Cargando…
Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA)
The antibacterial activity of two bisbenzylisoquinoline alkaloids, tetrandrine (Tet) and demethyltetrandrine (d-Tet), alone and in combination with the antibiotics ampicillin (AMP), azithromycin (AZM), cefazolin (CFZ) and levofloxacin (LEV) against 10 clinical isolates of staphylococcal chromosomal...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264781/ https://www.ncbi.nlm.nih.gov/pubmed/22117171 http://dx.doi.org/10.3390/molecules16129819 |
_version_ | 1783375566238384128 |
---|---|
author | Zuo, Guo-Ying Li, Yang Wang, Tao Han, Jun Wang, Gen-Chun Zhang, Yun-Ling Pan, Wei-Dong |
author_facet | Zuo, Guo-Ying Li, Yang Wang, Tao Han, Jun Wang, Gen-Chun Zhang, Yun-Ling Pan, Wei-Dong |
author_sort | Zuo, Guo-Ying |
collection | PubMed |
description | The antibacterial activity of two bisbenzylisoquinoline alkaloids, tetrandrine (Tet) and demethyltetrandrine (d-Tet), alone and in combination with the antibiotics ampicillin (AMP), azithromycin (AZM), cefazolin (CFZ) and levofloxacin (LEV) against 10 clinical isolates of staphylococcal chromosomal cassette mec (SCCmec) III type methicillin-resistant Staphylococcus aureus (MRSA) was studied. Susceptibility to each agent alone was tested using a broth microdilution method. The chequerboard and time-kill tests were used for the combined evaluations. The minimal inhibitory concentrations/minimal bactericidal concentrations (MICs/MBCs, μg/mL) ranges alone were 64–128/256–1,024 for both Tet and d-Tet. Significant synergies against 90% of the isolates were observed for the Tet/CFZ combination, with their MICs being reduced by 75–94% [fractional inhibitory concentration indices (FICIs) ranged from 0.188 to 0.625], respectively. An additive bactericidal result was also observed for the Tet (d-Tet)/CFZ combination in the time-kill experiments. These results demonstrated that Tet and d-Tet enhanced the in vitro inhibitory efficacy of CFZ. Their potential for combinatory therapy of patients infected with MRSA warrants further pharmacological investigation. |
format | Online Article Text |
id | pubmed-6264781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62647812018-12-10 Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA) Zuo, Guo-Ying Li, Yang Wang, Tao Han, Jun Wang, Gen-Chun Zhang, Yun-Ling Pan, Wei-Dong Molecules Article The antibacterial activity of two bisbenzylisoquinoline alkaloids, tetrandrine (Tet) and demethyltetrandrine (d-Tet), alone and in combination with the antibiotics ampicillin (AMP), azithromycin (AZM), cefazolin (CFZ) and levofloxacin (LEV) against 10 clinical isolates of staphylococcal chromosomal cassette mec (SCCmec) III type methicillin-resistant Staphylococcus aureus (MRSA) was studied. Susceptibility to each agent alone was tested using a broth microdilution method. The chequerboard and time-kill tests were used for the combined evaluations. The minimal inhibitory concentrations/minimal bactericidal concentrations (MICs/MBCs, μg/mL) ranges alone were 64–128/256–1,024 for both Tet and d-Tet. Significant synergies against 90% of the isolates were observed for the Tet/CFZ combination, with their MICs being reduced by 75–94% [fractional inhibitory concentration indices (FICIs) ranged from 0.188 to 0.625], respectively. An additive bactericidal result was also observed for the Tet (d-Tet)/CFZ combination in the time-kill experiments. These results demonstrated that Tet and d-Tet enhanced the in vitro inhibitory efficacy of CFZ. Their potential for combinatory therapy of patients infected with MRSA warrants further pharmacological investigation. MDPI 2011-11-25 /pmc/articles/PMC6264781/ /pubmed/22117171 http://dx.doi.org/10.3390/molecules16129819 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Zuo, Guo-Ying Li, Yang Wang, Tao Han, Jun Wang, Gen-Chun Zhang, Yun-Ling Pan, Wei-Dong Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA) |
title | Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA) |
title_full | Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA) |
title_fullStr | Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA) |
title_full_unstemmed | Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA) |
title_short | Synergistic Antibacterial and Antibiotic Effects of Bisbenzylisoquinoline Alkaloids on Clinical Isolates of Methicillin-Resistant Staphylococcus Aureus (MRSA) |
title_sort | synergistic antibacterial and antibiotic effects of bisbenzylisoquinoline alkaloids on clinical isolates of methicillin-resistant staphylococcus aureus (mrsa) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264781/ https://www.ncbi.nlm.nih.gov/pubmed/22117171 http://dx.doi.org/10.3390/molecules16129819 |
work_keys_str_mv | AT zuoguoying synergisticantibacterialandantibioticeffectsofbisbenzylisoquinolinealkaloidsonclinicalisolatesofmethicillinresistantstaphylococcusaureusmrsa AT liyang synergisticantibacterialandantibioticeffectsofbisbenzylisoquinolinealkaloidsonclinicalisolatesofmethicillinresistantstaphylococcusaureusmrsa AT wangtao synergisticantibacterialandantibioticeffectsofbisbenzylisoquinolinealkaloidsonclinicalisolatesofmethicillinresistantstaphylococcusaureusmrsa AT hanjun synergisticantibacterialandantibioticeffectsofbisbenzylisoquinolinealkaloidsonclinicalisolatesofmethicillinresistantstaphylococcusaureusmrsa AT wanggenchun synergisticantibacterialandantibioticeffectsofbisbenzylisoquinolinealkaloidsonclinicalisolatesofmethicillinresistantstaphylococcusaureusmrsa AT zhangyunling synergisticantibacterialandantibioticeffectsofbisbenzylisoquinolinealkaloidsonclinicalisolatesofmethicillinresistantstaphylococcusaureusmrsa AT panweidong synergisticantibacterialandantibioticeffectsofbisbenzylisoquinolinealkaloidsonclinicalisolatesofmethicillinresistantstaphylococcusaureusmrsa |