14 research outputs found
Human germline genes most similar to the genes encoding the BoNT/E3 specific scFv.
<p>Human germline genes most similar to the genes encoding the BoNT/E3 specific scFv.</p
<i>Ex vivo</i> mouse phrenic nerve-hemidiaphragm assay with ELC18.
<p>A) Neutralization of BoNT/E3 holotoxin (330 pg/mL; 20LD<sub>50</sub>/mL) by different concentrations of ELC18. Neutralization properties of ELC18 as scFv at 165 nM, 16.5 nM, 3.3 nM, and 0.3 nM were evaluated. B) Neutralization properties of ELC18 as scFv-Fc at 9.4 nM, 4.7 nM, and 0.9 nM were evaluated. Each neutralization set is from a single hemidiaphragm preparation per concentration.</p
Inhibition of BoNT/E3 endopeptidase activity.
<p>Inhibition of BoNT/E3 endopeptidase activity.</p
<i>In vivo</i> mouse paralysis assay with ELC18 as scFv-Fc.
<p>A) The neutralization activity of ELC18 was determined in the mouse paralysis assay <i>in vivo</i>. BoNT/E3 holotoxin (1LD<sub>50</sub> per dose) was pre-mixed with each antibody at 0.064 ng, 0.32 ng, 1.6 ng, 8 ng, 40 ng, 0.2 μg and 1 μg per dose. Animals were scored at 24 h post injection. Results are expressed as mean score for 4 mice ± SEM. Positive control group of mice were injected with BoNT/E3 toxin alone and negative control group of mice received the maximum concentration of antibody in the absence of toxin. B) Schema of the <i>in vivo</i> mouse paralysis assay. Formation of abdominal ptosis after injection of botulinum neurotoxin.</p
<i>Ex vivo</i> phrenic nerve-hemidiaphragm assay.
<p>Neutralization of BoNT/E3 toxicity (20LD<sub>50</sub>/mL) by the BoNT/E3 specific scFv ELC18, ELC51 and ELC76.</p
Schema of macaque immunization.
<p>Immunization was performed with five subcutaneous injections of recombinant BoNT/E3 light chain and sera were sampled to estimate the immunization titer.</p
<i>In vitro</i> endopeptidase assay.
<p>Concentration-dependent inhibition of the endopeptidase activity of BoNT/E3 holotoxin (330 pg/mL; 20LD<sub>50</sub>/mL) <i>in vitro</i> by several scFv targeting the light chain of BoNT/E3. As control, SNAP–25 cleavage by BoNT/E3 without inhibiting scFv and buffer without toxin. Each data point is a mean of triplicate determinants from two separate experiments (n = 6) ± SEM.</p
Description of the sequences tiled on the PathogenID v2.0 microarray for the detection and characterization of BoNT-producing clostridia.
<p>Description of the sequences tiled on the PathogenID v2.0 microarray for the detection and characterization of BoNT-producing clostridia.</p
Phylogenetic tree of the <i>bont/A</i> sequence retrieved in contaminated food and several toxinotype A strains.
<p>A neighbor-joining tree was constructed based on the <i>bont/A</i> sequence retrieved by the RMA for the enrichment culture of the <i>C. botulinum</i> strain in a naturally contaminated salad specimen, and the corresponding sequences of 6 strains representative of 5 known <i>C. botulinum</i> toxinotype A subtypes: strain Hall (A1), NCTC 2916 (A[B]), Kyoto (A2), Loch Maree (A3), 657 (Ba4) and A661222 (A5). Bootstrap values and genetic distance (bar) are shown. The Genbank accession number of each strain is indicated in parentheses. The <i>bont</i> sequence obtained from the contaminated salad specimen is marked in bold.</p