Dengue Virus Overview
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![Page 1: Dengue Virus Overview](https://reader036.fdocuments.us/reader036/viewer/2022062514/55a205681a28abe4648b4632/html5/thumbnails/1.jpg)
DENGUE VIRUS
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Case-study
17 year-old female admitted into Princeton Plainsborough Hospital. The patient present the following symptoms:
• High Fever• Severe nausea • Mild nosebleeds • Joint pain • New appearance of skin rashes
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Case-study
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BACKGROUND INFORMATION
• Word origin may be derived from Swahili or Spanish
• 3 forms of dengue:
• Dengue fever (DF), dengue haemorrhagic fever (DHF), and
dengue shock syndrome (DSS)
• Arboviral infection transmitted by the Aedes aegypti mosquito
• Originates in African forests independent of humans breeds in water
storage containers slave and commerce trade brought it to South-East
Asia & “New World” in 17th-19th centuries 1800 in global tropical coasts
(Comprehensive Guidelines for Prevention and
Control of Dengue and Dengue Haemorrhagic
Fever, 2011)
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GLOBAL DISTRIBUTION
• Found in tropical and subtropical regions of the world, 2.5 billion at risk
• Endemic in more than 100 countries in the WHO regions:
• Africa, Americas, Eastern Mediterranean, South-East Asia, and Western Pacific
• South-East Asia and Western Pacific regions are the most seriously affected
(Comprehensive Guidelines for Prevention and Control of Dengue and Dengue Haemorrhagic Fever, 2011)
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EPIDEMIOLOGY
• ~ 50-100 million infections occur worldwide, 0.5 million hospitalized for DHF
• ~ 90% are children under 5 years
• Classical DF more common in adults
• frequency of epidemics observed, infection rates of the previously unexposed is 40% - 50%,
can reach 80% - 90%
• Needs coincidence of many vector mosquitoes, many people with no immunity to ¼ virus types, and
opportunity for contact
• Infection with any 1 of 4 serotypes lifelong immunity to that 1 serotype
• Provides 1-3 years of cross-protection against other 3 serotypes
• Reoccurring infection with different serotypes severe dengue
(DHF/DSS)
(CDC, 2014)
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EPIDEMIOLOGY CONT’D
• Ae. aegypti strongly attracted to humans, domesticated, and is a nervous feeder
• Bites more than one host to complete blood meal and gonotropic cycle
• Breeds in safe clean water, feeds at dusk and dawn
• Results in multiple cases in cities
• Transmission usually occurs in rainy seasons when humidity
and temperature are conducive for survival and breeding
• transport, human contact, urbanization,
drinking water supply in rural areas brought DF to
urban and rural areas globally
(Comprehensive Guidelines for Prevention and Control of Dengue and Dengue
Haemorrhagic Fever, 2011)
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PREVENTION
• Key is disease surveillance to detect epidemics
• Dengue-endemic regions should be educated about the virus,
recognize symptoms, and prevent transmission:
• Regularly remove sources of stagnant water to prevent breeding
• Use mosquito repellent, coils, and nets
• Wear long, loose clothing in the daytime
• Use nets and coils on those with DF to prevent mosquitoes
transmitting infections
• Stay in AC or well-screened housing
• Infected mosquitoes like to live in/around homes
with clean water
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EVOLUTION
• Genus: Flavivirus
• Diverse
• 4 serotypes
• 1970: Central America and Africa (DEN 1 & 2) Southeast Asia (Den1-4)
• 2004: Worldwide (Den1-4)
• 65% genome shared
• Clinical characteristics conserved
(Holmes,E & Twiddy, S, 2003)
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VIRUS STRUCTURE & COMPONENTS
Dengue
• Class IV: Positive Sense Single Stranded RNA Virus
DNA Components
• Internal Structure: 10 genes (3 structural and 7 non-structural )
Molecular Structure
• External Structure : icosahedral & 50 nm in diameter
(Kuhn, R.J. et al. , 2002)
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TRANSMISSION
• Mosquito (female mosquito)• Possibly through blood transfusions• Human incubation period ~ 4 days • Viremia lasts ~5 days • During viremia biting mosquitos are
susceptible to infection • Mosquitos incubation period ~8-12
days, which then it is infectious for life• Virus resides in salivary glands of
infected mosquito (anti-clotting factors, ect)
(Nishiura, H., & Halstead, 2007; Rodenhuis-Zybert, 2011).
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THE DENGUE VIRUS
RNA Genome
Capsid
Lipid Bilayer
Envelope Proteins
DENGUE LIFE CYCLE
1. 1. Receptor-Mediated Endocytosis
2. 2. Fusion
3. 3. Nucleocapsid Release
4. 4. RNA Replication
5. 5. Translation
6. 6. Budding
7. 7. Furin Cleavage
8. 8. Progeny Release
(Martina, B. et al, 2009)
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DENGUE LIFE CYCLE
Infected Mosquito Biting
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DENGUE LIFE CYCLEExtracellular Matrix
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DENGUE LIFE CYCLE
Cognate receptor
Dengue virus
Receptor BindingEndocytosis
Cell Membrane
Cytoplasm
Extracellular Space
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DENGUE LIFE CYCLE
Endosome
Proton Pump
Fusion
H+H+
Lowered pHConformational Change
Cytoplasm
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DENGUE LIFE CYCLE
Endosome
Proton Pump H+H+
Conformational ChangeFusion
Cytoplasm
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DENGUE LIFE CYCLE
FusionNucleocapsid Release
Cytoplasm
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DENGUE LIFE CYCLE
Nucleocapsid Release Cytoplasm
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DENGUE LIFE CYCLECytoplasm
Viral RNA
Viral RNA Translation
Ribosomes
Rough Endoplasmic Reticulum
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DENGUE LIFE CYCLECytoplasm
Viral RNA
Viral RNA Translation
Ribosomes
Rough Endoplasmic Reticulum
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DENGUE LIFE CYCLECytoplasm
Viral RNA Translation
Envelope Proteins
Capsid Proteins
RNA dependent RNA Polymerase
Rough Endoplasmic Reticulum
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DENGUE LIFE CYCLECytoplasm
Viral RNA Translation
RdRp
Envelope Proteins
Capsid Proteins
RNA dependent RNA Polymerase
Proteases
Peptidases
Cell Membrane
Rough Endoplasmic Reticulum
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DENGUE LIFE CYCLE
RNA Replication
Cytoplasm
RdRp
RNA dependent RNA Polymerase
Double stranded RNASingle stranded RNA
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DENGUE LIFE CYCLE
RNA Transcription
Cytoplasm
Double stranded RNA
RdRp
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DENGUE LIFE CYCLECytoplasm
Viral RNA
Viral RNA Translation
Ribosomes
Rough Endoplasmic Reticulum
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DENGUE LIFE CYCLECytoplasm
Viral RNA
Viral RNA Translation
Ribosomes
Rough Endoplasmic Reticulum
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R
DENGUE LIFE CYCLECytoplasm
Viral RNA Translation
Envelope Proteins
Capsid ProteinsRdRp
Rough Endoplasmic Reticulum
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DENGUE LIFE CYCLE
Cytoplasm
Viral RNA TranslationBudding
Rough Endoplasmic Reticulum
Cell Membrane
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DENGUE LIFE CYCLE
RER
Golgi Apparatus
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Golgi Apparatus
Furin Cleavage
Furin
DENGUE LIFE CYCLE
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Golgi Apparatus Cytoplasm
Extracellular Space
Cognate receptor
Progeny Release
Molecular Structure
• External Structure : icosahedral
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PATHOPHYSIOLOGY
Complement Activation
ADE of virus
T-cell Immunology
Plasma Leakage Bleeding Diathesis
Hypovolemic Shock(Nishiura, H., & Halstead, 2007; Halstead & O’rourke, 1977) ).
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PATHOPHYSIOLOGY- ADE Activation
Heterotypic antibodies
- Low concentration
- Partial neutralization
- Ie. prM
Main Result: Increase in virus replication and numbers
(Halstead et al. 2010)
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PATHOPHYSIOLOGY- ADE Activation
Heterotypic antibodies
- Low concentration
- Partial neutralization
- Ie. prM
Virus uptake- Delivery to Fcɣ receptor cells
Main Result: Increase in virus replication and numbers
(Halstead et al. 2010)
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PATHOPHYSIOLOGY- ADE Activation
Heterotypic antibodies
- Low concentration
- Partial neutralization
- Ie. prM
Virus uptake- Delivery to Fcɣ receptor cells
Replication
- Increased viral
replication compared
to virus alone
Main Result: Increase in virus replication and numbers
(Halstead et al. 2010)
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PATHOPHYSIOLOGY- Complement Activation
Anaphylatoxins
• NS1- Glycoprotein secreted by dengue
infected cells
• Activation of innate immune system on
endothelial cell surface
1) Classical complement
2) Alternative complement
Result:1) Apoptosis of endothelial cell
2) Inflammation = CYTOKINES!
(Guzman & Kouri, 2002)
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PATHOPHYSIOLOGY- T-Lymphocyte Pathogenesis
Primary Infection
DENV-1T- cell selection
(Dejnirattisai et al., 2010)
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PATHOPHYSIOLOGY- T-Lymphocyte Pathogenesis
Primary Infection
Secondary Infection
DENV-1T- cell selection
DENV-2 Clonal Expansion
Cross-Reaction(Dejnirattisai et al., 2010)
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PATHOPHYSIOLOGY- T-Lymphocyte Pathogenesis
Primary Infection
Secondary Infection
DENV-1T- cell selection
DENV-2 Clonal Expansion
Cross-Reaction
TNF-α
IFN-ɣ
IL-2
CYTOKINE
STORM
(Dejnirattisai et al.,
2010)
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ENDOTHELIAL CELL ACTIVATION
http://www.scielo.br/img/revistas/rb/v43n6/en_a13fig01.jpg
Cytokines induce changes in
endothelial morphology:
• Loss of vascular integrity
• Increased adhesion molecules
• Increased cytokine production
IMPLICATIONS: Plasma leakage
Edema Hypovolemic shock Thrombocytopenia
(Manson et al. 2003)
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COAGULOPATHY
Loss of Plasma Components
- Platelets
- Plasma fibrinogen
Immune-mediated
Destruction of Platelets
GlycocalyxDamage
- Anti-coagulation via heparansulphate
(Sellahewa, K, 2012)
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SYMPTOMS
Febrile: • Hallmark trait is fever • Convulsions may occur due to high fever (DHF)• Thrombocytopenia, leukopenia (levels more drastic
with DHF)
Critical• Plasma leakage into pleural cavities, ascites (DHF)• Subnormal temperatures, defervescence• Varying degrees of hemorrhage (worsened for DHF)
Recovery • Reabsorption of accumulated fluids• Improved vital signs• Important to monitor
Dengue Fever and Dengue Hemorrhagic Fever
(CDC, 2010)
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Case-study
Back at Princeton Plainsborough, House has ordered his team to perform an
endoscopy to check for internal hemorrhaging …
New symptom: Vomiting blood, excessive bleeding in gastrointestinal tract…
Complications: Excessive loss of fluid, increased lymphatic return, overcompensation of
cardiovascular/adrenal/renal mechanisms, anoxia = DENGUE SHOCK SYNDROME
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DIAGNOSIS
• Clinical symptoms• Often misdiagnosed with influenza,
malaria, Typhoid fever, Leptospirosis• Travel history • Viral markers IgG, IgM, and NS1 • Laboratory confirmation:
• IgM Capture ELISA• NS-1 specific assays• Lateral flow test to detect IgM & IgG
antibody, NS1 antigen
(CDC, 2010; Mayo Clinic, 2013)
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ANTIVIRAL THERAPY
DENVax
AG129 Mouse Model
7-deaza-2′- C-methyl-adenosine
• deficient for interferon-α/β/ϒ receptors• one of only models that permit infection by all 4 serotypes• used to target virus entry, membrane fusion, RNA genome
replication, assembly, & release from infected cell• targets protein E to interfere with viral replication
(Schul et al., 2007; Wilder-Smith et al., 2010)
N-nonyl-deoxynojirimycin
6-O-butanoyl
castanospermine
• treatment tested in viremia mouse model (AG129 mice) during acute phase • block viral replication
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LIVE-ATTENUATED VACCINATION
DENVax
DENVax
LATV
• based on the PDK53 DENV-2 backbone• containing pre-membrane & E genes of serotypes 1-4• tested in cynomolgus macaques• Immunogenicity & efficacy results
(Durbin et al., 2013; Osorio et al., 2011)
• contains 30 nucleotide deletion; tetravalent• tested in flavivirus-naïve adults • no significant difference in adverse events between
vaccines and placebo-recepients• Race factor influencing infectivity of LATV virus
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CHIMERIC LIVE-ATTENUATED VACCINATION
DENVax
ChimeriVax Vaccine (Sanofi Pasteur)
Mahidol
• uses 17D yellow fever vaccine virus • Phase I, II, III
• shows 57% overall efficacy • reduction of hospitalization by 80%• 89% reduction of dengue haemorrhagic fever
(Fink & Shi, 2014; Wilder-Smith et al., 2010)
• PDK-53 DEN-2 backbone
• Phase 1 trial (U.S. & Columbia)
• protective when administered in monkeys and
mice
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REFERENCES
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(2007). Secreted NS1 of dengue virus attaches to the surface of cells via interactions with heparan sulfate and chondroitin
sulfate E. Plos Pathogens 3, 183.
Avirutnan, P., Punyadee, N., Noisakran, S., Komoltri, C., Thiemmeca, S., Auethavornanan, K., Jairungsri, A., Kanlaya, R.,
Tangthawornchaikul, N., and Puttikhunt, C. et al. (2006). Vascular leakage in severe dengue virus infections: a potential role for
the nonstructural viral protein NS1 and complement. Journal Of Infectious Diseases 193, 1078-1088.
Centers for Disease Control and Prevention. (2010). Dengue. Retrieved from: http://www.cdc.gov/dengue/clinicallab/clinical.html
Comprehensive Guidelines for Prevention and Control of Dengue and Dengue Haemorrhagic Fever: Revised and Expanded
Edition. (2011). Retrieved 13 October 2014, from http://apps.searo.who.int/pds_docs/B4751.pdf?ua=1
Dejnirattisai, W., Jumnainsong, A., Onsirisakul, N., Fitton, P., Vasanawathana, S., Limpitikul, W., Puttikhunt, C., Edwards, C.,
Duangchinda, T., and Supasa, S. et al. (2010). Cross-reacting antibodies enhance dengue virus infection in humans.
Science 328, 745-748.
Dejnirattisai, W., Jumnainsong, A., Onsirisakul, N., Fitton, P., Vasanawathana, S., Limpitikul, W., Puttikhunt, C., Edwards, C.,
Duangchinda, T., and Supasa, S. et al. (2010). Enhancing cross-reactive anti-prM dominates the human antibody response in
dengue infection. Science (New York, NY) 328.
Fink, M. (2005). Dengue. Textbook of critical care (Philadelphia: Elsevier Saunders).
Guzman, M., and Kouri, G. (2002). Dengue: an update. The Lancet Infectious Diseases 2, 33-42.
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REFERENCES
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Holmes, E. & Twiddy, S. (2003). The origin, emergence an evolutionary genetics of dengue virus. Infections,
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In, L. (2003). Howard Hughes Medical Institute
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Manson, P., Cook, G., Zumla, A., and Manson, P. (2003). Manson's tropical diseases (London: Saunders).
Martina, B., Koraka, P., & Osterhaus, A. (2009). Dengue virus pathogenesis: an integrated view.Clinical
Microbiology Reviews, 22(4), 564--581.
Nature.com,. (2014). Retrieved 14 October 2014, from
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Nimmannitya, S. (1999). Dengue hemorrhagic fever: disorders of hemostasis. 184-187.
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REFERENCES
Nishiura, H., & Halstead, S. (2007). Natural History of Dengue Virus (DENV)—1 and DENV—4
Infections: Reanalysis of Classic Studies. Journal Of Infectious Diseases, 195(7), 1007--1013.
Rodenhuis-Zybert, I., Wilschut, J., & Smit, J. (2010). Dengue virus life cycle: viral and host factors
modulating infectivity. Cellular And Molecular Life Sciences, 67(16), 2773--2786.
Sellahewa, K. (2012). Pathogenesis of Dengue Haemorrhagic Fever and Its Impact on Case
Management. ISRN Infectious Diseases 2013.
Seynhaeve, A., Vermeulen, C., Eggermont, A., and ten Hagen, T. (2006). Cytokines and vascular
permeability. Cell Biochemistry And Biophysics 44, 157-169.
Srikiatkhachorn, A., and others, (2009). Plasma leakage in dengue haemorrhagic fever. Thromb
Haemost 102, 1042-9.
Srikiatkhachorn, A., and others, (2009). Plasma leakage in dengue haemorrhagic fever. Thromb
Haemost 102, 1042-9.
Stoermer, K., and Morrison, T. (2011). Complement and viral pathogenesis. Virology 411, 362-373.
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REFERENCES
Zompi, S., and Harris, E. (2013). Original antigenic sin in dengue revisited. Proceedings Of The
National Academy Of Sciences 110, 8761-8762.