Department of Biotechnology and Food Microbiology, Poznan University of Life Sciences, 60-627 Poznan, Poland.
Int J Mol Sci. 2023 Feb 3;24(3):3051. doi: 10.3390/ijms24033051.
Human blood contains low biomass of circulating microbial cell-free DNA (cfmDNA) that predominantly originates from bacteria. Numerous studies have detected circulating cfmDNA in patients with infectious and non-infectious diseases, and in healthy individuals. Remarkable differences were found in the microbial composition of healthy subjects and patients compared to cohorts with various diseases or even patients with diversified prognoses, implying that these alterations may be associated with disease development. Although the function of circulating cfmDNA needs to be elucidated (whether it acts as a bystander of dysbiosis or a key player in disease development), several studies have demonstrated its potential as a non-invasive biomarker that may improve diagnosis and treatment efficacy. The origin of circulating cfmDNA is still the subject of much deliberation, but studies have identified members of various microbiome niches, including the gut, oral cavity, airways, and skin. Further studies investigating the origin and function of circulating cfmDNA are needed. Moreover, low-biomass microbiome studies are prone to contamination, therefore stringent negative experimental control reactions and decontamination frameworks are advised in order to detect genuine circulating cfmDNA.
人体血液中的循环微生物无细胞游离 DNA(cfmDNA)含量较低,主要来源于细菌。许多研究已经在感染性和非感染性疾病患者以及健康个体中检测到了循环 cfmDNA。与各种疾病患者甚至预后多样化的患者相比,健康受试者和患者的微生物组成存在显著差异,这表明这些改变可能与疾病的发展有关。尽管循环 cfmDNA 的功能尚待阐明(它是肠道菌群失调的旁观者还是疾病发展的关键参与者),但已有多项研究表明其作为一种非侵入性生物标志物具有潜在的应用价值,可能改善诊断和治疗效果。循环 cfmDNA 的来源仍然是人们关注的焦点,但研究已经确定了来自各种微生物组生态位的成员,包括肠道、口腔、气道和皮肤。需要进一步研究以探讨循环 cfmDNA 的来源和功能。此外,由于低生物量微生物组研究容易受到污染,因此建议采用严格的阴性实验对照反应和去污框架,以检测真正的循环 cfmDNA。