三株鸡与寄生虫共感染期间的组织特异性转录组适应。

IF 4 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Oyekunle John Oladosu, Henry Reyer, Nares Trakooljul, Solvig Görs, Cornelia C Metges, Gürbüz Daş
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引用次数: 0

摘要

背景:非笼养生产系统的广泛采用有助于胃肠道线虫和肉鸡组织单胞菌共感染的发病机制,引发鸡局部和全身免疫和代谢反应。本研究研究了罗曼布朗(LB)、罗曼双生(LD)和罗斯308 (R)不同生长速度(R b> LD b> LB)的雄性鸡,在实验中同时感染鸡蛔虫、鸡异源绦虫和meleagridis两周后组织的转录组适应性。结果:空肠、盲肠和肝脏组织的RNA测序揭示了组织特异性、菌株依赖性的转录反应。在尸检中证实了共感染,感染的鸟类中蛔虫特异性抗体和α -1-酸性糖蛋白显著升高(p结论:一般来说,表现较慢的菌株有效地启动了有利于蠕虫排出和空肠组织修复的反应,而表现较好的菌株主要在盲肠和肝脏中表现出炎症反应。这些发现强调了对混合寄生虫共感染的菌株依赖耐受的组织特异性适应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue-specific transcriptomic adaptation in three strains of chickens during coinfections with parasites.

Background: The widespread adoption of non-caged production systems contributes to the pathogenesis of coinfections with gastrointestinal nematodes and Histomonas meleagridis, triggering local and systemic immune and metabolic responses in chickens. This study investigated transcriptomic adaptation of tissues two weeks after experimental coinfections with Ascaridia galli, Heterakis gallinarum, and H. meleagridis in Lohmann Brown (LB), Lohmann Dual (LD), and Ross-308 (R) male chickens, which differ in growth rates (R > LD > LB).

Results: RNA sequencing of the jejunum, caecum, and liver tissues revealed tissue-specific, strain-dependent transcriptional responses. Coinfection was confirmed during necropsy, and Ascaris-specific antibodies as well as alpha-1-acid glycoprotein were significantly higher in infected birds (p < 0.01). The caecum exhibited the highest unique differentially expressed genes, DEGs (n = 4,094), corresponding to significant activation of complex immune pathways and inhibition of metabolic pathways (p < 0.01). Jejunum DEGs (n = 760) primarily related to muscle contraction, collagen metabolism notably in LB and LD strains. The liver displayed fewer unique DEGs (n = 266) but prominently activated immune responses, especially in R chickens.

Conclusion: In general, slower-performing strains effectively initiated responses favouring worm expulsion and tissue repair in the jejunum, whereas high-performing strains predominantly showed inflammatory responses in the caecum and liver. These findings highlight tissue-specific adaptations underlying strain-dependent tolerance to coinfections with mixed parasites.

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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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