HOME
COMPANY
PRODUCTS
MSDS DATA
LAB PRO.
FAQ
PARA-SITE ONLINE


LABORATORY
P
ROCEDURES


BACTI-STAIN

Auramine O Staining
Auramine-Rhodamine Staining

Gram Staining
Kinyoun Acid Fast Staining
Phenolic Acridine Orange Staining
Ziehl-Neelson Acid Fast Staining

CONCENTRATION SYSTEMS

SED-CONNECT™ (Illustrated)
SED-CONNECT™
PARA-SED™(Illustrated)
PARA-SED™
MICRO-SED™


PARASITOLOGY

Modified Acid Fast Staining
Para-Fix™: PVA
Para-Fix™: SAF
Trichrome Blue Staining

Wheatley's (modification of Gomori)
Trichrome
Wrights Dip Stat Staining
Wrights One Step Staining


OTHER PROCEDURES
(in PDF FORMAT)

Auramine O
Buffy Coat Protocol
Combination Modified Acid Fast, Modified Trichrome
Combination Thick-Thin Blood Film
Determination of Parasitemia
Fecal Concentration, Micro-Sed
Fecal Concentration, Para-Sed
Fecal Concentration, Sed-Connect
Giemsa Blood Stain
Gram Stain Table
Gram Stain
Modified Kinyoun (Cold)
Modified Trichrome Stain
(Ryan Blue)

Wheatley's Trichrome Stain
Wright's Dip STAT Kit
Wright's Dip STAT Stain
Wright's ONE-STEP Stain


 

 

 

 

MODIFIED ACID FAST STAINING

INTRODUCTION

Cryptosporidium and Isospora species have been identified as causes of severe diarrhea in immunocompromised hosts, but they can also cause diarrhea in the immunocompetent host. Oocysts in clinical specimens may be difficult to identify with out special staining. Various cyanobacterium-like bodies (CLBS) have also been reported to be acid- fast. Modified acid-fast (partial acid-fast) stains are recommended for identifying these organisms.

REAGENTS

PRODUCT # DESCTRIPTION
PACKAGING
482K 

Partial AFB Stain Kit

4 x 8 oz. bottles

483A-8oz

Kinyoun Carbol Fuchsin

8 oz.  
483A-1gl  

1 gallon

341A-8oz Sulfuric acid, 1% v/v

8 oz.

341A-1gl

  1 gallon

675A-8oz

Methylene Blue 1% 8oz  

675A-1gl

  1 gallon  

3715A-8oz

Reagent Alcohol, 50% v/v 8oz  
3715A-1gl   1 gallon      

 

 

SPECIMEN COLLECTION

Concentrated sediment of fresh or formalin preserved stool may be used. Other types of clinical specimens such as bile , duodenal fluid, pulmonary fluid (induced sputum, bronchial washings, biopsy specimens may also be used to stain for organisms.

 

RESULTS

With this method the background will stain blue CLBs and the oocysts of Cryptosporidium sp. and Isospora sp. will stain pink to red to deep purple. All or some of the sporozoites may be visible in the Cryptosporidium oocysts. Some of the two sporocysts within the mature Isospora oocyst wall will stain pink to purple with a clear area between the stained sporocysts and the oocysts wall. The oocysts in the immature Isospora will sometimes stain completely.

 

PROCEDURE

1. Place the fixed smear on a staining rack and flood with Kinyoun carbol fuchsin for about 3 minutes.

2. Rinse briefly with 50% v/v reagent alcohol.

3. Rinse with tap water and decolorize for about 2 minutes with 1% v/v sulfuric acid.

4. Rinse thoroughly with distilled water and drain.

5 Counterstain for 0.5 minute to 1 minute with 1% w/v methylene blue.

6. Examine under high dry magnification and verified under oil immersion. Partially acid fast organisms show reddish to purple filaments as opposed to non-acid fast organisms, which stain only blue.

Note: Staining times may vary to suit the individual.

 

NOTES

1. Some Nocardia spp., and acid-fast bacteria will stain positive.

2. Smears should not be to thick. After air drying, examine under a microscope. If there are no areas of bacteria separation, more water should be added to dilute the smear.

3. After staining it is essential that the back surface of the slide is wiped clean.

4. If washing with distilled water is not done adequately, crystallization of the stain may appear on the slide.

 

   
Back To:    LAB PROCEDURES    TOP           

 

HOME | COMPANY | PRODUCTS | MSDS DATA | LAB PROCEDURES | FAQ | PARA-SITE ONLINE

© Copyright 2005 Medical Chemical Corporation (MCC). All rights reserved.
Web site developed by Xcite Marketing Services