Fifteen healthy adult volunteers received in their drinking water a lower Escherichia coli phage T4 dose (10(3) PFU/ml), a higher phage dose (105 PFU/ml), and placebo. Fecal coliphage was detected in a dose-dependent way in volunteers orally exposed to phage. All volunteers receiving the higher phage dose showed fecal phage 1 day after exposure; this prevalence was only 50% in subjects receiving the lower phage dose. No fecal phage was detectable a week after a 2-day course of oral phage application. Oral phage application did not cause a decrease in total fecal E. coli counts. In addition, no substantial phage T4 replication on the commensal E. coli population was observed. No adverse events related to phage application were reported. Serum transaminase levels remained in the normal range, and neither T4 phage nor T4-specific antibodies were observed in the serum of the subjects at the end of the study. This is, to our knowledge, the first safety test in the recent English literature which has measured the bioavailability of oral phage in humans and is thus a first step to the rational evaluation of phage therapy for diarrheal diseases.
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BABALOVA E G, 1968, Zhurnal Mikrobiologii Epidemiologii i Immunobiologii, V45, P143
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RUHR UNIV BOCHUM,ST JOSEF HOSP,KINDERKLIN,INST MED MICROBIOL & VIROL,D-4630 BOCHUM,FED REP GERRUHR UNIV BOCHUM,ST JOSEF HOSP,KINDERKLIN,INST MED MICROBIOL & VIROL,D-4630 BOCHUM,FED REP GER
BRUSSOW, H
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WERCHAU, H
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WERCHAU, H
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LIEDTKE, W
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LIEDTKE, W
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LERNER, L
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LERNER, L
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MIETENS, C
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MIETENS, C
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SIDOTI, J
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SOTEK, J
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RUHR UNIV BOCHUM,ST JOSEF HOSP,KINDERKLIN,INST MED MICROBIOL & VIROL,D-4630 BOCHUM,FED REP GERRUHR UNIV BOCHUM,ST JOSEF HOSP,KINDERKLIN,INST MED MICROBIOL & VIROL,D-4630 BOCHUM,FED REP GER
BRUSSOW, H
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WERCHAU, H
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WERCHAU, H
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LIEDTKE, W
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RUHR UNIV BOCHUM,ST JOSEF HOSP,KINDERKLIN,INST MED MICROBIOL & VIROL,D-4630 BOCHUM,FED REP GERRUHR UNIV BOCHUM,ST JOSEF HOSP,KINDERKLIN,INST MED MICROBIOL & VIROL,D-4630 BOCHUM,FED REP GER
LIEDTKE, W
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LERNER, L
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MIETENS, C
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SIDOTI, J
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SIDOTI, J
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