Evidence map›Paper›PMID 40739242›Full record

ArticleVirology journal2025

Isolation and characterization of phages ΦZC2 and ΦZC3 against carbapenem-resistant Acinetobacter baumannii, and efficacy of ΦZC3 on A549 cells.

Kareem Essam, Azza G Kamel, Bishoy Maher Zaki, Mohamed Elhadidy, Amal Ahmed Abdel Aziz, Aysam Fayed, Tamer Roshdy, Ayman El-Shibiny

Abstract read
In one paragraph

Article in Virology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Revisiting the Fight AgainstAntibiotics (Basel, Switzerland) · 2026
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Genomic and functional characterization ofFrontiers in microbiology · 2026
    Article
  12. 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

8 authors.

Kareem EssamCenter for Microbiology and Phage Therapy, Zewail City of Science and Technology, Giza, 12578, Egypt.
Azza G KamelCenter for Microbiology and Phage Therapy, Zewail City of Science and Technology, Giza, 12578, Egypt.
Bishoy Maher ZakiCenter for Microbiology and Phage Therapy, Zewail City of Science and Technology, Giza, 12578, Egypt.
Mohamed ElhadidyBiomedical Sciences Program, University of Science and Technology, Zewail City of Science and Technology, October Gardens, 6th of October City, Giza, 12578, Egypt.
Amal Ahmed Abdel AzizGenetic Engineering and Biotechnology Research Institute, University of Sadat City, El Sadat City, Egypt.
Aysam FayedGenetic Engineering and Biotechnology Research Institute, University of Sadat City, El Sadat City, Egypt.
Tamer RoshdyGenetic Engineering and Biotechnology Research Institute, University of Sadat City, El Sadat City, Egypt.
Ayman El-ShibinyCenter for Microbiology and Phage Therapy, Zewail City of Science and Technology, Giza, 12578, Egypt. aelshibiny@zewailcity.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcinetobacter baumannii is an opportunistic pathogen and a major causative agent of hospital-acquired infections. This pathogen can acquire various antibiotic resistance genes, including those conferring resistance to last-resort antibiotics such as carbapenems. MDR A. baumannii is known to cause several infections, including pneumonia and urinary tract infections. Consequently, there is an urgent need to explore alternative therapies, and bacteriophage (phage) has emerged as a promising therapeutic approach for combating multidrug-resistant (MDR) infections. MATERIALS AND

methodsThis study investigates the therapeutic potential of specific bacteriophages against MDR, particularly carbapenem-resistant A. baumannii, and evaluates lytic activity against 41 clinical isolates of MDR A. baumannii. The phages morphotypes were identified by transmission electron microscope. The stability of these phages was assessed under different conditions, including pH (2, 3, 4, 7, and 10-12), temperature (-80, -20, 4, 37, 50, 60, 70, and 80

resultsTwo phages, vB_AbaP_ZC2 (ΦZC2) and vB_AbaM_ZC3 (ΦZC3), were isolated from hospital wastewater in Egypt. The phages demonstrated lytic activity against 24.3% (n = 10) and 31.7% (n = 13) of the isolates, respectively. Phage ΦZC2 demonstrated high EOP values (0.75-1) against AB23 and AB26, moderate activity on AB34 and AB35 (EOP = 0.19), and low or no activity on AB10, AB24, and AB31. Similarly, phage ΦZC3 exhibited high EOP on AB24 (EOP = 1), moderate levels on AB12, AB29, and AB38, while showing low or no efficacy against the remaining tested isolates. The morphotypes of ΦZC2 and ΦZC3 are podovirus and myovirus, respectively. The two phages were amplified using a bioreactor and reached titers of approximately 10¹⁰ PFU/ml in 2 L.ΦZC2 was stable at a pH range from 3 to 12 approximately 10

conclusionIn this study, the two lytic phages have antibacterial activity against MDR A. baumannii. particularly, ΦZC3 can be a potential therapy for pulmonary infections.

Indexed as

Acinetobacter baumanniiBacteriophagesCarbapenemsA549 CellsAcinetobacter InfectionsAnti-Bacterial AgentsDrug Resistance, Multiple, BacterialGenome, ViralHumansPhage TherapyAnti-Bacterial AgentsCarbapenemsAcinetobacter baumanniiAntibiotic resistanceESKAPEEMultidrug-resistant bacteriaPhage therapy

Identifiers

PMID40739242
PMCPMC12308983

What OpenQuestion holds

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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.