Evidence map›Paper›PMID 33495565›Full record

ArticleThe ISME journal2021

Efficient dilution-to-extinction isolation of novel virus-host model systems for fastidious heterotrophic bacteria.

Holger H Buchholz, Michelle L Michelsen, Luis M Bolaños, Emily Browne, Michael J Allen, Ben Temperton

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 42 citations in OpenAlex.

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  9. Genome sequences of the firstMicrobial genomics · 2024
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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

6 authors at 1 institution in 1 country.

Holger H BuchholzSchool of Biosciences, University of Exeter, Exeter, UK.
Michelle L MichelsenSchool of Biosciences, University of Exeter, Exeter, UK.
Luis M BolañosSchool of Biosciences, University of Exeter, Exeter, UK.ORCID http://orcid.org/0000-0002-0832-016X
Emily BrowneSchool of Biosciences, University of Exeter, Exeter, UK.
Michael J AllenSchool of Biosciences, University of Exeter, Exeter, UK.ORCID http://orcid.org/0000-0001-8504-7171
Ben TempertonSchool of Biosciences, University of Exeter, Exeter, UK. b.temperton@exeter.ac.uk.ORCID http://orcid.org/0000-0002-3667-8302
University of Exeter · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K003240/1Biotechnology and Biological Sciences Research Council BB/L024209/1Wellcome Trust WT097835MFWellcome Trust WT101650MA
6 · The paper itself

Abstract

Microbes and their associated viruses are key drivers of biogeochemical processes in marine and soil biomes. While viruses of phototrophic cyanobacteria are well-represented in model systems, challenges of isolating marine microbial heterotrophs and their viruses have hampered experimental approaches to quantify the importance of viruses in nutrient recycling. A resurgence in cultivation efforts has improved the availability of fastidious bacteria for hypothesis testing, but this has not been matched by similar efforts to cultivate their associated bacteriophages. Here, we describe a high-throughput method for isolating important virus-host systems for fastidious heterotrophic bacteria that couples advances in culturing of hosts with sequential enrichment and isolation of associated phages. Applied to six monthly samples from the Western English Channel, we first isolated one new member of the globally dominant bacterial SAR11 clade and three new members of the methylotrophic bacterial clade OM43. We used these as bait to isolate 117 new phages, including the first known siphophage-infecting SAR11, and the first isolated phage for OM43. Genomic analyses of 13 novel viruses revealed representatives of three new viral genera, and infection assays showed that the viruses infecting SAR11 have ecotype-specific host ranges. Similar to the abundant human-associated phage ɸCrAss001, infection dynamics within the majority of isolates suggested either prevalent lysogeny or chronic infection, despite a lack of associated genes, or host phenotypic bistability with lysis putatively maintained within a susceptible subpopulation. Broader representation of important virus-host systems in culture collections and genomic databases will improve both our understanding of virus-host interactions, and accuracy of computational approaches to evaluate ecological patterns from metagenomic data.

Indexed as

BacteriophagesSeawaterBacteriaHeterotrophic ProcessesHumansLysogeny

Identifiers

PMID33495565
PMCPMC8163748
OpenAlexW3121674341

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.