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使用针对外膜脂蛋白P6的单克隆抗体对痰液中流感嗜血杆菌进行非培养检测。

Nonculture detection of Haemophilus influenzae in sputum with monoclonal antibodies specific for outer membrane lipoprotein P6.

作者信息

Groeneveld K, van Alphen L, van Ketel R J, Geelen-van den Broek L, Eijk P P, Zanen H C

机构信息

Department of Medical Microbiology, University of Amsterdam, The Netherlands.

出版信息

J Clin Microbiol. 1989 Oct;27(10):2263-7. doi: 10.1128/jcm.27.10.2263-2267.1989.

Abstract

Isolation of Haemophilus influenzae from sputum is hampered by overgrowth by other microorganisms or by antibiotic treatment of the patient. To overcome this problem in the detection of H. influenzae, an in situ immunoperoxidase staining technique was developed with monoclonal antibody (MAb) 8BD9, immunoglobulin subclass G2a. MAb 8BD9 appeared to be directed to an epitope on the outer membrane lipoprotein P6 of H. influenzae. The species specificity of MAb 8BD9 was analyzed by staining isolates from different bacterial species. MAb 8BD9 reacted with all 300 H. influenzae strains tested and with H. aegyptius and H. haemolyticus. Twenty-six of 30 H. parainfluenzae strains, other Haemophilus species, and other bacterial species often isolated from sputum were not stained. The staining technique was compared with culture of 845 routinely obtained sputum samples from patients with respiratory tract infections. In 829 sputa (98.1%), the results of both techniques were in agreement; 173 were positive for H. influenzae, and 656 were negative. With 14 sputum samples, the staining method gave a positive result for H. influenzae, but the bacterium was not cultured. This could be ascribed to antibiotic treatment of the patient (n = 7), the presence of other MAb 8BD9-positive Haemophilus species in the sputum (n = 5), and overgrowth by swarming Proteus mirabilis or by Branhamella catarrhalis. In the immunoperoxidase- and Gram-stained smears of two sputum samples, no bacteria were seen, although some H. influenzae was cultured. On the basis of these results, we conclude that immunoperoxidase staining with MAb 8BD9 is a fast and reliable extension of the available detection techniques for H. influenzae.

摘要

痰液中流感嗜血杆菌的分离会受到其他微生物过度生长或患者接受抗生素治疗的阻碍。为了克服在检测流感嗜血杆菌时的这一问题,研发了一种使用单克隆抗体(MAb)8BD9(免疫球蛋白亚类G2a)的原位免疫过氧化物酶染色技术。MAb 8BD9似乎针对流感嗜血杆菌外膜脂蛋白P6上的一个表位。通过对不同细菌种类的分离株进行染色,分析了MAb 8BD9的种属特异性。MAb 8BD9与所检测的全部300株流感嗜血杆菌菌株以及埃及嗜血杆菌和溶血嗜血杆菌发生反应。30株副流感嗜血杆菌菌株、其他嗜血杆菌种类以及其他经常从痰液中分离出的细菌种类中有26株未被染色。将该染色技术与对845份从呼吸道感染患者常规获取的痰液样本进行培养的结果进行了比较。在829份痰液样本(98.1%)中,两种技术的结果一致;173份对流感嗜血杆菌呈阳性,656份呈阴性。对于14份痰液样本,染色方法对流感嗜血杆菌给出阳性结果,但该细菌未培养出来。这可能归因于患者接受了抗生素治疗(n = 7)、痰液中存在其他MAb 8BD9阳性的嗜血杆菌种类(n = 5)以及奇异变形杆菌群游或卡他布兰汉菌过度生长。在两份痰液样本的免疫过氧化物酶染色涂片和革兰氏染色涂片中,未见到细菌,尽管培养出了一些流感嗜血杆菌。基于这些结果,我们得出结论,使用MAb 8BD9进行免疫过氧化物酶染色是现有流感嗜血杆菌检测技术的一种快速且可靠的补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c534/267007/2a1e1b4a08c8/jcm00070-0132-a.jpg

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