Impact of ciprofloxacin and chloramphenicol on the lipid bilayer of staphylococcus aureus: Changes in membrane potential

BioMed Research International

Volumn 2013, Issue , 2013, Pages

  Páez, Paulina L ^a   Becerra, María C ^a   Albesa, Inés ^a  

^a UNIVERSIDAD NACIONAL DE CÓRDOBA   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

8 ANILINO 1 NAPHTHALENESULFONIC ACID; CHLORAMPHENICOL; CIPROFLOXACIN; 1-ANILINO-8-NAPHTHALENESULFONATE; LIPID BILAYER;

ANTIBIOTIC SENSITIVITY; ARTICLE; BACTERIAL CELL; BACTERIAL MEMBRANE; BINDING AFFINITY; BINDING SITE; CONTROLLED STUDY; DISSOCIATION; DRUG BINDING; ELECTRICAL PARAMETERS; ELECTROSTATIC SURFACE POTENTIAL; LIPID BILAYER; MEMBRANE POTENTIAL; MODULATION; NONHUMAN; STAPHYLOCOCCUS AUREUS; DRUG EFFECTS; METABOLISM; MICROBIAL SENSITIVITY TEST; PHYSIOLOGY; DRUG EFFECT;

BACTERIA (MICROORGANISMS); STAPHYLOCOCCUS AUREUS;

ANILINO NAPHTHALENESULFONATES; CHLORAMPHENICOL; CIPROFLOXACIN; LIPID BILAYERS; MEMBRANE POTENTIALS; MICROBIAL SENSITIVITY TESTS; STAPHYLOCOCCUS AUREUS;

EID: 84878705424     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2013/276524     Document Type: Article

References (27)

1. David F., Hebeisen M., Schade G., Franco-Lara E., Di Berardino M., Viability and membrane potential analysis of Bacillus megaterium cells by impedance flow cytometry. Biotechnology & Bioengineering 2012 109 2 483 492
2. Wolf M. K., Konisky J., Increased binding of a hydrophobic, photolabile probe to Escherichia coli inversely correlates to membrane potential but not adenosine 5'-triphosphate levels. Journal of Bacteriology 1981 145 1 341 347 2-s2.0-0019508293 (Pubitemid 11140311)
3. Montero M. T., Pijoan M., Merino-Montero S., Vinuesa T., Hernández-Borrell J., Interfacial membrane effects of fluoroquinolones as revealed by a combination of fluorescence binding experiments and atomic force microscopy observations. Langmuir 2006 22 18 7574 7578 2-s2.0-33748569107 10.1021/la060633c (Pubitemid 44373428)
4. Dinsdale M. G., Lloyd D., Jarvis B., Yeast vitality during cider fermentation: two approaches to the measurement of membrane potential. Journal of the Institute of Brewing 1995 101 6 453 458 10.1002/j.2050-0416.1995.tb00883. x
5. Mason D. J., Allman R., Stark J. M., Lloyd D., Rapid estimation of bacterial antibiotic susceptibility with flow cytometry. Journal of Microscopy 1994 176 1 8 16 2-s2.0-0028033780 (Pubitemid 24352251)
6. Lloyd D., Mason D. J., Suller M. T. E., McCarthy D. A., Macey M. G., Microbial infections. Cytometric Analysis of Cell Phenotype and Function 2001 1st Cambridge, UK Cambridge University Press 2982 3213
7. Lloyd D., Harris J. C., Biagini G. A., Hughes M. R., Maroulis S., Bernard C., Wadley R. B., Edwards M. R., The plasma membrane of microaerophilic protitsts: oxidative and nitrosative stress. Microbiology 2004 150 5 1183 1190 2-s2.0-2942555098 (Pubitemid 38744719)
8. Scott J. A., Rabito C. A., Oxygen radicals and plasma membrane potential. Free Radical Biology and Medicine 1988 5 4 237 246 2-s2.0-0023768432 (Pubitemid 18264467)
9. +) reduce mitochondrial membrane potential and trigger apoptosis in neuronal PC12 cells. Biochemical Society Transactions 1998 26 4 S340 2-s2.0-0032199866
10. Lloyd D., Harris J. C., Maroulis S., Mitchell A., Hughes M. N., Wadley R. B., Edwards M. R., Nitrosative stress induced cytotoxicity in Giardia intestinalis. Journal of Applied Microbiology 2003 95 3 576 583 2-s2.0-0042381392 10.1046/j.1365-2672.2003.02008.x (Pubitemid 37041090)
11. Kohanski M. A., Dwyer D. J., Hayete B., Lawrence C. A., Collins J. J., A common mechanism of cellular death induced by bactericidal antibiotics. Cell 2007 130 5 797 810 2-s2.0-34548213103 10.1016/j.cell.2007.06.049 (Pubitemid 47332566)
12. Albesa I., Becerra M. C., Battán P. C., Páez P. L., Oxidative stress involved in the antibacterial action of different antibiotics. Biochemical and Biophysical Research Communications 2004 317 2 605 609 2-s2.0-1842583592 10.1016/j.bbrc.2004.03.085 (Pubitemid 38452525)
13. Becerra M. C., Páez P. L., Laróvere L. E., Albesa I., Lipids and DNA oxidation in Staphylococcus aureus as a consequence of oxidative stress generated by ciprofloxacin. Molecular and Cellular Biochemistry 2006 285 1-2 29 34 2-s2.0-33646151166 10.1007/s11010-005-9051-0
14. Páez P. L., Becerra M. C., Albesa I., Antioxidative mechanisms protect resistant strains of Staphylococcus aureus against ciprofloxacin oxidative damage. Fundamental and Clinical Pharmacology 2010 24 6 771 776 2-s2.0-78349287753 10.1111/j.1472-8206.2009.00806.x
15. Aiassa V., Barnes A. I., Albesa I., Resistance to ciprofloxacin by enhancement of antioxidant defenses in biofilm and planktonic Proteus mirabilis. Biochemical and Biophysical Research Communications 2010 393 1 84 88 2-s2.0-77249155990 10.1016/j.bbrc.2010.01.083
16. Páez P. L. P., Becerra M. C., Albesa I., Comparison of macromolecular oxidation by reactive oxygen species in three bacterial genera exposed to different antibiotics. Cell Biochemistry and Biophysics 2011 61 3 467 472 10.1007/s12013-011-9227-z
17. Clinical and Laboratory Standards Institute, Performance standards for antimicrobial susceptibility testing, 18th informational supplement, Clinical and Laboratory Standards Institute), p. approved standard M100-S18, Clinical and Laboratory Standards Institute, Wayne, Pennsylvania, 2008
18. Verma I., Rohilla A., Khuller G. K., Alterations in macromolecular composition and cell wall integrity by ciprofloxacin in Mycobacterium smegmatis. Letters in Applied Microbiology 1999 29 2 113 117 2-s2.0-0032832833 10.1046/j.1365-2672.1999.00597.x (Pubitemid 29423826)
19. Robertson D. E., Rottenberg H., Membrane potential and surface potential in mitochondria. Fluorescence and binding of 1-anilinonaphthalene-8-sulfonate. The Journal of Biological Chemistry 1983 258 18 11039 11048 2-s2.0-0021112558
20. Zamzami N., Hirsch T., Dallaporta B., Petit P. X., Kroemer G., Mitochondrial implication in accidental and programmed cell death: apoptosis and necrosis. Journal of Bioenergetics and Biomembranes 1997 29 2 185 193 2-s2.0-0030848374 10.1023/A:1022694131572 (Pubitemid 27314976)
21. Gyulkhandanyan A. V., Feeney C. J., Pennefather P. S., Modulation of mitochondrial membrane potential and reactive oxygen species production by copper in astrocytes. Journal of Neurochemistry 2003 87 2 448 460 2-s2.0-0141884372 10.1046/j.1471-4159.2003.02029.x (Pubitemid 37255252)
22. Dalhoff A., Adam H., Hahn W., Opferkuch W., Interaction of aminoglycosides and ciprofloxacin with bacterial membrane. The Influence of Antibiotics on the Host Parasite Relationship 1985 Berlin, Germany Springer 16 27
23. Lewin C. S., Howard B. M. A., Smith J. T., Protein- and RNA-synthesis independent bactericidal activity of ciprofloxacin that involves the a subunit of DNA gyrase. Journal of Medical Microbiology 1991 34 1 19 22 2-s2.0-0026017127
24. Merino S., Vázquez J. L., Domènech O., Berlanga M., Viñas M., Montero M. T., Hernández-Borrell J., Fluoroquinolone- biomembrane interaction at the DPPC/PG lipid-bilayer interface. Langmuir 2002 18 8 3288 3292 2-s2.0-0037117910 10.1021/la015627p (Pubitemid 35383790)
25. Vázquez J. L., Montero M. T., Merino S., Domènech O., Berlanga M., Viñas M., Hernández-Borrell J., Location and nature of the surface membrane binding site of ciprofloxacin: a fluorescence study. Langmuir 2001 17 4 1009 1014 2-s2.0-0035249616 10.1021/la0008582 (Pubitemid 32252586)
26. Grancelli A., Morros A., Cabañas M. E., Domenech O., Merino S., Vázquez J. L. V., Montero M. T., Hernández-Borrell J., Interaction of 6-fluoroquinolones with dipalmitoylphosphatidylcholine monolayers and liposomes. Langmuir 2002 18 9177 9182 10.1021/la025837h (Pubitemid 35458173)
27. Domenech O., Dufrêne Y. F., Van Bambeke F., Tukens P. M., Mingeot-Leclercq M. P., Interactions of oritavancin, a new semi-synthetic lipoglycopeptide, with lipids extracted from Staphylococcus aureus. Biochimica et Biophysica Acta 2010 1798 10 1876 1885 2-s2.0-77955664812 10.1016/j.bbamem.2010.06.011