Temple G S, Ayling P D, Wilkinson S G
Microbios. 1986;45(183):93-104.
Typing phages of the Colindale typing set for Pseudomonas aeruginosa have been tested for the use of lipopolysaccharide (LPS) as a receptor. Studies using the reference strains of the International Antigenic Typing Scheme for O-serotypes of P. aeruginosa supported earlier indications that none of the phages were O-specific. Studies of the adsorption of phages to LPS showed that typing phages 16, 44, F8, 68, 109, 352, and 1214 (as well as other phages 2 and H22) were LPS-specific, but were not consistently adsorbed by isolated LPS from all sensitive strains. Water-soluble fractions from LPS did not adsorb phages and did not inhibit their neutralization by whole LPS. No endoglycosidase activity against LPS was detected for any phage. The significance of these results for the roles of LPS in the adsorption process and phage sensitivity are discussed.
已对用于铜绿假单胞菌的科林代尔分型噬菌体进行了测试,以研究脂多糖(LPS)作为受体的用途。使用铜绿假单胞菌O血清型国际抗原分型方案的参考菌株进行的研究支持了早期的迹象,即没有一种噬菌体是O特异性的。噬菌体对LPS吸附的研究表明,分型噬菌体16、44、F8、68、109、352和1214(以及其他噬菌体2和H22)是LPS特异性的,但并非始终能被所有敏感菌株的分离LPS吸附。LPS的水溶性部分不吸附噬菌体,也不抑制其被全LPS中和。未检测到任何噬菌体对LPS有内切糖苷酶活性。讨论了这些结果对于LPS在吸附过程和噬菌体敏感性中的作用的意义。