Evidence map›Paper›PMID 28201991›Full record

ArticleBMC genomics2017

Plasmid diversity and phylogenetic consistency in the Lyme disease agent Borrelia burgdorferi.

Sherwood R Casjens, Eddie B Gilcrease, Marija Vujadinovic, Emmanuel F Mongodin, Benjamin J Luft, Steven E Schutzer, Claire M Fraser, Wei-Gang Qiu

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 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

  1. Article
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  7. Virulence Regulation inMicroorganisms · 2025
    Review
  8. Article
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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

8 authors.

Sherwood R CasjensDivision of Microbiology and Immunology, Pathology Department and Biology Department, University of Utah School of Medicine, Room 2200 K Emma Eccles Jones Medical Research Building, 15 North Medical Drive East, Salt Lake City, UT, 84112, USA. sherwood.casjens@path.utah.edu.
Eddie B GilcreaseDivision of Microbiology and Immunology, Pathology Department and Biology Department, University of Utah School of Medicine, Room 2200 K Emma Eccles Jones Medical Research Building, 15 North Medical Drive East, Salt Lake City, UT, 84112, USA.
Marija VujadinovicDivision of Microbiology and Immunology, Pathology Department and Biology Department, University of Utah School of Medicine, Room 2200 K Emma Eccles Jones Medical Research Building, 15 North Medical Drive East, Salt Lake City, UT, 84112, USA.
Emmanuel F MongodinInstitute for Genome Sciences, University of Maryland BioPark, Baltimore, MD, USA.
Benjamin J LuftDepartment of Medicine, Health Science Center, Stony Brook University, Stony Brook, NY, USA.
Steven E SchutzerDepartment of Medicine, New Jersey Medical School, Rutgers, the State University of New Jersey, Newark, NJ, 07103, USA.
Claire M FraserInstitute for Genome Sciences, University of Maryland BioPark, Baltimore, MD, USA.
Wei-Gang QiuDepartment of Biology, The Graduate Center, City University of New York City, New York, NY, USA.

Funding

Basic and Translational Research Center for Reducing Health DisparitiesG12MD007599 · NIMHD · HUNTER COLLEGE · PI ANGULO, JESUS A · 2012 to 2017
$14.6M
DNA packaging and delivery by dsDNA virusesR01GM114817 · NIGMS · UNIVERSITY OF UTAH · PI CASJENS, SHERWOOD R. · 2014 to 2017
$1.5M
Genome Variability and Population Processes of Lyme Disease PathogensSC1AI107955 · NIAID · HUNTER COLLEGE · PI QIU, WEIGANG · 2013 to 2016
$1.1M
NIAID NIH HHS SC1 AI107955NIGMS NIH HHS R01 GM114817NIMHD NIH HHS G12 MD007599
6 · The paper itself

Abstract

backgroundBacteria from the genus Borrelia are known to harbor numerous linear and circular plasmids. We report here a comparative analysis of the nucleotide sequences of 236 plasmids present in fourteen independent isolates of the Lyme disease agent B. burgdorferi.

resultsWe have sequenced the genomes of 14 B. burgdorferi sensu stricto isolates that carry a total of 236 plasmids. These individual isolates carry between seven and 23 plasmids. Their chromosomes, the cp26 and cp32 circular plasmids, as well as the lp54 linear plasmid, are quite evolutionarily stable; however, the remaining plasmids have undergone numerous non-homologous and often duplicative recombination events. We identify 32 different putative plasmid compatibility types among the 236 plasmids, of which 15 are (usually) circular and 17 are linear. Because of past rearrangements, any given gene, even though it might be universally present in these isolates, is often found on different linear plasmid compatibility types in different isolates. For example, the arp gene and the vls cassette region are present on plasmids of four and five different compatibility types, respectively, in different isolates. A majority of the plasmid types have more than one organizationally different subtype, and the number of such variants ranges from one to eight among the 18 linear plasmid types. In spite of this substantial organizational diversity, the plasmids are not so variable that every isolate has a novel version of every plasmid (i.e., there appears to be a limited number of extant plasmid subtypes).

conclusionsAlthough there have been many past recombination events, both homologous and nonhomologous, among the plasmids, particular organizational variants of these plasmids correlate with particular chromosomal genotypes, suggesting that there has not been rapid horizontal transfer of whole linear plasmids among B. burgdorferi lineages. We argue that plasmid rearrangements are essentially non-revertable and are present at a frequency of only about 0.65% that of single nucleotide changes, making rearrangement-derived novel junctions (mosaic boundaries) ideal phylogenetic markers in the study of B. burgdorferi population structure and plasmid evolution and exchange.

Indexed as

Genetic VariationGenomicsPhylogenyBorrelia burgdorferiChromosomes, BacterialGenome, BacterialLyme DiseasePlasmidsB. burgdorferiGenome rearrangementLinear plasmidPlasmid

Identifiers

PMID28201991
PMCPMC5310021

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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.