Evidence map›Paper›PMID 40757481›Full record

ArticleThe ISME journal2025

Global dominance of Haloquadratum walsbyi by a single genomovar with distinct gene content and viral cohorts from close relatives.

Esteban Bustos-Caparros, Tomeu Viver, Juan F Gago, Juanita R Avontuur, Souad Amiour, Bonnie K Baxter, María E Llames, Mehmet B Mutlu, Aharon Oren, Ana S Ramírez and 9 more

Abstract read
In one paragraph

Article in The ISME journal, 2025. 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. Archaeal symbioses all the way down.Nature microbiology · 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

19 authors.

Esteban Bustos-CaparrosMarine Microbiology Group (MMG), Department of Animal and Microbial Biodiversity, Mediterranean Institute for Advanced Studies (IMEDEA, CSIC-UIB), 07190 Esporles, Illes Balears, Spain.ORCID 0000-0002-9489-4441
Tomeu ViverMarine Microbiology Group (MMG), Department of Animal and Microbial Biodiversity, Mediterranean Institute for Advanced Studies (IMEDEA, CSIC-UIB), 07190 Esporles, Illes Balears, Spain.
Juan F GagoMarine Microbiology Group (MMG), Department of Animal and Microbial Biodiversity, Mediterranean Institute for Advanced Studies (IMEDEA, CSIC-UIB), 07190 Esporles, Illes Balears, Spain.
Juanita R AvontuurMarine Microbiology Group (MMG), Department of Animal and Microbial Biodiversity, Mediterranean Institute for Advanced Studies (IMEDEA, CSIC-UIB), 07190 Esporles, Illes Balears, Spain.
Souad AmiourLaboratory of Bioengineering, National Higher School of Biotechnology, Ali Mendjeli University Town, E66 P.O. Box. Constantine 25100, Constantine, Algeria.
Bonnie K BaxterGreat Salt Lake Institute, Westminster University, 1840 S 1300 E, Salt Lake City, UT 84105, United States.
María E LlamesLaboratorio de Ecología Microbiana Ambiental, Instituto Tecnológico de Chascomús (CONICET-UNSAM), Escuela de Bio y Nanotecnologías (UNSAM), Cam. Circunvalación Km. 8,2, B7130 Chascomús, Buenos Aires, Argentina.
Mehmet B MutluDepartment of Biology, Eskisehir Technical University, 26470 Eskisehir, Turkey.
Aharon OrenDepartment of Plant and Environmental Sciences, The Institute of Life Sciences, The Hebrew University of Jerusalem, Edmond J. Safra Campus, Givat Ram, Jerusalem 9190401, Israel.
Ana S RamírezUnidad de Epidemiología y Medicina Preventiva, IUSA, Facultad de Veterinaria, Universidad de Las Palmas de Gran Canaria, C/ Trasmontaña s/n, Arucas, 35413 Canary Islands, Spain.
Matthew B StottSchool of Biological Sciences, University of Canterbury, Christchurch, 20 Kirkwood Avenue, Upper Riccarton, 8041 Christchurch, New Zealand.
Stephanus N VenterDepartment of Biochemistry, Genetics and Microbiology, and Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Hatfield, 0028, Pretoria, South Africa.ORCID 0000-0002-5726-4918
Fernando SantosDepartment of Physiology, Genetics and Microbiology, University of Alicante, 03690 San Vicent del Raspeig, Alicante, Spain.ORCID 0000-0002-6281-7310
Josefa AntónDepartment of Physiology, Genetics and Microbiology, University of Alicante, 03690 San Vicent del Raspeig, Alicante, Spain.ORCID 0000-0002-5823-493X
Luis M Rodriguez-RDepartment of Microbiology and Digital Science Center (DiSC), University of Innsbruck, Innrain 15, 6020 Innsbruck, Austria.
Rafael BoschMicrobiologia, Departament de Biologia, Edifici Guillem Colom, Universitat de les Illes Balears, Campus UIB, 07122 Palma de Mallorca, Illes Balears, Spain.
Brian P HedlundSchool of Life Sciences, University of Nevada, 4505 S. Maryland Pkwy, Las Vegas, NV 89154-4004, United States.
Konstantinos T KonstantinidisSchool of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, United States.
Ramon Rossello-MoraMarine Microbiology Group (MMG), Department of Animal and Microbial Biodiversity, Mediterranean Institute for Advanced Studies (IMEDEA, CSIC-UIB), 07190 Esporles, Illes Balears, Spain.ORCID 0000-0001-8253-3107

Funding

NASA 80NSSC18M0027Spanish Ministry of Science, Innovation and Universities PGC2018-096956-B-C41Spanish Ministry of Science, Innovation and Universities PID2021-126114NB-C41Spanish Ministry of Science, Innovation and Universities PID2021-126114NB-C42Spanish Ministry of Science, Innovation and Universities PID2024-158829NB-C42
6 · The paper itself

Abstract

Haloquadratum walsbyi is generally the dominant species in hypersaline ecosystems at salt saturation conditions. Here, we followed the dynamics of its genomovars and associated viruses during recurrent evaporation-dilution disturbances of varying intensities at the mesocosm scale over 813 days. The diversity observed within a single mesocosm was also compared with that in a global-scale inventory of hypersaline environments of thalassohaline origin. The 140 binned metagenome assembled genomes (MAGs) together with the genomes of the (only) two available of H. walsbyi isolates grouped into four highly related (98.25% > Average Nucleotide Identity [ANI] > 99.5%) dominant genomovars (intra-genomovar ANI > 99.5%). In mesocosm experiments, moderate disturbances (i.e. recurrent dilution from saturation to 20% salts) enhanced the abundance of the already-dominant genomovar Hqrw1, resulting in reduced intraspecific diversity. This genomovar also dominated in almost all sites sampled around the globe. In contrast, more intense disturbance (i.e. recurrent dilution from saturation to 13% salts) decreased the abundance of Hqrw1 to lower levels than genomovar Hqrw2 by the end of the incubation, which seems to resist better osmotic changes. Further, our results showed that genomovars were followed by their viral cohorts, who play a significant role in the global dominance of the four H. walsbyi genomovars and their replacement under unfavorable conditions. We propose that the global dominance of H. walsbyi in thalassohaline hypersaline sites is enabled by both the success of Hqrw1 in high but stable salinities and the larger resistance of Hqrw2 to extreme osmotic stress, safeguarding the presence of the species in the system.

Indexed as

HalobacteriaceaeVirusesEcosystemMetagenomePhylogenySalinitygenomovarHaloquadratum walsbyihalovirusintraspecies diversitymetagenomicsosmotic disturbancestime-series

Identifiers

PMID40757481
PMCPMC12400929

What OpenQuestion holds

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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.