Evidence map›Paper›PMID 41345956›Full record

ArticleBiology direct2025

ssDNA phage FLiP resides in dsDNA form in resistant Flavobacterium host.

Kati Mäkelä, Reetta Penttinen, Janne Ravantti, Elina Laanto, Lotta-Riina Sundberg

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In one paragraph

Article in Biology direct, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

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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

5 authors.

Kati MäkeläDepartment of Biological and Environmental Science and Nanoscience Center, University of Jyväskylä, P.O. Box 35, Jyväskylä, FI-40014, Finland.ORCID http://orcid.org/0000-0001-5574-9738
Reetta PenttinenDepartment of Biological and Environmental Science and Nanoscience Center, University of Jyväskylä, P.O. Box 35, Jyväskylä, FI-40014, Finland.ORCID http://orcid.org/0000-0003-2152-9889
Janne RavanttiMolecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, 00014, Finland.ORCID http://orcid.org/0000-0002-8578-7230
Elina LaantoDepartment of Biological and Environmental Science and Nanoscience Center, University of Jyväskylä, P.O. Box 35, Jyväskylä, FI-40014, Finland.ORCID http://orcid.org/0000-0003-4172-3128
Lotta-Riina SundbergDepartment of Biological and Environmental Science and Nanoscience Center, University of Jyväskylä, P.O. Box 35, Jyväskylä, FI-40014, Finland. lotta-riina.sundberg@jyu.fi.ORCID http://orcid.org/0000-0003-3510-4398

Funding

Emil Aaltosen Säätiö #200260HORIZON EUROPE European Research Council No 101117204OLVI-Säätiö #201910409Research Council of Finland #346772Research Council of Finland #354982Suomalainen Konkordia-liitto #20200077
6 · The paper itself

Abstract

backgroundBacteria in the genus Flavobacterium play a key role in organic matter decomposition in the aquatic environment. Phages infecting these bacteria regulate the host populations and thereby the ecosystem functions. However, bacterial resistance against phage may cause changes in bacterial phenotypic characteristics. The single stranded DNA phage Finnlakevirus FLiP infects three known environmental Flavobacterium sp. isolates: B330, B167, and B114. Building on our previous FLiP-host interaction studies, we investigated resistance mechanisms from the host perspective, aiming to understand how Flavobacterium strains resist FLiP and related phages.

resultsWe assessed the fitness effects of phage resistance by comparing growth dynamics between ancestral and resistant variants. In the absence of phage, no significant differences in growth was observed, indicating that resistance to single stranded DNA phage FLiP does not impose a detectable fitness cost under laboratory conditions. Next, we screened host genomes for anti-phage systems and compared host genomes across strains and between ancestral and resistant variants. Genomic comparisons revealed resistance-related mutations, although no single mutation or anti-phage system consistently explained FLiP resistance across strains. Furthermore, we evaluated the possibility of lysogeny and superinfection immunity using sequence analysis, PCR, and nuclease treatments. Notably, resistant B114 host harbored the FLiP genome as a circular extrachromosomal double stranded DNA element, suggesting potential for lysogeny. Surprisingly, low levels of FLiP sequences were detected in bacterial populations not exposed to FLiP in the laboratory.

conclusionsOur findings suggest that FLiP-type phages may persist in host populations as extrachromosomal double stranded DNA elements in a subset of cells. This strategy could allow phages to endure unfavorable conditions and regulate infection timing. As detected in previous experiments, rather than requiring optimal conditions, FLiP is capable of productive infection even under stress, with infection stalling only when host growth is severely limited. The constant persistence within the host population, and capability to start particle production as soon as conditions improve, may represent an evolutionary adaptation for survival and transmission in fluctuating environments.

Indexed as

BacteriophagesDNA, Single-StrandedFlavobacteriumDNA, ViralDNA, Single-StrandedDNA, ViralDefence systemsInteractionsLysogenyPseudolysogenyResistancessDNA phageSuperinfection exclusion

Identifiers

PMID41345956
PMCPMC12781566

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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.