Evidence map›Paper›PMID 35049139›Full record

ArticleEnvironmental microbiology2022

Isolation and characterization of a novel Lambda-like phage infecting the bloom-forming cyanobacteria Cylindrospermopsis raciborskii.

Emmanuelle Laloum, Esther Cattan-Tsaushu, Daniel A Schwartz, Hanaa Shaalan, Hagay Enav, Dikla Kolan, Sarit Avrani

Open access · hybridAbstract read
In one paragraph

Article in Environmental microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
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

3 citing papers in PubMed, 10 citations in OpenAlex.

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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

7 authors at 3 institutions in 3 countries.

Emmanuelle Laloum *Department of Evolutionary and Environmental Biology and The Institute of Evolution, University of Haifa, Haifa, Israel.
Esther Cattan-Tsaushu *Department of Evolutionary and Environmental Biology and The Institute of Evolution, University of Haifa, Haifa, Israel.
Daniel A Schwartz *Department of Biology, Indiana University, Bloomington, IN, USA.ORCID 0000-0002-8959-3070
Hanaa ShaalanDepartment of Evolutionary and Environmental Biology and The Institute of Evolution, University of Haifa, Haifa, Israel.
Hagay EnavDepartment of Microbiome Science, Max Planck Institute for Developmental Biology, Tübingen, Germany.
Dikla KolanDepartment of Evolutionary and Environmental Biology and The Institute of Evolution, University of Haifa, Haifa, Israel.
Sarit AvraniDepartment of Evolutionary and Environmental Biology and The Institute of Evolution, University of Haifa, Haifa, Israel.ORCID 0000-0002-3622-6779
University of Haifa · ILIndiana University Bloomington · USMax Planck Institute for Developmental Biology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cylindrospermopsis raciborskii is a central bloom-forming cyanobacteria. However, despite its ecological significance, little is known of its interactions with the phages that infect it. Currently, only a single sequenced genome of a Cylindrospermopsis-infecting phage is publicly available. Here we describe the isolation and characterization of Cr-LKS3, a second phage infecting Cylindrospermopsis. Cr-LKS3 is a siphovirus with a higher genome similarity to prophages within heterotrophic bacteria genomes than to any other cyanophage/cyano-prophage, suggesting that it represents a novel cyanophage group. The function, order and orientation of the 72 genes in the Cr-LKS3 genome are highly similar to those of Escherichia virus Lambda (hereafter Lambda), despite the very low sequence similarity between these phages, showing high evolutionary convergence despite the substantial difference in host characteristics. Similarly to Lambda, the genome of Cr-LKS3 contains various genes that are known to be central to lysogeny, suggesting it can enter a lysogenic cycle. Cr-LKS3 has a unique ability to infect a host with a dramatically different GC content, without carrying any tRNA genes to compensate for this difference. This ability, together with its potential lysogenic lifestyle shed light on the complex interactions between C. raciborskii and its phages.

Indexed as

BacteriophagesCyanobacteriaCylindrospermopsisSiphoviridaeProphages

Identifiers

PMID35049139
PMCPMC9303873
OpenAlexW4206212716

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.