Evidence map›Paper›PMID 35756049›Full record

ArticleFrontiers in microbiology2022

A Novel and Secure Pseudovirus Reporter System Based Assay for Neutralizing and Enhancing Antibody Assay Against Marburg Virus.

Jinhao Bi, Haojie Wang, Hongyan Pei, Qiuxue Han, Na Feng, Qi Wang, Xinyue Wang, Zhenshan Wang, Shimeng Wei, Liangpeng Ge and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

16 authors at 5 institutions in 1 country.

Jinhao BiCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, China.
Haojie WangChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Hongyan PeiChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Qiuxue HanChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Na FengChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Qi WangChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Xinyue WangChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Zhenshan WangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, China.
Shimeng WeiChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Liangpeng GeChongqing Academy of Animal Sciences, Chongqing, China.
Meng WuChongqing Academy of Animal Sciences, Chongqing, China.
Hao LiangChongqing Academy of Animal Sciences, Chongqing, China.
Songtao YangCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, China.
Feihu YanChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Yongkun ZhaoChangchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun, China.
Xianzhu XiaCollege of Veterinary Medicine, Jilin Agricultural University, Changchun, China.
Chinese Academy of Agricultural Sciences · CNChongqing Academy of Animal Science · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNGuangzhou Experimental Station · CNShihezi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Marburg virus (MARV) is one of the principal members of the filovirus family, which can cause fatal hemorrhagic fever in humans. There are currently no prophylactic and therapeutic drugs on the market, and the high pathogenicity and infectivity of MARV make its research highly dependent on biosafety level 4 conditions, severely hindering the development of vaccines and therapies. Therefore, the development of medicines, such as MARV serological diagnosis, vaccines, and therapeutic antibody drugs, urgently needs a safe, convenient, and biosafety level 2 detection method to measure the neutralizing activity of MARV antibodies. To this end, we report a neutralization assay relying on a Rabies virus (RABV) reverse genetic operating system. We constructed infectious clones carrying the eGFP reporter gene and the full length of the original unmodified MARV GP gene. Based on the critical parameters of phylogenetic analysis, recombinant viruses targeting representative strains in the two major MARV lineages were successfully rescued. These pseudoviruses are safe in mice, and their inability to infect cells after being neutralized by antibodies can be visualized under a fluorescence microscope. We tested the system using the neutralizing antibody MR191. MR191 can significantly block the infection of BSR cells with pseudovirus. We compared it with the traditional lentivirus-type pseudovirus system to verify the system's credibility and obtained the same results as reported in the literature. In general, we have established a safe and visualized method for evaluating the neutralizing activity of MARV antibodies. Compared with traditional methods, it has the advantages of convenient operation, short cycle, and low cost. It is a candidate method that can replace actual viruses for a neutralization assay.

Indexed as

Marburg virusMR191neutralization assaypseudovirusreplicable pseudovirus

Identifiers

PMID35756049
PMCPMC9224600
OpenAlexW4285744147

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.