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犬类针对有害沙蝇唾液重组蛋白的抗体:犬利什曼病流行区的纵向研究

Canine Antibodies against Salivary Recombinant Proteins of Phlebotomus perniciosus: A Longitudinal Study in an Endemic Focus of Canine Leishmaniasis.

作者信息

Kostalova Tatiana, Lestinova Tereza, Sumova Petra, Vlkova Michaela, Rohousova Iva, Berriatua Eduardo, Oliva Gaetano, Fiorentino Eleonora, Scalone Aldo, Gramiccia Marina, Gradoni Luigi, Volf Petr

机构信息

Department of Parasitology, Faculty of Science, Charles University in Prague, Prague, Czech Republic.

Animal Health Department, Universidad de Murcia, Murcia, Spain.

出版信息

PLoS Negl Trop Dis. 2015 Jun 25;9(6):e0003855. doi: 10.1371/journal.pntd.0003855. eCollection 2015.

Abstract

BACKGROUND

Phlebotomine sand flies are vectors of Leishmania parasites. During blood feeding, sand flies deposit into the host skin immunogenic salivary proteins which elicit specific antibody responses. These anti-saliva antibodies enable an estimate of the host exposure to sand flies and, in leishmaniasis endemic areas, also the risk for Leishmania infections. However, the use of whole salivary gland homogenates as antigen has several limitations, and therefore, recombinant salivary proteins have been tested to replace them in antibody detection assays. In this study, we have used for the first time sand fly salivary recombinant proteins in a longitudinal field study on dogs.

METHODOLOGY/PRINCIPAL FINDINGS: Sera from dogs naturally exposed to P. perniciosus bites over two consecutive transmission seasons in a site endemic for canine leishmaniasis (CanL) were tested at different time points by ELISA for the antibodies recognizing whole saliva, single salivary 43 kDa yellow-related recombinant protein (rSP03B), and a combination of two salivary recombinant proteins, 43 kDa yellow-related protein and 35.5 kDa apyrase (rSP01). Dogs were also tested for Leishmania infantum positivity by serology, culture, and PCR and the infection status was evaluated prospectively. We found a significant association between active CanL infection and the amount of anti-P. perniciosus saliva antibodies. Importantly, we detected a high correlation between IgG antibodies recognizing rSP03B protein and the whole salivary antigen. The kinetics of antibody response showed for both a whole saliva and rSP03B a similar pattern that was clearly related to the seasonal abundance of P. perniciosus.

CONCLUSIONS

These results suggest that P. perniciosus rSP03B protein is a valid alternative to whole saliva and could be used in large-scale serological studies. This novel method could be a practical and economically-sound tool to detect the host exposure to sand fly bites in CanL endemic areas.

摘要

背景

白蛉是利什曼原虫寄生虫的传播媒介。在吸血过程中,白蛉会将具有免疫原性的唾液蛋白注入宿主皮肤,从而引发特异性抗体反应。这些抗唾液抗体能够评估宿主接触白蛉的情况,并且在利什曼病流行地区,还能评估感染利什曼原虫的风险。然而,使用全唾液腺匀浆作为抗原有几个局限性,因此,已经测试了重组唾液蛋白以在抗体检测试验中取代它们。在本研究中,我们首次在对犬类的纵向现场研究中使用了白蛉唾液重组蛋白。

方法/主要发现:在犬利什曼病(CanL)流行地区,采集在两个连续传播季节自然暴露于有害白蛉叮咬的犬的血清,在不同时间点通过酶联免疫吸附测定(ELISA)检测识别全唾液、单一唾液43 kDa黄色相关重组蛋白(rSP03B)以及两种唾液重组蛋白(43 kDa黄色相关蛋白和35.5 kDa腺苷三磷酸双磷酸酶(rSP01))组合的抗体。还通过血清学、培养和聚合酶链反应(PCR)检测犬的婴儿利什曼原虫阳性,并前瞻性评估感染状况。我们发现活动性CanL感染与抗有害白蛉唾液抗体的量之间存在显著关联。重要的是,我们检测到识别rSP03B蛋白的IgG抗体与全唾液抗原之间存在高度相关性。抗体反应动力学显示,全唾液和rSP03B的模式相似,这与有害白蛉的季节性丰度明显相关。

结论

这些结果表明,有害白蛉rSP03B蛋白是全唾液的有效替代物,可用于大规模血清学研究。这种新方法可能是一种实用且经济合理的工具,用于检测CanL流行地区宿主接触白蛉叮咬的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d3/4482481/0609cae02c8e/pntd.0003855.g001.jpg

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