Metagenomic analysis of the impact of nitrofurantoin treatment on the human faecal microbiota

Author:

Vervoort Jascha12,Xavier Basil Britto12,Stewardson Andrew34,Coenen Samuel12,Godycki-Cwirko Maciek5,Adriaenssens Niels12,Kowalczyk Anna5,Lammens Christine12,Harbarth Stephan3,Goossens Herman12,Malhotra-Kumar Surbhi12

Affiliation:

1. 1  Department of Medical Microbiology, Universiteit Antwerpen, Antwerp, Belgium

2. 2  Vaccine & Infectious Disease Institute, Universiteit Antwerpen, Antwerp, Belgium

3. 3  Infection Control Program, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland

4. 4  Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia

5. 5  Centre for Family and Community Medicine, Medical University of Lodz, Lodz, Poland

Abstract

Abstract Objectives The objective was to study changes in the faecal microbiota of patients with uncomplicated urinary tract infections (UTIs) treated with nitrofurantoin and of non-treated healthy controls using 16S rRNA analysis. Methods Serial stool samples were collected from patients receiving nitrofurantoin treatment at different timepoints [before treatment (day 1; T1), within 48 h of end of treatment (days 5–15; T2) and 28 days after treatment (days 31–43; T3)], as well as from healthy controls. Direct DNA extraction (PowerSoil DNA Isolation Kit, MoBio Laboratories, Carlsbad, CA, USA) from stool samples was followed by pyrosequencing (454 GS FLX Titanium) of the V3–V5 region of the bacterial 16S rRNA gene. Results Among UTI patients, mean proportions of the Actinobacteria phylum increased by 19.6% in the first follow-up sample (T2) in comparison with the pretreatment baseline stool sample (T1) (P = 0.026). However, proportions of Actinobacteria reversed to ‘normal’ pre-antibiotic levels, with a mean difference of 1.0% compared with baseline proportions, in the second follow-up sample (T3). The increase in Actinobacteria was specifically due to an increase in the Bifidobacteriaceae family (Bifidobacterium genus), which constituted 81.0% (95% CI ±7.4%) of this phylum. Conclusions No significant impact was observed other than a temporary increase in the beneficial Bifidobacterium genus following nitrofurantoin treatment, which supports its reintroduction into clinical use.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

Reference18 articles.

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2. The pharmacokinetics of nitrofurantoin and its related bioavailability;Conklin;Antibiot Chemother,1978

3. Nitrofurantoin: mechanism of action and implications for resistance development in common uropathogens;McOsker;J Antimicrob Chemother,1994

4. Isolation of nitrofurantoin-resistant mutants of nitroreductase-producing Clostridium sp. strains from the human intestinal tract;Rafii;Antimicrob Agents Chemother,1998

5. An in vitro deletion in ribE encoding lumazine synthase contributes to nitrofurantoin resistance in Escherichia coli;Vervoort;Antimicrob Agents Chemother,2014

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