Key words: E. coli O 157: H7, fosfomycin, verotoxin, mouse infection

Similar documents

Key words: Antibiotics, Intestinal bacterial flora, Germfree mouse


VOL. 34 S-2 CHEMOTH8RAPY 913


CHEMOTHERAPY

Key words : 7432-S, Oral cephem, Urinary tract infection Fig. 1. Chemical structure of 7432-S.

CHEMOTHERAPY JUN Citrobacter freundii 27, Enterobacter aerogenes 26, Enterobacter cloacae 27, Proteus rettgeri 7, Proteus inconstans 20, Proteus

CHEMOTHERAPY JUNE 1993 Table 1. Background of patients in pharmacokinetic study

THE JAPANESE JOURNAL OF ANTIBIOTICS 65 6 Dec LVFX 100 mg 3 / mg 2 / LVFX PK PD mg mg 1 1 AUC/MIC

CHEMOTHERAPY JUNE 1986

CHEMOTHERAPY OCT Fig. 1 Chemical structure of CVA-K

Nippon Suisan Gakkaishi 64(4), (1998) Biodegradation of Raw Silk in Seawater Akihiko Nakayama,*1,*3 Yoshihiro Inoue,*2 Yozo Tahara,*2,*4 Shozo


CHEMOTHERAPY aureus 0.10, Enterococcus faecalis 3.13, Escherichia coli 0.20, Klebsiella pneumoniae, Enterobacter spp., Serratia marcescens 0.78, Prote

Fig. 1 Chemical structure of DL-8280

VOL.42 S-1

1272 CHEMOTHERAPY MAR. 1975


988 CHEMOTHERAPY NOV. 1971

CHEMOTHERAPY Fig. 1 Chemical structure of CXM-AX


CHEMOTHERAPY Table 1 Urinary excretion of mezlocillin Fig. 4 Urinary excretion of mezlocillin Fig. 3 Blood levels of mezlocillin

Key words : candidemia, endotoxin, D-arabinitol, Candida antigen, serological examination

明海大学歯学雑誌 37‐2/1.秦泉寺

Table 1. Antibacterial spectrum SBT ABPC ABPC CPZ : sulbactamiampicillin : ampicillin : cefoperazone

Fig.2. Sensitivity distribution of clinical isolates of S. epidermidis (24 strains, 106 CFU/ml) Staphylococcus aureus Staphylococcus epider- midis Ent

Clostridium difficile ciprofloxacin, ofloxacin, norfloxacin Bifidobacterium Lactobacillus Lactobacillus Bacteroides fragilis B. fragilis C. difficile

CHEMOTHERAPY FEB Table 1. Activity of cefpirome and others against clinical isolates


Fig.1 Chemical structure of BAY o 9867


日本消化器外科学会雑誌第31巻第7号

VOL.32 S-7 CHEMOTHERAPY Table 1 MIC of standard strains of CTRX Fig. 2 Cumulative curves of MIC S. aureus (26 strains )

Key words : Adverse reactions, Egg allergy, IgG antibody, Mills allergy, FAST

CHEMOTHERAPY Table 1 Clinical effect of Sultamicillin

Fig. 1 Chemical structure of KW-1070


日本化学療法学会雑誌第51巻第2号

Effects of Isomaltooligosaccharides Intake on Defecation and Intestinal Environment in Healthy Volunteers Toshiyuki KANEKO, Takanobu KOHMOTO, Hiroe KI

CHEMOTHERAPY

Fig. 1 Chemical structure of TE-031 Code number: TE-031 Chemical name: (-) (3R, 4S, 5S, 6R, 7R, 9R, 11R, 12R, 13S, 14R)-4-[(2, 6-dideoxy-3-C-methyl-3-

VOL. 20 NO. 5 CHEMOTHERAPY Methoxy-4-sulfanilamidopyrimidine (OS-3376) Sulfadimethoxine (SDM) Table 1. In vitro antibacterial activities of OS-3

J. Soc. Cosmet. Chem. Jpn. 7-chome, Edogawa-ku, Tokyo 132, Japan 2.1 J. Soc. Cosmet. Chem. Japan. Vol. 31, No


Dec. THE JAPANESE JOURNAL OF ANTIBIOTICS XXXVII (45)

48 皮 膚 第29巻 第1号 昭 和62年2月 第1-b図 第1-a図 第1図Micro Trak法 アッ 皮 細 胞 中あ るいは細 pin point sizeの による 胞 外に,アッ 粒子と 直 接 塗 抹 標本から プル グ リ ー ン に光 プル し てelelnentary る 粒子

semen quality or those without WBC in semen. In the patients with azoospermia and normal FSH levels (normogonadotropic azzospermia), the antibody (IgG

Table 1. Antibacterial activitiy of grepafloxacin and other antibiotics against clinical isolates

CHEMOTHERAPY Fig. 1 Body weight changes of pregnant mice treated orally with AM- 715 Day of sestation

Title 歯性病巣の関連する皮膚疾患におけるビオチンの効用 Author(s) 高橋, 愼一 ; 川島, 淳子 ; 森本, 光明 ; 山根, 源之 Journal, (): - URL Right Posted at the Inst

coccus aureus Corynebacterium sp, Haemophilus parainfluenzae Klebsiella pneumoniae Pseudornonas aeruginosa Pseudomonas sp., Xanthomonas maltophilia, F


CHEMOTHERAPY APR. 1984


過去26年間のスギ花粉飛散パターンのクラスター分析


VOL.39 S-3


Fig. 1 Trends of TB incidence rates for all forms and smear-positive pulmonary TB in Kawasaki City and Japan. Incidence=newly notified cases of all fo

Jan THE JAPANESE JOURNAL OF ANTIBIOTICS XL-1 Table 1. Outline of administering doses, routes and sampling times *: 4 ml/hr/kg Bacillus subtilis

日本消化器外科学会雑誌第24巻第12号

VOL.47 NO.5 Table 1. Susceptibility distribution of Ĉ- lactams against clinical isolates of MRSA MRSA: rnethicillin- resistant Staphylococcus aureus

Key words: Antibodies to Leptospira, Tokyo, Uveitis

CHEMOTHERAPY DEC Table 1 Antibacterial spectra of T-1982, CTT, CMZ, CTX, CPZ and CEZ 106 CFU/ml Note: P; Peptococcus, S; Streptococcus, G; Gaffk

Title 泌尿器科領域に於ける17-Ketosteroidの研究 17-Ketosteroidの臨床的研究 第 III 篇 : 尿 Author(s) 卜部, 敏入 Citation 泌尿器科紀要 (1958), 4(1): 3-31 Issue Date URL

CHEMOTHERAPY

Jpn.J.Leprosy 67, (1998)

<95DB8C9288E397C389C88A E696E6462>

Table 1. Concentration of ritipenem in plasma, gallbladder tissue and bile after ritipenem acoxil administration (200 mg t.i.d., 3 days) N.D.: not det


320 Nippon Shokuhin Kagaku Kogaku Kaishi Vol. /., No.1, -,* -,/ (,**1) 8 * ** *** * ** *** E#ect of Superheated Steam Treatment on the Preservation an

_’£”R‡Ù‡©



Table 1 Characteristics of the study participants in Imari municipal hospital

CHEMOTHERAPY APR Fig. 1 Chemical structure of cefotetan (CTT, YM09330)

日本消化器外科学会雑誌第25巻第11号

CHEMOTHERAPY APR Fig. 2 The inactivation of aminoglycoside antibiotics by PC-904 Fig. 3 Serum concentration of PC-904 (1) Fig. 4 Urinary recover

News from City Hospital




40B: Satoshi Shimai 1 and Shigehiro Fujimoto 2 1 Center for Liberal Arts and Education, Minami-Kyushu University, Miyakonojo,

Endocrinological and statistical analysis of ovarian function in hysterectomized patients Masaya HAYAFUJI, Kazuaki KATAYAMA and Matsuto MOCHIZUKI Depa

_念3)医療2009_夏.indd

8 The Bulletin of Meiji University of Integrative Medicine API II 61 ASO X 11 7 X-4 6 X m 5 X-2 4 X 3 9 X 11 7 API 0.84 ASO X 1 1 MR-angio

JJRM5005/04.短報.責了.indd

VOL. 23 NO. 3 CHEMOTHERAPY 1067 Table 2 Sensitivity of gram positive cocci isolated from various diagnostic materials Table 3 Sensitivity of gram nega

Key words: Surfactant, Tween, Legionella

Fig. 2 Body weight curves rats treated orally with DL-8280 for 4 weeks

Key words: bacterial meningitis, Haemophilus influenzae type b, Streptococcus pneumoniae, rapid diagnosis, childhood

untitled

VOL.35 S-2 CHEMOTHERAPY Table 1 Sex and age distribution Table 2 Applications of treatment with carumonam Table 3 Concentration of carumonam in human

Changes in Electrodermal Activity Associated with Candies and Chewing Gum Chewing Satoshi Beppu, Takeshi Morita*, Susumu Igarashi **, Kanichi Seto* an

The Eevaluation One Bottle Type Silane Coupling Agents Masahiro Aida, Hideo Kanaya, Taira Kobayashi, Keiji Utsugizaki, Yoshizumi Murata, Tohru Hayakaw

untitled

udc-3.dvi

VOL. 40 S- 1 Table 1. Susceptibility of methicillin-resistant Staphylococcus aureus to meropenem Table 2. Coagulase typing of methicillin-resistant St

epidermidis, Enterococcus faecalis, Enterococcus Klebsiella pneumoniae, Proteus mirabilis, indolepositive Proteus spp., Enterobacter spp., Serratia

Transcription:

Key words: E. coli O 157: H7, fosfomycin, verotoxin, mouse infection

Table 1. Bacterial cell counts in feces of mice infected with Esclwrichia coli O 157: H7 NK2 before and during oral dosing with fosfomycin for 6 days

Table 2. Bacterial cell counts in feces of mice infected with Escherichia coli O157: H7 NK2 after the final oral dosing with fosfomycin Mice nos. 1 to 3 were treated with 1,200 mg/kg/day of fosfomycin and nos. 4 to 6 were not treated CFU/g N.D.: <2.0 ~ 10 Table 3. Bacterial cell counts and verotoxin in the intestinal contents of Escherichia coil O157: H7-infected mice sacrificed 7 days after the final fosfomycin treatment Mice nos. 1 to 3 were treated with 1,200 mg/kg/day of fosfomycin and nos. 4 to 6 were not treated CFU/g N.D.: <78 ng/g VT1, VT2: verotoxin 1, verotoxin 2 Table 4. Fosfomycin concentrations in feces and intestinal contents of mice infected with Escherichia call O157: H7 Mice lios. 1 to 3 were treated with 1,200 mg/kg/day of fosfomycin and nos. 4 to 6 were not treated N.L.: < 25

3) Walterspiel J N, Ashkenazi S, Morrow A L, et al.: Effect of subinhibitory concentrations of antibiotics extracellular shiga-like toxin I. Infection 20: 25 29, 1992 5) Forbes B A, Granato P A: Processing specimens for bacteria. In Manual of Clinical Microbiology 6th ed. (Murray P R et al. ed.), p.265-281, American Society for Microbiology, Washington D. C., 1995 6) March S B, Ratnam S: Latex agglutination test for derection of Escherichia coli serotype 0157. J Clin Microbiol. 27: 1675 `1677, 1989

Therapeutic effect of fosfomycin against interstinal infection with Escherichia coli Intetsu Kobayashi1), Hiroe Muraoka1), Kaoru Matsuzaki1), Takeshi Saika1), Minoru Nishida1), Hironobu Akita2), Satoshi Iwata3) Yoshitake Sato4), Keisuke Sunakawa5) ) Chemotherapy Division, Mitsubishi-Kagaku Bio-Clinical Laboratories, Shimura 3-30-1, Itahashi-ku, Tokyo 174-8555, Japan ) Department of Pediatrics, St. Marianna University, Yokohama City Seibu Hospital ) Department of Pediatrics, Kasumigaura National Hospital ) Ota General Hospital National Tokyo Medical Center (Department of Infectious Disease, School of Medicine, Kitasato University) The therapeutic effect of fosfomycin at a large oral dose against intestinal infection with Escherichia coli O157: H7 was investigated in a mouse model previously described. Three ICR strain (IQI, germ free) mice aged 5 weeks were challenged orally with a verotoxin-producing strain NK2 of E. coli O157: H7. The high levels of viable cells, 3.0 X 101"-3.4 X 10 CFU/g, were excreted into the feces of the untreated mice for 3-10 days after bacterial challenge. Fosfomycin was given at an oral dose of 600 mg/kg twice a day for 6 days to 3 mice infected with E. coli 0157: H7, beginning 3 days after the challenge, to investigate changes in viable cell counts and to measure fecal concentrations of fosfomycin. Results were that the viable cells decreased markedly, (from about 1010 CFU/g before dosing) to 10-10' CFU/g on day 1 of dosing, and no viable cells were detected in the feces from day 2 of dosing onwards. During the period, no verotoxin was detected in fecal samples collected from all 6 test mice (including 3 control mice). Concentrations of fosfomycin in the feces after dosing were 34.6-47.4 Đg/g in all the mice on day 1 of dosing, and 62.4 and 131.1 in 2 of the mice on day 6 after dosing, but nondetectable otherwise. These results suggested that a marked decrease in viable cells without the liberation of verotoxin was observed in the feces of infected mice after fosfomycin was given orally in a massive dose.