||It has been suggested that Ziehl–Neelsen stain be merged into this article. (Discuss) Proposed since November 2011.|
Acid-fast organisms are easy to characterize using standard microbiological techniques (e.g. Gram stain - if an acid-fast bacillus (AFB) was gram stained, the result would be an abnormal gram positive organism, which would indicate that further testing wasn't necessary), though they can be stained using concentrated dyes, particularly when the staining process is combined with heat. Once stained, these organisms resist the dilute acid and/or ethanol-based de-colorization procedures common in many staining protocols, hence the name acid-fast.
The high mycolic acid content of certain Protozoa cell walls, and those of Mycobacteria, is responsible for the staining pattern of poor absorption followed by high retention. The most common staining technique used to identify acid-fast genetically engineered bacteria are the Ziehl-Neelsen stain, in which the acid fast mycobacterium are stained bright red and stand out clearly against a blue background. Another method is the Kinyoun method, in which the bacteria are stained bright red and stand out clearly against a green background. Acid-fast Mycobateria can also be visualized by fluorescence microscopy using specific fluorescent dyes (auramine-rhodamine stain, for example). Some bacteria may also be partially acid-fast. The eggs of the parasitic lung fluke Paragonimus westermani are actually destroyed by the stain, which can hinder diagnosis in patients who present with TB-like symptoms.
Some Acid Fast Staining techniques
- Ziehl–Neelsen stain (Classic and modified bleach types)
- Kinyoun stain
- For color blind people (or in backgrounds where detecting red bacteria is difficult) Victoria Blue can be substituted for carbol fuchsin and Picric acid can be used as the counter stain instead of methylene blue, and rest of Kinyoun technique can be used.
- Fite stain
- Ellis and Zabrowarny stain (no Phenol/carbolic acid)
- Auramine-rhodamine stain
- Auramine phenol stain
Notable acid-fast structures
Very few structures are acid fast; this makes staining for acid-fastness particularly useful in diagnosis. The following are notable examples of structures which are acid fast:
- All Mycobacteria - M. tuberculosis, M. leprae, M. smegmatis and atypical Mycobacterium
- Actinomycetes (especially some aerobic ones) with Mycolic acid in their cell wall (note Streptomyces do NOT have); not to be confused with Actinomyces, which is a non-acid fast genera of Actinomycetes
- Head of sperm
- Bacterial spores, see Endospore
- Certain cellular inclusions e.g.
- Cytoplasmic inclusion bodies seen in
- Neurons in layer 5 of cerebral cortex neuronal ceroid-lipofuscinoses (Batten disease).
- Nuclear inclusion bodies seen in
- Lead poisoning
- Bismuth poisoning.
- Cytoplasmic inclusion bodies seen in
- Oocysts of some coccidian parasites in faecal matter, such as:
- A few other parasites:
- Taenia saginata eggs stain well but Taenia solium eggs don't (Can be used to distinguish)
- Hydatid cysts, especially their "hooklets" stain irregularly with ZN stain but emanate bright red fluorescence under green light, and can aid detection in moderately heavy backgrounds or with scarce hooklets.
- Fungal yeast forms are inconsistently stained with Acid-fast stain which is considered a narrow spectrum stain for fungi. In a study on acid-fastness of fungi, 60% of blastomyces and 47% of histoplasma showed positive cytoplasmic staining of the yeast-like cells, and Cryptococcus or candida did not stain, and very rare staining was seen in Coccidioides endospores.
- Madison B (2001). "Application of stains in clinical microbiology". Biotech Histochem 76 (3): 119–25. doi:10.1080/714028138. PMID 11475314.
- Ryan KJ; Ray CG (editors) (2004). Sherris Medical Microbiology (4th ed.). McGraw Hill. ISBN 0-8385-8529-9.
- Abe C (2003). "[Standardization of laboratory tests for tuberculosis and their proficiency testing]". Kekkaku 78 (8): 541–51. PMID 14509226.
- Theory and Practice of Histological Techniques, John D Bancroft, 6th ed, p314
- Dorner, W. 1926. Un procédé simple pour la colouration des spores. Le Lait 6:8-12.
- Schaeffer, A. B., and M. Fulton. 1933. A simplified method of staining endospores. Science 77:194.
- Endospore Stain Protocol from American Society for Microbiology website
- stain's file entry on Fite
- stains file entry on Fite Faraco
- stains file entry on Wade Fite
- Ellis, R. C.; Zabrowarny, L. A. (1993). "Safer staining method for acid fast bacilli". Journal of Clinical Pathology 46 (6): 559–560. doi:10.1136/jcp.46.6.559. PMC 501296. PMID 7687254.
- Garcia LS, Bruckner DA, Brewer TC, Shimizu RY (July 1983). "Techniques for the recovery and identification of Cryptosporidium oocysts from stool specimens". J. Clin. Microbiol. 18 (1): 185–90. PMC 270765. PMID 6193138.
- Ng E, Markell EK, Fleming RL, Fried M (September 1984). "Demonstration of Isospora belli by acid-fast stain in a patient with acquired immune deficiency syndrome". J. Clin. Microbiol. 20 (3): 384–6. PMC 271334. PMID 6208216.
- Ortega YR, Sterling CR, Gilman RH, Cama VA, Díaz F (May 1993). "Cyclospora species--a new protozoan pathogen of humans". N. Engl. J. Med. 328 (18): 1308–12. doi:10.1056/NEJM199305063281804. PMID 8469253.
- J Clin Microbiol. 1999 May; 37(5): 1561–1563. Visualization of Hydatid Elements: Comparison of Several Techniques
- Wages ds, Wear dJ. acid-fastness of fungi in blastomycosis and histoplasmosis. Arch Pathol Lab Med 1982; 106:440-41.
Online protocol examples