A Pilot Single Cell Analysis of the Zebrafish Embryo Cellular Responses to Uropathogenic Escherichia coli Infection.

Q1 Medicine Pathogens and Immunity Pub Date : 2022-02-04 eCollection Date: 2022-01-01 DOI:10.20411/pai.v7i1.479
Ashley Rawson, Vijay Saxena, Hongyu Gao, Jenaya Hooks, Xiaoling Xuei, Patrick McGuire, Takashi Hato, David S Hains, Ryan M Anderson, Andrew L Schwaderer
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Abstract

Background: Uropathogenic Escherichia coli (UPEC) infections are common and when they disseminate can be of high morbidity.

Methods: We studied the effects of UPEC infection using single cell RNA sequencing (scRNAseq) in zebrafish. Bulk RNA sequencing has historically been used to evaluate gene expression patterns, but scRNAseq allows gene expression to be evaluated at the single cell level and is optimal for evaluating heterogeneity within cell types and rare cell types. Zebrafish cohorts were injected with either saline or UPEC, and scRNAseq and canonical pathway analyses were performed.

Results: Canonical pathway analysis of scRNAseq data provided key information regarding innate immune pathways in the cells determined to be thymus cells, ionocytes, macrophages/monocytes, and pronephros cells. Pathways activated in thymus cells included interleukin 6 (IL-6) signaling and production of reactive oxygen species. Fc receptor-mediated phagocytosis was a leading canonical pathway in the pronephros and macrophages. Genes that were downregulated in UPEC vs saline exposed embryos involved the cellular response to the Gram-negative endotoxin lipopolysaccharide (LPS) and included Forkhead Box O1a (Foxo1a), Tribbles Pseudokinase 3 (Trib3), Arginase 2 (Arg2) and Polo Like Kinase 3 (Plk3).

Conclusions: Because 4-day post fertilization zebrafish embryos only have innate immune systems, the scRNAseq provides insights into pathways and genes that cell types utilize in the bacterial response. Based on our analysis, we have identified genes and pathways that might serve as genetic targets for treatment and further investigation in UPEC infections at the single cell level.

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斑马鱼胚胎细胞对尿路致病性大肠杆菌感染反应的中试单细胞分析。
背景:尿路致病性大肠杆菌(UPEC)感染是常见的,当它们传播时可以有很高的发病率。方法:采用单细胞RNA测序(scRNAseq)技术对斑马鱼UPEC感染的影响进行研究。批量RNA测序历来用于评估基因表达模式,但scRNAseq允许在单细胞水平评估基因表达,是评估细胞类型和罕见细胞类型异质性的最佳选择。斑马鱼组注射生理盐水或UPEC,并进行scRNAseq和典型通路分析。结果:scRNAseq数据的典型通路分析提供了胸腺细胞、离子细胞、巨噬细胞/单核细胞和肾原细胞固有免疫通路的关键信息。胸腺细胞中激活的途径包括白细胞介素6 (IL-6)信号传导和活性氧的产生。Fc受体介导的吞噬是原肾细胞和巨噬细胞的主要典型途径。与生理盐水暴露的胚胎相比,UPEC中下调的基因涉及革兰氏阴性内毒素脂多糖(LPS)的细胞反应,包括Forkhead Box O1a (Foxo1a)、Tribbles Pseudokinase 3 (Trib3)、Arginase 2 (Arg2)和Polo Like Kinase 3 (Plk3)。结论:由于受精后4天的斑马鱼胚胎只有先天免疫系统,scRNAseq提供了细胞类型在细菌应答中利用的途径和基因的见解。根据我们的分析,我们已经确定了可能作为治疗和进一步研究单细胞水平UPEC感染的遗传靶点的基因和途径。
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来源期刊
Pathogens and Immunity
Pathogens and Immunity Medicine-Infectious Diseases
CiteScore
10.60
自引率
0.00%
发文量
16
审稿时长
10 weeks
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