Evidence map›Paper›PMID 26323462›Full record

ArticleMolecular medicine reports2015

Evaluation of a combinatorial RNAi lentivirus vector targeting foot-and-mouth disease virus in vitro and in vivo.

Xiaoxi Zhang, Haixue Zheng, Minjun Xu, Yu Zhou, Xiangping Li, Fan Yang, Qingyou Liu, Deshun Shi

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 10 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

8 authors at 3 institutions in 1 country.

Xiaoxi ZhangState Key Laboratory for Conservation and Utilization of Subtropical Agro‑Bioresources, Guangxi University, Nanning, Guangxi 530005, P.R. China.
Haixue ZhengState Key Laboratory of Veterinary Etiological Biology, National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu 730046, P.R. China.
Minjun XuState Key Laboratory of Veterinary Etiological Biology, National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu 730046, P.R. China.
Yu ZhouState Key Laboratory for Conservation and Utilization of Subtropical Agro‑Bioresources, Guangxi University, Nanning, Guangxi 530005, P.R. China.
Xiangping LiState Key Laboratory for Conservation and Utilization of Subtropical Agro‑Bioresources, Guangxi University, Nanning, Guangxi 530005, P.R. China.
Fan YangState Key Laboratory for Conservation and Utilization of Subtropical Agro‑Bioresources, Guangxi University, Nanning, Guangxi 530005, P.R. China.
Qingyou LiuState Key Laboratory for Conservation and Utilization of Subtropical Agro‑Bioresources, Guangxi University, Nanning, Guangxi 530005, P.R. China.
Deshun ShiState Key Laboratory for Conservation and Utilization of Subtropical Agro‑Bioresources, Guangxi University, Nanning, Guangxi 530005, P.R. China.
Guangxi University · CNChinese Academy of Agricultural Sciences · CNLanzhou Veterinary Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foot-and-mouth disease virus (FMDV) causes a highly contagious disease of cloven‑hoofed animals, which leads to serious economical losses. FMDV is not adequately controlled by vaccination or biosecurity measures. To generate genetically modified FMDV‑resistant animals, a combinatorial expression cassette producing three short hairpin (sh)RNAs was constructed using the lentivirus (LV) vector, LV‑3shRNA. The three shRNAs were expressed under the regulation of DNA polymerase III promoters from a buffalo and a bovine source, with one targeted to the non‑structural protein 3B, and the other two targeted to the viral polymerase protein 3D of FMDV, respectively. The role of LV‑3shRNA in the inhibition of the replication of FMDV was determined in BHK‑21 cells and in suckling mice. The results revealed that LV‑3shRNA reduced viral growth 3‑fold (24 h post‑infection) when the cells were challenged with 107‑times the tissue culture infective dose (TCID50)/ml of O serotype FMDV. The suckling mice pretreated with LV‑3shRNA were completely protected on administration of 5‑times the dose of FMDV otherwise sufficient to kill 50% of the experimental animals (LD50). These results demonstrated that the LV‑mediated dual expression of three FMDV‑specific shRNAs provided a novel strategy towards combating FMDV, which facilitates the permanent introduction of novel disease-resistance traits into the buffalo and bovine genomes in the future.

Indexed as

RNAi TherapeuticsAnimalsCattleCell LineFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusGenetic VectorsHumansLentivirusMiceRNA InterferenceRNA, Small InterferingViral ProteinsVirus ReplicationRNA, Small InterferingViral Proteins

Identifiers

PMID26323462
PMCPMC4626173
OpenAlexW2125930806

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.