Oyekunle John Oladosu, Henry Reyer, Rosemarie Weikard, Beatrice Grafl, Dieter Liebhart, Cornelia C Metges, Christa Kühn, Gürbüz Daş
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The mixed infections reduced feed intake and the average daily weight gain (P < 0.001). The infections also increased the plasma concentrations of alpha (1)-acid glycoprotein and the antibody titre against H. meleagridis (P = 0.049), with no strain differences (P > 0.05). For host molecular response, 1887 genes were differentially expressed in LD, while 275 and 25 genes were differentially expressed in R and LB, respectively. The up-regulated genes in R and LD were mostly related to inflammatory and adaptive immune responses, while down-regulated genes in LD were involved in metabolic pathways, including gluconeogenesis. Despite performance differences among the strains, worm burdens were similar, but hepatic molecular responses differed significantly. Moreover, there was an indication of a shift in hepatic functions towards immune-related pathways. We, therefore, conclude that the liver shifts its functions from metabolic to immune-related activities in chickens when challenged with mixed parasite species.</p>","PeriodicalId":23658,"journal":{"name":"Veterinary Research","volume":"55 1","pages":"125"},"PeriodicalIF":3.7000,"publicationDate":"2024-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11439216/pdf/","citationCount":"0","resultStr":"{\"title\":\"Hepatic transcriptomic analysis reveals differential regulation of metabolic and immune pathways in three strains of chickens with distinct growth rates exposed to mixed parasite infections.\",\"authors\":\"Oyekunle John Oladosu, Henry Reyer, Rosemarie Weikard, Beatrice Grafl, Dieter Liebhart, Cornelia C Metges, Christa Kühn, Gürbüz Daş\",\"doi\":\"10.1186/s13567-024-01378-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>During parasite infections, the liver may prioritise immune-related pathways over its metabolic functions. Intestinal infections caused by Ascaridia galli and Heterakis gallinarum impair feed intake, nutrient absorption, and weight gain. Histomonas meleagridis, vectored by H. gallinarum, can also damage liver tissues, potentially impairing liver functions. This study examined the hepatic gene expression in three strains of chickens: Ross-308 (R), Lohmann Brown Plus (LB), and Lohmann Dual (LD), 2 weeks after an experimental infection (n = 18) with both A. galli and H. gallinarum or kept as uninfected control (n = 12). Furthermore, H. gallinarum infection led to a co-infection with H. meleagridis. The mixed infections reduced feed intake and the average daily weight gain (P < 0.001). The infections also increased the plasma concentrations of alpha (1)-acid glycoprotein and the antibody titre against H. meleagridis (P = 0.049), with no strain differences (P > 0.05). For host molecular response, 1887 genes were differentially expressed in LD, while 275 and 25 genes were differentially expressed in R and LB, respectively. The up-regulated genes in R and LD were mostly related to inflammatory and adaptive immune responses, while down-regulated genes in LD were involved in metabolic pathways, including gluconeogenesis. Despite performance differences among the strains, worm burdens were similar, but hepatic molecular responses differed significantly. Moreover, there was an indication of a shift in hepatic functions towards immune-related pathways. 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引用次数: 0
摘要
在寄生虫感染期间,肝脏可能会优先考虑免疫相关途径,而不是代谢功能。由五倍子蛔虫(Ascaridia galli)和五倍子杂环虫(Heterakis gallinarum)引起的肠道感染会损害饲料摄入、营养吸收和体重增加。由H. gallinarum传播的组织单胞菌(Histomonas meleagridis)也会破坏肝组织,从而可能损害肝功能。本研究检测了三种鸡品系的肝脏基因表达:Ross-308 (R)、Lohmann Brown Plus (LB) 和 Lohmann Dual (LD)三个品系的鸡在实验性感染五倍子甲虫和五倍子母虫 2 周后(n = 18),或作为未感染对照(n = 12)。此外,H. gallinarum 感染会导致 H. meleagridis 同时感染。混合感染降低了采食量和平均日增重(P 0.05)。在宿主分子反应方面,1887 个基因在 LD 中有差异表达,而在 R 和 LB 中分别有 275 和 25 个基因有差异表达。R和LD中上调的基因大多与炎症和适应性免疫反应有关,而LD中下调的基因则涉及代谢途径,包括葡萄糖生成。尽管各菌株的表现不同,但蠕虫负担相似,但肝脏分子反应却有显著差异。此外,有迹象表明肝脏功能转向了免疫相关途径。因此,我们得出结论,当鸡受到混合寄生虫物种的挑战时,肝脏功能会从代谢活动转向免疫相关活动。
Hepatic transcriptomic analysis reveals differential regulation of metabolic and immune pathways in three strains of chickens with distinct growth rates exposed to mixed parasite infections.
During parasite infections, the liver may prioritise immune-related pathways over its metabolic functions. Intestinal infections caused by Ascaridia galli and Heterakis gallinarum impair feed intake, nutrient absorption, and weight gain. Histomonas meleagridis, vectored by H. gallinarum, can also damage liver tissues, potentially impairing liver functions. This study examined the hepatic gene expression in three strains of chickens: Ross-308 (R), Lohmann Brown Plus (LB), and Lohmann Dual (LD), 2 weeks after an experimental infection (n = 18) with both A. galli and H. gallinarum or kept as uninfected control (n = 12). Furthermore, H. gallinarum infection led to a co-infection with H. meleagridis. The mixed infections reduced feed intake and the average daily weight gain (P < 0.001). The infections also increased the plasma concentrations of alpha (1)-acid glycoprotein and the antibody titre against H. meleagridis (P = 0.049), with no strain differences (P > 0.05). For host molecular response, 1887 genes were differentially expressed in LD, while 275 and 25 genes were differentially expressed in R and LB, respectively. The up-regulated genes in R and LD were mostly related to inflammatory and adaptive immune responses, while down-regulated genes in LD were involved in metabolic pathways, including gluconeogenesis. Despite performance differences among the strains, worm burdens were similar, but hepatic molecular responses differed significantly. Moreover, there was an indication of a shift in hepatic functions towards immune-related pathways. We, therefore, conclude that the liver shifts its functions from metabolic to immune-related activities in chickens when challenged with mixed parasite species.
期刊介绍:
Veterinary Research is an open access journal that publishes high quality and novel research and review articles focusing on all aspects of infectious diseases and host-pathogen interaction in animals.