Viljanen M K, Linko L, Lehtonen O P
Department of Medical Microbiology, University of Turku, Finland.
J Clin Microbiol. 1988 Mar;26(3):448-52. doi: 10.1128/jcm.26.3.448-452.1988.
A total of 1,897 clinical specimens (1,019 aspirates and 876 swabs) were studied by indirect immunofluorescence (IF) with a mouse monoclonal antibody (MAb) against a D-galactose oligomer of Bacteroides fragilis lipopolysaccharide. The MAb has been shown to react with 96% of clinical B. fragilis isolates and with about 50% of Bacteroides ovatus and Bacteroides thetaiotaomicron isolates but not with other aerobic or anaerobic organisms tested. The sensitivity of IF in comparison with culturing was 78.9% for all three species. Of the 32 strains originating from culture-positive, IF-negative specimens, 13 lacked the target determinant for the MAb. Sensitivity was highest with specimens taken from the perineal area (87.1%) and lowest with those taken from undefined sites (56.6%). Sensitivity was better with aspirates (86.8%) than with swabs (72.6%). The specificity of IF was 95.6% for all of the material. Positive and negative predictive values were 51.1 and 98.0%, respectively. Neither long transportation times of specimens nor antimicrobial therapy seemed to correlate with the occurrence of IF-positive, culture-negative specimens. This study shows that a single MAb can be used to establish an IF assay that can complement isolation in the detection of these three members of the B. fragilis group.
采用抗脆弱拟杆菌脂多糖D-半乳糖寡聚物的小鼠单克隆抗体,通过间接免疫荧光法(IF)对总共1897份临床标本(1019份吸出物和876份拭子)进行了研究。该单克隆抗体已被证明可与96%的临床脆弱拟杆菌分离株、约50%的卵形拟杆菌和多形拟杆菌分离株发生反应,但不与其他检测的需氧或厌氧生物发生反应。与培养法相比,IF对所有这三种菌的敏感性为78.9%。在来自培养阳性但IF阴性标本的32株菌株中,有13株缺乏该单克隆抗体的靶标决定簇。来自会阴区域的标本敏感性最高(87.1%),来自未明确部位的标本敏感性最低(56.6%)。吸出物的敏感性(86.8%)优于拭子(72.6%)。IF对所有材料的特异性为95.6%。阳性和阴性预测值分别为51.1%和98.0%。标本的长时间运输和抗菌治疗似乎均与IF阳性、培养阴性标本的出现无关。本研究表明,一种单克隆抗体可用于建立一种IF检测方法,该方法可在检测脆弱拟杆菌组的这三个成员时补充分离培养法。