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评估猪感染后选定分子因素及17-β雌二醇剂量的情况。

Assessment of selected molecular factors and 17-β estradiol dosage in response to infection in swine.

作者信息

Castello Annamaria, Fazio Esterina, Alfonzetti Tiziana, Giunta Renato Paolo, Salvaggio Antonio, Ferlazzo Alida Maria, Cravana Cristina, Bruschetta Giuseppe, Medica Pietro, Marino Anna Maria Fausta

机构信息

Department of Catania, Istituto Zooprofilattico Sperimentale Della Sicilia, Catania, Italy.

Department of Veterinary Sciences, University of Messina, Polo Universitario dell'Annunziata, Messina, Italy.

出版信息

Vet World. 2022 Jul;15(7):1641-1649. doi: 10.14202/vetworld.2022.1641-1649. Epub 2022 Jul 13.

DOI:10.14202/vetworld.2022.1641-1649
PMID:36185508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9394144/
Abstract

BACKGROUND AND AIM

is a global zoonotic parasite infecting virtually all warm-blooded species, although a species-specific variability is evident referring to symptoms frame. Both the success of and the outcome of infection depend on a delicate balance between host cellular pathways and the evasion or modulation strategies elicited by the parasite. The hormonal and molecular mechanisms involved in this delicate host-parasite balance are still unclear, especially when considering intermediate host species other than mouse. This study aimed to assess any correlation between infection and selected molecular and hormonal factors involved in responses to infection in susceptible species such as swine. Moreover, blood counts and hematochemical assays (glucose, total cholesterol, and triglycerides dosage) were performed to evaluate the overall health condition of animals.

MATERIALS AND METHODS

Toxoplasmosis was diagnosed by enzyme-linked immunosorbent assay for antibodies determination and real-time polymerase chain reaction (RT-PCR) for DNA detection. Target genes coding for key factors of cell responses to infection were selected, and their transcription was assessed in various tissues by quantitative RT-PCR. 17-β estradiol concentrations were assessed by and the AIA-360 automated immunoassay analyzer. Blood count and hematochemical analyses were performed by a blood cell counter and a spectrophotometer, respectively.

RESULTS

The present research highlighted significant differences among infected and uninfected swine (control group) for both transcription profiles of some of the molecular factors considered and 17-β estradiol concentrations. Referring to the assessed hematological and biochemical parameters, no statistically significant differences were observed in infected swine compared to the control group.

CONCLUSION

Our results contribute to the enrichment of data available about the subject and could be useful for a deeper knowledge of the interaction between this parasite and its hosts. However, more aspects are still unclear, such as the effective response of downstream molecules from the same pathways to the variation of factors observed in this study either assessing how the same factors respond to infection in other host speciesand further analyses should be performed on other host species.

摘要

背景与目的

[病原体名称]是一种全球范围内的人畜共患寄生虫,几乎感染所有温血动物物种,不过在症状表现方面存在明显的物种特异性差异。[病原体名称]的感染成功与否及感染结果取决于宿主细胞通路与寄生虫引发的逃避或调节策略之间的微妙平衡。参与这种宿主 - 寄生虫微妙平衡的激素和分子机制仍不清楚,尤其是在考虑除小鼠之外的中间宿主物种时。本研究旨在评估[病原体名称]感染与易感物种(如猪)感染反应中涉及的选定分子和激素因素之间的任何相关性。此外,进行了血细胞计数和血液生化分析(葡萄糖、总胆固醇和甘油三酯测定)以评估动物的整体健康状况。

材料与方法

通过酶联免疫吸附测定法检测抗体来诊断弓形虫病,通过实时聚合酶链反应(RT-PCR)检测[病原体名称]DNA。选择编码细胞对[病原体名称]感染反应关键因子的靶基因,并通过定量RT-PCR评估其在各种组织中的转录情况。通过[具体方法]和AIA - 360自动免疫分析仪评估17-β雌二醇浓度。血细胞计数和血液生化分析分别通过血细胞计数器和分光光度计进行。

结果

本研究突出显示,在所考虑的一些分子因素的转录谱和17-β雌二醇浓度方面,感染猪与未感染猪(对照组)之间存在显著差异。就评估的血液学和生化参数而言,与对照组相比,感染猪未观察到统计学上的显著差异。

结论

我们的结果有助于丰富关于该主题的现有数据,可能有助于更深入了解这种寄生虫与其宿主之间的相互作用。然而,仍有更多方面尚不清楚,例如同一通路下游分子对本研究中观察到的因素变化的有效反应,或者评估相同因素在其他宿主物种中对[病原体名称]感染的反应,并且应对其他宿主物种进行进一步分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/27d49925e0d2/Vetworld-15-1641-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/142fe062b6d1/Vetworld-15-1641-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/27d49925e0d2/Vetworld-15-1641-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/976f8c4b94d9/Vetworld-15-1641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/474a89c9ac73/Vetworld-15-1641-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/1b2621c1b63f/Vetworld-15-1641-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/c932b0950068/Vetworld-15-1641-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/9cf96bfe00ae/Vetworld-15-1641-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/142fe062b6d1/Vetworld-15-1641-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a015/9394144/27d49925e0d2/Vetworld-15-1641-g008.jpg

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