下一代测序技术在恙虫病感染病原学诊断中的应用

Nannan Xu , Lintao Sai , Gang Wang , Gregory A. Dasch , Marina E. Eremeeva
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引用次数: 0

摘要

背景恙虫病是由恙虫病原虫(Orientia tsutsugamushi)引起的一种急性发热性疾病,通过受感染的恙螨传播给人类。我们报告了一例山东省健康男性恙虫病病例,该病例通过新一代测序(NGS)和 PCR 诊断,并回顾了近期有关 NGS 诊断恙虫病的文献。采用 ELISA 方法检测急性期和恢复期血清中的 IgM 和 IgG 抗体。结果47-kDa蛋白基因TaqMan和恙虫病56-kDa蛋白基因片段的测序证实了NGS诊断。对该序列和 NGS 数据的分析表明,恙虫病菌株 Cheeloo2020 是一种新型基因型。将 NGS 数据与 O. tsutsugamushi Gilliam 菌株基因组序列进行比对,发现了 304 个具有高度相似性的读数。由于普遍存在不向数据库提交序列的情况,因此很难确定用于临床标本中Orientia DNA阳性鉴定的NGS数据的最低数量和质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utility of next-generation sequencing for the etiological diagnosis of Orientia tsutsugamushi infection

Background

Scrub typhus, an acute febrile disease caused by Orientia tsutsugamushi, is transmitted to humans through infected chigger mites. We present a case of scrub typhus in a previously healthy man from Shandong Province diagnosed using next-generation sequencing (NGS) and PCR and review recent literature on NGS for scrub typhus diagnosis.

Methods

NGS was utilized for testing whole blood collected on admission. Confirmatory testing was done by detecting IgM and IgG antibodies to Orientia in acute and convalescent sera by ELISA. Orientia 47-kDa protein gene TaqMan and standard PCR of the 56-kDa protein gene and Sanger sequencing were performed on eschar scab DNA.

Results

The NGS diagnosis was confirmed by 47-kDa protein gene TaqMan and sequencing of a fragment of the O. tsutsugamushi 56-kDa protein gene from the eschar scab. Analysis of this sequence and the NGS data indicated O. tsutsugamushi strain Cheeloo2020 is a novel genotype. Mapping of the NGS data against the O. tsutsugamushi Gilliam strain genome sequence identified 304 reads with high similarity.

Conclusions

NGS is not only useful for multiplex diagnosis of scrub typhus, but also provides insight into the genetic diversity of O. tsutsugamushi. The common failure to submit sequences to databases makes it difficult to determine the minimal quantity and quality of NGS data being used for the positive identification of Orientia DNA in clinical specimens.

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