Lec3 Flashcards

1
Q

is the M.O that can cause a disease.

A

Pathogen

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2
Q

is the M.O that take the opportunity of a reduced host defense to cause a disease.

A

Opportunistic pathogen

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3
Q

is a quantitative measure of pathogenicity

A

Virulence

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4
Q

which is the number of M.O cells needed to kill half of the hosts.

A

LD50

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5
Q

which is the number of M.O cells needed to cause infection in half of the hosts.

A

ID50

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6
Q

Infection dose of shigella

A

100 cells

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7
Q

Infectious dose of salmonella

A

100,000 cells

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8
Q

Why the LD50 and ID50 values varies among bacteria?

A

1: Presence of pili allow them adhering the mucous
membranes easily.
2: Presence of a capsule protect them from phagocytosis.
3: Ability to survive host defenses such as stomach acid.
4: Ability to produce exotoxins or endotoxins.
5: Ability to produce lytic enzymes.

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9
Q

can grow within cells, outside cells, or on bacteriologic media.

A

Facultative parasites

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10
Q

Chlamydia and Rickettsia, can grow only within host cells.

A

Obligate intracellular parasites

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11
Q

conditions required for infection

A
  1. The correct portal of entry.
  2. High number of microbial cells.
  3. The virulence of M.O.
  4. Weak immune system increases the chance of infection.
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12
Q

Bacteria cause diseases by two major mechanisms:

A
  1. Invasion and inflammation.
  2. Toxin production
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13
Q

Stages of bacterial pathogenesis

A
  1. Transmission from an external source into the portal of
    entry.
  2. Overcome the primary host defenses such as skin, mucous, saliva, stomach acid.
  3. Adherence to mucous membranes (by pili or capsule).
    4.Colonization of the site of adherence (invasion and
    inflammation).
  4. Toxin and enzyme production.
  5. Appearance of symptoms.
  6. Host responses during the previous steps.
  7. Progression or resolution of the disease.
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14
Q

mode of transmission:

A

Human to human
Nonhuman to human

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15
Q

Human to human transmission

A
  1. Direct contact (sex, hand shaking).
  2. Indirect contact (Fecal—oral)
  3. Transplacental (Bacteria cross the placenta and infect the fetus).
  4. Blood-borne (through blood transfusion).
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16
Q

Nonhuman to human transmission

A
  1. Soil source
  2. Water source
  3. Fomite source
  4. Animal source
17
Q

Transmission of microbes drom=mother=tomofispring: via
placenta, birth ‘canal, and breast milk called

A

vertical transmission.

18
Q

by contrast, include person-to-person transmission.

A

Horizontal transmission

19
Q

mediate the attachment to the urinary tract epithelium.

A

pili of E. coli

20
Q

mediate the attachment to the heart valves endothelium.

A

glycocalyx of viridans streptococci

21
Q

play an important role in the formation of dental plaque.

22
Q

strains have surface proteins called

23
Q

protects bacteria from phagocytosis by walling off the infected area and coating the organisms.

24
Q

destroy both neutrophilic leukocytes and macrophages.

A

Leukocidins

25
Q

M protein of St pyogenes

A

antiphagocytic.

26
Q

binds to IgG and prevents the activation of complement.

A

Protein A of Staph. aureus

27
Q

Pyogenic (pus-producing) inflammation

A

where neutrophils are the predominant cells (most cells)

28
Q

Granulomatous inflammation

A

where macrophages and T cells predominate.

29
Q

Obligate intracellular parasites

A

(Chlamydia and Rickettsia)

30
Q

Escape from the phagosome into the cytoplasm, where there are no degradative enzymes.

31
Q

specific bacterial surface proteins called

A

invasins or adhesins

32
Q

are virulence factors that inhibit phagocytosis and cytokine production.

A

“Yops” (Yersinia outer-membrane proteins)

33
Q

is a “master controller” of many virulence factors in several pathogens.

A

DNA adenine methylase (Dam)

34
Q

inability of hydrophilic drugs to enter the lipid-rich brain parenchyma, whereas lipophilic (lipid-soluble) drugs enter well.

A

“blood-brain barrier”

35
Q

Endotoxin source

A

Cell wall of G-ve bacteria

36
Q

Exotoxins toxicity