Haemonchus contortus alters distribution and utilization of protein and amino acids in different tissues of host sheep

IF 2 2区 农林科学 Q2 PARASITOLOGY Veterinary parasitology Pub Date : 2024-08-14 DOI:10.1016/j.vetpar.2024.110289
Hai Xiang , Bao Zhao , Yi Fang , Linshu Jiang , Rongzhen Zhong
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Abstract

The objective was to determine host animal protein/amino acid redistribution and use among the abomasum, duodenum and muscle of sheep infected with Haemonchus contortus. Sixteen male Ujumqin sheep (32.4 ± 3.9 kg) were dewormed and randomly assigned to two groups, infected or not infected with H. contortus (GIN and CON). The GIN group had lower (P < 0.05) dry matter intake, average daily gain, and live body weight than CON, with extensive focal infiltration of lymphocytes in the lamina propria and bottom of the abomasal epithelium. In the abomasum and duodenum, there were 100 and 220 genes, respectively, that were up-regulated, whereas 56 and 149 were down-regulated. In the abomasum, the most enriched KEGG pathways were related to immunity and inflammation reaction, including: viral protein interaction with cytokine and cytokine receptor (P = 0.017), influenza A (P = 0.030), IL-17 signaling pathway (P = 0.030). In the duodenum, KEGG pathways were more enriched in nutrient metabolism, including pancreatic secretion (P < 0.001), protein digestion and absorption (P < 0.001), graft-versus-host disease (P = 0.004). Furthermore, most genes related with the above KEGG pathways were increased in the abomasum but decreased in the duodenum. Amino acid profiles in abomasum and duodenum of CON and GIN groups were clustered in a partial least-squares discriminant analysis model, with significant changes in 36 and 19 metabolites in abomasal and duodenal chyme, respectively. Further confirmed by transcriptome-targeted metabolome association analysis, GIN mainly enhanced metabolism of arginine and sulphur amino acids in abomasum and those metabolic pathways were associated. Meanwhile, GIN mainly decreased pyruvate related amino acid metabolism in duodenum. Moreover, concentrations of Arg (P = 0.036), His (P = 0.027), and Cys (P = 0.046) in longissimus thoracis et lumborum were decreased in GIN, whereas concentrations of Gly (P = 0.012) and Ala (P = 0.046) were increased. In conclusion, H. contortus enhanced metabolism of arginine and sulphur amino acids in the abomasum; decreased pyruvate metabolism in the duodenum; and drove more protein/amino acids for abomasal tissues to resist physical and immune damage, reducing protein and amino acids in duodenum and muscle for support host growth. Specific nutrients (such like arginine, histidine, and cysteine) may play important role in control gastrointestinal nematode infection for ruminant.

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口蹄疫改变了蛋白质和氨基酸在宿主绵羊不同组织中的分布和利用率
目的是确定感染了口蹄疫的绵羊的腹腔、十二指肠和肌肉中宿主动物蛋白/氨基酸的再分布和使用情况。16 只雄性乌珠穆沁绵羊(32.4 ± 3.9 千克)被驱虫后随机分配到两组,即感染或未感染线虫病组(GIN 组和 CON 组)。GIN 组的干物质摄入量、平均日增重和活体重均低于 CON 组(P < 0.05),腹腔上皮固有层和底部有广泛的淋巴细胞灶性浸润。在腹腔和十二指肠中,分别有100个和220个基因上调,56个和149个基因下调。在腹腔,与免疫和炎症反应相关的KEGG通路最为丰富,包括:病毒蛋白与细胞因子和细胞因子受体的相互作用(P = 0.017)、甲型流感(P = 0.030)、IL-17信号通路(P = 0.030)。在十二指肠中,KEGG通路更多地与营养代谢有关,包括胰腺分泌(P < 0.001)、蛋白质消化与吸收(P < 0.001)、移植物抗宿主疾病(P = 0.004)。此外,与上述 KEGG 通路相关的大多数基因在腹腔中增加,而在十二指肠中减少。在偏最小二乘判别分析模型中,CON组和GIN组腹腔和十二指肠中的氨基酸谱发生了聚类,腹腔和十二指肠食糜中分别有36种和19种代谢物发生了显著变化。转录组靶向代谢组关联分析进一步证实,GIN主要增强了精氨酸和含硫氨基酸在腹腔中的代谢,这些代谢通路与GIN相关。同时,GIN 主要降低了十二指肠中丙酮酸相关氨基酸的代谢。此外,GIN 还降低了胸腰长肌中 Arg(P = 0.036)、His(P = 0.027)和 Cys(P = 0.046)的浓度,而增加了 Gly(P = 0.012)和 Ala(P = 0.046)的浓度。总之,H. contortus 增强了腹腔内精氨酸和含硫氨基酸的代谢;降低了十二指肠内丙酮酸的代谢;驱动更多的蛋白质/氨基酸用于腹腔组织以抵抗物理和免疫损伤,减少了十二指肠和肌肉中用于支持宿主生长的蛋白质和氨基酸。特定营养物质(如精氨酸、组氨酸和半胱氨酸)可能在控制反刍动物胃肠道线虫感染中发挥重要作用。
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来源期刊
Veterinary parasitology
Veterinary parasitology 农林科学-寄生虫学
CiteScore
5.30
自引率
7.70%
发文量
126
审稿时长
36 days
期刊介绍: The journal Veterinary Parasitology has an open access mirror journal,Veterinary Parasitology: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. This journal is concerned with those aspects of helminthology, protozoology and entomology which are of interest to animal health investigators, veterinary practitioners and others with a special interest in parasitology. Papers of the highest quality dealing with all aspects of disease prevention, pathology, treatment, epidemiology, and control of parasites in all domesticated animals, fall within the scope of the journal. Papers of geographically limited (local) interest which are not of interest to an international audience will not be accepted. Authors who submit papers based on local data will need to indicate why their paper is relevant to a broader readership. Parasitological studies on laboratory animals fall within the scope of the journal only if they provide a reasonably close model of a disease of domestic animals. Additionally the journal will consider papers relating to wildlife species where they may act as disease reservoirs to domestic animals, or as a zoonotic reservoir. Case studies considered to be unique or of specific interest to the journal, will also be considered on occasions at the Editors'' discretion. Papers dealing exclusively with the taxonomy of parasites do not fall within the scope of the journal.
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