Evidence map›Paper›PMID 35986252›Full record

ArticleBMC genomics2022

Genomic features of Mycoplasma bovis subtypes currently circulating in France.

Chloé Ambroset, Aurélie Peticca, Agnès Tricot, Florence Tardy

Abstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Integrative and conjugative elements inFrontiers in veterinary science · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Pathogenicity and molecular characterization of Mycoplasma bovis isolate from calves in Morocco.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2023
    Review
  7. 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

4 authors.

Chloé AmbrosetUniversité de Lyon, VetAgro Sup, Anses laboratoire de Lyon, UMR Mycoplasmoses Animales, 69280, Marcy l'Etoile, France.
Aurélie PeticcaUniversité de Lyon, VetAgro Sup, Anses laboratoire de Lyon, UMR Mycoplasmoses Animales, 69280, Marcy l'Etoile, France.
Agnès TricotUniversité de Lyon, VetAgro Sup, Anses laboratoire de Lyon, UMR Mycoplasmoses Animales, 69280, Marcy l'Etoile, France.
Florence TardyUniversité de Lyon, Anses Laboratoire de Lyon, VetAgro Sup, UMR Mycoplasmoses Animales, 69007, Lyon, France. florence.tardy@anses.fr.ORCID http://orcid.org/0000-0003-3968-4801

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMycoplasma (M.) bovis is a major etiological agent of bovine respiratory disease, which is the most economically costly disease of cattle worldwide. Cattle disease surveillance on M. bovis is increasingly using gene-based techniques, such as multilocus sequence typing (MLST), or genome-based techniques such as core genome MLST that both require only partial genomic data. However, accurate up-to-date surveillance also demands complete, circular genomes that can be used as reference to track the evolution of the different lineages. Yet, in France, two of the main subtypes currently circulating still have no representing genome in public databases. Here, to address this gap, we provide and compare three new complete M. bovis genomes obtained from recent clinical isolates that represent major subtypes circulating in France and Europe.

resultsGenomes were obtained using a hybrid assembly strategy (Illumina and Nanopore) with fine-tuning of settings and inputs used in the Unicycler assembly pipeline, such as size selection of reads and quality trimming of the FASTQ files. The main characteristics and synteny of the genomes were compared. The three genomes mainly differed by their content in terms of mobile genetic elements, i.e. integrative conjugative elements (ICE) and insertion sequences (IS), a feature that impacts their structure. For instance, strain L15527, representing subtype3 (st3), harbours an exceptionally high number of ICEs, which results in a bigger-sized genome than all those previously described and could be associated with the propensity of st3 to gain and fix mutations through chromosomal transfer mechanisms. In contrast, strain F9160, of st1, is very close to the PG45 type strain isolated in 1961 in the USA, and harbours a huge number of IS. These features may be associated with an evolution towards a host-restricted state or in a "closed" host or environment reservoir until a recent re-emergence.

conclusionsWhole-genome comparison of the three French M. bovis subtypes provides valuable resources for future studies combining epidemiology, phylogenetic data, and phylodynamic methods.

Indexed as

Cattle DiseasesMycoplasma bovisAnimalsCattleDNA Transposable ElementsGenomicsMultilocus Sequence TypingPhylogenyDNA Transposable ElementsGenome assemblyMobile genetic elementsMycoplasma bovisSubtypeWhole-genome comparison

Identifiers

PMID35986252
PMCPMC9392320

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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.