Time-Resolved Multiomics Illustrates Host and Gut Microbe Interactions during Salmonella Infection.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-11-01 Epub Date: 2024-10-07 DOI:10.1021/acs.jproteome.4c00172
Yongseok Kim, Katherine Kokkinias, Anice Sabag-Daigle, Ikaia Leleiwi, Mikayla Borton, Michael Shaffer, Maryam Baniasad, Rebecca Daly, Brian M M Ahmer, Kelly C Wrighton, Vicki H Wysocki
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引用次数: 0

Abstract

Salmonella infection, also known as Salmonellosis, is one of the most common food-borne illnesses. Salmonella infection can trigger host defensive functions, including an inflammatory response. The provoked-host inflammatory response has a significant impact on the bacterial population in the gut. In addition, Salmonella competes with other gut microorganisms for survival and growth within the host. Compositional and functional alterations in gut bacteria occur because of the host immunological response and competition between Salmonella and the gut microbiome. Host variation and the inherent complexity of the gut microbial community make understanding commensal and pathogen interactions particularly difficult during a Salmonella infection. Here, we present metabolomics and lipidomics analyses along with the 16S rRNA sequence analysis, revealing a comprehensive view of the metabolic interactions between the host and gut microbiota during Salmonella infection in a CBA/J mouse model. We found that different metabolic pathways were altered over the four investigated time points of Salmonella infection (days -2, +2, +6, and +13). Furthermore, metatranscriptomics analysis integrated with metabolomics and lipidomics analysis facilitated an understanding of the heterogeneous response of mice, depending on the degree of dysbiosis.

时间分辨多组学图解沙门氏菌感染过程中宿主与肠道微生物的相互作用
沙门氏菌感染又称沙门氏菌病,是最常见的食源性疾病之一。沙门氏菌感染会引发宿主的防御功能,包括炎症反应。被激起的宿主炎症反应会对肠道中的细菌数量产生重大影响。此外,沙门氏菌还与其他肠道微生物争夺在宿主体内的生存和生长。由于宿主的免疫反应以及沙门氏菌与肠道微生物群之间的竞争,肠道细菌的组成和功能发生了改变。宿主的变异和肠道微生物群落固有的复杂性使得了解沙门氏菌感染期间共生菌和病原体之间的相互作用变得尤为困难。在这里,我们将代谢组学和脂质组学分析与 16S rRNA 序列分析结合起来,揭示沙门氏菌感染 CBA/J 小鼠模型期间宿主与肠道微生物群之间代谢相互作用的全貌。我们发现,在沙门氏菌感染的四个调查时间点(第 -2、+2、+6 和 +13天),不同的代谢途径都发生了改变。此外,元转录组学分析与代谢组学和脂质组学分析相结合,有助于了解小鼠因菌群失调程度不同而产生的不同反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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