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Antibacterial activity of Australian plant extracts against methicillin‐resistant Staphylococcus aureus (MRSA) and vancomycin‐resistant enterococci (VRE)
Author(s) -
Palombo Enzo A.,
Semple Susan J.
Publication year - 2002
Publication title -
journal of basic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.58
H-Index - 54
eISSN - 1521-4028
pISSN - 0233-111X
DOI - 10.1002/1521-4028(200212)42:6<444::aid-jobm444>3.0.co;2-8
Subject(s) - staphylococcus aureus , microbiology and biotechnology , antibacterial activity , methicillin resistant staphylococcus aureus , enterococcus faecalis , enterococcus , biology , traditional medicine , bacteria , medicine , antibiotics , genetics
Ethanolic extracts of five traditional Australian medicinal plants, previously shown to display antibacterial activity against laboratory strains of the Gram positive bacteria Staphylococcus aureus and Enterococcus faecalis , were investigated for their abilities to inhibit clinical isolates of methicillin‐resistant Staphylococcus aureus (MRSA) and vancomycin‐resistant enterococci (VRE). Using plate‐hole diffusion assays, the following results were obtained: (a) extract from the leaves of Eremophila alternifolia ( Myoporaceae ) showed activity against MRSA; (b) extract from the leaves of Acacia kempeana ( Mimosaceae ) showed incomplete inhibition of VRE; (c) extracts from the leaves of Amyema quandong ( Loranthaceae ) and Eremophila duttonii ( Myoporaceae ) were active against both types of bacteria; (d) extract from the stem base of Lepidosperma viscidum ( Cyperaceae ) was active against MRSA and exhibited incomplete inhibition of VRE. All active extracts were evaluated using time‐kill assays. Most of the extracts showed bactericidal effects and reduced the number of viable cells by 4–6 logs within four hours, while the extracts from Acacia kempeana leaves and Lepidosperma viscidum stem base exhibited bacteriostatic activity against VRE. The extract from the leaves of Eremophila duttonii was the most active and reduced the number of viable cells of MRSA and VRE to undetectable levels within 1 hour.