Replication of ds RNA Viruses Flashcards

1
Q

Name the characteristics and genera of Reoviridae

A

Genera: Orbivirus (bluetounge virus), Rotavirus, Orthovirus
genome: segmented ds RNA, 10-12 segments, 18-27kb, eg Bluetongue 19.2 kB in 10 segments
Virion structure: komplex, 3-layered protein shell, insensitive to detergents, glycoproteins

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2
Q

Describe the replicative cycle of reoviridae

A
  • Receptor binding and endocytosis
  • Acid-induced proteolysis of the virion within the endosome (see 6) = conversion of the virion into the infectious subviral particle (ISVP)
  • Proteolytic conversion can take place already in the intestine (see 3)
  • Can penetrate through endosomal membrane into cytoplasm
  • Cytoplasm: Conversion from ISVP to core particle
  • Synthesis of capped viral mRNAs takes place in the core particle
  • Association of mRNAs with newly translated proteins to RNase-sensitive subviral particles SVP
  • „Transcription“ of mRNAs into (-)-strand RNA and formation of RNase resistent SVP with 10 dsRNA segments (reassortment?)
  • Formation of virions by assembly of preformed outer capsid proteins
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3
Q

Where does the mRNA synthesis take place in reoviridae?

A

The RNA synthesis occurs right at the tunnel structures (Turret) of the core particle. Each turret has a polymerase bound and the synthesised mRNA leaves the particle stretchy through the tunnel.

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4
Q

What are the steps of the cell entry of reovirus?

A
  • Hemagglutinin binds cellular receptor
  • Receptor mediates endocytosis into the endosome
  • Proteolysis leads to ISVP and allows penetration through endosomal membrane
  • Conversion into core particle; place of mRNA synthesis
  • RNase insensitive
  • Allows entry of nucleotides and start of mRNA transcription
    →turrets have to be selective due to dsRNA being a danger signal for the host cell, functional homolog to membrane system of +ssRNA viruses
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5
Q

What are the functions of the rotavital structural proteins?

A

VP1: RdRp, forms protein bridge between 5 ́and 3 ́ends of the genome segments
VP2: RNA binding; essential for activity of VP1
VP3: Guanylyltranserfase, methyltransferase, ssRNA binding, in complex with VP1
VP4: Hemagglutinin, fusion protein (?), cleavage required before fusion
VP6: Trimer, essential for transcription, transcriptional pore
VP7: Ca2+ dep. trimeric membrane glycoprotein in the outer capsid

Virion: VP1, 2, 3, 4, 6, 7
ISVP: VP1, 2, 3, 6
Core: VP1, 2, 3

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6
Q

What are the functions of the non-structural proteins of rotavirus?

A

NSP1: Zn-finger, RNA binding, IRF3 (interferon system) antagonist
NSP2: RNA binding, oligomer, helicase/NTPase, forms viroplasm with NSP5
NSP3: Dimer, binds 3 ́end of viral mRNAs, competes with PABP for
eIF4G-1 binding, so prevents cyclization and translation of cell. mRNAs
NSP4: Membrane glycoprotein at ER, involved in assembly, interacts with viroplasm NSP5: Phosphoprotein, RNA binding, protein kinase, forms viroplasm with NSP2 NSP6: Interacts with NSP5, is inside the viroplasm
Naked RNA ist not infectious! dsRNA is never naked, always together with viral proteins

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7
Q

explain the genome replication process of reovirus.

A
  • Conserved UGUG motif recognized in all segments by RdRp
  • Panhandle structure: interaction of 5 ́and 3 ́end of each segment (base pairing)
  • Non-coding sequences contain packaging- and assembly-signals
  • dsRNA is synthesized in simultaniously forming subviral particles→hiding dsRNA from innate immune system
  • Viroplasm: area of RNA replication in the cytoplasm
  • Subviral particles mature at the viroplasm, bud into the ER
    and receive thereby the outer capsid proteins (glycoproteins)
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8
Q

What are the characteristics of the Blue tongue virus (orbivirus)?

A

Virions
Size: 60-80 nm; non enveloped Capsid (Icosahedron)
several protein shells; ISVP
Genome: dsRNA, 18-27 kb 10-12 segments; reassortment
Replication: in cytoplasm

A mainly acute developing, seasonal disease of sheep, cattle, goat and wild ruminants
transmission via gnats
Pathogen is very variable
(24 serotypes with different virulence) need of 24 different vaccines
Distribution: Africa, North- and Middle-America, Asia, Australia, southern Europa (Spain, Portugal, Greek, Italy, Bulgary, Turkey, …)

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9
Q

How can blue tongue disease be detected?

A
  • RT-PCR: detection of viral genome - in currently infected animals detectable between 2 days to 8 months past infection (hidden genome)
  • ELISA: detection of viral proteins and antibodies- can be detected during infection and after recovery from disease (detectable from 14 days past infection onwards)
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10
Q

What actions are required after detection of blue tongue virus in cattle?

A

-disclosure
-introduction of hazard zone and monitoring zone
-prohibition of animal transport
-monitoring of suspected animals:
1. Sentinel animals
Serological testing of BTV-negative cattle since March 2007 (monthly)
2. Wild animal monitoring
3. Entomological monitoring
- Federal territory wide
- Morphological sorting and characterisation of gnats - Monitoring of the gnat pools via real-time RT-PCR

-insect killing
→immunisation of farm animals with killed vaccine

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