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直接RNA测序揭示了鸡对空肠弯曲菌接种的转录后修饰反应。

Direct RNA sequencing reveals chicken post-transcriptional modifications in response to Campylobacter jejuni inoculation.

作者信息

Zhao Yanan, Wang Yuanmei, Ren Yanru, Liu Long, Wang Tianyi, Liu Liying, Li Xianyao

机构信息

Shandong Provincial Key laboratory for Livestock Germplasm Innovation & Utilization, College of Animal Science and Technology, Shandong Agricultural University, Tai'an, 271017, Shandong, China.

College of Life Sciences, Shandong Agricultural University, Tai'an, 271017, Shandong, China.

出版信息

BMC Genomics. 2025 Apr 14;26(1):374. doi: 10.1186/s12864-025-11564-3.

Abstract

BACKGROUND

Campylobacter jejuni (C. jejuni), is a leading cause of food-borne pathogen, poses significant threats to poultry industry and public health. Post-transcriptional modifications play crucial roles in regulating the immune system and cell functions. However, the epigenetic regulation in response to C. jejuni inoculation in chicken remains elusive.

RESULTS

The RNA transcriptional profiles and base modification alterations in the chicken cecum following C. jejuni inoculation were characterized using direct RNA sequencing and analyzed by bio-informatics and expression analysis. We identified 40,755 transcripts and 23,877 genes following C. jejuni inoculation in the chicken cecum. Of which, 10,503 novel transcripts across 8,560 genes were identified. The number of significantly differential alternative splicing events and poly(A) tails was 192 and 426, respectively (P < 0.05). Particularly, 121 significantly differentially expressed transcripts which were enriched in defense response to gram-negative bacteria, positive regulation of interleukin-6 production, innate immune response, macrophage activation (P < 0.05). Among these, 29 transcripts contained mC sites, and 37 transcripts contained mA sites. The transcripts containing mA/mC modifications displayed higher expression levels and shorter poly(A) tails than those without modifications. Functional analysis of these modules including differentially expressed transcripts (DETs), transcripts with differentially significant poly(A) tail length, mC modified DETs, and mA modified DETs showed that the negative regulation of interferon-beta production was enriched (P < 0.05). Specially, ENSGALT00000020390 (novel transcript), and ENSGALT00000053962 (IFIH1-202) were significantly enriched.

CONCLUSIONS

This study provided a post-transcriptional modification profile in the chicken cecum post C. jejuni inoculation, including alternative splicing, poly(A) tail length, mA and mC modifications. ENSGALG00000012480 and IFIH1 could be potential candidate genes as epigenetic markers following C. jejuni inoculation. The findings provide new insights into the complexity of expression regulation and data resource of the epitranscriptome, enhancing our understanding on epigenetic modification regulating C. jejuni inoculation.

摘要

背景

空肠弯曲菌是食源性病原体的主要病因,对家禽业和公众健康构成重大威胁。转录后修饰在调节免疫系统和细胞功能中起关键作用。然而,鸡在接种空肠弯曲菌后的表观遗传调控仍不清楚。

结果

利用直接RNA测序对鸡盲肠接种空肠弯曲菌后的RNA转录谱和碱基修饰变化进行了表征,并通过生物信息学和表达分析进行了分析。我们在鸡盲肠接种空肠弯曲菌后鉴定出40,755个转录本和23,877个基因。其中,鉴定出跨越8,560个基因的10,503个新转录本。显著差异的可变剪接事件和多聚腺苷酸尾的数量分别为192个和426个(P < 0.05)。特别地,121个显著差异表达的转录本富集于对革兰氏阴性菌的防御反应、白细胞介素-6产生的正调控、先天免疫反应、巨噬细胞激活(P < 0.05)。其中,29个转录本含有5-甲基胞嘧啶(mC)位点,37个转录本含有N6-甲基腺苷(mA)位点。含有mA/mC修饰的转录本比未修饰的转录本显示出更高的表达水平和更短的多聚腺苷酸尾。对这些模块的功能分析,包括差异表达转录本(DETs)、多聚腺苷酸尾长度差异显著的转录本、mC修饰的DETs和mA修饰的DETs,表明干扰素-β产生的负调控得到富集(P < 0.05)。特别地,ENSGALT00000020390(新转录本)和ENSGALT00000053962(IFIH1-202)显著富集。

结论

本研究提供了鸡盲肠接种空肠弯曲菌后的转录后修饰谱,包括可变剪接、多聚腺苷酸尾长度、mA和mC修饰。ENSGALG00000012480和IFIH1可能是空肠弯曲菌接种后作为表观遗传标记的潜在候选基因。这些发现为表达调控的复杂性和表观转录组的数据资源提供了新的见解,增强了我们对表观遗传修饰调节空肠弯曲菌接种的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/292d/11998244/f8c5f3d812ae/12864_2025_11564_Fig1_HTML.jpg

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