Bacterial Diagnosis - Hunter Flashcards

1
Q

T/F: a physician should begin treatment when an infectious disease is suspected BEFORE lab confirmation

A

yes

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2
Q

What is the most common reason to fail to establish an etiologic diagnosis or a wrong diagnosis of an infectious organism?

A

Failure to properly collect a specimen

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3
Q

In diagnosing a bacterial infection, what is the primary problem?

A

distinguishing normal flora from those causing infection

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4
Q

What is a direct specimen?

A

microbes are in sterile site that can be accessed directly (e.g., needle aspiration of deep abscess, or blood collection)

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5
Q

What is an indirect specimen?

A

microbes are in sterile site but must be collected through a non-sterile site (e.g., voided urine sample)

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6
Q

What is a contaminated specimen?

A

Microbes are in site contaminated with normal flora (e.g., throat or stool culture)

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7
Q

what two factors will dictate how the micro lab will approach isolating and identifying the bacteria?

A

the type of specimen you collected and your presumptive diagnosis

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8
Q

T/F: transport of bacterial specimens is aerobic only

A

false, it can be either

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9
Q
Microscopy
Broth and Agar Culture (antibiotic sensitivity testing)
Biochemical Characterization
Antibody Detection
Antigen Detection
Nucleic Acid-Based Tests

These are all methods of what?

A

identifying specific microbes in the lab

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10
Q

What type of microscopy focuses directly on the specimen?

A

brightfield

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11
Q

What type of microscopy has the central light blocked and peripeheral light is collected as scatter from the microbes?

A

darkfield

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12
Q

What type of microscopy has microbes labeled with fluorescent dye that interacts at a certain wavelength?

A

fluorescence

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13
Q

What type of microscopy is most common?

A

brightfield

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14
Q

What power mag do you need to see bacteria?

A

100x under oil immersion

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15
Q

What is the point of simple staining?

A

to just visualize bacteria

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16
Q

what is the point of differential staining?

A

to distinguish different groups of bacteria, such as gram pos/neg

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17
Q

what are special stains used for?

A

detect bacterial structures such as capsules, flagella, and endospores

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18
Q

what are the two most common stains?

A

Gram stain and acid fast

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19
Q

what medium is commonly used to grow bacteria?

A

agar

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20
Q

T/F: a single microbes can grow to visible amounts

A

true

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21
Q

T/F: almost all medically important microbes can be cultured

A

true

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22
Q

How do you describe the colony form?

A

Circular
irregular
filamentous
rhizoid

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23
Q

how do you describe colony elevation?

A
raised
convex
flat
umbonate
cateriform
24
Q

how do you describe colony margins

A
entire
undulate
filiform
curled
lobate
25
Q

What is the difference between nutrient, selective, and indicator media?

A

nutrient used to grow microbes, selective include antimicrobials to limit overgrowth of undesired bacteria, and indicator media has stuff that demonstrates specific activities of certain bacteria

26
Q

what type of media should you use if you have a sample of intestinal flora?

A

selective media to limit floral overgrowth to SELECT for you bacteria

27
Q

media that has a pH indicator of fermentation of sugars or RBC hemolysis is what type of media?

A

indicator media

28
Q

MacConkey agar is what type of media and is used to grow what?

A

Selective and indicator, gram negative, shows lactose fermentation

29
Q

Eosin Methylene blue agar is what type of media and is used to grow what?

A

Selective and indicator, gram negative, also shows lactose fermentation

30
Q

Hektoen Enteric agar is what type of media and is used to grow what?

A

Selective and indicator, SPECIFICALLY salmonella and Shigella, shows lactose fermentation and HYDROGEN SULFIDE production

31
Q

what does capnophilic mean?

A

bacteria grows in air but requires CO2

32
Q

Strictly (blank) bacteria die in the presence of air

33
Q

What are the factors that must be accounted for to grow bacteria? (3)

A
  1. Broth/solid media
  2. aerobic vs. anaerobic
  3. CO2 levels
34
Q

What allows the selection of most effective chemotherapeutic agent against the bacterial isolate?

A

Antimicrobial sensitivity testing

35
Q

What is used to determine the minimum inhibitory concentration (MIC) of an abx?

A

broth dilutions and agar diffusion

36
Q

Bacitracin A disk is used to ID what bacteria?

A

Strep pyogenes

37
Q

Bile solubility allow for rapid differentiation of (blank) from other streptococci

A

pneumococci

38
Q

Catalase activity differentiates what two major groups?

A

staph (catalase pos) from strep and enterococci (catalase neg)

39
Q

Coagulase positive is KEY for what bacteria?

A

staph aureus

40
Q

Hippurate hydrolysis will ID group (blank) streptococci

41
Q

An (blank) rapid test will detect E. coli in the urine

A

Indole A (hippurate hydrolysis)

42
Q

Optochin (P) disk can be used to ID what?

A

strep PNEUMONIAE; P for P

43
Q

Oxidase activity differentiates what type of rods?

A

gram negative rods from each other

44
Q

Enterobacteriaceae, Acinetobacter, and Stenotrophomonas are oxidase pos/neg?

A

oxidase negative

45
Q

Pseudomonas and Burkholderia are oxidase pos/neg?

A

oxidase positive

46
Q

S. pyogenes and Enterococcus can be determined via rapid test using what?

A

PYR hydrolysis

47
Q

What detection lab methods do you use to visualize sera Abs?

A

ELISA, westerns, or immunofluorescence

48
Q

The Ab response to some bacteria can take (days/weeks)?

49
Q

Serology is mostly useful in what type of studies?

A

epidemiologic

50
Q

T/F: Abs are a good detection mechanism of bacterial infection in immunocompromised patients?

51
Q

Can Abs detect whole bacteria or bacterial toxins?

52
Q

How does a non-amplified nucleic acid assay work?

A

hybridization of nucleic acids FROM pathogens TO labeled probes

53
Q

Are rapid non-amplified nucleic acid tests sensitive?

A

NO; but they are fast

54
Q

what is the amplifed NA test?

55
Q

IS PCR sensitive?

56
Q

T/F: the genomes of most bacterial pathogens are known

57
Q

When would sensitivity not be an issue when IDing bacteria?

A

after the bacteria has bee grown up in vitro so you have a lot of it vs. trying to test in vivo