Immunophenotyping of peripheral circulating lymphocytes and serum selenium levels in calves with neonatal diarrhea

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY
Murat Uztimür , Ömer Kizil , Hatice Handan Akbulut
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引用次数: 0

Abstract

This work aims to: (1) elucidate the immune response exhibited by CD4 + and CD8 + T lymphocyte cells in response to various infectious agents in calves suffering with neonatal diarrhea; and (2) determine and investigate the association between serum selenium levels and T lymphocyte subtypes in neonatal calves afflicted with neonatal diarrhea and infected with various infectious agents. The study encompassed a cohort of 50 calves, encompassing both sexes and various breeds, within the neonatal age range (1–28 days old). Subdivided into distinct groups, the calves were categorized based on the causative agents of neonatal diarrhea, including Rotavirus (n = 10), Cryptosporidium parvum (C.parvum) (n = 10), Coronavirus (n = 5), Rotavirus+C.parvum (n = 5), and a Control group (n = 20). Blood samples were meticulously obtained from the vena jugularis of all animals utilizing specific techniques—8 ml in tubes devoid of anticoagulant and 3 ml in blood collection tubes containing EDTA. Serum selenium levels were analyzed by ICP-MS. Flow Cytometry device was used to determine CD4 + and CD8 +T lymphocyte levels. In this study, although there was no statistically significant difference in serum selenium levels between all study groups, it was found that the selenium level in the control group was not sufficient. CD4 T lymphocyte levels, the rotavirus+C.parvum group exhibited a statistically significant elevation compared to the coronavirus group. Regarding CD8 + T lymphocyte levels, the coronavirus group demonstrated a statistically significant increase when compared to the control group. In intragroup analyses of CD8 + T lymphocyte levels, the coronavirus group exhibited a significant elevation compared to the rotavirus group, C.parvum group, and the C.parvum + Rotavirus group. A significant negative correlation was detected between selenium levels and CD4 + T lymphocytes, while no correlation was found between CD8 + T lymphocytes. Fibrinogen concentration exhibited statistical significance, being higher in the Rotavirus group (p < 0.008) compared to the control group, in the C.parvum group (p < 0.004) compared to the control group, and in the Coronavirus group (p < 0.001) compared to the control group. The leukocyte count demonstrated statistical significance, being higher in the Rotavirus group compared to the control group (p < 0.001), in the Rotavirus+C.parvum group compared to the control group (p < 0.002), and in the Coronavirus group compared to the control group (p < 0.011). In conclusion, the data derived from this study illuminate discernible disparities in CD4 + and CD8 + T lymphocyte immune responses, contingent upon the specific etiological agent associated with neonatal diarrhea. Furthermore, the study underscores the importance of considering selenium deficiency as a relevant factor in calves affected by neonatal diarrhea.

新生儿腹泻犊牛外周循环淋巴细胞的免疫分型和血清硒含量
本研究旨在:(1) 阐明 CD4 + 和 CD8 + T 淋巴细胞对新生儿腹泻犊牛感染各种传染病病原体所表现出的免疫反应;(2) 确定并研究新生儿腹泻犊牛和感染各种传染病病原体的犊牛血清硒水平与 T 淋巴细胞亚型之间的关系。这项研究涵盖了 50 头新生儿年龄段(1-28 天)的小牛,包括雌雄和不同品种。根据新生儿腹泻的病原体将犊牛分为不同的组别,包括轮状病毒组(10 头)、副猪嗜血杆菌组(10 头)、冠状病毒组(5 头)、轮状病毒+副猪嗜血杆菌组(5 头)和对照组(20 头)。利用特定技术从所有动物的颈静脉仔细采集血样--8 毫升装在不含抗凝剂的试管中,3 毫升装在含 EDTA 的采血管中。采用 ICP-MS 分析血清硒水平。使用流式细胞仪测定 CD4 + 和 CD8 +T 淋巴细胞水平。在这项研究中,虽然所有研究组之间的血清硒水平没有显著的统计学差异,但发现对照组的硒水平不足。与冠状病毒组相比,轮状病毒+C.parvum 组的 CD4 T 淋巴细胞水平出现了统计学意义上的显著升高。在 CD8 + T 淋巴细胞水平方面,冠状病毒组与对照组相比有显著的统计学增长。在对 CD8 + T 淋巴细胞水平进行组内分析时,冠状病毒组比轮状病毒组、C.parvum 组和 C.parvum + 轮状病毒组明显升高。硒水平与 CD4 + T 淋巴细胞之间存在明显的负相关,而与 CD8 + T 淋巴细胞之间则没有相关性。纤维蛋白原浓度具有统计学意义,轮状病毒组(p <0.008)高于对照组,C.parvum 组(p <0.004)高于对照组,冠状病毒组(p <0.001)高于对照组。白细胞计数具有统计学意义,轮状病毒组高于对照组(p <0.001),轮状病毒+C.parvum 组高于对照组(p <0.002),冠状病毒组高于对照组(p <0.011)。总之,本研究得出的数据表明,CD4 + 和 CD8 + T 淋巴细胞免疫反应存在明显差异,这取决于与新生儿腹泻相关的特定病原体。此外,该研究还强调了将缺硒作为受新生儿腹泻影响的犊牛的一个相关因素的重要性。
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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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