, such as membranes and lipids, to assemble viral replicase complexes (VRCs) that drive viral replication. The host lipins (phosphatidate phosphatases) are particularly interesting because these proteins play key roles in cellular decisions about membrane biogenesis versus lipid storage. Therefore, we examined the relationship between host lipins and tombusviruses, based on yeast model host. We show that deletion of PAH1 (phosphatidic acid phosphohydrolase), which is the single yeast homolog of the lipin gene family of phosphatidate phosphatases, whose inactivation is responsible for proliferation and expansion of the endoplasmic reticulum (ER) membrane, facilitates robust RNA virus replication in yeast. We document increased tombusvirus replicase activity in pah1Δ yeast due to the efficient assembly of VRCs. We show that the ER membranes generated in pah1Δ yeast is efficiently subverted by this RNA virus, thus emphasizing the connection between host lipins and RNA viruses. Thus, instead of utilizing the peroxisomal membranes as observed in wt yeast and plants, TBSV readily switches to the vastly expanded ER membranes in lipin-deficient cells to build VRCs and support increased level of viral replication. Over-expression of the Arabidopsis Pah2p in Nicotiana benthamiana decreased tombusvirus accumulation, validating that our findings are also relevant in a plant host. Over-expression of AtPah2p also inhibited the ER-based replication of another plant RNA virus, suggesting that the role of lipins in RNA virus replication might include several more eukaryotic viruses.
Vyšlo v časopise: Inactivation of the Host Lipin Gene Accelerates RNA Virus Replication through Viral Exploitation of the Expanded Endoplasmic Reticulum Membrane. PLoS Pathog 10(2): e32767. doi:10.1371/journal.ppat.1003944
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003944Souhrn
RNA viruses take advantage of cellular resources, such as membranes and lipids, to assemble viral replicase complexes (VRCs) that drive viral replication. The host lipins (phosphatidate phosphatases) are particularly interesting because these proteins play key roles in cellular decisions about membrane biogenesis versus lipid storage. Therefore, we examined the relationship between host lipins and tombusviruses, based on yeast model host. We show that deletion of PAH1 (phosphatidic acid phosphohydrolase), which is the single yeast homolog of the lipin gene family of phosphatidate phosphatases, whose inactivation is responsible for proliferation and expansion of the endoplasmic reticulum (ER) membrane, facilitates robust RNA virus replication in yeast. We document increased tombusvirus replicase activity in pah1Δ yeast due to the efficient assembly of VRCs. We show that the ER membranes generated in pah1Δ yeast is efficiently subverted by this RNA virus, thus emphasizing the connection between host lipins and RNA viruses. Thus, instead of utilizing the peroxisomal membranes as observed in wt yeast and plants, TBSV readily switches to the vastly expanded ER membranes in lipin-deficient cells to build VRCs and support increased level of viral replication. Over-expression of the Arabidopsis Pah2p in Nicotiana benthamiana decreased tombusvirus accumulation, validating that our findings are also relevant in a plant host. Over-expression of AtPah2p also inhibited the ER-based replication of another plant RNA virus, suggesting that the role of lipins in RNA virus replication might include several more eukaryotic viruses.
Zdroje
1. den BoonJA, DiazA, AhlquistP (2010) Cytoplasmic viral replication complexes. Cell Host Microbe 8 : 77–85.
2. MillerS, Krijnse-LockerJ (2008) Modification of intracellular membrane structures for virus replication. Nat Rev Microbiol 6 : 363–374.
3. NagyPD, PoganyJ (2012) The dependence of viral RNA replication on co-opted host factors. Nature Reviews Microbiology 10 : 137–149.
4. BelovGA, van KuppeveldFJ (2012) (+)RNA viruses rewire cellular pathways to build replication organelles. Curr Opin Virol 2 : 740–747.
5. McCartneyAW, GreenwoodJS, FabianMR, WhiteKA, MullenRT (2005) Localization of the tomato bushy stunt virus replication protein p33 reveals a peroxisome-to-endoplasmic reticulum sorting pathway. Plant Cell 17 : 3513–3531.
6. BarajasD, JiangY, NagyPD (2009) A Unique Role for the Host ESCRT Proteins in Replication of Tomato bushy stunt virus. PLoS Pathog 5: e1000705.
7. NovoaRR, CalderitaG, ArranzR, FontanaJ, GranzowH, et al. (2005) Virus factories: associations of cell organelles for viral replication and morphogenesis. Biol Cell 97 : 147–172.
8. SalonenA, AholaT, KaariainenL (2005) Viral RNA replication in association with cellular membranes. Curr Top Microbiol Immunol 285 : 139–173.
9. BartenschlagerR, CossetFL, LohmannV (2010) Hepatitis C virus replication cycle. Journal of Hepatology 53 : 583–585.
10. CherryS, DoukasT, ArmknechtS, WhelanS, WangH, et al. (2005) Genome-wide RNAi screen reveals a specific sensitivity of IRES-containing RNA viruses to host translation inhibition. Genes Dev 19 : 445–452.
11. KushnerDB, LindenbachBD, GrdzelishviliVZ, NoueiryAO, PaulSM, et al. (2003) Systematic, genome-wide identification of host genes affecting replication of a positive-strand RNA virus. Proc Natl Acad Sci U S A 100 : 15764–15769.
12. ServieneE, JiangY, ChengCP, BakerJ, NagyPD (2006) Screening of the yeast yTHC collection identifies essential host factors affecting tombusvirus RNA recombination. J Virol 80 : 1231–1241.
13. PanavasT, ServieneE, BrasherJ, NagyPD (2005) Yeast genome-wide screen reveals dissimilar sets of host genes affecting replication of RNA viruses. Proc Natl Acad Sci U S A 102 : 7326–7331.
14. KrishnanMN, NgA, SukumaranB, GilfoyFD, UchilPD, et al. (2008) RNA interference screen for human genes associated with West Nile virus infection. Nature 455 : 242–245.
15. CastorenaKM, StaplefordKA, MillerDJ (2010) Complementary transcriptomic, lipidomic, and targeted functional genetic analyses in cultured Drosophila cells highlight the role of glycerophospholipid metabolism in Flock House virus RNA replication. BMC Genomics 11 : 183.
16. BelovGA, EhrenfeldE (2007) Involvement of cellular membrane traffic proteins in poliovirus replication. Cell Cycle 6 : 36–38.
17. HsuNY, IlnytskaO, BelovG, SantianaM, ChenYH, et al. (2010) Viral reorganization of the secretory pathway generates distinct organelles for RNA replication. Cell 141 : 799–811.
18. SasvariZ, NagyPD (2010) Making of Viral Replication Organelles by Remodeling Interior Membranes. Viruses-Basel 2 : 2436–2442.
19. BergerKL, CooperJD, HeatonNS, YoonR, OaklandTE, et al. (2009) Roles for endocytic trafficking and phosphatidylinositol 4-kinase III alpha in hepatitis C virus replication. Proc Natl Acad Sci U S A 106 : 7577–7582.
20. HeatonNS, PereraR, BergerKL, KhadkaS, LacountDJ, et al. (2010) Dengue virus nonstructural protein 3 redistributes fatty acid synthase to sites of viral replication and increases cellular fatty acid synthesis. Proc Natl Acad Sci U S A 107 : 17345–17350.
21. NagyPD, PoganyJ (2006) Yeast as a model host to dissect functions of viral and host factors in tombusvirus replication. Virology 344 : 211–220.
22. RajendranKS, NagyPD (2006) Kinetics and functional studies on interaction between the replicase proteins of Tomato Bushy Stunt Virus: Requirement of p33:p92 interaction for replicase assembly. Virology 345 : 270–279.
23. ServieneE, ShapkaN, ChengCP, PanavasT, PhuangratB, et al. (2005) Genome-wide screen identifies host genes affecting viral RNA recombination. Proc Natl Acad Sci U S A 102 : 10545–10550.
24. NagyPD, BarajasD, PoganyJ (2012) Host factors with regulatory roles in tombusvirus replication. Curr Opin Virol 2 : 685–692.
25. NagyPD, PoganyJ (2010) Global genomics and proteomics approaches to identify host factors as targets to induce resistance against Tomato bushy stunt virus. Adv Virus Res 76 : 123–177.
26. PanavieneZ, BakerJM, NagyPD (2003) The overlapping RNA-binding domains of p33 and p92 replicase proteins are essential for tombusvirus replication. Virology 308 : 191–205.
27. OsterSK, WuB, WhiteKA (1998) Uncoupled expression of p33 and p92 permits amplification of tomato bushy stunt virus RNAs. J Virol 72 : 5845–5851.
28. ScholthofKB, ScholthofHB, JacksonAO (1995) The tomato bushy stunt virus replicase proteins are coordinately expressed and membrane associated. Virology 208 : 365–369.
29. WhiteKA, NagyPD (2004) Advances in the molecular biology of tombusviruses: gene expression, genome replication, and recombination. Prog Nucleic Acid Res Mol Biol 78 : 187–226.
30. PanavieneZ, PanavasT, NagyPD (2005) Role of an internal and two 3′-terminal RNA elements in assembly of tombusvirus replicase. J Virol 79 : 10608–10618.
31. PanavieneZ, PanavasT, ServaS, NagyPD (2004) Purification of the cucumber necrosis virus replicase from yeast cells: role of coexpressed viral RNA in stimulation of replicase activity. J Virol 78 : 8254–8263.
32. PoganyJ, NagyPD (2012) p33-Independent Activation of a Truncated p92 RNA-Dependent RNA Polymerase of Tomato Bushy Stunt Virus in Yeast Cell-Free Extract. J Virol 86 : 12025–12038.
33. MonkewichS, LinHX, FabianMR, XuW, NaH, et al. (2005) The p92 polymerase coding region contains an internal RNA element required at an early step in Tombusvirus genome replication. J Virol 79 : 4848–4858.
34. PanavasT, HawkinsCM, PanavieneZ, NagyPD (2005) The role of the p33:p33/p92 interaction domain in RNA replication and intracellular localization of p33 and p92 proteins of Cucumber necrosis tombusvirus. Virology 338 : 81–95.
35. PoganyJ, WhiteKA, NagyPD (2005) Specific binding of tombusvirus replication protein p33 to an internal replication element in the viral RNA is essential for replication. J Virol 79 : 4859–4869.
36. StorkJ, KovalevN, SasvariZ, NagyPD (2011) RNA chaperone activity of the tombusviral p33 replication protein facilitates initiation of RNA synthesis by the viral RdRp in vitro. Virology 409 : 338–347.
37. PoganyJ, StorkJ, LiZ, NagyPD (2008) In vitro assembly of the Tomato bushy stunt virus replicase requires the host Heat shock protein 70. Proc Natl Acad Sci U S A 105 : 19956–19961.
38. RussoM, BurgyanJ, MartelliGP (1994) Molecular biology of tombusviridae. Adv Virus Res 44 : 381–428.
39. PanavasT, HawkinsCM, PanavieneZ, NagyPD (2005) The role of the p33:p33/p92 interaction domain in RNA replication and intracellular localization of p33 and p92 proteins of Cucumber necrosis tombusvirus. Virology 338 : 81–95.
40. PathakKB, SasvariZ, NagyPD (2008) The host Pex19p plays a role in peroxisomal localization of tombusvirus replication proteins. Virology 379 : 294–305.
41. JonczykM, PathakKB, SharmaM, NagyPD (2007) Exploiting alternative subcellular location for replication: tombusvirus replication switches to the endoplasmic reticulum in the absence of peroxisomes. Virology 362 : 320–330.
42. XuK, HuangTS, NagyPD (2012) Authentic in vitro replication of two tombusviruses in isolated mitochondrial and endoplasmic reticulum membranes. J Virol 86 : 12779–12794.
43. CarmanGM, HanGS (2011) Regulation of phospholipid synthesis in the yeast Saccharomyces cerevisiae. Annu Rev Biochem 80 : 859–883.
44. CsakiLS, ReueK (2010) Lipins: multifunctional lipid metabolism proteins. Annu Rev Nutr 30 : 257–272.
45. LoewenCJ (2012) Lipids as conductors in the orchestra of life. F1000 Biol Rep 4 : 4.
46. ReueK, DwyerJR (2009) Lipin proteins and metabolic homeostasis. J Lipid Res 50 Suppl: S109–114.
47. ReueK, DonkorJ (2007) Genetic factors in type 2 diabetes: all in the (lipin) family. Diabetes 56 : 2842–2843.
48. CarmanGM, HanGS (2006) Roles of phosphatidate phosphatase enzymes in lipid metabolism. Trends Biochem Sci 31 : 694–699.
49. HanGS, SiniossoglouS, CarmanGM (2007) The cellular functions of the yeast lipin homolog PAH1p are dependent on its phosphatidate phosphatase activity. J Biol Chem 282 : 37026–37035.
50. ChoiHS, SuWM, HanGS, PloteD, XuZ, et al. (2012) Pho85p-pho80p phosphorylation of yeast pah1p phosphatidate phosphatase regulates its activity, location, abundance, and function in lipid metabolism. J Biol Chem 287 : 11290–11301.
51. MietkiewskaE, SilotoRM, DewaldJ, ShahS, BrindleyDN, et al. (2011) Lipins from plants are phosphatidate phosphatases that restore lipid synthesis in a pah1Delta mutant strain of Saccharomyces cerevisiae. FEBS J 278 : 764–775.
52. ChaeM, HanGS, CarmanGM (2012) The Saccharomyces cerevisiae Actin Patch Protein App1p Is a Phosphatidate Phosphatase Enzyme. J Biol Chem 287 : 40186–40196.
53. ChoiHS, SuWM, MorganJM, HanGS, XuZ, et al. (2011) Phosphorylation of phosphatidate phosphatase regulates its membrane association and physiological functions in Saccharomyces cerevisiae: identification of SER(602), THR(723), AND SER(744) as the sites phosphorylated by CDC28 (CDK1)-encoded cyclin-dependent kinase. J Biol Chem 286 : 1486–1498.
54. HanGS, O'HaraL, SiniossoglouS, CarmanGM (2008) Characterization of the yeast DGK1-encoded CTP-dependent diacylglycerol kinase. J Biol Chem 283 : 20443–20453.
55. HanGS, O'HaraL, CarmanGM, SiniossoglouS (2008) An unconventional diacylglycerol kinase that regulates phospholipid synthesis and nuclear membrane growth. J Biol Chem 283 : 20433–20442.
56. JaagHM, StorkJ, NagyPD (2007) Host transcription factor Rpb11p affects tombusvirus replication and recombination via regulating the accumulation of viral replication proteins. Virology 368 : 388–404.
57. WangRY, StorkJ, PoganyJ, NagyPD (2009) A temperature sensitive mutant of heat shock protein 70 reveals an essential role during the early steps of tombusvirus replication. Virology 394 : 28–38.
58. WangRY, StorkJ, NagyPD (2009) A key role for heat shock protein 70 in the localization and insertion of tombusvirus replication proteins to intracellular membranes. J Virol 83 : 3276–3287.
59. PoganyJ, NagyPD (2008) Authentic replication and recombination of Tomato bushy stunt virus RNA in a cell-free extract from yeast. J Virol 82 : 5967–5980.
60. NavarroB, RussoM, PantaleoV, RubinoL (2006) Cytological analysis of Saccharomyces cerevisiae cells supporting cymbidium ringspot virus defective interfering RNA replication. J Gen Virol 87 : 705–714.
61. PathakKB, PoganyJ, XuK, WhiteKA, NagyPD (2012) Defining the Roles of cis-Acting RNA Elements in Tombusvirus Replicase Assembly In Vitro. J Virol 86 : 156–171.
62. PathakKB, PoganyJ, NagyPD (2011) Non-template functions of the viral RNA in plant RNA virus replication. Curr Opin Virol 1 : 332–338.
63. HwangYT, McCartneyAW, GiddaSK, MullenRT (2008) Localization of the Carnation Italian ringspot virus replication protein p36 to the mitochondrial outer membrane is mediated by an internal targeting signal and the TOM complex. BMC Cell Biol 9 : 54.
64. Weber-LotfiF, DietrichA, RussoM, RubinoL (2002) Mitochondrial targeting and membrane anchoring of a viral replicase in plant and yeast cells. J Virol 76 : 10485–10496.
65. KovalevN, PoganyJ, NagyPD (2012) A Co-Opted DEAD-Box RNA Helicase Enhances Tombusvirus Plus-Strand Synthesis. PLoS Pathog 8: e1002537.
66. PoganyJ, PanavasT, ServieneE, Nawaz-Ul-RehmanMS, NagyPD (2010) A high-throughput approach for studying virus replication in yeast. Current Protocols in Microbiology 19 : 16J.11.11–16J.11.15.
67. PriceBD, EckerleLD, BallLA, JohnsonKL (2005) Nodamura virus RNA replication in Saccharomyces cerevisiae: heterologous gene expression allows replication-dependent colony formation. J Virol 79 : 495–502.
68. EastmondPJ, QuettierAL, KroonJT, CraddockC, AdamsN, et al. (2011) A phosphatidate phosphatase double mutant provides a new insight into plant membrane lipid homeostasis. Plant Signal Behav 6 : 526–527.
69. EastmondPJ, QuettierAL, KroonJT, CraddockC, AdamsN, et al. (2010) Phosphatidic acid phosphohydrolase 1 and 2 regulate phospholipid synthesis at the endoplasmic reticulum in Arabidopsis. Plant Cell 22 : 2796–2811.
70. NakamuraY, KoizumiR, ShuiG, ShimojimaM, WenkMR, et al. (2009) Arabidopsis lipins mediate eukaryotic pathway of lipid metabolism and cope critically with phosphate starvation. Proc Natl Acad Sci U S A 106 : 20978–20983.
71. MineA, OkunoT (2012) Composition of plant virus RNA replicase complexes. Curr Opin Virol 2 : 669–675.
72. HenrySA, KohlweinSD, CarmanGM (2012) Metabolism and regulation of glycerolipids in the yeast Saccharomyces cerevisiae. Genetics 190 : 317–349.
73. GrangeonR, JiangJ, LaliberteJF (2012) Host endomembrane recruitment for plant RNA virus replication. Curr Opin Virol 2 : 683–690.
74. LaliberteJF, SanfaconH (2010) Cellular remodeling during plant virus infection. Annu Rev Phytopathol 48 : 69–91.
75. de CastroIF, VolonteL, RiscoC (2013) Virus factories: biogenesis and structural design. Cell Microbiol 15 : 24–34.
76. SharmaM, SasvariZ, NagyPD (2011) Inhibition of phospholipid biosynthesis decreases the activity of the tombusvirus replicase and alters the subcellular localization of replication proteins. Virology 415 : 141–152.
77. HarrisTE, FinckBN (2011) Dual function lipin proteins and glycerolipid metabolism. Trends Endocrinol Metab 22 : 226–233.
78. van HarmelenV, RydenM, SjolinE, HoffstedtJ (2007) A role of lipin in human obesity and insulin resistance: relation to adipocyte glucose transport and GLUT4 expression. J Lipid Res 48 : 201–206.
79. Yao-BorengasserA, RasouliN, VarmaV, MilesLM, PhanavanhB, et al. (2006) Lipin expression is attenuated in adipose tissue of insulin-resistant human subjects and increases with peroxisome proliferator-activated receptor gamma activation. Diabetes 55 : 2811–2818.
80. SasvariZ, IzotovaL, KinzyTG, NagyPD (2011) Synergistic Roles of Eukaryotic Translation Elongation Factors 1Bgamma and 1A in Stimulation of Tombusvirus Minus-Strand Synthesis. PLoS Pathog 7: e1002438.
81. LiZ, BarajasD, PanavasT, HerbstDA, NagyPD (2008) Cdc34p ubiquitin-conjugating enzyme is a component of the tombusvirus replicase complex and ubiquitinates p33 replication protein. J Virol 82 : 6911–6926.
82. Shah Nawaz-Ul-RehmanM, Reddisiva PrasanthK, BakerJ, NagyPD (2013) Yeast screens for host factors in positive-strand RNA virus replication based on a library of temperature-sensitive mutants. Methods 59 : 207–216.
83. PathakKB, JiangZ, OchanineV, SharmaM, PoganyJ, et al. (2013) Characterization of dominant-negative and temperature-sensitive mutants of tombusvirus replication proteins affecting replicase assembly. Virology 437 : 48–61.
84. PanavasT, NagyPD (2003) Yeast as a model host to study replication and recombination of defective interfering RNA of Tomato bushy stunt virus. Virology 314 : 315–325.
85. BarajasD, LiZ, NagyPD (2009) The Nedd4-type Rsp5p ubiquitin ligase inhibits tombusvirus replication by regulating degradation of the p92 replication protein and decreasing the activity of the tombusvirus replicase. J Virol 83 : 11751–11764.
86. RiederSE, EmrSD (2001) Isolation of subcellular fractions from the yeast Saccharomyces cerevisiae. Curr Protoc Cell Biol Chapter 3: Unit 3 8.
87. PanavasT, ServieneE, PoganyJ, NagyPD (2008) Genome-wide screens for identification of host factors in viral replication. Methods Mol Biol 451 : 615–624.
88. ChengCP, JaagHM, JonczykM, ServieneE, NagyPD (2007) Expression of the Arabidopsis Xrn4p 5′-3′ exoribonuclease facilitates degradation of tombusvirus RNA and promotes rapid emergence of viral variants in plants. Virology 368 : 238–248.
Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium
Článek Structure of the Membrane Anchor of Pestivirus Glycoprotein E, a Long Tilted Amphipathic HelixČlánek Iron Acquisition in : The Roles of IlsA and Bacillibactin in Exogenous Ferritin Iron MobilizationČlánek AvrBsT Acetylates ACIP1, a Protein that Associates with Microtubules and Is Required for ImmunityČlánek Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden HamstersČlánek Genome-Wide RNAi Screen Identifies Broadly-Acting Host Factors That Inhibit Arbovirus Infection
Článok vyšiel v časopisePLOS Pathogens
Najčítanejšie tento týždeň
2014 Číslo 2- 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?
-
Všetky články tohto čísla
- Viral Enhancer Mimicry of Host Innate-Immune Promoters
- The Epstein-Barr Virus-Encoded MicroRNA MiR-BART9 Promotes Tumor Metastasis by Targeting E-Cadherin in Nasopharyngeal Carcinoma
- Implication of PMLIV in Both Intrinsic and Innate Immunity
- The Consequences of Reconfiguring the Ambisense S Genome Segment of Rift Valley Fever Virus on Viral Replication in Mammalian and Mosquito Cells and for Genome Packaging
- Substrate-Induced Unfolding of Protein Disulfide Isomerase Displaces the Cholera Toxin A1 Subunit from Its Holotoxin
- Male-Killing Induces Sex-Specific Cell Death via Host Apoptotic Pathway
- Highly Active Antiretroviral Therapies Are Effective against HIV-1 Cell-to-Cell Transmission
- The microRNAs in an Ancient Protist Repress the Variant-Specific Surface Protein Expression by Targeting the Entire Coding Sequence
- Transmission-Blocking Antibodies against Mosquito C-Type Lectins for Dengue Prevention
- Type III Secretion Protein MxiI Is Recognized by Naip2 to Induce Nlrc4 Inflammasome Activation Independently of Pkcδ
- Lundep, a Sand Fly Salivary Endonuclease Increases Parasite Survival in Neutrophils and Inhibits XIIa Contact Activation in Human Plasma
- Induction of Type I Interferon Signaling Determines the Relative Pathogenicity of Strains
- Structure of the Membrane Anchor of Pestivirus Glycoprotein E, a Long Tilted Amphipathic Helix
- Foxp3 Regulatory T Cells Delay Expulsion of Intestinal Nematodes by Suppression of IL-9-Driven Mast Cell Activation in BALB/c but Not in C57BL/6 Mice
- Iron Acquisition in : The Roles of IlsA and Bacillibactin in Exogenous Ferritin Iron Mobilization
- MicroRNA Editing Facilitates Immune Elimination of HCMV Infected Cells
- Reversible Silencing of Cytomegalovirus Genomes by Type I Interferon Governs Virus Latency
- Identification of Host-Targeted Small Molecules That Restrict Intracellular Growth
- A Cyclophilin Homology Domain-Independent Role for Nup358 in HIV-1 Infection
- Engagement of NKG2D on Bystander Memory CD8 T Cells Promotes Increased Immunopathology following Infection
- Suppression of RNA Silencing by a Plant DNA Virus Satellite Requires a Host Calmodulin-Like Protein to Repress Expression
- CIB1 Synergizes with EphrinA2 to Regulate Kaposi's Sarcoma-Associated Herpesvirus Macropinocytic Entry in Human Microvascular Dermal Endothelial Cells
- A Gammaherpesvirus Bcl-2 Ortholog Blocks B Cell Receptor-Mediated Apoptosis and Promotes the Survival of Developing B Cells
- Metabolic Reprogramming during Purine Stress in the Protozoan Pathogen
- The Post-transcriptional Regulator / Activates T3SS by Stabilizing the 5′ UTR of , the Master Regulator of Genes, in
- Tailored Immune Responses: Novel Effector Helper T Cell Subsets in Protective Immunity
- AvrBsT Acetylates ACIP1, a Protein that Associates with Microtubules and Is Required for Immunity
- Epstein-Barr Virus Large Tegument Protein BPLF1 Contributes to Innate Immune Evasion through Interference with Toll-Like Receptor Signaling
- The Major Cellular Sterol Regulatory Pathway Is Required for Andes Virus Infection
- Insights into the Initiation of JC Virus DNA Replication Derived from the Crystal Structure of the T-Antigen Origin Binding Domain
- Domain Shuffling in a Sensor Protein Contributed to the Evolution of Insect Pathogenicity in Plant-Beneficial
- Lectin-Like Bacteriocins from spp. Utilise D-Rhamnose Containing Lipopolysaccharide as a Cellular Receptor
- A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects
- Exploits Asparagine to Assimilate Nitrogen and Resist Acid Stress during Infection
- Interleukin-33 Increases Antibacterial Defense by Activation of Inducible Nitric Oxide Synthase in Skin
- Protective Vaccination against Papillomavirus-Induced Skin Tumors under Immunocompetent and Immunosuppressive Conditions: A Preclinical Study Using a Natural Outbred Animal Model
- Gem-Induced Cytoskeleton Remodeling Increases Cellular Migration of HTLV-1-Infected Cells, Formation of Infected-to-Target T-Cell Conjugates and Viral Transmission
- Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters
- Genome-Wide RNAi Screen Identifies Broadly-Acting Host Factors That Inhibit Arbovirus Infection
- Inflammatory Monocytes Orchestrate Innate Antifungal Immunity in the Lung
- Quantitative and Qualitative Deficits in Neonatal Lung-Migratory Dendritic Cells Impact the Generation of the CD8+ T Cell Response
- Human Genome-Wide RNAi Screen Identifies an Essential Role for Inositol Pyrophosphates in Type-I Interferon Response
- The Master Regulator of the Cellular Stress Response (HSF1) Is Critical for Orthopoxvirus Infection
- Code-Assisted Discovery of TAL Effector Targets in Bacterial Leaf Streak of Rice Reveals Contrast with Bacterial Blight and a Novel Susceptibility Gene
- Competitive and Cooperative Interactions Mediate RNA Transfer from Herpesvirus Saimiri ORF57 to the Mammalian Export Adaptor ALYREF
- The Type III Secretion Chaperone Slc1 Engages Multiple Early Effectors, Including TepP, a Tyrosine-phosphorylated Protein Required for the Recruitment of CrkI-II to Nascent Inclusions and Innate Immune Signaling
- Yeasts: How Many Species Infect Humans and Animals?
- Clustering of Pattern Recognition Receptors for Fungal Detection
- Distinct Antiviral Responses in Pluripotent versus Differentiated Cells
- Igniting the Fire: Virulence Factors in the Pathogenesis of Sepsis
- Inactivation of the Host Lipin Gene Accelerates RNA Virus Replication through Viral Exploitation of the Expanded Endoplasmic Reticulum Membrane
- Inducible Deletion of CD28 Prior to Secondary Infection Impairs Worm Expulsion and Recall of Protective Memory CD4 T Cell Responses
- Clonal Expansion during Infection Dynamics Reveals the Effect of Antibiotic Intervention
- The Secreted Triose Phosphate Isomerase of Is Required to Sustain Microfilaria Production
- Unifying Viral Genetics and Human Transportation Data to Predict the Global Transmission Dynamics of Human Influenza H3N2
- ‘Death and Axes’: Unexpected Ca Entry Phenologs Predict New Anti-schistosomal Agents
- PLOS Pathogens
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Reversible Silencing of Cytomegalovirus Genomes by Type I Interferon Governs Virus Latency
- Implication of PMLIV in Both Intrinsic and Innate Immunity
- Transmission-Blocking Antibodies against Mosquito C-Type Lectins for Dengue Prevention
- Lundep, a Sand Fly Salivary Endonuclease Increases Parasite Survival in Neutrophils and Inhibits XIIa Contact Activation in Human Plasma
Prihlásenie#ADS_BOTTOM_SCRIPTS#Zabudnuté hesloZadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.
- Časopisy