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与白羽鸡综合征相关的鸡星状病毒自然感染1日龄雏鸡的分子特征及相关细胞因子表达测定

Molecular Characterization and Determination of Relative Cytokine Expression in Naturally Infected Day-Old Chicks with Chicken Astrovirus Associated to White Chick Syndrome.

作者信息

Naranjo Nuñez Luis F, Santander-Parra Silvana H, Kyriakidis Nicolaos C, Astolfi-Ferreira Claudete S, Buim Marcos R, De la Torre David, Piantino Ferreira Antonio J

机构信息

Department of Pathology, School of Veterinary Medicine, University of São Paulo (USP), Av. Prof. Dr. Orlando M. Paiva 87, São Paulo CEP 05508-270, SP, Brazil.

Facultad de Ciencias de la Salud, Carrera de Medicina Veterinaria, Universidad de Las Américas (UDLA), Av. Jose Queri, Quito 170513, Ecuador.

出版信息

Animals (Basel). 2020 Jul 14;10(7):1195. doi: 10.3390/ani10071195.

DOI:10.3390/ani10071195
PMID:32674433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7401566/
Abstract

White chick syndrome (WCS) is an emergent disease that affects hatchability and hatched chicks, resulting in high mortality and economic losses, and is related to chicken astrovirus (CAstV). This syndrome has been reported in several countries worldwide, and groups and of CAstV have been determined; however, in Brazil, the virus has not been genotyped. The innate immunity of chicks affected by WCS or any CAstV is poorly understood and studied, and it is important to determine whether relative cytokine expression occurs during the early stages of the life of chicks. The aim of the present investigation is to detect and molecularly characterize CAstV associated with WCS, examine the macroscopic and microscopic lesions in the jejunum and spleen, and determine cytokine expression in the jejunum, liver, spleen and thymus of chicks naturally infected with WCS. To do so, we applied a pathological and molecular approach for CAstV detection and characterization, as well as the quantification of the relative mRNA expression of several cytokine genes. The phylogenetic analyses of the sequences obtained herein classified CAstV as uniquely belonging to group , showing a high similarity of nucleotides (NT) (75.7-80.6%) and amino acids (AA) (84.2-89.9%) with the members of group and a low similarity of NT (46.7-47.9%) and AA (37.8-38.9%) with the virus belonging in group . CAstV was also detected and quantified in the serum, spleen, thymus and jejunum, the latter being the organ where CAstV had the highest viral concentration. However, this organ did not present any microscopical alterations. In contrast, we observed necrotic hepatitis in the liver of the affected subjects. On the other hand, we observed the activation of several T helper 1 (Th1)- and T helper 2 (Th2)-cytokines ( and ), without being able to control the viral replication due to the high concentration of viral particles in some organs, principally in the gut. One possible role of these cytokines is contributing to the control of inflammation and cell protection of intestinal cells, principally during the early activation of immune responses. However, the fact that these responses are not mature enough to control the viral infection means that more studies need to be carried out to elucidate this topic.

摘要

白羽鸡综合征(WCS)是一种影响孵化率和雏鸡的新发疾病,会导致高死亡率和经济损失,且与鸡星状病毒(CAstV)有关。这种综合征在世界上多个国家都有报道,并且已经确定了CAstV的群组;然而,在巴西,该病毒尚未进行基因分型。受WCS或任何CAstV影响的雏鸡的先天免疫了解和研究较少,确定雏鸡生命早期阶段是否发生相关细胞因子表达很重要。本研究的目的是检测与WCS相关的CAstV并进行分子特征分析,检查空肠和脾脏的宏观和微观病变,并确定自然感染WCS的雏鸡空肠、肝脏、脾脏和胸腺中的细胞因子表达。为此,我们采用了病理和分子方法进行CAstV检测和特征分析,以及几种细胞因子基因相对mRNA表达的定量分析。本文获得的序列的系统发育分析将CAstV归类为仅属于群组,与群组成员的核苷酸(NT)(75.7 - 80.6%)和氨基酸(AA)(84.2 - 89.9%)具有高度相似性,与属于群组的病毒的NT(46.7 - 47.9%)和AA(37.8 - 38.9%)相似性较低。在血清、脾脏、胸腺和空肠中也检测到并定量了CAstV,空肠是CAstV病毒浓度最高的器官。然而,该器官未出现任何微观改变。相反,我们在受影响个体的肝脏中观察到坏死性肝炎。另一方面,我们观察到几种辅助性T细胞1(Th1)和辅助性T细胞2(Th2)细胞因子(和)的激活,但由于某些器官(主要是肠道)中病毒颗粒浓度高,无法控制病毒复制。这些细胞因子的一个可能作用是有助于控制炎症和保护肠道细胞,主要是在免疫反应的早期激活期间。然而,这些反应不够成熟以控制病毒感染这一事实意味着需要进行更多研究来阐明这一主题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/4409982e58e2/animals-10-01195-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/111ab958d821/animals-10-01195-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/c67d9210a3ff/animals-10-01195-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/8e8938f17ddf/animals-10-01195-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/6b0157f3b763/animals-10-01195-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/4409982e58e2/animals-10-01195-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/111ab958d821/animals-10-01195-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/c67d9210a3ff/animals-10-01195-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/8e8938f17ddf/animals-10-01195-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/6b0157f3b763/animals-10-01195-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3338/7401566/4409982e58e2/animals-10-01195-g005.jpg

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