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virus

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卡片总数: 21内容版本: v4公开卡包更新时间: 8/1/2026

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#1
正面 (问题)

characteristics of viruses (june paper)

背面 (解答)

• living/non-living • small, 10nm to 300nm • acellular (no membrane bound organelles) • organelles, cytoplasm • capsid capsomeres • geometric shape, crystalline • metabolic processes, respiration • genetic material, RNA/DNA • reproduce and replicate • host cells’ enzymes, RNA polymerase for transcription, ribosome for translation • obligate parasite • show metabolic activity • can grow and develop

#2
正面 (问题)

what is genome’s structure

背面 (解答)

• single/several, circular/linear • DNA/RNA • ss/ds

#3
正面 (问题)

capsid structure

背面 (解答)

• determined by the viral genome • composed of p subunits called capsomeres • capsid and viral NA= nucleocapsid

#4
正面 (问题)

envelope structure

背面 (解答)

• composed of phospholipids and glycoproteins arranged to form the lipid bilayer • derived from the host cell membrane by budding • embedded with viral glycoprotein spikes - involved in host cell recognition

#5
正面 (问题)

what are the five stages for viral replication

背面 (解答)

• attachment • penetration (digest cell wall) • replication (genome) • maturation (assembly) • release

#6
正面 (问题)

how does the viral nucleic acid enters a bacterial cell

背面 (解答)

• when tail fibres of t4 bacteriophage attaches to receptors on the bacterial host cell wall, • it will release lysozyme, an enzyme that digests the bacterial cell wall resulting in release of molecules that changes the base plate conformation • in turn causes the tail sheath to contract and thurst the hollow tube through the bacterial cell • viral DNA genome will then be injected into the bacterial host cell via the hollow tube

#7
正面 (问题)

where is the lysogenic cycle found

背面 (解答)

lambda phage: undergoes both lytic and lysogenic cycles (aka temperate phage)

#8
正面 (问题)

function of temperate phage

背面 (解答)

incorporate its DNA into the bacterium’s DNA to form a (non-infectious) prophage OR replicate by means of the lytic life cycle and cause lysis of the host bacterium

#9
正面 (问题)

what possible defense mechanisms of bacteria against phages?

背面 (解答)

• mutant bacteria with receptor sites that are no longer complementary to the phage attachment sites • develop restriction enzymes that recognize foreign phage DNA and cleave them. Modify bacteria’s own DNA to prevent attack by restriction enzymes

#10
正面 (问题)

what organ does the influenza virus target

背面 (解答)

epithelial cells of the respiratory tract; virus binds to the sialic acid receptor

#11
正面 (问题)

what is a retrovirus

背面 (解答)

• RNA virus • contains reverse transcriptase • produces DNA from its RNA genome • dsDNA incorporated into host genome (provirus)

#12
正面 (问题)

what is an obligate parasite

背面 (解答)

• cannot live independently of its host • depends on its host to complete its life cycle

#13
正面 (问题)

why can viruses be regarded as non-living organisms?

背面 (解答)

• acellular and lack cellular organelles • do not carry out metabolism • lack ability to REPRODUCE on their own independently and only undergo REPLICATION in living cells • do not GROW and undergo developmental changes and require a host cell–> new products such as coat protein and nucleic acids • do not respond to stimuli when outside the host cell • ONLY EVOLVE by natural selection WITHIN A HOST CELL

#14
正面 (问题)

describe the replication process

背面 (解答)

• inside the cell, the bacteriophage DNA is IMMEDIATELY TRANSCRIBED –> mRNA using host RNA polymerase • high virulent phages–> early proteins that completely TAKE CONTROL –> degrade host cell DNA into nucleotides • e coded take over BACTERIUM’S MACROMOLECULAR synthesising machinery for own use • use host cell NucLEOtiDES to synthesise many copies of phage DNA

#15
正面 (问题)

define antigenic drift

背面 (解答)

a mechanism of variation by viruses that involves the accumulation of mutations in the genes encoding the surface glycoproteins of the virus. resulting viruses have surface antigens/glycoproteins that have a different conformation from prev virus strain

#16
正面 (问题)

define antigenic drift

背面 (解答)

a mechanism of variation by viruses that involves the accumulation of mutations in the genes encoding the surface glycoproteins of the virus. resulting viruses have surface antigens/glycoproteins that have a different conformation from prev virus strain

#17
正面 (问题)

define antigenic shift

背面 (解答)

sudden and major change in surface antigens of a virus and occurs; when 2/more different strains of a virus/strains of 2/more diff viruses combine to form new subtype specific type of genetic reassortment that confers a phenotypic change; enabling a flu strain jump from animal specieis to another

#18
正面 (问题)

characteristics of viruses

背面 (解答)

• obligate parasites: totally dependent on a host cell for replication • genome is made up of only 1 type of nucleic acid: DNA/RNA • viral components MUST ASSEMBLE into complete viruses to be able to infect another cell

#19
正面 (问题)

describe the maturation process of lysogenic process

背面 (解答)

phage genome no longer repressed–> phage components produced using host metabolic machinery more copies of viral genome produced by DNA replication using host cell machinery bacteriophage components then assemble into complete virions

#20
正面 (问题)

describe the genome in an influenza (enveloped) virus

背面 (解答)

influenza genome organised into 8 segments of ssRNA RNA genome is a -ve strand; packaged with protein–> helical nucleoprotein form: 3 RNA segments coding for 3 different polymerases–> enzyme complex: RNA-dependent-RNA-polymerase/ RNA replicase: replication and transcription other 5 RNA segments code for haemaglutinin, neuraminidase, nucleoprotein etc

#21
正面 (问题)

how does new strains of influenza virus arise (drift)

背面 (解答)

new strains of viruses are formed as a result of the accumulation of mutations in the gene leading to changes in ribonucleotide sequences known as antigenic drift due to lack of proof reading ability of RNA-dependent-RNA polymerase in influenza, HIGH RATE of replication and the viral RNA is ss and do not have backup copy to carry out REPAIR MECHANISM–> changes in the conformation of the glycoproteins