The plasma viral communities associate with clinical profiles in a large-scale haematological patients cohort.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-07-23 DOI:10.1186/s40168-024-01855-4
Shuai Ma, Yuyao Yin, Yifan Guo, Chaoqun Yao, Siqi Xu, Qingqing Luo, Guankun Yin, Shuyi Wang, Qi Wang, Hongbin Chen, Ruobing Wang, Longyang Jin, Guanxiang Liang, Hui Wang
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Abstract

Background: Haematological patients exhibit immune system abnormalities that make them susceptible to viral infections. Understanding the relationship between the virome in the blood plasma of haematological patients and their clinical characteristic is crucial for disease management. We aimed to explore the presence of viral pathogens and identify close associations between viral infections and various clinical features.

Results: A total of 21 DNA viruses and 6 RNA viruses from 12 virus families were identified from 1383 patients. Patients with haematological diseases exhibited significantly higher diversity, prevalence, and co-detection rates of viral pathogens. During fever episodes, pathogen detection was notably higher, with Epstein-Barr virus (EBV) and Mucorales infections being the most probable culprits for fever symptoms in non-haematological patients. The detection rate of torque teno virus (TTV) significantly increases in haematological patients after transplantation and during primary lung infections. Additionally, TTV-positive patients demonstrate significantly higher absolute neutrophil counts, while C-reactive protein and procalcitonin levels are notably lower. Furthermore, TTV, cytomegalovirus, and parvovirus B19 (B19V) were found to be more prevalent in non-neutropenic patients, while non-viral pathogenic infections, such as Gram-negative bacteria and Mucorales, were more common in neutropenic patients. Pegivirus C (HPgV-C) infection often occurred post-transplantation, regardless of neutropenia. Additionally, some viruses such as TTV, B19V, EBV, and HPgV-C showed preferences for age and seasonal infections.

Conclusions: Analysis of the plasma virome revealed the susceptibility of haematological patients to plasma viral infections at specific disease stages, along with the occurrence of mixed infections with non-viral pathogens. Close associations were observed between the plasma virome and various clinical characteristics, as well as clinical detection parameters. Understanding plasma virome aids in auxiliary clinical diagnosis and treatment, enabling early prevention to reduce infection rates in patients and improve their quality of life. Video Abstract.

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大规模血液病患者队列中的血浆病毒群与临床特征的关联。
背景:血液病患者免疫系统异常,容易受到病毒感染。了解血液病患者血浆中病毒组与临床特征之间的关系对疾病管理至关重要。我们的目的是探索病毒病原体的存在,并确定病毒感染与各种临床特征之间的密切联系:结果:我们从 1383 名患者中鉴定出了 12 个病毒家族中的 21 种 DNA 病毒和 6 种 RNA 病毒。血液病患者的病毒病原体多样性、流行率和共同检测率都明显较高。在发热期间,病原体的检出率明显较高,其中 Epstein-Barr 病毒(EBV)和粘菌感染是非血液病患者出现发热症状的罪魁祸首。血液病患者在移植后和原发性肺部感染期间,Torque Teno 病毒(TTV)的检出率明显升高。此外,TTV 阳性患者的绝对中性粒细胞计数明显升高,而 C 反应蛋白和降钙素原水平则明显降低。此外,研究发现 TTV、巨细胞病毒和副病毒 B19(B19V)在非中性粒细胞减少的患者中更为常见,而非病毒性病原体感染,如革兰氏阴性菌和粘菌,在中性粒细胞减少的患者中更为常见。无论中性粒细胞减少与否,移植后经常会发生宿主病毒 C(HPgV-C)感染。此外,一些病毒,如TTV、B19V、EBV和HPgV-C显示出对年龄和季节性感染的偏好:对血浆病毒组的分析表明,血液病患者在特定疾病阶段易受血浆病毒感染,同时还会发生与非病毒病原体的混合感染。血浆病毒群与各种临床特征以及临床检测参数之间存在密切联系。了解血浆病毒组有助于辅助临床诊断和治疗,实现早期预防,降低患者感染率,提高生活质量。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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