Rajendran Ramya, Srinivasan Jaisree, Natarajan Jayanthi, Govindan Kalaiselvi, Kumaragurubaran Karthik, Muthukrishnan Madhanmohan, Seeralan Manoharan, Subbiah Madhuri, Sundaram Revathi Shunmuga, Rao Pachineella Lakshmana, Ramasamy Sridhar
Central University Laboratory, Centre for Animal Health Studies, Tamil Nadu Veterinary and Animal Sciences University, Madhavaram Milk Colony, Chennai, 600051, India.
Vaccine Research Centre-Viral Vaccines, Centre for Animal Health Studies, Tamil Nadu Veterinary and Animal Sciences University, Madhavaram Milk Colony, Chennai, 600051, India.
Vet Res Commun. 2023 Sep;47(3):1231-1241. doi: 10.1007/s11259-022-10063-0. Epub 2023 Jan 3.
Sudden death of ducklings was reported in a duck farm located at Tiruvallur district in Tamil Nadu, India. Disease investigation began with post mortem findings of dead birds revealing enlarged pale-pink / pale-yellow liver with multifocal petechiae and ecchymosis. A positive amplification with duck hepatitis A virus specific primers by reverse transcription-polymerase chain reaction (RT-PCR) on the tissue samples collected from dead birds indicated infection by duck hepatitis A virus (DHAV), an avian picornavirus, known to cause acute and high-mortality in ducklings. The virus isolation was successful in 9-days old embryonated chicken eggs, in primary chicken embryo fibroblast (CEF) cells and from experimentally infected ducklings. The embryonic death on day 5 to 7 post inoculation in chicken embryos with signs of cutaneous hemorrhage, edema and greenish yellow liver together with histopathology of embryonic liver and kidney further confirmed DHAV infection. TEM analysis of the infected allantoic fluid and infected CEF cell culture supernatant showed the presence of spherical shaped, non-enveloped virion particles of ~ 20-38 nm diameter, typical for DHAV. Experimental infection of ducklings with RT-PCR positive tissue supernatant caused 40% to 50% mortality with typical petechial hemorrhages on the surface of liver. Further, histopathological analysis and RT-PCR of the inoculated duckling's tissues confirmed the presence of DHAV. Nucleotide sequencing of the 5'UTR region and VP1 region confirmed duck hepatitis A virus genotype 2 (DHAV-2). To the best of our knowledge, this is the first report of laboratory confirmation of DHAV-2 in India. This study warrants the need for the extensive epidemiological surveillance to understand the prevalence of DHAV-2 in India and to take appropriate control measures to curtail the disease spread.
据报道,印度泰米尔纳德邦蒂鲁瓦勒尔区的一个养鸭场出现了雏鸭突然死亡的情况。疾病调查始于对死鸭的尸检结果,发现肝脏肿大,呈淡粉色/淡黄色,有多处瘀点和瘀斑。对从死鸭采集的组织样本进行逆转录-聚合酶链反应(RT-PCR),用鸭甲型肝炎病毒特异性引物进行扩增呈阳性,表明感染了鸭甲型肝炎病毒(DHAV),这是一种禽微小核糖核酸病毒,已知可导致雏鸭急性高死亡率。该病毒在9日龄鸡胚、原代鸡胚成纤维细胞(CEF)以及经实验感染的雏鸭中成功分离。接种后第5至7天,鸡胚出现胚胎死亡,伴有皮肤出血、水肿和黄绿色肝脏等症状,同时胚胎肝脏和肾脏的组织病理学检查进一步证实了DHAV感染。对感染的尿囊液和感染的CEF细胞培养上清液进行透射电镜分析,显示存在直径约20 - 38纳米的球形、无包膜病毒粒子,这是DHAV的典型特征。用RT-PCR阳性组织上清液对雏鸭进行实验性感染,导致40%至50%的死亡率,肝脏表面出现典型的瘀点出血。此外,对接种雏鸭的组织进行组织病理学分析和RT-PCR,证实了DHAV的存在。对5'UTR区域和VP1区域进行核苷酸测序,确认了鸭甲型肝炎病毒2型(DHAV-2)。据我们所知,这是印度首次对DHAV-2进行实验室确诊的报告。本研究有必要进行广泛的流行病学监测,以了解DHAV-2在印度的流行情况,并采取适当的控制措施来遏制疾病传播。