McArthur W P, Stroup S, Wilson L
J Clin Periodontol. 1986 Aug;13(7):684-91. doi: 10.1111/j.1600-051x.1986.tb00866.x.
A combination of blotting of bacterial colonies on nitrocellulose paper discs and immunoenzymatic detection of bound antigens with specific monoclonal antibodies was used to detect and serotype Actinobacillus actinomycetemcomitans directly off the initial agar culture dish. The A. actinomycetemcomitans antigens, representative of specific colonies, were identified immunoenzymatically using monoclonal antibody specific for a species-specific antigen. The serotype of the bacteria in colonies was identified by dividing the blotting paper into sections and immunoenzymatically identifying the serotype antigens with serotype-specific monoclonal antibodies. This procedure provides for simple, rapid, sensitive and accurate identification and characterization of A. actinomycetemcomitans isolates from the initial isolation agar plates.
将细菌菌落印迹在硝酸纤维素纸盘上,并使用特异性单克隆抗体对结合抗原进行免疫酶检测,以此直接从初始琼脂培养皿中检测伴放线放线杆菌并进行血清分型。使用针对种特异性抗原的单克隆抗体,通过免疫酶法鉴定代表特定菌落的伴放线放线杆菌抗原。将印迹纸分成几部分,并用血清型特异性单克隆抗体通过免疫酶法鉴定菌落中细菌的血清型。该方法能够对来自初始分离琼脂平板的伴放线放线杆菌分离株进行简单、快速、灵敏且准确的鉴定和特征描述。