Q74 | Match the test in Group I with its application in Group II
| Group I | Group II |
|---|---|
| P. Ouchterlony-Fulthorpe test
Q. Limulus amoebocyte lysate test R. Weil-Felix reaction test S. Complement-fixation test |
1. IgM detection
2. Determining antigen-antibody specificity 3. Endotoxin detection 4. Rickettsial infection diagnosis |
CSIR NET Life Sciences: Ouchterlony Test Matching with Immunological Applications
The correct matching for the immunological tests in Group I with their applications in Group II is option (A): P-2, Q-3, R-4, S-1. This pairs each test accurately based on standard serological principles used in diagnostics and research.
Test Matching Explained
Group I tests are classic immunological assays, while Group II lists specific diagnostic applications. Here’s the detailed rationale for the correct pairing:
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P. Ouchterlony-Fulthorp test (2. Determining antigen-antibody specificity): This double immunodiffusion technique places antigen and antibody in adjacent agar gel wells, allowing diffusion and precipitation line formation to reveal reaction patterns like identity, non-identity, or partial identity, confirming specificity.
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Q. Limulus amebocyte lysate test (3. Endotoxin detection): Extract from horseshoe crab amebocytes clots specifically with gram-negative bacterial endotoxins (LPS), enabling sensitive pyrogen detection in pharmaceuticals and samples.
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R. Weil-Felix reaction test (4. Rickettsial infection diagnosis): Uses Proteus OX strains (OX19, OX2, OXK) to detect cross-reacting antibodies in rickettsial diseases like typhus or scrub typhus via agglutination.
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Q. Complement fixation test (1. Ig detection): Detects antigen-antibody complexes by measuring complement fixation; if patient serum antibodies bind test antigen, complement is consumed, preventing indicator red cell hemolysis—used for Ig/antibody presence.
Why Other Options Fail
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(B) P-2, Q-1, R-4, S-3: Swaps Q (LAL, endotoxin-specific) with S (CFT, not for endotoxins) and misplaces others; LAL does not detect Ig.
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(C) P-1, Q-3, R-2, S-4: Assigns Ouchterlony to Ig detection (it’s for specificity patterns, not direct Ig quantitation) and Weil-Felix to specificity (it’s rickettsial serology).
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(D) P-4, Q-3, R-2, S-1: Wrongly links Ouchterlony to rickettsia (uses ELISA/IFA instead) and CFT to specificity (focuses on presence, not detailed patterns).
Introduction to Keyphrase Test Matching
Ouchterlony test matching Group I Group II CSIR NET questions test core immunology knowledge for competitive exams. These assess precipitation, coagulation, agglutination, and fixation principles in diagnostics.
Core Applications Breakdown
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Ouchterlony-Fulthorp excels in visualizing antigen-antibody specificity via precipitin lines.
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Limulus amebocyte lysate revolutionized endotoxin detection for sterile products.
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Weil-Felix remains vital for presumptive rickettsial infection diagnosis despite modern alternatives.
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Complement fixation quantifies Ig through hemolysis inhibition.
Exam Preparation Strategy
Practice by diagramming diffusion patterns and reaction cascades. Focus on CSIR NET patterns where mispairing specificity versus detection trips candidates.


