# Dairy Farm Streptococcus agalactiae in a Region of Northeast Brazil: Genetic Diversity, Resistome, and Virulome

**Authors:** Vinicius Pietta Perez, Fernanda Zani Manieri, Luciana Roberta Torini, Carlos Gabriel Andrade Barbosa, Fabio Campioni, Fabiana Caroline Zempulski Volpato, Eloíza Helena Campana, Artur Cezar de Carvalho Fernandes, Afonso Luís Barth, Eduardo Sergio Soares Sousa, Celso Jose Bruno de Oliveira, Ilana Lopes Baratella da Cunha Camargo

PMC · DOI: 10.3390/pathogens15020128 · Pathogens · 2026-01-24

## TL;DR

This study examines the genetic diversity and resistance patterns of Streptococcus agalactiae in Brazilian dairy farms, highlighting the spread of antibiotic resistance and the need for better surveillance.

## Contribution

The study provides new insights into the molecular epidemiology and antimicrobial resistance of S. agalactiae in a specific Brazilian region.

## Key findings

- High genetic diversity was observed among S. agalactiae isolates, but resistance and virulence profiles were homogeneous within herds.
- Tetracycline and macrolide resistance was common, mediated by tetO, ermB, and tetM genes.
- Genome analysis revealed resistance genes in mobile elements and identified ST-103 as a multi-host-adapted lineage.

## Abstract

Streptococcus agalactiae is a major cause of bovine mastitis, which affects the quality and yield of milk. The main strategy for controlling this pathogen on dairy farms is the use of antibiotics. This study investigated the clonality, serotype distribution, antimicrobial susceptibility, and presence of resistance and virulence genes in 46 S. agalactiae isolates obtained from raw bovine milk in northeastern Brazil. Capsular types were determined using multiplex PCR and antibiotic susceptibility profiles were determined using disc diffusion or the gradient strip method. Clonal diversity was evaluated via pulsed-field gel electrophoresis. Eight isolates were sequenced using short- and long-read methods. There was high overall genetic diversity, whereas the resistance and virulence profiles were largely homogeneous within herds. Tetracycline and macrolide resistance was frequent and mediated by tetO and ermB and less frequently by tetM. Genome analysis demonstrated that resistance genes are present in mobile genetic elements that are also present in human isolates, and phylogenomic analyses identified ST-103 as the predominant and multi-host-adapted lineage, whereas ST-91 clustered with the bovine-adapted lineage. These findings expand the molecular epidemiology of S. agalactiae in dairy farms of a region in northeast Brazil and highlight the importance of surveillance strategies for guiding mastitis control and mitigating the spread of antimicrobial resistance.

## Linked entities

- **Genes:** tet(O) (tetracycline resistance ribosomal protection protein Tet(O)) [NCBI Gene 8154417], erm(B) (23S rRNA (adenine(2058)-N(6))-methyltransferase Erm(B)) [NCBI Gene 8154416], tet(M) (tetracycline resistance ribosomal protection protein Tet(M)) [NCBI Gene 8154447]
- **Diseases:** bovine mastitis (MONDO:0025100)
- **Species:** Streptococcus agalactiae (taxon 1311), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, pbsP (plasminogen-binding protein PbsP) [NCBI Gene 66885367] {aka AMM49_02300}, fbsB (fibrinogen-binding surface protein FbsB) [NCBI Gene 66885783] {aka AMM49_04510}, RepA [NCBI Gene 1263208], hylB (hyaluronate lyase) [NCBI Gene 66886121] {aka AMM49_06240}
- **Diseases:** injury to (MESH:D014947), perinatal infections (MESH:D003586), SLV (MESH:D012640), mastitis (MESH:D008413), Streptococcus infections (MESH:D011008), COVID-19 (MESH:D000086382), bacteremia (MESH:D016470), neonatal meningitis (MESH:D007232), TET (MESH:C535269)
- **Chemicals:** MgCl2 (MESH:D015636), aminoglycosides (MESH:D000617), polysaccharide (MESH:D011134), EDTA (MESH:D004492), lincosamides (MESH:D055231), CLI (MESH:D002981), VAN (MESH:D014640), LEV (MESH:D064704), ERY (MESH:D004917), Mueller-Hinton agar (-), S (MESH:D013455), TET (MESH:D013752), glycerol (MESH:D005990), PEN (MESH:D010406), streptogramin B (MESH:D025381), macrolide (MESH:D018942), LZD (MESH:D000069349), Chelex-100 (MESH:C024997), agarose (MESH:D012685), Beta-lactams (MESH:D047090), CHL (MESH:D002701)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Ovis aries (domestic sheep, species) [taxon 9940], Streptococcus sp. 'group B' (species) [taxon 1319], Veillonella nakazawae (species) [taxon 2682456], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Streptococcus agalactiae (species) [taxon 1311], Delphinidae (marine dolphins, family) [taxon 9726], Bos taurus (bovine, species) [taxon 9913]
- **Cell lines:** XM_1 — Xiphophorus hellerii x Xiphophorus maculatus (Hybrid swordtail), Xiphophorus melanoma, Cancer cell line (CVCL_R938)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942680/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942680/full.md

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Source: https://tomesphere.com/paper/PMC12942680