Evidence map›Paper›PMID 40650819›Full record

ArticleVeterinary research communications2025

Establishment of an ELISA for the detection of antibodies against Stenotrophomonas maltophilia.

Qian Zhang, Lu Dai, Fuxian Zhang, Zijie Xu, Xiangrui Yang, Hong Chu, Guangmou Yan, Na Li, Fengyang Li, Liancheng Lei

Abstract read
PubMed Publisher
In one paragraph

Article in Veterinary research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Qian ZhangCollege of Animal Science and Technology, Yangtze University, Jingzhou, China.
Lu DaiCollege of Animal Science and Technology, Yangtze University, Jingzhou, China.
Fuxian ZhangCollege of Animal Science and Technology, Yangtze University, Jingzhou, China.
Zijie XuState Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Qinglong Road 818, Changchun, 130062, China.
Xiangrui YangState Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Qinglong Road 818, Changchun, 130062, China.
Hong ChuState Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Qinglong Road 818, Changchun, 130062, China.
Guangmou YanState Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Qinglong Road 818, Changchun, 130062, China.
Na LiState Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Qinglong Road 818, Changchun, 130062, China.
Fengyang LiState Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Qinglong Road 818, Changchun, 130062, China. fengyangli@jlu.edu.cn.
Liancheng LeiState Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Qinglong Road 818, Changchun, 130062, China. leiliancheng@163.com.

Funding

National Key Research and Development Program of China 2022YFD1800905National Natural Science Foundation of China 32102670
6 · The paper itself

Abstract

backgroundStenotrophomonas maltophilia (S. maltophilia) is a conditionally pathogenic bacterium around the world. In humans, it mainly harms patients with immunodeficient or chronic diseases, leading to high mortality rate of patients with pneumonia and bacteremia. In the veterinary medicine, it caused respiratory infections or mixed infections with other common pathogens in pigs. However, infection of S. maltophilia has been overlooked and the prevalence of S. maltophilia in porcine remains unknown due to a lack of diagnosis method.

methodsIn this study, an indirect ELISA was established using the purified Phospholipase C (PLC) protein of S. maltophilia SMFZ-01 strain as the coating antigen. Checkerboard titration was performed for the optimization of the coating concentration of the recombinant PLC (rPLC) protein, the dilution and incubation time of serum and the IgG-HRP secondary antibody. The specificity, repeatability and sensitivity of established ELISA was also optimized. The positive rate of S. maltophilia antibodies was calculated using 305 clinical porcine sera samples by either established indirect ELISA or a nested PCR.

resultsrPLC was successfully purified and identified by Western blot. The optimal coating concentration of rPLC was 2.5 µg/mL. The optimal dilutions of serum samples and secondary antibody were 1:400 and 1:2500, respectively. The analytical sensitivity was 1:1600, with no cross-reaction with the positive sera of other common porcine pathogens. The intra-assay and inter-assay reproducibility coefficients of variation was less than 10%. Detection of 305 clinical porcine sera samples revealed a high positive rate by established ELISA (12.01%) and nested PCR (29.87%).

conclusionsTo our knowledge, this is the first study to develop an indirect ELISA for the detection and epidemiological analysis of S. maltophilia in porcine. Our findings indicate that S. maltophilia may be more prevalent in porcine populations than previously recognized, though further studies are needed to confirm this. The established indirect ELISA enhances our understanding of S. maltophilia infections in pig herds and provides valuable insights for designing future prevention and control strategies, along with considerations regarding the health and welfare of porcine.

Indexed as

Antibodies, BacterialGram-Negative Bacterial InfectionsStenotrophomonas maltophiliaSwine DiseasesAnimalsEnzyme-Linked Immunosorbent AssayReproducibility of ResultsSensitivity and SpecificitySwineAntibodies, BacterialIndirect ELISAPhospholipase CPigPRDCStenotrophomonas maltophilia

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.