Expression of sialylated Lex, involved in SabA-mediated adherence of H. pylori, was mainly observed in the body. Of known canine non-H. pylori Helicobacter

species, H. heilmannii sensu stricto presented the highest adherence scores to the antral mucosa in canine paraffin-embedded sections. The relationship between pet ownership or frequent exposure to dogs and infection with different gastric Helicobacter species was assessed [35]. A significant correlation was found between human and canine infection for H. felis and to a lesser extent for H. bizzozeronii. The poultry gut microbiota was little studied, while chickens are a major meat source worldwide and are considered as important reservoirs for foodborne pathogens. High abundance of Campylobacter species H. pullorum and Megamonas species

was found in the buy MLN0128 cecal microbiome of Ross broiler chickens housed indoors under standard commercial conditions [36]. The gastrointestinal tract microbiota was characterized in king, gentoo, macaroni, and little penguin species [37]. 16S rRNA gene pyrosequencing revealed that Helicobacteriaceae was the third dominant family in king penguins (8%) in contrast to other penguin species. In the Proteobacteria phylum, Helicobacter INCB024360 in vitro species ranged from 1 to 11% in these four marine seabird species. Of 3889 16S rRNA sequences analyzed from the feces of migrating birds (migratory stopover, Delaware Bay, USA), 6.5% corresponded to Epsilonproteobacteria, that is, Campylobacter (82.3%) and Helicobacter (17.7%) species.

Most Helicobacter-like sequences were closely related to H. pametensis and H. anseris, while the low percentage of sequence identity (92%) with H. anseris suggests a different Helicobacter species [38]. Helicobacters were detected at low frequence in feces and intestinal tissues of tropical terrestrial wild birds (Venezuela) by molecular methods [39], suggesting that these bacteria may be uncommon in the populations studied. PCR selleck compound arrays for commonly reported rodent infectious agents were used in naturally infected index mice and sentinel mice exposed by contact and soiled-bedding transfer [40]. Helicobacters and pinworms were detected in fewer than half of the soiled-bedding sentinels. Of the four Helicobacter species identified in index mice, only H. ganmani was found in soiled-bedding and contact sentinels. The prevalence of enterohepatic Helicobacter (EHH) infection was determined in a study on old rhesus monkeys [41]. Helicobacter infection (PCR, culture) was present in 97% of the monkeys; 13 of 14 monkeys diagnosed with intestinal adenocarcinoma were infected. H. macacae and “Helicobacter sp. rhesus monkey” taxons 2 and 4 were detected on the epithelial colonic surface. In vitro experiments showed bacterial adherence to epithelia, invasion as well as induction of proinflammatory gene expression, while genes involved in the inflammasome were downregulated.