Evidence map›Paper›PMID 39434132›Full record

ArticleBMC veterinary research2024

Whole-genome sequencing of toxigenic Clostridioides difficile reveals multidrug resistance and virulence genes in strains of environmental and animal origin.

Daniela Tercero-Guerrero, José L Blanco, Marta Hernández, Laura Torre-Fuentes, Julio Alvarez, Marta E García

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Article in BMC veterinary research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Daniela Tercero-GuerreroDepartment of Animal Health, Faculty of Veterinary Medicine, Complutense University of Madrid, 28039, Madrid, Spain.
José L BlancoDepartment of Animal Health, Faculty of Veterinary Medicine, Complutense University of Madrid, 28039, Madrid, Spain. jlblanco@ucm.es.
Marta HernándezArea of Microbiology, Faculty of Medicine, University of Valladolid, Valladolid, Spain.
Laura Torre-FuentesVISAVET Health Surveillance Centre, Complutense University of Madrid, Madrid, Spain.
Julio AlvarezDepartment of Animal Health, Faculty of Veterinary Medicine, Complutense University of Madrid, 28039, Madrid, Spain.
Marta E GarcíaDepartment of Animal Health, Faculty of Veterinary Medicine, Complutense University of Madrid, 28039, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClostridioides difficile has been recognized as an emerging pathogen in both humans and animals. In this context, antimicrobial resistance plays a major role in driving the spread of this disease, often leading to therapeutic failure. Moreover, recent increases in community-acquired C. difficile infections have led to greater numbers of investigations into the animal origin of the disease. The aim of this study was to evaluate the genetic similarities between 23 environmental and animal isolates by using whole-genome sequencing and to determine antimicrobial resistance and virulence factor genes in toxigenic C. difficile strains to provide important data for the development of diagnostic methods or treatment guidelines.

resultsThe most common sequence type was ST11 (87%), followed by ST2 (9%) and ST19 (4%). In addition, 86.95% of the strains exhibited multidrug resistance, with antimicrobial resistance to mainly aminoglycosides, fluoroquinolones, tetracycline and B-lactams; nevertheless, one strain also carried other resistance genes that conferred resistance to lincosamide, macrolides, streptogramin a, streptogramin b, pleuromutilin, oxazolidinone and amphenicol. In addition, a wide range of virulence factor genes, such as those encoding adherence factors, exoenzymes and toxins, were found. However, we observed variations between toxinotypes, ribotypes and sequence types.

conclusionsThe results of this study demonstrated significant genetic similarity between ST11 strains isolated from environmental sampling and from animal origin; these strains may represent a reservoir for community-acquired C. difficile infection, which is becoming a growing public health threat due to the development of multridug resistant (MDR) bacteria and the number of virulence factors detected.

Indexed as

Anti-Bacterial AgentsClostridioides difficileClostridium InfectionsDrug Resistance, Multiple, BacterialVirulence FactorsWhole Genome SequencingAnimalsGenome, BacterialVirulenceAnti-Bacterial AgentsVirulence FactorsAntimicrobial resistance genesClostridioides difficileOne HealthToxinVirulence genesWhole-genome sequencing

Identifiers

PMID39434132
PMCPMC11492571

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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.