TY - JOUR
T1 - Immunological identification of Vibrio parahaemolyticus
T2 - Staphylococcal coagglutination test and enzyme-linked immunosorbent assay
AU - Shinoda, Sumio
AU - Ikeda, Mitsuyo
AU - Yamada, Sanae
AU - Kane, Haruaki
AU - Miyoshi, Noriko
PY - 1985/9
Y1 - 1985/9
N2 - The species-specific antigenicity of the lateral flagella of Vibrio parahaemolyticus was applied to techniques for immunological identification of the vibrio. One was a coagglutination test using staphylococcal cells sensitized with anti-lateral-flagella antibody bound to protein A located in the staphylococcal cell wall. The other technique was an enzyme-linked immunosorbent assay (ELISA) using a four-layer sandwich procedure. By means of the staphylococcal coagglutination technique, about 106 vibrio cells or 60 ng of flagellar protein could be detected and the whole procedure was performed within 1 h. The sandwich ELISA procedure was more sensitive, but the time required for the whole procedure was about 8 h. Both techniques were specific for V. parahaemolyticus, because no cross-reactivity was observed with other related vibrios, and the tests were not inhibited by heterologous bacterial cells. These results suggest that both techniques are useful for the rapid identification of V. parahaemolyticus in complex samples.
AB - The species-specific antigenicity of the lateral flagella of Vibrio parahaemolyticus was applied to techniques for immunological identification of the vibrio. One was a coagglutination test using staphylococcal cells sensitized with anti-lateral-flagella antibody bound to protein A located in the staphylococcal cell wall. The other technique was an enzyme-linked immunosorbent assay (ELISA) using a four-layer sandwich procedure. By means of the staphylococcal coagglutination technique, about 106 vibrio cells or 60 ng of flagellar protein could be detected and the whole procedure was performed within 1 h. The sandwich ELISA procedure was more sensitive, but the time required for the whole procedure was about 8 h. Both techniques were specific for V. parahaemolyticus, because no cross-reactivity was observed with other related vibrios, and the tests were not inhibited by heterologous bacterial cells. These results suggest that both techniques are useful for the rapid identification of V. parahaemolyticus in complex samples.
KW - ELISA
KW - Immunological identification
KW - Staphylococcal coagglutination
KW - Vibrio parahaemolyticus
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U2 - 10.1016/0168-1605(85)90043-1
DO - 10.1016/0168-1605(85)90043-1
M3 - Article
AN - SCOPUS:0021933759
SN - 0168-1605
VL - 2
SP - 301
EP - 309
JO - International Journal of Food Microbiology
JF - International Journal of Food Microbiology
IS - 5
ER -