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The CM1032 is a laboratory centrifuge designed for general purpose applications. It features a robust construction and can accommodate a variety of sample tubes and microplates. The centrifuge provides consistent and reliable performance to meet the needs of various laboratory workflows.

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4 protocols using cm1032

1

Bacterial Strains Preparation and Validation

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Two bacterial strains were used for this study, S. aureus ATCC 29213 and P. aeruginosa S0599 (internal reference). These bacteria were stored at −80 °C in glycerol-BHI (VWR 24388.295; Brain Heart Infusion, Oxoid CM1032). Bacterial strains were revived by inoculating 10 µl into BHI broth (Oxoid) and incubated at 37 °C overnight and under agitation (Unimax 2010; Heidolph) to obtain 108–109 CFU ml−1. Ten microlitres of the solution was spread on plate count agar (PCA, 3564475; Bio-Rad) to control the purity of the bacterial strains and the absence of contamination.
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2

Enrichment and Isolation of E. coli from Swab Samples

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On the same day, each swab sample was enriched with 10 mL of Buffered Peptone Water (BPW, Oxoid, CM0509, Basingstoke, Hampshire, England), homogenized by a Masticator (IUL instruments, S.A., Barcelona, Spain) and incubated for 24 h at 37 °C for the detection of E. coli. After incubation, 10 μL of the BPW fraction was plated on Rapid’E. coli 2 agar plates (Bio-Rad, 356–4024, Marnes-la-Coquette, France) and incubated at 44 °C for 24 h. From each positive Rapid’E. coli 2 plate one isolate was purified and stored at − 80 °C on brain heart infusion (BHI, Oxoid, CM1032) supplemented with 15% (v/v) glycerol. In total, 67 and 183 E. coli isolates were obtained during the longitudinal study at the broiler pilot farm and the experimental pig farm, respectively.
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3

Culturing Fusobacterium nucleatum

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F. nucleatum (ATCC 10953) was grown on heart infusion (HI) agar, containing HI broth (Oxoid, CM1032, Thebarton, SA, Australia), 0.5% haemin (Sigma-Aldrich, 51280, Bayswater, VIC, Australia) and 1% bacteriological agar (Oxoid, LP0011, Thebarton, SA, Australia). The culture was grown in anaerobic conditions using anaerobic generating sachets (AnaeroGenTM 2.5L, AN0025A, Oxoid, Thebarton, SA, Australia) at 37 °C for 48 h.
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4

Rapid E. coli Isolation Protocol

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After sampling, swabs were transported to the lab in a cool box with ice packs. Upon their arrival in the lab (± 2 h after sampling), 10 mL of Buffered Peptone Water (BPW, Oxoid, CM0509, Basingstoke, Hampshire, England) was immediately added to each sample, homogenized by a Masticator (IUL instruments, S.A., Barcelona, Spain) and incubated for 24 h at 37 °C for enrichment of E. coli. After incubation, 10 μL of the enriched BPW fraction was plated on Rapid’E. coli 2 agar plates (Biorad, 356–4024, Marnes-la-Coquettes, France) and incubated at 44 °C for 24 h. From positive Rapid’E. coli 2 plates purified isolates were obtained and stored at − 80 °C on brain heart infusion (BHI, Oxoid, CM1032) supplemented with 15% (v/v) glycerol.
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