| A | B |
|---|
| Auramine and rhodamine is a basic fluorescent dye that binds to the mycolic acids in teh cell walls of mycobacteria | Mycobacteria stains |
| This microscopy does not allow light to pass directly though condenser | Darkfield |
| Bacteria with thick peptioglycan and numerous teichoic acid cross linkages are | gram positive |
| Overdecolorizing a GP bacteria during gram stain procedure will give the bacteria this appearance | gram negative |
| This media supports the growth of many types of organisms | nutrative |
| This media contains one or more agents that are inhibitory to all organisms except the organism in question | selective |
| Reading a hemolytic reaction on a BAP requires the technologist | to hold the plate up to light for the transmitted light to pass through the ager |
| This genetic makeup has a higher melting temperature | 50% C-G bonds |
| analysis or quantitation of the number of target molecules occurs in this molecular technique | quantitative PCR |
| Growth behavior of microorganism and proteins, enzymes, and toxins are considered | phenotypic diagnostic techniques |
| molecular behavior of microorganisms are | genotypic diagnostic techniques |
| I am produced by the offspring of a single hybrid cell | Monoclonal cells |
| I am produced by immunizing animals | polyclonal cells |
| I am used to determine hemolysis patterns | blood agar plates |
| I am an agar that provides hemin | chocolate agar |
| I contain antibiotics colistin and NA | CNA agar |
| In contain eosin Y and methylane blue to inhibit GP bacteria | EMB agar |
| N. gonorrhoea grows well on me | MTM agar |
| used to describe microorganisms that have enhanced growth in atmospher with increased CO2 | Capnophilic |
| Microorganism that grows under reduced O2 (5-10%) and increased CO2 (8-10%) | Microaerophilic |
| I am performed using hydrogen peroxide as my reagent | catalase test |
| This test provides a visual assessment of the adequacy of a specimen | immunofluorescent microscopy |
| I will stain bright apple green using FITC dye | Legionella pneumphilia |
| Common latex aggutination test for Cryptococcus is performed on this specimen | CSF |
| I bind to and block surface receptors for host cells | neutralizing antibodies |
| I attach to the surface of pathogens and contribute to their destruction by lytic action of complement | complement-fixing antibodies |
| I use electrophoresis and then transfer the proteins to solid support matrix for identification. | Western blot assay |
| I can kill organisms | bactericidal |
| I inhibit growth of organisms | bacteriostatic |
| We are known to inhibit cell wall synthesis | beta-lactams |
| We are known to inhibit cell membrane function | lipopeptides |
| We inhibit protein synthesis | aminoglycosides |
| I have an intrinsic resistance to ampicillin | Klebsiella |
| I have an intrinsic resistance to aminoglycosides | Enterococci |
| I am an antibiotic that works well for UTI's | Nitrofurantoin |
| I am an antibiotic that works well for GN bacteria | Polymyxins |
| In this assay the correlation of the MIC with serum-achievable levels of common doses of antimicrobial agents | microdilution broth dilution |
| If S. aureus is resistant to cefoxitin this should be prescribed instead. | Vancomycin |
| If Viridans streptococci is resistant to penicillin this can be given instead | erythromycin |
| I use a series of plaste with different antimicrobial concentrations inoculated with multiple bacterial isolates per plate | agar dilution |
| I inhibit cell wall synthesis | beta-lactams, fosfomycin, glycopeptides |
| I inhibit cell membrane function | lipopeptides |
| I inhibit protein synthesis | aminoglycosides, macrolide-lincosamides, ketolides, tetracyclines, |
| I inhibit nucleic acid synthesis | fluoroquinolones, metronidazole, rifamycin |
| We disrupt the folic acid pathway | Sulfonamides and Trimethoprim |
