班氏梭菌感染的循环无细胞核酸检测

Marisa Salazar, Paul Schaughency, Thomas B Nutman, Sasisekhar Bennuru
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摘要

人淋巴丝虫病(LF)主要由班氏乌氏丝虫病(Wb)和马来布鲁氏丝虫病(Bm)引起。检测血浆中游离寄生循环细胞核酸(ccfDNA/ccfRNA)是一种很有前途的检测活动性感染的方法。血浆rnaseq分析来自活动性Wb感染和未感染对照的个体,鉴定出6个特异性针对Wb和/或Bm的RNA靶标。用于检测ccfDNA和ccfRNA的检测方法已成功地用于感染Wb的个体,但以dna为基础的针对WbTR1的检测被发现是Wb循环游离核酸最敏感的生物标志物。在来自印度、库克群岛、马里、海地和圭亚那的71%(所有阳性个体)的Wb感染中鉴定出血浆来源的ccfDNA。在最终治疗后,时间过程分析表明,一年内无法检测到WbTR1 ccfDNA水平。总之,ccfDNA/RNA在LF中的检测有望评估Wb和Bm感染的感染和治疗反应。
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Circulating cell-free Nucleic Acid Detection for W. bancrofti infections
Human lymphatic filariasis (LF) is primarily caused by helminth parasites Wuchereria bancrofti (Wb) and Brugia malayi (Bm). Detecting parasitic circulating cell free nucleic acids (ccfDNA/ccfRNA) in plasma is a promising approach for detection of active infections. Plasma-RNAseq analyses from individuals with active Wb infection and uninfected controls identified 6 RNA targets that were specific to Wb and/or Bm. Assays developed to detect either ccfDNA and ccfRNA were successfully used in Wb-infected individuals, but DNA-based assays targeting WbTR1 was found to be the most sensitive biomarker of Wb circulating cell free nucleic acids. Plasma-derived ccfDNA was identified in 71 % (of all mf-positive individuals) Wb infection from India, Cook Islands, Mali, Haiti and Guyana. Following definitive treatment, time course analyses indicated that WbTR1 ccfDNA levels were undetectable within a year. Overall, ccfDNA/RNA detection in LF holds promise for assessment of infection and treatment response in Wb and Bm infections.
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