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弗吉尼亚海湾扇贝血清对霍乱弧菌凝集作用的发生及特征

Occurrence and characteristics of agglutination of Vibrio cholerae by serum from the eastern oyster, Crassostrea virginica.

作者信息

Tamplin M L, Fisher W S

机构信息

Fishery Research Branch, U.S. Food and Drug Administration, Dauphin Island, Alabama 36528.

出版信息

Appl Environ Microbiol. 1989 Nov;55(11):2882-7. doi: 10.1128/aem.55.11.2882-2887.1989.

Abstract

Cell-free hemolymph (serum) of the eastern oyster, Crassostrea virginica, agglutinated Vibrio cholerae, including all O1 serovars and biovars. Seventy-nine other strains of bacteria, including 14 genera and 26 species, were not agglutinated. The A, B, and C factors of O1 antigen were not involved in agglutination. Bacterial agglutinating (BA) activity was demonstrated for oysters inhabiting different environments of the U.S. Atlantic and Gulf coasts. Oyster serum BA titers showed high individual variation. The serum component(s) involved in BA was inhibited by 80 degrees C heat, pronase, EDTA, mucin, and fetuin treatments. N-Acetylneuraminic acid (10 mg/ml) weakly inhibited BA activity. Ligands of V. cholerae were sensitive to neuraminidase and resistant to 80 degrees C and pronase. High salinities (24 and 30%) enhanced BA. Cross-adsorption tests with V. cholerae and human O+ erythrocytes indicated that BA and hemagglutinating activities may involve different serum components. These results imply that the ecology of V. cholerae in C. virginica is influenced by agglutinating activity of oyster serum.

摘要

美国东海岸牡蛎(Crassostrea virginica)的无细胞血淋巴(血清)能够凝集霍乱弧菌,包括所有O1血清型和生物型。其他79种细菌菌株,包括14个属和26个种,均未被凝集。O1抗原的A、B和C因子不参与凝集反应。对栖息于美国大西洋和墨西哥湾沿岸不同环境的牡蛎进行检测,均显示出细菌凝集(BA)活性。牡蛎血清BA效价存在较高的个体差异。参与BA的血清成分经80℃加热、链霉蛋白酶、乙二胺四乙酸(EDTA)、粘蛋白和胎球蛋白处理后受到抑制。N - 乙酰神经氨酸(10 mg/ml)对BA活性有微弱抑制作用。霍乱弧菌的配体对神经氨酸酶敏感,对80℃和链霉蛋白酶有抗性。高盐度(24%和30%)可增强BA。用霍乱弧菌和人O + 红细胞进行的交叉吸附试验表明,BA和血凝活性可能涉及不同的血清成分。这些结果表明,牡蛎血清的凝集活性会影响霍乱弧菌在弗吉尼亚牡蛎中的生态。

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Diseases of humans (other than cholera) caused by vibrios.由弧菌引起的人类疾病(霍乱除外)。
Annu Rev Microbiol. 1980;34:341-67. doi: 10.1146/annurev.mi.34.100180.002013.
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Appl Environ Microbiol. 1982 Nov;44(5):1047-58. doi: 10.1128/aem.44.5.1047-1058.1982.
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