A new evolutionary variant of the streptogramin A resistance protein, Vga(A)LC, from Staphylococcus haemolyticus with shifted substrate specificity towards lincosamides
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
N01-AI-95359
NIAID NIH HHS - United States
PubMed
17015629
PubMed Central
PMC1693986
DOI
10.1128/aac.00799-06
PII: AAC.00799-06
Knihovny.cz E-zdroje
- MeSH
- bakteriální geny MeSH
- bakteriální proteiny chemie genetika metabolismus fyziologie MeSH
- DNA bakterií genetika izolace a purifikace MeSH
- genetická variace * MeSH
- lidé MeSH
- linkosamidy MeSH
- makrolidy farmakologie MeSH
- mikrobiální testy citlivosti MeSH
- mnohočetná bakteriální léková rezistence MeSH
- molekulární evoluce * MeSH
- sekvence aminokyselin MeSH
- sekvence nukleotidů MeSH
- sekvenční analýza DNA MeSH
- Staphylococcus aureus účinky léků genetika MeSH
- Staphylococcus haemolyticus účinky léků genetika izolace a purifikace MeSH
- streptogramin A farmakologie MeSH
- substituce aminokyselin MeSH
- substrátová specifita MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- srovnávací studie MeSH
- Názvy látek
- bakteriální proteiny MeSH
- DNA bakterií MeSH
- linkosamidy MeSH
- makrolidy MeSH
- streptogramin A MeSH
We found a new variant of the streptogramin A resistance gene, vga(A)LC, in clinical isolates of Staphylococcus haemolyticus resistant to lincomycin and clindamycin but susceptible to erythromycin and in which no relevant lincosamide resistance gene was detected. The gene vga(A)LC, differing from the gene vga(A) at the protein level by seven amino acid substitutions, was present exclusively in S. haemolyticus strains resistant to both lincosamides and streptogramin A (LS(A) phenotype). Antibiotic resistance profiles of the ATP-binding cassette (ABC) proteins Vga(A)(LC) and Vga(A) in the antibiotic-susceptible host S. aureus RN4220 were compared. It was shown that Vga(A)LC conferred resistance to both lincosamides and streptogramin A, while Vga(A) conferred significant resistance to streptogramin A only. Detailed analysis of the seven amino acid substitutions, distinguishing the two related ABC proteins with different substrate specificities, identified the substrate-recognizing site: four clustered substitutions (L212S, G219V, A220T, and G226S) in the spacer between the two ATP-binding cassettes altered the substrate specificity and constituted the lincosamide-streptogramin A resistance phenotype. A transport experiment with radiolabeled lincomycin demonstrated that the mechanism of lincosamide resistance in S. haemolyticus was identical to that of the reported macrolide-streptogramin B resistance conferred by Msr(A).
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Structural basis for antibiotic resistance mediated by the Bacillus subtilis ABCF ATPase VmlR
Mutasynthesis of lincomycin derivatives with activity against drug-resistant staphylococci
