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Question #46491

Difficulty: 8/10 | 🟢 Free

The Question

To detect Plasmodium infection during the early stages of low parasitemia, a biotechnology firm developed a PCR-based molecular diagnostic kit. The primers were designed to be complementary to the gene encoding a major merozoite surface protein. However, clinical trials in endemic areas frequently produced false-negative results in patients with active malaria. Which of the following best explains this molecular diagnostic failure?

Options

  • A.

    High polymorphism in the target gene due to immune selection pressure causes primer-template mismatch and failed annealing.

  • B.

    The target gene is absent in the sporozoite stage genome, making PCR detection impossible during early liver infection.

  • C.

    Hemozoin pigment released during the erythrocytic phase irreversibly denatures Taq polymerase during the extension step.

  • D.

    The merozoite surface protein is an RNA transcript, requiring Reverse Transcriptase PCR (RT-PCR) for successful amplification.

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Correct Answer

Step-by-Step Solution

Explanation

How the Examiner Thinks

Regulatory_Failure

Understand how NOT, EXCEPT, and logical constraints are used to manipulate exam results.

Concepts Behind This Question

Plasmodium|PCR Primer Design|Molecular Diagnosis by ELISA

Why This Question Is Tricky

Common Mistakes

Conceptual Pivot: Students often assume PCR is a foolproof method for low parasitemia (as per NCERT Biotechnology applications) but fail to integrate the concept of genetic polymorphism and primer specificity.

A common misconception tested here is 'Genomic Equivalence' (Option B) - students often confuse the absence of a protein in a specific life stage with the absence of the gene itself.

Quick Facts About This Question

Question Information

SubjectBiology
ChapterHuman Health and Disease - Class 12
ConceptLife Cycle of Plasmodium
Difficulty8
Cognitive Load5
Target Solve Time120 sec
AccessFree