Virology - 1 Fundamentals

Skern - Coffee House Notes on Virology

Skern - Coffee House Notes on Virology


Iris Bachtrog
Diese Lernkarten bieten einen umfassenden Überblick über die Grundlagen der Virologie auf Universitätsniveau. Sie behandeln die Struktur und Klassifizierung von Viren, einschließlich ihrer Symmetrie, Proteine und genetischen Codes. Die Karteikarten erklären auch die Replikation, Evolution und Pathogenität von Viren sowie ihre Rolle bei Krankheiten und Krebs. Ideal für Studierende und Forscher, die ihr Verständnis der Virologie vertiefen möchten.
Cartes-fiches
29
Utilisateurs
0
Langue
Allemand
Catégorie
Biologie
Niveau
Université
Créé / Mis à jour
28.01.2017 / 28.01.2017

Cartes-fiches

What are viruses?

*obligate intracellular parasites

*made up pf nucleic adic, protein, sometimes lipid

*does not code for ribosomes, mitochondria

*do not reproduce by division, they are assembled from pre-formed complexes

Key steps in viral life-cycles

*Attachment

*Entry

*Uncoating

*Expression of genetic information

*Replication of genetic information

*Assembly

*Maturation

*Release

Uncoating can occur...

*at the plasma membrane

*in the cytosol

*at the nuclear membrane

Expression of genetic information produces proteins for

*virus particle

*nucleic acid synthesis

*virus-host interactions

example for Class I Virus:

ds DNA Virus:

eg Herpes simplex virus type 1

example for Class II Virus:

(-)ssDNA

eg feline parovirus

example for Class III virus:

ds RNA Virus:

eg human rotavirus

example for Class IV Virus:

+ssRNA Virus

eg Hepatitis C Virus

example for Class V Virus:

-ssRNA Virus:

Measles Virus

example for Class VI Virus:

+ssRNA Virus with a DNA intermediate (Retrovirus)

Human immunodeficiency virus type 1 (HIV)

Why do viruses keep their genomes small?

*the larger the genome, the longer the time needed to replicate it

*....the larger the capsid must be

*...the higher the probability of mutations

Four strategies to keep viral genomes small:

*all viruses use cellular machinery to generate energy and synthesise proteins - viral genomes do not need to code for such machinery

*some viruses use the same region of nucleic acid to code for different proteins
----more than 1 ORF in same region of nucleic acid

----using different reading frames on one strand

---- encoding proteins on both strands

 

*some viruses produce one large RNA (PRIMARY TRANSCRIPT) which is spliced by cellular splicing machinery to generate several mRNAs

*some viruses produce single large protein POLYPROTEIN which is cleaved by viral and cellular proteases to mature proteins

What characteristics drive viral evolution?

*viruses produce a large number of descendants - viral replication generates a large number of mutants

*viruses can evolve by recombination of genomes

*certain viruses can evolve by reassortment of genome segments

large numbers of mutant viruses can be selected for fitness in new environments and hosts - new possibilities often provided by human behaviour

*high density agriculture

*water regulation

*drug abuse

*sexual practices

emerging viruses are generated from existing ones:

*known viruses change to become able to infect an immune population

*known virus is exposed to a naive population

* nown viruses changes its host range to enter a different species

which perameters limit the evolution of viruses?

*icosahedral viral capsids limit size of nucleid acid

*virus is dependent on host systems for decoding genetic information

*mutations may adversly affect activity of viral proteins

*an extremely virulent virus kills its host and therefore itself

*too many mutations lead to a non-viable virus

two types of symmtetry, found in virus particles:

*icosahedral symmetry

*helical symmetry

icosahedral symmetry:

*regular polyhedron with 20 faces
   *polyhedron has 3 types of symmetry axes: 12 five fold, 20 three fold, 30 two fold axes

VIRUS PARTICLES MUST HAVE AT LEAST 60 COPIES OF ONE PROTEIN TO OBEY ICOSAHEDRAL SYMMETRY

or multiples of 60

helical symmetry:

*proteins arranged in simple repeating unit around nucleic acid

*each protein occupies the same position, makes identical interactions with its neighbours and the nucleic acid

consequences of icosahedral symmetry:

* volume of icosahedral limits size of nucleic acid
-rules of symmetry must still be obeyed - limits number of proteins to certain multiples of 60 - 180, 240, 420, etc

difference in proteins on surface of icosahedron allows antigenic variation

consequences of helical symmetry:

helical structure formed around nucleic acid - theoretically no limit to lenght

proteins occupying identical position makes antigenic variation difficult 

viruses present in blood

Hepatitis B

Hepatitis C

viruses present in semen

HIV1

HTLV1

viruses present in feces:

poliovirus

human rotavirus

viruses present in respiratory droplets:

measles

influenza A

viruses in saliva:

Epstein.Barr virus

herpes simplex 1

viruses which are risk factors for cancer:

Hepatitis B, C

HTLV1

Epstein-Barr 

HPV

viruses which can cause long-term infections

Hepatitis B, C

HSV1

HIV1

HTLV1

Epstein-Barr

Which properties should a viral vaccine have to make it sage and efficient?

*should induce protection against a pathogenic virus without itself causing disease

*immune response generated by vaccine should resemble as closely as possible the response generated by pathogenic agent

*vaccines should induce the production of memory B and memory T  cell

*vaccines should induce long-term production with just one or few inoculations

*should be cheap

*should be seen as a clear advantage by society

Étudier