Evidence map›Paper›PMID 38864950›Full record

ArticleMarine biotechnology (New York, N.Y.)2024

Shotgun Metagenomics Reveals Taxonomic and Functional Patterns of the Microbiome Associated with Barbour's Seahorse (Hippocampus barbouri).

Rose Chinly Mae H Ortega-Kindica, Chinee S Padasas-Adalla, Sharon Rose M Tabugo, Joey Genevieve T Martinez, Olive A Amparado, Carlo Stephen O Moneva, Rodelyn Dalayap, Carlos O Lomeli-Ortega, Jose Luis Balcazar

Abstract read
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In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2024. 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. Draft genome sequence ofMicrobiology resource announcements · 2025
    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

9 authors.

Rose Chinly Mae H Ortega-KindicaDepartment of Biology and Environmental Science, University of the Philippines Cebu, Lahug, Cebu City, 6000, Philippines. rosechinlymae.ortega@g.msuiit.edu.ph.
Chinee S Padasas-AdallaDepartment of Biological Sciences, College of Science and Mathematics, MSU-Iligan Institute of Technology, Iligan City, 9200, Philippines.
Sharon Rose M TabugoDepartment of Biological Sciences, College of Science and Mathematics, MSU-Iligan Institute of Technology, Iligan City, 9200, Philippines.
Joey Genevieve T MartinezDepartment of Biological Sciences, College of Science and Mathematics, MSU-Iligan Institute of Technology, Iligan City, 9200, Philippines.
Olive A AmparadoDepartment of Biological Sciences, College of Science and Mathematics, MSU-Iligan Institute of Technology, Iligan City, 9200, Philippines.
Carlo Stephen O MonevaDepartment of Biological Sciences, College of Science and Mathematics, MSU-Iligan Institute of Technology, Iligan City, 9200, Philippines.
Rodelyn DalayapDepartment of Biology, Sultan Kudarat State University, Tacurong City, Sultan Kudarat, 9800, Philippines.
Carlos O Lomeli-OrtegaCatalan Institute for Water Research (ICRA), Girona, 17003, Spain.
Jose Luis BalcazarCatalan Institute for Water Research (ICRA), Girona, 17003, Spain. jlbalcazar@icra.cat.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate the taxonomic and functional patterns of the microbiome associated with Barbour's seahorse (Hippocampus barbouri) using a combination of shotgun metagenomics and bioinformatics. The analyses revealed that Pseudomonadota and Bacillota were the dominant phyla in the seahorse skin microbiome, whereas Pseudomonadota and, to a lesser extent, Bacillota and Bacteroidota were the dominant phyla in the seahorse gut microbiome. Several metabolic pathway categories were found to be enriched in the skin microbiome, including amino acid metabolism, carbohydrate metabolism, cofactor and vitamin metabolism, energy metabolism, nucleotide metabolism, as well as membrane transport, signal transduction, and cellular community-prokaryotes. In contrast, the gut microbiome exhibited enrichment in metabolic pathways associated with the metabolism of terpenoids and polyketides, biosynthesis of other secondary metabolites, xenobiotics biodegradation and metabolism, and quorum sensing. Additionally, although the relative abundance of bacteriocins in the skin and gut was slightly similar, notable differences were observed at the class level. Specifically, class I bacteriocins were found to be more abundant in the skin microbiome, whereas class III bacteriocins were more abundant in the gut microbiome. To the best of our knowledge, this study represents the first comprehensive examination of the taxonomic and functional patterns of the skin and gut microbiome in Barbour's seahorse. These findings can greatly contribute to a deeper understanding of the seahorse-associated microbiome, which can play a pivotal role in predicting and controlling bacterial infections, thereby contributing to the success of aquaculture and health-promoting initiatives.

Indexed as

BacteriaGastrointestinal MicrobiomeMetagenomicsMicrobiotaSkinSmegmamorphaAnimalsBacteriocinsMetabolic pathwaysMicrobiomePhilippinesSeahorse

Identifiers

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Read underepoch 390

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.