Complete genome sequence of an Enterococcus devriesei strain isolated from Zophobas morio larvae: Complete genome of Enterococcus devriesei Ed-CK-24.

Background .Enterococcus spp. are typically found in multiple settings and are sometimes responsible for difficult-to-treat infections. In this context, very little is known about E. devriesei, a rare species first isolated from a river lamprey. Importantly, no complete genome of E. devriesei currently exists in public repositories.Methods . An E. devriesei strain (Ed-CK-24) was isolated from homogenized Zophobas morio larvae. Initial species identification (ID) was performed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Antimicrobial susceptibility testing (AST) was performed by broth microdilution. Whole-genome sequencing (WGS) was done using both Illumina NovaSeq 6000 and Nanopore MinION to generate a complete genome assembly. WGS data were used to confirm species ID, antimicrobial resistance genes (ARGs) and plasmid replicon sequences screening. A database search for other E. devriesei genomes in NCBI was performed and used for 16S rRNA and core-genome phylogeny analyses.Results . WGS and bioinformatic analyses were performed, resulting in a complete genome assembly and allowing accurate taxonomic classification of Ed-CK-24 strain as E. devriesei. Alignment of 16S rRNA sequences of representative Enterococcus spp. further supported the ID of Ed-CK-24. A core-genome phylogenetic analysis revealed no clonal relationships between Ed-CK-24 and other E. devriesei derived from multiple sources. The Ed-CK-24 strain was resistant to clindamycin and quinupristin/dalfopristin. ARG screening identified the lsa(A) gene, carried on a 633,497-bp circular megaplasmid.Conclusions . WGS of Ed-CK-24 allowed high-resolution genomic comparison and epidemiologic analysis of E. devriesei. Its isolation from Z. morio larvae, commonly used in pet food, warns for further surveillance as the human pathogenic potential of this species remains unknown.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2025-02-17
DOI
https://doi.org/10.48620/85407
Primary Topic
Urban Green Space and Health
Type
article
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article

Complete genome sequence of an Enterococcus devriesei strain isolated from Zophobas morio larvae: Complete genome of Enterococcus devriesei Ed-CK-24.

Open Access CRIS of the University of Bern
Urban Green Space and Health
article

Complete genome sequence of an Enterococcus devriesei strain isolated from Zophobas morio larvae: Complete genome of Enterococcus devriesei Ed-CK-24.

article en

Abstract

Background .Enterococcus spp. are typically found in multiple settings and are sometimes responsible for difficult-to-treat infections. In this context, very little is known about E. devriesei, a rare species first isolated from a river lamprey. Importantly, no complete genome of E. devriesei currently exists in public repositories.Methods . An E. devriesei strain (Ed-CK-24) was isolated from homogenized Zophobas morio larvae. Initial species identification (ID) was performed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Antimicrobial susceptibility testing (AST) was performed by broth microdilution. Whole-genome sequencing (WGS) was done using both Illumina NovaSeq 6000 and Nanopore MinION to generate a complete genome assembly. WGS data were used to confirm species ID, antimicrobial resistance genes (ARGs) and plasmid replicon sequences screening. A database search for other E. devriesei genomes in NCBI was performed and used for 16S rRNA and core-genome phylogeny analyses.Results . WGS and bioinformatic analyses were performed, resulting in a complete genome assembly and allowing accurate taxonomic classification of Ed-CK-24 strain as E. devriesei. Alignment of 16S rRNA sequences of representative Enterococcus spp. further supported the ID of Ed-CK-24. A core-genome phylogenetic analysis revealed no clonal relationships between Ed-CK-24 and other E. devriesei derived from multiple sources. The Ed-CK-24 strain was resistant to clindamycin and quinupristin/dalfopristin. ARG screening identified the lsa(A) gene, carried on a 633,497-bp circular megaplasmid.Conclusions . WGS of Ed-CK-24 allowed high-resolution genomic comparison and epidemiologic analysis of E. devriesei. Its isolation from Z. morio larvae, commonly used in pet food, warns for further surveillance as the human pathogenic potential of this species remains unknown.

Open Access CRIS of the University of Bern
Infectious Disease Research Institute (US), Infectious Diseases Institute (UG), Max Planck Institute for Gravitational Physics (DE), National Center for Infectious Diseases (US)
Openalex Percentile: Top 47%
Urban Green Space and Health
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