Evidence map›Paper›PMID 37167330›Full record

ArticlePloS one2023

A minisatellite-based MLVA for deciphering the global epidemiology of the bacterial cassava pathogen Xanthomonas phaseoli pv. manihotis.

Leidy Rache, Laurence Blondin, Paula Diaz Tatis, Carolina Flores, Andrea Camargo, Moussa Kante, Issa Wonni, Camilo López, Boris Szurek, Stephane Dupas and 5 more

Abstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

15 authors.

Leidy RacheDepartment of Biological Sciences, Universidad de los Andes, Bogotá D.C., Colombia.
Laurence BlondinCIRAD, UMR PHIM, Montpellier, France.
Paula Diaz TatisFacultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.ORCID 0000-0001-8334-966X
Carolina FloresPlant Health Institute of Montpellier (PHIM), Université Montpellier, IRD, CIRAD, INRAE, Institut Agro, Montpellier, France.
Andrea CamargoFacultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.
Moussa KantePlant Health Institute of Montpellier (PHIM), Université Montpellier, IRD, CIRAD, INRAE, Institut Agro, Montpellier, France.ORCID 0000-0002-9925-155X
Issa WonniINERA, LMI Pathobios, Bobo Dioulasso, Burkina Faso.
Camilo LópezDepartamento de Biología, Universidad Nacional de Colombia, Bogotá, Colombia.
Boris SzurekPlant Health Institute of Montpellier (PHIM), Université Montpellier, IRD, CIRAD, INRAE, Institut Agro, Montpellier, France.
Stephane DupasDepartment of Biological Sciences, Universidad de los Andes, Bogotá D.C., Colombia.
Olivier PruvostCIRAD, UMR PVBMT, Saint-Pierre, La Réunion, France.
Ralf KoebnikPlant Health Institute of Montpellier (PHIM), Université Montpellier, IRD, CIRAD, INRAE, Institut Agro, Montpellier, France.
Silvia RestrepoDepartment of Biological Sciences, Universidad de los Andes, Bogotá D.C., Colombia.
Adriana BernalDepartment of Biological Sciences, Universidad de los Andes, Bogotá D.C., Colombia.ORCID 0000-0002-3557-697X
Christian VernièrePlant Health Institute of Montpellier (PHIM), Université Montpellier, IRD, CIRAD, INRAE, Institut Agro, Montpellier, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cassava Bacterial Blight (CBB) is a destructive disease widely distributed in the different areas where this crop is grown. Populations studies have been performed at local and national scales revealing a geographical genetic structure with temporal variations. A global epidemiology analysis of its causal agent Xanthomonas phaseoli pv. manihotis (Xpm) is needed to better understand the expansion of the disease for improving the monitoring of CBB. We targeted new tandem repeat (TR) loci with large repeat units, i.e. minisatellites, that we multiplexed in a scheme of Multi-Locus Variable number of TR Analysis (MLVA-8). This genotyping scheme separated 31 multilocus haplotypes in three clusters of single-locus variants and a singleton within a worldwide collection of 93 Xpm strains isolated over a period of fifty years. The major MLVA-8 cluster 1 grouped strains originating from all countries, except the unique Chinese strain. On the contrary, all the Xpm strains genotyped using the previously developed MLVA-14 microsatellite scheme were separated as unique haplotypes. We further propose an MLVA-12 scheme which takes advantage of combining TR loci with different mutation rates: the eight minisatellites and four faster evolving microsatellite markers, for global epidemiological surveillance. This MLVA-12 scheme identified 78 haplotypes and separated most of the strains in groups of double-locus variants (DLV) supporting some phylogenetic relationships. DLV groups were subdivided into closely related clusters of strains most often sharing the same geographical origin and isolated over a short period, supporting epidemiological relationships. The main MLVA-12 DLV group#1 was composed by strains from South America and all the African strains. The MLVA-12 scheme combining both minisatellite and microsatellite loci with different discriminatory power is expected to increase the accuracy of the phylogenetic signal and to minimize the homoplasy effects. Further investigation of the global epidemiology of Xpm will be helpful for a better control of CBB worldwide.

Indexed as

ManihotMinisatellite RepeatsBacterial Typing TechniquesGenotypeMicrosatellite RepeatsPhylogenyXanthomonas

Identifiers

PMID37167330
PMCPMC10174486

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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.