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Authors Ducatelle

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Ducatelle, R.


Publications
6

CitationNamesAbstract
Prevalence of ‘Candidatus Helicobacter suis’ in pigs of different ages Hellemans et al. (2007). Veterinary Record 161 (6) Ca. Helicobacter suis
Experimental Infection of Pigs with ‘Candidatus Helicobacter suis’ Hellemans et al. (2006). Veterinary Research Communications 31 (4) Ca. Helicobacter suis
Protective immunization against “Candidatus Helicobacter suis” with heterologous antigens of H. pylori and H. felis Hellemans et al. (2006). Vaccine 24 (14) Ca. Helicobacter suis
Evaluation of Antibiotic Treatment against “ Candidatus Helicobacter suis” in a Mouse Model Hellemans et al. (2005). Antimicrobial Agents and Chemotherapy 49 (11) Ca. Helicobacter suis
‘Candidatus Helicobacter suis’, a gastric helicobacter from pigs, and its phylogenetic relatedness to other gastrospirilla De Groote et al. (1999). International Journal of Systematic and Evolutionary Microbiology 49 (4) Ca. Helicobacter suis
Phylogenetic characterization of ‘Candidatus Helicobacter bovis’, a new gastric helicobacter in cattle De Groote et al. (1999). International Journal of Systematic and Evolutionary Microbiology 49 (4) Ca. Helicobacter bovis

Evaluation of Antibiotic Treatment against “ Candidatus Helicobacter suis” in a Mouse Model
ABSTRACT “ Helicobacter heilmannii ” (proposed name) type 1 colonizes the human stomach. It has been shown to be identical to“ Candidatus Helicobacter suis,” a Helicobacter species colonizing the stomachs of >60% of slaughter pigs. This bacterium has not been isolated in vitro until now. Antibiotic susceptibility testing of “ Candidatus Helicobacter suis” has not been carried out so far. For the present study, a mouse model was adopted to evaluate the antibiotic susceptibility of this organism. Mice infected with“ Candidatus Helicobacter suis” were treated with amoxicillin and omeprazole, a therapy which is used to treat H. heilmannii infections in humans. Two different isolates of“ Candidatus Helicobacter suis” were tested. The excretion of bacterial DNA was assessed during treatment, using PCR on fecal samples. At the end of the experiment, 8 days after the cessation of treatment, the presence of infection was evaluated using a urease test and a PCR test on stomach samples. A marked decrease in the excretion of bacterial DNA was observed a few days after the onset of treatment, and the level remained low until the end of the experiment. A difference in susceptibility between the two“ Candidatus Helicobacter suis” isolates was pointed out. The in vivo mouse model infected with“ Candidatus Helicobacter suis” will be useful for further screening of potential therapeutic regimens.
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