Purpose <p>Vancomycin-resistant <i>Enterococcus faecium</i> is listed in the 2024 WHO Bacterial Priority Pathogens List as a high-priority agent of hospital-acquired infections. Its persistence is supported by marked genomic plasticity across human, animal, food, and environmental sources. We aimed to map antimicrobial resistance genes, virulence determinants, and clonal lineages of <i>Enterococcus</i> spp. reported in Brazil across these four sampling contexts.</p> Methods <p>Scoping review following JBI methodological guidance and reported per PRISMA-ScR. Four databases (PubMed, Embase, SciELO, LILACS) were searched without time restrictions in English, Portuguese, and Spanish. Two reviewers screened studies in Rayyan and extracted data using a standardised instrument.</p> Results <p>A total of 133 studies (1999 to 2025) were included. Evidence was concentrated in the Southeast and South. Sixty-seven acquired resistance genes and 11 chromosomal mutations were identified across 14 species, predominantly <i>E. faecalis</i> and <i>E. faecium</i>. Twelve broadly reported genes, including <i>vanA</i>, <i>erm(B)</i>, and <i>tet(M)</i>, spanned all four One Health contexts. Of 67 <i>E. faecium</i> sequence types, 28 (42%) were assigned to CC17 according to the current PubMLST classification and were reported across 26 studies in six states. Forty-six virulence determinants were mapped, with nine adhesion- and biofilm-associated genes shared across all four contexts.</p> Conclusion <p><i>Enterococcus</i> resistance, virulence, and lineage diversity in Brazil show a structured but unevenly characterised distribution with substantial surveillance gaps relevant to infection control and antimicrobial stewardship. The co-occurrence of PubMLST-assigned CC17 STs and last-resort resistance genes across compartments underscores the need for coordinated genomic surveillance.</p> Graphical Abstract <p>The map gradient indicates the number of included studies per state (darker blue, more studies; grey, no included studies). Context colours are human (blue), animal (green), food (pink), and environmental (amber). The hospital-adapted lineage panel highlights PubMLST-assigned <i>E. faecium</i> CC17 STs reported outside human hospital settings: environmental ST32, ST168, and ST1893 in RJ and ST203 and ST412 in SP; animal ST22, ST25, ST56, and ST1274 in RJ and ST612 in SP; and food ST1336 in SP. Assignments use the clonal_complex field of the original <i>E. faecium</i> MLST scheme in PubMLST, accessed on 5 July 2026. Individual ST-level data are provided in Online Resource 5</p> <p></p>

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Genotypic features of antimicrobial resistance, virulence determinants, and clonal lineages of Enterococcus spp. reported in Brazil: a scoping review with marked regional asymmetry

  • Josiane Trevisol Leal,
  • Matheus Negri Boschiero,
  • Luciana Sartori,
  • Ana Cristina Gales

摘要

Purpose

Vancomycin-resistant Enterococcus faecium is listed in the 2024 WHO Bacterial Priority Pathogens List as a high-priority agent of hospital-acquired infections. Its persistence is supported by marked genomic plasticity across human, animal, food, and environmental sources. We aimed to map antimicrobial resistance genes, virulence determinants, and clonal lineages of Enterococcus spp. reported in Brazil across these four sampling contexts.

Methods

Scoping review following JBI methodological guidance and reported per PRISMA-ScR. Four databases (PubMed, Embase, SciELO, LILACS) were searched without time restrictions in English, Portuguese, and Spanish. Two reviewers screened studies in Rayyan and extracted data using a standardised instrument.

Results

A total of 133 studies (1999 to 2025) were included. Evidence was concentrated in the Southeast and South. Sixty-seven acquired resistance genes and 11 chromosomal mutations were identified across 14 species, predominantly E. faecalis and E. faecium. Twelve broadly reported genes, including vanA, erm(B), and tet(M), spanned all four One Health contexts. Of 67 E. faecium sequence types, 28 (42%) were assigned to CC17 according to the current PubMLST classification and were reported across 26 studies in six states. Forty-six virulence determinants were mapped, with nine adhesion- and biofilm-associated genes shared across all four contexts.

Conclusion

Enterococcus resistance, virulence, and lineage diversity in Brazil show a structured but unevenly characterised distribution with substantial surveillance gaps relevant to infection control and antimicrobial stewardship. The co-occurrence of PubMLST-assigned CC17 STs and last-resort resistance genes across compartments underscores the need for coordinated genomic surveillance.

Graphical Abstract

The map gradient indicates the number of included studies per state (darker blue, more studies; grey, no included studies). Context colours are human (blue), animal (green), food (pink), and environmental (amber). The hospital-adapted lineage panel highlights PubMLST-assigned E. faecium CC17 STs reported outside human hospital settings: environmental ST32, ST168, and ST1893 in RJ and ST203 and ST412 in SP; animal ST22, ST25, ST56, and ST1274 in RJ and ST612 in SP; and food ST1336 in SP. Assignments use the clonal_complex field of the original E. faecium MLST scheme in PubMLST, accessed on 5 July 2026. Individual ST-level data are provided in Online Resource 5