Evidence map›Paper›PMID 40240972›Full record

ArticleBMC microbiology2025

Antimicrobial, antibiofilm, cytotoxicity, and anti-DNA topoisomerase activity of Streptomyces sp. 22SH with ADME and in silico study.

Mervat G Hassan, Mohamed O Abdel-Monem, Al Shaimaa M A Sleem, Mohamed E El Awady, Ahmed A Hamed

Abstract read
In one paragraph

Article in BMC microbiology, 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
  2. Aquatic-derived Streptomyces cavourensis BA1 as a promising source of antibacterial metabolites against multidrug-resistant gram-negative pathogens.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2026
    Article
  3. 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

5 authors.

Mervat G HassanBotany and Microbiology Department, Faculty of Science, Benha Univ., Benha, Egypt. mervat.hassan@fsc.bu.edu.eg.
Mohamed O Abdel-MonemBotany and Microbiology Department, Faculty of Science, Benha Univ., Benha, Egypt.
Al Shaimaa M A SleemBotany and Microbiology Department, Faculty of Science, Benha Univ., Benha, Egypt.
Mohamed E El AwadyMicrobial Biotechnology Department, National Research Centre, El-Buhouth St. 33, Dokki-Cairo, 12622, Egypt.ORCID http://orcid.org/0000-0001-5155-3949
Ahmed A HamedMicrobial Chemistry Department, National Research Centre, El-Buhouth St. 33, Dokki-Cairo, 12622, Egypt. ahmedshalbio@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genus Streptomyces has been recently proven to be a valuable and rich source of producing several bioactive compounds with substantial biological activity and applications in many fields such as medicine, environmental science, food industries, and agronomy. This study highlights the importance of Streptomyces as an antimicrobial, antibiofilm, and anticancer. Out of the 75 actinobacteria isolated from both marine and soil habitats, one isolate, HG2, was selected based on its potent antimicrobial activity. The isolate has been identified morphologically by studying colony and spore chain morphology using TEM and genetically by sequencing their 16 sr RNA gene as Streptomyces sp. 22SH with Accession number OK326829.1. Bioassay-guided fractionation of the Streptomyces sp. 22SH crude extract led to the isolation and purification of Cis-9-Octadecenoic. Biological evaluation including antimicrobial and antibiofilm activity of the crude and purified compound was performed on four clinical microbes (S. aureus ATCC6538-P, B. subtilis ATCC6633, and P. aeruginosa ATCC27853). The compound showed the ability to eradicate the biofilm formation by the tested pathogens. Additionally, the antitumor activity was assessed, and the compound showed a cytotoxic effect against liver carcinoma and breast cancer cells, with IC50 values of 17.48 ± 0.94 and 88.73 ± 4.78 µg/ml, respectively. While it displayed anti-topoisomerase activity with an IC

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsAntineoplastic AgentsBiofilmsStreptomycesTopoisomerase InhibitorsBacillus subtilisCell Line, TumorComputer SimulationDNA TopoisomerasesHumansMicrobial Sensitivity TestsMolecular Docking SimulationPseudomonas aeruginosaStaphylococcus aureusAnti-Bacterial AgentsAnti-Infective AgentsAntineoplastic AgentsDNA TopoisomerasesTopoisomerase InhibitorsAntibacterialAntibiofilmanti-DNA topoisomeraseBioactive metabolitesStreptomyces sp.

Identifiers

PMID40240972
PMCPMC12001559

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Registered trials

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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.