Evidence map›Paper›PMID 42288735›Full record

ArticleBMC microbiology2026

Comparison and correlation of in vitro and in vivo approaches for determining Pseudomonas aeruginosa bacteriophages activity.

Pedro Henrique Takata, Giovana Nicolete Pereira, Jhonatan Macedo Ribeiro, Laura Pierobão, Gabriel Henrique Maximino Santos, Bruna Carolina Gonçalves, Pedro Ademário Lima E Silva, Mariana Marques Bertozzi, Rafael Reis de Rezende, Giarlã Cunha da Silva and 5 more

Abstract readComparative Study
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Pedro Henrique TakataLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil. pedro.takata23@uel.br.
Giovana Nicolete PereiraLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.
Jhonatan Macedo RibeiroLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.
Laura PierobãoLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.
Gabriel Henrique Maximino SantosLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.
Bruna Carolina GonçalvesLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.
Pedro Ademário Lima E SilvaLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.
Mariana Marques BertozziLaboratory of Pain, Inflammation, Neuropathy and Cancer, Department of Immunology, Parasitology and General Pathology, Department of Pathological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Rafael Reis de RezendeInstitute of Biotechnology Applied to Agriculture (BIOAGRO), Department of Microbiology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Giarlã Cunha da SilvaInstitute of Biotechnology Applied to Agriculture (BIOAGRO), Department of Microbiology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Ruither Arthur Loch GomesInstitute of Biotechnology Applied to Agriculture (BIOAGRO), Department of Microbiology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Waldiceu A VerriLaboratory of Pain, Inflammation, Neuropathy and Cancer, Department of Immunology, Parasitology and General Pathology, Department of Pathological Sciences, State University of Londrina, Londrina, Paraná, Brazil.
Poliane Alfenas-ZerbiniInstitute of Biotechnology Applied to Agriculture (BIOAGRO), Department of Microbiology, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Renata Katsuko Takayama KobayashiLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.
Gerson NakazatoLaboratory of Basic and Applied Bacteriology, Department of Microbiology, State University of Londrina, Londrina, Paraná, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico #309633/2021-4, #305938/2026-6
6 · The paper itself

Abstract

The rise of infections caused by multidrug-resistant bacteria has driven the search for alternative therapies, with Pseudomonas aeruginosa representing a major target. Among these alternatives, the use of bacteriophages (phage therapy) employs these viruses that specifically infect bacteria to fight infections. Although phage efficacy has been demonstrated both in vitro and in vivo, few studies have directly correlated these two dimensions. This study aimed to evaluate, compare, and correlate in vitro and in vivo phage activity. For this, three strictly lytic bacteriophages (ph9027, ph1461, and ph3678) were isolated and tested against 15 clinical isolates and three reference strains of P. aeruginosa. Their in vitro activity was assessed through Spot-Test, Efficiency of Plating, Local Virulence, and Virulence Index assays, followed by in vivo assays in Galleria mellonella larvae and Balb/C mice in a peritonitis model with bacteremia induction. Virulence Index and animal treatments were performed using a phage cocktail (1:1:1 ratio, 1.0 × 10⁹ PFU/mL). In vitro assays revealed varying phage activity, with the Virulence Index showing the strongest correlation with in vivo results in G. mellonella (rs = 0.7648). Larval treatment achieved up to 100% survival, significantly different (p < 0.05) from bacteria-only controls. In mice, phage therapy reduced bacterial loads by up to 3 logs in blood, spleen, peritoneal lavage, liver, and lung (p < 0.05) in comparison with control groups. Therefore, the present study, in addition to reiterating the safety and therapeutic efficacy of phage therapy in animal models, presents evidence that Virulence Index techniques, associated with the survival results of G. mellonella larvae, can be excellent tools for directing preclinical assays due to the strong statistical correlation observed between these data and those obtained in mouse experiments.

Indexed as

Phage TherapyPseudomonas aeruginosaPseudomonas InfectionsPseudomonas PhagesAnimalsBacteremiaDisease Models, AnimalHumansLarvaMiceMice, Inbred BALB CMothsPeritonitisVirulenceCorrelation coefficientGalleria mellonellaHost rangeMice modelMultidrug-resistant bacteriaPeritonitisPhage therapy

Identifiers

PMID42288735
PMCPMC13374203

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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.