Virginiamycin S1
Also known as: Ostreogrycin B (related), Pristinamycin IA (analog), Staphylomycin S1, Virginiamycin S, VS1
Summary
Virginiamycin S1 is the streptogramin B component of the virginiamycin complex, a natural antibiotic mixture produced by Streptomyces virginiae. It is a cyclic hexadepsipeptide that inhibits prokaryotic protein synthesis. Alone it is bacteriostatic, but in combination with the type A component (virginiamycin M1) the mixture is bactericidal. The combination has been used as a growth promotant in livestock and as an agricultural antibiotic; it is closely related to quinupristin, the streptogramin B component of the approved drug quinupristin/dalfopristin (Synercid).
Mechanism of Action
Binds to the 50S ribosomal subunit at the peptidyl transferase center, blocking the exit tunnel and inhibiting elongation and translocation of peptide chains; acts synergistically with streptogramin A components (e.g., virginiamycin M1) to produce irreversible, bactericidal inhibition
Routes of Administration
Goals & Uses
- Gram-positive bacterial infection treatmentAntimicrobialModerate
- MRSA and resistant Gram-positive infectionsAntimicrobial ResistanceLow
- Livestock growth promotionVeterinary/agriculturalHigh
- Ribosomal biology research toolResearchHigh
Contraindications
- Concurrent use with drugs metabolized by CYP3A4Drug InteractionModerate
- Hypersensitivity to streptogramin antibioticsAllergyHigh
Adverse Effects
- HepatotoxicityHepaticUncommonLiver injury or dysfunction
- Arthralgia/myalgiaMusculoskeletalUncommon
- Injection site reactionsLocalCommon
- Gastrointestinal disturbanceGastrointestinalCommon
Drug Interactions
- CYP3A4 substrates (e.g., cyclosporine, tacrolimus, statins)High
- WarfarinModerate
- Chloramphenicol / lincosamidesModerate
Population Constraints
- PregnancyReproductive SafetyRelative
- Hepatic impairmentOrgan FunctionRelative
- Pediatric populationAgeRelative
Regulatory Status
- European UnionWithdrawnVirginiamycin combination as veterinary growth promotant banned in EU since 1999 (Regulation EC No 2821/98) due to cross-resistance concerns with quinupristin/dalfopristin
- United StatesUnapprovedNot approved as a standalone pharmaceutical in the US; virginiamycin combination used in some veterinary/agricultural contexts under USDA/FDA framework
- United KingdomUnapprovedNo approved human pharmaceutical use; agricultural use mirroring EU restrictions post-Brexit
Virginiamycin as a combination product (M1 + S1) has been used as a veterinary/agricultural growth promotant in several countries but has faced bans or restrictions in the EU due to concerns over cross-resistance with quinupristin/dalfopristin. The isolated S1 component alone is not an approved pharmaceutical agent in any major jurisdiction.
Evidence & Sources
No sources recorded yet.