Colitose

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Colitose[edit | edit source]

Colitose molecule structure

Colitose is a rare sugar molecule that is primarily found in the lipopolysaccharides (LPS) of certain bacteria. It is classified as a 6-deoxyhexose, meaning it is a hexose sugar with a hydroxyl group missing from the sixth carbon atom. Colitose is known for its unique structure and its role in the virulence of certain bacterial pathogens.

Structure[edit | edit source]

The chemical structure of colitose consists of a six-carbon backbone with five hydroxyl groups and one keto group. It is structurally similar to other hexose sugars, such as glucose and mannose, but with the absence of the hydroxyl group at the sixth carbon. This structural difference gives colitose its distinct properties and functions.

Function[edit | edit source]

Colitose plays a crucial role in the virulence of certain bacteria, particularly those belonging to the Enterobacteriaceae family. It is a component of the O-antigen, which is the outermost part of the lipopolysaccharide (LPS) molecule found in the bacterial cell wall. The O-antigen is responsible for the antigenic specificity of the LPS and is involved in host-pathogen interactions.

Role in Bacterial Pathogenesis[edit | edit source]

Bacterial Pathogenesis

Colitose contributes to the pathogenicity of bacteria by aiding in the evasion of the host immune system and promoting bacterial colonization. It has been shown to enhance bacterial resistance to complement-mediated killing, a process by which the host immune system eliminates invading pathogens. Additionally, colitose has been implicated in the adherence of bacteria to host cells, facilitating the establishment of infection.

Clinical Significance[edit | edit source]

The presence of colitose in bacterial pathogens has important clinical implications. It has been associated with increased virulence and severity of infections caused by certain bacteria, including Escherichia coli and Salmonella enterica. Understanding the role of colitose in bacterial pathogenesis can aid in the development of targeted therapies and vaccines against these pathogens.

References[edit | edit source]


See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD