Virology test 1 lecture 6 Flashcards

2/05

Last week went over DNA ss, ds, and ds with reverse transcription

Today/wed will go over RNA viruses

DNA -> replication (dna polymerase) -> more DNA

DNA -> transcription (rna polymerase) -> mRNA

mrna -> translation (ribosomes in cytoplasm) -> protein

in RNA viruses, both replication and transcription use RNA templates (both are RNA-dependent)

• only RNA genome
• use RNA replicates, so must be RNA dependent

didnt go over this

• is labile and transient
  • DNA is NOT. DNA is more stable
• most RNA replicate in cytoplasm
  • DNA usually replicate in nucleus (except poxvirus)
• cells cannot replicate RNA, thus all RNA viruses (except retroviruses) must encode an RNA dependent RNA polymerase (replicase and transcriptase)
• genome structure determines mechanisms of transcription/replication
• RNA viruses highly prone to mutations and lack proofreading activity (higher mutation rate and less stability/higher polymerase activity)
• majority of human viral pathogens are RNA viruses

• cell produces its own mRNA in nucleus (transcription of its own DNA)
  • cell does DNA -> RNA (DNA dependent RNA polymerase)
• cells infected by RNA viruses lack enzymes to make mRNA from viral RNA genome (the cell itself cannot do this)
• thus, RNA viruses had to develop their own enzymes to generate mRNA
  • viral RNA dependent RNA polymerase (RdRp)

viral RNA dependent RNA polymerase

in order to make RNA from RNA, bc cell itself only carries DNA dependent RNA polymerase normally

identical to coding DNA strand

complementary to template DNA strand

plus (+) configuration

minus (-) configuration

+ strand rna virus

- strand RNA virus

Based on relationship btw genomes of viruses and mRNA

mRNA by definition = coding strand (remember from before)

- complementary to template strand in DNA

So mRNA = (+) configuration (+ RNA)

And mRNA’s complement has (-) configuration

Virus w/ ssRNA genome in same orientation as its mRNA is called a + strand RNA virus

So + rna viruses are ready to translate

= they immediately infect you, they do not need anything in order to translate except the cell functioning (what I said myself)

- strand RNA viruses go thru diff mechanism, they do not directly translate (they must first transcribe)

+ RNA virus

functional

• bc they can translate themselves directly, dont need to transcribe

• (-) strand RNA viruses
• DS RNA viruses

for these, 1st event after genome penetration is transcription

• done by viral proteins (like RdRp) that enter cell together with genome in virion particle

(+) RNA, bc just coding for RdRp is sufficient, since it can directly translate and make proteins after entering cell

• thus, it will make RdRp after it translates

(-) strand and DS RNA viruses, because they require RdRp for initial TRANSCRIPTION of (-) strand to make mRNA (+) after entering the cell

• their first event in the cell is transcription, so they need to bring RdRp in order to be able to

+ mRNA that contain mRNA genomes, but DO NOT TRANSLATE THEIR mRNA

-> reverse trancsription

• 4th group – retroviruses - are + strand RNA viruses - they don’t translate - do reverse transcription (RNA -> DNA)

1. (+) - viral genome can be directly used as mRNA
2. (-) - viral genome must first be transcribed into mRNA

• virus containing mRNA in their genome
  • they first translate
• those that dont (- strand RNA, ds RNA)
  • they first transcribe

• do not carry mRNA as genome
• require viral-encoded transcriptases contained in their virions
• virion genomic RNA = template for transcription, not translation

Only + strand can translate

Other 2, transcribe

Retrovirus exception ( use DNA as intermediate)

exception to written above

carry mRNA genome

BUT use DNA as intermediate in their replication

- and ds rna are NOT immediately infectious like the + rna is (bc it directly translates)

Replicase uses original genome as template to produce mRNA (make RNA of opposite sense, so - produce + and + produce - rna)

- these intermediate RNAs serve as templates

1. input strand
   
   • transcribed into complementary sequence of opposite polarity, type 1 replicative intermediate (RI-1)
2. -> this complementary strand
   • template for formation of genomic-sense RNA strand (type 2 replicative intermediate, RI-2)

Mechanism of replication

Input -> complementary strand -> make more of original strand using complementary strand (I think this is what last slide showed too)

• virion RNA is the template in RI-1
• RI-1 produce RNA of opposite sense to virion RNA
• RNA that is complementary to virion RNA is template in RI-2
• RI-2 is intermediate for expression of RNA of the same sense of the virion

RNA virus replication -> error frequency of RNA-directed replication -> quite high compared to DNA

• mismatch base incorporation in DNA is 10^-7 to 10^-9
• mismatch base incorporation in RNA is 10^-4 to 10^-5
• also no proofreading or editing repair in RNA like there is in DNA
• thus, infection of cells w/ RNA viruses can lead to generation of defective/mutated viruses -> significant role in viral pathogenesis and evol

RNA virus replication has high frequency for mistakes

• much more than DNA

(+) sense RNA viruses

polio, common cold, Hep A

(+) sense RNA viruses

rubella

(+) sense RNA viruses

yellow fever, Hep C, dengue

(+) sense RNA viruses

COVID, SARS, MERS, common cold

retroviruses

HTLV is oncogenic -> leukemia in humans

(-) sense RNA viruses

measles, mumps, RSV

(-) sense RNA viruses

rabies

(-) sense RNA viruses

flu

(-) sense RNA viruses

resp distress hemorrhagic fevers

DS RNA viruses

resp/GI infections

Rna viruses can be enveloped or naked

Enveloped

- ss genome

- segmented (can do reassortment)

- flu

- nonsegmented

- MMR, rsv

- rabies

- ss reverse transcriptase

Nonenveloped

- ssrna

- picornavirus

- ds rna

-reoviruses

• (+) RNA strand which is = mRNA
• infectious
• can be capped/polyadenylated
  • ex: some RdRps make mRNA caps and make poly A mRNAs
• this (+) RNA encodes -> virus specific RNA-dependent RNA polymerase (RdRp)
• RdRp is NOT already present bc not needed IN the virion - it is created by the viral mRNA
• mRNA bind ribosomes -> viral proteins
• translation -> polyproteins -> post translationally cleaved into diff proteins w/ viral proteases
• after RNA polymerase is created by the viral mRNA
  • -> (-) strand RNA template (RI) is made
    • RNA template - generates more mRNA + to replicate viral genome

Not in virion bc directly infectious, so it makes it (protein)

- after RNA pol translated, the (-) template is made, as a template to make more mRNA + replicate genome

the enzyme ENCODED by (+) RNA viruses

• created when the (+) RNA is directly translated (on host cell ribosomes) to make the proteins and cleaved = gives rise to this polymerase
• not in viron bc not required for mRNA translation
• used for replication of viral RNA
• this and other viral proteins are needed for viral RNA synthesis
• encoded as polyprotein that is cleaved by virally encoded proteases

• acts as mRNA -> directly translate to make viral proteins
• serve as template for replication to make more viral RNAs

directly/right away

shortly after penetration into the cell

Example of how this happens in polio

1.virion release the mRNA into host cell

2.Go directly to ribosomes to translate

3.Then cleaved by proteases

4.In nucleus, viral mRNA do genomic replication

5.Exit membrane (mRNA) w/ capsid proteins and etc. all formed correctly

Block synth of host cell proteins

Don’t have 5’ cap, but have “ VpG” - allows virus to stop synth of host cell proteins

Translation -> make polyprotein

- produced thru autocleavages (see proteases 3C and 2A)

= make P1, P2, P3

- P1 -> capsid proteins

- P2/P3 make other regulatory proteins

Polio virus – 1st viral capsid completely elucidated in structure

Capsid proteins assemble into protomer, then pentamer, then procapsid, provirion, then virion

cellular mRNA has 5' cap to protect from degradation + assist ribosomal binding in translation and has 3' end poly A tail, also protects from degradation

cap-dependent translation involves recognition of cap structure by elF4F cao-binding complex that recruits ribosomes to the mRNA for translation initiation

but, (+) RNA (like picornaviruses) - use cap-independent mechanism to use internal ribosome entry sites (IRES)

Used by many RNA viruses

5’ cap structure – allow recognition by ribosome (cap recognition site allow binding)

These viruses destroy possibility …

• viral proteinase 2A cleaves eIF4G to inhibit cap-dependent translation (cleaves important factor that recruits ribosomes_
  • host translation system becomes unusable to translate its own cellular mRNA
  • viral genome contains region 5' to AUG initiation codon
  • internal ribosome entry site (IRES) directs ribosomes to initiate translation that is independent of CAP structure and internal to mRNA

2A cleaves important factor that recruits ribosomes

- host can no longer translate own cellular mRNA

Block synth In host cell of proteins

shut down cellular protein synthesis

• unusual mechanism for turning off translation of cellular mRNA
  • viral proteinase 2A inactivate cellular cap translation initiation factor elF-4F which is needed for binding of 5' capped mRNA to ribosomes
  • ribosomes cannot recognize capped mRNA -> so cellular mRNA cannot be translated
  • while picornavirus does NOT have capped mRNA
    • so they have translation of their uncapped viral mRNA, which is exclusively occuring

= THUS ribosomes cannot recognize capped mRNA, so cell mRNA cant be translated

what i wrote:

2A inactivate cellular cap transl. initiation factor

ribosomes cant recognize capped mRNA -> BUT picornaviruses/these types of viruses usa LEADER signal instead that enables ribosomal recognition

= thus translation of uncapped viral mRNA occurs