Microbiological analysis of medicinal raw materials revealed capsular bacteria. What stain method was used to detect the capsules?

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microbiology an introduction 12th edition test bank Questions

Question 1 of 5

Microbiological analysis of medicinal raw materials revealed capsular bacteria. What stain method was used to detect the capsules?

Correct Answer: A

Rationale: The correct answer is A: Gin's stain method. Gin's stain method is specifically used to detect capsules of bacteria. This method involves staining the bacteria with crystal violet and copper sulfate, which highlights the capsules as a clear halo around the stained bacterial cells. Ziehl-Neelsen's stain is used for acid-fast bacteria like Mycobacterium tuberculosis, Neisser's stain is for detecting Neisseria species, and Gram's stain is for differentiating bacteria based on their cell wall composition (Gram-positive vs. Gram-negative). Therefore, choices B, C, and D are incorrect for this scenario.

Question 2 of 5

Which bacteria are capable of forming spores to survive in extreme conditions?

Correct Answer: C

Rationale: The correct answer is C because both Clostridium botulinum and Bacillus anthracis are capable of forming spores to survive in extreme conditions. Clostridium botulinum is known for causing botulism and produces highly heat-resistant spores, while Bacillus anthracis is the causative agent of anthrax and also forms spores. Choice A is incorrect because only Clostridium botulinum is mentioned, not Bacillus anthracis. Choice B is incorrect because only Bacillus anthracis is mentioned, not Clostridium botulinum. Choice D is incorrect as it states that none of the bacteria can form spores, which is false based on the characteristics of Clostridium botulinum and Bacillus anthracis.

Question 3 of 5

Which of the following proteins are encoded by herpesviruses and required for viral DNA replication

Correct Answer: A

Rationale: The correct answer is A: viral DNA polymerase. Herpesviruses require viral DNA polymerase for viral DNA replication. This enzyme is responsible for synthesizing new DNA strands using existing viral DNA as a template. Ribonucleotide reductase (B) is not directly involved in DNA replication but in the synthesis of deoxyribonucleotides. Neuraminidase (C) is an enzyme found in influenza viruses, not herpesviruses. Thymidine kinase (D) is involved in nucleotide metabolism but is not essential for viral DNA replication in herpesviruses.

Question 4 of 5

In a bacteriological laboratory some bacterial smears had to be stained by Gram's method. For this purpose the following reagents were prepared: gentian violet, Lugol's solution, aqueous fuchsin solution. What other reagent is required?

Correct Answer: A

Rationale: The correct answer is A: 96% ethanol. In Gram's staining method, after applying gentian violet, Lugol's solution, and aqueous fuchsin, the next step is to use a decolorizing agent like 96% ethanol to wash away the excess stain from the Gram-negative bacteria. This step is crucial as it helps differentiate between Gram-positive and Gram-negative bacteria based on their cell wall properties. The other choices are incorrect because sulfuric acid is not used in Gram's staining method, methylene blue is typically used in other staining techniques like the simple stain, and carbolic fuchsin is not a standard reagent in the Gram's staining process.

Question 5 of 5

A wound smear from a patient revealed Gram-positive cocci arranged in clusters. The culture was catalase-positive and coagulase-positive. What is the causative agent?

Correct Answer: A

Rationale: The correct answer is A: Staphylococcus aureus. 1. Gram-positive cocci in clusters suggest staphylococci. 2. Catalase-positive indicates staphylococci since streptococci are catalase-negative. 3. Coagulase-positive further confirms Staphylococcus aureus, distinguishing it from other staphylococci. Summary: B is incorrect as Streptococcus pyogenes is catalase-negative. C is incorrect as Micrococcus luteus is catalase-negative and coagulase-negative. D is incorrect as Enterococcus faecalis is catalase-negative and coagulase-negative.

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