Evidence map›Paper›PMID 31208333›Full record

ArticleBMC microbiology2019

Characterization of a bacteriophage with broad host range against strains of Pseudomonas aeruginosa isolated from domestic animals.

Anna Cristhina Carmine de Melo, Amanda da Mata Gomes, Fernando L Melo, Daniel M P Ardisson-Araújo, Agueda Palmira Castagna de Vargas, Valessa Lunkes Ely, Elliot W Kitajima, Bergmann M Ribeiro, José Luiz Caldas Wolff

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 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 1 country.

Anna Cristhina Carmine de MeloCCBS - Curso de Ciências Biológicas, Laboratório de Biologia Molecular e Virologia, Prédio 28, primeiro andar, Universidade Presbiteriana Mackenzie, Rua da Consolação, 896, Consolação, São Paulo, SP, CEP 01302-907, Brazil.
Amanda da Mata GomesCCBS - Curso de Ciências Biológicas, Laboratório de Biologia Molecular e Virologia, Prédio 28, primeiro andar, Universidade Presbiteriana Mackenzie, Rua da Consolação, 896, Consolação, São Paulo, SP, CEP 01302-907, Brazil.
Fernando L MeloDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, Brasília, DF, Brazil.
Daniel M P Ardisson-AraújoDepartamento de Bioquímica e Biologia Molecular, Universidade Federal de Santa Maria, Av. Roraima, 1000, Cidade Universitária, Santa Maria, RS, CEP 97105-900, Brazil.
Agueda Palmira Castagna de VargasDepartamento de Medicina Veterinária Preventiva (DMVP), Centro de Ciências Rurais (CCR)Avenida Roraima, Universidade Federal de Santa Maria, 1000. Prédio 44, Sala 5137, Santa Maria, RS, CEP 97105-900, Brazil.
Valessa Lunkes ElyDepartamento de Medicina Veterinária Preventiva (DMVP), Centro de Ciências Rurais (CCR)Avenida Roraima, Universidade Federal de Santa Maria, 1000. Prédio 44, Sala 5137, Santa Maria, RS, CEP 97105-900, Brazil.
Elliot W KitajimaNAP/MEPA, Departamento de Fitopatologia e Nematologia, ESALQ, Universidade de São Paulo, Piracicaba, SP, Brazil.
Bergmann M RibeiroDepartamento de Biologia Celular, Instituto de Ciências Biológicas, Universidade de Brasília, Brasília, DF, Brazil.
José Luiz Caldas WolffCCBS - Curso de Ciências Biológicas, Laboratório de Biologia Molecular e Virologia, Prédio 28, primeiro andar, Universidade Presbiteriana Mackenzie, Rua da Consolação, 896, Consolação, São Paulo, SP, CEP 01302-907, Brazil. joseluiz.wolff@mackenzie.br.ORCID 0000-0002-0541-5286
Universidade Federal de Santa Maria · BRUniversidade Presbiteriana Mackenzie · BRUniversidade de Brasília · BRUniversidade Metodista de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPseudomonas aeruginosa is an opportunistic pathogen and one of the leading causes of nosocomial infections. Moreover, the species can cause severe infections in cystic fibrosis patients, in burnt victims and cause disease in domestic animals. The control of these infections is often difficult due to its vast repertoire of mechanisms for antibiotic resistance. Phage therapy investigation with P. aeruginosa bacteriophages has aimed mainly the control of human diseases. In the present work, we have isolated and characterized a new bacteriophage, named Pseudomonas phage BrSP1, and investigated its host range against 36 P. aeruginosa strains isolated from diseased animals and against P. aeruginosa ATCC strain 27853.

resultsWe have isolated a Pseudomonas aeruginosa phage from sewage. We named this virus Pseudomonas phage BrSP1. Our electron microscopy analysis showed that phage BrSP1 had a long tail structure found in members of the order Caudovirales. "In vitro" biological assays demonstrated that phage BrSP1 was capable of maintaining the P. aeruginosa population at low levels for up to 12 h post-infection. However, bacterial growth resumed afterward and reached levels similar to non-treated samples at 24 h post-infection. Host range analysis showed that 51.4% of the bacterial strains investigated were susceptible to phage BrSP1 and efficiency of plating (EOP) investigation indicated that EOP values in the strains tested varied from 0.02 to 1.72. Analysis of the phage genome revealed that it was a double-stranded DNA virus with 66,189 bp, highly similar to the genomes of members of the genus Pbunavirus, a group of viruses also known as PB1-like viruses.

conclusionThe results of our "in vitro" bioassays and of our host range analysis suggested that Pseudomonas phage BrSP1 could be included in a phage cocktail to treat veterinary infections. Our EOP investigation confirmed that EOP values differ considerably among different bacterial strains. Comparisons of complete genome sequences indicated that phage BrSP1 is a novel species of the genus Pbunavirus. The complete genome of phage BrSP1 provides additional data that may help the broader understanding of pbunaviruses genome evolution.

Indexed as

AnimalsAnimals, DomesticDNADNA, ViralGenome SizeMicroscopy, ElectronOpen Reading FramesPseudomonas aeruginosaPseudomonas PhagesSewageSpecies SpecificityWhole Genome SequencingDNADNA, ViralSewage

Identifiers

PMID31208333
PMCPMC6580649
OpenAlexW2950891768

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.