Prophage φEr670 and Genomic Island GI_Er147 as Carriers of Resistance Genes in Erysipelothrix rhusiopathiae Strains

In this study we employed nanopore whole genome sequencing to analyze the resistance genes, genomic islands and prophage DNA in two multidrug resistant <i>E. rhusiopathiae</i> strains, i.e., 670 and 147, isolated from domestic geese. MLST profiles and core-genome phylogeny were determined to assess strain relatedness. In strain 670 (serotype 8, ST 113), a novel 53 kb prophage φEr670 carrying the <i>lnuB</i> and <i>lsaE</i> resistance genes was identified. Regions highly homologous to the φEr670 prophage were detected in 36 of 586 (6.14%) publicly available <i>E. rhusiopathiae</i> genomes, as well as in some other Gram-positive bacteria, and usually contained resistance genes. <i>E. rhusiopathiae</i> strain 147 (serotype 5, ST 243) was found to contain a composite 98 kb genomic island (GI_Er147) carrying the <i>ant(6)-Ia</i> and <i>spw</i> genes, as well as gene encoding a putative lincosamide nucleotidyltransferase designated <i>lnu(J)</i> and a <i>vat</i> family gene encoding a putative streptogramin A O-acetyltransferase. The <i>lnu(J)</i> gene exhibited 83.6% homology to the <i>lnu(D)</i> gene, and <i>lnu(J)</i>-positive <i>E. rhusiopathiae</i> strains displayed intermediate susceptibility to lincomycin. <i>Vat</i>-positive strain 147 and <i>vat</i>-negative <i>E. rhusiopathiae</i> strains showed similar susceptibility to quinupristin/dalfopristin. The presence of the Tn916 transposon carrying the <i>tetM</i> gene was confirmed in the genomes of both <i>E. rhusiopathiae</i> strains; in strain 147, however, Tn916 was located within ICEEr1012. Based on analyses of additional <i>E. rhusiopathiae</i> genomes, the integration sites of Tn916, ICEEr1012, and GI_Er147 were identified as genomic "hot spots," contributing to the genome plasticity of <i>E. rhusiopathiae</i>. Prophage φEr670 and GI_Er147 as well as the Tn916 transposon and ICEEr1012 are most likely responsible for the dissemination of resistance genes in <i>E. rhusiopathiae</i>. Prophages highly homologous to φEr670 act as carriers of resistance genes in various Gram-positive bacteria. However, the transferability of the identified genetic elements and the functional role of the <i>lnu(J)</i> gene require further investigation. This study provides new insights into the diversity of MGEs in <i>E. rhusiopathiae</i> and advances understanding of the genomic mechanisms driving antimicrobial resistance in Gram-positive bacteria.

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Journal
International Journal of Molecular Sciences
Published
2025-12-25
DOI
https://doi.org/10.3390/ijms27010250
Primary Topic
Microbial infections and disease research
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article

Prophage φEr670 and Genomic Island GI_Er147 as Carriers of Resistance Genes in Erysipelothrix rhusiopathiae Strains

R. Urban-Chmiel, Marta Dec, Aldert Zomer, Marian J. Broekhuizen-Stins
International Journal of Molecular Sciences
Microbial infections and disease research
article

Prophage φEr670 and Genomic Island GI_Er147 as Carriers of Resistance Genes in Erysipelothrix rhusiopathiae Strains

R. Urban-Chmiel, Marta Dec, Aldert Zomer, Marian J. Broekhuizen-Stins
article en

Abstract

In this study we employed nanopore whole genome sequencing to analyze the resistance genes, genomic islands and prophage DNA in two multidrug resistant <i>E. rhusiopathiae</i> strains, i.e., 670 and 147, isolated from domestic geese. MLST profiles and core-genome phylogeny were determined to assess strain relatedness. In strain 670 (serotype 8, ST 113), a novel 53 kb prophage φEr670 carrying the <i>lnuB</i> and <i>lsaE</i> resistance genes was identified. Regions highly homologous to the φEr670 prophage were detected in 36 of 586 (6.14%) publicly available <i>E. rhusiopathiae</i> genomes, as well as in some other Gram-positive bacteria, and usually contained resistance genes. <i>E. rhusiopathiae</i> strain 147 (serotype 5, ST 243) was found to contain a composite 98 kb genomic island (GI_Er147) carrying the <i>ant(6)-Ia</i> and <i>spw</i> genes, as well as gene encoding a putative lincosamide nucleotidyltransferase designated <i>lnu(J)</i> and a <i>vat</i> family gene encoding a putative streptogramin A O-acetyltransferase. The <i>lnu(J)</i> gene exhibited 83.6% homology to the <i>lnu(D)</i> gene, and <i>lnu(J)</i>-positive <i>E. rhusiopathiae</i> strains displayed intermediate susceptibility to lincomycin. <i>Vat</i>-positive strain 147 and <i>vat</i>-negative <i>E. rhusiopathiae</i> strains showed similar susceptibility to quinupristin/dalfopristin. The presence of the Tn916 transposon carrying the <i>tetM</i> gene was confirmed in the genomes of both <i>E. rhusiopathiae</i> strains; in strain 147, however, Tn916 was located within ICEEr1012. Based on analyses of additional <i>E. rhusiopathiae</i> genomes, the integration sites of Tn916, ICEEr1012, and GI_Er147 were identified as genomic "hot spots," contributing to the genome plasticity of <i>E. rhusiopathiae</i>. Prophage φEr670 and GI_Er147 as well as the Tn916 transposon and ICEEr1012 are most likely responsible for the dissemination of resistance genes in <i>E. rhusiopathiae</i>. Prophages highly homologous to φEr670 act as carriers of resistance genes in various Gram-positive bacteria. However, the transferability of the identified genetic elements and the functional role of the <i>lnu(J)</i> gene require further investigation. This study provides new insights into the diversity of MGEs in <i>E. rhusiopathiae</i> and advances understanding of the genomic mechanisms driving antimicrobial resistance in Gram-positive bacteria.

International Journal of Molecular SciencesVol. 27(1)
University of Life Sciences in Lublin (PL), Utrecht University (NL)
Life below water
Openalex Percentile: Top 32%
Microbial infections and disease research
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