Evidence map›Paper›PMID 41856082›Full record

ArticleAnimal bioscience2026

ASAP1 gene InDel variants are associated with enhanced goat resistance against Brucella infection.

Xiaoyu Liu, Congliang Wang, Xiaoyuan Ren, Zhaofei Ren, Yanyan Li, Wangye Liu, Rongrong Li, Xiaoyue Song, Helin Li, Lei Zhang and 4 more

Abstract read
In one paragraph

Article in Animal bioscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Xiaoyu Liu *Shaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Congliang Wang *Shaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Xiaoyuan RenShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Zhaofei RenShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Yanyan LiShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Wangye LiuManagement Committee of Yulin Modern Agricultural Science and Technology Demonstration Zone, Yulin, China.
Rongrong LiManagement Committee of Yulin Modern Agricultural Science and Technology Demonstration Zone, Yulin, China.
Xiaoyue SongShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Helin LiShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Lei ZhangShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Shenghui ChenShaanxi Shenao Agricultural Biotechnology Development Co., Ltd., Yulin, China.
Xiaomin DuShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China.
Jinlian HuaCollege of Veterinary Medicine/Shaanxi Centre of Stem Cells Engineering & Technology, Northwest Agriculture & Forestry University, Yangling, China. jinlianhua@nwsuaf.edu.cn.
Haijing ZhuShaanxi Provincial Engineering and Technology Research Center of Shaanbei Cashmere Goats, College of Advanced Agricultural Sciences, Yulin University, Yulin, China. haijingzhu@yulinu.edu.cn.

Funding

Doctoral Research Foundation of Yulin University 2023GK12Doctoral Research Foundation of Yulin University 2025GK22Key Area Project of the Shaanxi Provincial Department of Science and Technology 2025NCYBXM-095Key Scientific Research Program Project of Shaanxi Provincial Department of Education 22JY074Key Scientific Research Program Project of Shaanxi Provincial Department of Education 22JY075Key Scientific Research Program Project of Shaanxi Provincial Department of Education 23JY087Key Scientific Research Program Project of Shaanxi Provincial Department of Education 23JY090Natural Science Basic Research Program of Shaanxi Province 2024JC-YBQN-0239Yulin Youth Talent Promotion Plan 20240601
6 · The paper itself

Abstract

objectiveThis study aimed to investigate the potential of the ASAP1 gene as a genetic biomarker for brucellosis resistance/susceptibility in goats.

methodsThis study collected samples from female Shaanbei white cashmere (SBWC) goats to investigate the association between the ASAP1 gene and brucellosis susceptibility. Peripheral blood mononuclear cells (PBMCs) were isolated from goats with various haplo types and Brucella statuses, and the association was evaluated using polymerase chain re action (PCR), quantitative reverse transcription (qRT)-PCR, and lipopolysaccharide (LPS) stimulation assays.

resultsThe ASAP1 gene was expressed most in th e spleen, significantly more than in the kidney and heart (p<0.05). In the SBWC goats population, three genotypes insertion/insertion (II), insertion/deletion (ID), and deletion/deletion (DD) were identified at the P2, P5, and P7 sites of goat ASAP1 gene. Association analysis showed that P2 and P7 sites variants were associated with host resistance to Brucella infection with the II genotype used as reference (p<0.05; p<0.01) and maintained after multiple testing correction. The ASAP1 gene was observed lower expression in testicular tissues of Brucella-infected adult SBWC goats compared to healthy controls (p<0.01). Haplotype analysis revealed Hap3 and Hap5 were associated with brucellosis-resistant compared to Hap1 (p<0.05). PBMCs were isolated from goats carrying Hap1, Hap3, and Hap5. After LPS stimulation, significantly reduced ASAP1 expression was detected in the susceptible haplotype Hap1 compared to the resistant haplotypes. The highest expression level was exhibited by the most resistant haplotype, Hap5. Furthermore, resistant haplotypes showed more rapid activation of key inflammatory pathways and pro-inflammatory cytokines (NF-κB, IL-6, TNF-α, IFN-γ) compared to susceptible Hap1, with faster resolution of the inflammatory response observed, particularly in the most resistant haplotype Hap5.

conclusionThe present study demonstrates that ASAP1 gene InDel variants influence brucellosis resistance in SBWC goats, providing a theoretical basis for breeding resistant populations.

Indexed as

ASAP1BrucellaGoatsResistance

Identifiers

PMID41856082
PMCPMC13353162

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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.