Lysine iron agar
Lysine Iron Agar (LIA) is a type of agar medium used in microbiology to differentiate Enterobacteriaceae based on their ability to decarboxylate or deaminate lysine and to produce hydrogen sulfide. It is a valuable tool in the identification of Salmonella, Shigella, and other members of the Enterobacteriaceae family.
Composition[edit | edit source]
Lysine Iron Agar consists of lysine, iron sulfate, sodium thiosulfate, agar, sugars, and a pH indicator. The medium is designed to detect two main reactions: the decarboxylation of lysine to produce cadaverine and the production of hydrogen sulfide (H2S).
Principle[edit | edit source]
The principle behind LIA is to test the organism's ability to decarboxylate lysine and to produce hydrogen sulfide. The medium contains lysine as a substrate for decarboxylation, which, if utilized by the organism, will raise the pH and change the color of the medium due to the pH indicator. The production of hydrogen sulfide, on the other hand, is indicated by the formation of a black precipitate in the medium, resulting from the reaction of H2S with iron sulfate.
Interpretation of Results[edit | edit source]
- Purple Slant/Purple Butt: Indicates lysine decarboxylation, suggesting the organism is capable of utilizing lysine and producing cadaverine, which raises the pH. - Yellow Slant/Yellow Butt: Indicates fermentation of glucose with acid production, lowering the pH. - Black Precipitate: Indicates the production of hydrogen sulfide. - Purple Slant/Yellow Butt: This combination can indicate that the organism is capable of glucose fermentation but not lysine decarboxylation.
Applications[edit | edit source]
Lysine Iron Agar is primarily used in the differentiation of members of the Enterobacteriaceae family, particularly in distinguishing Salmonella and Shigella from other enteric pathogens. It is a standard test in the identification schemes for these bacteria.
Limitations[edit | edit source]
While LIA is a useful diagnostic tool, it is not definitive on its own. Results should be interpreted in conjunction with other biochemical and serological tests for accurate identification of bacterial species.
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Contributors: Prab R. Tumpati, MD