ArticleBMC microbiology2025
Biological characterization and genomic analysis of the newly discovered mycobacteriophage WST1.
Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.
What it found
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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.
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.
Who cites it
2 citing papers in PubMed.
- Advances in mycobacteriophage research: from lytic mechanisms to one health applications.Frontiers in cellular and infection microbiology · 2026Review
- Correction: Biological characterization and genomic analysis of the newly discovered mycobacteriophage WST1.BMC microbiology · 2025Article
Corrections and comments
- Erratum issued
Authors and funding
9 authors.
Funding
Abstract
The rising prevalence of multidrug-resistant mycobacteria necessitates novel therapeutic strategies. Phages targeting clinically relevant mycobacteria remain scarce, lytic phages represent promising alternatives. In this study, we isolated mycobacterium phage WST1 from wastewater, exhibiting strict lytic specificity for Mycobacterium smegmatis. Genomic analysis revealed a 38,120 bp dsDNA genome (64.60% GC) with 59 ORFs, including tyrosine integrase, hicA/B toxin-antitoxin, but no virulence or resistance genes. WST1 demonstrated broad thermal stability (4–60℃) and pH (4–9) stability, but is UV-sensitive. Phylogenetically, WST1 formed a distinct clade with mycobacterium phage IdentityCrisis, the average nucleotide identity is 83.9%, WST1 possesses a terminase which shows 100% amino acid identity to IdentityCrisis, while its endolysin shows over 90% identity to other distant phages, showcasing the modular evolution of WST1.We discovered a new, safe phage candidate useful for both phage diversity studying and genetic engineering, thereby expanding the resources for mycobacteriophage therapeutic development.
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Registered trials
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.