Evidence map›Paper›PMID 29037147›Full record

ArticleBMC genomics2017

De novo assembly of genomes from long sequence reads reveals uncharted territories of Propionibacterium freudenreichii.

Paulina Deptula, Pia K Laine, Richard J Roberts, Olli-Pekka Smolander, Helena Vihinen, Vieno Piironen, Lars Paulin, Eija Jokitalo, Kirsi Savijoki, Petri Auvinen and 1 more

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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  9. Red-Brown Pigmentation ofMicroorganisms · 2019
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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

11 authors.

Paulina DeptulaDepartment of Food and Environmental Sciences, University of Helsinki, 00014, Helsinki, Finland. paulina.deptula@helsinki.fi.
Pia K LaineInstitute of Biotechnology, University of Helsinki, 00014, Helsinki, Finland.
Richard J RobertsNew England Biolabs, Ipswich, MA, 01938-2723, USA.
Olli-Pekka SmolanderInstitute of Biotechnology, University of Helsinki, 00014, Helsinki, Finland.
Helena VihinenInstitute of Biotechnology, University of Helsinki, 00014, Helsinki, Finland.
Vieno PiironenDepartment of Food and Environmental Sciences, University of Helsinki, 00014, Helsinki, Finland.
Lars PaulinInstitute of Biotechnology, University of Helsinki, 00014, Helsinki, Finland.
Eija JokitaloInstitute of Biotechnology, University of Helsinki, 00014, Helsinki, Finland.
Kirsi SavijokiDepartment of Food and Environmental Sciences, University of Helsinki, 00014, Helsinki, Finland.
Petri AuvinenInstitute of Biotechnology, University of Helsinki, 00014, Helsinki, Finland.
Pekka VarmanenDepartment of Food and Environmental Sciences, University of Helsinki, 00014, Helsinki, Finland. pekka.varmanen@helsinki.fi.ORCID http://orcid.org/0000-0002-4508-3060

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPropionibacterium freudenreichii is an industrially important bacterium granted the Generally Recognized as Safe (the GRAS) status, due to its long safe use in food bioprocesses. Despite the recognized role in the food industry and in the production of vitamin B12, as well as its documented health-promoting potential, P. freudenreichii remained poorly characterised at the genomic level. At present, only three complete genome sequences are available for the species.

resultsWe used the PacBio RS II sequencing platform to generate complete genomes of 20 P. freudenreichii strains and compared them in detail. Comparative analyses revealed both sequence conservation and genome organisational diversity among the strains. Assembly from long reads resulted in the discovery of additional circular elements: two putative conjugative plasmids and three active, lysogenic bacteriophages. It also permitted characterisation of the CRISPR-Cas systems. The use of the PacBio sequencing platform allowed identification of DNA modifications, which in turn allowed characterisation of the restriction-modification systems together with their recognition motifs. The observed genomic differences suggested strain variation in surface piliation and specific mucus binding, which were validated by experimental studies. The phenotypic characterisation displayed large diversity between the strains in ability to utilise a range of carbohydrates, to grow at unfavourable conditions and to form a biofilm.

conclusionThe complete genome sequencing allowed detailed characterisation of the industrially important species, P. freudenreichii by facilitating the discovery of previously unknown features. The results presented here lay a solid foundation for future genetic and functional genomic investigations of this actinobacterial species.

Indexed as

Adaptation, PhysiologicalGenome, BacterialGenomic IslandsGenomicsPlasmidsPropionibacterium freudenreichiiSequence AnalysisBacteriophageComparative genomicsComplete genomeCRISPR-CasGrasMobile elementsPacBioPilusPropionibacterium freudenreichiiRestriction and modificationVitamin B12

Identifiers

PMID29037147
PMCPMC5644110

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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.