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循环游离 DNA 作为日本血吸虫病诊断的生物标志物。

Circulating cell-free DNA as a biomarker for diagnosis of Schistosomiasis japonica.

机构信息

Transplantation Center, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.

Engineering and Technology Research Center for Transplantation Medicine, of National Health Commission, Changsha, Hunan, China.

出版信息

Parasit Vectors. 2024 Mar 6;17(1):114. doi: 10.1186/s13071-024-06203-x.

Abstract

BACKGROUND

Schistosomiasis, a neglected tropical disease, remains an important public health problem. Although there are various methods for diagnosing schistosomiasis, many limitations still exist. Early diagnosis and treatment of schistosomiasis can significantly improve survival and prognosis of patients.

METHODOLOGY

Circulating cell-free (cf)DNA has been widely used in the diagnosis of various diseases. In our study, we evaluated the diagnostic value of circulating cfDNA for schistosomiasis caused by Schistosoma japonicum. We focused on the tandem sequences and mitochondrial genes of S. japonicum to identify highly sensitive and specific targets for diagnosis of Schistosomiasis japonica.

RESULTS

Through data screening and analysis, we ultimately identified four specific tandem sequences (TD-1, TD-2, TD-3. and TD-4) and six mitochondrial genes (COX1(1), COX1(2), CYTB, ATP6, COX3, and ND5). We designed specific primers to detect the amount of circulating cfDNA in S. japonicum-infected mouse and chronic schistosomiasis patients. Our results showed that the number of tandem sequences was significantly higher than that of the mitochondrial genes. A S. japonicum infection model in mice suggested that infection of S. japonicum can be diagnosed by detecting circulating cfDNA as early as the first week. We measured the expression levels of circulating cfDNA (TD-1, TD-2, and TD-3) at different time points and found that TD-3 expression was significantly higher than that of TD-1 or TD-2. We also infected mice with different quantities of cercariae (20 s and 80 s). The level of cfDNA (TD-3) in the 80 s infection group was significantly higher than in the 20 s infection group. Additionally, cfDNA (TD-3) levels increased after egg deposition. Meanwhile, we tested 42 patients with chronic Schistosomiasis japonica and circulating cfDNA (TD-3) was detected in nine patients.

CONCLUSIONS

We have screened highly sensitive targets for the diagnosis of Schistosomiasis japonica, and the detection of circulating cfDNA is a rapid and effective method for the diagnosis of Schistosomiasis japonica. The levels of cfDNA is correlated with cercariae infection severity. Early detection and diagnosis of schistosomiasis is crucial for patient treatment and improving prognosis.

摘要

背景

作为一种被忽视的热带病,血吸虫病仍然是一个重要的公共卫生问题。尽管有各种方法诊断血吸虫病,但仍存在许多局限性。早期诊断和治疗血吸虫病可以显著改善患者的生存和预后。

方法

循环无细胞(cf)DNA 已广泛用于各种疾病的诊断。在我们的研究中,我们评估了循环 cfDNA 对日本血吸虫引起的血吸虫病的诊断价值。我们专注于日本血吸虫的串联序列和线粒体基因,以确定用于诊断日本血吸虫病的高度敏感和特异的靶标。

结果

通过数据筛选和分析,我们最终确定了四个特定的串联序列(TD-1、TD-2、TD-3 和 TD-4)和六个线粒体基因(COX1(1)、COX1(2)、CYTB、ATP6、COX3 和 ND5)。我们设计了特异性引物来检测感染日本血吸虫的小鼠和慢性血吸虫病患者循环 cfDNA 的含量。我们的结果表明,串联序列的数量明显高于线粒体基因。日本血吸虫感染小鼠模型表明,早在第一周即可通过检测循环 cfDNA 诊断日本血吸虫感染。我们测量了不同时间点循环 cfDNA(TD-1、TD-2 和 TD-3)的表达水平,发现 TD-3 的表达明显高于 TD-1 或 TD-2。我们还感染了不同数量尾蚴(20 个和 80 个)的小鼠。80 个尾蚴感染组的 cfDNA(TD-3)水平明显高于 20 个尾蚴感染组。此外,在产卵后 cfDNA(TD-3)水平增加。同时,我们检测了 42 例慢性日本血吸虫病患者,在 9 例患者中检测到循环 cfDNA(TD-3)。

结论

我们筛选出了用于诊断日本血吸虫病的高度敏感靶标,检测循环 cfDNA 是一种快速有效的日本血吸虫病诊断方法。cfDNA 水平与尾蚴感染严重程度相关。早期发现和诊断血吸虫病对于患者的治疗和改善预后至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5f1/10918879/68a4ae1ae1a6/13071_2024_6203_Fig1_HTML.jpg

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