Enhanced Morphological Visualization and Diagnostic Reliability of Entamoeba histolytica Using 0.1% Methylene Blue-Glycerol Vital Stain
Authors
School of Medical Laboratory Science, The Manila Times College of Subic (Philippines)
School of Medical Laboratory Science, The Manila Times College of Subic (Philippines)
School of Medical Laboratory Science, The Manila Times College of Subic (Philippines)
Article Information
DOI: 10.51244/IJRSI.2026.1304000134
Subject Category: Biology
Volume/Issue: 13/4 | Page No: 1493-1501
Publication Timeline
Submitted: 2026-04-12
Accepted: 2026-04-18
Published: 2026-05-07
Abstract
Microscopic identification of Entamoeba histolytica in traditional saline wet mounts is frequently compromised by poor refractive contrast and rapid specimen desiccation. This study evaluated 0.1% Methylene Blue-Glycerol as a specialized vital stain designed to enhance morphological visualization and extend the diagnostic window in resource-limited settings. A comparative analysis was conducted on 100 Entamoeba-positive fecal specimens. Each sample was evaluated via 0.85% saline wet mount and 0.1% Methylene Blue-Glycerol. Morphological quality was quantified using a 5-point Likert scale targeting Nuclear Definition, Cytoplasmic Detail, and Contrast Ratio. Statistical significance was determined using the Wilcoxon Signed-Rank Test, while inter-observer reliability among three independent microscopists was assessed using Fleiss’ Kappa. The Methylene Blue-Glycerol method yielded a statistically significant improvement over saline across all parameters. Nuclear definition increased by 148.3%, while the contrast ratio improved by 191.7%. Cytoplasmic detail rose by 87.2%, significantly improving the detection of erythrophagocytosis. Specimen longevity extended from a mean of 12 minutes in saline to over 120 minutes in Methylene Blue-Glycerol. Inter-observer reliability was "Almost Perfect" with an overall Fleiss’ Kappa of 0.84. The 0.1% Methylene Blue-Glycerol reagent provides a superior, low-cost alternative for amebiasis screening. By utilizing the cationic affinity of Methylene Blue for chromatin and the optical clearing properties of glycerol, this method standardizes morphological identification and offers a reliable bridge between traditional microscopy and costly molecular diagnostics.
Keywords
Entamoeba histolytica, Fecal Microscopy
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References
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