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通过大鼠模型中监测的感染动力学揭示曲霉病的早期和非侵入性诊断

Early and Non-invasive Diagnosis of Aspergillosis Revealed by Infection Kinetics Monitored in a Rat Model.

作者信息

Skriba Anton, Pluhacek Tomas, Palyzova Andrea, Novy Zbynek, Lemr Karel, Hajduch Marian, Petrik Milos, Havlicek Vladimir

机构信息

Institute of Microbiology of the Czech Academy of Sciences, Prague, Czechia.

Department of Analytical Chemistry, Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacký University Olomouc, Olomouc, Czechia.

出版信息

Front Microbiol. 2018 Oct 8;9:2356. doi: 10.3389/fmicb.2018.02356. eCollection 2018.

Abstract

is a ubiquitous saprophytic airborne fungus responsible for more than one million deaths every year. The siderophores of represent important virulence factors that contribute to the microbiome-metabolome dialog in a host. From a diagnostic point of view, the monitoring of secondary metabolites in urine of a host is promising due to the non-invasiveness, rapidity, sensitivity, and potential for standardization. Using a model of experimental aspergillosis in immunocompromised Lewis rats, the fungal siderophores ferricrocin (FC) and triacetylfusarinine C (TAFC) were monitored in rat urine before and after lung inoculation with conidia. Molecular biomarkers in high-dose (HD) and low-dose (LD) infection models were separated using high performance liquid chromatography (HPLC) and were detected by mass spectrometry (MS). In the current work, we corroborated the MS infection kinetics data with micro-positron emission tomography/computed tomography (μPET/CT) kinetics utilizing Ga-labeled TAFC. In the HD model, the initial FC signal reflecting aspergillosis appeared as early as 4 h post-infection. The results from seven biological replicates showed exponentially increasing metabolite profiles over time. In , TAFC was found to be a less produced biomarker that exhibited a kinetic profile identical to that of FC. The amount of siderophores contributed by the inoculating conidia was negligible and undetectable in the HD and LD models, respectively. In the μPET/CT scans, the first detectable signal in HD model was recorded 48 h post-infection. Regarding the MS assay, among nine biological replicates in the LD model, three animals did not develop any infection, while one animal experienced an exponential increase of metabolites and died on day 6 post-infection. All remaining animals had constant or random FC levels and exhibited few or no symptoms to the experiment termination. In the LD model, the TAFC concentration was not statistically significant, while the μPET/CT scan was positive as early as 6 days post-infection. Siderophore detection in rat urine by MS represents an early and non-invasive tool for diagnosing aspergillosis caused by . μPET/CT imaging further determines the infection location and allows the visualization of the infection progression over time.

摘要

是一种普遍存在的腐生空气传播真菌,每年导致超过100万人死亡。其铁载体是重要的毒力因子,有助于宿主中的微生物组 - 代谢组对话。从诊断角度来看,由于非侵入性、快速性、敏感性和标准化潜力,监测宿主尿液中的次生代谢产物很有前景。使用免疫受损的Lewis大鼠的实验性曲霉病模型,在肺接种分生孢子前后,对大鼠尿液中的真菌铁载体铁曲霉素(FC)和三乙酰铁载体素C(TAFC)进行监测。使用高效液相色谱(HPLC)分离高剂量(HD)和低剂量(LD)感染模型中的分子生物标志物,并通过质谱(MS)进行检测。在当前工作中,我们利用镓标记的TAFC通过微正电子发射断层扫描/计算机断层扫描(μPET/CT)动力学证实了MS感染动力学数据。在HD模型中,反映曲霉病的初始FC信号在感染后4小时就出现了。七个生物学重复的结果显示代谢产物谱随时间呈指数增加。在实验中,发现TAFC是一种产生较少的生物标志物,其动力学特征与FC相同。接种分生孢子贡献的铁载体量在HD和LD模型中分别可忽略不计且无法检测到。在μPET/CT扫描中,HD模型中第一个可检测到的信号记录在感染后48小时。关于MS检测,在LD模型的九个生物学重复中,三只动物未发生任何感染,而一只动物代谢产物呈指数增加并在感染后第6天死亡。所有其余动物的FC水平保持恒定或随机,在实验结束时几乎没有或没有症状。在LD模型中,TAFC浓度无统计学意义,而μPET/CT扫描早在感染后6天就呈阳性。通过MS检测大鼠尿液中的铁载体是诊断由该菌引起的曲霉病的一种早期且非侵入性的工具。μPET/CT成像进一步确定感染位置,并允许可视化感染随时间的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1235/6186828/2bf25eefb7f6/fmicb-09-02356-g001.jpg

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