A novel cystatin in Psoroptes ovis var. cuniculi: molecular characterization, serodiagnostic potential, and its anti-inflammatory property on rabbit peripheral blood mononuclear cells

IF 3 2区 医学 Q1 PARASITOLOGY Parasites & Vectors Pub Date : 2024-09-19 DOI:10.1186/s13071-024-06483-3
Xiaobin Gu, Fusheng Yang, Ce Wang, Jing Xu, Yane Li, Youping Liang, Je Fan, Fangyan Wu, Ran He, Hui Wang, Yue Xie
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Abstract

The ectoparasite Psoroptes ovis var. cuniculi causes substantial economic losses to the global rabbit industry. Currently, microscopy for identifying Psoroptes mite in skin scrapings, as the “diagnosis gold standard,” remains a challenge owing to its poor sensitivity in detecting low-level and/or early stage mite infestations. Additionally, Psoroptes infestations rapidly trigger cutaneous inflammation, thus the mites might produce some molecules to deal with the harmful effects of inflammation for their long-time survival on the host skin, but these molecules are still mostly unknown. To seek a sensitive diagnostic method and illuminate the new antiinflammatory molecules, we characterized a novel cystatin of P. ovis var. cuniculi (PsoCys) using bioinformatics and molecular biology methods. The results showed that PsoCys comprised the classical features of the type II cystatin superfamily including an N-terminal glycine residue, a central QXVXG motif, and a C-terminal LW motif. In mixed stages of mites, the transcription level of PsoCys was significantly higher in “fed” mites than in “starved” mites (P < 0.001), and among the different life-cycle stages of “fed” mites, the expression of PsoCys was higher in adult males than in larva, nymph, and adult females (P < 0.001). The established indirect ELISA based on recombinant PsoCys (rPsoCys-iELISA) presented 95.4% sensitivity and 95.7% specificity. The area under the receiver operating characteristic curve (AUC) for this method was 0.991, indicating its excellent diagnostic performance. Moreover, rPsoCys-iELISA had advantages over microscopy for detecting low-level and/or early stage mite infestations (90% versus 40% in artificial infestation cases at 3 weeks post-infestation; 61.9% versus 22.6% in clinical cases). In addition, rPsoCys could inhibit the activity of papain and cathepsin B in vitro, and significantly suppressed mRNA levels of toll-like receptors (TLR 1, 2, 4, and 6) and downstream molecules (NF-κB, p38, MyD88, IL-10, and IFN-γ) in LPS-stimulated rabbit PBMCs, indicating its anti-inflammatory property. Our findings indicated that PsoCys was a novel type II cystatin of Psoroptes mites, and it served as a potential serological diagnostic antigen for detecting low-level and/or early stage mite infestations, as well as a novel anti-inflammatory molecule of Psoroptes mites.
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猫鼬变种中的一种新型胱抑素:分子特征、血清诊断潜力及其对兔外周血单核细胞的抗炎特性
外寄生虫 Psoroptes ovis var. cuniculi 给全球养兔业造成了巨大的经济损失。目前,显微镜作为 "诊断金标准",在皮肤刮片中识别Psoroptes螨仍然是一项挑战,因为它在检测低水平和/或早期螨虫感染方面灵敏度较低。此外,螨虫感染会迅速引发皮肤炎症,因此螨虫可能会产生一些分子来应对炎症的有害影响,以便在宿主皮肤上长期存活,但这些分子大多仍不为人所知。为了寻求一种灵敏的诊断方法并揭示新的抗炎分子,我们利用生物信息学和分子生物学方法对一种新型的猫螨胱抑素(PsoCys)进行了表征。结果表明,PsoCys 具有 II 型胱抑素超家族的经典特征,包括一个 N 端甘氨酸残基、一个中央 QXVXG 矩阵和一个 C 端 LW 矩阵。在混合阶段的螨虫中,"喂养 "螨虫的 PsoCys 转录水平明显高于 "饥饿 "螨虫(P < 0.001),而且在 "喂养 "螨虫的不同生命周期阶段中,成年雄螨的 PsoCys 表达高于幼虫、若螨和成年雌螨(P < 0.001)。基于重组 PsoCys 的间接 ELISA(rPsoCys-iELISA)灵敏度为 95.4%,特异性为 95.7%。该方法的接收者操作特征曲线下面积(AUC)为 0.991,表明其诊断性能极佳。此外,与显微镜相比,rPsoCys-iELISA 在检测低水平和/或早期螨虫感染方面更具优势(在感染后 3 周的人工感染病例中,检测率为 90% 对 40%;在临床病例中,检测率为 61.9% 对 22.6%)。此外,rPsoCys 还能在体外抑制木瓜蛋白酶和 cathepsin B 的活性,并能显著抑制 LPS 刺激的兔 PBMC 中的收费样受体(TLR 1、2、4 和 6)和下游分子(NF-κB、p38、MyD88、IL-10 和 IFN-γ)的 mRNA 水平,这表明它具有抗炎特性。我们的研究结果表明,PsoCys 是一种新型的 Psoroptes 螨虫 II 型胱抑素,可作为一种潜在的血清学诊断抗原用于检测低水平和/或早期阶段的螨虫感染,同时也是一种新型的 Psoroptes 螨虫抗炎分子。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
期刊最新文献
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