Evidence map›Paper›PMID 41999489›Full record

ArticleMicrobial ecology2026

Gut Microbial Nitrate Reduction to Ammonia: A Possible Pathway of Biological Nitrogen Provisioning in Freshwater Insects.

Kiera Nelson, Nick Peterson, Rozlyn Olson, Hanna Castillo, Charles Antwi, Stephanie Cromwell, M Eric Benbow, Paul Ayayee

Abstract read
In one paragraph

Article in Microbial ecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Kiera NelsonDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA.
Nick PetersonDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA.
Rozlyn OlsonDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA.
Hanna CastilloDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA.
Charles AntwiDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA.
Stephanie CromwellDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA.
M Eric BenbowDepartment of Entomology, Michigan State University, East Lansing, MI, USA.
Paul AyayeeDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA. payayee@nebraska.edu.

Funding

UNMC Structural Biology CoreP20GM103427 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Heather Colleen Jensen-Smith · 2012 to 2026
$59.2M
UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI James Eudy · 1985 to 2026
$55.0M
NCI NIH HHS P30 CA036727NIGMS NIH HHS P20 GM103427
6 · The paper itself

Abstract

Biologically provided nitrogen (from diet or symbionts) is overwhelmingly vital to animal life on Earth. Biological nitrogen provisioning (BNP), mainly via nitrogen fixation and recycling, is a well-established function of the gut microbiomes of various terrestrial insects but remains less well-studied in freshwater insects. One possible route for BNP in freshwater insects is microbial nitrate reduction to ammonium (NRA), which produces the same intermediate metabolite, ammonium, as microbial nitrogen fixation in terrestrial insects. In this study, we characterized gut microbiome composition using 16S amplicon sequencing, followed by compound-specific stable isotope analyses (CSIA), to examine gut microbial NRA as a possible function in nymphs of the herbivorous, filter-feeding mayfly (Hexagenia bilineata) and the predatory dragonfly (Tetragoneuria spinigera). We first uncovered significant differences in microbiome community composition and elevated NRA potential in mayflies compared with dragonflies. We subsequently determined significantly greater 15N-signatures across essential amino acids (δ15NEAA) and non-essential amino acids (δ15NNEAAs) in the herbivorous mayfly than the predatory dragonfly, after incubation in K15NO3 for 5 days. This is interpreted as insect host uptake and incorporation of microbe-derived 15NH4 into amino acids following NRA. Taken together, the results presented here suggest that gut microbial NRA may be a potential mechanism for supplying biological nitrogen to freshwater insects, potentially helping alleviate nitrogen limitations. This work advances our understanding of freshwater insect host-gut microbe associations (nature and function) and the potential impacts of these associations on host and ecosystem processes.

Indexed as

AmmoniaBacteriaEphemeropteraGastrointestinal MicrobiomeInsectaNitratesNitrogenOdonataAnimalsFresh WaterNitrogen IsotopesNymphOxidation-ReductionRNA, Ribosomal, 16SAmmoniaNitratesNitrogenNitrogen IsotopesRNA, Ribosomal, 16SAmmoniumFreshwater insectsGut microbiomeNitrate reductionStable isotopes

Identifiers

PMID41999489
PMCPMC13222897

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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.