M2-Group 5 (Non-segmented) Flashcards

1
Q

Are Paramyxoviridae enveloped or non enveloped and what capsid do they have?

A

-Enveloped
-helical

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2
Q

What group are Paramyxoviridae in?

A

Group 5–> (-) ssRNA

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3
Q

Are Paramyxoviridae segmented or non-segmented?

A

Non-segmented

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4
Q

What does it mean to be segmented or non-segmented

A

Non-segmented: Only 1 strand of RNA
Segmented: Multiple strands of RNA that makes up genome

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5
Q

What pathogens are in Paramyxoviridae?

A

-Measles & mumps
-Parainfluenza
-Nipah & Hendra
-Rabies–>Rhabdoviridae

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6
Q

True or false: Before the measles vaccine, it did not kill many people

A

False
-Before vaccine measles killed 2 million kids per year

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7
Q

True or false: Measles has a low R0 value compared to other viruses

A

False
-Measles has the HIGHEST R0 value for a virus
-R0 = 12-18

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8
Q

What are the reservoirs and amplifying host for Nipah and Hendra

A

Reservoir: bats
Nipah host: Pigs
Hendra host: Horses

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9
Q

True or false: Nipah, Hendra, and Rabies can easily pass human to human

A

False
-usually dead end host because of high fatality rate

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10
Q

Explain Paramyxovirus life cycle

A
  1. Enters through fusion–>neutral pH
  2. Polymerase is brought with virus
  3. Buds off plasma membrane–>syncytia
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11
Q

True or False: In Paramyxoviridae the genome is not bound by proteins

A

False
-Since helical genome is always wrapped in viral proteins
-Genome size is divisible by 6

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12
Q

Differences between Icosahedral and Helical capsids

A

Icosahedral: Genome is not associated with proteins–>naked RNA
Can be immediately translated
Helical: Genome is bound by proteins –>Nucleocapsid, phosphoprotein, polymerase
Must be transcribed to make mRNA

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13
Q

Where are structural and non structural proteins found on mRNA?

A

-Structural (nucleocapsid) at the beginning 3’ end –> N
-Non-structural (polymerase)–> 5’ end –>L

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14
Q

What does polymerase stuttering do?

A

-Pol stutters at polyU to form polyA so that pol can reinitiate at start in intergenic region or go back to the beginning at 3’end

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15
Q

What determines the switch from making short mRNA transcription to the whole genome replication

A

Levels of N protein –> nucleocapsid proteins
-when there is enough N proteins to coat the genome, pol will stop reinitiating & read the entire genome

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16
Q

The expression of what protein cause infected cells to fuse with uninfected cells forming a?

A

-fusion (F) proteins
-form syncytia
-Paraymyxovirus

17
Q

Filoviridae: group, enveloped/non, capsid, segmented/non

A

-Group 5–>(-)ssRNA
-Enveloped
-Helical
-Non-segmented

18
Q

What pathogens are in Filoviridae?

A

Ebola and Marburg

19
Q

Filovirus life cycle

A
  1. Entry through endosomes –> Low pH triggers
  2. Viral polymerase is always brought with virus
  3. Virus buds off plasma membrane–>secretes 2 types of glycoprotein from polymerase stuttering
20
Q

What is Ebola’s host receptor that is used to access cytoplasm?

A

NPC1

21
Q

True or false: Once viruses spillover they adapt to humans and replicate less in original reservoir

A

True
-Ex: virus binds better to human NPC1 than bat NPC1

22
Q

What does the P/C/V gene do?

A

Polymerase stuttering that causes “editing” or insertion of either 1 or 2 As
-changes frameshift–>causes overlapping reading frames & alternative starts

23
Q

In Filoviridae, how are 2 alternative versions of GP made?

A

-Full length GP is made ONLY when polymerase stutters & adds an extra base
-secreted sGP is made in high conc to be a decoy for antibodies–>nothing happens when it binds

24
Q

Ebola viral protein?

A

Glycoprotein

25
Q

Difference in stuttering for Paramyxoviridae and Filoviridae

A

-Paramyxoviridae: addition of As not essential for making proteins, happens occasionally
-Filoviridae: Glycoprotein is ONLY made when there is stuttering