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本文引用的文献

1
parasites block the activation of the inflammasome by inhibiting maturation of IL-1β.寄生虫通过抑制白细胞介素-1β的成熟来阻断炎性小体的激活。
Microb Cell. 2018 Jan 14;5(3):137-149. doi: 10.15698/mic2018.03.619.
2
Type I interferons induced by endogenous or exogenous viral infections promote metastasis and relapse of leishmaniasis.内源性或外源性病毒感染诱导产生的I型干扰素会促进利什曼病的转移和复发。
Proc Natl Acad Sci U S A. 2017 May 9;114(19):4987-4992. doi: 10.1073/pnas.1621447114. Epub 2017 Apr 24.
3
Leishmaniavirus-Dependent Metastatic Leishmaniasis Is Prevented by Blocking IL-17A.通过阻断白细胞介素-17A预防利什曼病毒依赖性转移性利什曼病。
PLoS Pathog. 2016 Sep 22;12(9):e1005852. doi: 10.1371/journal.ppat.1005852. eCollection 2016 Sep.
4
Mammalian Innate Immune Response to a Leishmania-Resident RNA Virus Increases Macrophage Survival to Promote Parasite Persistence.哺乳动物对利什曼原虫寄生RNA病毒的先天性免疫反应可提高巨噬细胞存活率,从而促进寄生虫持续存在。
Cell Host Microbe. 2016 Sep 14;20(3):318-328. doi: 10.1016/j.chom.2016.08.001. Epub 2016 Sep 1.
5
Leishmaniasis in immunosuppressed individuals.免疫抑制个体中的利什曼病。
Clin Microbiol Infect. 2014 Apr;20(4):286-99. doi: 10.1111/1469-0691.12556. Epub 2014 Feb 20.
6
Leishmania RNA virus controls the severity of mucocutaneous leishmaniasis.利什曼原虫 RNA 病毒可控制黏膜皮肤利什曼病的严重程度。
Science. 2011 Feb 11;331(6018):775-8. doi: 10.1126/science.1199326.
7
Retention and loss of RNA interference pathways in trypanosomatid protozoans.RNA 干扰途径在原生动物锥虫中的保留和丢失。
PLoS Pathog. 2010 Oct 28;6(10):e1001161. doi: 10.1371/journal.ppat.1001161.

通过生物发光对小鼠模型中的寄生虫进行定量分析。

Parasite Quantification by Bioluminescence in Murine Models.

作者信息

Reverte Marta, Fasel Nicolas

机构信息

Department of Biochemistry, University of Lausanne, Epalinges, Switzerland.

出版信息

Bio Protoc. 2019 Nov 20;9(22):e3431. doi: 10.21769/BioProtoc.3431.

DOI:10.21769/BioProtoc.3431
PMID:33654927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7853991/
Abstract

Leishmaniasis remains a major public health problem worldwide with a prevalence of 12 million, an incidence of 1 million persons, and 350 million people being at risk. Murine models have been largely used for studying the host-pathogen relationship and developing effective chemotherapies against parasites. Thus, preclinical imaging is crucial for monitoring the disease outcome. The aim of this protocol is to quantify parasite burden using bioluminescence imaging. Here, we describe a high-throughput imaging workflow, together with data acquisition and analysis ideal to assess parasite load in mouse models.

摘要

利什曼病仍然是全球一个主要的公共卫生问题,全球有1200万人患病,100万人发病,3.5亿人面临风险。鼠类模型在很大程度上已被用于研究宿主与病原体的关系以及开发针对寄生虫的有效化疗方法。因此,临床前成像对于监测疾病结果至关重要。本方案的目的是使用生物发光成像来量化寄生虫负荷。在此,我们描述了一种高通量成像工作流程,以及用于评估小鼠模型中寄生虫负荷的数据采集和分析方法。