Exam 1 study guide Flashcards

1
Q
  1. There are 6 steps in the infectious disease process
A

encounter, 2. entry, 3. spread, 4. multiplication, 5. damage and 6. outcome. (You should know what each step is).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q
  1. Entry into a host can be thought of as two different processes
A

1) ingress of microorganisms into body cavities that are contiguous with the outside (inhalation or ingestion) 2) penetration of microorganisms into deeper tissues after crossing an epithelial barrier (insect bites, cuts and wounds, organ transplants, blood transfusions)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q
  1. The nose, mouth, respiratory tract, alimentary canal, anus, female genital tract and urinary tract are all in
A

direct contact with the exterior and are therefore generally not considered inside the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q
  1. Penetration of bacteria into epithelial cells usually involves two steps
A

attachment to specific receptors followed by internalization

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q
  1. The spread of infection can have two meanings
A

the lateral propagation (or movement) to contiguous tissues or dissemination to distant sites.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q
  1. Microbes must overcome host defenses in order to
A

multiply and spread

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q
  1. Inoculum size is important in establishing an
A

infection (it varies with different organisms).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q
  1. There are 4 possible outcomes of a host-parasite interaction
A

: 1) the host wins out and clears the infection. 2) the parasite overcomes the host. 3) the host and parasite adapt to each other. 4) neither host or parasite win. This chronic infection can continue indefinitely.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q
  1. Damage to the host can be caused by the
A

infectious agent or by the host response (immune system) or both.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q
  1. The great majority of microorganisms are
A

commensal. They coexist without causing harm. It can be difficult to identify a bacterium as a commensal.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q
  1. Gram positive bacteria have
A

a thick cell wall made up of murein (peptidoglycan). Murein is made up of long chains of N-acetylmuramic acid and N-acetylglucosamine linked together by short polypeptides.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
  1. Gram negative bacteria have a thin
A

layer of murein between two membranes (lipid bilayers).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q
  1. The outside of the outer membrane of gram negative bacteria is made up of
A

lipopolysaccharide (LPS) that is different for different bacteria.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

LPS

A

toxic (endotoxin) even in its purified form. LPS is made up of a lipid region (fatty acids attached to a phosphorylated disaccharide) that faces into the membrane and a polysaccharide region face out. The outer (O-antigen) region in highly variable and antigenic.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q
  1. Bactericidal agents kill
A

baceteria - bacteriostatic do not.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q
  1. Penicillins and other beta-lactams are
A

antibiotics that affect the cell wall. They are bactericidal.

17
Q
  1. Antibiotics often work by targeting
A

bacterial ribosomes

18
Q
  1. There are 2 subunits to bacterial ribosomes
A

the 30S and 50S subunit

19
Q
  1. The 30S subunit is primarily responsible for
A

translation of mRNA

20
Q
  1. The 50S subunit is primarily responsible for
A

joining amino acids together and moving the complex along the mRNA molecule.

21
Q
  1. Antibiotics can target either the
A

30S or 50S subunit.

22
Q
  1. Sulfonamides and trimethoprim inhibit
A

folic acid metabolism

23
Q
  1. Aminoglycosides (streptomycin, kanamycin etc.) tetracyclines and erythromycin inhibit
A

protein synth

24
Q
  1. Metronidazole inhibits
A

DNA synthesis.

25
1. Pili (or fimbriae) are specialized structures on the surface of bacteria that are involved in
adhesion to cells or other surfaces
26
1. Sex pili are specialized pili that
link a donor cell to a recipient cell during transfer of DNA.
27
1. Flagella are surface structures used for
locomotion. They cause movement when they rotate counterclockwise and tumbling when they rotate clockwise
28
1. Flagellar movement is used by bacteria for
chemotaxis - the movement towards substances that attract and away from substances that repel
29
1. Obligate intracellular parasites can only grow
inside host cells
30
1. The therapeutic index is the
1. ratio between the effective and toxic dose of an antibiotic
31
1. Antibiotics tend to target structures that are
“unique” in bacteria compared to structures found in host cells. You should know what those targets are.
32
1. The sulfa drugs interact with an
enzyme to prevent the production of a metabolite. You should know what that metabolite is, why it’s important, and why this competition is damaging to the host.
33
1. Bacteria can become resistant to antibiotics by
synthesizing enzymes that inactivate the drug, inhibiting uptake of the drug, increasing secretion of the drug (pumping it out of the cell), modifying the target of the drug
34
1. Drug resistant genes are often found on
plasmids that can be transferred readily from one bacteria to another.
35
1. In order to survive as an infectious agent, bacteria must:
1) avoid being washed away, 2) find a nutritionally compatible niche, 3) survive host defenses, 4) transfer to a new host.
36
1. Damage to a host as a result of infection can be caused by
cell death, pharmacological alterations of metabolism, mechanical causes, host responses, or bacterial toxins.
37
1. Many structures on the microbial surface consists of repeated molecules---
referred to as pathogen associated molecular patterns
38
1. Pattern recognition receptors recognize
pathogen associated molecular patterns.
39
1. Bacteria are often classified via their
surface antigens (referred to as the serotype). In this scheme, O refers to LPS, H refers to flagella, and K refers to a capsule.