Module 2 Flashcards

1
Q

difference between enveloped and non enveloped viruses

A

nonenveloped- have just a protein coat (capsid) surrounding their nucleic acid

enveloped- have a lipoid membrane consisting of lipids and carbohydrates (from hosts) and embedded viral proteins

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2
Q

a virus that infects bacteria is a

A

bacteriophage

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2
Q

steps of bacteriophage infection

A

Infection: binds and injects viral genetic material

replication of viral genetic information

production of viral proteins

assembly of viruses

lysis of bacterium

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3
Q

lytic vs lysogenic cycle

only for viruses that infect bacteria

A

lytic: always lyse

lysogenic: may or may not enter a lytic phase in the future, integrate their genomes into the host genome to be passed down

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4
Q

how do nonenveloped viruses infect a eukaryotic cell

A

bind to receptor to enter via endocytosis, where the capsid is degraded to release the viral genome

taken to nucleus to replicate, then leaves nucleus for assembly

released by lysis

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5
Q

their proteinaceous outer structure makes ___ viruses more tolerant to harsh conditions and disinfectants

A

nonenveloped

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6
Q

how does an enveloped virus infect a eukaryotic cell

A

attach via receptors to membrane, and since it can a lipid it fuses with the membrane and the virus is uncoated

genome replication (RNA to DNA in reverse transcription)

proteolytic processing: breaks large polypeptide into individual proteins to be functional

budding: viral particle encased in host membrane

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7
Q

what is a retrovirus

A
  • Transcribe their RNA into DNA after entering a cell and then integrating into the chromosomal DNA of the host cell
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8
Q

describe the cell wall components of gram + bacteria

A

Structural but not barrier functions

Thick peptidoglycan layer (PG)
□ A polymer of alternating NAG and NAM (Glycan chain) that is bridged by short amino acid chains (Covalent cross links)

Teichoic and Lipoteichoic Acid
□ Help to maintain the entire cell envelope structure by anchoring the peptidoglycan layer to the cytoplasmic membrane
□ Net negative change to the cell wall and can be recognized during infections by the immune system

Size of Periplasmic space is smaller

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9
Q

describe the cell wall components of gram - bacteria

A

Thin PG layer

outer membrane: barrier function

large periplasmic space

outer membrane
-porins: protein channels
-lipoproteins: links PG to OM
-LPS: net negative charge, highly immunogenic

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10
Q

ways to cross the bacterial membrane

A

facilitated diffusion
-concentration graident

primary active transport
-low to high
-ATP

Secondary active transport
-movement of one molecule down CG lets other molecule move against its CG

Group translocation
-organic molecule (glucose) transported across membrane in conjunction with chemical modification

iron uptake
-strip iron off cell surfaces or use scavenger proteins (siderophores)

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11
Q

extracellular structures: capsules, slime and biofilms

A

Capsule
○ Layer of material firmly attached to an individual bacterium

Slime layer
○ Diffused, unorganized material that is easy to remove
- Offer protection by masking the bacteria from the immune system

Biofilm
○ Polysaccharides surrounding groups of bacteria
○ Heterogenous - contain different types of organisms
○ Important for bacterial colonization of both environmental and host surfaces
○ Get an environmental signal to do this

S-layer
-proteinaceous

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12
Q

flagella vs pili

A

flagella is movement in liquids
-basal body in cell membrane, hook and filament

pili is movement on solid surfaces via twitching
-thinner and shorter than flagella
-assembled on cell surface

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13
Q

archaeal wall types

A

s-layers
pseudomurein

simple

monolayer: very heat and chemical resistant, corresponds to unique habitats

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14
Q

how do bacterial biofilms contribute to virulence

A

protection from host defences
-immune evasion (physical barrier)
-antibiotic resistance (lessened penetration and HGT of resistant genes)

enhanced adhesion
-EPS help bind to surfaces including host tissue, leading to persistant infection

quorum sensing:
-coordinate expression of virulence factors based on population density, enhancing their pathogenicity

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15
Q

what are the two ways HIV attaches to the host cell

A

non-specifically with negatively charged proteins on the host cell surface

interation with the host cell surface: proteins bring the two membranes/surfaces together
-antiviral strategies target antibodies that recognize proteins suc has CD4

16
Q

adenoviruses tend to infect what function of the host

A

respiratory

17
Q

adenovirus binding

A

Spike on virus binds to CAR on membrane, then is endocytosed
-strong association occurs via irreversible binding of integrin to the base of the spike

vesicle is acidified and the virus is released into the cell

18
Q

antigenic shift vs antigenic drift

A

Shift:
- Associated with large scale virus epidemics
- Occurs when there is a major change in the HA or NA antigens
- New strain

Drift
- Virus undergoes a gradual change in genetic makeup
- Similar genetic makeup to parent virus

19
Q

how do pili enhance bacteria infection

A

‘sticky bits’ to bind bacteria to substrates, viruses use this as first step of infection

help form biofilms and shelter bacteria from immune system and target the cell

can elicit an immune response from the host

20
Q

why is peptidoglycan structure an effective antimicrobial target

A
  • It is unique to prokaryotes
    ○ So drugs less likely to be toxic to eukaryotes
  • Many pathogens have it, so it is an ubiquitous target
  • Antibiotics targeting peptidoglycan do not need to cross the cytoplasmic membrane as the drug target is readily accessible
21
Q

major difference between immune response to bacteria and to viruses

A

○ Viral infection is inside of host cell

○ Bacterial infection is extracellular