Liao Wei, Zuo Xiaoyu, Lin Guowang, Zhou Yaqing, Fu Yonghong, Cai Shaohang, Wei Pan-Pan, Liu Yu-Xiang, Liu Yang, Ma Gang, Bei Jin-Xin
Intensive Care Unit, Sun Yat-sen University Cancer Center, Guangzhou, 510060, Guangdong, China.
Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, Guangdong, China.
Discov Med. 2020 Mar-Apr;29(157):129-137.
Sepsis is a life-threatening clinical condition demanding accurate and rapid diagnosis of the culprit pathogen, thereby to improve prognosis. Pathogen determination through blood culture is the gold standard for diagnosis but has limitations due to low sensitivity. Recently, circulating DNAs derived from pathogenic organisms were found in the plasma of patients with sepsis and were further proved to be more sensitive biomarkers for the diagnosis of the pathogen origin in sepsis. However, the fundamental molecular characteristics of circulating DNA in patients with sepsis remain unclear. Here, we used specific PCR and Sanger sequencing to verify the microbiology culture results via the corresponding plasma circulating DNA. We analyzed the composition and molecular characteristics of circulating DNA in septic patients using next-generation sequencing technology. We showed the presence of pathogen-derived circulating DNA in the plasma of patients with sepsis. The sizes of circulating DNA fragments derived from pathogenic bacteria showed a skewed unimodal distribution, while those derived from host cells showed a normal unimodal distribution. Lengths of fragments at peak concentration for both origins ranged from 150 bp to 200 bp, and reads mapping to pathogenic bacteria genome distributed uniformly on the reference. Our findings have improved our understanding of microbial circulating DNA in patients with sepsis as a potential methodology for the accurate diagnosis of sepsis, especially in light of an urgent need for such a diagnosis associated with the COVID-19 infection.
脓毒症是一种危及生命的临床病症,需要准确快速地诊断出致病病原体,从而改善预后。通过血培养确定病原体是诊断的金标准,但由于敏感性低而存在局限性。最近,在脓毒症患者的血浆中发现了源自致病生物体的循环DNA,并且进一步证明其是诊断脓毒症病原体来源的更敏感生物标志物。然而,脓毒症患者循环DNA的基本分子特征仍不清楚。在此,我们使用特异性PCR和桑格测序通过相应的血浆循环DNA来验证微生物培养结果。我们使用下一代测序技术分析了脓毒症患者循环DNA的组成和分子特征。我们证明了脓毒症患者血浆中存在病原体来源的循环DNA。源自致病细菌的循环DNA片段大小呈偏态单峰分布,而源自宿主细胞的片段呈正态单峰分布。两种来源的峰值浓度片段长度范围为150 bp至200 bp,并且映射到致病细菌基因组的读数在参考序列上均匀分布。我们的研究结果增进了我们对脓毒症患者微生物循环DNA的理解,其作为一种准确诊断脓毒症的潜在方法,尤其是鉴于与COVID-19感染相关的此类诊断的迫切需求。