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利用针对脆弱拟杆菌脂多糖的单克隆抗体通过免疫荧光法检测临床标本中的脆弱拟杆菌、多形拟杆菌和卵形拟杆菌。

Detection of Bacteroides fragilis, Bacteroides thetaiotaomicron, and Bacteroides ovatus in clinical specimens by immunofluorescence with a monoclonal antibody to B. fragilis lipopolysaccharide.

作者信息

Viljanen M K, Linko L, Lehtonen O P

机构信息

Department of Medical Microbiology, University of Turku, Finland.

出版信息

J Clin Microbiol. 1988 Mar;26(3):448-52. doi: 10.1128/jcm.26.3.448-452.1988.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8726/266311/d5da6cc25501/jcm00075-0077-a.jpg

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