Parasite Circulating Cell-free DNA in the Blood of Alveolar Echinococcosis Patients as a Diagnostic and Treatment-Status Indicator

Author:

Fan Haining1,Gai Wei2,Zhang Lingqiang1,Ma Yanyan1,Wang Haijiu1,Chen Xiaoping3,Dong Jiahong4,Zhang Yan2,Bao Haihua1,Zhou Ying1,Ren Li1,Cairang Yangdan1,Hou Lizhao1,Ren Bin1,Wang Zhan1,Wang Zhixin1,Song Cuidan2

Affiliation:

1. Qinghai University Affiliated Hospital, Xining, China, Qinghai Province Key Laboratory of Hydatid Disease Research, Xining, China

2. Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou, China, National Engineering Research Center for Beijing Biochip Technology, Beijing, China, CapitalBio Corporation, Beijing, China

3. Tongji Hospital, Tongji Medical College Huazhong University of Science and Technology, Wuhan, China

4. Beijng Tsinghua Changgung Hospital, Belling, China

Abstract

Abstract Background Alveolar echinococcosis (AE) is a serious parasitic disease caused by the larvae of Echinococcus multilocularis. It is the less common but substantially more deadly of the 2 major echinococcosis diseases that can occur globally but are concentrated in central Asia. Methods We analyzed parasite circulating cell-free DNA (cfDNA) in 149 plasma samples using a DNA sequencing–based method (105 AE, 16 cystic echinococcosis, 4 liver cancer, 4 gallstones, and 20 healthy volunteers). After identifying the Echinococcus-specific cfDNA (Em-cfDNA) sequences in the samples, we determined whether Em-cfDNA could be used for AE diagnosis and as a potential indicator of the effectiveness of surgical treatment. We also examined potential associations between Em-cfDNA levels and clinical features of AE patients. Results Our work demonstrates that varying reads of Em-cfDNA were detectable in the plasma of 100% of preoperative AE patients and that all of the non-AE patients and healthy volunteers were negative. Em-cfDNA has good sensitivity and specificity for the diagnosis of AE. We also found that Em-cfDNA levels apparently have reference value for evaluating the therapeutic efficacy of surgery interventions for AE lesions. Finally, our analysis revealed that Em-cfDNA levels can reflect meaningful information about lesion size in preoperative AE patients. Conclusions We demonstrate that sequencing-based monitoring of Em-cfDNA can be used in the clinic as a powerful diagnostic indicator for AE. We also note that there is a strong potential for use of this liquid-biopsy method to monitor ongoing disease status in postintervention AE patients.

Funder

Echinococcosis Clinical Medical Research Center of Qinghai Province

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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