pathogens + immune system Flashcards

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1
Q

list the living organisms that can cause disease

A

bacteria, fungi, protozoa

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2
Q

list acellular agents that can cause disease

A

viruses, viroids, prions

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3
Q

what is a viroid pathogenic to

A

plants

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4
Q

what are viroids composed of

A

small, circular RNA

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5
Q

T or F: viroids encode proteins

A

false; even though they’re RNA, they don’t encode proteins

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6
Q

how do viroids replicate

A

using a host cell enzyme

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7
Q

structure of viroid

A

nucleotides are often paired = RNA has a closed 3D structure

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8
Q

how do viroids cause disease

A

by RNA silencing of host genes

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9
Q

how were prions named

A

proteinaceous infectious particle

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10
Q

what is a prion

A

an abnormally folded protein that can cause disease

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11
Q

where are prions found within the human body

A

on the PM of neurons

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12
Q

function of prions in humans?

A

unknown

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13
Q

list the two ways in which a prion can stably fold

A
  1. into the normal (cellular) form: PrpC
  2. into the diseased (abnormal) form: PrPSc
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14
Q

list 3 ways that diseases can occur due to prions

A
  1. spontaneous conf change of the protein into the abnormal form
  2. mutation in the gene that results in a conf change to the abnormal form
  3. through ingestion/injection of the abnormal prion protein
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15
Q

describe what happens when the body encounters one abnormal prion

A

chain reaction occurs. Abnormal prions cause normal ones to change into abnormal ones = build up of PrPSc in the brain = plaques = spongiform brain

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16
Q

what are prion diseases known as

A

TSEs (transmissible spongiform encephalopathies)

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17
Q

features of prion diseases?

A

can occur in humans and animals, fatal, long incubation period, no immune response, victims lose motor function/become demented/death follows

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18
Q

list 3 animal TSEs

A

mad cow, scrapie, chronic wasting

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19
Q

list 3 human TSEs

A

Kuru, fatal familial insomnia, Creuztfelt-jacob disease (CJD)

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20
Q

describe CJD

A

most common human TSE, found among 55-75 year olds
symptoms: progressive dementia, visual/speech problems, tremors, moderate plaques, spongiform brain
incubation time is 3-20 years

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21
Q

what are the three different forms of CJD

A

sporadic, familial, iatrogenic (caused by medical treatment)

22
Q

describe the new variant of CJD (nvCJD)

A

patients are younger and have larger plaques. It is the human form of mad cow disease

23
Q

list some ways that prions are NOT destroyed

A

boiling or cooking, standard autoclave sterilization, radiation, alcohol disinfectants (alcohol or aldehyde)

24
Q

list some ways that prions ARE destroyed

A

incineration (super high heat), high heat/pressure autoclaving, autoclaving with alkali

25
Q

T or F: some people are born with inherited immunodeficiency diseases

A

true

26
Q

what is X-SCID + what does it cause

A

an immunodeficiency disease; there’s a gene defect so you can’t make WBCs

27
Q

what are the two types of immune responses

A

innate and adaptive

28
Q

features of the innate response

A

it is present from birth
it provides a rapid response to a foreign substance
it’s a general response (no specificity)
does not have a memory response

29
Q

what two lines of defense is the innate response composed of

A

first and second lines of defense

30
Q

what is the first line of defense composed of

A

skin, mucous membranes, normal microbiota
(it’s the physical + chemical ways of protection)

31
Q

how does the skin protect us from infection (via physical means)

A

The outer layer consists of tightly packed keratinocytes which constantly shed, removing any microbes that have attached to them

32
Q

describe how chemical factors of the skin protect us

A

sweat from sweat glands flushes microorganisms off the skin. release of sebum from oil glands + secretions from sweat glands keep the pH of the skin low (5-6)
presence of lysozyme in sweat

33
Q

list physical ways that mucous membranes protect us

A
  • epithelial cells are packed tightly + constantly replaced
  • saliva dilutes microbes present + flushes them away
  • lacrimal apparatus in the eye produces tears that flush them
  • mucus traps microbes (present in mouth, coats the hairs of the nose)
  • mucociliary blanket in lower resp tract traps microbes and moves them away from lungs
  • peristalsis of intestines minimizes establishment of harmful microbes
  • flow of urine in genitourinary tract prevents colonization
34
Q

list chemical ways that mucous membranes protect us

A
  • lysozyme in nasal secretions, saliva, tears, urine
  • IgA in saliva prevents attachment of microbes
  • gastric juice in stomach
  • vaginal secretions = acidic environment
  • acidity of urine
  • presence of lactoferrin in tears inhibit growth by sequestering iron
  • production of lactoperoxidase which is responsible for production of superoxide radicals
35
Q

how can the normal microbiota protect us

A

inhibiting pathogens from colonizing through competition (use up nutrients, receptors, iron), bacteriocins are produced that are harmful to pathogens, alteration of the physical environment so pathogen cannot survive (ie pH, oxygen availability)

36
Q

what is the second line of defense composed of

A

cells (phagocytes) and antimicrobial chemicals (complement system)

37
Q

describe how cells in the second line of defense can protect us

A

they can engulf microbes (called phagocytes)

38
Q

list the different phagocytes in the blood

A

macrophages, dendritic cells, eosinophils, monocytes

39
Q

how do antimicrobial chemicals protect us in the second line of defense

A

the complement system is a group of 30 proteins found in the blood. Consequences of complement activation: inflammatory response, cytolysis, phagocytosis

40
Q

features of the adaptive immune response

A

it’s a specific response to a specific pathogen
it’s slower to respond
it has a memory response

41
Q

T or F: the innate and adaptive immune responses work independently

A

false; they do NOT work independently

42
Q

list the two branches of the adaptive response + what they use as weapons against pathogens

A

humoral immunity: uses antibodies
cell-mediated immunity: uses T cells

43
Q

describe humoral immunity

A

uses antibodies that are located in blood, mucus secretions, tears, saliva, breast milk. They act by binding to an antigen.
5 classes of antibodies: IgG, IgM, IgD, IgA, IgE

44
Q

list 4 ways that antibodies protect us from disease

A

agglutination, neutralization, opsonization, complement activation

45
Q

what is agglutination

A

phagocytes can engulf more pathogens

46
Q

what is neutralization

A

antibodies block adhesion of pathogens to host cell receptors

47
Q

what is opsonization

A

microbe is coated with antibody, thereby enhancing its ability to be recognized by a phagocyte

48
Q

what is complement activation

A

antigen-antibody binding can activate a component of the complement system which can lead to inflammation and cytolysis

49
Q

what are the two types of T cells in cell mediated immunity

A

cytotoxic T cells and helper T cells

50
Q

what do cytotoxic T cells do

A

directly kill an infected cell

51
Q

what do helper T cells do

A

provide help to Tc cells and B cells through the release of signaling molecules (cytokines). They’re needed for B cells to produce antibodies and for Tc cells to kill infected targets