Sociedad Americana de Hirudoterapia

RK22 Antimicrobial Peptide (MRSA-Active)

11-mer antimicrobial peptide RK22 from Hirudinaria manillensis salivary-gland transcriptome — Lu 2023 demonstrates MRSA killing + biofilm eradication.

Preclínico / mecanísticoLast updated: 2026-05-28 · Reviewed by ASH Editorial Board
Molecular weight of RK22 Antimicrobial Peptide (MRSA-Active) compared with other characterized leech-derived compoundsHementerin80 kDaHementin80 kDaHementin-Like Protein (HLP-1)80 kDaLeech Collagenase70 kDaHaemadipsa yanyuanensis Progr…70 kDaLeech Apyrase67 kDaCalin65 kDaHyaluronidase60 kDaAntithrombin III binding prot…58 kDaCollagenolytic Fibrinolysin55 kDaLeech Thrombospondin-Like Pro…50 kDaRK22 Antimicrobial Peptide (M…1.4 kDa
Molecular weight (kilodaltons) of RK22 Antimicrobial Peptide (MRSA-Active) (highlighted) alongside other characterized leech salivary compounds. Smaller proteins/peptides generally diffuse and act faster.

Mechanistic Evidence Box

Preclinical / mechanistic
Page type
Compound profile
Evidence type
11-mer antimicrobial peptide RK22 from Hirudinaria manillensis salivary-gland transcriptome — Lu 2023 demonstrates MRSA killing + biofilm eradication.
Evidence level
Preclinical (animal)
Drug vs leech
Synthetic analog
Safety domains
Antibiotic stewardship · Aeromonas infection

Clinical translation limit

RK22's antimicrobial activity in vitro + animal MRSA model does NOT establish clinical efficacy in humans. No FDA-approved derivative; H. manillensis is not on the FDA K040187 cleared device species list.

Molecular Profile

Category
Antimicrobial
Evidence tier
Preclinical
Molecular weight
1,400 Da
Source species
Hirudinaria manillensis
Discovered
2023 · Lu X et al.
RK22 Antimicrobial Peptide (MRSA-Active) molecular structure

Biological Targets

  • Staphylococcus aureus (incl. methicillin-resistant strains); biofilm matrix

Key Citations

  1. Lu X et al. (2023), Int J Mol Sci · PMID 37686259

External Resources

    Related Antimicrobial Compounds

    Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.