Vagnozzi Ariel E, Espinosa Rodrigo, Cheng Sunny, Brinson Denise, O'Kane Peter, Wilson Jeanna, Zavala Guillermo
a Instituto de Virología, Centro de Investigaciones en Ciencias Veterinarias y Agronómicas , Instituto Nacional de Tecnología Agropecuaria , Argentina.
b Department of Population Health, Poultry Diagnostic and Research Center , University of Georgia , USA.
Avian Pathol. 2018 Oct;47(5):489-496. doi: 10.1080/03079457.2018.1492089. Epub 2018 Jul 25.
Chicken infectious anaemia virus (CIAV) is a widely distributed immunosuppressive agent. SPF flocks and eggs used for vaccine production and diagnostics must be CIAV-free. Detection of CIAV infection in SPF flocks involves primarily serology or other invasive methods. In order to evaluate different types of samples for rapid detection of CIAV infection, a trial was conducted in serologically negative broiler breeder pullets vaccinated with a commercial live-attenuated CIAV vaccine. Controls and vaccinated groups were sampled before and after vaccination. Invasive and non-invasive samples were used for CIAV DNA detection by real-time PCR. Seroconversion occurred at 14 days post-inoculation (DPI) in the vaccinated group, whereas CIAV genome was detected by qPCR at 7 DPI in both invasive and non-invasive samples. Only invasive samples remained qPCR positive for CIAV DNA by 21 DPI despite seroconversion of the chickens.
鸡传染性贫血病毒(CIAV)是一种广泛传播的免疫抑制因子。用于疫苗生产和诊断的无特定病原体(SPF)鸡群和鸡蛋必须无CIAV。检测SPF鸡群中的CIAV感染主要涉及血清学或其他侵入性方法。为了评估不同类型的样本用于快速检测CIAV感染,在接种了商业减毒活CIAV疫苗的血清学阴性肉种鸡青年母鸡中进行了一项试验。对照组和接种组在接种前后进行采样。通过实时PCR使用侵入性和非侵入性样本检测CIAV DNA。接种组在接种后14天(DPI)出现血清转化,而在接种后7天,在侵入性和非侵入性样本中均通过定量PCR(qPCR)检测到CIAV基因组。尽管鸡发生了血清转化,但到21 DPI时,只有侵入性样本的CIAV DNA的qPCR检测仍为阳性。