bacteriology Flashcards

microbiological diagnosis: explain the concept of best-guess diagnosis and the contribution of the laboratory to it, recall how a microbiology laboratory works and what investigations may be performed

1
Q

what is syphilis and associated symptom

A

STI with skin rash

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2
Q

how does endocarditis present

A

fever and weight loss

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3
Q

what type of bacteria is toxoplasma

A

opportunistic

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4
Q

how does bacterial tuberculosis present

A

weight loss, fever, co-infection with HIV

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5
Q

common diagnostic techniques

A

culture (sterile sites e.g. blood, CSF - no bacteria should be present; non-sterile sites - commensal bacteria present), serology, molecular techniques (screening, identify resistance genes), antimicrobial susceptibility testing (main reason persist with culture; likelihood to respond to antibiotics)

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6
Q

what to do with specific clinical details (e.g. history, travel)

A

look for specific bacteria matching symptoms

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7
Q

where are normal bacteria

A

nasopharynx, skin, upper bowel, lower bowel, vagina

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8
Q

blood culture sterile sites: steps

A

placed into plastic bottles with growth media (anaerobic and aerobic; paeds normally optimised for aerobic as not much blood) -> machine warms it, agitates so bathe in broth for optimal conditions to grow -> toxic metabolites produced which interact with indictor at bottom to change colour -> machine detects colour change and notifies of positive growth (usually 16-20 hours) -> removed for rapid identification testing -> placed on agar plates for susceptibility testing to antibiotics

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9
Q

when to give blood culture to lab, and affect of sample

A

give before treating with antibiotics (skew results); where plated pus/sample, can inhibit growth, giving false negative

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10
Q

gram +ve vs gram -ve; staining

A

gram +ve: thick peptidoglycan cell wall, gram -ve: thin peptidoglycan cell wall, LPS polysaccharide membrane outside this; gram +ve stain more purple as stains peptidoglycan cell wall

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11
Q

what else is observed after gram type

A

shape and division (clumps or chains)

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12
Q

how to separate Staphylococci types

A

divide in clumps; coagulase test (+ve and -ve): ability of bacteria to produce clot in plasma

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13
Q

S. aureus complex: infections, gram and coagulase test

A

major pathogen (includes MRSA) responsible for severe infections e.g. skin/soft tissue, endocarditis, osteomyelitis; gram +ve and coagulase -ve

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14
Q

type and division of Streptococci, and how it is separated into groups

A

gram +ve and divide chain to chain; haemolytic (B is main pathogens; within which is group A which is Strep pathogens); group C and G like group A but less virelent

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15
Q

what is S. pnueomoniae

A

gram -ve bacilli

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16
Q

non-sterile site: diarrhoea - what bacteria to look for after request and why

A

common after food poisoning; Salmonella (incl. S. typhi), Shigella, Campylobacter, E. coli O157, C. dificile (if recent antibiotic use), Cholera

17
Q

non-sterile site: diarrhoea - what else to look for after request because of travel/other history

A

parasites: Amoeba, Giardia, Cryptosporidium; viruses e.g. norovirus

18
Q

bacterial investigations of stool sample

A

culture on agar plate, only Salmonella, Shigella, Campylobacter looked for routinely; PCR initially as less sensitive (if positive, then do sensitivity test); different culture requirements to suppress growth (only grow pathogens to kill other bacteria); C. difficile detected by toxin/PCR toxin gene as difficult to grow

19
Q

parasitic investigations of stool sample

A

don’t grow, so concentration in faeces then special strains (for different parasites)

20
Q

why are there different agar

A

optimal for different bacteria

21
Q

what must be thought of before requesting test

A

pre-test probability (based on clinical judgement), as if this is low, then low positive predictive value (sensitivity)

22
Q

what does sensitivity testing do

A

tests bacteria against antibiotics to determine resistance and MIC (minimum inhibitory concentrations; minimal amount of antibiotic needed to inhibit growth in vivo)

23
Q

how is antibiotic senstivity or resistance determined

A

based on MIC and pharmacodynamics and pharmacokinetics by usual dose of drug

24
Q

how is MIC, and therefore sensitivity or resistance, calculated

A

gradient, disc diffusion

25
why would you genotype entire genome
to determine genotype and associated phenotype, preventing need of culture for and sensitivity testing
26
gold standard for serology
seroconversion (seronegative to seropositive when specific antibody develops and becomes detectable in blood)