Evidence map›Paper›PMID 39287214›Full record

ArticleVeterinary medicine and science2024

RNA-Seq analysis reveals the different mechanisms triggered by bovine and equine after infection with FMDV.

Yi Wu, Lu Li, Wanfu Bai, Tao Li, Xiaoying Qian, Yiyi Liu, Shenyuan Wang, Chunxia Liu, Fang Wan, Dong Zhang and 7 more

Abstract read
In one paragraph

Article in Veterinary medicine and science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Yi WuCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.ORCID 0009-0003-9615-6105
Lu LiCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Wanfu BaiBaoTou Medical College, Baotou, China.
Tao LiCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Xiaoying QianInstitute of Agriculture and Animal Husbandry, Xing'an League, China.
Yiyi LiuCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Shenyuan WangCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Chunxia LiuCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Fang WanCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Dong ZhangCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Yingchun LiuCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Kaifeng WuCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Yu LingCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Huanmin ZhouCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Fanhua MengCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.
Yanru ZhangSchool of Medicine, Hainan Vocational University of Science and Technology, Haikou, China.
Junwei CaoCollege of Life Sciences, Inner Mongolia Agricultural University, Hohhot, China.ORCID 0009-0005-8205-4364

Funding

Natural Science Foundation of Inner Mongolia, China 2020MS03048
6 · The paper itself

Abstract

backgroundFoot-and-mouth disease virus (FMDV) is an important pathogen of the MicroRNA virus family. Infection of livestock can cause physical weakness, weight loss, reduced milk production, and a significant reduction in productivity for an extended period. It also causes a high mortality rate in young animals, seriously affecting livestock production. The host range of FMDV is mainly limited to cloven-hoofed animals such as cattle and sheep, while odd-toed ungulates such as horses and donkeys have natural resistance to FMDV. The mechanism underlying this resistance in odd-toed ungulates remains unclear.

objectiveThis study aimed to analyze the differences between FMDV-infected cattle and horses to provide valuable insights into the host-FMDV interaction mechanisms, thereby contributing to the control of foot-and-mouth disease and promoting the development of the livestock industry.

methodsWe observed the distribution of integrins, which help FMDV enter host cells, in the nasopharyngeal tissues of cattle and horses using immunohistochemistry. Then, we employed high-throughput RNA sequencing (RNA-Seq) to study the changes in host gene expression in the nasopharyngeal epithelial tissues of cattle and horses after FMDV infection. We performed enrichment analysis of GO and KEGG pathways after FMDV infection and validated related genes through qPCR.

resultsThe immunohistochemical results showed that both cattle and horses had four integrin receptors that could assist FMDV entry into host cells. The transcriptome analysis revealed that after FMDV infection, pro-apoptotic genes such as caspase-3 (CASP3) and cytochrome C (CYCS) were upregulated in cattle, while apoptosis-inhibiting genes such as NAIP and BCL2A1 were downregulated. In contrast, the expression trend of related genes in horses was opposite to that in cattle. Additionally, autophagy-related genes such as beclin 1, ATG101, ATG4B, ATG4A, ATG13, and BCL2A1 were downregulated in cattle after FMDV infection, indicating that cattle did not clear the virus through autophagy. However, key autophagy genes including ATG1, ATG3, ATG9, ATG12, and ATG16L1 were significantly upregulated in horses after viral infection.

conclusionBoth water buffaloes and Mongolian horses express integrin receptors that allow FMDV entry into cells. Therefore, the resistance of Mongolian horses to FMDV may result from more changes in intracellular mechanisms, including processes such as autophagy and apoptosis. Significant differences were observed between water buffaloes and Mongolian horses in these processes, suggesting that these processes influence FMDV replication and synthesis.

Indexed as

Cattle DiseasesFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusRNA-SeqAnimalsCattleHorse DiseasesHorsesapoptosisautophagyFMDVRNA‐Seq

Identifiers

PMID39287214
PMCPMC11406511

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.