Unit 1: Core Concepts In Pathogen Biology And Immunology Flashcards
What are the 7 Baltimore classifications?
1) dsDNA
2) ssDNA
3)dsRNA
4)ssRNA (+ve)
5)ssRNA (-ve)
6)ssRNA +ve RT
7)dsDNA RT
What is the general sequence of events for virus replication?
Attachment (spike proteins) - entry - uncoating - gene expression - replication - assembly - release
(DNA pretends to be chromosome, RNA pretends to be mRNA)
What is the difference between positive and negative sense RNA?
-ve sense like dsRNA requires use of RNA dependant RNA polymerase (RdRp)
Positive can be read by ribosomes
Negative is the copy of the positive
Chemically the same, different coding ability
Why do viruses gain entry to cells via endocytosis?
Entry without killing the cell - eg can present as a ligand to a receptor without alerting immune responses
What class of virus integrate into the host genome?
Retroviruses
All RNA viruses require what as an intermediate?
dsRNA intermediate - except retroviruses
Plus strand translated directly, complementary copy transcribed to messenger senses before translation (neg sense)
Enzymes that copy nucleic acid work in what direction?
5’ to 3’
Why do cells take up virus particles?
Endocytosis normal process (activated receptors internalises), maturation + fusion with lysosomes
What examples of viruses have a lipid bilayer and what is present here?
Virally encoded proteins
Hepatitis C, influenza A…
Rabies has matrix protein
what is the function of virus particles?
- protect viral nucleic acid from degradation
- machinery to deliver n.acid to uninfected cell
- transport from one host to another
transport from one cell to another - factor for determining virus tropism
- some protect n.acid from degradation inside cell; machine for efficient replication
what processes occur in order to drive virus binding to host cell surface receptors?
decrease in pH = conformation shift in r.binding protein = fusion to v.membrane to surface membrane
first c.change to embed into host membrane, second c.change brings 2 membranes = pore formation and membrane fusion
give some examples of fusion triggers and an example virus/ fusion protein
receptor binding - HIV (gp41)
low pH - Influenza A (HA)
how do non-enveloped viruses enter cells?
nucleic acid ‘injected’ into cell: attachment - conformational shift = pore through cell membrane - translocation across membrane into cell - replication
OR
attachment - endocytosis - acidification = fusion proteins make membrane pore - nucleocapsid core released in cytoplasm - transcription
features of Baltimore group 1 viruses
-large genome
-nucleus replication
-replicates as an episome
-herpesvirus, chichenpox
-poxvirus replicates solely in cytoplasm
features of Baltimore group 2 viruses
-smaller genome
-dsDNA intermediate circle mechanism
nonenveloped
-in rapidly dividing cells
-parvovirus
features of Baltimore group 3 viruses
-genome 10-12 segments of dsRNA
-replicate in cytoplasm
-icosahedral capsid doesn’t completely disassemble during cell entry
-bluetongue virus
features of Baltimore group 4 viruses
-most common type
-messenger sense RNA genome
-replication in cytoplasm
-Polio, FMDV, Flavivirus