Study for the CAMLPR Histology Practice Test. Study with flashcards and multiple choice questions, each question has hints and explanations. Get ready for your exam!

Multiple Choice

Which sequence describes Wade-Fites stain steps?

Wade-Fite staining is an acid-fast technique used to visualize lepra bacilli (Mycobacterium leprae) in tissue, and it uses a lipid-preserving deparaffinization step with peanut oil before staining. The sequence begins with deparaffinization using peanut oil and xylene, which helps keep the lipid-rich organisms intact so they can take up the stain. Next, the primary stain Carbol Fuchsin is applied to penetrate the waxy cell wall of acid-fast bacteria. After staining, an acid-alcohol decolorizer is used; this removes the stain from non–acid-fast organisms while the lipid-rich, acid-fast bacilli retain it. Finally, a contrasting counterstain like Methylene Blue is applied to color the background and non–acid-fast elements, making the acid-fast organisms stand out in red-pink against a blue background. This aligns with the option that uses peanut oil/xylene deparaffinization, Carbol Fuchsin, Acid Alcohol, and Methylene Blue. The other sequences differ in the staining reagent (alkaline Fuchsin vs Carbol Fuchsin), the decolorizer (ethanol instead of acid-alcohol), or the counterstain, which are not consistent with the Wade-Fite protocol.

Wade-Fite staining is an acid-fast technique used to visualize lepra bacilli (Mycobacterium leprae) in tissue, and it uses a lipid-preserving deparaffinization step with peanut oil before staining. The sequence begins with deparaffinization using peanut oil and xylene, which helps keep the lipid-rich organisms intact so they can take up the stain. Next, the primary stain Carbol Fuchsin is applied to penetrate the waxy cell wall of acid-fast bacteria. After staining, an acid-alcohol decolorizer is used; this removes the stain from non–acid-fast organisms while the lipid-rich, acid-fast bacilli retain it. Finally, a contrasting counterstain like Methylene Blue is applied to color the background and non–acid-fast elements, making the acid-fast organisms stand out in red-pink against a blue background.

This aligns with the option that uses peanut oil/xylene deparaffinization, Carbol Fuchsin, Acid Alcohol, and Methylene Blue. The other sequences differ in the staining reagent (alkaline Fuchsin vs Carbol Fuchsin), the decolorizer (ethanol instead of acid-alcohol), or the counterstain, which are not consistent with the Wade-Fite protocol.