Evidence map›Paper›PMID 31791238›Full record

ArticleBMC genomics2019

CRISPR elements provide a new framework for the genealogy of the citrus canker pathogen Xanthomonas citri pv. citri.

Kwanho Jeong, Alejandra Muñoz-Bodnar, Nathalia Arias Rojas, Lucie Poulin, Luis Miguel Rodriguez-R, Lionel Gagnevin, Christian Vernière, Olivier Pruvost, Ralf Koebnik

Abstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Pathogens (Basel, Switzerland) · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Riboswitch theo/Microorganisms · 2021
    Article
  7. Article
  8. 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

9 authors.

Kwanho JeongIRD, Cirad, Université de Montpellier, IPME, Montpellier, France.
Alejandra Muñoz-BodnarIRD, Cirad, Université de Montpellier, IPME, Montpellier, France.
Nathalia Arias RojasIRD, Cirad, Université de Montpellier, IPME, Montpellier, France.
Lucie PoulinIRD, Cirad, Université de Montpellier, IPME, Montpellier, France.
Luis Miguel Rodriguez-RIRD, Cirad, Université de Montpellier, IPME, Montpellier, France.
Lionel GagnevinIRD, Cirad, Université de Montpellier, IPME, Montpellier, France.
Christian VernièreCIRAD, UMR PVBMT, 97410, Saint Pierre, La Réunion, France.
Olivier PruvostCIRAD, UMR PVBMT, 97410, Saint Pierre, La Réunion, France.
Ralf KoebnikIRD, Cirad, Université de Montpellier, IPME, Montpellier, France. Ralf.Koebnik@ird.fr.ORCID http://orcid.org/0000-0002-4419-0542

Funding

Agence Nationale de la Recherche ANR-2010-BLAN-1723Direction Générale de l'Armement 2011 60 091
6 · The paper itself

Abstract

backgroundXanthomonads are an important clade of Gram-negative bacteria infecting a plethora of economically important host plants, including citrus. Knowledge about the pathogen's diversity and population structure are prerequisite for epidemiological surveillance and efficient disease management. Rapidly evolving genetic loci, such as Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR), are of special interest to develop new molecular typing tools.

resultsWe analyzed CRISPR loci of 56 Xanthomonas citri pv. citri strains of world-wide origin, a regulated pathogen causing Asiatic citrus canker in several regions of the world. With one exception, 23 unique sequences built up the repertoire of spacers, suggesting that this set of strains originated from a common ancestor that already harbored these 23 spacers. One isolate originating from Pakistan contained a string of 14 additional, probably more recently acquired spacers indicating that this genetic lineage has or had until recently the capacity to acquire new spacers. Comparison of CRISPR arrays with previously obtained molecular typing data, such as amplified fragment length polymorphisms (AFLP), variable-number of tandem-repeats (VNTR) and genome-wide single-nucleotide polymorphisms (SNP), demonstrated that these methods reveal similar evolutionary trajectories. Notably, genome analyses allowed to generate a model for CRISPR array evolution in X. citri pv. citri, which provides a new framework for the genealogy of the citrus canker pathogen.

conclusionsCRISPR-based typing will further improve the accuracy of the genetic identification of X. citri pv. citri outbreak strains in molecular epidemiology analyses, especially when used concomitantly with another genotyping method.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Associated ProteinsGenotyping TechniquesMolecular TypingPhylogenyPolymerase Chain ReactionXanthomonasCRISPR-Associated ProteinsClustered regularly interspaced short palindromic repeatsEpidemiologyEvolutionGenetic diversityMolecular typingPhylogenySpoligotypingVariable numbers of tandem repeatsXanthomonas citri pv. citri

Identifiers

PMID31791238
PMCPMC6889575

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.