samira mubareka , md dept. microbiology and division of infectious diseases
DESCRIPTION
Samira Mubareka , MD Dept. Microbiology and Division of Infectious Diseases Sunnybrook HSC and Research Institute [email protected]. Mandell Field’s Virology Clinical Virology (Hayden) Red Book TWIV: This Week In Virology (iTunes) http://www.twiv.tv/ - PowerPoint PPT PresentationTRANSCRIPT
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Samira Mubareka, MD
Dept. Microbiology and Division of Infectious Diseases Sunnybrook HSC and Research Institute
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Mandell Field’s Virology Clinical Virology (Hayden) Red Book TWIV: This Week In Virology (iTunes)
• http://www.twiv.tv/ Persiflager’s Infectious Diseases
Puscast (iTunes)
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DNA RNA
AcuteAdenovirusParvovirusPoxvirusHHV6/7
LatencyHSV, VZV, CMVPolyomaviruses
OncogenicEBV, HHV8HBVPapillomaviruses
Arthropod-borne/zoonoticArenavirusesAlphavirusesBunyavirusesFlavivirusesRhabdoviruses
P2P
RetrovirusesHIV I/IIHTLV I/II
RespOrthomyxovirusesParamyxovirusesFiloviruses
GIPicornavirusesCalicivirusesHCV
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Reverse genetics
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New platforms:• Mass spec• High-throughput screening• Confocal and immunofluorescence
microscopy• Flow cytommetry• Tissue culture, VLPs
Sequence databases, bioinformatics RNAi Genomics and novel animal models
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Nature Reviews Microbiology 5, 453-463 (June 2007)
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Fields’ (Skip Virgin):• Sequential: more readily correlated with disease• Stochastic events and bottlenecks
Viral determinants vs. host selection• Integrated effects of host genetic variations
Immunogenetics• Other considerations:
Tissue tropism Viral inoculum (effect on incubation period & outcome;
eg. ebola) Route of transmission Socioeconomic factors/poverty
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• Entry via: •contact /MM (incl sexual)•Parenteral• oral (organ infectivity=109 pfu/g)
•Target cells: monos, macrophages, DCs GP binds host cell receptor (DC-SIGN?) hepatocytes, splenocytes, fibroblasts, adrenal cortical cells
• Viremia: 106-108 pfu/ml; direct EM+RNA polymerase
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Extensive liver, spleen, adrenal, gonadal necrosis without infiltration:
• Hepatcellular necrosis with ghostlike cells• Intracytoplasmic inclusion bodies• Tissue damage correlates with viral Ag and
NA• Elevated LFTs; coagulation
dysfunctionhemorrhage (GI bleeding)• Adrenal involvementhypotension
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Lymphoid depletion in lymphatic tissues with minimal infiltrate; lymphopenia (T cells and NKs)• TNF-related apoptosis-inducing ligand (TRAIL)• Fas death receptor pathways• Pro-apoptotic NO
Proinflammatory cytokines• IL-6/8/10/12, IP-10, MCP-1, RANTES, TNF-α,
reactive oxygen and nitrogen spp.increased vascular permeability
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IFN-antagonism: VP35 (block IRF-3) & VP24
GP, secreted (putative): vascular injury & hemorrhagic diathesis
Endovascular lesions not consistently seen in humans; intact vascular endothelium in animal models, though increased permeability noted
Persistence: viral RNA identified in semen up to 100d post-infection
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Horimoto, T. Nature Microbiology Reviews 2005;3:351-600
Subtyping:16 HA9 NA
A/Toronto/R8557/2009(H1N1)
Virus typeGeographic origin
Virus subtype
Strain #Year
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K. Shinya, Nature, 2006;440:435-436
Nasal mucosa
Paranasal sinuses
Bronchus
Bronchiole
Alveolus
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Krug, RM, Lamb, RA Orthomyxoviridae: The Viruses and Their Replication 2001 Fields Virology. 4th edition, editors: Knipe DM, Howley PM,. Philadelphia: Lippincott Williams & Wilkins.
NA
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Hale, et al. J Gen Virol 2008;89:2359-2376
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1918 HA (Ian Wilson,Scripps)Connenello & Palese. Cell Host & Microbe, 2007;2(4):207-209
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www.clinical-virology.org/gallery/images/em/rabies2.jpg
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Bites: local replication in striated muscle Other routes: aerosol, parenteral, Tx, oral,
vertical Viral GP binds host cell receptors in NMJ:
• post-synaptic nicotinic ACH receptor; hence fox is susceptible & possums are resistant
• CD56• Neurotrophin receptor p75
Retrograde motor neuron transport (50-100mm/d) via viral P protein-dynein interactiontransynaptic transfer of nucleocapsid (viral G protein)
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Diffuse centrifugal spread (NOT viremia)
Viral shedding in lacrimal & salivary glands
Immune response: none until symptom onset
Neutralizing antibody CD4+ T cells and B cells central; viral
N protein epitopes
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Furious rabies (brainstem, CN, limbic)
Paralytic rabies(medulla, spinal cord)
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PV capsid interacts with host cell receptor CD155
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Virology. 2006 Jan 5;344(1):9-16
100 TCID50infection
Resistance to acid
Fecal shedding=6 weeks
Replication in tonsils/Peyer’s patches (1-3d)
Deep cervical/mesentericnodes with minor viremia
RES (LN/BM/liver/speen)With major viremia
CNS invasion(across BBB & retrograde)
Cutter’s vaccine incident & provocation poliomyelitis
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Virus Res. 2005 Aug;111(2):175-93
Immunofluorescence analysis of CD155
tonsil Peyer’s
appendix rectum
PV1 capsid proteins in L ant horn of spinal cord 33h post- gastoc
Infection of CD155tg mouse
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Virus Res. 2005 Aug;111(2):175-93
PV incorporated into endosomes at NMJ
after viremia and muscle seeding or
GIvagal nerve
Neurovirulence
• Sabin strains• 5’ UTR mutations destabilize secondary structure• VP 1,3,4 (PV1)• VP 1 (PV2)• VP 1,3 (PV3)
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Innate immunity (type 1 IFNs)
Humoral immunity (not sterilizing)• Persistent enteroviral infections in Ig-
deficient states• Neutralizing epitope in capsid protein
VP1 and 2C protease contain T cell epitopes
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Nature Reviews Microbiology 5, 453-463 (June 2007)
Viral E2 binds putative host cell receptor CD81
Primary replication in liver within 2d of infectionviremia
vRNA isolated from PBMCs, LN, spleen, brain, adrenals, BM, pancreas, thyroid
Quasispecies result of stochastic events
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http://www.nature.com/onc/journal/v25/n51/fig_tab/1209941f4.html
K/O in HCV-permissive cells
K/O
in
HC
V-
per
mis
siv
e ce
lls
NS5 & E2 interfere in JAK/STAT
pathway
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Nature Reviews Immunology 5, 215-229 (March 2005)
T cells key: hosts who have robust CD4+ response clear virus
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Elevated AST temporally relates to CD8+ cytotoxic activity and fall in VL
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Inflammation & Fibrosis Periportal lymphocytic
infiltration, hepatocellular necrosis
Mediated by NK and T cells as well as hepatic stellate cells (fibrogenic, synthesis of collagen)
Steatosis Core protein & genotype 3 are
key viral determinants Block assembly & release of
VLDL, interfere with PPARα Mitochondrial injury
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Hepatocellular carcinoma HCV does not integrate into the host genome HCC due to ongoing fibrosis, oxidative stress, etc… Core protein, S3, NS5A/B may be oncogenic by
modulating cell proliferation
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Lymphoproliferative disorders• Mixed cryoglobulinemia (polyclonal IgG & IgM,
types II and III respectively) due to clonal B cell expansion Small vessel vasculitis Peripheral neuropathy MPGN
• NHL *Porphyria cutanea tarda, lichen planus Sjogren’s syndrome Chronic polyarthritis
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