van Santen V L, Joiner K S, Murray C, Petrenko N, Hoerr F J, Toro H
Department of Pathobiology, College of Veterinary Medicine, 166 Greene Hall, Auburn University, Auburn, AL 36849-5519, USA.
Avian Dis. 2004 Sep;48(3):494-504. doi: 10.1637/7155-010904R.
The events during the pathogenesis of chicken anemia virus (CAV) infection following intramuscular (IM) and oral inoculation were further elucidated and compared by sequential clinical, pathologic, and morphometric histopathologic evaluations, and by sequential determination of CAV genome concentrations in different organs. Specific-pathogen-free chickens were inoculated by IM or oral routes with the same dose (2 x 10(6) mean tissue culture infective dose [TCID50]) of CAV isolate 03-4876 at 1 day of age. Weights and hematocrits were obtained at 7, 10, 14, 18, 21, 25, and 28 days postinoculation (DPI). Seven birds from each group were necropsied at 7, 10, 14, and 28 DPI, and samples of thymus, Harderian gland, and cecal tonsils (CT) were obtained for histopathologic examination and CAV genome quantification by real-time polymerase chain reaction. Peak CAV genome concentrations were detected in the thymus at 10 and 14 DPI in the IM and orally infected chickens, respectively. High CAV DNA concentrations were maintained throughout the experimental period until 28 DPI, despite specific seroconversion occurring by 14 DPI in the IM-inoculated chickens. CAV was isolated from both orally and IM-infected chickens 28 DPI. Peak CAV genomes in the thymuses of IM and orally infected chickens coincided with peak lymphocyte depletion in these organs. Lymphocyte repopulation of the thymus occurred by 28 DPI in spite of the presence of the virus in the organs of both infected chicken groups. CAV genomes were detected in the CT, but histopathologic changes were not observed. Compared with the IM route of infection, orally infected chickens did not show apparent signs of illness. Clinical parameters, including reduction of weight gains and hematocrits, and gross and histopathologic changes were delayed and less severe in the orally inoculated chickens. This was concurrent with a delay in accumulation of CAV genomes in the thymus of these chickens.
通过连续的临床、病理和形态计量组织病理学评估,以及连续测定不同器官中鸡贫血病毒(CAV)基因组浓度,进一步阐明并比较了肌肉注射(IM)和口服接种后CAV感染发病过程中的相关事件。1日龄的无特定病原体鸡通过IM或口服途径接种相同剂量(2×10⁶平均组织培养感染剂量[TCID₅₀])的CAV分离株03 - 4876。在接种后7、10、14、18、21、25和28天(DPI)获取体重和血细胞比容数据。每组7只鸡在7、10、14和28 DPI进行剖检,采集胸腺、哈德氏腺和盲肠扁桃体(CT)样本用于组织病理学检查和通过实时聚合酶链反应进行CAV基因组定量分析。IM感染和口服感染的鸡分别在10和14 DPI时在胸腺中检测到CAV基因组浓度峰值。尽管IM接种的鸡在14 DPI时出现特异性血清转化,但在整个实验期直至28 DPI期间,CAV DNA浓度一直维持在较高水平。在28 DPI时,从口服和IM感染的鸡中均分离到CAV。IM感染和口服感染鸡的胸腺中CAV基因组峰值与这些器官中淋巴细胞耗竭峰值一致。尽管两个感染鸡组的器官中都存在病毒,但胸腺中的淋巴细胞在28 DPI时重新增殖。在CT中检测到CAV基因组,但未观察到组织病理学变化。与IM感染途径相比,口服感染的鸡未表现出明显的疾病迹象。口服接种的鸡的临床参数,包括体重增加和血细胞比容降低,以及大体和组织病理学变化出现延迟且程度较轻。这与这些鸡胸腺中CAV基因组积累延迟同时发生。