Evidence map›Paper›PMID 40450297›Full record

ArticleBMC veterinary research2025

Development of an indirect ELISA based on a new specific lipoprotein LP53 for the detection of antibodies against Mycoplasma synoviae.

Haoran Li, Zengjin Hu, Guijun Wang, Yu Wang, Shaohui Wang, Mingxing Tian, Yanqing Bao, Jingjing Qi, Shengqing Yu

Abstract read
In one paragraph

Article in BMC veterinary research, 2025. 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

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

1 citing paper in PubMed.

  1. 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

9 authors.

Haoran Li *Shanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China.
Zengjin Hu *Shanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China.
Guijun WangCollege of Animal Science and Technology, Anhui Agricultural University, No. 130, Changjiangxilu, Hefei, Anhui, 230061, PR China.
Yu WangShanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China.
Shaohui WangShanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China.
Mingxing TianShanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China.
Yanqing BaoShanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China.
Jingjing QiShanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China. qijingjing@shvri.ac.cn.
Shengqing YuShanghai Veterinary Research Institute, the Chinese Academy of Agricultural Sciences (CAAS), 518 Ziyue Road, Shanghai, 200241, P. R. China. yus@shvri.ac.cn.

Funding

National Key Research and Development Program of China 2023YFD1800602National Natural Science Foundation of China 31902244
6 · The paper itself

Abstract

backgroundMycoplasma synoviae (MS) is considered to be one of the main mycoplasma pathogens of poultry, causing arthritis, airsacculitis, eggshell apex abnormalities and production drops in chickens and turkeys. Infection by MS usually results in considerable economic losses to the poultry industry worldwide. Therefore, it is essential to develop a highly sensitive and accurate diagnostic method in the livestock production.

resultsThe MSLP53 was predicted as a highly conserved and specific membrane associated lipoprotein of MS by bioinformatics analysis. The His-tagged MSLP53 (rMSLP53) protein was expressed and purified using E. coli expression system, and was confirmed by Western blotting to react with each MS-positive serum, but not react with positive sera against other avian pathogens, suggesting that the rMSLP53 had strong immunoreactivity and specificity. An rMSLP53-based indirect ELISA was developed, compared to IDEXX kit with a pool of 277 chicken sera samples, and showed high sensitivity (85.54%), specificity (89.19%) and coincidence rate (87.00%) within these two methods. When detecting the sera from experimentally infected chickens, the newly established rMSLP53-ELISA had certain advantages over the IDEXX kit, that is, it could identify the serum 3–18 weeks after infection as MS-positive serum, while IDEXX kit could only identify the serum 3–12 weeks after infection as positive serum.

conclusionThe MSLP53 protein is a specific immunogenic lipoprotein of MS, which was confirmed to be a promising antigen target for the detection of serum antibodies of MS. A rMSLP53-based indirect ELISA assay was successfully established in this study, showed high sensitivity, specificity and consistency with the commercial IDEXX kit, and could recognize the serum as MS-positive in a longer period after MS infection than IDEXX kit. This newly established rMSLP53-ELISA may be used as an effective detection method for MS serological monitoring and epidemiological investigation.

Indexed as

Antibodies, BacterialLipoproteinsMycoplasma InfectionsMycoplasma synoviaePoultry DiseasesAnimalsBacterial ProteinsChickensEnzyme-Linked Immunosorbent AssaySensitivity and SpecificityAntibodies, BacterialBacterial ProteinsLipoproteinsImmunogenic lipoproteinIndirect ELISAInfection serum detectionLP53Mycoplasma synoviae

Identifiers

PMID40450297
PMCPMC12125734

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.