Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, China; Scientific Observing and Experimental Station of Veterinary Pharmacology and Diagnostic Technology, Ministry of Agriculture, Yangling, Shaanxi, China.
Xi'an Center for Animal Disease Control and Prevention, Xi'an, Shaanxi, China.
Poult Sci. 2020 Mar;99(3):1287-1296. doi: 10.1016/j.psj.2019.10.067. Epub 2019 Dec 28.
Hens of a commercial Hy-line brown layer flock in China exhibited increased mortality and decreased egg production at 47 wk of age. From 47 to 57 wk, average weekly mortality increased from 0.11 to 3.0%, and egg production decreased from 10 to 30%, with a peak mortality rate (3.0%) observed at 54 wk of age. Necropsy of 11 birds demonstrated tissue damage that included hepatitis, liver hemorrhage, rupture, and/or enlarged livers. Microscopic liver lesions exhibited hepatocytic necrosis, lymphocytic periphlebitis, and myeloid leukosis. While no bacteria were recovered from liver and spleen samples, avian hepatitis E virus (HEV) RNA was detected in all 11 tested hens by nested reverse transcription-polymerase chain reaction. Of these, subgroup J avian leukosis virus (ALV-J) proviral DNA was detected in 5 hens by PCR. Alignments of partial ORF2 gene sequences obtained here demonstrated shared identity (76 to 97%) with corresponding sequences of other known avian HEV isolates. Env sequences of ALV-J isolates obtained here shared 50.1 to 55% identity with other ALV subgroups and 91.8 to 95.5% identity with other known ALV-J isolates. Phylogenetic tree analysis of selected sequences obtained here grouped an avian HEV sequence with genotype 3 HEV and assigned an ALV-J sequence to a branch separate from known ALV-J subgroups. Immunohistochemical results confirmed the presence of avian HEV and ALV-J in livers. Therefore, these results suggest that avian HEV and ALV-J co-infection caused the outbreak of hepatitis and liver hemorrhagic syndrome observed in the layer hen flock analyzed in this study.
中国某商业海兰褐蛋鸡群在 47 周龄时出现死亡率增加和产蛋量下降。47 至 57 周龄时,平均每周死亡率从 0.11%增加到 3.0%,产蛋量从 10%下降到 30%,54 周龄时死亡率达到峰值(3.0%)。对 11 只病死鸡进行剖检发现,组织损伤包括肝炎、肝出血、破裂和/或肝脏肿大。显微镜下肝脏病变表现为肝细胞坏死、淋巴细胞性门静脉周围炎和髓样白血病。虽然未从肝和脾样本中分离到细菌,但巢式逆转录聚合酶链反应检测到所有 11 只检测母鸡的禽戊型肝炎病毒(HEV)RNA。其中,5 只母鸡通过 PCR 检测到 J 亚群禽白血病病毒(ALV-J)前病毒 DNA。这里获得的部分 ORF2 基因序列的比对显示,与其他已知禽 HEV 分离株的相应序列具有共享同一性(76%至 97%)。这里获得的 ALV-J 分离株的Env 序列与其他 ALV 亚群共享 50.1%至 55%的同一性,与其他已知的 ALV-J 分离株共享 91.8%至 95.5%的同一性。这里选择的序列的系统发育树分析将禽 HEV 序列与基因型 3 HEV 分组,并将 ALV-J 序列分配到与已知 ALV-J 亚群分开的分支。免疫组织化学结果证实肝脏中存在禽 HEV 和 ALV-J。因此,这些结果表明,禽 HEV 和 ALV-J 的共同感染导致了所分析蛋鸡群中观察到的肝炎和肝出血综合征的爆发。