Evidence map›Paper›PMID 40011297›Full record

ArticleWorld journal of microbiology & biotechnology2025

Amphibian skin bacteria contain a wide repertoire of genes linked to their antifungal capacities.

Francisco González-Serrano, Yordan J Romero-Contreras, Alberto H Orta, M Delia Basanta, Hugo Morales, Gabriela Sandoval García, Elena Bello-López, A S Escobedo-Muñoz, Víctor H Bustamante, Víctor Ávila-Akerberg and 3 more

Abstract read
In one paragraph

Article in World journal of microbiology & biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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

13 authors.

Francisco González-SerranoCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México.ORCID http://orcid.org/0000-0002-7740-3727
Yordan J Romero-ContrerasCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México.ORCID http://orcid.org/0000-0002-1836-9215
Alberto H OrtaCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México.ORCID http://orcid.org/0000-0002-3997-9514
M Delia BasantaDepartment of Biology, University of Nevada, Reno, 1664 N. Virginia St, Reno, NV, 89557, USA.ORCID http://orcid.org/0000-0002-1633-0691
Hugo MoralesFacultad de Ciencias, Universidad Autónoma del Estado de México, Carretera Toluca - Ixtlahuaca Km 15.5, Piedras Blancas, Toluca de Lerdo, 50200, México.
Gabriela Sandoval GarcíaFacultad de Ciencias, Universidad Nacional Autónoma de México, Av. Universidad 3000, Circuito Exterior s/n Alcaldía Coyoacán, Mexico City, Ciudad Universitaria, 04510, México.ORCID http://orcid.org/0009-0003-6613-3607
Elena Bello-LópezCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México.ORCID http://orcid.org/0000-0002-5508-9714
A S Escobedo-MuñozCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México.ORCID http://orcid.org/0009-0002-0149-1481
Víctor H BustamanteDepartamento de Microbiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Apdo. Postal 510-3, Cuernavaca, Morelos, 62251, México.ORCID http://orcid.org/0000-0002-8852-150X
Víctor Ávila-AkerbergInstituto de Ciencias Agropecuarias y Rurales, Universidad Autónoma del Estado de México, Toluca, México.ORCID http://orcid.org/0000-0001-5369-0920
Miguel Ángel CevallosCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México.ORCID http://orcid.org/0000-0002-0447-812X
Mario SerranoCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México.ORCID http://orcid.org/0000-0002-1510-756X
Eria A RebollarCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Av. Universidad s/n, Cuernavaca, Morelos, 62210, México. rebollar@ccg.unam.mx.ORCID http://orcid.org/0000-0001-8827-023X

Funding

Consejo Nacional de Humanidades, Ciencias y Tecnologías 373914Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica (PAPIIT-DGAPA) IG200224
6 · The paper itself

Abstract

Emerging diseases caused by fungi are a serious threat to wildlife biodiversity. The widespread fungal pathogen Batrachochytrium dendrobatidis (Bd) has caused dramatic amphibian population declines and species extinctions worldwide. While many amphibians have been negatively affected by Bd, some populations/species have persisted despite its presence. One factor contributing to amphibian protection against this fungus is the host-associated skin microbiome. In this study, we aimed to identify gene clusters associated with the antifungal activity of amphibian skin bacteria. Specifically, we explored skin bacteria isolated from species that have persisted in the wild despite the presence of Bd: the frogs Agalychnis callidryas, Craugastor fitzingeri, Dendropsophus ebraccatus, and the axolotl Ambystoma altamirani. Bacterial isolates were tested in vitro for their capacity to inhibit the growth of two fungal pathogens: Bd and the phytopathogen Botrytis cinerea (Bc). Genome mining of these bacterial isolates revealed a diverse repertoire of Biosynthetic Gene Clusters (BGCs) and chitin-degrading gene families (ChDGFs) whose composition and abundance differed among bacterial families. We found specific BGCs and ChDGFs that were associated with the capacity of bacteria to inhibit the growth of either Bd or Bc, suggesting that distinct fungi could be inhibited by different molecular mechanisms. By using similarity networks and machine learning, we identified BGCs encoding known antifungal compounds such as viscosin, fengycin, zwittermicin, as well as siderophores and a novel family of beta-lactones. Finally, we propose that the diversity of BGCs found in amphibian skin bacteria comprise a substantial genetic reservoir that could collectively explain the antifungal properties of the amphibian skin microbiome.

Indexed as

AmphibiansAntibiosisAntifungal AgentsBacteriaSkinAnimalsAnuraBatrachochytriumMicrobiotaMultigene FamilyPhylogenyAntifungal AgentsAmphibiansAntifungal activityBatrachochytrium dendrobatidisBiosynthetic gene clusterBotrytis cinereaChytridiomycosisSkin microbiome

Identifiers

PMID40011297
PMCPMC11865118

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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.