Evidence map›Paper›PMID 39034380›Full record

ArticleScientific reports2024

An untargeted cultivation approach revealed Pseudogemmatithrix spongiicola gen. nov., sp. nov., and sheds light on the gemmatimonadotal mode of cell division: binary fission.

Tom Haufschild, Nicolai Kallscheuer, Jonathan Hammer, Timo Kohn, Moses Kabuu, Mareike Jogler, Nicole Wohlfarth, Manfred Rohde, Muriel C F van Teeseling, Christian Jogler

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 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

10 authors.

Tom Haufschild *Department of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany.
Nicolai Kallscheuer *Department of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany.
Jonathan HammerDepartment of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany.
Timo KohnLeibniz Institute DSMZ, Brunswick, Germany.
Moses KabuuDepartment of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany.
Mareike JoglerDepartment of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany.
Nicole WohlfarthDepartment of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany.
Manfred RohdeCentral Facility for Microscopy, Helmholtz Centre for Infection Research, Brunswick, Germany.
Muriel C F van TeeselingDepartment of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany.
Christian JoglerDepartment of Microbial Interactions, Institute of Microbiology, Friedrich Schiller University, Jena, Germany. christian.jogler@uni-jena.de.

Funding

Deutsche Forschungsgemeinschaft 239748522Deutsche Forschungsgemeinschaft 390713860
6 · The paper itself

Abstract

Members of the phylum Gemmatimonadota can account for up to 10% of the phylogenetic diversity in bacterial communities. However, a detailed investigation of their cell biology and ecological roles is restricted by currently only six characterized species. By combining low-nutrient media, empirically determined inoculation volumes and long incubation times in a 96-well plate cultivation platform, we isolated two strains from a limnic sponge that belong to this under-studied phylum. The characterization suggests that the two closely related strains constitute a novel species of a novel genus, for which we introduce the name Pseudogemmatithrix spongiicola. The here demonstrated isolation of novel members from an under-studied bacterial phylum substantiates that the cultivation platform can provide access to axenic bacterial cultures from various environmental samples. Similar to previously described members of the phylum, the novel isolates form spherical appendages at the cell poles that were believed to be daughter cells resulting from asymmetric cell division by budding. However, time-lapse microscopy experiments and quantitative image analysis showed that the spherical appendages never grew or divided. Although the role of these spherical cells remains enigmatic, our data suggests that cells of the phylum Gemmatimonadota divide via FtsZ-based binary fission with different division plane localization patterns than in other bacterial phyla.

Indexed as

PhylogenyAnimalsBacterial ProteinsCell DivisionRNA, Ribosomal, 16SBacterial ProteinsRNA, Ribosomal, 16SAquatic microbiologyBinary fissionBuddingCell divisionFreshwater spongeGemmatimonas

Identifiers

PMID39034380
PMCPMC11271474

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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.