Evidence map›Paper›PMID 37971221›Full record

ArticleJournal of virology2023

A recombination-resistant genome for live attenuated and stable PEDV vaccines by engineering the transcriptional regulatory sequences.

Xiaoyu Niu, Mingde Liu, Shaomin Yang, Jiayu Xu, Yixuan J Hou, Dongxiao Liu, Qiyi Tang, Hua Zhu, Qiuhong Wang

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 13 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

9 authors at 4 institutions in 2 countries.

Xiaoyu NiuCenter for Food Animal Health, Department of Animal Sciences, College of Food, Agricultural and Environmental Sciences, The Ohio State University, Wooster, Ohio, USA.ORCID 0000-0002-6412-7348
Mingde Liu *Center for Food Animal Health, Department of Animal Sciences, College of Food, Agricultural and Environmental Sciences, The Ohio State University, Wooster, Ohio, USA.
Shaomin Yang *Department of Pain Medicine, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Guangdong Medical University, Shenzhen, China.ORCID 0000-0001-7932-4777
Jiayu XuDepartment of Veterinary Preventive Medicine, College of Veterinary Medicine, The Ohio State University, Columbus, Ohio, USA.
Yixuan J HouCenter for Food Animal Health, Department of Animal Sciences, College of Food, Agricultural and Environmental Sciences, The Ohio State University, Wooster, Ohio, USA.
Dongxiao LiuDepartment of Microbiology, Howard University College of Medicine, Washington, DC, USA.
Qiyi TangDepartment of Microbiology, Howard University College of Medicine, Washington, DC, USA.ORCID 0000-0002-6487-2356
Hua ZhuDepartment of Microbiology and Molecular Genetics, UMDNJ-New Jersey Medical School, Newark, New Jersey, USA.ORCID 0000-0002-6087-3175
Qiuhong WangCenter for Food Animal Health, Department of Animal Sciences, College of Food, Agricultural and Environmental Sciences, The Ohio State University, Wooster, Ohio, USA.ORCID 0000-0002-8238-417X
The Ohio State University · USHoward University · USGuangdong Medical College · CNRutgers, The State University of New Jersey · US

Funding

U.S. Department of Agriculture (USDA) 2019-67015-29843
6 · The paper itself

Abstract

importanceCoronaviruses are important pathogens of humans and animals, and vaccine developments against them are imperative. Due to the ability to induce broad and prolonged protective immunity and the convenient administration routes, live attenuated vaccines (LAVs) are promising arms for controlling the deadly coronavirus infections. However, potential recombination events between vaccine and field strains raise a safety concern for LAVs. The porcine epidemic diarrhea virus (PEDV) remodeled TRS (RMT) mutant generated in this study replicated efficiently in both cell culture and in pigs and retained protective immunogenicity against PEDV challenge in pigs. Furthermore, the RMT PEDV was resistant to recombination and genetically stable. Therefore, RMT PEDV can be further optimized as a backbone for the development of safe LAVs.

Indexed as

Coronavirus InfectionsPorcine epidemic diarrhea virusRecombination, GeneticSwineSwine DiseasesVaccines, AttenuatedViral VaccinesAnimalsCells, CulturedMutationVirus ReplicationVaccines, AttenuatedViral Vaccinescoronaviruslive attenuated vaccinesporcine epidemic diarrhea virus (PEDV)recombinationtranscriptional regulatory sequences (TRS)

Identifiers

PMID37971221
PMCPMC10734454
OpenAlexW4388729344

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.