Ract infections in adults and children. It has been shown that the fecal microbiota of adults displays a major shift in dominant species upon an amoxicillin treatment, starting 24 h after antibiotic initiation and persisting during treatment [17,18]. Limited information is ML-281 biological activity available about the effects of oral amoxicillin alone or combined with clavulanic acid on the Bifidobacterium species balance [19]. It seems important to assess whether microbial community composition is resistant, resilient or functionally redundant in response to this disturbance. “Resistance” refers toBifidobacterium Monitoring after AMC Exposurethe ability of a community to maintain a given structure in the setting of a perturbation while “resilience” is the ability of a community to return to its baseline structure following a perturbation in community structure [20]. To date, several molecular methods are available to analyse microbial diversity : fingerprinting methods such as Temporal Temperature Gradient gel Electrophoresis (TTGE) and Denaturing Gradient Gel Electrophoresis (DGGE), molecular inventories (PCR, cloning and sequencing of 16S rRNA genes), and more recently, high throughput sequencing such as pyrosequencing. Considering the number of samples to analyse, molecular inventories were not possible. Pyrosequencing could have been used [21,22]. Nevertheless we decided to use PCR-TTGE since it was less expensive and allowed a greater number of samples to be analysed. 
Indeed, methods such as TTGE and DGGE based on 1662274 sequence-specific separation of 16S rRNA gene amplicons, are among the best methods for rapid high throughput comparison of bacterial communities or bifidobacterial species over time [23,24,25]. In the present study, we explored, on a 76-day period, the quantitative and qualitative changes occurring in total microbiota and also in the Bifidobacterium genus, in 18 adult men after a 5-day amoxicillin-clavulanic acid (AMC) treatment, using specific real-time PCR (qPCR) and PCR-TTGE combined with cloned sequence 194423-15-9 manufacturer analysis.total DNA using the chemical guanidium isothiocyanate and the mechanical bead beating method as previously described [24,26].Real-time PCR for total bacteria and Bifidobacterium quantificationReactions were performed in duplicate in a volume of 25 ml within 96-well twin-tech PCR plates, using the Platinum SYBR Green qPCR SuperMix-UDG (Invitrogen, Cergy Pontoise, France). The forward and reverse primers used were Bia339f, Bia788r for total bacteria [23] and Bif164f, Bif662r for Bifidobacterium genus [27]. Amplifications were performed in a Mastercycler ep Realplex4 (excitation source 470 nm, emission 520/550 nm) (Eppendorf AG, Hamburg, Germany) with the following temperature profile: one cycle at 50uC (2 min) for uracyl-DNA glycosylase action, one cycle at 96uC (2 min), 40 cycles of denaturation at 96uC (15 seconds), primer annealing at 55uC (1 min) for total bacteria and at 62uC (1 min) for bifidobacteria, and elongation step at 68uC (2 min) with fluorescence measure. Finally, the melting curve was made by slowly heating the PCR mixtures from 60 to 96uC (20 min) with simultaneous measurements of the SYBR Green I signal intensities. A standard curve made from known amounts of plasmid DNA containing a 16S rRNA gene insert from E. coli or Bifidobacterium sp. allowed quantifications.Materials and Methods Bacterial strains and growth conditionsThe reference strains used in this study were purchased in lyophilized form from the Pasteur.Ract infections in adults and children. It has been shown that the fecal microbiota of adults displays a major shift in dominant species upon an amoxicillin treatment, starting 24 h after antibiotic initiation and persisting during treatment [17,18]. Limited information is available about the effects of oral amoxicillin alone or combined with clavulanic acid on the Bifidobacterium species balance [19]. It seems important to assess whether microbial community composition is resistant, resilient or functionally redundant in response to this disturbance. “Resistance” refers toBifidobacterium Monitoring after AMC Exposurethe ability of a community to maintain a given structure in the setting of a perturbation while “resilience” is the ability of a community to return to its baseline structure following a perturbation in community structure [20]. To date, several molecular methods are available to analyse microbial diversity : fingerprinting methods such as Temporal Temperature Gradient gel Electrophoresis (TTGE) and Denaturing Gradient Gel Electrophoresis (DGGE), molecular inventories (PCR, cloning and sequencing of 16S rRNA genes), and more recently, high throughput sequencing such as pyrosequencing. Considering the number of samples to analyse, molecular inventories were not possible. Pyrosequencing could have been used [21,22]. Nevertheless we decided to use PCR-TTGE since it was 
less expensive and allowed a greater number of samples to be analysed. Indeed, methods such as TTGE and DGGE based on 1662274 sequence-specific separation of 16S rRNA gene amplicons, are among the best methods for rapid high throughput comparison of bacterial communities or bifidobacterial species over time [23,24,25]. In the present study, we explored, on a 76-day period, the quantitative and qualitative changes occurring in total microbiota and also in the Bifidobacterium genus, in 18 adult men after a 5-day amoxicillin-clavulanic acid (AMC) treatment, using specific real-time PCR (qPCR) and PCR-TTGE combined with cloned sequence analysis.total DNA using the chemical guanidium isothiocyanate and the mechanical bead beating method as previously described [24,26].Real-time PCR for total bacteria and Bifidobacterium quantificationReactions were performed in duplicate in a volume of 25 ml within 96-well twin-tech PCR plates, using the Platinum SYBR Green qPCR SuperMix-UDG (Invitrogen, Cergy Pontoise, France). The forward and reverse primers used were Bia339f, Bia788r for total bacteria [23] and Bif164f, Bif662r for Bifidobacterium genus [27]. Amplifications were performed in a Mastercycler ep Realplex4 (excitation source 470 nm, emission 520/550 nm) (Eppendorf AG, Hamburg, Germany) with the following temperature profile: one cycle at 50uC (2 min) for uracyl-DNA glycosylase action, one cycle at 96uC (2 min), 40 cycles of denaturation at 96uC (15 seconds), primer annealing at 55uC (1 min) for total bacteria and at 62uC (1 min) for bifidobacteria, and elongation step at 68uC (2 min) with fluorescence measure. Finally, the melting curve was made by slowly heating the PCR mixtures from 60 to 96uC (20 min) with simultaneous measurements of the SYBR Green I signal intensities. A standard curve made from known amounts of plasmid DNA containing a 16S rRNA gene insert from E. coli or Bifidobacterium sp. allowed quantifications.Materials and Methods Bacterial strains and growth conditionsThe reference strains used in this study were purchased in lyophilized form from the Pasteur.
