Evidence map›Paper›PMID 24516427›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2013

In vitro and in vivo inhibition of rabies virus replication by RNA interference.

Ekaterina A Durymanova Ono, Keila Iamamoto, Juliana G Castilho, Pedro Carnieli, Rafael de Novaes Oliveira, Samira M Achkar, Maria L Carrieri, Ivanete Kotait, Paulo E Brandão

Open access · hybridAbstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2013. 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
0.4field-weighted citation impact, top 38% 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.

  1. Article
  2. Review
  3. Article
  4. Evaluation of short-interfering RNAs treatment in experimental rabies due to wild-type virus.The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases
    Article
  5. Short interfering RNAs targeting a vampire-bat related rabies virus phosphoprotein mRNA.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]
    Article
  6. Article
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 2 institutions in 1 country.

Ekaterina A Durymanova OnoFaculdade de Medicina Veterinária, Universidade de São Paulo, São Paulo, SP, Brazil. ; Instituto Pasteur, São Paulo, SP, Brazil.
Keila IamamotoFaculdade de Medicina Veterinária, Universidade de São Paulo, São Paulo, SP, Brazil. ; Instituto Pasteur, São Paulo, SP, Brazil.
Juliana G CastilhoInstituto Pasteur, São Paulo, SP, Brazil.
Pedro CarnieliInstituto Pasteur, São Paulo, SP, Brazil.
Rafael de Novaes OliveiraInstituto Pasteur, São Paulo, SP, Brazil.
Samira M AchkarInstituto Pasteur, São Paulo, SP, Brazil.
Maria L CarrieriInstituto Pasteur, São Paulo, SP, Brazil.
Ivanete KotaitInstituto Pasteur, São Paulo, SP, Brazil.
Paulo E BrandãoFaculdade de Medicina Veterinária, Universidade de São Paulo, São Paulo, SP, Brazil.
Instituto PasteurUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rabies is a zoonotic disease that affects all mammals and leads to more than 55,000 human deaths every year, caused by rabies virus (RABV) (Mononegavirales: Rhabdoviridae: Lyssavirus). Currently, human rabies treatment is based on the Milwaukee Protocol which consists on the induction of coma and massive antiviral therapy. The aim of this study was to assess the decrease in the titer of rabies virus both in vitro and in vivo using short-interfering RNAs. To this end, three siRNAs were used with antisense strands complementary to rabies virus nucleoprotein (N) mRNA. BHK-21 cells monolayers were infected with 1000 to 0.1 TCID50 of PV and after 2 hours the cells were transfected with each of tree RNAs in separate using Lipofectamine-2000. All three siRNAs reduced the titer of PV strain in a least 0.72 logTCID50/mL and no cytotoxic effect was observed in the monolayers treated with Lipofectamine-2000. Swiss albino mice infected with 10.000 to 1 LD of PV strain by the intracerebral route were also transfected after two hours of infection with a pool 3 siRNAs with Lipofectamine-2000 by the intracerebral route, resulting in a survival rate of 30% in mice inoculated with 100 LD50, while the same dose led to 100% mortality in untreated animals. Lipofectamine-2000 showed no toxic effect in control mice. These results suggest that intracerebral administration of siRNAs might be an effective antiviral strategy for rabies.

Indexed as

RNA InterferenceAnimalsAntiviral AgentsCell LineCricetinaeDisease Models, AnimalMiceNucleocapsid ProteinsRabiesRabies virusRNA, Small InterferingSurvival AnalysisViral LoadVirus CultivationVirus ReplicationAntiviral Agentsnucleocapsid protein, Rabies virusNucleocapsid ProteinsRNA, Small InterferingantiviralrabiesRNA interferencesiRNAstreatment

Identifiers

PMID24516427
PMCPMC3910205
OpenAlexW2128262400

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.