Evidence map›Paper›PMID 40696756›Full record

ArticleEnvironmental microbiology2025

Cyanophage Infections in a Sponge Intracellular Cyanobacterial Symbiont.

Tzipora Peretz, Esther Cattan-Tsaushu, Chiara Conti, Benyamin Rosental, Laura Steindler, Sarit Avrani

Abstract read
In one paragraph

Article in Environmental microbiology, 2025. 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

6 authors.

Tzipora PeretzDepartment of Evolutionary and Environmental Biology, Faculty of Natural Sciences, University of Haifa, Israel.ORCID https://orcid.org/0009-0007-2764-936X
Esther Cattan-TsaushuDepartment of Evolutionary and Environmental Biology, Faculty of Natural Sciences, University of Haifa, Israel.ORCID https://orcid.org/0009-0001-4885-1045
Chiara ContiDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Israel.ORCID https://orcid.org/0000-0003-1363-0223
Benyamin RosentalThe Shraga Segal Department of Microbiology, Immunology, and Genetics, Faculty of Health Sciences, Center for Regenerative Medicine and Stem Cells, Ben Gurion University of the Negev, Beer Sheva, Israel.ORCID https://orcid.org/0000-0002-3974-3296
Laura SteindlerDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Israel.ORCID https://orcid.org/0000-0002-0188-101X
Sarit AvraniDepartment of Evolutionary and Environmental Biology, Faculty of Natural Sciences, University of Haifa, Israel.ORCID https://orcid.org/0000-0002-3622-6779

Funding

Gordon and Betty Moore Foundation GBMF9352Israel Science Foundation 1386/20Israel Science Foundation 933/23
6 · The paper itself

Abstract

Sponges are sessile animals that play crucial roles in marine ecosystems by facilitating nutrient cycling, enhancing biodiversity, and structuring benthic habitats. Microbial symbionts, including cyanobacteria, are vital to sponges, aiding in nutrient cycling, metabolism, and defence. However, due to the sponge's ability to concentrate phages from seawater, extracellular sponge symbionts are particularly vulnerable to phage infection. By contrast, little is known about the susceptibility of intracellular sponge symbionts to phage predation. Here, we present evidence that Candidatus Synechococcus feldmannii, a facultative, horizontally transmitted cyanobacterial endosymbiont of the sponge Petrosia ficiformis, is susceptible to cyanophages. We analysed four Ca. S. feldmannii genomes and found evidence for phage interactions in two, including CRISPR spacers matching sipho- and T4-like cyanophages. One genome harboured a prophage region resembling freshwater cyanobacterial prophages, featuring conserved regions associated with Type VI secretion systems, similar to Wolbachia endosymbionts prophages. Additionally, we developed a method for isolating cyanophages directly from purified sponge bacteriocytes (specialised sponge cells harbouring symbionts) and identified nine T4-like cyanophages with less than 60% similarity to known relatives. Collectively, our findings indicate that Ca. S. feldmannii is susceptible to cyanophages and suggest potential functional parallels between phages infecting endosymbionts across different animal hosts.

Indexed as

BacteriophagesCyanobacteriaPoriferaSymbiosisSynechococcusAnimalsGenome, ViralProphageslysogenyphagesponge endosymbiontsymbiotic cyanobacteriatripartite interactions

Identifiers

PMID40696756
PMCPMC12284385

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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.