Christersson L A, Wikesjö U M, Albini B, Zambon J J, Genco R J
J Periodontol. 1987 Aug;58(8):540-5. doi: 10.1902/jop.1987.58.8.540.
Recent immunohistological studies have suggested that Actinobacillus actinomycetemcomitans is present in the gingival tissues in juvenile periodontitis lesions. The present study examined tissue bound A. actinomycetemcomitans by bacterial culture and immunohistological demonstration of antigen in tissue. A total of 14 periodontitis lesions were examined. Eleven biopsies were obtained from gingiva adjacent to A. actinomycetemcomitans infected pockets, while the remaining three control biopsies were obtained from gingiva adjacent to pockets where subgingival A. actinomycetemcomitans infection could not be detected. Each biopsy was hemisected, one half was used for immunofluorescence microscopic examination while the other half was processed for culture of A. actinomycetemcomitans. The latter section was surface-disinfected, repeatedly washed and then minced to release bacteria from within the tissues. Aliquots from the serial washings and the minced tissue suspension were cultured on medium selective for A. actinomycetemcomitans. Surface disinfection and serial washings gradually decreased cultivable A. actinomycetemcomitans in the washings aliquots. Following tissue disruption, an increase in colony-forming units of A. actinomycetemcomitans was seen from eight of the 11 test biopsies. This bacterium could not be detected in washings or minced tissue suspensions from the control biopsies obtained from lesions in which subgingival A. actinomycetemcomitans was previously not detected. A positive correlation was seen between the presence of A. actinomycetemcomitans antigens in the gingival biopsies and; (1) A. actinomycetemcomitans colony-forming units released from the minced tissues (r = 0.90, p = 0.000), as well as; (2) the colony-forming units from the periodontal pocket (r = 0.62, P = 0.017).(ABSTRACT TRUNCATED AT 250 WORDS)
近期的免疫组织学研究表明,伴放线放线杆菌存在于青少年牙周炎病变的牙龈组织中。本研究通过细菌培养和组织中抗原的免疫组织学检测来检查组织内的伴放线放线杆菌。共检查了14个牙周炎病变。11份活检样本取自与伴放线放线杆菌感染袋相邻的牙龈,其余3份对照活检样本取自未检测到龈下伴放线放线杆菌感染的袋相邻的牙龈。每份活检样本均切成两半,一半用于免疫荧光显微镜检查,另一半用于伴放线放线杆菌培养。后一部分进行表面消毒、反复冲洗,然后切碎以从组织中释放细菌。将连续冲洗液和切碎组织悬液的等分试样接种在对伴放线放线杆菌有选择性的培养基上培养。表面消毒和连续冲洗逐渐减少了冲洗液等分试样中可培养的伴放线放线杆菌。组织破碎后,11份测试活检样本中有8份可见伴放线放线杆菌菌落形成单位增加。在先前未检测到龈下伴放线放线杆菌的病变中获取的对照活检样本的冲洗液或切碎组织悬液中未检测到这种细菌。在牙龈活检样本中伴放线放线杆菌抗原的存在与以下方面之间存在正相关:(1)从切碎组织中释放的伴放线放线杆菌菌落形成单位(r = 0.90,p = 0.000),以及;(2)牙周袋中的菌落形成单位(r = 0.62,P = 0.017)。(摘要截断于250字)