Yu Guanliu, Wang Aihua, Tang Yi, Diao Youxiang
College of Animal Science and Technology, Shandong Agricultural UniversityTai'an, China.
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural UniversityTai'an, China.
Front Microbiol. 2017 Aug 15;8:1559. doi: 10.3389/fmicb.2017.01559. eCollection 2017.
During a study on high mortality cases of goose embryo in Shandong Province, China (2014-2015), we isolated an H9N2 avian influenza virus (AIV) strain (A/goose/Shandong/DP01/2014, DP01), which was supposedly the causative agent for goose embryo death. Sequence analysis revealed that DP01 shared 99.9% homology in the HA gene with a classic immune suppression strain SD06. To study the potential vertical transmission ability of the DP01 strain in breeder goose, a total of 105 Taizhou breeder geese, which were 360 days old, were equally divided into five groups (A, B, C, D, and E) for experimental infection. H9N2 AIV (DP01) was used for inoculating through intravenous (group A), intranasal instillation (group B), and throat inoculation (group C) routes, respectively. The geese in group D were inoculated with phosphate buffer solution (PBS) and those in group E were the non-treated group. At 24 h post inoculation, H9N2 viral RNA could be detected at vitelline membrane, embryos, and allantoic fluid of goose embryos from H9N2 inoculated groups. Furthermore, the HA gene of H9N2 virus from vitelline membrane, embryo, allantoic fluid, and gosling shared almost 100% homology with an H9N2 virus isolated from the ovary of breeder goose, which laid these eggs, indicating that H9N2 AIV can be vertically transmitted in goose. The present research study provides evidence that vertical transmission of H9N2 AIV from breeding goose to goslings is possible.
在中国山东省(2014 - 2015年)进行的一项关于鹅胚高死亡率病例的研究中,我们分离出一株H9N2禽流感病毒(AIV)毒株(A/鹅/山东/DP01/2014,简称DP01),推测它是导致鹅胚死亡的病原体。序列分析显示,DP01的血凝素(HA)基因与经典免疫抑制毒株SD06的同源性为99.9%。为研究DP01毒株在种鹅中的潜在垂直传播能力,将105只360日龄的泰州种鹅平均分为五组(A、B、C、D和E组)进行实验感染。分别通过静脉注射(A组)、滴鼻(B组)和咽喉接种(C组)途径用H9N2 AIV(DP01)进行接种。D组鹅接种磷酸盐缓冲液(PBS),E组鹅不做处理。接种后24小时,在接种H9N2组的鹅胚卵黄膜、胚胎和尿囊液中可检测到H9N2病毒RNA。此外,从卵黄膜、胚胎、尿囊液和雏鹅中分离的H9N2病毒的HA基因与从产下这些蛋的种鹅卵巢中分离的H9N2病毒几乎具有100%的同源性,这表明H9N2 AIV可在鹅中垂直传播。本研究为H9N2 AIV从种鹅垂直传播给雏鹅提供了证据。