TY - JOUR
T1 - Antibacterial activity of highly negative charged polyoxotungstates, K 27[KAs4W40O140] and K 18[KSb9W21O86], and Keggin-structural polyoxotungstates against Helicobacter pylori
AU - Inoue, Miyao
AU - Segawa, Keiko
AU - Matsunaga, Sae
AU - Matsumoto, Nobuhiro
AU - Oda, Mayumi
AU - Yamase, Toshihiro
PY - 2005/5
Y1 - 2005/5
N2 - The antibacterial activity of polyoxometalates (PMs) against Helicobacter pylori was investigated based on determinations of minimum inhibitory concentration (MIC) and fractional inhibitory concentration (FIC), time-killing of the bacteria, bacterial morphology and PM-uptake into the bacteria cell. The result of MIC values revealed that, of 13 PMs used in this study, highly negative-charged polyoxotungstates, such as K27[KAs4W 40O140] and K18[KSb9W 21O86], and Keggin-structural polyoxotungstates exhibited a potent antibacterial activity with the MIC values of less than 256 μg/ml. The former was the most active, and superior to metronidazole (MTZ) against MTZ-susceptible and resistant strains and also to clarithromycin (CLR) against CLR-resistant strains. In contrast, most of polyoxomolybdates showed little antibacterial activity with the MIC values of more than 256 μg/ml. The result of FIC index values indicated that the antibacterial polyoxotungstates had partially synergistic effect in combination with MTZ and CLR but indifferent effect in combination with amoxicillin (AMX). From the results of the time-killing and scanning elctron microscope images, K27[KAs 4W40O140] and K18[KSb 9W21O86] proved the concentration-dependent bactericidal activity with the morphological change from bacillary form to coccoid form, while Keggin-structural K5[SiVVW 11O40] showed the bacteriostatic activity with small change of morphology to coccoid form. The fluorescent X-ray analysis demonstrated that these polyoxotungstates were taken into the bacteria cell. It is pointed out that the Keggin-structure and/or high negativity polyoxotungstates are an important factor for the antibacterial activity against H. pylori.
AB - The antibacterial activity of polyoxometalates (PMs) against Helicobacter pylori was investigated based on determinations of minimum inhibitory concentration (MIC) and fractional inhibitory concentration (FIC), time-killing of the bacteria, bacterial morphology and PM-uptake into the bacteria cell. The result of MIC values revealed that, of 13 PMs used in this study, highly negative-charged polyoxotungstates, such as K27[KAs4W 40O140] and K18[KSb9W 21O86], and Keggin-structural polyoxotungstates exhibited a potent antibacterial activity with the MIC values of less than 256 μg/ml. The former was the most active, and superior to metronidazole (MTZ) against MTZ-susceptible and resistant strains and also to clarithromycin (CLR) against CLR-resistant strains. In contrast, most of polyoxomolybdates showed little antibacterial activity with the MIC values of more than 256 μg/ml. The result of FIC index values indicated that the antibacterial polyoxotungstates had partially synergistic effect in combination with MTZ and CLR but indifferent effect in combination with amoxicillin (AMX). From the results of the time-killing and scanning elctron microscope images, K27[KAs 4W40O140] and K18[KSb 9W21O86] proved the concentration-dependent bactericidal activity with the morphological change from bacillary form to coccoid form, while Keggin-structural K5[SiVVW 11O40] showed the bacteriostatic activity with small change of morphology to coccoid form. The fluorescent X-ray analysis demonstrated that these polyoxotungstates were taken into the bacteria cell. It is pointed out that the Keggin-structure and/or high negativity polyoxotungstates are an important factor for the antibacterial activity against H. pylori.
KW - Antibacterial activity
KW - Helicobacter pylori
KW - Highly negative charge
KW - Keggin structure
KW - Polyoxotungstates
UR - http://www.scopus.com/inward/record.url?scp=17044388244&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=17044388244&partnerID=8YFLogxK
U2 - 10.1016/j.jinorgbio.2005.01.010
DO - 10.1016/j.jinorgbio.2005.01.010
M3 - Article
C2 - 15833325
AN - SCOPUS:17044388244
SN - 0162-0134
VL - 99
SP - 1023
EP - 1031
JO - Journal of Inorganic Biochemistry
JF - Journal of Inorganic Biochemistry
IS - 5
ER -