Evidence map›Paper›PMID 24926861›Full record

ArticleThe ISME journal2015

From community approaches to single-cell genomics: the discovery of ubiquitous hyperhalophilic Bacteroidetes generalists.

María Gomariz, Manuel Martínez-García, Fernando Santos, Francisco Rodriguez, Salvador Capella-Gutiérrez, Toni Gabaldón, Ramon Rosselló-Móra, Inmaculada Meseguer, Josefa Antón

Abstract read
In one paragraph

Article in The ISME journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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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

9 authors.

María Gomariz1] Department of Materials, Optics and Electronics, University Miguel Hernández of Elche, Alicante, Spain [2] Department of Physiology, Genetics, and Microbiology, University of Alicante, Alicante, Spain.
Manuel Martínez-GarcíaDepartment of Physiology, Genetics, and Microbiology, University of Alicante, Alicante, Spain.
Fernando SantosDepartment of Physiology, Genetics, and Microbiology, University of Alicante, Alicante, Spain.
Francisco RodriguezDepartament of Applied Mathematics, University of Alicante, Alicante, Spain.
Salvador Capella-GutiérrezBioinformatics and Genomics Programme, Centre for Genomic Regulation (CRG), Barcelona, Spain.
Toni Gabaldón1] Bioinformatics and Genomics Programme, Centre for Genomic Regulation (CRG), Barcelona, Spain [2] Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra (UPF), Barcelona, Spain.
Ramon Rosselló-MóraMarine Microbiology Group, Department of Ecology and Marine Resources, Institut Mediterrani d'Estudis Avançats IMEDEA (CSIC-UIB), Esporles, Spain.
Inmaculada MeseguerDepartment of Materials, Optics and Electronics, University Miguel Hernández of Elche, Alicante, Spain.
Josefa AntónDepartment of Physiology, Genetics, and Microbiology, University of Alicante, Alicante, Spain.

Funding

European Research Council 310325
6 · The paper itself

Abstract

The microbiota of multi-pond solar salterns around the world has been analyzed using a variety of culture-dependent and molecular techniques. However, studies addressing the dynamic nature of these systems are very scarce. Here we have characterized the temporal variation during 1 year of the microbiota of five ponds with increasing salinity (from 18% to >40%), by means of CARD-FISH and DGGE. Microbial community structure was statistically correlated with several environmental parameters, including ionic composition and meteorological factors, indicating that the microbial community was dynamic as specific phylotypes appeared only at certain times of the year. In addition to total salinity, microbial composition was strongly influenced by temperature and specific ionic composition. Remarkably, DGGE analyses unveiled the presence of most phylotypes previously detected in hypersaline systems using metagenomics and other molecular techniques, such as the very abundant Haloquadratum and Salinibacter representatives or the recently described low GC Actinobacteria and Nanohaloarchaeota. In addition, an uncultured group of Bacteroidetes was present along the whole range of salinity. Database searches indicated a previously unrecognized widespread distribution of this phylotype. Single-cell genome analysis of five members of this group suggested a set of metabolic characteristics that could provide competitive advantages in hypersaline environments, such as polymer degradation capabilities, the presence of retinal-binding light-activated proton pumps and arsenate reduction potential. In addition, the fairly high metagenomic fragment recruitment obtained for these single cells in both the intermediate and hypersaline ponds further confirm the DGGE data and point to the generalist lifestyle of this new Bacteroidetes group.

Indexed as

MicrobiotaActinobacteriaArchaeaBacteriaBacteroidetesBiodiversityGenome, BacterialHalobacteriaceaeMetagenomicsPondsSalinity

Identifiers

PMID24926861
PMCPMC4274432

What OpenQuestion holds

Textmetadata
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.