Evidence map›Paper›PMID 41198758›Full record

ArticleScientific reports2025

Isolation and characterization of bacteriophages for carbapenem resistant Enterobacter cloacae complex strains.

Matthew Imanaka, Wakana Yamashita, Shinjiro Ojima, Aa Haeruman Azam, Michiyo Kataoka, Tadaki Suzuki, Yo Sugawara, Motoyuki Sugai, Yoshimasa Takahashi, Koichi Watashi and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

12 authors.

Matthew ImanakaResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Wakana YamashitaResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Shinjiro OjimaResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Aa Haeruman AzamResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Michiyo KataokaDepartment of Infectious Disease Pathology, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan.
Tadaki SuzukiDepartment of Infectious Disease Pathology, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, 162-8640, Japan.
Yo SugawaraAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Motoyuki SugaiAntimicrobial Resistance Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Yoshimasa TakahashiResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Koichi WatashiResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Satoshi TsunedaDepartment of Life Science and Medical Bioscience, Waseda University, 2-2 Wakamatsu-cho, Shinjuku-ku, 162-8480, Tokyo, Japan.
Kotaro KigaResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan. k-kiga@niid.go.jp.

Funding

Japan Agency for Medical Research and Development JP23wm0325065Japan Society for the Promotion of Science 21H02110
6 · The paper itself

Abstract

There has been an increased interest in phage therapy for the treatment of antimicrobial resistant bacterial infections due to the decreasing effectiveness of antibiotics. While phage therapy has been successful, it often requires time to isolate and characterize phages suitable for phage therapy. Here, we isolated and characterized three phages against carbapenem-resistant Enterobacter cloacae complex (ECC) strains to potentially be applied in phage therapy. ECC strains commonly cause sepsis and urinary tract infections in hospitals and are designated as a pathogen of critical importance for its global prevalence and high instance of antimicrobial resistance. Initially, a total of 96 phages were isolated using a collection of diverse clinical ECC strains. Three phages were selected for genome sequencing and additional characterization based on their broad host range and lytic activity. Based on average nucleotide identity (ANI), vB_ECC_YI837 and vB_ECC_MY742 were considered strains of previously isolated phages vB_CsaM_leN and Entb_45, respectively. One phage had an ANI of 92.65% and was therefore considered novel and named vB_ECC_CW742. Furthermore, none of the phages carried toxin, antimicrobial resistance, or lysogeny-related genes. Collectively, the phages covered 82% (108/131) of our carbapenem-resistant ECC strain library. These findings suggest that the three phages are promising candidates for phage therapy against carbapenem-resistant ECC infections.

Indexed as

BacteriophagesCarbapenem-Resistant EnterobacteriaceaeCarbapenemsEnterobacter cloacaeAnti-Bacterial AgentsEnterobacteriaceae InfectionsGenome, ViralHost SpecificityHumansPhage TherapyAnti-Bacterial AgentsCarbapenems

Identifiers

PMID41198758
PMCPMC12592470

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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.