Topic 6- microbiology and pathogens Flashcards

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1
Q

define aseptic technique

A

a way of working , designed to prevent contamination from other microorganisms

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2
Q

describe how you would carry out aseptic technique

A

Provide culture with required nutrients in sterile medium.
Inoculate culture- streak or spread plate

Equipment is sterilised in Bunsen burner

Lids replaced as quickly as possible

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3
Q

explain the differences between ; broth, agar and selective medium

A

agar is solid (jelly)
broth is liquid
(both have nutrients added)

selective medium contains certain nutrients so that only specific bacteria can grow (contains specific selective agent)

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4
Q

bacteria invade and destroy host tissue by producing toxins. (this incapacitates organism/immune system)

explain exotoxins

A

Excreted by organisms (living cells)

Found in gram positive and negative bacteria

Highly antigenic

Unstable, heat liable at 60 degrees

Highly toxic

Denatured on boiling

No enzymatic activity

Usually binds to specific receptors

Toxoids can be made by treating with formalin

Polypeptide, soluble proteins

e.g staphylococcus

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5
Q

bacteria invade and destroy host tissue by producing toxins. (this incapacitates organism/immune system)

explain endotoxins

A

Integral part of cell wall

Mostly found in gram negative bacteria

Lipopolysaccharide complex

Relatively stable and heat tolerant

Moderately toxic , rarely fatal

Weakly immunogenic

Toxoids can not be made

Specific receptors not found

Mostly enzymatic activity

On boiling, cannot be denatured

e.g salmonella

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6
Q

explain the difference between bacteriostatic and bactericidal antibiotics

A

Bactericidal antibiotics – kill bacteria by destroying their cell wall, causing them to burst (e.g penicillin)

Bacteriostatic antibiotics- inhibit growth/reproduction, by stopping photosynthesis so cell division can’t happen. (e.g tetracycline)

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7
Q

influenza

A

transmission - direct contact/droplets/coughs/sneezes

mode of infection- Effects epithelial cells in lungs
Viral RNA is continually produced – new virus particles

pathogenic effects-Sore throat/Headache/Cough/sneeze /5-7 days

treatment- antivirals

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8
Q

stem rust fungus

A

transmission- pores from infected plant transported by wind

mode of infection-
Pores germinate on plant due to water producing hyphae

Hyphae enter plant via stomata

Hyphae grows into mycelium

This surrounds all tissues in the plant, producing enzymes

(these digest plant/make fungus absorb needed nutrients)

pathogenic effects- Weakened stem
Less transpiration and photosynthesis
Pustules on epidermis eventually burst, producing more spores

treatment-fungicide

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9
Q

explain social, economic and ethical considerations for the control of the endemic malaria

A

Ethical: informed consent difficult, spraying mosquitos may harm them, money spent on vaccines could be spent on education/preventing famine

Social: vaccines need to become accepted , social changes to reduce infection are difficult to bring about

Economical: treatment and control is expensive , malnutrition may be more of a threat to human life than malaria

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10
Q

define endemic

A

Widespread disease in one particular area/region

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11
Q

malaria

A

transmission:
Vector of female mosquito

mode of infection:
Parasite transmitted from mosquito travels to liver
Infects RBC
Asexually reproduce in erythrocytes – lysis
Malaria bursts out of RBC every 2-3 days

pathogenic effects:
(paroxysm)
Sweating, shaking, liver damage

treatment/control:
Prevent bites using insect repellent/net, water treatment (introduce predators)

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12
Q

physical barriers

A

Skin has keratin

Stomach acid

Gut and skin flora (pathogens have to compete for food and space)

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13
Q

non-specific immune response

A

Kills anything foreign

Size of response = size of infection

Inflammation, fever, phagocytosis

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14
Q

specific immune response- cell mediated response

A

Relies on lymphocytes produced in bone marrow – B cells ( humoural) and T cell ( cell mediated)
T cells move to thymus gland to mature

Cell mediated response:

Pathogen invades host cell
Antigen attaches to MHC markers and becomes APC (antigen presenting cell)
T killer cells (with complimentary receptors) bind to APC
Cytokines (from T helper) stimulate T killer to divide by mitosis
T killer divides into active T killer and T killer memory cells
Active T killers bind to APCs, secreting chemicals which cause pores to form in cell membrane
Infected cell dies

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15
Q

explain how the structures of erythrocytes and monocytes are related to their functions

A

erythrocytes have no nucleus to free up space to carry more haemoglobin (to transport oxygen) , monocytes have a nucleus to synthesise proteins.

shape:
erythrocytes are a biconcave shape, increasing SA to allow more absorption of oxygen and are smaller to pass through capillaries.
monocytes can change shape (are larger) to engulf pathogens

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16
Q

specific immune response - humoural response

A

T helper activation:

Bacteria engulfed by macrophage
Macrophage acts as APC , presenting antigens on MHCs
APC binds to T helper (has complimentary receptor proteins)
T helped is ‘activated’, divides by mitosis into T memory and T helper

effector stage:
Antigens on APCs that are complimentary to receptors on B cells bind and are taken in by endocytosis
B cell acts as APC and presents antigens on MHCs
Activated T helper cell binds to APC to produce cytokines
Cytokines stimulate B cell to divide by mitosis into B memory and B effector
B effector differentiate into plasma cells
Plasma cells synthesis antibodies
Antibodies have an effect – e.g agglutination means antibodies clump antigens together to make phagocytosis easier
T supressor cells stop immune response

17
Q

what are the different typed of vaccines you can get?

A

live (living pathogens)
dead (killed pathogens)
attenuated (weakened pathogens)
toxoids (toxins made harmless)
DNA
edible vaccines

18
Q

blood taken from a patient may have an unusually high proportion of eosinophils - why?

A

the patient is producing more of these cells, so more is being released into blood stream

because patient has allergic inflammation due to parasitic infection

19
Q

why would people infected with staphylococcus present symptoms quicker than those infected with salmonella?

A

staphylococcus produces exotoxins whereas salmonella produces endotoxins.

endotoxins are produced much later, takes longer

20
Q

describe techniques microbiologists could use to prove what food poisoning was caused by?

A

take a sample of sick/faeces
look at colonies to see if they have specific characteristic
use gram staining
grow on selective media
use antibodies specific to the suspected bacteria

21
Q

on nutrient agar plates , if an antibiotic is not effective , what will the outcome be?

A

there will be no clear zone (zone of inhibition)

22
Q

why may a sample tube be sealed?

A

prevent microorganisms entering

maintain conditions (e.g humidity)

23
Q

name the property of cells that may allow them to develop new shoots

A

totipotency

24
Q

describe how bacteria should be added to a petri dish.

A

use sterile equipment

uniform spreading e.g lawn spreading

25
Q

why may a lid of a petri dish be secured with tape?

A

prevent microorganisms entering and contaminating the dish

allow for aerobic conditions, reducing the growth of harmful anaerobic bacteria.

26
Q

how would you calculate the mean diameter of a zone of inhibition if it was not circular?

A

record several measurements
divide that number by the number of measurements.

27
Q

why is it good safety practice to incubate bacteria at a temperature BELOW 37 degrees?

A

37 degrees is the human body temp

encourages more rapid growth of potentially dangerous bacteria.