Evidence map›Paper›PMID 40711470›Full record

ArticleMicrobial genomics2025

Genomic potential of crustose coralline algae-associated bacteria for the biosynthesis of novel antimicrobials.

Diego Lera-Lozano, Jordan S Ruiz-Toquica, Samantha A Kratman, Matthew W Holt, Clancy A McIntyre, Elizabeth K Jones, Mateo Lopez-Victoria, Kim B Ritchie, Mónica Medina, Raúl A González-Pech

Abstract read
In one paragraph

Article in Microbial genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Diego Lera-LozanoDepartment of Biology, The Pennsylvania State University, University Park, PA, USA.
Jordan S Ruiz-ToquicaFaculty of Natural Sciences and Engineering, Universidad de Bogotá Jorge Tadeo Lozano, Bogota, Colombia.
Samantha A KratmanDepartment of Biology, The Pennsylvania State University, University Park, PA, USA.
Matthew W HoltDepartment of Natural Sciences, University of South Carolina Beaufort, Beaufort, SC, USA.
Clancy A McIntyreDepartment of Biology, The Pennsylvania State University, University Park, PA, USA.
Elizabeth K JonesDepartment of Natural Sciences, University of South Carolina Beaufort, Beaufort, SC, USA.
Mateo Lopez-VictoriaDepartment of Natural Sciences and Mathematics, Pontificia Universidad Javeriana, Cali, Colombia.
Kim B RitchieDepartment of Natural Sciences, University of South Carolina Beaufort, Beaufort, SC, USA.
Mónica MedinaDepartment of Biology, The Pennsylvania State University, University Park, PA, USA.
Raúl A González-PechDepartment of Biology, The Pennsylvania State University, University Park, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global rise of antimicrobial resistance has intensified efforts in bioprospecting, with researchers increasingly exploring unique marine environments for novel antimicrobials. In line with this trend, our study focused on bacteria isolated from the unique microbiome of crustose coralline algae (CCA), which has yet to be investigated for antimicrobial discovery. In the present work, bacteria were isolated from a CCA collected from Varadero Reef located in Cartagena Bay, Colombia. After performing antimicrobial assays against antibiotic-resistant human and marine pathogens, three isolates were selected for genome sequencing using the Oxford Nanopore technology. Genome mining of the high-quality assemblies revealed 115 putative biosynthetic gene clusters (BGCs) and identified genes in relevant biosynthetic pathways across the three genomes. Nonetheless, we hypothesize that the biosynthesis of antimicrobial compounds results from the expression of undescribed BGCs. Further analysis revealed the absence of genes pertaining to the synthesis of coral larvae settling molecule tetrabromopyrrole, commonly produced by CCA-associated bacteria. We also discuss how differential representation of gene functions between the three isolates may be attributed to the distinct ecological niches they occupy within the CCA. This study provides valuable resources for future research aimed at the discovery of novel antimicrobials, particularly in the face of the antibiotic-resistance global crisis, and highlights the potential of specialized marine environments like CCA.

Indexed as

AnthozoaAnti-Bacterial AgentsAnti-Infective AgentsBacteriaRhodophytaAnimalsBiosynthetic PathwaysGenome, BacterialGenomicsMicrobiotaMultigene FamilyPhylogenyAnti-Bacterial AgentsAnti-Infective Agentsantimicrobial activitybioprospectingcrustose coralline algaecrustose coralline algae (CCA) bacteriamicrobial ecology

Identifiers

PMID40711470
PMCPMC12452183

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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.