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Diagnosis of Human Ehrlichiosis by PCR Assay of Acute-Phase Serum

机译:急性血清PCR检测对人类埃希氏病的诊断

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摘要

A PCR assay of 43 acute-phase serum samples was evaluated as a method for early detection of human granulocytic ehrlichiosis (HGE) and determination of etiology when serologic testing is inconclusive. Sequence-confirmed products of the HGE agent were amplified from three individuals residing or having exposure history in Minnesota or Wisconsin, and similarly confirmed products from Ehrlichia chaffeensis were amplified from three individuals from Florida or Maryland. Etiology, as determined by PCR and serology, was the same whenever there was a fourfold difference between the maximum titers of antibodies to both antigens, indicating that presumptive determination of etiology may be based on fourfold differences in titers. PCR testing determined that E. chaffeensis was the etiologic agent for one individual who had similar titers of antibodies to both agents. PCR assay of acute-phase serum in the absence of whole blood specimens may be a useful method for early detection of human ehrlichiosis and determination of etiology when serologic testing is inconclusive.
机译:评估43种急性期血清样品的PCR测定方法,可作为早期检测人粒细胞性埃希氏病(HGE)的方法,并在血清学检查尚无定论时确定病因。从明尼苏达州或威斯康星州居住或有接触史的三名个体中扩增出HGE试剂的序列确认产物,同样从佛罗里达州或马里兰州的三名个体中扩增出 Ehrlichia chaffeensis 的产物。通过PCR和血清学确定的病因学是相同的,只要针对两种抗原的抗体的最大效价之间存在四倍的差异,这表明病因学的推定确定可能是基于效价的四倍差异。 PCR测试确定为 E。 chaffeensis 是一个个体的病原体,该个体对两种药物的效价相似。在没有全血标本的情况下,急性期血清的PCR检测可能是有用的方法,可用于早期检测人类埃希氏病和在血清学检测尚无定论时确定病因。

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