Chen Lu, Wang Jingjing, Liu Yufeng, Chen Yuteng, Wang Haiming, Li Jinping, Jiang Wenming, Yu Xiaohui, Liu Hualei
China Animal Health and Epidemiology Center, Qingdao, Shandong, China.
Qingdao Agricultural University, Qingdao, Shandong, China.
PLoS One. 2025 Sep 19;20(9):e0330417. doi: 10.1371/journal.pone.0330417. eCollection 2025.
Pigeon virus diarrhea is very common in the clinic, which has caused great damage to the pigeon industry. Pigeon adenovirus constitutes a significant pathogen responsible for pigeon viral diarrhea. Among them, Pigeon adenovirus 1 (PiAdV-1) and Pigeon adenovirus 2 (PiAdV-2) are the most common adenoviruses discovered in pigeon diseases in recent years. Infection with these viruses is common in clinical settings, which makes differential diagnosis more difficult. At present, real-time PCR is one of the most widely used techniques for the identification and detection of pathogens. This study presents the development of a dual real-time PCR assay designed specifically for the detection of PiAdV-1 and PiAdV-2. The dual real-time PCR assay developed in this study demonstrated satisfactory specificity, sensitivity, repeatability, and reproducibility, while showing no cross-reactivity with unrelated pathogens. The limit of detection (LOD) for PiAdV-1 is 94.8 copies/µL, and the LOD for PiAdV-2 is 88.4 copies/µL. This method was then used to analyze 20 liver tissue samples collected from dead pigeons, and the results were verified by genome sequencing. To understand the current epidemic status of pigeon adenovirus in China, the dual real-time PCR method established in this study was used to detect 500 pigeon swab samples collected from 10 provinces in China from 2022 to 2023. The results showed that the positive rates of PiAdV detected by the real-time PCR was 27.00% (135/500). PiAdV-1 single infection was detected in 8 cases (1.6%), PiAdV-2 single infection in 123 cases (24.6%), and PiAdV-1 and PiAdV-2 co-infection in 4 cases (0.8%). This study established a valuable tool for differentiating between PiAdV-1 and PiAdV-2 in practical applications and provided significant insights into the prevalence of these viruses in China.
鸽病毒性腹泻在临床上非常常见,给养鸽业造成了巨大损失。鸽腺病毒是引起鸽病毒性腹泻的重要病原体。其中,鸽腺病毒1型(PiAdV-1)和鸽腺病毒2型(PiAdV-2)是近年来在鸽病中发现的最常见的腺病毒。这些病毒感染在临床环境中很常见,这使得鉴别诊断更加困难。目前,实时荧光定量聚合酶链反应(real-time PCR)是病原体鉴定和检测中应用最广泛的技术之一。本研究介绍了一种专门用于检测PiAdV-1和PiAdV-2的双重实时荧光定量聚合酶链反应检测方法的开发。本研究开发的双重实时荧光定量聚合酶链反应检测方法具有令人满意的特异性、敏感性、重复性和再现性,同时与无关病原体无交叉反应。PiAdV-1的检测限(LOD)为94.8拷贝/微升,PiAdV-2的检测限为88.4拷贝/微升。然后用该方法分析了从死鸽采集的20份肝脏组织样本,并通过基因组测序验证了结果。为了解中国鸽腺病毒的当前流行状况,本研究建立的双重实时荧光定量聚合酶链反应方法用于检测2022年至2023年从中国10个省份采集的500份鸽拭子样本。结果显示,实时荧光定量聚合酶链反应检测到的PiAdV阳性率为27.00%(135/500)。检测到PiAdV-1单感染8例(1.6%),PiAdV-2单感染123例(24.6%),PiAdV-1和PiAdV-2混合感染4例(0.8%)。本研究建立了一种在实际应用中区分PiAdV-1和PiAdV-2的有价值工具,并为这些病毒在中国的流行情况提供了重要见解。