Evidence map›Paper›PMID 31603945›Full record

ArticlePloS one2019

Amphibian skin-associated Pigmentiphaga: Genome sequence and occurrence across geography and hosts.

Molly C Bletz, Boyke Bunk, Cathrin Spröer, Peter Biwer, Silke Reiter, Falitiana C E Rabemananjara, Stefan Schulz, Jörg Overmann, Miguel Vences

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Gene functions of theMicrobial genomics · 2024
    Article
  4. Article
  5. Thiol Metabolism and Volatile Metabolome ofFrontiers in microbiology · 2022
    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 at 5 institutions in 3 countries.

Molly C BletzDepartment of Biology, University of Massachusetts Boston, Boston, MA, United States of America.ORCID 0000-0003-4120-9356
Boyke BunkDSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Cathrin SpröerDSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Peter BiwerInstitute of Organic Chemistry, Technische Universität Braunschweig, Braunschweig, Germany.
Silke ReiterInstitute for Insect Biotechnology, Justus Liebig University Giessen, Giessen, Germany.
Falitiana C E RabemananjaraDepartment of Zoology and Animal Biodiversity, University of Antananarivo, Antananarivo, Madagascar.
Stefan SchulzInstitute of Organic Chemistry, Technische Universität Braunschweig, Braunschweig, Germany.ORCID 0000-0002-4810-324X
Jörg OvermannDSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Miguel VencesZoological Institute, Technische Universitt Braunschweig, Braunschweig, Germany.
Leibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures · DETechnische Universität Braunschweig · DEJustus-Liebig-Universität Gießen · DEUniversity of Antananarivo · MGUniversity of Massachusetts Boston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bacterial communities colonizing amphibian skin have been intensively studied due to their interactions with pathogenic chytrid fungi that are causing drastic amphibian population declines. Bacteria of the family Alcaligenaceae, and more specifically of the genus Pigmentiphaga, have been found to be associated specifically to arboreal frogs. Here we analyze their occurrence in a previously assembled global skin microbiome dataset from 205 amphibian species. Pigmentiphaga made up about 5% of the total number of reads in this global dataset. They were mostly found in unrelated arboreal frogs from Madagascar (Mantellidae and Hyperoliidae), but also occurred at low abundances on Neotropical frogs. Based on their 16S sequences, most of the sequences belong to a clade within Pigmentiphaga not assignable to any type strains of the five described species of the genus. One isolate from Madagascar clustered with Pigmentiphaga aceris (>99% sequence similarity on 16S rRNA gene level). Here, we report the full genome sequence of this bacterium which, based on 16S sequences of >97% similarity, has previously been found on human skin, floral nectar, tree sap, stream sediment and soil. Its genome consists of a single circular chromosome with 6,165,255 bp, 5,300 predicted coding sequences, 57 tRNA genes, and three rRNA operons. In comparison with other known Pigmentiphaga genomes it encodes a higher number of genes associated with environmental information processing and cellular processes. Furthermore, it has a biosynthetic gene cluster for a nonribosomal peptide syntethase, and bacteriocin biosynthetic genes can be found, but clusters for β-lactones present in other comparative Pigmentiphaga genomes are lacking.

Indexed as

AlcaligenaceaeAnimalsAnuraBiosynthetic PathwaysGenome, BacterialGenome SizeMultigene FamilyPhylogeographyPlant NectarRNA, Ribosomal, 16SSkinSoil MicrobiologyWhole Genome SequencingPlant NectarRNA, Ribosomal, 16S

Identifiers

PMID31603945
PMCPMC6788695
OpenAlexW2980190371

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.