-
Články
- Časopisy
- Kurzy
- Témy
- Kongresy
- Videa
- Podcasty
Characterisation of a Multi-ligand Binding Chemoreceptor CcmL (Tlp3) of
Campylobacter jejuni is the leading cause of human gastroenteritis worldwide with over 500 million cases annually. Chemotaxis and motility have been identified as important virulence factors associated with C. jejuni colonisation. Group A transducer-like proteins (Tlps) are responsible for sensing the external environment for bacterial movement to or away from a chemical gradient or stimulus. In this study, we have demonstrated Cj1564 (Tlp3) to be a multi-ligand binding chemoreceptor and report direct evidence supporting the involvement of Cj1564 (Tlp3) in the chemotaxis signalling pathway via small molecule arrays, surface plasmon and nuclear magnetic resonance (SPR and NMR) as well as chemotaxis assays of wild type and isogenic mutant strains. A modified nutrient depleted chemotaxis assay was further used to determine positive or negative chemotaxis with specific ligands. Here we demonstrate the ability of Cj1564 to interact with the chemoattractants isoleucine, purine, malic acid and fumaric acid and chemorepellents lysine, glucosamine, succinic acid, arginine and thiamine. An isogenic mutant of cj1564 was shown to have altered phenotypic characteristics of C. jejuni, including loss of curvature in bacterial cell shape, reduced chemotactic motility and an increase in both autoagglutination and biofilm formation. We demonstrate Cj1564 to have a role in invasion as in in vitro assays the tlp3 isogenic mutant has a reduced ability to adhere and invade a cultured epithelial cell line; interestingly however, colonisation ability of avian caeca appears to be unaltered. Additionally, protein-protein interaction studies revealed signal transduction initiation through the scaffolding proteins CheV and CheW in the chemotaxis sensory pathway. This is the first report characterising Cj1564 as a multi-ligand receptor for C. jejuni, we therefore, propose to name this receptor CcmL, Campylobacter chemoreceptor for multiple ligands. In conclusion, this study identifies a novel multifunctional role for the C. jejuni CcmL chemoreceptor and illustrates its involvement in the chemotaxis pathway and subsequent survival of this organism in the host.
Vyšlo v časopise: Characterisation of a Multi-ligand Binding Chemoreceptor CcmL (Tlp3) of. PLoS Pathog 10(1): e32767. doi:10.1371/journal.ppat.1003822
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003822Souhrn
Campylobacter jejuni is the leading cause of human gastroenteritis worldwide with over 500 million cases annually. Chemotaxis and motility have been identified as important virulence factors associated with C. jejuni colonisation. Group A transducer-like proteins (Tlps) are responsible for sensing the external environment for bacterial movement to or away from a chemical gradient or stimulus. In this study, we have demonstrated Cj1564 (Tlp3) to be a multi-ligand binding chemoreceptor and report direct evidence supporting the involvement of Cj1564 (Tlp3) in the chemotaxis signalling pathway via small molecule arrays, surface plasmon and nuclear magnetic resonance (SPR and NMR) as well as chemotaxis assays of wild type and isogenic mutant strains. A modified nutrient depleted chemotaxis assay was further used to determine positive or negative chemotaxis with specific ligands. Here we demonstrate the ability of Cj1564 to interact with the chemoattractants isoleucine, purine, malic acid and fumaric acid and chemorepellents lysine, glucosamine, succinic acid, arginine and thiamine. An isogenic mutant of cj1564 was shown to have altered phenotypic characteristics of C. jejuni, including loss of curvature in bacterial cell shape, reduced chemotactic motility and an increase in both autoagglutination and biofilm formation. We demonstrate Cj1564 to have a role in invasion as in in vitro assays the tlp3 isogenic mutant has a reduced ability to adhere and invade a cultured epithelial cell line; interestingly however, colonisation ability of avian caeca appears to be unaltered. Additionally, protein-protein interaction studies revealed signal transduction initiation through the scaffolding proteins CheV and CheW in the chemotaxis sensory pathway. This is the first report characterising Cj1564 as a multi-ligand receptor for C. jejuni, we therefore, propose to name this receptor CcmL, Campylobacter chemoreceptor for multiple ligands. In conclusion, this study identifies a novel multifunctional role for the C. jejuni CcmL chemoreceptor and illustrates its involvement in the chemotaxis pathway and subsequent survival of this organism in the host.
Zdroje
1. AllosBM (2001) Campylobacter jejuni Infections: update on emerging issues and trends. Clin Infect Dis 32 : 1201–1206.
2. MurphyC, CarrollC, JordanKN (2006) Environmental survival mechanisms of the foodborne pathogen Campylobacter jejuni. J Appl Microbiol 100 : 623–632.
3. Verhoeff-BakkenesL, HazelegerWC, de JongeR, ZwieteringMH (2009) Campylobacter jejuni: a study on environmental conditions affecting culturability and in vitro adhesion/invasion. J Appl Microbiol 106 : 924–931.
4. SkirrowMB (1991) Epidemiology of Campylobacter enteritis. Int J Food Microbiol 12 : 9–16.
5. YoungKT, DavisLM, DiritaVJ (2007) Campylobacter jejuni: molecular biology and pathogenesis. Nat Rev Microbiol 5 : 665–679.
6. Schmidt-OttR, SchmidtH, FeldmannS, BrassF, KroneB, et al. (2006) Improved serological diagnosis stresses the major role of Campylobacter jejuni in triggering Guillain-Barre syndrome. Clin Vaccine Immunol 13 : 779–783.
7. ZautnerAE, HerrmannS, CorsoJ, TareenAM, AlterT, et al. (2011) Epidemiological association of different Campylobacter jejuni groups with metabolism-associated genetic markers. Appl Environ Microbiol 77 : 2359–2365.
8. RhodesKM, TattersfieldAE (1982) Guillain-Barre syndrome associated with Campylobacter infection. Br Med J (Clin Res Ed) 285 : 173–174.
9. JanssenR, KrogfeltKA, CawthrawSA, van PeltW, WagenaarJA, et al. (2008) Host-pathogen interactions in Campylobacter infections: the host perspective. Clin Microbiol Rev 21 : 505–518.
10. JosenhansC, SuerbaumS (2002) The role of motility as a virulence factor in bacteria. Int J Med Microbiol 291 : 605–614.
11. DastiJI, TareenAM, LugertR, ZautnerAE, GrossU (2010) Campylobacter jejuni: a brief overview on pathogenicity-associated factors and disease-mediating mechanisms. Int J Med Microbiol 300 : 205–211.
12. SzymanskiCM, KingM, HaardtM, ArmstrongGD (1995) Campylobacter jejuni motility and invasion of Caco-2 cells. Infect Immun 63 : 4295–4300.
13. MorookaT, UmedaA, AmakoK (1985) Motility as an intestinal colonization factor for Campylobacter jejuni. J Gen Microbiol 131 : 1973–1980.
14. NachamkinI, YangXH, SternNJ (1993) Role of Campylobacter jejuni flagella as colonization factors for three-day-old chicks: analysis with flagellar mutants. Appl Environ Microbiol 59 : 1269–1273.
15. WassenaarTM, Bleumink-PluymNM, van der ZeijstBA (1991) Inactivation of Campylobacter jejuni flagellin genes by homologous recombination demonstrates that flaA but not flaB is required for invasion. EMBO J 10 : 2055–2061.
16. YaoR, BurrDH, DoigP, TrustTJ, NiuH, et al. (1994) Isolation of motile and non-motile insertional mutants of Campylobacter jejuni: the role of motility in adherence and invasion of eukaryotic cells. Mol Microbiol 14 : 883–893.
17. EverestPH, GoossensH, ButzlerJP, LloydD, KnuttonS, et al. (1992) Differentiated Caco-2 Cells as a Model for Enteric Invasion by Campylobacter jejuni and Campylobacter coli. Journal of Medical Microbiology 37 : 319–325.
18. HugdahlM, BeeryJ, DoyleM (1988) Chemotactic behavior of Campylobacter jejuni. Infection and immunity 56 : 1560–1566.
19. TakataT, FujimotoS, AmakoK (1992) Isolation of Nonchemotactic Mutants of Campylobacter jejuni and Their Colonization of the Mouse Intestinal Tract. Infection and Immunity 60 : 3596–3600.
20. YaoR, BurrDH, GuerryP (1997) CheY-mediated modulation of Campylobacter jejuni virulence. Mol Microbiol 23 : 1021–1031.
21. ChangC, MillerJF (2006) Campylobacter jejuni colonization of mice with limited enteric flora. Infect Immun 74 : 5261–5271.
22. PavlovskisOR, RollinsDM, HaberbergerRLJr, GreenAE, HabashL, et al. (1991) Significance of flagella in colonization resistance of rabbits immunized with Campylobacter spp. Infect Immun 59 : 2259–2264.
23. GoldenNJ, AchesonDW (2002) Identification of motility and autoagglutination Campylobacter jejuni mutants by random transposon mutagenesis. Infect Immun 70 : 1761–1771.
24. MisawaN, BlaserMJ (2000) Detection and characterization of autoagglutination activity by Campylobacter jejuni. Infection and Immunity 68 : 6168–6175.
25. FalkeJJ, BassRB, ButlerSL, ChervitzSA, DanielsonMA (1997) The two-component signaling pathway of bacterial chemotaxis: a molecular view of signal transduction by receptors, kinases, and adaptation enzymes. Annu Rev Cell Dev Biol 13 : 457–512.
26. DjordjevicS, StockAM (1998) Structural analysis of bacterial chemotaxis proteins: components of a dynamic signaling system. J Struct Biol 124 : 189–200.
27. SandersDA, Gillece-CastroBL, StockAM, BurlingameAL, KoshlandDEJr (1989) Identification of the site of phosphorylation of the chemotaxis response regulator protein, CheY. J Biol Chem 264 : 21770–21778.
28. Stock JB, Surette MG (1996) Chemotaxis. In: F. C. Neidhardt RCI, J. L. Ingraham, E. C. C. Lin, K. B. Low, B. Magasanik, W. S. Reznikoff, M. Riley, M. Schaechter, and H. E. Umbarger, editor. Escherichia coli and Salmonella: cellular and molecular biology. 2nd ed ed. Washington, D.C: ASM Press. pp. 1103–1129.
29. BakerMD, WolaninPM, StockJB (2006) Signal transduction in bacterial chemotaxis. Bioessays 28 : 9–22.
30. MarchantJ, WrenB, KetleyJ (2002) Exploiting genome sequence: predictions for mechanisms of Campylobacter chemotaxis. Trends in Microbiology 10 : 155–159.
31. ZhangW, BroounA, McCandlessJ, BandaP, AlamM (1996) Signal transduction in the archaeon Halobacterium salinarium is processed through three subfamilies of 13 soluble and membrane-bound transducer proteins. Proc Natl Acad Sci U S A 93 : 4649–4654.
32. ParkhillJ, WrenBW, MungallK, KetleyJM, ChurcherC, et al. (2000) The genome sequence of the food-borne pathogen Campylobacter jejuni reveals hypervariable sequences. Nature 403 : 665–668.
33. DayCJ, Hartley-TassellLE, ShewellLK, KingRM, TramG, et al. (2012) Variation of chemosensory receptor content of Campylobacter jejuni strains and modulation of receptor gene expression under different in vivo and in vitro growth conditions. BMC Microbiol 12 : 128.
34. KorolikV, KetleyJ (2008) Chemosensory Signal Transduction Pathway of Campylobacter jejuni. Campylobacter, 3rd Edition 351–366.
35. Hartley-TassellLE, ShewellLK, DayCJ, WilsonJC, SandhuR, et al. (2010) Identification and characterization of the aspartate chemosensory receptor of Campylobacter jejuni. Mol Microbiol 75 : 710–730.
36. TareenAM, DastiJI, ZautnerAE, GrossU, LugertR (2010) Campylobacter jejuni proteins Cj0952c and Cj0951c affect chemotactic behaviour towards formic acid and are important for invasion of host cells. Microbiology 156 : 3123–3135.
37. MarchantJ, WrenB, KetleyJ (2002) Exploiting genome sequence: predictions for mechanisms of Campylobacter chemotaxis. Trends Microbiol 10 : 155–159.
38. Hartley-TassellLE, ShewellLK, DayCJ, WilsonJC, SandhuR, et al. (2010) Identification and characterization of the aspartate chemosensory receptor of Campylobacter jejuni. Mol Microbiol 75 : 710–730.
39. RingoirDD, KorolikV (2003) Colonisation phenotype and colonisation potential differences in Campylobacter jejuni strains in chickens before and after passage in vivo. Vet Microbiol 92 : 225–235.
40. FieldsS (1993) The two-hybrid system to detect protein-protein interactions. Methods; A companion to Methods in Enzymology 5 : 116–124.
41. AmesP, ParkinsonJS (1994) Constitutively signaling fragments of Tsr, the Escherichia coli serine chemoreceptor. J Bacteriol 176 : 6340–6348.
42. BilwesAM, AlexLA, CraneBR, SimonMI (1999) Structure of CheA, a signal-transducing histidine kinase. Cell 96 : 131–141.
43. GegnerJA, GrahamDR, RothAF, DahlquistFW (1992) Assembly of an MCP receptor, CheW, and kinase CheA complex in the bacterial chemotaxis signal transduction pathway. Cell 70 : 975–982.
44. TirodeF, MalagutiC, RomeroF, AttarR, CamonisJ, et al. (1997) A conditionally expressed third partner stabilizes or prevents the formation of a transcriptional activator in a three-hybrid system. J Biol Chem 272 : 22995–22999.
45. AbdollahiH, TadjrobehkarO (2012) The Role of Different Sugars, Amino Acids and Few Other Substances in Chemotaxis Directed Motility of Helicobacter pylori. Iranian Journal of Basic Medical Sciences 15 : 787–794.
46. de JongMH, van der DriftC, VogelsGD (1975) Receptors for chemotaxis in Bacillus subtilis. J Bacteriol 123 : 824–827.
47. StorchKF, RudolphJ, OesterheltD (1999) Car: a cytoplasmic sensor responsible for arginine chemotaxis in the archaeon Halobacterium salinarum. EMBO J 18 : 1146–1158.
48. TaguchiK, FukutomiH, KurodaA, KatoJ, OhtakeH (1997) Genetic identification of chemotactic transducers for amino acids in Pseudomonas aeruginosa. Microbiology 143(Pt 10): 3223–3229.
49. AdlerJ, HazelbauerGL, DahlMM (1973) Chemotaxis toward sugars in Escherichia coli. J Bacteriol 115 : 824–847.
50. BakkerRG, LiC, MillerMR, CunninghamC, CharonNW (2007) Identification of specific chemoattractants and genetic complementation of a Borrelia burgdorferi chemotaxis mutant: flow cytometry-based capillary tube chemotaxis assay. Appl Environ Microbiol 73 : 1180–1188.
51. GlekasGD, MulhernBJ, KrocA, DuelferKA, LeiV, et al. (2012) The Bacillus subtilis chemoreceptor McpC senses multiple ligands using two discrete mechanisms. J Biol Chem 287 : 39412–39418.
52. MesibovR, AdlerJ (1972) Chemotaxis toward amino acids in Escherichia coli. J Bacteriol 112 : 315–326.
53. LeeA, O'RourkeJL, BarringtonPJ, TrustTJ (1986) Mucus colonization as a determinant of pathogenicity in intestinal infection by Campylobacter jejuni: a mouse cecal model. Infect Immun 51 : 536–546.
54. ParsonsCM, PotterLM, BrownRDJr (1983) Effects of dietary carbohydrate and of intestinal microflora on excretion of endogenous amino acids by poultry. Poult Sci 62 : 483–489.
55. VelayudhanJ, JonesMA, BarrowPA, KellyDJ (2004) L-serine catabolism via an oxygen-labile L-serine dehydratase is essential for colonization of the avian gut by Campylobacter jejuni. Infect Immun 72 : 260–268.
56. LiuX, GaoB, NovikV, GalanJE (2012) Quantitative Proteomics of Intracellular Campylobacter jejuni Reveals Metabolic Reprogramming. PLoS Pathog 8: e1002562.
57. LuxR, ShiW (2004) Chemotaxis-guided movements in bacteria. Crit Rev Oral Biol Med 15 : 207–220.
58. WeingartenRA, TaveirneME, OlsonJW (2009) The dual-functioning fumarate reductase is the sole succinate:quinone reductase in Campylobacter jejuni and is required for full host colonization. J Bacteriol 191 : 5293–5300.
59. LineJE, HiettKL, Guard-BouldinJ, SealBS (2010) Differential carbon source utilization by Campylobacter jejuni 11168 in response to growth temperature variation. J Microbiol Methods 80 : 198–202.
60. ElliottKT, ZhulinIB, StuckeyJA, DiRitaVJ (2009) Conserved residues in the HAMP domain define a new family of proposed bipartite energy taxis receptors. J Bacteriol 191 : 375–387.
61. HendrixsonDR, AkerleyBJ, DiRitaVJ (2001) Transposon mutagenesis of Campylobacter jejuni identifies a bipartite energy taxis system required for motility. Mol Microbiol 40 : 214–224.
62. AmesP, YuYA, ParkinsonJS (1996) Methylation segments are not required for chemotactic signalling by cytoplasmic fragments of Tsr, the methyl-accepting serine chemoreceptor of Escherichia coli. Molecular Microbiology 19 : 737–746.
63. VeggeCS, BrondstedL, LiYP, BangDD, IngmerH (2009) Energy taxis drives Campylobacter jejuni toward the most favorable conditions for growth. Appl Environ Microbiol 75 : 5308–5314.
64. GoldenNJ, AchesonDWK (2002) Identification of Motility and Autoagglutination Campylobacter jejuni Mutants by Random Transposon Mutagenesis. Infection and Immunity 70 : 1761–1771.
65. FrirdichE, BiboyJ, AdamsC, LeeJ, EllermeierJ, et al. (2012) Peptidoglycan-modifying enzyme Pgp1 is required for helical cell shape and pathogenicity traits in Campylobacter jejuni. PLoS Pathog 8: e1002602.
66. HendrixsonDR, DiRitaVJ (2004) Identification of Campylobacter jejuni genes involved in commensal colonization of the chick gastrointestinal tract. Molecular Microbiology 52 : 471–484.
67. Korolik V, Ketley JM (2008) Chemosensory signal transduction pathway of Campylobacter jejuni. In: Nachamkin I, Symanski C, Blaser MJ, editors. Campylobacter. third ed. Washington, DC: ASM Press. pp. 351–366.
68. DayCJ, TiralongoJ, HartnellRD, LogueCA, WilsonJC, et al. (2009) Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions. PLoS One 4: e4927.
69. WrenBW, HendersonJ, KetleyJM (1994) A PCR-based strategy for the rapid construction of defined bacterial deletion mutants. Biotechniques 16 : 994–996.
70. WostenMMSM, BoeveM, KootMGA, van NuenenAC, van der ZeijstBAM (1998) Identification of Campylobacter jejuni Promoter Sequences. Journal of Bacteriology 180 : 594–599.
71. GaynorEC, CawthrawS, ManningG, MacKichanJK, FalkowS, et al. (2004) The genome-sequenced variant of Campylobacter jejuni NCTC 11168 and the original clonal clinical isolate differ markedly in colonization, gene expression, and virulence-associated phenotypes. J Bacteriol 186 : 503–517.
72. MisawaN, BlaserMJ (2000) Detection and characterization of autoagglutination activity by Campylobacter jejuni. Infect Immun 68 : 6168–6175.
73. ReeserRJ, MedlerRT, BillingtonSJ, JostBH, JoensLA (2007) Characterization of Campylobacter jejuni biofilms under defined growth conditions. Appl Environ Microbiol 73 : 1908–1913.
74. TramG, KorolikV, DayCJ (2013) MBDS as solvent: an improved method for assessment of biofilms. Advances in Microbiology 3 : 200–204.
Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium
Článek Serotonin Signaling in : A Serotonin–Activated G Protein-Coupled Receptor Controls Parasite MovementČlánek Regulators of Cell Cycle Progression and Differentiation Identified Using a Kinome-Wide RNAi ScreenČlánek IFNγ/IL-10 Co-producing Cells Dominate the CD4 Response to Malaria in Highly Exposed ChildrenČlánek Functions of CPSF6 for HIV-1 as Revealed by HIV-1 Capsid Evolution in HLA-B27-Positive SubjectsČlánek Decreases in Colonic and Systemic Inflammation in Chronic HIV Infection after IL-7 Administration
Článok vyšiel v časopisePLOS Pathogens
Najčítanejšie tento týždeň
2014 Číslo 1- 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
- HIV-1 Accessory Proteins Adapt Cellular Adaptors to Facilitate Immune Evasion
- Ranaviruses: Not Just for Frogs
- Effectors and Effector Delivery in
- Plasmacytoid Dendritic Cell Dynamics Tune Interferon-Alfa Production in SIV-Infected Cynomolgus Macaques
- Lu/BCAM Adhesion Glycoprotein Is a Receptor for Cytotoxic Necrotizing Factor 1 (CNF1)
- A Substrate-Fusion Protein Is Trapped inside the Type III Secretion System Channel in
- Parvovirus-Induced Depletion of Cyclin B1 Prevents Mitotic Entry of Infected Cells
- Red Blood Cell Invasion by : Structural Basis for DBP Engagement of DARC
- NsrR, GadE, and GadX Interplay in Repressing Expression of the O157:H7 LEE Pathogenicity Island in Response to Nitric Oxide
- Loss of Circulating CD4 T Cells with B Cell Helper Function during Chronic HIV Infection
- TREM-1 Deficiency Can Attenuate Disease Severity without Affecting Pathogen Clearance
- Origin, Migration Routes and Worldwide Population Genetic Structure of the Wheat Yellow Rust Pathogen f.sp.
- Glutamate Utilization Couples Oxidative Stress Defense and the Tricarboxylic Acid Cycle in Phagosomal Escape
- Serotonin Signaling in : A Serotonin–Activated G Protein-Coupled Receptor Controls Parasite Movement
- Recovery of an Antiviral Antibody Response following Attrition Caused by Unrelated Infection
- Regulators of Cell Cycle Progression and Differentiation Identified Using a Kinome-Wide RNAi Screen
- Absence of Intestinal PPARγ Aggravates Acute Infectious Colitis in Mice through a Lipocalin-2–Dependent Pathway
- Induction of a Stringent Metabolic Response in Intracellular Stages of Leads to Increased Dependence on Mitochondrial Metabolism
- CTCF and Rad21 Act as Host Cell Restriction Factors for Kaposi's Sarcoma-Associated Herpesvirus (KSHV) Lytic Replication by Modulating Viral Gene Transcription
- Gammaherpesviral Gene Expression and Virion Composition Are Broadly Controlled by Accelerated mRNA Degradation
- The Arabidopsis Silencing Pathway Modulates PAMP- and Effector-Triggered Immunity through the Post-transcriptional Control of Disease Resistance Genes
- Inflammatory Stimuli Reprogram Macrophage Phagocytosis to Macropinocytosis for the Rapid Elimination of Pathogens
- Alphavirus Mutator Variants Present Host-Specific Defects and Attenuation in Mammalian and Insect Models
- Phosphopyruvate Carboxylase Identified as a Key Enzyme in Erythrocytic Carbon Metabolism
- IFNγ/IL-10 Co-producing Cells Dominate the CD4 Response to Malaria in Highly Exposed Children
- Electron Tomography of HIV-1 Infection in Gut-Associated Lymphoid Tissue
- Characterisation of a Multi-ligand Binding Chemoreceptor CcmL (Tlp3) of
- Single Cell Stochastic Regulation of Pilus Phase Variation by an Attenuation-like Mechanism
- Cell Tropism Predicts Long-term Nucleotide Substitution Rates of Mammalian RNA Viruses
- Functions of CPSF6 for HIV-1 as Revealed by HIV-1 Capsid Evolution in HLA-B27-Positive Subjects
- RNA-seq Analysis of Host and Viral Gene Expression Highlights Interaction between Varicella Zoster Virus and Keratinocyte Differentiation
- Kaposi's Sarcoma Associated Herpesvirus Tegument Protein ORF75 Is Essential for Viral Lytic Replication and Plays a Critical Role in the Antagonization of ND10-Instituted Intrinsic Immunity
- DAMP Molecule S100A9 Acts as a Molecular Pattern to Enhance Inflammation during Influenza A Virus Infection: Role of DDX21-TRIF-TLR4-MyD88 Pathway
- Variable Suites of Non-effector Genes Are Co-regulated in the Type III Secretion Virulence Regulon across the Phylogeny
- Reengineering Redox Sensitive GFP to Measure Mycothiol Redox Potential of during Infection
- Preservation of Tetherin and CD4 Counter-Activities in Circulating Alleles despite Extensive Sequence Variation within HIV-1 Infected Individuals
- KSHV 2.0: A Comprehensive Annotation of the Kaposi's Sarcoma-Associated Herpesvirus Genome Using Next-Generation Sequencing Reveals Novel Genomic and Functional Features
- Nutrient Limitation Governs Metabolism and Niche Adaptation in the Human Nose
- Decreases in Colonic and Systemic Inflammation in Chronic HIV Infection after IL-7 Administration
- Investigation of Acetylcholine Receptor Diversity in a Nematode Parasite Leads to Characterization of Tribendimidine- and Derquantel-Sensitive nAChRs
- Intranasal Vaccination Promotes Detrimental Th17-Mediated Immunity against Influenza Infection
- -Mediated Inhibition of Iron Export Promotes Parasite Replication in Macrophages
- Variation in RNA Virus Mutation Rates across Host Cells
- A Single Amino Acid in the Stalk Region of the H1N1pdm Influenza Virus HA Protein Affects Viral Fusion, Stability and Infectivity
- Group B Engages an Inhibitory Siglec through Sialic Acid Mimicry to Blunt Innate Immune and Inflammatory Responses
- Synthesis and Biological Properties of Fungal Glucosylceramide
- HIV Protective KIR3DL1/S1-HLA-B Genotypes Influence NK Cell-Mediated Inhibition of HIV Replication in Autologous CD4 Targets
- Recruitment of PfSET2 by RNA Polymerase II to Variant Antigen Encoding Loci Contributes to Antigenic Variation in
- Human and Plant Fungal Pathogens: The Role of Secondary Metabolites
- Lyme Disease: Call for a “Manhattan Project” to Combat the Epidemic
- Enhancing Virus-Specific Immunity by Combining Therapeutic Vaccination and PD-L1 Blockade in Chronic Hepadnaviral Infection
- Suppression of Interferon Lambda Signaling by SOCS-1 Results in Their Excessive Production during Influenza Virus Infection
- Inflammation Fuels Colicin Ib-Dependent Competition of Serovar Typhimurium and in Blooms
- Host-Specific Enzyme-Substrate Interactions in SPM-1 Metallo-β-Lactamase Are Modulated by Second Sphere Residues
- STING-Dependent Type I IFN Production Inhibits Cell-Mediated Immunity to
- From Scourge to Cure: Tumour-Selective Viral Pathogenesis as a New Strategy against Cancer
- Lysine Acetyltransferase GCN5b Interacts with AP2 Factors and Is Required for Proliferation
- Narrow Bottlenecks Affect Populations during Vertical Seed Transmission but not during Leaf Colonization
- Targeted Cytotoxic Therapy Kills Persisting HIV Infected Cells During ART
- Murine Gammaherpesvirus M2 Protein Induction of IRF4 via the NFAT Pathway Leads to IL-10 Expression in B Cells
- iNKT Cell Production of GM-CSF Controls
- Malaria-Induced NLRP12/NLRP3-Dependent Caspase-1 Activation Mediates Inflammation and Hypersensitivity to Bacterial Superinfection
- Detection of Host-Derived Sphingosine by Is Important for Survival in the Murine Lung
- PLOS Pathogens
- Archív čísel
- Aktuálne číslo
- Informácie o časopise
Najčítanejšie v tomto čísle- Lyme Disease: Call for a “Manhattan Project” to Combat the Epidemic
- Origin, Migration Routes and Worldwide Population Genetic Structure of the Wheat Yellow Rust Pathogen f.sp.
- IFNγ/IL-10 Co-producing Cells Dominate the CD4 Response to Malaria in Highly Exposed Children
- Human and Plant Fungal Pathogens: The Role of Secondary Metabolites
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