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在诊断性酶联免疫吸附测定(ELISA)试验中使用重组沙眼衣原体OMP2作为抗原。

Using recombinant Chlamydia trachomatis OMP2 as antigen in diagnostic ELISA test.

作者信息

Javaherian Mahdieh, Sharifnia Zarin, Taheripanah Robabeh, Bandepour Mojgan, Soleimani Mohammad, Kazemi Bahram

机构信息

Microbiology Department, Islamic Azad University, Qom, Iran.

Cellular and Molecular Biology Research center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Microbiol. 2014 Feb;6(1):8-13.

Abstract

BACKGROUND AND OBJECTIVES

The obligate intracellular bacterium Chlamydia trachomatis causes sexually transmissible diseases in human. Timely and sensitive detection of this pathogen is very important. There are many cross-reactions in bacteriological and serological methods in detection of this type of pathogens. The aim of this study was to achieve a more specific antigen for serological tests.

MATERIALS AND METHODS

Blood samples were taken from 192 women with suspected chlamydial infection and sera were isolated. ELISA plate wells were coated with recombinant C. trachomatis OMP2 as antigen. Cut-off system was determined with 40 negative sera. The final results of this research were compared with Euroimmun commercial kit.

RESULTS

The ELISA system cut-off was calculated at 0.27 using negative sera samples. ODs of positive samples were higher than 0.27 and negative samples were lower than it. We obtained 30 samples (15.62%) as positive and 162 cases (84.37%) as negative. Sensitivity and specificity of the recombinant antigen were 90% and 86%, respectively. This antigen showed no cross-reactivity with sera of patients infected with Hydatid cyst, HCV, Epstein barr virus, HBV, Helicobacter pylori, Toxoplasma gondii, Cytomegalovirus, Mycoplasma, Measles and Varicella zoster virus.

CONCLUSION

The sensitivity and specificity of rOMP2 in ELISA for detection of C. trachomatis were 90% and 86%, respectively. Though the sensitivity was higher than results of Euroimmun commercial kit, its specificity was calculated lower than reference kit.

摘要

背景与目的

专性胞内细菌沙眼衣原体可引起人类性传播疾病。及时、灵敏地检测该病原体非常重要。在检测这类病原体时,细菌学和血清学方法存在许多交叉反应。本研究的目的是获得一种用于血清学检测的更具特异性的抗原。

材料与方法

采集192例疑似衣原体感染女性的血样并分离血清。用重组沙眼衣原体OMP2作为抗原包被酶联免疫吸附测定(ELISA)板孔。用40份阴性血清确定临界值系统。将本研究的最终结果与欧蒙(Euroimmun)商用试剂盒进行比较。

结果

使用阴性血清样本计算得出ELISA系统的临界值为0.27。阳性样本的光密度(OD)高于0.27,阴性样本低于此值。我们获得30份阳性样本(15.62%)和162例阴性样本(84.37%)。重组抗原的敏感性和特异性分别为90%和86%。该抗原与感染包虫囊肿、丙型肝炎病毒(HCV)、EB病毒、乙型肝炎病毒(HBV)、幽门螺杆菌、弓形虫、巨细胞病毒、支原体、麻疹病毒和水痘带状疱疹病毒患者的血清无交叉反应。

结论

ELISA法中重组OMP2检测沙眼衣原体的敏感性和特异性分别为90%和86%。虽然其敏感性高于欧蒙商用试剂盒的结果,但其特异性经计算低于参考试剂盒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e81c/4419049/9c0536711cf1/IJM-6-8f1.jpg

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