week 2 material Flashcards

1
Q

what are 2 ways to define MICROBIOLOGY?

A
  1. by the organism we’re studying
  2. the mechanism we’re using to look at the organism
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2
Q

what does acellular mean?

A

organism can NOT replicate on its own/ does not contain cells

they do have genetic material and proteins

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3
Q

what are 2 acellular agents that transmit and cause disease ?

A

virus + prions
they are not free-living

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4
Q

what is aseptic technique?

A

a method used to look at species and doesn’t contaminate other species

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5
Q

why is it called microbiology?

A

you can only see the organism with the help of a microscope

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6
Q

what microbes represent all 3 domains of life?

A

Bacteria = single-celled microorganisms

Eucarya = multicellular organisms (plants, animals, fungi and protists)

Archaea = single-celled microorganisms that can survive in all types of environments

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7
Q

How did people used to think diseases were spread?

A

MIASMA THEORY
that diseases were caused by bad air/harmful vapor and rotten food/organic material

this led to clean cities, better sanitation and the building of better drainage systems

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8
Q

what did Antoni Van Leeuwenhoek discover?

A

he made and used microscopes

he found animacules in pond water

  • single-celled protozoa/eukaryotes
  • fungi
  • algae
  • tiny animals

now known as microorganisms

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9
Q

what were some indirect evidence that MICROBES cause disease

A

JOSEPH LISTER
- surgeon
- thought disease was caused by pollen-like dust
- incorporated disinfection -> increased survival post-op + decreased post-op infections

  • disinfection = use of phenol to disinfect skin and instruments

ROBERT KOCH
- looked at the bacterium BACILLUS ANTHRACIS
- was observing mice and how they got sick

EXPERIMENT
- took the tissue of an infected mouse and inserted it into a healthy mouse
- took the spleen (organ) of infected mouse and passed it through 20 mice
- took spleen from mouse #20 who HAD SYMPTOMS OF ANTHRAX and made a broth culture
- isolated bacillus anthracis from the culture

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10
Q

what were Robert Koch’s 4 postulates (statements that he claimed to be true without any evidence) and why may they not be true

A
  1. the suspected agent had to be present in all infected individuals
  2. the agent has to be isolated + grown in pure culture (it’s only the one agent in the culture)
  3. the cultured agent will cause the disease once injected into a healthy and susceptible host
  4. the agent that was injected into the host can then be reisolated
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11
Q

why might Koch’s postulates not be true?

A

PATHOGENS ARE ONLY FOUND IN DISEASED INDIVIDUALS
- people can have the agent but also not develop the disease - depends on the host’s susceptability

ALL HEALTHY TEST SUBJECTS ARE EQUALLY SUSCEPTIBLE TO DISEASE
- subjects have different susceptibility and different reasons/causes/factors that allow them to have that disease
- can be based on their immune system in that moment

ALL PATHOGENS CAN GROW IN A PURE CULTURE
- some can’t be cultured in labs
- some microbes can NOT grow on their own or are intracellular organisms and can only grow with the help of a cell

ANIMALS CAN SERVE AS A RELIABLE MODEL FOR HUMAN DISEASES
- some diseases only affect people

  • injecting people with human-specific diseases are not ethical

PATHOGENS CAUSE THE SAME DISEASE PRESENTATIONS
- a pathogen can cause more than 1 presentation (can be shown in someone in different ways)
- diseases can have multiple causes

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12
Q

what was the update to Koch’s postulates

A

it included molecular tests to see if the pathogen or the gene that caused for the organism to be pathogenic was present

the molecular tests help to see if the organism is intracellular/can’t grow or if it can be present in harmless + pathogenic strain

  • helps to see if the organism is intracellular and can’t grow or if it’s a harmless pathogen ??
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13
Q

what are the groups of microbes?

A
  • viruses
  • bacteria
  • fungi
  • parasites (protozoa, helminths - worms)
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14
Q

what is bacteria

A
  • prokaryotes (unicellular)
  • makes yogurt, cheese
  • there can be bad and good bacteria (can keep intestines happy or cause food poisoning and infectious diseases)
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15
Q

what are viruses

A
  • depends on host cells to survive and replicate
  • can infect bacteria (ex. bacteriophage)
  • causes infectious diseases (severe)
  • different shapes
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16
Q

what is fungi

A
  • sizes vary
  • different shapes - can be single-cells or multicellular
  • eukaryotic
  • heterotrophic - relies on organic material for food
  • important for decomposition and fermentation
  • causes a range of diseases
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17
Q

what are parasites?

A
  • sizes vary
  • different shapes - can be unicellular or multicellular
  • eukaryotic
  • relies on host to survive
  • can have multiple hosts + has complicated lifecycles
  • causes a range of diseases (mild-severe)
  • usually a protozoan (unicellular eukaryotes) or worm
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18
Q

what were semmelweis’ initial observations?

A

there had been a lot of deaths among his patients

division I had a higher mortality rate and it was run by male medical students and doctors

division II had a lower mortality rate and it was run by female midwifery students

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19
Q

what is infectious disease

A

growth of a microbe or the microbe’s products causes damage to the host

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20
Q

what is a pathogen and examples of a pathogen

A

a microbe that can cause a infectious disease
= virus, bacteria, fungi, protozoa, prion, or worm

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21
Q

what are the steps for a pathogen to cause an infectious disease?

A

there are 7 steps
1. maintain a reservoir
2. has to be transported and enter a host
3. adhere, colonize, and/or invade host cells/tissues
4. evades/fights against the host’s defenses
5. multiples and completes its life cycle
6. mechanically or chemically damages the host
7. leave the host and returns to its reservoir or finds a new host

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22
Q

what does it mean for a pathogen to maintain a reservoir?

A

it’s present/circulates in low concentrations in susceptible hosts or in water

it also maintains population in a non-susceptible host

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23
Q

how does a pathogen get transported and enter a host?

A

through direct contact
- fecal-oral
- droplets
- aerosols
- sexual contact

through indirect contact
- fomites (inanimate objects that can house pathogens)

through vectors
- insect vectors (malaria parasite - the pathogen that carries the agent to the host)

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24
Q

what are some routes of entry for pathogens

A
  • eye
  • nose
  • mouth
  • ear
  • placenta
  • vagina
  • anus
  • urethra
  • insect bite
  • needle
  • broken skin
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25
Q

what does it mean for the pathogen to colonize or invade host cells/tissues

A

pathogens can attach to their hosts
- viruses = has specific receptors/glycoproteins to enter the host
- bacteria = has adhesion molecules to attach to tissues

pathogens can enter their host/host cells
- not ALL pathogens can enter host cells
- ALL VIRUSES CAN
- TB, malaria, and salmonella CAN

26
Q

how do pathogens move into the host?

A

they can attach to the host using ATTACHMENT PROTEINS

  • found on viruses and bacteria
  • the ligands of viruses and bacteria bind to the host cell’s receptors - this determines host cell specificity (b/ the ligand is specific for the specific receptor on the host cell)
  • bacterial pathogens attach to each other to create a BIOFILM
27
Q

what causes for the prevention of an infection?

A

changing or blocking the ligand or its corresponding receptor

the pathogen isn’t able to make attachment proteins making the pathogen not virulent

28
Q

what does a pathogen do to fight against the host’s defenses

A

it forms a CAPSULE
- bacteria has a polysaccharide coat - prevents it from being digested by host WBC

!! pathogens that do NOT have capsules - are NOT virulent

it reproduces inside of the host cell

changes it’s surface antigens to blend in with the host cells

29
Q

How do viruses, bacteria, and protozoa multiply/reproduce

A

VIRUS
- takes over the host cell’s system to create a new virus

BACTERIA
- binary fission

PROTOZOA
- asexually or sexually

30
Q

how does the pathogen mechanically or chemically damage the host?

A

using toxigenicity - pathogens can create enzymes that then create toxins - exotoxins and endotoxins

EXOTOXINS = small protein toxins that damage the host

ENDOTOXINS = components of the bacterial cell wall trigger a strong immune response that damage the host

the toxins is what brings on the immune response

31
Q

what is microbiota

A

a population of microbes that are in a area of an individual (example: GI tract)

the microbiota can be different across different sites of the body and can be different from person to person

changes in microbiota can influence health

32
Q

what is a microbiome

A

all of the genomes and genes of a microbiota

33
Q

what does it mean when microbes are colonized on host

A

microbes are present on the body but do not cause disease

this is due to the host’s diet, environment and genetic factors

34
Q

what are benefits of normal microbiota

A

prevents bad bacteria from infecting/limits the opportunistic pathogen from colonizing and infecting

creates vitamins, essential amino acids + other metabolic co-factors

gives 10-15% of calories from food

helps to control digestion efficiency and control body weight/digests things that are hard to digest

35
Q

what is dysbiosis

A

a change in the microbiota’s structure or function which creates a disruption in the homeostasis/balance between the microbial community and its host

36
Q

what are the molecular aspects of bacteria?

A

bacteria is a prokaryote
- prokaryotes lack a nucleus
- prokaryotes have a single circular chromosome in a nucleoid
- prokaryotes are smaller than eukaryotes
- prokaryotes do not have membrane-bound organelles
- prokaryotes have plasmids (another form of genetic material)

37
Q

what is vertical gene transfer

A

genes get passed from generation to generation
- bacteria has asexual reproduction
- doesn’t have genetic diversity b/ its the exact same DNA being passed down

38
Q

what is horizontal gene transfer

A

genetic material gets transferred from one organism to another organism in the same generation

  • specifically plasmid
  • allows for genetic diversity
  • genetic diversity is important for antibiotic resistance
39
Q

what is the bacterial cell wall made out of and what does it do

A

one major component = peptidoglycan (protein + sugar)

  • protects bacteria from harsh external environment
  • targeted by antibiotics
40
Q

what is the peptidoglycan composition for gram-positive bacteria and gram-negative bacteria

A

gram-positive = thick peptidoglycan
gram-negative = thin peptidoglycan + outer cell membrane
- it’s in between the cytoplasmic membrane and the outer cell membrane

41
Q

what does a gram stain do and what are the stains for gram-positive and gram-negative bacteria

A

gram stain = stains organism based on the characteristics of its cell wall

gram-positive = stains purple

gram-negative = stains pink

42
Q

what is the gram stain process

A

step 1: add crystal violet -> stains cells purple or blue

step 2: add iodine -> makes crystal violet less soluble and makes it stick to the cell wall better -> cells are still either purple or blue

step 3: add alcohol -> washes the stain away from the gram-negative cell wall -> GP remains blue or purple + GN are colourless

step 4: add safranin -> stains anything that is not stained with crystal violet, allows dye to stick to GN -> GP remains blue or purple + GN appears pink or red

43
Q

how is bacteria identified and named

A

based on its shape, cell arrangement, and gram stain

the same shape can cause different diseases

same shape does not mean same properties

44
Q

what are the bacteria shapes called

A

coccus
bacillus
vibrio
coccobacillus
spirillum
spirochete

45
Q

what are the different arrangements of bacterial cells and which are the most common arrangements

A

single coccus
pair of cocci
4 cells arranged in a square
chain of cocci
cluster of cocci

chain and cluster is the most common arrangements

46
Q

what are the characteristics of a bacteria causing disease

A

pathogenicity = when a microorganism is able to cause disease

virulence = the degree of pathogenicity/the severity of the disease

  • this is based on case fatality rates + its ability to invade the tissues of the host
  • the ability for the infectious agent to create pathological effects
47
Q

what does bacteria have that increases its ability to cause disease

A

virulence factors - molecules or structures that increase this ability

48
Q

what factors affect the outcome of host-pathogen interaction

A
  1. host’s health state
    - depends on age (very young and very old being the most susceptible to the pathogen)
    - its nutrition
    - its state of immunosuppression (due to other diseases or drugs)
  2. virulence of pathogen
    - how infectious the pathogen is
    - how invasive the pathogen is
    - the toxigenicity of the pathogen
49
Q

what are indicators of virulence

A

ID50 = median infectious dose = the amount of pathogen cells or virus particles needed to cause an active infection in 50% of vaccinated/inoculated animals

this dose does not correlate to the disease severity

LD50 = median lethal dose = the amount of pathogen cells or virus particles required to kill 50% of infected animals/hosts

50
Q

can a bacteria be virulent without being pathogenic or causing disease

51
Q

what are some virulence factors

A

extracellular enzymes
- secreted by pathogens
- dissolves structural chemicals
- helps pathogen maintain the infection, invade and avoid the body’s defence mechanism

toxins - endotoxin and exotoxin
- chemicals harm tissues
- chemicals that trigger the host’s immune response which causes damage

  • bacterial capsule
  • antiphagocytic chemicals
52
Q

what is toxemia

A

toxins in the bloodstream that get carried from the site of infection to other areas of the body

53
Q

what is endotoxin

A

part of the bacterial cell wall
released when cell dies

54
Q

what is exotoxin

A

proteins that get secreted by bacteria
meant to target something

55
Q

how does virulence factors prevent the pathogen from going through phagocytosis by the host cell’s phagocytic cells?

A

using bacterial capsules or antiphagocytic chemicals

bacterial capsules
- made up of chemicals that are not seen as foreign
- slippery making it hard for phagocytes to take in bacteria

antiphagocytic chemicals
- prevents the lysosome to merge with the phagocyte
- leukocidins specifically destroy phagocytic WBC directly

56
Q

what are mechanisms that allow for the bacteria to survive in harsh environments?

A

they create endospores and biofilms

57
Q

what is endospore

A

it’s a structure that is tough, non-reproductive and inactive and allows for bacteria to survive in harsh environments

very resistant to heat-drying + chemicals

58
Q

what are biofilms

A

structured communities of bacteria that are embedded into extracellular matrix

the community of bacteria sticks to the surface

protects the bacteria from environmental stresses + antimicrobial agents

59
Q

where do biofilms form

A

on tissues -> wounds, airways, etc.

on foreign bodies -> prosthetic joint

does this to cause infections

60
Q

list smallest to biggest: worms, bacteria, virus, protozoa

A

viruses
bacteria
protozoa
worms