Tuesday, July 3, 2012

July 3 Lytic Cycle continued






T2 viruses attacking an <em>E-coli</em> bacterium
T2 bacteriophage virus attacking E. coli bacterium

*** diagram handdrawn: ds DNA, ss RNA - sense; ss RNA + sense, ds RNA

Lytic Cycle: Step 3: Synthesis 

Host genome:
Genome of virus:

2 main molecule types that must be produced during synthesis:
--------------------------------------------- and ----------------------------------------------------------
*Drug targets: nucleotide analogue

SEE DNA REVIEW SLIDE POSTED ON BLACKBOARD
Master strand of DNA:
 + sense strand of RNA:
-sense strand of RNA:
---------------------------------------------------------------------------------------------------------
(SEE HANDOUT DONE IN CLASS using “Synthesis stage of viral life cycle” review item, also Fig. 13.13)
[Summarize the Steps of Synthesis for each genome type below]
- ds DNA genome



-ss DNA genome (not covered in class, use text)



- sense (non-sense) ssRNA genome



+ sense ssRNA genome



ds RNA genome (not covered in class, use text)



Lytic Cycle: Step 4: Assembly (Maturation)
*drug target: protease inhibitors
* vital parts are put together
  • capsomeres form capsid
  • genetic
    material in capsid
  • Enzymes in capsid
  • enveloped peplomers go to membrane
*Drug target: protease inhibitors


Lytic Cycle: Step 5: Release(Lysis)
* Cell releases virus particles
Phages: host cell explodes, host cell dies

Naked: host cell explodes
Enveloped:viruses bud out, gain envelope and peplomers


 Fig. 13.14 
AIDS virus budding from a white blood cell

http://www.microbiologyonline.org.uk/about-microbiology/introducing-microbes/viruses 

*** Drug: tamiflu prevents budding so the envelope can't form

Lysogenic Life Cycle  Fig. 13.11
Step 1 -Attachment (same as lytic)
Step 2 -Penetration (same as lytic)

Step 3 - Incorporation:
Viral genes: join host cell genome (integrase)****integrase inhibitors is a drug target***
Incorporated Virus genes is now called: Provirus (or called prophage)
Some known triggers which activate expression of viral genes: 
  • Chemical, physical, emotional trauma, age, hormones, immune system weak, UV radiation, AA arginine, etc.



*drug target: integrase inhibitors
Step 4 – Synthesis
_______________________________________________________________________
[Summarize the Steps of Synthesis for each genome type below]
+ sense ssRNA genome – retrovirus (NOTE: see diagram done in class)  *drug target: reverse transcriptase inhibitors


DNA genome – (not covered in class, use text)


Step 5 - Assembly
Step 6 - Release
*******

Lysogenic Life Cycle
*DNA viruses
*(RNA viruses) Retroviruses
*** draw on diagram***

Animal Virus options: 
Lystic Cycle.... imediate replication with host cell death
Lysogenic cycle (3 options): 
  1. Dormant/latent infection- triggered later
  2. Persistent infection: continous release- cell lives
  3. Tumor formation: oncogene activation
normal and abnormal (potentially cancerous cell)

Viral connection to cancer:
* Cancer is a result of uncontrolled cellular reproduction
* Proto-oncogene (prexisting) gene converted to oncogene by mutation: at least 2 mutations to change
Figure 13.15

http://www.youtube.com/watch?feature=player_embedded&v=U6QwtBl870I


Specific viruses and cancer:

*Example cancer-causing viruses:
  • Human papilloma virus = genital warts and cervical cancer
  • Hepatitis B and C viruses = liver cancer
  • human herpes virus 4= Burkitt's lymphoma (coinfection with malaria) 
  • human Herpes Virus B = Kaposi's sarcoma (coinfection with HIV-1) purple spots that attack connective tissue
Known oncogenes (turned OFF or ON to cause cancerous behavior)
  •  Loss of tumor suppressor genes
    • Normally on- inhibit mitosis in abnormal cells
  • Loss of apoptosis 
    • Normally on - cause abnormal cells to commit suicide
    • Example p53 tumor suppressor.... picture..of development of figure and toes that use apoptosis to divide them, example of child who have two fused fingers instead of seperating
  •  Angiogenesis
    • Normally off - growth of new blood vessels into mass of new cells
    • What is Tumor Angiogenesis? picture: small localized tumor.... angiogenesis causes tumor that can grow and reproduce becuse new blood vessels to bring nutrients
  •  Metastasis
    • normally off- separation and spread of cells

July 2 classnotes: Virus Lytic Life cycle

**** Test !**** until 1:15 pm
 
Bio 280 Test 2 study notes:
Lecture notes: 7/2/2012

Lytic life cycle:  Fig. 13.8
Step 1: Attachment / Adhesion
 
Receptor proteins on host cell surface (specificity)
virus binds by ligand proteins:
Phage:tail fibers
Naked:capsomeres
Enveloped:peplomers

*drug target: attachment antagonists
********* group activity*********


* Label diagram:
A. peplomer
B. envelope (made from a cell membrane)
C. capsid
d. Capsomeres
e. genomen

* cde = nucleocapsid
* which of the lettered parts would b the ligand for the host cell surface proteins? A = peplomer
* not transmitted to water because enveloped so vulnerable outside body


****** print out sheet for after exam*****







Lytic Cycle: Stage 2
PENETRATION:

Phages: lysozymes: tail fibers (uncoating not needed)

Naked virus:
1. Endocytosis or phagocytosis: *uncoating in cytoplasm
2. Direct entry: capsomeres make a hole and inserts genome (does not need uncoating)
- attachment, insert, only genome enters
Fig 13.12
*** end result: genome floating in cytoplasm***

Enveloped: 1. Fusion of envelope and cell membrane fig 13.12
*must be uncoated in cytoplasm, can’t happen with naked virus because they don’t have envelope which used to be part of old host cell membrane
Ex. Herpoviruses, paramyxoviruses, HIV
2. Endocytosis
**** uncoating in cytoplasm****
***some drugs as uncoating inhibitors***
3, direct entry
Picture: entry>> uncoating>> (viral uncoating/ effective against influenza A virus) Amantadine and Flimantadine are two uncoating inhibitors>>> nucleic acid synthesis (virus enzyme directed) >>> viral particles production>>> exit
Lytic cycle: Step 3 Synthesis
Host genome shut down
·         may break up (phages, some animal viruses)
Genome of virus directs all cell activities:
·         produces viral parts:
o    genome copies
o    proteins
§  capsomeres
§  optional enzymes
§  peoplomeres and matrix , enveloped
Nucleic acid synthesis inhibitors: acyclovir, valcyclovir (vatrox), AZT… work against VIRAL synthesis of material but not our own….
Fig. 7.1
Fig 7.7
Master strand…. With start codon AUG….positive RNA makes sense to ribosome… + sense strand… starts with 3’ which is the master strand…. 5’ Holder strand….
Starts with UAC = negative sense RNA.. some viruses have negative sense RNA.. enzymes..
Posted blackboard outlines: