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Microbiology

20 cards from 2 lessons in Microbiology, each linking to the passage it came from.

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Urinary Tract Bacteriology and Identification Methods

Antimicrobial Susceptibility Testing and Resistance Mechanisms

  • What is the minimum inhibitory concentration (MIC)?

    The lowest antimicrobial concentration that prevents visible growth under the specified test conditions.

    It measures growth inhibition only. A susceptible, intermediate, or resistant category comes from comparing it with the breakpoint for that organism and drug.

    Read the passage: Interpretation: MIC, breakpoints, and categories

  • What measurement is read from a disk-diffusion susceptibility test?

    The diameter of the growth-inhibition zone, in millimeters.

    Compare the diameter with the interpretive criteria for that organism, drug, and method.

    Read the passage: Disk diffusion

  • How does broth microdilution expose an isolate to different antimicrobial concentrations?

    It uses a series of drug dilutions in small broth wells.

    The lowest concentration with no visible growth is the MIC.

    Read the passage: Dilution and gradient-diffusion methods

  • Why does an MIC alone not provide a clinical susceptibility category?

    The category comes from comparing the MIC with the breakpoint for that organism and drug.

    Breakpoints also depend on the dose given and the infection site, such as meningitis.

    Read the passage: Interpretation: MIC, breakpoints, and categories

  • How does the CLSI intermediate category help when measurements fall near a breakpoint?

    It acts as a buffer between the susceptible and resistant categories where measurement is uncertain.

    This reduces the risk of calling a resistant isolate susceptible, or the reverse.

    Read the passage: Interpretation: MIC, breakpoints, and categories

  • What does the CLSI susceptible-dose dependent category communicate?

    Susceptibility depends on a dosing regimen higher than the standard one.

    The laboratory reports the category with the exposure its breakpoint requires, and the clinical team uses that report to select the regimen.

    Read the passage: Interpretation: MIC, breakpoints, and categories

  • What does *mecA* encode in methicillin-resistant staphylococci?

    The altered penicillin-binding protein PBP2a.

    Its low affinity for many β-lactams underlies the resistance.

    Read the passage: Staphylococcal methicillin resistance

  • Why is cefoxitin useful for phenotypic detection of methicillin resistance in *S. aureus*?

    It is a strong inducer of *mecA* expression and gives clear endpoints.

    Read the result against the cefoxitin criteria for that staphylococcal species and method.

    Read the passage: Staphylococcal methicillin resistance

  • Why does a negative *mecA* PCR result not rule out methicillin resistance?

    A targeted assay misses mechanisms outside its target, such as *mecC*.

    A cefoxitin phenotype or PBP2a test resolves the disagreement, and an unresolved conflict in *S. aureus* is reported as resistant.

    Read the passage: Staphylococcal methicillin resistance

  • What kind of susceptibility result is needed for vancomycin against *S. aureus*?

    A true MIC value in µg/mL.

    Vancomycin disk diffusion misses vancomycin-intermediate *S. aureus* (MIC 4 to 8 µg/mL).

    Read the passage: Vancomycin-intermediate and -resistant S. aureus

  • What do you check when an *S. aureus* isolate shows unexpected reduced vancomycin susceptibility?

    Culture purity, the organism identification, and a repeat MIC.

    A mixed culture can create a misleading resistance result.

    Read the passage: Vancomycin-intermediate and -resistant S. aureus

  • What do antimicrobial susceptibility testing (AST) control results have to show before affected patient results are reported?

    Each control strain's result must fall inside its published QC range for that drug.

    Investigate an out-of-range result and document corrective action before reporting resumes.

    Read the passage: Quality control and verification

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