Evidence map›Paper›PMID 36918910›Full record

ArticleVeterinary research2023

Clearance of bacteria from lymph nodes in sheep immunized with Brucella suis S2 vaccine is associated with M1 macrophage activation.

Si Chen, Yuanyuan Chen, Zizhuo Jiao, Chengqiang Wang, Dantong Zhao, Yongbin Liu, Wenguang Zhang, Shihua Zhao, Bin Yang, Qinan Zhao and 8 more

Open access · goldFull text read
In one paragraph

Article in Veterinary research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 20% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. mSphere · 2025
    Article
  3. An SNP-based diagnostic method forFrontiers in veterinary science · 2025
    Article
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

18 authors at 4 institutions in 1 country.

Si ChenHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China.
Yuanyuan ChenHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China.
Zizhuo JiaoHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China.
Chengqiang WangHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China.
Dantong ZhaoJinyu Baoling Bio-Pharmaceutical Co., Ltd., Hohhot, Inner Mongolia, China.
Yongbin LiuInner Mongolia University, College Road No. 235, Hohhot, Inner Mongolia, China.
Wenguang ZhangCollege of Life Science, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia, China.
Shihua ZhaoInner Mongolia Academy of Agriculture and Animal Husbandry Sciences, Hohhot, Inner Mongolia, China.
Bin YangInner Mongolia Academy of Agriculture and Animal Husbandry Sciences, Hohhot, Inner Mongolia, China.
Qinan ZhaoInner Mongolia Academy of Agriculture and Animal Husbandry Sciences, Hohhot, Inner Mongolia, China.
Shaoyin FuInner Mongolia Academy of Agriculture and Animal Husbandry Sciences, Hohhot, Inner Mongolia, China.
Xiaolong HeInner Mongolia Academy of Agriculture and Animal Husbandry Sciences, Hohhot, Inner Mongolia, China.
Qiaoling ChenHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China.
Churiga ManHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China.
Guoying LiuJinyu Baoling Bio-Pharmaceutical Co., Ltd., Hohhot, Inner Mongolia, China.
Xuefeng WeiJinyu Baoling Bio-Pharmaceutical Co., Ltd., Hohhot, Inner Mongolia, China.
Li DuHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China. Kych2008dl@163.com.
Fengyang WangHainan Key Lab of Tropical Animal Reproduction, Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Lab of Haikou, School of Animal Science and Technology, Hainan University, Haikou, Hainan, China. fywang68@163.com.ORCID http://orcid.org/0000-0002-2043-2703
Hainan University · CNInner Mongolia Academy of Agricultural & Animal Husbandry Sciences · CNInner Mongolia Agricultural University · CNInner Mongolia University · CN

Funding

Academician Innovation Platform Project of Hainan Province No. YSPTZX202013Natural Science Foundation of China 32160831Special Funding Projects for Local Science and Technology Development Guided by the Central Committee ZY2022HN09
6 · The paper itself

Abstract

Ovine brucellosis is a global zoonotic disease of sheep caused by Brucella melitensis, which inflicts a significant burden on human and animal health. Brucella suis strain S2 (B. suis S2) is a smooth live attenuated vaccine for the prevention of ovine brucellosis in China. However, no previous studies have assessed the immunogenicity of B. suis S2 vaccine after oral immunization in sheep. Here, we attempted to evaluate the ovine immune response over the course of B. suis S2 immunization and to identify in vivo predictors for vaccine development. Body temperature, serum Brucella antibodies, serum cytokines (IL-12p70 and interferon [IFN]-γ), and bacterial load in the mandibular lymph nodes (LN), superficial cervical LN, superficial inguinal LN, and spleen were investigated to determine the safety and efficacy of the vaccine. The abnormal body temperature of sheep occurred within 8 days post-infection (dpi). Brucella suis S2 persisted for a short time (< 21 dpi) in the mandibular LN. The highest level of IL-12p70 was observed at 9 dpi, whereas serum IFN-γ levels peaked at 12 dpi. Transcriptome analysis and quantitative reverse transcription PCR were performed to determine gene expression profiles in the mandibular LN of sheep. Antigen processing and presentation pathway was the dominant pathway related to the dataset. Our studies suggest that the immune response in ovine LN resembled type 1 immunity with the secretion of IL-12p70 and IFN-γ after B.suis S2 immunization and the vaccine may eliminate Brucella via stimulation of M1 macrophages through the course of Th cells.

Indexed as

Brucella melitensisBrucella suisBrucella VaccineBrucellosisSheep DiseasesAnimalsLymph NodesMacrophage ActivationMacrophagesSheepVaccines, AttenuatedBrucella VaccineVaccines, AttenuatedBrucellalymphatic nodesmacrophagessheepvaccine

Identifiers

PMID36918910
PMCPMC10013293
OpenAlexW4324193921

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read9
table measurements read2
Read underepoch 390

Registered trials

None linked

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.