8 research outputs found
Distribution (%) of MIC values (in µg/mL) of group n°2 antimicrobials.
<p>MICs of marbofloxacin, danofloxacin, gamithromycin, tildipirosin, tulathromycin, valnemulin for 27 <i>M. bovis</i> strains isolated in 1978–1979 (white bars) and 30 <i>M. bovis</i> strains isolated in 2010–2012 (black bars). When available, CLSI breakpoints for bovine <i>Pasteurellaceae</i> are given under the X axis: - strains with MIC values less than or equal to the dilution indicated in the dotted-line arrow are susceptible, - strains with MIC values greater than the dilution indicated in the full-line arrow are resistant, all other strains are intermediate.</p
Distribution (%) of MIC values (in µg/mL) of group n°1 antimicrobials.
<p>MICs of tylosin, tilmicosin, spectinomycin, oxytetracycline and florfenicol for 27 <i>M. bovis</i> strains isolated in 1978–1979 (white bars) and 46 isolated in 2010–2012 (black bars). MICs of enrofloxacin, for 27 <i>M. bovis</i> strains isolated in 1978- 1979 (white bars) and 143 <i>M. bovis</i> strains isolated in 2010–2012 (black bars). When available, CLSI breakpoints for bovine <i>Pasteurellaceae</i> are given under the X axis: - strains with MIC values less than or equal to the dilution indicated in the dotted-line arrow are susceptible, - strains with MIC values greater than the dilution indicated in the full-line arrow are resistant, - all other strains are intermediate.</p
Variation in <i>Mmm</i> colony opacity associated to antigenic variation of the glucose PTS permease.
<p><b>A: </b><i>Mmm</i> strain Afadé colonies on PPLO supplemented agar observed under stereomicroscope with indirect light. <b>B:</b> Colony-blotting performed from the same plate using the 3F3 monoclonal antibody. (Magnification: x10).</p
Exopolysaccharide (EPS) secretion by <i>Mmm</i> strain Afadé in supplemented PPLO broth and CMRL-1066 medium.
<p>EPS extracted either from <i>Mmm</i> culture (Afadé) or from unseeded medium used as negative control (Neg) were spotted onto a nylon membrane and either stained with a glycoprotein detection reagent (<b>A</b>) or immunodetected using a serum from a CBPP-positive bovine (<b>B</b>).</p
PG1<sup>T</sup> colony opacity is related to the presence of capsular material.
<p><b>A:</b> Colony morphology of PG1<sup>T</sup> opaque (OP) and translucent (TR) colony variants grown on PPLO supplemented agar with (right) or without (left) Congo red. Magnification: x30. <b>B:</b> Electron microscopy of Ruthenium red-stained PG1<sup>T</sup> OP and TR colonies. CM: cytoplasmic membrane.</p
Kinetics of exopolysaccharides secretion and viability of <b><i>Mmm</i></b><b> strain Afadé following transfer into CMRL-1066 medium with (red) or without (blue) glucose supplementation.</b>
<p>Glucose (1 g/L) was added at 24, 48 and 72 h (arrows).</p
NMR spectra of EPS produced by <i>Mmm</i>.
<p><b>A: <sup>1</sup>H NMR spectrum, B: 2D COSY NMR spectrum and C: 2D HSQC NMR spectrum.</b></p
Growth, pH and exopolysaccharide (EPS) secretion of translucent (blue) and opaque (red) colony variants in CMRL-1066 medium.
<p>50 ml of CMRL-1066 medium were inoculated with 10<sup>8</sup>–10<sup>9</sup> CFU/mL and incubated for 96 hours. Viable titer, pH and EPS production were determined every 24 h.</p