Detecting antimicrobial resistance: Difference between revisions
From IDWiki
m (Aidan moved page Antimicrobial Detecting antimicrobial resistance to Detecting antimicrobial resistance without leaving a redirect) |
No edit summary |
||
Line 1: | Line 1: | ||
= Phenotypic methods = |
|||
= Detecting antimicrobial resistance = |
|||
== |
== Broth dilution tests == |
||
=== Broth dilution tests === |
|||
* Gold standard |
* Gold standard |
||
Line 13: | Line 11: | ||
** Trailing can occur; the MIC is read at the first spot where trailing begins |
** Trailing can occur; the MIC is read at the first spot where trailing begins |
||
== Agar dilution == |
|||
* Concentration of antibiotic is incorporated into the agar |
* Concentration of antibiotic is incorporated into the agar |
||
Line 20: | Line 18: | ||
** Final inoculum of 10^4^ CFU per spot |
** Final inoculum of 10^4^ CFU per spot |
||
== Disk diffusion == |
|||
* Drug released from disk with an antimicrobial agent diffuses through the agar |
* Drug released from disk with an antimicrobial agent diffuses through the agar |
||
Line 27: | Line 25: | ||
* If on blood agar, must be read from the front |
* If on blood agar, must be read from the front |
||
== Other == |
|||
* Potentiation using standard methods |
* Potentiation using standard methods |
||
Line 33: | Line 31: | ||
* Lateral flow assay |
* Lateral flow assay |
||
= Genotypic methods = |
|||
* Detected resistance may not predict antibiotic failure if genes are non-functional or not expressed, or may be expressed in insignificant levels |
* Detected resistance may not predict antibiotic failure if genes are non-functional or not expressed, or may be expressed in insignificant levels |
||
Line 41: | Line 39: | ||
** Sequencing |
** Sequencing |
||
= Other methods = |
|||
⚫ | |||
[[Category:Antimicrobials]] |
|||
⚫ | |||
[[Category:Microbiology]] |
Revision as of 00:12, 15 August 2019
Phenotypic methods
Broth dilution tests
- Gold standard
- Uses serial two-fold dilutions of the antimicrobial agent
- Macrobroth has a final volume of 1-2 mL
- Microbroth has a final volume of 50 µL
- Determines an MIC and MBC (min. bactericidal concentration)
- Read at lowest concentration that inhibits growth (i.e. no obvious growth)
- Trailing can occur; the MIC is read at the first spot where trailing begins
Agar dilution
- Concentration of antibiotic is incorporated into the agar
- Each agar plate has a different concentration
- Multiple inocula are set up on each plate
- Final inoculum of 10^4^ CFU per spot
Disk diffusion
- Drug released from disk with an antimicrobial agent diffuses through the agar
- Zone diameter is inversely proportional to the log of the MIC
- Interpretation usually uses reflected light reading above a black, nonreflective background; measured using a ruler on the back of an inverted dish
- If on blood agar, must be read from the front
Other
- Potentiation using standard methods
- Colorimetric methods
- Lateral flow assay
Genotypic methods
- Detected resistance may not predict antibiotic failure if genes are non-functional or not expressed, or may be expressed in insignificant levels
- Similarly, a negative results may not indicate susceptibility given genetic variation, novel mechanisms of resistance, or inhibition of amplification
- Genotypic methods
- PCR
- Sequencing