Differentiating media are:
- A. Lowenstein-Jensen and Petraniani
- B. Apoholate-citrate aga and Brilliant-green phenol-red Lactose Agar
- C. Endo, Gassner and Levin
- D. None of the above
Correct Answer: C
Rationale: The correct answer is C because Endo, Gassner, and Levin are all examples of differential media used in microbiology. These media contain specific components that allow for the differentiation of different types of microorganisms based on their metabolic characteristics or biochemical reactions. Lowenstein-Jensen and Petraniani (choice A) are selective media for mycobacteria, not differential. Apoholate-citrate agar and Brilliant-green phenol-red Lactose agar (choice B) are selective media for Salmonella and E. coli, respectively, not differential. Therefore, the correct choice is C as it includes examples of differential media commonly used for microbial identification.
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Agents associated with human disease but generally not a serious health risk are classified in which of the following risk groups?
- A. RG1
- B. RG2
- C. RG3
- D. RG4
Correct Answer: B
Rationale: The correct answer is B: RG2. RG2 is appropriate for agents associated with human disease that pose a moderate health risk. These agents may cause disease of varying severity, but generally do not result in serious health consequences. Other choices are incorrect because: A: RG1 is for agents not associated with disease in healthy adults, C: RG3 is for agents associated with serious or lethal human disease, and D: RG4 is for agents that pose a high risk of life-threatening disease and for which there are no treatments.
A smear of a patient's sputum suspected for tuberculosis was prepared and stained. The smear showed red bacilli against a blue background. What staining method was used?
- A. Ziehl-Neelsen
- B. Gram
- C. Giemsa
- D. Neisser
Correct Answer: A
Rationale: The correct answer is A: Ziehl-Neelsen staining method. This method is used to detect acid-fast bacteria like Mycobacterium tuberculosis. Step-by-step rationale: 1. Acid-fast bacteria resist decolorization with acid-alcohol. 2. The red bacilli seen in the smear indicate acid-fast bacteria. 3. Ziehl-Neelsen stain uses carbol fuchsin to stain acid-fast bacteria red. 4. The blue background is likely the counterstain methylene blue. Incorrect choices: B: Gram stain is for categorizing bacteria into Gram-positive or Gram-negative, not specific for acid-fast bacteria. C: Giemsa stain is used for blood films and detecting parasites, not acid-fast bacteria. D: Neisser stain is not a standard microbiological staining method.
The discipline addressing issues associated with the choice and application of drugs to be used for disease prevention, treatment, and/or diagnosis is:
- A. pharmacotherapeutics
- B. toxicology
- C. pharmacokinetics
- D. pharmacy
Correct Answer: A
Rationale: The correct answer is A: pharmacotherapeutics. Pharmacotherapeutics focuses on the selection and use of drugs for disease prevention, treatment, and diagnosis. It involves determining the most effective and safe medications for specific conditions based on patient factors. Toxicology (B) is the study of the adverse effects of chemicals, including drugs. Pharmacokinetics (C) focuses on drug absorption, distribution, metabolism, and excretion in the body. Pharmacy (D) involves the preparation and dispensing of medications, but does not specifically address drug selection and application for disease management. Therefore, pharmacotherapeutics is the most suitable discipline for addressing the use of drugs in disease management.
Aflatoxins are produced by:
- A. Genus Cryptococcus
- B. Genus Actinomyces
- C. Genus Streptococcus
- D. Genus Aspergillus
Correct Answer: D
Rationale: The correct answer is D: Genus Aspergillus. Aflatoxins are toxic compounds produced by certain species of fungi, particularly Aspergillus species. Aspergillus flavus and Aspergillus parasiticus are well-known producers of aflatoxins. These fungi can contaminate crops such as peanuts, corn, and tree nuts, leading to potential health risks. Cryptococcus (A), Actinomyces (B), and Streptococcus (C) are not known to produce aflatoxins. It is important to be aware of the sources and implications of aflatoxin contamination to ensure food safety and public health.
Which bacteria are known for their ability to fix nitrogen?
- A. Bacillus cereus
- B. Azotobacter species
- C. Clostridium botulinum
- D. Escherichia coli
Correct Answer: B
Rationale: The correct answer is B: Azotobacter species. Azotobacter are known for their ability to fix nitrogen through the process of nitrogen fixation, converting atmospheric nitrogen into a form that plants can use. Bacillus cereus is not known for nitrogen fixation. Clostridium botulinum is a bacterium that causes botulism and does not fix nitrogen. Escherichia coli is a common gut bacterium but does not have the ability to fix nitrogen. Thus, Azotobacter species is the correct choice based on its unique ability to fix nitrogen.