Evidence map›Paper›PMID 33028866›Full record

ArticleScientific reports2020

Establishment of a fluorescence staining method for Schistosoma japonicum miracidia.

Yuanxi Shen, Rongyi Ji, Man Yang, Jiaojiao Lin, Hairong Wang, Chuangang Zhu, Qinkun Xu

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Yuanxi ShenKey Laboratory of Animal Parasitology, Ministry of Agricultμre of China, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 518, Ziyue Road, Min Hang District, Shanghai, 200241, China.
Rongyi JiKey Laboratory of Animal Parasitology, Ministry of Agricultμre of China, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 518, Ziyue Road, Min Hang District, Shanghai, 200241, China.
Man YangKey Laboratory of Animal Parasitology, Ministry of Agricultμre of China, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 518, Ziyue Road, Min Hang District, Shanghai, 200241, China.
Jiaojiao LinKey Laboratory of Animal Parasitology, Ministry of Agricultμre of China, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 518, Ziyue Road, Min Hang District, Shanghai, 200241, China.
Hairong WangShandong Provincial Engineering Technology Research Center of Animal Disease Control and Prevention, Shandong Agricultural University, 61 Daizong Road, Tai'an City, 271018, Shandong Province, China.
Chuangang ZhuKey Laboratory of Animal Parasitology, Ministry of Agricultμre of China, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 518, Ziyue Road, Min Hang District, Shanghai, 200241, China. zcg@shvri.ac.cn.
Qinkun XuHenry Fok College of Biology and Agriculture, Shaoguan University, No. 288, University Road, Zhenjiang District, Shaoguan City, Guangdong Province, China. xuqinkun@sgu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently the diagnosis of schistosomiasis is mainly determined by observing the presence of eggs in host stool samples. Because of the overwhelming number of impurities in the stool, eggs are rarely observed. Therefore, the stool hatching method is used to observe the miracidia in the water. However, the miracidia of Schistosoma japonicum are small and difficult to detect, and missed detection is likely to occur when the infection level is low. In this study, recombinant streptococcal protein G-enhanced green fluorescent protein (rSPG-EGFP) was expressed, purified, and used as a fluorescence staining reagent for miracidia. A preliminary miracidium fluorescence staining method based on antigen and antibody bindingwas established by combining recombinant protein staining with the stool hatching method. The stool hatching method was used to collect the miracidia of S. japonicum, and Schistosoma-positive serum and the recombinant protein were mixed to assess the feasibility of fluorescence staining of miracidia. The miracidia of S. japonicum and Schistosoma turkestanicum were incubated with S. japonicum-positive serum and S. turkestanicum-positive serum, respectively, to identify miracidia species. When the fluorescence staining method was used to observe living miracidia, the miracidiawere labelled by the recombinant protein, and their motility status was not affected.

Indexed as

Staining and LabelingAnimalsFluorescenceHumansSchistosoma japonicumSchistosomiasis japonica

Identifiers

PMID33028866
PMCPMC7542450

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