Evidence map›Paper›PMID 38539229›Full record

ArticleMicrobiome2024

Phenology and ecological role of aerobic anoxygenic phototrophs in freshwaters.

Cristian Villena-Alemany, Izabela Mujakić, Livia K Fecskeová, Jason Woodhouse, Adrià Auladell, Jason Dean, Martina Hanusová, Magdalena Socha, Carlota R Gazulla, Hans-Joachim Ruscheweyh and 7 more

Abstract read
In one paragraph

Article in Microbiome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  4. Do carotenoids protect phytodetritus-associated bacteria from oxidative stress?Environmental science and pollution research international · 2025
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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

17 authors.

Cristian Villena-AlemanyLaboratory of Anoxygenic Phototrophs, Institute of Microbiology of the Czech Academy of Sciences, Třeboň, Czechia. cristian.villena.alemany@hotmail.com.
Izabela MujakićLaboratory of Anoxygenic Phototrophs, Institute of Microbiology of the Czech Academy of Sciences, Třeboň, Czechia.
Livia K FecskeováAssociated Tissue Bank, Faculty of Medicine, Pavol Jozef Safarik University in Košice, Košice, Slovakia.
Jason WoodhouseDepartment of Plankton and Microbial Ecology, Leibniz Institute of Freshwater Ecology and Inland Fisheries, Stechlin, Germany.
Adrià AuladellFunctional Genomics and Evolution Department, Institute of Evolutionary Biology, CSIC-UPF, Barcelona, Catalonia, Spain.
Jason DeanLaboratory of Anoxygenic Phototrophs, Institute of Microbiology of the Czech Academy of Sciences, Třeboň, Czechia.
Martina HanusováLaboratory of Anoxygenic Phototrophs, Institute of Microbiology of the Czech Academy of Sciences, Třeboň, Czechia.
Magdalena SochaDepartment of Fisheries Oceanography and Marine Ecology, National Marine Fisheries Research Institute, Gdynia, Poland.
Carlota R GazullaCentro Oceanográfico de Málaga, Instituto Español de Oceanografía, IEO-CSIC, 29640, Fuengirola, Málaga, Spain.
Hans-Joachim RuscheweyhDepartment of Biology, Institute of Microbiology and Swiss Institute of Bioinformatics, ETH Zurich, Zurich, Switzerland.
Shinichi SunagawaDepartment of Biology, Institute of Microbiology and Swiss Institute of Bioinformatics, ETH Zurich, Zurich, Switzerland.
Vinicius Silva KavaguttiDepartment of Ecosystem Biology, Faculty of Science, University of South Bohemia, České Budějovice, Czechia.
Adrian-Ştefan AndreiLimnological Station, Department of Plant and Microbial Biology, University of Zurich, Kilchberg, Switzerland.
Hans-Peter GrossartDepartment of Plankton and Microbial Ecology, Leibniz Institute of Freshwater Ecology and Inland Fisheries, Stechlin, Germany.
Rohit GhaiDepartment of Aquatic Microbial Ecology, Institute of Hydrobiology, Biology Center CAS, České Budějovice, Czech Republic.
Michal KoblížekLaboratory of Anoxygenic Phototrophs, Institute of Microbiology of the Czech Academy of Sciences, Třeboň, Czechia.
Kasia PiwoszDepartment of Fisheries Oceanography and Marine Ecology, National Marine Fisheries Research Institute, Gdynia, Poland. kpiwosz@mir.gdynia.pl.

Funding

Grantová Agentura České Republiky 19-28778XPolska Akademia Nauk 2021/03/Y/NZ8/00076
6 · The paper itself

Abstract

backgroundAerobic anoxygenic phototrophic (AAP) bacteria are heterotrophic bacteria that supply their metabolism with light energy harvested by bacteriochlorophyll-a-containing reaction centers. Despite their substantial contribution to bacterial biomass, microbial food webs, and carbon cycle, their phenology in freshwater lakes remains unknown. Hence, we investigated seasonal variations of AAP abundance and community composition biweekly across 3 years in a temperate, meso-oligotrophic freshwater lake.

resultsAAP bacteria displayed a clear seasonal trend with a spring maximum following the bloom of phytoplankton and a secondary maximum in autumn. As the AAP bacteria represent a highly diverse assemblage of species, we followed their seasonal succession using the amplicon sequencing of the pufM marker gene. To enhance the accuracy of the taxonomic assignment, we developed new pufM primers that generate longer amplicons and compiled the currently largest database of pufM genes, comprising 3633 reference sequences spanning all phyla known to contain AAP species. With this novel resource, we demonstrated that the majority of the species appeared during specific phases of the seasonal cycle, with less than 2% of AAP species detected during the whole year. AAP community presented an indigenous freshwater nature characterized by high resilience and heterogenic adaptations to varying conditions of the freshwater environment.

conclusionsOur findings highlight the substantial contribution of AAP bacteria to the carbon flow and ecological dynamics of lakes and unveil a recurrent and dynamic seasonal succession of the AAP community. By integrating this information with the indicator of primary production (Chlorophyll-a) and existing ecological models, we show that AAP bacteria play a pivotal role in the recycling of dissolved organic matter released during spring phytoplankton bloom. We suggest a potential role of AAP bacteria within the context of the PEG model and their consideration in further ecological models.

Indexed as

LakesPhototrophic ProcessesBacteriaBacteria, AerobicBiomassPhytoplanktonAerobic anoxygenic phototrophsAquatic microbial ecologyFreshwatersLong-term samplingMicrobial seasonal successionPEG modelPhotoheterotrophspufM gene

Identifiers

PMID38539229
PMCPMC10976687

What Socratic holds

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LicenceCC BY
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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 Socratic graph.