Evidence map›Paper›PMID 41786613›Full record

ArticleThe ISME journal2026

Hypoosmolarity inhibits ammonia oxidation by terrestrial and freshwater Nitrosopumilaceae members.

Joo-Han Gwak, Adebisi Olabisi, Ui-Ju Lee, Christiana Abiola, Seongjun Lee, Hackwon Do, Yun Ji Choi, Jay-Jung Lee, Man-Young Jung, Nico Jehmlich and 5 more

Abstract read
In one paragraph

Article in The ISME journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Joo-Han GwakDepartment of Life Science, Hallym University, Chuncheon 24252, Gangwon-do, Republic of Korea.ORCID 0000-0002-0464-4722
Adebisi OlabisiDepartment of Biological Sciences and Biotechnology, Chungbuk National University , Cheongju 28644, Chungcheongbuk-do, Republic of Korea.ORCID 0009-0002-2713-6111
Ui-Ju LeeDepartment of Biological Sciences and Biotechnology, Chungbuk National University , Cheongju 28644, Chungcheongbuk-do, Republic of Korea.ORCID 0009-0008-5921-8852
Christiana AbiolaDepartment of Biological Sciences and Biotechnology, Chungbuk National University , Cheongju 28644, Chungcheongbuk-do, Republic of Korea.ORCID 0000-0001-6251-4486
Seongjun LeeDepartment of Biological Sciences and Biotechnology, Chungbuk National University , Cheongju 28644, Chungcheongbuk-do, Republic of Korea.ORCID 0009-0005-2178-1082
Hackwon DoDivision of Life Sciences, Korea Polar Research Institute, Incheon 21990, Republic of Korea.
Yun Ji ChoiInterdisciplinary Graduate Program in Advanced Convergence Technology and Science, Jeju National University, Jeju 63243, Jeju-do, Republic of Korea.ORCID 0000-0002-6097-3141
Jay-Jung LeeGeum River Environment Research Center, National Institute of Environmental Research, Okcheon 29027, Chungcheongbuk-do, Republic of Korea.
Man-Young JungInterdisciplinary Graduate Program in Advanced Convergence Technology and Science, Jeju National University, Jeju 63243, Jeju-do, Republic of Korea.ORCID 0000-0002-5244-5197
Nico JehmlichDepartment of Molecular Systems Biology, Helmholtz Centre for Environmental Research-Zentrum für Umweltforschung GmbH, Leipzig 04318, Germany.ORCID 0000-0002-5638-6868
Martin von BergenDepartment of Molecular Systems Biology, Helmholtz Centre for Environmental Research-Zentrum für Umweltforschung GmbH, Leipzig 04318, Germany.ORCID 0000-0003-2732-2977
Michael WagnerCentre for Microbiology and Environmental Systems Science, Department of Microbiology and Ecosystem Science, University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-9778-7684
Samuel Imisi AwalaDepartment of Biological Sciences, University of Calgary, Calgary, AB T2N 1N4, Canada.ORCID 0000-0002-2553-1604
Zhe-Xue QuanSchool of Life Sciences, Fudan University, Shanghai 200438, China.ORCID 0000-0002-7561-8572
Sung-Keun RheeDepartment of Biological Sciences and Biotechnology, Chungbuk National University , Cheongju 28644, Chungcheongbuk-do, Republic of Korea.ORCID 0000-0003-2111-7999

Funding

Austrian Science Fund (FWF) Cluster of Excellence Microbiomes drive Planetary Health 10.55776/COE7Korea Institute of Marine Science & Technology PromotionMinistry of Education 2020R1A6A1A06046235Ministry of Oceans and Fisheries RS-2025-02307311Ministry of Science and ICT RS-2023-00213601Ministry of Science and ICT RS-2025-000518246Ministry of Science and ICT RS-2026-25480345National Institute of Environmental Research, Ministry of Environment, Republic of Korea NIER-2022-01-01-075National Research Foundation of Korea
6 · The paper itself

Abstract

Salinity strongly influences the physiology and distribution of nitrifying microorganisms, yet the effects of low salinity remain understudied. This study investigates the impact of hypoosmolarity on different groups of ammonia oxidizers in soil and freshwater reservoirs, as well as in pure culture isolates. In soil microcosms amended with ammonium, at low salinity levels (~120 μS/cm), comparable to values commonly found in pristine terrestrial and freshwater environments, the abundance of ammonia-oxidizing bacteria (AOB), dominated by Nitrosomonas oligotropha, significantly increased. In contrast, the growth of ammonia-oxidizing archaea (AOA), dominated by "Candidatus Nitrosotenuis" of the Nitrosopumilaceae family, was stimulated by high salinity (~760 μS/cm). In ammonium-fed freshwater microcosms, the abundance of AOB, dominated by N. oligotropha, significantly increased under both low (~170 μS/cm) and high salinity (~850 μS/cm) conditions. In the presence of allylthiourea (50 μM), used to inhibit bacterial ammonia oxidation, AOA were sensitive to low salinity in both soil and freshwater microcosms. Consistently, culture-dependent studies revealed marked growth inhibition of terrestrial AOA, especially members of Nitrosopumilaceae, under hypoosmolarity, unlike AOB and complete ammonia oxidizer (comammox) strains. Genomic analyses, along with transcriptomic studies, suggested that the sensitivity of AOA to hypoosmolarity stress was possibly due to a lack of osmoregulatory transport systems and their S-layer cell wall structure. Overall, this study indicates hypoosmolarity as an important factor shaping the ecological niches and distribution of ammonia oxidizers, as well as nitrification activities, in terrestrial and freshwater environments that are increasingly affected by intensified water cycles due to global change.

Indexed as

AmmoniaArchaeaFresh WaterSoil MicrobiologyBacteriaNitrificationOxidation-ReductionSalinityAmmoniaammonia-oxidizing archaeahypoosmolaritynitrificationsoil and freshwater ecosystems

Identifiers

PMID41786613
PMCPMC13037477

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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.