巴贝虫病
巴贝虫
病毒学
金标准(测试)
血涂片
生物
多路复用
实时聚合酶链反应
寄生虫寄主
聚合酶链反应
医学
免疫学
内科学
基因
生物信息学
疟疾
万维网
生物化学
计算机科学
作者
Guiqing Wang,Gary P. Wormser,Jian Zhuge,Patrick Villafuerte,Dawn Ip,Christine Zeren,John T. Fallon
标识
DOI:10.1016/j.ttbdis.2015.03.001
摘要
Babesiosis is an emerging tick-borne disease mainly caused Babesia microti, a protozoan that infects erythrocytes. Microscopic examination of blood smears is the current gold standard for detection of Babesia infection, but this diagnostic test has several limitations. We developed and assessed the clinical utilization of a multiplex real-time PCR assay targeting the 18S rRNA gene of B. microti and the human gapdh gene. The limit of detection of this PCR assay was approximately 1–3 parasites/μl of blood. The assay showed a diagnostic sensitivity and probable specificity of 100% based on testing 145 retrospective and 185 prospective blood specimens from controls and patients with confirmed babesiosis. Notably, the PCR assay was more sensitive than blood smear examination in patients during and following anti-babesia drug therapy. Our study suggests that PCR testing is as good or better than a blood smear for detection of B. microti in routine clinical practice. PCR testing may confirm the presence of babesiosis in patients whose level of infection is too low for reliable microscopic detection.
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