Exam #1 Flashcards

1
Q

What is microbiology

A

The study of organisms too small to be seen with the naked eye

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2
Q

What are prokaryotes

What are some examples

A

Prokaryotes have no nucleus and have less complexity
Examples:
- bacteria
- archea

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3
Q

What are eukaryotes

What are some examples

A
Eukaryotes have a nucleus and are subcellular organelles
Examples:
- Protozoa(parasite)
- fungi
- works/neliminthus
-true algi
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4
Q

What are viruses and prions(?) ?

A

They are acellular
They are not a structure
They are shells of protein
They carry nucleic acid

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5
Q

What are the 3 domains of life

A

Bacteria
Archea
Eukarya

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6
Q

How old is the science of microbiology

A

Only about 150 years old

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7
Q

What needed to occur in order for science to be well established

A

1) discovery of bacteria
2) debunking of spontaneous generation
3) germ theory of disease

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8
Q

Who was the first person to publish established descriptions of microorganisms ?

A

Antony Van Leewenheok

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9
Q

What kind of bacteria did Antony van leeuwenheok find under the microscope

A
Rod
Bacteria conemove
Coxeyed
Spirokeet
Larger bacteria
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10
Q

Who is Luis pasteur and what did he do

A

He preformed Swan necked flask experiments that proved that bacteria did not spontaneously generate

He said instead bacteria that grew on an animal carcass, for example, originated from the soil, air, feces, etc.

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11
Q

What is the miasma theory of disease

A

Miasma: “bad or poisonous air” thought to cause disease

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12
Q

What is the germ theory of disease

A

Microorganisms are the cause of infectious disease

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13
Q

What did Robert Koch do?

A

He was a German physician who first linked bacteria with illness
- he linked the bacteria Bacillus Anthracis with the disease anthrax

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14
Q

How did Robert koch preform his experiment

A

1) he took an anthrax infected rodent, exposed a healthy rodent to the diseased material. The healthy rodent and he kept repeating that
2) he isolated the bacteria from the sick rodent
3) he exposed healthy rodent to anthrax bacteria and animals would get sick
3) he isolated some bacteria from experimentally infected host

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15
Q

Microbiology developments were also hampered by limitations in culturing then

A

Know this

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16
Q

What did Angelina hesse do

A

People before her would use gelatin as a solidifying but high enough temp, it would liquify

Angelina developed the use of agar as a solidifying agent
This remained solid at high temps.

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17
Q

What were Koch’s postulates

A

1) microorganisms must be present in every case of the disease
2) the organism must be grown in pure culture from the diseased animal
3) the same disease must be reproduced when a pure culture is introduced into a susceptible host
4) the organism must be recovered from experimentally infected hosts

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18
Q

What were the exceptions to Koch’s postulates

A

1) viruses cannot be cultured on standard media
2) some bacteria are difficult/impossible to grow on standard media
3) for some diseases there are asymptomatic carriers

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19
Q

Today we use modified Koch’s molecular postulates that focus on linking genetic material(DNA) wirh infection, instead of culturing

A

Know this

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20
Q

What were some further microbiological advances for immunity?
(3)

A

1) Edward Jenner - English Physician 1796: cowpox infection prevents smallpox infection (1st vaccine for smallpox)
2) Louis Pasteur: attenuated (weakened strains) used for vaccines
3) Daniel Salmon & Theobald Smith: heat killed microbes & fragments used for vaccines

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21
Q

What were some further microbiological advances for public hygiene ?
(5)

A

1) sewage disposal practices
2) hand washing

3) use of antiseptics
- ignaz semmelweis disinfects physicians hands

4) medical statistics
- Florence nightengale links infectious disease to war-related deaths

5) pasteurization
- heat food products to kill most pathogens

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22
Q

Who was martinis Beijernick

A

He discovered that mashed up filtered extract from plants infected with tobacco mosaic disease could infect healthy plants

Coined the term virus

It was not until the development of the electron microscope in the 1930’s thay the viruses were visualized

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23
Q

What were the reaping benefits of advancement in microbiology

A
Eradication 
   - smallpox 
Reductions 
    - bubonic Plague
    - cholera
    - polio
Food production
Bioremediation
Microbial ecology
Microbiome studies
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24
Q

Whag are some present and future challenges from infectious disease

A

HIV - spillover/species jump
TB - antibiotic resistance & HIV/AID
West Nile - bird movement
Whooping Cough - vaccine change
Measles - lack of vaccination
Lyme Disease - change in animal population (deer; mouse)
Chikungunya, dengue fever, zika - global travel, climate change, mosquitoes spread

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25
Q

What are the options for the objective lens?

A

4x, 10x, 20x, 40x, 60x, 100x

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26
Q

What are the options for the ocular lens?

A

10x

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27
Q

The lens on a microscope is

A

Convex (thicker in the middle and thinner on the edges)

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28
Q

How does a microscope work

A

When light enters and leaves the lens, it refracts and bends.

Where rays of light
emerge=magnified image

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29
Q

How is the resolution of magnification?

A

The resolution is defined by the sharpness of an image

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30
Q

What is the resolution of the magnification influenced by

A

1) size of lens (bigger is better)
2) wavelength of light (shorter is better)
3) use of oil (captured more light, more info)

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31
Q

What is the contrast in the magnification?

A

The contrast = difference in light intensity

Can achieve contrast in microscopy with the use of stain

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32
Q

What are the simple stains

A

Basic and acidic

33
Q

What are some basic stains

A

Basic is +

Methylene blue
Basicfuchin
Crystal violet
Safranin

It will bind to somethinb negatively charged In the cell

34
Q

What is Acidic stains

A

Acidic is -

Eosin
Rose bengal
Acid fuchsin

Will hind to + charged

35
Q

What are the differential stains-acid fast stain

A

1) used to detect mycobacteria
2) harsh stain that uses heat and phenol to drive the stain into cell and acid to rinse it away
3) mycobacteria hold onto the stain in the presence of acid, hence they are acid fast

36
Q

What is the differential stain - gram stain

A

Gram stain = distinguish gram positive (purple) from gram negative (pink)

37
Q

What does a gram positive stain have

A

If has a plasma membrane and a thick pephodlogin

38
Q

What does a gram negative stain have

A

Plasma membrane
Thin pephologylth and
Outer membrane

39
Q

What is the gram stain procedure

A

1) add crystal violet which makes all cells purple
2) add iodine and all cells are purple
3) add decolorizer all gram positive are purple and all gram negative are clear
4) add safranin all gram positive are purple all gram negative are pink

40
Q

What are other ways to achieve contrast with light microscopy

A

1) fluorescence microscopy = use antibodies to make cells grow
The secondary antibody has a yellow tag thay will glow when light is shown on it

41
Q

What are the types of prokaryotic shapes

A

Cocci - spheres
Rods (bacilli)
Vibrio - comma shape
Spirila - flangilla at the end and little wavy
Spirochetes - has internal flangilla makinh it very wavy
Pleomorphic - many shaped

42
Q

Is the nucleus an eukaryote or a bacteria or archea

Bacteria and archea are prokaryotes

A

Eukaryote

43
Q

Is a true chromosome an eukaryote or a bacteria or archea

Bacteria and archea are prokaryotes

A

Eukaryote & archea, histones are wrapped around the DNA

44
Q

Is the membrane around organelles an eukaryote or a bacteria or archea

(Bacteria and archea are prokaryotes)

A

Eukaryote

45
Q

Is the peptidoglycan cell wall an eukaryote or a bacteria or archea

(Bacteria and archea are prokaryotes)

A

Bacteria (most) & archea

46
Q

Why do most bacteria grow so fast?

A

Bacteria are small

  • they have a large surface area to volume ratio
  • compared to larger eukaryotic cell, there is relatively more surface to feed the volume
  • this Bactria can meet their nutritional needs more easily and will grow faster
47
Q

What is included of the structure of a typical bacterial cell

A

Pilus - tube for plasma DNA exchange

Plasmid - extrageonomic DNA

Ribosomes - makes protein

Fimbriae - stick to surfaces

Storage granule - store energy

Nucleoid - genomic DNA & associated proteins

Flagellum - matter that move bacteria as they spin

48
Q

What does the envelope consist of

A

The plasma membrane (inner) and cell wall ( outer)

49
Q

What is the function of the plasma membrane

A

Communication post
- responds to chemical cues (toxins, nutrients)
Major Metabolic Site
- electron transport enzymes (specific for bacteria)
Semi-permeable
- lets some substances in and keeps others out

50
Q

What does the plasma membrane structure consist of

A

Lipid bilayer

  • phosphate group
  • glycerol
  • fatty acid
51
Q

70 % of the plasma consists of what proteins

30 % consists of what proteins

A

70% = integral membrane protein, completely spans plasma membrane ( see pic in notes )

30% = peripheral membrane proteins

52
Q

Cholesterol can insert themselves between the bilayer membrane

A

Know this

53
Q

What is an ester bond

A

O
=
C-O-C

54
Q

What is an ether bond

A

C-O-C

55
Q

What are archeal plasma membranes

A

Archea has a phospholipid monolayer

The phospholipids are fused together

Very stable at high temperatures

56
Q

What are the primary catorgues bacterial cell wall

A
Gram positive
Gram negative 
Mycobacteria 
   - TB, Leprosy
Mycoplasmas
   - no cell wall,
57
Q

What does peotidoglycan structure

A

Peptid - chains of amino acid

Glycan - chains of sugar

58
Q

Peptidoglycan stricture has a D or L form

A

D-forms

59
Q

Teichoic acids do whag cod the gram positive cell wall

A

Stabilizes, anchors, cell wall

60
Q

What does the gram negative cell wall have

A

Lipopolysacxarride

- this allows things to go through the outer membrane

61
Q

Features of the outer membrane

A

Lipopolysaccharide
Clinically important
Lipid A = toxic
Polysaccaride

Porins
Forms passage for solutes to cross the outer membrane

62
Q

Why are porins needed

A

Allows transport across the outer membrane.

Polar and nonpolar molecules can not pass through, porins help that

63
Q

What is the clinical importance of gram negative cell wall

A

1) outer membrane protection
- harder for substances to penetrate, including some antibiotics and disinfectants

2) Endotoxin
- lipid A portion of LPS
- toxic to humans and other animals
- causes shock due to cytokine storm (massive release to immune signaling molecules)

64
Q

What does the mycobacteria cell wall contain

A

Mycolic acid

Which makes mycobacteria

65
Q

What is mycolic acid

And what is mycobacteria

A

Mycolic acid

  • long chain fatty acid (70 carbons in length)
    - wax-like consistency

Mycobacteria

  • slow growing
  • resistant to dessiccation(drying out)
  • hard to kill
66
Q

What are the 2 functions of the cell wall

A

1) maintains shape
- lysozyme is an enzyme that degrades cell wall. If you treat rod-shaped bacteria with lysozyme they become spherical

2) withstand turgor pressure
- pressure that builds up inside cell, prevents cell from bursting

67
Q

What are the structures outside the envelope?

A

Capsule

  • secreted from cell (gummy slimy substance)
  • protects against phagocytosis, allows adherence to surfaces

What is the clinical importance: makes disease more severe

68
Q

What are the structures inside the bacterial cell

A

1) cytoskeleton
2) storage granules
3) ribosomes
4) the nucleiod
5) plasmids

69
Q

FtsZ helps cell divide

Z-ring - contracts and gets smaller and splits the cell

A

Know this

70
Q

What is the MreB role in bacterial cytoskeleton?

A

MreB & cell wall help give the bacteria its shape and overall structure

71
Q

What are inorganic storage granules

A

Polyphosphate storage granules
Use for energy, and DNA/RNA nucleotide

Sulfite granules

72
Q

What are organic storage granules

A

Glycogen

Poly Beta-hydroxybutyrate(synthesize lipids)

73
Q

What are the special storage granules

A
Gas Vacuoles (air bags)
    - change buoyancy
74
Q

What is the magnstosomes (special storage granules)

A

1) found in magnetotactic bacteria
2) filled with magnetite(Fe3O4)
3) align bacteria with magnetic field
4) help find optimal nutrient level

75
Q

What are the ribosomes

A

1) site of protein synthesis
2) made of protein and RNA
3) bacteria have 70s ribosomes and eukaryotes have 80s

Very abundant in bacteria & very important

76
Q

What is the nucleiod

A

1) bacterial genomes
- supercoiled
- usually circular
- 1 single piece of dsDNA
2) exceptions
- some linear genomes
- some bacteria with multiple chromosomes

77
Q

What are plasmids?

A

1) extragenomic pieces of DNA
2) most bacteria have them (1-several)

3) contain few genes
- encode many beneficial traits
- required genes (e.g. DNA replication) are on genome

78
Q

Types of plasmids

A

1) conjugative plasmids
- allow for swapping of genetic material
2) resistance plasmids
- confer resistance to antibiotics
3) virulence plasmids
- contain genes that encode toxic products
4) metabolic plasmids
- allow bacteria to breakdown unusual energy sources

79
Q

Fertility plasma can swap antibiotic resistant genes and swap between cells of different species

A

Know this