Lecture 1 Flashcards

(49 cards)

1
Q

What are the 6 infectious microorganisms?

A

-HIV
-Influenza
-STAPHYLOCOCCUSAUREUS
-STREPTOCOCCUSPNEUMONIAE
-SALMONELLAENTERITIDIS
-MYCOBACTERIUM TUBERCULOSIS

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2
Q

What are the sizes of microorganisms?

A

-Viruses (0.03-0.3uM)
-Bacteria (0.1-10uM)
-Microscopic protozoa and fungi (4-10uM)

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3
Q

Naked Viruses contains what?

A

Capsid & Nucleic acid

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4
Q

Enveloped Viruses contain what?

A

-Envelope
-Spike
-Capsid
-Nucleic acid

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5
Q

T/F: Viruses are not cells

A

True

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6
Q

Slide 13 review differences between prokaryotes and eukaryotes

A
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7
Q

T/F: Bacteria are prokaryotes

A

True

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8
Q

Fungi and parasites are what?

A

eukaryotic organisms represented by single-cell and complex organisms

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9
Q

Sources and Sites of Infection

A

-Direct vs Indirect (contact)
-Horizontal vs Vertical (mother to fetus)

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10
Q

Slide 17 memorize

A
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11
Q

What are the classes of microorganisms?

A

Microbiome (normal flora)

Commensal (resident, symbiotic, core microbiome)

Transient colonization (transients, secondary microbiome)

Opportunistic (carrier state)

Pathogenic

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12
Q

Commensal Microorganisms ??

A

Endogenous flora
> 1000 species in the human body; billions of organisms
Microbiota – cohorts of microbes in specific body regions

Provide many benefits
Process digested food
Provide essential vitamins/growth factors
Protect against invasion of pathogens

In a constant state of flux dependent on age, diet, health
Microbial populations change in response to illness or treatment with antibiotics (dysbiosis)

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13
Q

What are Virulence?

A

Circumstances that allow a microorganism to achieve infection and cause disease with varying degrees of severity

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14
Q

Virulence factors are…

A

gaining access to the body
avoiding multiple host defenses
colonization of the host
parasitizing host resources
inducing toxicity and damage

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15
Q

Influences on the Microbiome

A

-Host physiology
-Environement
-Immune System
-Host genotype
-Lifestyle
-Pathobiology

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16
Q

Human Microbiome Project is

A

Effort to sample and analyze the genome of microbes from five sites on the human body

Nose
Oral cavity
Skin
Gastrointestinal tract
Urogenital tract

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17
Q

Viral Classification

A

All viruses are intracellular pathogens

All viruses must use some components of the hosts cellular biosynthetic machinery

All viruses are nucleic acid based

All viruses replicate by assembly of components

All viruses are composed of the viral genome, a protective coat & associated enzymes/proteins

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18
Q

All viruses are composed of

A

the viral genome, a protective coat & associated enzymes/proteins

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19
Q

Nucleic Acids consist of

A

DNA or RNA
single or double stranded
linear or circular
continuous or segmented genome

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20
Q

Outer layer consist of

A

capsid (naked)
envelope
VAPs (viral attachment proteins)

21
Q

Capsid shape

A

spherical
icosahedral (icosadeltahedral)
filamentous
brick-shaped
bullet-shaped

22
Q

+RNA

A

(N)-Picorna Calici
(E)-Toga Flavi Corona

23
Q

-RNA

A

(E)- Rhabdo Filo Orthomyxo Paramyxo Bunya Arena

24
Q

+/-RNA

A

(Double Capsid)- Reo

25
+RNA via DNA
(E) Retro
26
slide 45
27
Enveloped
Pox Herpes Hepadna
28
Naked Capsid
Polyoma Papilloma Adeno Parvo(ss)
29
Slide 48
30
Viral Replication steps
1) Recognize target cell 2) Attachment 3) Penetration/Fusion 4) Uncoating of virion 5) Transcription 6) Protein synthesis 7) Replication 8) Assembly 9) Release
31
Viruses can be
-Productive: Lyse the infected cell (lytic response) Non-productive Lysogenic– integration of viral genome into host genome or formation of extrachromosomal plasmid Oncogenic transformation Persistent – latent or chronic
32
Cells can be
Permissive Allow viral replication or integration Non-permissive Do not allow replication but may be transformative Abortive – no replication but cause cell death
33
Target recognition & attachment
VAPs, host range, tissue tropism
34
Penetration
receptor-mediated endocytosis (viropexis), membrane fusion
35
Uncoating
remove coat, deliver to site of replication
36
Synthesis
early gene products – non-structural proteins, replication late gene products – structural proteins
37
T/F: Most DNA Viruses generate mRNA thru splicing
TRUE From the same DNA, many different mRNA transcripts are translated into proteins
38
Segmented RNA genomes
one segment encodes one proteins
39
Some viruses have one long RNA(-) genomic strand from which mRNA can be directly transcribed
just know this
40
Protein synthesis
requires host ribosomes, tRNA & post-translational machinery
41
At Ribosomes:
produce giant, genome-spanning polyprotein produce smaller polypeptides produce individual proteins
42
achieve preferential translation by
block mRNAs degrade host DNA & mRNA decrease cellular transcript access/concentration
43
Assembly
recognition sequences allow protein:protein, protein:nucleic acid and protein:membrane interactions for budding, viral membrane proteins (like spike proteins) inserted into plasma membrane
44
Release
bud from plasma membrane bud through ER/Golgi (remain intracellular) pass through ER & transported to surface (endosomes) cell lysis cell-cell bridge
45
DNA viruses do what?
Uses the host cell DNA-dependent, RNA polymerase to make mRNA Uses freshly made DNA-dependent, DNA polymerase to copy DNA
46
(+) RNA VIRUSES do what?
(+)RNA viruses can begin translation by ribosomes as soon as the genome is uncoated Will still encode for a viral polymerase to copy the genome for replication (RNA-dependent, RNA polymerase)
47
(-) RNA VIRUSES
(-)RNA viruses must carry a viral RNA-dependent, RNA polymerase to transcribe the negative strand into mRNA *L PROTEIN*
48
Viral genetics are
Parental (wild-type) Mutants (change in coding sequences) viruses have terrible polymerases; lots of errors Lethal mutations Deletion mutants Plaque mutants Host range mutants Attenuated mutants Conditional mutants
49
Antigenic Drift
Codon should be UUU translated to AAA (Lysine); mutation created CUU which is translated to GAA (Glutamic acid