INI-CET EXAM -2025
Applied Microbiology & Infection control
Easy

A culture of Streptococcus pneumoniae shows alpha-hemolysis and draughtsman colonies on blood agar. Which test is most useful for its identification?

Appeared in: INI-CET EXAM -2025

Explanation

  • The bile solubility test is a key confirmatory test for Streptococcus pneumoniae.
  • S. pneumoniae possesses an autolytic enzyme (autolysin) that is activated by bile salts, causing the cells to lyse and the colony or suspension to clear.
  • This property distinguishes it from other alpha-hemolytic streptococci, such as the viridans group, which are bile insoluble.
  • The characteristic 'draughtsman' appearance of older colonies is also due to this autolytic activity, where the center of the colony collapses.

Why Other Options Were Wrong

  • Option A: This is a statement about prevention, not a diagnostic test. It is also factually incorrect, as highly effective pneumococcal vaccines (PCV13, PPSV23) exist.
  • Option B: Streptococcus pneumoniae is catalase-negative. The catalase test differentiates catalase-positive staphylococci from catalase-negative streptococci.
  • Option C: This test is not specific. While S. pneumoniae is usually sensitive to vancomycin, so are many other gram-positive bacteria, including the viridans streptococci from which it needs to be differentiated.

Related Visual

Visual explanation — Related Visual
  • Visual 1: Diagram - A side-by-side comparison of the bile solubility test. One test tube labeled 'S. pneumoniae' shows a clear liquid (positive result), while another labeled 'Viridans streptococci' shows a turbid liquid (negative result).
  • Visual 2: Image - A blood agar plate showing the characteristic alpha-hemolysis (greenish discoloration) and 'draughtsman' colonies (colonies with a depressed center and raised edges) of S. pneumoniae.
Clinical Relevance
  • Nursing practice connection: Knowing Microbiological identification of Streptococcus pneumoniae helps nurses interpret findings accurately and avoid errors in routine assessment, medication administration, and patient teaching.
  • Accurate and rapid identification of S. pneumoniae is critical because it is a major cause of community-acquired pneumonia, meningitis, otitis media, and sepsis.
  • Differentiating S. pneumoniae from the less pathogenic viridans streptococci (which are part of the normal oral flora) is essential for appropriate clinical management and antibiotic selection.
  • What if? If the alpha-hemolytic streptococcus was optochin-resistant and bile-insoluble, it would be identified as a member of the viridans group. This would have different clinical implications, as viridans streptococci are a common cause of subacute bacterial endocarditis but are less frequently associated with pneumonia or meningitis in immunocompetent individuals.
How to Approach the Question
  • First, identify the key information in the question stem: the organism is Streptococcus pneumoniae, and it shows alpha-hemolysis and draughtsman colonies.
  • Recognize that alpha-hemolysis is also produced by other bacteria (viridans streptococci), so a differentiating test is needed.
  • Evaluate each option as a potential identification test for S. pneumoniae.
  • Option A ('No vaccine') is about prevention, not identification, and is factually wrong.
  • Option B ('Catalase positive') is incorrect because streptococci are catalase-negative. This test distinguishes them from staphylococci.
  • Option C ('Vancomycin sensitivity') is not specific enough, as many gram-positive cocci are sensitive.
Concept Tested & Keywords
  • Concept Tested: Microbiological identification of Streptococcus pneumoniae
  • Stem keywords: Streptococcus pneumoniae, alpha-hemolysis, draughtsman colonies, blood agar
  • Lead-in keywords: most useful

Question ID

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