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Bactericidal, Bacteriolytic, and Antibacterial Virulence Activities of Boesenbergia pandurata (Roxb) Schltr Extract against Streptococcus pyogenes
Purpose: To determine the anti- Streptococcus pyogenes activity of the chloroform extract of Boesenbergia pandurata (Roxb.) Schltr. (Zingiberaceae) and investigate its possible antibacterial mechanisms of action. Methods: Minimum inhibitory concentration (MIC) and minimum bactericidal concentration...
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Published in: | Tropical journal of pharmaceutical research 2014-01, Vol.12 (6), p.1023 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Purpose: To determine the anti- Streptococcus pyogenes activity of
the chloroform extract of Boesenbergia pandurata (Roxb.) Schltr.
(Zingiberaceae) and investigate its possible antibacterial mechanisms
of action. Methods: Minimum inhibitory concentration (MIC) and minimum
bactericidal concentration (MBC) values were investigated against 47
clinical isolates of S. pyogenes. Time-kill study was performed to
determine how quickly the extract acts on S. pyogenes. The ability of
the extract to damage bacterial cell wall and effects on S. pyogenes
virulence factors including protease enzyme and haemolysin were
investigated. Results: The extract exhibited good antibacterial
activity against all of the clinical isolates of S. pyogenes with
similar MIC and MBC ranging from 3.91-62.50 µg/ml. Complete
killing of the bacterial cells by the extract at concentrations of
4MIC, 2MIC, and MIC occurred within 4, 8, and 12 h, respectively.
Treatment of the bacterial cells with the extract at 2MIC and 4MIC
caused cell lysis. All the test concentrations (1/32 - 1/2MIC) produced
no effects on protease and haemolysin enzymes. Conclusion: Boesenbergia
pandurata extract has powerful in vitro activity against S. pyogenes.
The ability of the extract to lyse the bacterial cells suggests that
the mechanism of action may be associated with cell wall and cell
membrane damage. |
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ISSN: | 1596-5996 1596-9827 |
DOI: | 10.4314/tjpr.v12i6.23 |