Falkler W A, Hawley C E
Infect Immun. 1977 Jan;15(1):230-8. doi: 10.1128/iai.15.1.230-238.1977.
Gingival isolates of oral Fusobacterium nucleatum strains (gram-negative anaerobic fusiform bacilli) have shown the characteristic ability to hemagglutinate a variety of erythrocytes (RBC) of human and animal origin. Other members of the genus tested (F. necrophorus, F. varium, and F. mortiferum) displayed little if any ability to hemagglutinate RBC. The hemagglutination (HA) activity could be observed in the F. nucleatum strains with the whole cells and in most instances with sonicated preparations of the organisms. The HA activity was observed in cell wall preparations of the organism and appeared dependent upon a heat-labile protein component of the cell wall. In decreasing order, the RBC that would hemagglutinate with the smallest concentration of HA preparations were rabbit, monkey, human, sheep, horse, and ox. No differences in HA activity of the preparations with cells from the various human blood types were noted. Absorption of the HA preparation of one strain with human cells removed HA moiety was bound to the cells via a Ca2+ binding site interaction since ethylenediaminetetraacetic acid and ethylene glycol-bis-N,N'-tetraacetic acid inhibited binding, and HA could be reestablished by the addition of Ca2+ but not Mg2+. Rabbit antisera to the F. nucleatum strains inhibited HA activity when tested with the HA preparation in the standard test, whereas anti-Leptotrichia buccalis sera or normal rabbit sera had no effect. A tanned-cell passive HA test with rabbit anti-F. nucleatum sera displayed reactivity between the homologous strains but little reactivity with the other Fusobacterium species tested.
口腔具核梭杆菌菌株(革兰氏阴性厌氧梭形杆菌)的牙龈分离株已显示出对多种人和动物来源的红细胞(RBC)进行血凝的独特能力。所测试的该属其他成员(坏死梭杆菌、多变梭杆菌和死亡梭杆菌)几乎没有或根本没有血凝红细胞的能力。具核梭杆菌菌株的全细胞以及大多数情况下该菌的超声破碎制剂都能观察到血凝(HA)活性。在该菌的细胞壁制剂中观察到了HA活性,且似乎依赖于细胞壁的一种热不稳定蛋白质成分。按血凝所需HA制剂浓度由低到高的顺序,能与之发生血凝的红细胞依次为兔、猴、人、羊、马和牛。未发现不同人类血型细胞的HA制剂活性有差异。用人体细胞吸收一种菌株的HA制剂可去除HA部分,HA通过Ca2 +结合位点相互作用与细胞结合,因为乙二胺四乙酸和乙二醇双(N,N'-四乙酸)可抑制结合,加入Ca2 +可恢复HA活性,而加入Mg2 +则不能。在标准试验中,用具核梭杆菌菌株的兔抗血清检测HA制剂时可抑制HA活性,而颊纤毛菌抗血清或正常兔血清则无作用。用兔抗具核梭杆菌血清进行的鞣酸细胞被动血凝试验显示,同源菌株之间有反应性,但与所测试的其他梭杆菌属物种反应性很小。