伊朗哈马丹省血清学阳性患者及其家属布鲁氏菌病调查与随访

M. Alikhani, M. Adabi, F. Keramat, Abbas Moghimbaigi, Sima Kazemi, Somayeh Shiralizadeh
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摘要

背景:布鲁氏菌病被认为是人类和动物中最流行的疾病之一。本研究通过培养和血清学方法对伊朗Hamadan省Famenin的布鲁氏菌病血清阳性参与者及其家庭进行了调查和随访。方法:采集66例受试者的血液样本,其中抗体滴度≥1:180的法氏杆菌病队列研究对象18例,抗体滴度<1:80的法氏杆菌病队列研究对象36例,抗体滴度<1:80的法氏杆菌病队列研究对象12例。血清学方法采用患者血清进行标准试管凝集试验(STAT阳性≥1:80)和2-硫醇(2-ME)试验(阳性≥1:40)。最后取所有受试者8cc的血液在BACTEC培养基中培养。结果:66份血清标本中STAT阳性20份(30.3%),分别为1:20、1:40、1:80稀释5份、4份、10份,1:160稀释1份,其中患者家属13份(65%)。2-ME检测血清标本阳性10例(15.2%),其中5例(50%)为患者家属。最终,66瓶BACTEC培养基中没有观察到布鲁氏菌的生长。结论:目前尚没有明确的诊断方法,必须综合运用多种方法进行诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation and Follow-up of Brucellosis in Seropositive Patients and Their Families in Hamadan Province, Iran
Background: Brucellosis is recognized as one of the most prevalent diseases among humans and animals. This study investigated and followed up brucellosis in seropositive participants in the Famenin (Hamadan province, Iran) cohort of brucellosis and their families by culture and serology methods. Methods: Blood samples were taken from 66 subjects, including 18 subjects in the Famenin brucellosis cohort study with antibody titers≥1:180 and 36 subjects from their families and 12 subjects in the Famenin brucellosis cohort study with antibody titers<1:80. In the serological method, standard tube agglutination test (STAT positive with≥1:80) and 2-mercaptoethanol (2-ME) test (positive with≥1:40) were performed using the patient serum. Finally, 8 cc of the blood of all subjects was used for culture in the BACTEC culture medium. Results: Of the 66 serum samples, 20 (30.3%) samples, including 5, 4, and 10 samples at 1:20, 1:40, and 1:80 dilution, respectively, and 1 sample at 1:160 dilution were positive by the STAT, of which 13 (65%) samples belonged to patients’ family members. Using the 2-ME test, 10 (15.2%) serum samples were positive, of which 5 (50%) cases were related to patients’ family members. Eventually, no growth of Brucella was observed in 66 flasks of the BACTEC culture medium. Conclusion: Considering that a definite diagnostic method is not yet accessible, a combination of methods must be applied to diagnose the disease.
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