The impact of age on vitamin D receptor expression, vitamin D metabolism and cytokine production in ex vivo Rhodococcus equi infection of equine alveolar macrophages

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY Veterinary immunology and immunopathology Pub Date : 2024-01-02 DOI:10.1016/j.vetimm.2023.110707
LJ. Berghaus , J. Cathcart , RD. Berghaus , C. Ryan , RE. Toribio , KA. Hart
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Abstract

Rhodococcus equi (R. equi), a pneumonia-causing intracellular bacterium, results in significant morbidity and mortality in young foals, while healthy adult horses rarely develop disease. Survival and replication within alveolar macrophages (AMφ) are the hallmarks of R. equi’s pathogenicity. The vitamin D receptor (VDR) and its ligand, the active vitamin D metabolite 1,25(OH)2D, are important in immune responses to intracellular bacteria. The vitamin D/VDR pathway regulates the downstream production of cytokines in infected human AMφ. The immunomodulatory role of the vitamin D/VDR pathway in equine leukocytes is unknown. The objective of the current study was to determine the impact of R. equi infection and age on synthesis of 1,25(OH)2D, VDR expression, and cytokine production in an ex vivo model of R. equi infection in equine AMφ. AMφ were collected from ten healthy foals at 2-, 4- and 8-weeks old and from nine healthy adult horses once via bronchoalveolar lavage. AMφ were mock infected (CONTROL) or infected with a virulent laboratory strain of R. equi for 7 days (INFECTED). VDR expression was determined via RT-qPCR from cell lysates. 1,25(OH)2D and cytokines were measured in cell supernatant by immunoassays. VDR expression was impacted by age (P = 0.001) with higher expression in AMφ from 8-week-old foals than from 2-week-old foals and adults. There was no significant effect of infection in foal AMφ, but in adults, relative VDR expression was significantly lower in INFECTED AMφ compared to CONTROL AMφ (P = 0.002). There was no effect of age or infection on 1,25(OH)2D concentration (P > 0.37). Mean TNFα production was significantly higher from INFECTED compared to CONTROL AMφ from 4- and 8-week-old foals and adults (P < 0.005). Mean IFNγ production was significantly higher from AMφ from foals at 8-weeks-old compared to 2-weeks-old (P = 0.013) and higher from INFECTED AMφ than from CONTROL AMφ in foals at 4-weeks-old and in adults (P < 0.027). The proportion of samples producing IL-1β and IL-10 was also significantly higher from INFECTED compared to CONTROL AMφ isolated from 4-week-old foals (P < 0.008). Similarly, in adult samples, IL-17 was produced from a greater proportion of INFECTED compared to CONTROL samples (P = 0.031). These data document age-associated changes in VDR expression and cytokine production in equine AMφ in response to R. equi infection. This preliminary investigation supports the need for further research to fully elucidate if the vitamin D pathway has an immunomodulatory role in the horse.

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马肺泡巨噬细胞体内外感染马霍多球菌时,年龄对维生素 D 受体表达、维生素 D 代谢和细胞因子产生的影响
马霍多球菌(R. equi)是一种引起肺炎的细胞内细菌,会导致幼驹严重发病和死亡,而健康的成年马却很少发病。在肺泡巨噬细胞(AMφ)中存活和复制是 R. equi 致病性的标志。维生素 D 受体(VDR)及其配体(活性维生素 D 代谢物 1,25(OH)2D)在对细胞内细菌的免疫反应中非常重要。维生素 D/VDR 通路调节受感染人类 AMφ 细胞因子的下游产生。维生素 D/VDR 通路在马白细胞中的免疫调节作用尚不清楚。本研究旨在确定在马 AMφ 感染 R. equi 的体外模型中,R. equi 感染和年龄对 1,25(OH)2D、VDR 表达和细胞因子产生的影响。通过支气管肺泡灌洗从 10 匹 2 周、4 周和 8 周大的健康马驹和 9 匹健康成年马身上收集 AMφ。对 AMφ 进行模拟感染(对照组)或用马癣菌实验室毒株感染 7 天(感染组)。通过对细胞裂解液进行 RT-qPCR 检测 VDR 表达。通过免疫测定法测定细胞上清液中的 1,25(OH)2D和细胞因子。VDR 的表达受年龄影响(P = 0.001),8 周龄马驹的 AMφ 表达高于 2 周龄马驹和成年马驹。马驹AMφ中的感染无明显影响,但在成年马驹中,与对照AMφ相比,感染AMφ中VDR的相对表达量明显较低(P = 0.002)。年龄或感染对 1,25(OH)2D 浓度没有影响(P > 0.37)。与控制 AMφ 相比,4 周龄和 8 周龄的小马驹和成年马驹感染 AMφ 产生的 TNFα 平均值明显更高(P < 0.005)。8 周龄马驹的 AMφ 产生的 IFNγ 平均值明显高于 2 周龄马驹(P = 0.013),4 周龄马驹和成年马驹的 INFECTED AMφ 产生的 IFNγ 平均值高于 CONTROL AMφ 产生的 IFNγ 平均值(P < 0.027)。从4周大的马驹中分离出的样本中,产生IL-1β和IL-10的比例也显著高于INFECTED AMφ和CONTROL AMφ(P < 0.008)。同样,在成年样本中,与对照样本相比,INFECTED样本产生IL-17的比例更高(P = 0.031)。这些数据记录了马 AMφ 中 VDR 表达和细胞因子产生与年龄相关的变化,以应对 R. equi 感染。这项初步调查支持了进一步研究的必要性,以充分阐明维生素 D 通路在马体内是否具有免疫调节作用。
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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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