Liang Suyun, Lu Meixi, Yu Daxin, Xing Guangnan, Ji Zhanqing, Guo Zhanbao, Zhang Qi, Huang Wei, Xie Ming, Hou Shuisheng
Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Comput Struct Biotechnol J. 2024 Jan 17;23:771-782. doi: 10.1016/j.csbj.2024.01.005. eCollection 2024 Dec.
Duck hepatitis A virus genotype 3 (DHAV-3) is the major cause of viral hepatitis in ducks in Asia. Previous studies have shown that ducklings younger than 21 days are more susceptible to DHAV-3. To elucidate the mechanism by which age affects the differential susceptibility of Pekin ducks to DHAV-3, intestinal ( = 520), liver ( = 40) and blood ( = 260) samples were collected from control and DHAV-3-infected ducks at 7, 10, 14, and 21 days of age. Comparisons of plasma markers, mortality rates, and intestinal histopathological data showed that the resistance of Pekin ducks to DHAV-3 varied with age. 16 S sequencing revealed that the ileal microbial composition was influenced by age, and this correlation was greater than that recorded for caecal microbes. , , , , , and were the differntially abundant microbes in the ileum at the genus level after DHAV-3 infection and were significantly correlated with 7 differentially expressed genes (DEGs) in 7- and 21-day-old ducklings. 3 immunity-related pathways were significantly different between 7- and 21-day-old ducklings, especially for -mediated induction of the interferon-alpha/beta pathway, which induces differential production of CD8(+) T cells and was influenced by a combination of differentially abundant microbiota and DEGs. We found that microbes in the ileum changed regularly with age. The intestinal microbiota was associated with the expression of genes in the liver through IFIH1-mediated induction of the interferon-alpha/beta pathway, which may partially explain why younger ducklings were more susceptible to DHAV-3 infection.
鸭甲型肝炎病毒3型(DHAV-3)是亚洲地区鸭病毒性肝炎的主要病因。先前的研究表明,21日龄以下的雏鸭对DHAV-3更易感。为阐明年龄影响北京鸭对DHAV-3易感性差异的机制,在7、10、14和21日龄时从对照鸭和感染DHAV-3的鸭中采集了肠道(n = 520)、肝脏(n = 40)和血液(n = 260)样本。血浆标志物、死亡率和肠道组织病理学数据的比较表明,北京鸭对DHAV-3的抵抗力随年龄而变化。16S测序显示,回肠微生物组成受年龄影响,且这种相关性大于盲肠微生物的相关性。DHAV-3感染后,在属水平上,[具体微生物名称1]、[具体微生物名称2]、[具体微生物名称3]、[具体微生物名称4]、[具体微生物名称5]和[具体微生物名称6]是回肠中丰度有差异的微生物,并且与7日龄和21日龄雏鸭中的7个差异表达基因(DEGs)显著相关。7日龄和21日龄雏鸭之间有3条免疫相关途径存在显著差异,特别是对于γ介导的α/β干扰素途径的诱导,该途径诱导CD8(+) T细胞的差异产生,并受到丰度有差异的微生物群和DEGs组合的影响。我们发现回肠中的微生物随年龄有规律地变化。肠道微生物群通过IFIH1介导的α/β干扰素途径的诱导与肝脏中的基因表达相关,这可能部分解释了为什么幼雏鸭对DHAV-3感染更易感。