1H-NMR based-metabolomics reveals alterations in the metabolite profiles of chickens infected with ascarids and concurrent histomonosis infection.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Oyekunle John Oladosu, Banny Silva Barbosa Correia, Beatrice Grafl, Dieter Liebhart, Cornelia C Metges, Hanne Christine Bertram, Gürbüz Daş
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引用次数: 0

Abstract

Background: Gut infections of chickens caused by Ascaridia galli and Heterakis gallinarum are associated with impaired host performance, particularly in high-performing genotypes. Heterakis gallinarum is also a vector of Histomonas meleagridis that is often co-involved with ascarid infections. Here, we provide a first insight into the alteration of the chicken plasma and liver metabolome as a result of gastrointestinal nematode infections with concomitant histomonosis. 1H nuclear magnetic resonance (1H-NMR) based-metabolomics coupled with a bioinformatics analysis was applied to explore the variation in the metabolite profiles of the liver (N = 105) and plasma samples from chickens (N = 108) experimentally infected with A. galli and H. gallinarum (+H. meleagridis). This was compared with uninfected chickens at different weeks post-infection (wpi 2, 4, 6, 10, 14, 18) representing different developmental stages of the worms.

Results: A total of 31 and 54 metabolites were quantified in plasma and aqueous liver extracts, respectively. Statistical analysis showed no significant differences (P > 0.05) in any of the 54 identified liver metabolites between infected and uninfected hens. In contrast, 20 plasma metabolites including, amino acids, sugars, and organic acids showed significantly elevated concentrations in the infected hens (P < 0.05). Alterations of plasma metabolites occurred particularly in wpi 2, 6 and 10, covering the pre-patent period of worm infections. Plasma metabolites with the highest variation at these time points included glutamate, succinate, trimethylamine-N-oxide, myo-inositol, and acetate. Differential pathway analysis suggested that infection induced changes in (1) phenylalanine, tyrosine, and tryptophan metabolism, (2) alanine, aspartate and glutamate metabolism; and 3) arginine and proline metabolism (Pathway impact > 0.1 with FDR adjusted P-value < 0.05).

Conclusion: In conclusion, 1H-NMR based-metabolomics revealed significant alterations in the plasma metabolome of high performing chickens infected with gut pathogens-A. galli and H. gallinarum. The alterations suggested upregulation of key metabolic pathways mainly during the patency of infections. This approach extends our understanding of host interactions with gastrointestinal nematodes at the metabolic level.

基于1H-NMR的代谢组学揭示了感染蛔虫和并发组织瘤病感染的鸡的代谢物谱的变化。
背景:鸡蛔虫和鸡异线虫引起的鸡肠道感染与宿主生产性能受损有关,特别是在高性能基因型中。鸡异线虫也是肉苁蓉组织单胞菌的载体,通常与蛔虫感染有关。在这里,我们提供了第一个洞察鸡血浆和肝脏代谢组的变化,作为胃肠道线虫感染合并组织吸虫病的结果。采用1H核磁共振(1H- nmr)代谢组学结合生物信息学分析方法,研究了实验感染鸡a . galli和H. gallinarum (+H.)的鸡(N = 108)肝脏(N = 105)和血浆样品的代谢物谱变化。meleagridis)。这与感染后不同周(wpi 2、4、6、10、14、18)的未感染鸡进行了比较,代表了蠕虫的不同发育阶段。结果:在血浆和肝水提取物中分别定量测定了31种和54种代谢物。统计分析表明,54种肝脏代谢物在感染和未感染母鸡之间均无显著差异(P > 0.05)。相比之下,20种血浆代谢物,包括氨基酸、糖和有机酸,在感染鸡体内的浓度显著升高(P值为FDR调整后的P值P值为0.1)。结论:基于1H-NMR的代谢组学分析显示,感染肠道病原体a的高性能鸡血浆代谢组学发生了显著变化。galli和H. gallinarum。这些变化表明主要在感染通畅期间关键代谢途径的上调。这种方法扩展了我们对宿主与胃肠道线虫在代谢水平上相互作用的理解。
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来源期刊
Gut Pathogens
Gut Pathogens GASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍: Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology. Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).
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