# Antimicrobial Resistance in Rhodococcus equi and the Promise of Synergistic Therapies

**Authors:** Farzaneh Javadimarand, Pablo Castañera, Blanca Lorente-Torres, Negar Mortazavi, Jesús Llano-Verdeja, Sergio Fernández-Martínez, Helena Á. Ferrero, Luis M. Mateos, Álvaro Mourenza, Michal Letek

PMC · DOI: 10.3390/antibiotics15030313 · Antibiotics · 2026-03-19

## TL;DR

This paper reviews antimicrobial resistance in Rhodococcus equi and explores new synergistic therapies to improve treatment outcomes.

## Contribution

The paper highlights novel synergistic strategies and molecular insights to combat multidrug resistance in R. equi.

## Key findings

- Multidrug resistance in R. equi involves mutations, efflux pumps, and biofilm formation.
- Synergistic therapies, including optimized antibiotic combinations, show promise in enhancing antibacterial efficacy.
- Molecular tools and experimental models reveal bacterial responses to oxidative and antibiotic stress.

## Abstract

Rhodococcus equi is an opportunistic intracellular pathogen responsible for severe pneumonia in foals and has emerged as an important cause of infection in immunocompromised humans. The treatment of R. equi infections in foals relies mainly on the combination of macrolides and rifampin. However, the increasing incidence of multidrug-resistant (MDR) isolates has raised significant therapeutic challenges. The mechanisms underlying this resistance include mutations in target genes, activation of efflux pumps, and biofilm formation, which collectively compromise the efficacy of conventional antibiotics. Recently, growing concern over antibiotic failure has accelerated research into alternative and synergistic strategies to enhance antibacterial efficacy and reduce the development of resistance. Natural and synthetic compounds, as well as optimized antibiotic combinations, have shown promising synergistic effects by enhancing intracellular accumulation, disrupting redox homeostasis, or inhibiting efflux systems. Experimental models employing checkerboard and time-kill assays, as well as redox-sensitive biosensors, have demonstrated that certain antibiotic combinations can influence bacterial susceptibility to antibiotic exposure. Furthermore, integrating molecular tools provides valuable insight into bacterial responses to oxidative and antibiotic stress, paving the way for novel therapeutic designs. This review summarizes the current understanding of the molecular factors contributing to antimicrobial resistance in R. equi and assesses new therapeutic approaches aimed at overcoming these challenges. It highlights recent findings on strategies to improve treatment outcomes and manage antimicrobial resistance.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249)

## Full-text entities

- **Genes:** VapA [NCBI Gene 1238336]
- **Diseases:** mycobacterial (MESH:C564468), R. equi (MESH:C580424), Infection (MESH:D007239), injury to (MESH:D014947), HIV/AIDS (MESH:D015658), pyogranulomatous bronchopneumonia (MESH:D001996), pulmonary infection (MESH:D012141), blood infections (MESH:D000086982), abscesses (MESH:D000038), R. equi infection (MESH:C000656949), R. equi pneumonia (MESH:D011014), cytotoxicity (MESH:D064420), marrow suppression (MESH:D001855), respiratory distress (MESH:D012128), pulmonary lesions (MESH:D008171), AMR (MESH:D060467), opportunistic infections (MESH:D009894), malakoplakia (MESH:D008287), dehydration (MESH:D003681), arthropathy (MESH:D007592), weight loss (MESH:D015431), fever (MESH:D005334), diarrhoea (MESH:D003967), cavitary lesions (MESH:C566924), colitis (MESH:D003092), granuloma (MESH:D006099), MDR (MESH:D018088), tubercular (MESH:D014390), granulomatous inflammation (MESH:D007249)
- **Chemicals:** Cyclic peptides (MESH:D010456), morusin (MESH:C057451), hydrogen (MESH:D006859), isoniazid (MESH:D007538), Curcumin (MESH:D003474), amikacin (MESH:D000583), MXene (MESH:C000723374), nitric oxide (MESH:D009569), HDT (-), cholesterol (MESH:D002784), meropenem (MESH:D000077731), gentisaldehyde (MESH:C112784), nitrate (MESH:D009566), oxygen (MESH:D010100), citral (MESH:C007076), 1,3-beta-glucan (MESH:C033363), terpenoids (MESH:D013729), Tetracyclines (MESH:D013754), geraniol (MESH:C007836), rifampicin (MESH:D012293), chloramphenicol (MESH:D002701), Azithromycin (MESH:D017963), heavy metal (MESH:D019216), enrofloxacin (MESH:D000077422), pyridomycin (MESH:C458999), mycolic acid (MESH:D009171), Poly(propylene sulfide) (MESH:C522256), hapalindole A (MESH:C568209), trans-cinnamaldehyde (MESH:C012843), PLGA (MESH:D000077182), berberine (MESH:D001599), nitrite (MESH:D009573), ginkgolic acid (MESH:C112485), gamithromycin (MESH:C552399), tildipirosin (MESH:C576258), Amoxicillin-clavulanate (MESH:D019980), phloroglucinaldehyde (MESH:C535196), Carbapenems (MESH:D015780), rifabutin (MESH:D017828), agar (MESH:D000362), rifamycin (MESH:C023808), beta-lactam (MESH:D047090), Lipid (MESH:D008055), clarithromycin (MESH:D017291), streptogramin B (MESH:D025381), ciprofloxacin (MESH:D002939), Macrolide (MESH:D018942), ERY (MESH:D004917), carvacrol (MESH:C073316), Doxycycline (MESH:D004318), ROS (MESH:D017382), lassomycin (MESH:C000595674), penicillin (MESH:D010406), H2O2 (MESH:D006861), Glu (MESH:D018698), Vancomycin (MESH:D014640), dichloromethane (MESH:D008752), Fluoroquinolones (MESH:D024841), methanol (MESH:D000432), isoliquiritigenin (MESH:C040920)
- **Species:** Bdellovibrio sp. ETA (species) [taxon 242951], Bos taurus (bovine, species) [taxon 9913], Prescottella equi (species) [taxon 43767], Nocardia (genus) [taxon 1817], Mus musculus (house mouse, species) [taxon 10090], Mycolicibacterium fortuitum (species) [taxon 1766], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Cervus elaphus (red deer, species) [taxon 9860], Rhodococcus (genus) [taxon 1827], Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773], Capra hircus (domestic goat, species) [taxon 9925], Mycobacteroides chelonae (species) [taxon 1774], Bacillus sp. CG (species) [taxon 1196795], Equus caballus (domestic horse, species) [taxon 9796], Suidae (boars, family) [taxon 9821], Mycobacterium tuberculosis variant bovis (biotype) [taxon 1765], Mycobacteroides abscessus (species) [taxon 36809]
- **Mutations:** Ser531Phe, Asp87 Gly
- **Cell lines:** THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006)

## Full text

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## References

183 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023593/full.md

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Source: https://tomesphere.com/paper/PMC13023593