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4 protocols using b uniformis

1

Anaerobic Cultivation of Bacteroides Species

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Bacterial species, B. cellulosilyticus WH2 (42 (link)) received as glycerol stocks from Washington University, St. Louis, B. fragilis NCTC 9343 (ATCC 25285), B. stercoris CC31F (ATCC 43183), and B. uniformis ATCC 8492 were received as glycerol stocks from BEI resources were used as bacterial hosts. All the bacteria were grown in brain-heart infusion media supplemented with 2 mM MgSO4, and 10 mM MgCl2 we denote as BHISMg. Culture plates were supplemented with 1.5 % w/v agar and incubated at 37 for 48 hrs under anaerobic conditions with 5 % H2, 5 % CO2, and 90 % N2. Following incubation, an isolated colony was transferred into a 12 hrs deoxygenated BHISMg broth. Following anaerobic incubation at 37 for 24 hrs the liquid cultures were further sub-cultured into another BHISMg broth and incubated overnight.
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2

Characterization of Bacteroides fragilis Strains

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Bacterial DNA from the 84 feces samples and 192 bacterial isolates was obtained
using, respectively, the commercial QIAmp DNA Stool Mini Kit and QIAmp DNA Mini Kit
(QIAGEN), according to the manufacturer's instructions. DNA was stored at −80 °C
until use.
The presence of B. fragilis in the fecal samples was detected by PCR
amplification with 16S rRNA primers. DNA from the bacterial isolates was amplified
with 16S-23S rRNA primers. All DNA samples positive for B. fragiliswere screened for the presence of ETBF and/or NTBF sequences. The oligonucleotide
pairs and amplification conditions used are described in Table 1.
All PCR assays were performed as follows: 1X PCR buffer, 50 mM MgCl2, 0.2
mM dNTP mix, 0.4 mM each primer, 0.5 U of Platinum Taq polymerase
(Invitrogen), and 1 ng of DNA. PCR products were analyzed by 1% agarose gel
electrophoresis, stained with 0.5 μg/mL of ethidium bromide and photographed under UV
light.
B. fragilis ATCC 43858 (ETBF pattern I, bft+) and ATCC 25285 (NTBF pattern III, bft-) were used, respectively, as positive and negative controls. The other
strains used as controls were: B. thetaiotaomicron ATCC 29741,
B. vulgatus ATCC 8482, B. caccae ATCC 43185,
B. ovatus ATCC 8483, B. eggerthii ATCC 27754,
B. uniformis ATCC 8492, B. stercoris ATCC 43183,
Parabacteroides distasonis ATCC 8503, and P.
merdae
ATCC 43184.
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3

Anaerobic Culture of Bacteroides Species

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Bacteroides species were grown in Tryptone Yeast Glucose broth (TYG) [16 (link)] in an anaerobic chamber (37°C, 5% CO2, 5% H2 and 90% N2) and included B. caccae ATCC 43185T, B. dorei JCM 13471, B. eggerthii ATCC 27754, B. fragilis NCTC 9343, B. finegoldii JCM13345, B. intestinalis JCM 13265, P. merdae ATCC 43184, B. ovatus JCM 5824, B. sartorii A-C2-0, B. stercoris ATCC 43183, B. thetaiotaomicron VPI 5482, B. uniformis JCM 5828T, and B. vulgatus ATCC 8482. Non-Bacteroides species included Prevotella stercorea JCM 13469T grown using Peptone Yeast Glucose broth (PYG, DSMZ Medium 104) and Escherichia coli grown in Luria Bertani broth (LB, BD 244620).
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4

Anaerobic Cultivation of Bacteroides Species

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Bacterial species, B. cellulosilyticus WH2 [33 (link)] received as glycerol stocks from Washington University, St. Louis, B. fragilis NCTC 9343 (ATCC 25285), B. stercoris CC31F (ATCC 43183), and B. uniformis (ATCC 8492) were received as glycerol stocks from BEI resources were used as bacterial hosts. All the bacteria were grown in brain-heart infusion media supplemented with 2 mM MgSO4, and 10 mM MgCl2 we denote as BHISMg. Culture plates were supplemented with 1.5% w/v agar and incubated at 37 °C for 48 h under anaerobic conditions with 5% H2, 5% CO2, and 90% N2. Following incubation, an isolated colony was transferred into a 12 h deoxygenated BHISMg broth. Following anaerobic incubation at 37 °C for 24 h the liquid cultures were further sub-cultured into another BHISMg broth and incubated overnight.
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