Evidence map›Paper›PMID 42897578›Full record

ArticleGenome medicine2026

Cumulative cgMLST provides increased discrimination of nested phylogenetic groups.

Armen Ovsepian, Jose F Delgado-Blas, Martin Rethoret-Pasty, Melissa J Martin, François Lebreton, Sylvain Brisse

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In one paragraph

Article in Genome medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Armen OvsepianInstitut Pasteur, Université Paris Cité, Biodiversity and Epidemiology of Bacterial Pathogens, Paris, France.
Jose F Delgado-BlasInstitut Pasteur, Université Paris Cité, Biodiversity and Epidemiology of Bacterial Pathogens, Paris, France.
Martin Rethoret-PastyInstitut Pasteur, Université Paris Cité, Biodiversity and Epidemiology of Bacterial Pathogens, Paris, France.
Melissa J MartinMultidrug-Resistant Organism Repository and Surveillance Network (MRSN), Diagnostics and Countermeasures Branch, CIDR, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
François LebretonMultidrug-Resistant Organism Repository and Surveillance Network (MRSN), Diagnostics and Countermeasures Branch, CIDR, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Sylvain BrisseInstitut Pasteur, Université Paris Cité, Biodiversity and Epidemiology of Bacterial Pathogens, Paris, France. sylvain.brisse@pasteur.fr.

Funding

Bill and Melinda Gates Foundation INV-025280Bill & Melinda Gates Foundation INV-025280French Government's Investissement d'Avenir program Laboratoire d'Excellence Integrative Biology of Emerging Infectious Diseases ANR-10-LABX-62-IBEIDISIDORe JRA CENTAUR project funded by European Union ISID_JRA_gun1
6 · The paper itself

Abstract

backgroundCore genome multilocus sequence typing (cgMLST) is a powerful method for bacterial strain genotyping. However, the size of the core genome decreases as the phylogenetic breadth of the target group increases, reducing discriminatory power. To overcome this discrimination/applicability tradeoff, here we developed a cumulative cgMLST approach, where sets of core loci conserved within nested phylogenetic entities are added. We illustrate this approach using the Klebsiella pneumoniae species complex (KpSC), for which a widely used cgMLST scheme (KpSC-cgMLST) comprises only 629 genes.

methodsWe created non-redundant cgMLST schemes for the individual species K. pneumoniae sensu stricto (Kpn-cgMLST scheme), and its multidrug resistant sublineages (SLs) SL147 and SL307. To extract core genes, we used 37,874 genome assemblies originating from over 80 countries worldwide. A methodology was set to filter redundant loci before importing them into the genotyping tool BIGSdb, where they were combined into schemes together with preexisting loci conserved at higher phylogenetic levels. The performance of the cumulative cgMLST schemes was evaluated on previously published datasets and on novel data from an inter-hospital outbreak of SL307.

resultsThe Kpn-cgMLST, SL147 and SL307 schemes comprise 2752, 852, and 947 additional loci, respectively. The mean allele call rate of the novel loci was > 99% in the validation datasets. Compared to the KpSC scheme used alone, pairwise allelic distances among isolates increased on average 5.6-fold using the Kpn scheme, and further by 1.2-fold and 1.3-fold using the SL147 and SL307 schemes, respectively. We demonstrated the added value of this increased discriminatory power for epidemiological analyses and observed a level of discrimination that approaches that of whole-genome single nucleotide polymorphism analysis.

conclusionsThe cumulative cgMLST strategy combines broad phylogenetic applicability and nearly complete genotyping resolution, expanding the utility of this harmonized approach for genomic epidemiology.

Indexed as

Genome, BacterialKlebsiella pneumoniaeMultilocus Sequence TypingPhylogenyCgMLSTCore genome MLSTCumulative cgMLSTGenomic epidemiologyGenotypingKlebsiella pneumoniae

Identifiers

PMID42897578
PMCPMC13682010

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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.