Who is usually credited with the discovery of penicillin? |
Fleming |
Whose discovery of streptomycin stimulated an intense search for other antibiotics? |
Waksman |
The use of arsenic compound Salvarsan as a treatment for syphilis is credited to |
Ehrlich. |
Chemotherapeutic agents that are natural products of microorganisms are most specifically referred to as __________. |
antibiotics |
Who is generally credited with the discovery of sulfanilamide as a chemotherapeutic agent? |
Gerhard Domagk |
__________ __________ are activities of a chemotherapeutic agent that damage the host either by inhibiting the same process in the host as in the target cell or by damaging other processes. |
Side effects |
The minimum lethal concentration (MLC) is the lowest concentration of drug from which organisms fail to recover when removed from the drug. |
true |
Agents that are static and, therefore, do not kill infecting microorganisms are not useful as chemotherapeutic agents. |
false |
A drug that disrupts a microbial function not found in animal cells usually has a higher therapeutic index. |
true |
The drug level required for the clinical treatment of a particular infection is called the |
therapeutic dose. |
Which of the following inhibits protein synthesis? |
erythromycin |
Which of the following is likely to have the most toxic side effects to humans? |
disrupters of cell membrane structure |
Isoniazid is a narrow-spectrum antibiotic that |
is one of the few drugs effective against Mycobacterium tuberculosis. |
Consider an antibacterial drug. In which of the following cases would the action of the drug be considered primarily bacteriostatic? |
The MLC is 10-20 times higher than the MIC. |
Chemotherapeutic agents that are chemically modified natural products of microorganisms are most specifically referred to as __________. |
semisynthetic drugs |
Chemotherapeutic agents that are artificially produced are most specifically referred to as __________. |
synthetic drugs |
The ratio of toxic dose to therapeutic dose is called the |
therapeutic index. |
The minimal lethal concentration (MLC) is the |
lowest concentration of a drug that kills a particular pathogen. |
The lowest concentration of an antibiotic that prevents growth is the |
minimal inhibitory concentration (MIC). |
Which of the following is a desirable general characteristic of antimicrobial drugs? |
selective toxicity, broad-spectrum of activity, and bactericidal rather than bacteriostatic |
When a chemotherapeutic agent is effective against many different pathogens, it is said to be a __________ antibiotic. |
broad-spectrum |
In a disk diffusion assay for drug susceptibility, a drug producing a larger clear zone is always more effective than a drug than to one producing a smaller clear zone. |
false |
Which of the following affects the size of the clear zone in a disk diffusion test of antimicrobial susceptibility? |
the initial concentration of the drug, the solubility of the drug, and the diffusion rate of the drug |
The E test is |
a quantitative antibiotic sensitivity test that utilizes plastic strips impregnated with an antibiotic of interest. |
In the broth dilution test, the highest concentration of the antibiotic resulting in no growth after 16 to 20 hours of incubation is the MIC. |
false |
Which of the following is not true about Kirby-Bauer disk diffusion method? |
Bacteria used to swab plate should be at least a week old. |
Which of the following does not inhibit protein synthesis? |
penicillin |
The most selective antibacterial agents are those that interfere with bacterial cell wall synthesis. This is because |
bacterial cell walls have a unique structure not found in eukaryotic host cells. |
In addition to inhibiting the transpeptidation reaction in cell wall synthesis, penicillins may also destroy bacteria by |
stimulating proteins to form holes in the plasma membrane. |
It is difficult to treat central nervous system infections because |
it is difficult for many drugs to penetrate the blood-brain barrier. |
Aminoglycoside antibiotics |
bind to the 30S ribosomal subunit. |
Sulfonamides and other drugs that inhibit folic acid synthesis have a high therapeutic index because |
humans do not synthesize folic acid but obtain it in their diets. |
Antibiotics that are given by injection are said to have a(n) __________ route of administration. |
parenteral |
Sulfonamides inhibit the production of folic acid and, therefore, inhibit the synthesis of __________. |
purines and pyrimidines |
Which of the following is (are) true about cephalosporins? |
They, like penicillin, inhibit bacterial cell wall synthesis, there are four generations of cephalosporins, and they can be given to patients with penicillin allergies. |
Bacitracin |
inhibits peptidoglycan synthesis. |
Vancomycin |
inhibits the transpeptidation reaction in peptidoglycan biosynthesis. |
Which of the following is a useful mechanism of action for an antibacterial drug? |
inhibition of cell wall synthesis, inhibition of protein synthesis, and interference with RNA and DNA synthesis |
Which of the following antibiotics specifically inhibits DNA synthesis? |
quinolones |
Protein synthesis inhibitors have a low therapeutic index because they usually cannot discriminate between prokaryotic and eukaryotic ribosomes. |
false |
Ampicillin, like penicillin, must be administered by injection because it is rapidly degraded in the stomach and cannot, therefore, be given orally. |
false |
A(n) __________ is a drug that blocks the function of a metabolic pathway. |
antimetabolite |
Which of the following is normally treated by antifungal creams and solutions? |
superficial mycoses |
The treatment for pneumonia caused by Pneumocystis jiroveci in AIDS patients is |
either atovaquone or pentamidine |
_______________ ________________ from Streptomyces spp. binds to the sterols in fungal membranes, disrupting membrane permeability and causing leakage of cell constituents. |
Amphotericin B |
Treatment of fungal infections is more difficult than treatment of bacterial infections because the greater metabolic similarity between the fungi and their hosts limits the ability of a drug to have a selective toxicity. |
true |
A neuraminidase inhibitor called __________ is sometimes used in the treatment of people infected with influenza viruses. |
Tamiflu |
Which of the following is sometimes useful against viral infections? |
zidovudine |
Which of the following is the major reason why it has been difficult to treat viral infections with chemotherapeutic agents? |
Viruses use the metabolic machinery of their hosts, which limits many of the potential points of attack. |
________ and ________ can be used to prevent influenza A infections, reducing the incidence of influenza by 50 to 70% in an exposed population. |
Amantadine, rimantadine |
All of the following are reverse transcriptase inhibitors used to treat HIV infection except |
acyclovir. |
The antiviral drugs currently approved for use in HIV disease include |
nucleoside reverse transcriptase inhibitors, nonnucleoside reverse transcriptase inhibitors, protease inhibitors, and fusion inhibitors. |
Drugs are used to treat malaria include |
chloroquine and qualaquin. |
Metronidazole is used to treat Entamoeba infections. |
true |
The antimicrobial action of artemisinin is not well understood but this chemical appears to |
form reactive oxygen intermediates inside Plasmodium-infected red blood cells. |
Most of the drugs used to treat protozoan infection have insignificant side effects; because protozoa are prokaryotes, the potential for drug action on host cells and tissues is less than it is when targeting bacteria. |
false |
________, which is used to treat Toxoplasma gondii, is an analog of ________, an integral component of the eukaryotic electron transport system. |
Atovaquone, ubiquinone |
Bacteria in biofilms or abscesses may be replicating very slowly and are therefore resistant to chemotherapy because many agents affect pathogens only if they are actively growing and dividing. |
true |
The chemotherapeutic agent must reach levels in the body that are ________ the pathogen’s MIC value if it is going to be effective. |
A. greater than |
The concentration of an antimicrobial drug that is reached in the body will depend on |
the amount of drug administered, the route of administration and speed of uptake, and the rate at which the drug is cleared or eliminated from the body. |
Penicillin is frequently injected but not normally given orally because it is rapidly degraded in the stomach. |
true |
Genes for drug resistance may be present |
both on the chromosome and on plasmids |
One way in which organisms may exhibit resistance to a drug is the ability to pump the drug out of the cell immediately after it has entered. |
true |
The effects of most antimicrobial drugs are greater if the microorganisms are actively growing. |
true |
R plasmids, transposons, integrons and gene cassettes have each contributed to the spread of bacterial antibiotic resistance. |
true |
One way that the development of drug resistance in viruses has been reduced has been by the use of a cocktail of several drugs at high doses. |
true |
The drug of last resort that is generally used in treating infections caused by methicillin resistant Staphylococcus aureus is |
vancomycin. |
Development of drug resistance is not discouraged by |
widespread use of broad-spectrum drugs. |
Which of the following is (are) used by microorganisms to become resistant to a particular drug? |
enzymatic inactivation of the drug, exclusion of the drug from the cell, and an alternate metabolic pathway that bypasses the drug-sensitive step |
A plasmid bearing one or more antibiotic resistance genes is a(n) |
R plasmid. |
Chapter 34 Microbiology
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