Porritt Robert J, Mercer Joanne L, Munro Rosemary
Department of Microbiology and Infectious Diseases, South Western Area Pathology Service, Sydney, NSW, Australia.
Pathology. 2003 Feb;35(1):61-4.
An ultrasonic instrument, the Immunosonic, was used to evaluate ultrasound-enhanced latex immunoagglutination testing (USELAT) for detection and serogroup determination of Neisseria meningitidis in clinical specimens.
Eighty-two CSF and EDTA blood specimens from patients with suspected meningococcal disease (MD) were tested by USELAT. Results were compared with routine laboratory tests for confirmation of MD and discrepant results were resolved by analysis of further laboratory and clinical data.
Using the Wellcogen Bacterial Antigen Kit, USELAT was positive in 20 (24%) specimens. The resolved sensitivity of USELAT was 49% compared with 67% for PCR. There were no discrepancies between serogroups indicated by USELAT and serogroups confirmed by PCR or culture grouping.
Although USELAT could be performed in laboratories without facilities for PCR testing, a specific ultrasonic instrument is necessary and some experience is required in interpreting results. The lower resolved sensitivity makes USELAT unsuitable as a stand-alone rapid test, and it added little value to standard laboratory culture with PCR testing.
使用一种名为免疫超声仪的超声仪器来评估超声增强乳胶免疫凝集试验(USELAT),以检测临床标本中的脑膜炎奈瑟菌并确定其血清群。
采用USELAT对82例疑似脑膜炎球菌病(MD)患者的脑脊液和乙二胺四乙酸(EDTA)血液标本进行检测。将结果与用于确诊MD的常规实验室检测结果进行比较,并通过进一步分析实验室和临床数据来解决结果不一致的问题。
使用Wellcogen细菌抗原试剂盒时,USELAT在20份(24%)标本中呈阳性。USELAT的确诊敏感性为49%,而聚合酶链反应(PCR)的确诊敏感性为67%。USELAT所指示的血清群与PCR或培养分组所确认的血清群之间没有差异。
尽管USELAT可以在没有PCR检测设施的实验室中进行,但需要特定的超声仪器,并且在解读结果方面需要一些经验。较低的确诊敏感性使得USELAT不适宜作为一种独立的快速检测方法,并且相对于标准实验室培养加PCR检测,它几乎没有增加价值。