Atmospheric-pressure scanning microprobe matrix-assisted laser desorption/ionization mass spectrometry imaging of Neospora caninum-infected cell monolayers.

IF 3 Q2 CHEMISTRY, ANALYTICAL
Analytical science advances Pub Date : 2022-08-30 eCollection Date: 2022-08-01 DOI:10.1002/ansa.202200016
Nils H Anschütz, Stefanie Gerbig, Alejandra M Peter Ventura, Liliana M R Silva, Camilo Larrazabal, Carlos Hermosilla, Anja Taubert, Bernhard Spengler
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Abstract

Neospora caninum is an obligate intracellular protozoan parasite of the phylum Alveolata (subphylum Apicomplexa) which has not been studied extensively in a biochemical context. N. caninum is a primary cause of reproductive disorders causing mummification and abortion not only in cattle but also in other small ruminant species resulting in a substantial economic impact on the livestock industry. In canids, which are the final hosts of N. caninum, clinical disease includes neuromuscular symptoms, ataxia, and ascending paralysis. Fatal outcomes of neosporosis have also been reported depending on the host species, age and immune status, however, its zoonotic potential is still uncertain. Therefore, N. caninum should be thoroughly investigated. Matrix-assisted laser desorption/ionisation (MALDI) mass spectrometry (MS) and MS imaging (MSI) were used, combined with high-performance liquid chromatography (HPLC) to investigate these intracellular parasites. The aim of this study was to identify molecular biomarkers for N. caninum tachyzoite-infected host cells and to further clarify their functions. By atmospheric-pressure scanning microprobe MALDI MS(I), sections of N. caninum-infected and non-infected host cell pellets were examined in order to determine potential markers. In vivo, N. caninum infects different types of nucleated cells, such as endothelial cells which represent a highly immunoreactive cell type. Therefore, primary bovine umbilical vein endothelial cells were here used as a suitable infection system. For comparison, the permanent MARC-145 cell line was used as an additional, simplified in vitro cell culture model. HPLC-tandem MS (HPLC-MS/MS) experiments combined with database search were employed for structural verification of markers. The statistically relevant biomarkers found by MS and identified by HPLC-MS/MS measurements were partly also found in infected monolayers. Marker signals were imaged in cell layers of N. caninum-infected and non-infected host cells at 5 µm lateral resolution.

犬新孢子虫感染细胞单层的常压扫描微探针基质辅助激光解吸/电离质谱成像
犬新孢子虫(Neospora caninum)是一种细胞内原生动物寄生虫,隶属于肺泡动物门(吸虫亚门),目前尚未对其进行广泛的生化研究。N. caninum 是导致繁殖障碍的主要原因,不仅会导致牛木乃伊化和流产,还会导致其他小型反刍动物的木乃伊化和流产,从而对畜牧业造成巨大的经济影响。犬科动物是 N. caninum 的最终宿主,临床疾病包括神经肌肉症状、共济失调和上行性麻痹。也有报道称新孢子虫病的致命后果取决于宿主的种类、年龄和免疫状态,但其人畜共患病的可能性仍不确定。因此,应对犬新孢子虫病进行彻底调查。本研究采用基质辅助激光解吸/电离(MALDI)质谱法(MS)和质谱成像(MSI),并结合高效液相色谱法(HPLC)来研究这些细胞内寄生虫。这项研究的目的是确定犬小甲虫感染宿主细胞的分子生物标志物,并进一步阐明它们的功能。通过常压扫描微探针 MALDI MS(I),对感染 N. caninum 和未感染 N. caninum 的宿主细胞颗粒切片进行了检测,以确定潜在的标记物。在体内,N. caninum 会感染不同类型的有核细胞,如内皮细胞,它是一种高度免疫反应的细胞类型。因此,原代牛脐静脉内皮细胞被用作合适的感染系统。为了进行比较,还使用了永久性 MARC-145 细胞系作为额外的简化体外细胞培养模型。采用高效液相色谱-串联质谱(HPLC-MS/MS)实验结合数据库搜索来验证标记物的结构。通过 MS 发现并通过 HPLC-MS/MS 测量确定的具有统计学意义的生物标记物也部分出现在受感染的单层细胞中。以 5 微米的横向分辨率对金线虫感染和未感染宿主细胞的细胞层中的标记信号进行了成像。
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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CiteScore
4.60
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