Module 7 Flashcards

1
Q

what is parasitic symbiosis

A

One party benefits while the other suffers

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2
Q

what is mutualistic symbiosis

A

both party’s benefit

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3
Q

what is commensal symbiosis

A

one party benefits while the other is neutral

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4
Q

what is a non pathogen

A

microorganism that does not cause disease
may be apart of the normal flora

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5
Q

what is an opportunitstic pathogen

A

capable of causing diseases only when the hosts resistance is impaired
immunocompromised

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6
Q

what is a pathogen

A

a microorganism capable of causing disease

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7
Q

what is pathogenicity

A

the ability of an infectious agent to to cause disease

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8
Q

what is toxigenicity

A

the ability of a microorganism to produce a toxin that contributes to the development of disease

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9
Q

what is adherence

A

the process by which a pathogen can stick to the surfaces of host cells

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10
Q

what is infection

A

multiplication of an infectious pathogenic agent within the body - even if person is asymptomatic

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11
Q

what is invasion

A

the process where by bacteria, parasites, fungi and viruses enter host cells or tissues and spread

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12
Q

what is a carrier

A

a person or animal with asymptomatic infections that can be transmitted to another person or animal

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13
Q

what is virulence

A

the quantitative ability of an agent to cause disease
virulent agents cause disease when introduced into the host in small numbers
virculence is the enchanced ability for adherence, invasion and toxigenicity

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14
Q

what are the four stages of infection

A

incubation
prodrome
specific illness period
recovery period

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15
Q

what is the incubation period

A

time between exposure and symptoms

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16
Q

what is the prodrome period

A

generalized symptoms

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17
Q

what is the specific illness period

A

illness specific symptoms

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18
Q

what is the recovery period

A

symptoms resolve and return to health

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19
Q

what are the aspects of pathogenesis

A

colonization and transmission
adherence
invassiveness
toxins

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20
Q

what is colonization

A

establishment of a pathogen at an appropriate site of entry

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21
Q

where does colonization normally happen

A

anything with exposure to outside -> eyes, nose, mouth, lungs
urogenetial tract

22
Q

what do body surfaces at sites of microbial infection do to protect body from infection

A

have defense mechanisms to prevent attachment and shed microbes
successful microorganisms possess mechanisms for attaching to and moving along surfaces

23
Q

describe respiratory/salivary transmission

A

hard to control
cover when sneeze/cough

24
Q

describe fecal-oral transmission

A

control with public health measures
wash hands/access to clean water

25
describe venereal transmission
hard to control as social factors involved increase public awareness/education
26
describe vector transmission
person to bug to another person malaria, zika, lyme disease
27
descrive vertebrate resevoir
vertebrate to vertebrate to person rabies
28
vector-vertebrate resevoir
vertebrate to bug to person the plague...
29
routes of infection for the fetus/newborn
prenatal/congenital perinatal postnatal
30
describe infectious dose
measures virulence amount needed for 50% of sample population to be infected
31
what does a pathogen need for adherence
receptor --> specific carb or peptide residues on host cell ashesin --> macromolecule on the pathogen surface that interacts with the host cell receptor
32
describe surface spread
comes and goes within 7 days innate immune defenses employed common cold
33
describe systemic spread
lasts more than 1 week adaptive immune defenses employed measles
34
what are pathogenic factors for invasiveness
hyalurnidase lipases coagulase collagenase
35
what are the two main types of toxins
endotoxin exotoxin
36
describe endotoxins
gram - part of the cell not used for immunization eg. lipopolysaccharide
37
describe exotoxins
on gram - and + can be released can be used for immunization can be specific to bacteria strains eg. tetanus
38
how do microbes evade the innate immune system
evade mechanical barriers evade phagocytosis
39
how do microbes evade adaptive immune defenses
concealment of antigens antigenic variation immunosuppression
40
how do pathogens evade mechanical barriers
fluid and mucous can remove most viruses, bacteria and protozoa from the surface of epithelial cells specific receptors or mechanical means to bind firmly to epithelial surface
41
how do pathogens evade phagocytosis
kill phagocyte by releasing toxins prevent phagocyte from engulfing microorganism (capsule) prevent the fusion between phagosome and lysosome escape from phagosome to cytoplasm: allow replication of microbe resistance to killing when inside phagolysome - production of antioxidants that neutralize hydrogen peroxide
42
describe concealment of antigens: latency
if a microbe can remain inside a cell without its antigens being displayed on the surface, it cannot be recognized --> even if antibody-mediated or cell-mediated response has been put into action, the microbe inside such a cell is unaffected --> persistenet latent viruses act this way --> during reactivation: re-exposure occurs and boostig of immune responses is inevitable
43
describe concealmet of antigens: microbes in privileged tissue sites
certain microbes colonize in tissues that are out of reach from circulating lymphocytes or have alternate drainage (not lymph) only effective if microbe does not induce innate immune inflammatory response Brain, anterior of eye, testes, placenta
44
describe genetic mutation
some pathogen antigens can repeatedly change their imporant surface structures so that host immunity is less effective can occur during course of infection or spread of a microbe in community --> reduces effectiveness fo T and B memory cells and requires new immune responses to new antigens of the flu virus
45
describegene recombination
sudden alterations in antigens take place by the exchange of genetic info between 2 subtypes of microbes
46
describe immunosupression
many viral and bacterial infections cause immunosupression that is normally temporary but can be long term
47
describe temporary immunosupression
release of immunosuppressive molecules that interfere with complement reduction in MHC I expression by infected cells
48
describe long term immunosuppression
interference with signalling between immune cells and cytotoxic cells
49
describe resistance to anti-microbial treatments
the microbe alters a function or acquires a new functional molecule that helps it resist the drug
50
describe immune function in pregnancy
pregnancy hormones result in reduced cellular immunity but maintain Ab immunity fetal tissue protected from immune rejection by specific functions of placenta and immune regulation some viruses can cross placenta, fetus only has maternal IgG antibodies and innate function
51
describes immune function in newborns
newborns have maternal IgG and IgA from milk --> rapidly develop B cell immunity on their own and eventually T cell mediated immunity Can be treated with immune globulins and some anti-microbial or anti-viral drugs