An isotonic protein solution favorably modulated the porcine intestinal immune response and cellular adhesion markers and reduced PEDV shedding in vivo

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY Veterinary immunology and immunopathology Pub Date : 2024-04-06 DOI:10.1016/j.vetimm.2024.110753
Dmytro M. Masiuk , Andrii V. Kokariev , Stefan G. Buzoianu , Ava M. Firth , Victor S. Nedzvetsky
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Abstract

Porcine epidemic diarrhea virus (PEDV) causes immensely large economic losses worldwide in the swine industry. PEDV attacks the intestine, disrupts intestinal epithelium morphology and barrier integrity, and results in profound diarrhea and high mortality. A commercially available isotonic protein solution (IPS) (Tonisity Px) has anecdotally been reported to be effective in supportive treatment of piglets with active PEDV infections. This study evaluated the effects of supplementing (or not) the drinking water of 14 day old PEDV-infected piglets with the IPS on the content of E-cadherin, fibronectin, interferon-alpha (IFN-α), and matrix metalloproteinase 9 (MMP-9) in duodenal tissue. The content of PEDV DNA in feces was also measured. Though both groups had similar PEDV shedding at day 1, IPS piglets had significantly lower PEDV shedding at day 5, 14 and 21. The IPS group also had a shorter duration of PEDV virus shedding.

Levels of E-cadherin and fibronectin, both of which are structural proteins in the intestine, remained unchanged from baseline in the IPS group, whereas the same molecules decreased significantly in the control group. IFN-α, an antiviral cytokine, and MMP-9, an enzyme that aids in tissue remodeling, were increased at days 5 and 14 post infection, and then decreased at day 21 post-infection in the IPS group compared to control.

Overall, the IPS used in this study enhanced epithelial intercellular adhesion (E-cadherin) and extracellular matrix structure (fibronectin), resulted in significantand favorable changes in MMP-9 activity, and favorably modulated IFN-α production.

This is the first report of this panel of biomarkers, especially MMP-9 and IFN-α, in the face of in vivo PEDV infection. This is also the first report to investigate a commercially available swine product that does not need to be administered in solid feed, and that is already registered for use throughout Asia, Europe, South America, and North America.

Overall, the results of this study serve to clarify the behavior of 4 key biomarkers in the presence of in vivo PEDV infection. The results also indicate that IPS (Tonisity Px) supplementation is a viable intervention to modulate the porcine intestinal immune response with favorable effects on the intestine.

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等渗蛋白溶液能有效调节猪肠免疫反应和细胞粘附标记物,减少猪瘟病毒在体内的脱落
猪流行性腹泻病毒(PEDV)给全球养猪业造成了巨大的经济损失。PEDV 攻击肠道,破坏肠道上皮细胞形态和屏障完整性,导致严重腹泻和高死亡率。据坊间报道,一种市售等渗蛋白溶液(IPS)(Tonisity Px)对活动性 PEDV 感染仔猪的辅助治疗有效。本研究评估了在 14 日龄 PEDV 感染仔猪的饮水中添加(或不添加)IPS 对十二指肠组织中 E-粘连蛋白、纤连蛋白、干扰素-α (IFN-α) 和基质金属蛋白酶 9 (MMP-9) 含量的影响。粪便中的 PEDV DNA 含量也进行了测定。虽然两组仔猪在第 1 天的 PEDV 感染率相似,但 IPS 组仔猪在第 5、14 和 21 天的 PEDV 感染率明显较低。IPS组的E-粘连蛋白和纤连蛋白(这两种蛋白都是肠道结构蛋白)水平与基线持平,而对照组则显著下降。与对照组相比,IPS组的抗病毒细胞因子IFN-α和有助于组织重塑的酶MMP-9在感染后第5天和第14天有所增加,在感染后第21天又有所减少。总体而言,本研究中使用的 IPS 增强了上皮细胞间粘附力(E-cadherin)和细胞外基质结构(纤连蛋白),导致 MMP-9 活性发生显著而有利的变化,并有利地调节了 IFN-α 的产生。这也是对一种无需在固体饲料中添加的商用猪产品进行调查的首份报告,该产品已在亚洲、欧洲、南美洲和北美洲注册使用。研究结果还表明,补充 IPS(Tonisity Px)是调节猪肠道免疫反应的可行干预措施,对肠道有良好的影响。
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来源期刊
CiteScore
3.40
自引率
5.60%
发文量
79
审稿时长
70 days
期刊介绍: The journal reports basic, comparative and clinical immunology as they pertain to the animal species designated here: livestock, poultry, and fish species that are major food animals and companion animals such as cats, dogs, horses and camels, and wildlife species that act as reservoirs for food, companion or human infectious diseases, or as models for human disease. Rodent models of infectious diseases that are of importance in the animal species indicated above,when the disease requires a level of containment that is not readily available for larger animal experimentation (ABSL3), will be considered. Papers on rabbits, lizards, guinea pigs, badgers, armadillos, elephants, antelope, and buffalo will be reviewed if the research advances our fundamental understanding of immunology, or if they act as a reservoir of infectious disease for the primary animal species designated above, or for humans. Manuscripts employing other species will be reviewed if justified as fitting into the categories above. The following topics are appropriate: biology of cells and mechanisms of the immune system, immunochemistry, immunodeficiencies, immunodiagnosis, immunogenetics, immunopathology, immunology of infectious disease and tumors, immunoprophylaxis including vaccine development and delivery, immunological aspects of pregnancy including passive immunity, autoimmuity, neuroimmunology, and transplanatation immunology. Manuscripts that describe new genes and development of tools such as monoclonal antibodies are also of interest when part of a larger biological study. Studies employing extracts or constituents (plant extracts, feed additives or microbiome) must be sufficiently defined to be reproduced in other laboratories and also provide evidence for possible mechanisms and not simply show an effect on the immune system.
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