A2.3: Viruses

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30 Terms

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Structure of Viruses (5)

Small Size: need to be small to enter host (20-300 nm)

Fixed Size: Do not grow, assembled in full size in host

Nucleic Acid as Genetic Material: either single/double stranded DNA/RNA, hosts machinery must read it to make proteins

Capsid: Protein coat that encloses genetic material

No cytoplasm, very few enzymes: Relies on hosts metabolism. Own enzymes used to replicate genetic material and infect/burst host

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Genetic Material Basics

Single or double-stranded DNA or RNA

Circular or linear

Genetic material varies greatly in length

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Positive-Sense RNA Virus

Genes are used directly as mRNA

Positive-sense is the complement to template/antisense strand, therefore looks like mRNA

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Negative-Sense RNA Virus

Genes need to be transcribed to mRNA

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Retrovirus

RNA gene changes to double-stranded DNA (w/ Reverse Transcriptase), then to mRNA

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Drawing of DNA to Showcase Template vs. Nontemplate

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Envelope in Viruses

-Envelope is membrane acquired during lysis, or bursting process

-Takes plasma membrane of animal cell host

-helps make contact w/ other hosts (b/c looks similar to disguise itself)

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Enveloped Viruses

Infect Animal cells

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Non-enveloped Viruses

Infect bacteria or plant cells

Lose envelope as break through cell wall

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Bacteriophage Lambda Characteristics (5)

Type: DNA Virus

Envelope: Non-envelope

Genetic Material: one double-stranded, positive & negative sense DNA (AKA regular DNA)

32 Genes code for 29 proteins, 4 enzymes

Features: can engage in lytic and lysogenic cycles

Host: Escherichia coli (E. coli)

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HIV (human immunodeficiency virus) Characteristics (5)

Type: Retrovirus

Envelope: Enveloped

Genetic Material: Two single-stranded positive-sense RNA (but must be reverse-transcribed)

9 Genes or 15 proteins, 4 enzymes

Features: Contains reverse transcriptase, makes DNA from RNA

Host: Human Helper T Cell

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Lytic Cycle Characteristics

Virus is virulent, or kills host, spreads extremely fast from host to host

Disease becomes more severe as it spreads

Disadvantages: Host can produce antibodies to destroy the virus, may kill host to fast and not be able to replicate

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Lytic Cycle Process (in Bacteriophage Lambda) (7)

Attachment: proteins on virus tail bind to maltoporin on host's (E. coli) membrane

DNA entry - viral DNA enters host

DNA replication - linear, viral DNA turns circular and replicates

DNA Transcription - mRNA produced

Protein Synthesis - Host ribosomes synthesize viral proteins, head and tail proteins self-assemble into capsid

Lysis - Viral proteins puncture host's cell wall

Spread - Host bursts, releasing about 100 viruses

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Lytic Cycle Process Image

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Lysogenic Cycle Characteristics

Virus is temperate, so host is not destroyed

-remains this way until lytic cycle induced, this occurs when a stimulate activates viral genes

Benefit to Host: due to prophage (viral + bacterial DNA), new host can receive previous host's DNA

-this increased bacterial genetic diversity

*Typically used w/ hosts w/ longer lifespans so the virus doesn't go through the host population too quickly and kill off all it's potential hosts*

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Lysogenic Cycle Process (in Bacteriophage Lambda (4)

Attachment, DNA Entry (same as Lytic)

Integration - linear, viral DNA turns circular

-enzyme Integrase inserts DNA into specific location in bacterial DNA

-now viral DNA only exists as prophage, or part of bacterial DNA

Cell Division: bacterial cell divides as normal, and prophage (viral genes) copy as well

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Lysogenic Cycle Image

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Viral Evolution

Viruses must have evolved from cells

Viruses evolved through convergent evolution (not common ancestor)

-bc high structural and genetic diversity suggests multiple origins

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Obligate Parasite

What a virus is, means that it requires a host to replicate

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Progressive Hypothesis

Viruses developed from cells via modification

Evidence: cells contain virus-like components such as retrotransposons

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Retrotransposons

-Sequence of nucleotides common in DNA

-Transcribed into mRNA, then translated into several enzymes

-Enzymes make copies of the transposon DNA in reverse transcription (similar to revers transcriptase)

-Transposon copies inserted into various chromosomes at random places, similar to HIV, a retrovirus

*basically just copies DNA to RNA, then back to DNA and put in random place*

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Regressive Hypothesis

Virus developed from cells via loss (basically just remove everything unnecessary in cell)

Evidence: Viruses vary regarding complexity and self-reliance

-ex. some larger/complex viruses (smallpox) perform host functions

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Rapid Evolution of Viruses Causes (3)

Quick Generation Time, High Mutation Rate, High Intensity for Natural Selection

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Quick Generation Time

Evolution occurs between generations, each virus generation is about 1 hour (very fast)

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High Mutation Rate

Variation must exist for evolution, RNA Polymerase doesn't proofread replication errors, leads to lots of variation

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High Intensity for Natural Selection

-Host has immune mechanisms for detection and disposal of viruses

-host's antibodies target viruses' antigens

-Viruses w/ new antigens can survive (leads to very fast natural selection)

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Influenza Virus Characteristics

Enveloped virus w/ negative-sense, single stranded RNA w/ a HIGH MUTATION RATE

Transmitted between species

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Why does Influenza mutate quickly? (6)

-Genome exists as 8 separate molecules

-Has two antigens on membrane surface:

-hemagglutinin - binds to host

-neuraminidase - used to break free form host

New strain/mutation surfaces if new combinations of genome or antigen evolve

Allows for high potential for a pandemic

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HIV (human immunodeficiency virus) Characteristics Part II

Retrovirus w/ reverse-transcriptase that converts single-stranded RNA into DNA

HIGH MUTATION RATE

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Why does HIV mutate quickly? (4)

-Reverse transcriptase does not proofread

-HIV affected by cytidine deaminase, enzyme in host that converts cytosine to uracil (relevant b/c viral DNA can be mutated more when incorporated into host DNA)

-env gene - surface protein used to enter host, mutations in it allow it to enter different human cells

-New strain surfaces from any different combinations, leads to resistance to antiretroviral drugs