Serotype

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Two serotypes 1a and 1b with antigens 2a and 2b on surface.

Serotype or serovar are distinct variations within a species of bacteria or viruses or among immune cells of different individuals. These microorganisms, viruses, or cells are classified together based on their cell surface antigens, allowing the epidemiologic classification of organisms to the sub-species level.[1][2][3] A group of serovars with common antigens is called a serogroup or sometimes serocomplex.

Serotyping often plays an essential role in determining species and subspecies. The Salmonella genus of bacteria, for example, has been determined to have over 2600 serotypes, including Salmonella enterica serovar Typhimurium, S. enterica serovar Typhi, and S. enterica serovar Dublin.[2] Vibrio cholerae, the species of bacteria that causes cholera, has over 200 serotypes, based on cell antigens. Only two of them have been observed to produce the potent enterotoxin that results in cholera: 0:1 and 0:139.

Serotypes were discovered by the American microbiologist Rebecca Lancefield in 1933.[4]

Role in organ transplantation

Agglutination of HLA-A3 positive red blood cells (RBCs) with anti-A3 alloreactive antisera containing Anti-A3 IgM

The immune system is capable of discerning a cell as being 'self' or 'non-self' according to that cell's serotype. In humans, that serotype is largely determined by human leukocyte antigen (HLA), the human version of the major histocompatibility complex. Cells determined to be non-self are usually recognized by the immune system as foreign, causing an immune response, such as hemagglutination. Serotypes differ widely between individuals; therefore, if cells from one human (or animal) are introduced into another random human, those cells are often determined to be non-self because they do not match the self-serotype. For this reason, transplants between genetically non-identical humans often induce a problematic immune response in the recipient, leading to transplant rejection. In some situations this effect can be reduced by serotyping both recipient and potential donors to determine the closest HLA match.[5]

Human leukocyte antigens

Serotypes according to HLA (MHC) locus
HLA Locus # of Serotypes Broad Antigens Split Antigens
A 25 4 15
B 50 9
C* 12 1
DR 21 4
DQ 8 2
DP*
*DP and many Cw require SSP-PCR for typing.

Serotyping of Salmonella

The Kauffmann-White classification Scheme is the basis for naming the manifold serovars of Salmonella. To date, more than 2600 different serotypes have been identified.[6] A Salmonella serotype is determined by the unique combination of reactions of cell surface antigens. The "O" antigen is determined by the outermost portion of the Lipopolysaccharide (LPS) and the "H" antigen is based on the flagellar (protein) antigens.[7] There are two species of Salmonella: Salmonella bongori and Salmonella enterica. Salmonella enterica can be subdivided into six subspecies. The process to identify the serovar of the bacterium consists of finding the formula of cell antigens which represent the variations of the bacteria. First of all, the use of the agglutination method on slides is required in order to get the antigen formula. The agglutination between the antigen and the antibody is made with a specific antisera, which reacts with the antigen to produce a mass. The antigen O is tested with a bacteria suspension from an agar plate whereas the antigen H is tested with a bacteria suspension from a broth culture. The scheme is used to classify the serovar depending on its antigen formula obtained with the reaction of the agglutination.[8][9]

See also

References

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  3. "serovar." The American Heritage Medical Dictionary. 2007. Houghton Mifflin Company 24 Oct. 2009 http://medical-dictionary.thefreedictionary.com/serovar
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  5. Christoph Frohn, Lutz Fricke, Jan-Christoph Puchta, and Holger Kirchner. The effect of HLA-C matching on acute renal transplant rejection. Nephrol. Dial. Transplant. 16: 355-360. http://ndt.oxfordjournals.org/cgi/content/full/16/2/355
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External links