Identification of biomarker candidates for filarial parasite infections by analysis of extracellular vesicles

Devyn Yates, Lucia S. Di Maggio, Bruce A. Rosa, Robert W. Sprung, Petra Erdmann-Gilmore, R. Reid Townsend, Philip J. Budge, Joseph Kamgno, Makedonka Mitreva, Gary J. Weil, Peter U. Fischer
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Abstract

Background Improved diagnostic tools are needed for detecting active filarial infections in humans. Tests are available that detect adult W. bancrofti circulating filarial antigen, but there are no sensitive and specific biomarker tests for brugian filariasis or loiasis. Here we explored whether extracellular vesicles released by filarial parasites contain diagnostic biomarker candidates. Methods Vesicles were isolated using VN96-affinity purification from supernatants of short-term in vitro cultured B. malayi microfilariae (Mf) and analyzed by mass spectrometry (Bruker timsTOF). Parasite-specific proteins were identified by bioinformatic analysis and a protein was called present if supported by ≥ 2 spectra. After validation with cultures parasites, this approach was then used to analyze vesicles isolated from plasma of animals infected with B. malayi and from humans with heavy Loa loa infections. Results Vesicles from Mf cultures contained more than 300 B. malayi proteins with high consistency across biological replicates. These included the known Mf excretory antigen BmR1 (AF225296). Over 150 B. malayi proteins were detected in vesicles isolated from plasma samples from two infected animals. Vesicles isolated from plasma from 10 persons with high L. loa Mf densities contained consistently 21 proteins, 9 of them were supported by at least 5 unique peptides and 7 with spectral counts above 10. The protein EN70_10600 (an orthologue of the B. malayi antigen BmR1, GenBank AF225296) was detected in all 10 samples with a total count of 91 spectra and a paralogue (EN70_10598) was detected in 6 samples with a total of 44 spectra. Discussion Extracellular vesicles released by filarial parasites in vitro and in vivo contain parasite proteins which can be reliably detected by mass spectrometry. This research provides the foundation to develop antigen detection assays to improve diagnosis of active filarial infections in humans.
通过细胞外囊泡分析鉴定丝虫病感染的生物标志物候选物
背景需要改进诊断工具来检测人类活动性丝虫病感染。现有检测成年班氏分枝杆菌循环丝虫病抗原的检测方法,但对于布鲁氏丝虫病或路易病尚无敏感和特异性的生物标志物检测方法。在这里,我们探讨了丝虫寄生虫释放的细胞外囊泡是否含有诊断生物标志物候选物。方法采用vn96亲和纯化法从短期体外培养的马来芽孢杆菌微丝蚴(Mf)上清液中分离出囊泡,并用质谱法(Bruker timsTOF)进行分析。通过生物信息学分析鉴定出寄生虫特异性蛋白,如果有≥2个光谱支持,则称为存在蛋白。在用培养寄生虫进行验证后,该方法随后用于分析从感染马来芽孢杆菌的动物和重度罗阿罗阿感染的人的血浆中分离的囊泡。结果Mf培养的囊泡中含有300多种马来芽孢杆菌蛋白,在不同的生物重复中具有较高的一致性。其中包括已知的Mf排泄抗原BmR1 (AF225296)。在从两只受感染动物的血浆样本中分离的囊泡中检测到150多种马来芽胞杆菌蛋白。从10个高L. loa Mf密度的人的血浆中分离到的小泡一致含有21个蛋白,其中9个蛋白被至少5个独特的肽支持,7个蛋白的光谱计数在10以上。在所有10份样品中检测到EN70_10600蛋白(与马来芽孢杆菌抗原BmR1同源,GenBank AF225296),共91个光谱;在6份样品中检测到EN70_10598蛋白,共44个光谱。讨论丝虫在体外和体内释放的细胞外囊泡中含有寄生虫蛋白,质谱法可以可靠地检测到这些蛋白。本研究为发展抗原检测方法以提高人类活动性丝虫病的诊断提供了基础。
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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