Evidence map›Paper›PMID 39585548›Full record

ArticleVeterinary research communications2024

Expression of chicken circovirus Cap protein and establishment of ELISA method for antibody detection.

Man Xu, Tingting Zhang, Weiyu Gao, Xinling Xu, Haoyan Yang, Hao Wang, Bin Xie, Xiang Liu, Baoshan Liu, Zeliang Chen

Abstract read
PubMed Publisher
In one paragraph

Article in Veterinary research communications, 2024. 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

10 authors.

Man XuKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China.
Tingting ZhangXinjiang Academy of Agricultural Sciences, No. 403, Nanchang Road, Bayi Street, Shaybak District, Urumqi, 830091, China.
Weiyu GaoKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China.
Xinling XuKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China.
Haoyan YangKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China.
Hao WangKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China.
Bin XieKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China.
Xiang LiuKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China.
Baoshan LiuKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China. lbslgy@syau.edu.cn.
Zeliang ChenKey Laboratory of Livestock Infectious Diseases, Ministry of Education, Shenyang Agricultural University, Shenyang, Liaoning Province, China. zeliangchen@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recently identified virus, chicken circovirus (ChCV), has been linked to the onset of acute gastroenteritis in chicks, a condition that can have a detrimental impact on the overall health and well-being of chickens in a farming setting. In this study, we developed an enzyme-linked immunosorbent assay (ELISA) method for the indirect detection of antibodies against the chicken circovirus (ChCV) through codon optimization, which effectively expressed the capsid protein of the ChCV and utilized it as an encapsulated antigen following purification. In establishing the ELISA method for detecting antibodies using the purified Cap protein as the antigen, the optimal concentration of the antigen was determined to be 1 µg/mL, the optimal blocking solution was identified as 1% bovine serum albumin, the optimal dilution ratio of the serum to be tested was established to be 1:100, and the dilution ratio of the secondary antibody was determined to be 1:5,000. At these thresholds, the sensitivity of the ELISA method was 94.44%, and the specificity was 100%. The testing of 203 clinical samples yielded a positivity rate of 46.8%, indicating that the virus is endemic in chickens. In conclusion, this study established an ELISA method to detect antibodies against chicken circovirus using recombinant Cap protein as antigen, demonstrating good specificity and sensitivity. This lays the foundation for the development of related kits and the detection of infection and epidemiology of chicken circovirus. Meanwhile, the analysis concluded that chicken circovirus infection is more common, and the prevention and control of this disease should be emphasised and strengthened.

Indexed as

Antibodies, ViralCapsid ProteinsChickensCircoviridae InfectionsCircovirusEnzyme-Linked Immunosorbent AssayPoultry DiseasesAnimalsSensitivity and SpecificityAntibodies, ViralCapsid ProteinsAntibodyCap ProteinChicken circovirusELISA

Identifiers

What OpenQuestion holds

Textmetadata
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.