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Arginine-Glucose Yeast extract Agar M1869

Composition**Ingredients Gms / LitrePeptone 5.000Yeast Extract 3.000Tryptone 10.000Sodium Chloride 20.000Dextrose (Glucose) 1.000L-Arginine hydrochloride 5.000Ferric ammonium citrate 0.500Sodium thiosulphate 0.300Bromocresol purple 0.020Agar 13.500Final pH ( at 25°C) 6.9±0.1**Formula adjusted, standardized to suit performance parameters

DirectionsSuspend 58.32 grams in 1000 ml purified / distilled water. Heat to boiling to dissolve the medium completely. Dispense in 5 ml amount into test tubes and sterilize by autoclaving at 15 lbs pressure (121°C) for 10-12 minutes. Cool to 45-50°C and allow the medium to set in a sloped form giving butt and slant.

Principle And InterpretationVibrio species are asporogenus, motile rods with polar flagella. Amongst the different species V. cholerae, V.

parahaemolyticus, V.vulnificus and V. mimicus are well-documented human pathogens especially in intestinal diseases

such as cholera, whereas V. alginolyticus, V. fluvialis, V. furnissii, V. metschnikovii and V. hollisae are reported to be opportunistic pathogens. Arginine-Glucose Yeast Extract Agar is used for the screening and confirmation of Vibrio species from food specimens in accordance with FDA BAM (4).

Peptone, Tryptone and yeast extract provide the necessary carbonaceous, nitrogenous compounds, long chain amino acids and vitamin B complex to the organisms. Dextrose (Glucose) acts as the fermentable carbon source. Ferric ammonium citrate and sodium thiosulphate are the indicators for H2S production and bromocresol purple acts as the pH indicator. This medium contains L- Arginine HCl. The organisms which do not decarboxylate L- Arginine HCl but ferment glucose, gives an alkaline slant and an acid butt (3).

Inoculate the suspect culture identified through presumptive method to the Arginine-Glusose Yeast Extract Agar slants by streaking and stabbing the butt. Incubate it with loose cap overnight at 35° ±2°C. Organisms that ferment glucose produce a variety of acids, turning the colour of the medium from purple to yellow. More amounts of acids are liberated in butt

(fermentation) than in the slant (respiration). Growing bacteria that can hydrolyse Arginine give more alkaline products that neutralize the acid present in the butt making the medium purple.V. cholera, V. mimicus, V. parahaemolyticus and V.

vulnificus cultures will have an alkaline (purple) slant and an acid (yellow) butt, as arginine is not hydrolyzed. Whereas V.

fluvialis, V. furnissii and V. hollisae show positive arginine hydrolysis indicated by the purple slants and butt. No gas or H2S is produced by any of the organisms.

Intended Use:Recommended for screening and confirmation of Vibrio species in accordance with FDA BAM, 1998

Type of specimen Food samples

HiMedia Laboratories Technical Data

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Firm, comparable with 1.35% Agar gel.Colour and Clarity of prepared mediumPurple coloured clear to slightly opalescent gel forms in tubes as slants with a butt.ReactionReaction of 5.83 % w/v aqueous solution at 25°C. pH : 6.9±0.1pH6.80-7.00Cultural ResponseCultural characteristics observed after an incubation at 33-37°C for 18-24 hours.

Organism Inoculum(CFU)

Growth Slant Butt Gas H2S

Vibrio cholerae ATCC15748

50-100 luxuriant Alkalinereaction,Purplish colour

acidic reaction,yellowing ofthe medium

negativereaction

negativereaction, noblackening ofthe medium

Vibrio parahaemolyticus ATCC 17802 (00037*)

50-100 luxuriant Alkalinereaction,Purplish colour

acidic reaction,yellowing ofthe medium

positivereaction

negative, noblackening ofmedium

Vibrio vulnificus ATCC29306

50-100 luxuriant Alkalinereaction,Purplish colour

acidic reaction,yellowing ofthe medium

positivereaction

negative, noblackening ofmedium

Vibrio fluvialis ATCC 33809 (00137*)

50-100 luxuriant Alkalinereaction,purplish colour

acidic reaction,yellowing ofthe medium

positivereaction

negative, noblackening ofmedium

Quality ControlAppearanceLight yellow to greenish yellow homogeneous free flowing powderGelling

Warning and Precautions Read the label before opening the container. Wear protective gloves/protective clothing/eye protection/ face protection. Follow good microbiological lab practices while handling specimens and culture. Standard precautions as per established guidelines should be followed while handling specimens. Safety guidelines may be referred in individual safety data sheets.

Limitations 1. Due to nutritional variations certain strains may show poor growth.

Key : (*) Corresponding WDCM numbers.

Storage and Shelf LifeStore between 10-30°C in a tightly closed container and the prepared medium at 20-30°C. Use before expiry date on the label. On opening, product should be properly stored dry, after tightly capping the bottle in order to prevent lump formation due to the hygroscopic nature of the product. Improper storage of the product may lead to lump formation. Store in dry ventilated area protected from extremes of temperature and sources of ignition. Seal the container tightly after use. Use before expiry date on the label.Product performance is best if used within stated expiry period.

Disposal

User must ensure safe disposal by autoclaving and/or incineration of used or unusable preparations of this product. Follow established laboratory procedures in disposing of infectious materials and material that comes into contact with sample must be decontaminated and disposed of in accordance with current laboratory techniques (1, 2).

For food samples, follow appropriate techniques for sample collection and processing as per guidelines (5). After use, contaminated materials must be sterilized by autoclaving before discarding.

Specimen Collection and Handling

Disclaimer :

User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained inthis and other related HiMedia™ publications. The information contained in this publication is based on our research and developmentwork and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes tospecifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use butfor laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should notbe considered as a warranty of any kind, expressed or implied, and no liability is accepted for infringement of any patents.

HiMedia Laboratories Technical Data

Reference

Revision : 02 / 2019

1. Isenberg, H.D. Clinical Microbiology Procedures Handbook. 2nd Edition.2. Jorgensen, J.H., Pfaller, M.A., Carroll, K.C., Funke, G., Landry, M.L., Richter, S.S and Warnock., D.W. (2015) Manualof Clinical Microbiology, 11th Edition. Vol. 1.3. Murray PR, Baron EJ, Jorgensen JH, Pfaller MA, Yolken RH. Manual of Clinical Microbiology. 8 ed. Washington,D.C:ASM; 2003.4. US FDA. Bacteriological Analytical Manual. 18 ed. Washington, DC: AOAC; 2005.

HiMedia Laboratories Pvt. Ltd. Reg.office : 23, Vadhani Ind.Est., LBS Marg, Mumbai-400086, India. Customer care No.: 022-6116 9797 Corporate office : A-516,Swastik Disha Business Park,Via Vadhani Ind. Est., LBS Marg, Mumbai-400086, India. Customer care No.: 022-6147 1919 Email: techhelp@himedialabs.com Website: www.himedialabs.com

5. Salfinger Y., and Tortorello M.L. Fifth (Ed.), 2015, Compendium of Methods for the Microbiological Examination ofFoods, 5th Ed., American Public Health Association, Washington, D.C.