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Antimicrobial Agents and Chemotherapy, September 2001, p. 2450-2454, Vol. 45, No. 9
Medicinal Biology Research Laboratories,
Fujisawa Pharmaceutical Co., Ltd., Osaka,1
and Nagasaki University, Nagasaki,2
Japan
Received 1 December 2000/Returned for modification 22 March
2001/Accepted 31 May 2001
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.9.2450-2454.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Mechanism of Therapeutic Effectiveness of Cefixime against
Typhoid Fever
-Lactams have been considered ineffective against organisms
growing inside mammalian cells because of their poor penetration into
cells. However, cefixime has been shown to be clinically effective
against typhoid fever. The probable mechanism of therapeutic effectiveness of cefixime against typhoid fever was investigated using
Salmonella enterica serovar Typhimurium instead of S. enterica serovar Typhi both in a cellular and in a mouse
infection model. Cefixime was able to inhibit the growth of serovar
Typhimurium inhabiting monocyte-derived THP-1 cells. Elongation of
serovar Typhimurium in THP-1 cells was observed microscopically.
Apparent morphological changes of serovar Typhimurium in THP-1 cells
were also observed by electron microscopy. The concentration of
cefixime inside THP-1 cells was almost half (46 to 48%) of the
concentration outside the cells when serovar Typhimurium coexisted in
the solution. The length of time after oral dosing (8 mg/kg)
that cefixime was present
calculated from levels in serum
at a
concentration above the MIC at which 90% of the serovar Typhi
organisms inside human cells were inhibited was presumed to be more
than 12 h. Cefixime also showed excellent activity in the mouse
systemic and oral infection models based on infections caused by
serovar Typhimurium. It is concluded that a fair amount of
cefixime can enter mammalian cells and inhibit the growth of
bacteria inside cells when the bacteria are sensitive enough to
cefixime, as are serovars Typhimurium and Typhi.
*
Corresponding author. Mailing address: Post-Marketing
Surveillance II, Fujisawa Pharmaceutical Co., Ltd., 1-6, 2-Chome,
Kashima, Yodogawa-ku, Osaka 532-8514, Japan. Phone: (06) 6390-1548. Fax: (06) 6304-1452. E-mail:
yoshimi_matsumoto{at}po.fujisawa.co.jp.
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