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对组织活检样本进行分子谱分析揭示了与链球菌坏死性软组织感染相关的独特特征。

Molecular profiling of tissue biopsies reveals unique signatures associated with streptococcal necrotizing soft tissue infections.

机构信息

Microbial Interactions and Processes Research Group, Helmholtz Center for Infection Research, Braunschweig, Germany.

Department of Intensive Care, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

出版信息

Nat Commun. 2019 Aug 26;10(1):3846. doi: 10.1038/s41467-019-11722-8.

Abstract

Necrotizing soft tissue infections (NSTIs) are devastating infections caused by either a single pathogen, predominantly Streptococcus pyogenes, or by multiple bacterial species. A better understanding of the pathogenic mechanisms underlying these different NSTI types could facilitate faster diagnostic and more effective therapeutic strategies. Here, we integrate microbial community profiling with host and pathogen(s) transcriptional analysis in patient biopsies to dissect the pathophysiology of streptococcal and polymicrobial NSTIs. We observe that the pathogenicity of polymicrobial communities is mediated by synergistic interactions between community members, fueling a cycle of bacterial colonization and inflammatory tissue destruction. In S. pyogenes NSTIs, expression of specialized virulence factors underlies infection pathophysiology. Furthermore, we identify a strong interferon-related response specific to S. pyogenes NSTIs that could be exploited as a potential diagnostic biomarker. Our study provides insights into the pathophysiology of mono- and polymicrobial NSTIs and highlights the potential of host-derived signatures for microbial diagnosis of NSTIs.

摘要

坏死性软组织感染(NSTIs)是由单一病原体(主要为化脓性链球菌)或多种细菌引起的破坏性感染。更好地了解导致这些不同类型 NSTI 的发病机制,可以促进更快的诊断和更有效的治疗策略。在这里,我们将微生物群落分析与宿主和病原体转录分析相结合,在患者活检中剖析化脓性链球菌和混合微生物 NSTI 的病理生理学。我们观察到,混合微生物群落的致病性是由社区成员之间的协同相互作用介导的,从而推动了细菌定植和炎症性组织破坏的循环。在化脓性链球菌 NSTIs 中,专门的毒力因子的表达是感染病理生理学的基础。此外,我们还发现了一种针对化脓性链球菌 NSTIs 的强烈干扰素相关反应,这可能被用作潜在的诊断生物标志物。我们的研究提供了对单微生物和混合微生物 NSTI 病理生理学的深入了解,并强调了宿主来源特征在 NSTI 微生物诊断中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e677/6710258/7595570bef09/41467_2019_11722_Fig1_HTML.jpg

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