Bacteriology Flashcards

1
Q

Common diagnostic techniques for bacteria

A

Cultures
Serology
Molecular techniques
Antimicrobial susceptobility testing

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2
Q

2 different types of culture

A

Sterile- like blood and CSF
Non sterile sites- sites of infection
NOTE- skin is not sterile as million of commensal bacteria here

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3
Q

How are blood cultures tested as positive

A

The blood is put in tubs containing nutrients for bacteria and intubated at 37C- they are left and after time the bacteria produce waste products that change the colour of indicator at the bottom of the tubs

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4
Q

What happens to tubs containing blood cultures after their intubation

A

They are put in a machine with sensors to tell if there is a change in the colour of the indicator

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5
Q

What do you do if blood tests positive for bacteria and why

A

Carry out gram staining to work out what antibiotics would be best appropriate

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6
Q

Gnerally speaking where do gram positive infect

A

Skin and soft tissue

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7
Q

Generally speaking where do gram negative bacteria infect

A

abdomen and urinary tract

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8
Q

Cases where should give antibiotics regardless of if tests have come back

A

Meningitis and meningococcoal spticaemia

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9
Q

Why can you use non-selective agar plates for blood cultures

A

Blood should be sterile anyway

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10
Q

What is chocolate agar

A

Where the blood on agar is cooked

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11
Q

Why is chocolate agar cooked

A

Some bacteria are unable to lyse to RBCs to gain nutrients so cooking blood does this for them

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12
Q

Common example of bacteria growing on chocolate agar

A

Haemophilus influenzae

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13
Q

What grows on macconkey agar

A

Gram negative bacteria

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14
Q

Problem of gram negative bacteria

A

Most antibiotics target cell wall which in gram negative bacteria antibiotics are unable to reach because of its lipopolysaccaride outer membrane

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15
Q

Most common bacteria seen

A

gram positive cocci- easy to identify on cultures as have distinguishable growing pattens which can help drive antibiotic treatment

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16
Q

Growing pattern of staphylococci

A

Divide in 2 and from clumps of four- they look like a bunch of grapes

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17
Q

Growing pattern of streptococci

A

Divide end on end so form chains

18
Q

Test carried out on staphylococci bacteria

A

Coagulase test

19
Q

What is purpose of coagulase test

A

Distinguish between virulent staphylococci and commensal bacteria

20
Q

Positive coagulase test

A

This indicates virulence as coagulase is virulence factor

21
Q

Negative coagulase tests

A

Sign of commensal bacteria

22
Q

Test carried on streptococci bacteria

A

Haemolytic test- depends on how they appear on blood agar

23
Q

Potential results of haemolytic agar tests

A

Can either be alpha or beta haemolysis

24
Q

Alpha haemolysis test result

A

Appear green as there is incmplete haemolysis

25
Beta haemolysis
Clear agar as complete heamolysus
26
3 main bacteria stool is tested for in diarrorhoea
Salmonella Shigella Campylobacter
27
What tests are used to diagnose C.difficile
Antigen and toxin gene PCR
28
Why arent cultures used to diagnose C.difficile
Very difficult to grow hence the name so use detection of their toxin
29
Test for salmonella
Grow on XLD agar
30
Positive salmonella test
Goes pink as unable to ferment xylose. Black colonies also form as salmonella forms hydrogen sulfide VERY SPECIFIC TEST
31
Negative salmonella test
Goes yellow as other bacteria are unalbe to ferment Xylose
32
Campylobacter test
Intubate stool sample at 42 degrees as campylobacter able to grow at this temperature. Then put remaining bacteria on a selvetive agar and see if grows
33
Test for cholera
Grow on TCBS agar- green if postive
34
What is minimum inhibitory concentration (MIC)
Lowest amount of antibiotic required to inhibit growth of bacteria in vitro
35
How is MIC used clinically
Set breakpoints and if concentration is below breakpoint then will have postive clinical success in treating bacteria If above then then should be reported as resistant
36
Traditional way of testing sensitivity of antibiotics
Disc diffusion
37
What is carbapenemase
Beta lactamase- breaks down all beta lactams making it untreatable
38
Benefits of disc diffusion
Able to test multiple antibiotics quickly
39
How does disc diffusion work
* There is a set concentration of antibiotic on each disc which is then placed on the agar and incubated for 24 hours * The zone size is interpreted using the breakpoints in the above table (interpretation of zone diameters) * The zone diameter can be used to determine whether it is sensitive or resistant
40
What do disc diffusion and MIC test
Sensitivity of antibiotics