Isolation and characterization of Helicobacter suis from human stomach

• Published in: Proceedings of the National Academy of Sciences - PNAS 2021-03, Vol.118 (13), p.1-8
• Main Authors: Rimbara, Emiko, Suzuki, Masato, Matsui, Hidenori, Nakamura, Masahiko, Morimoto, Misako, Sasakawa, Chihiro, Masuda, Hiroki, Nomura, Sachiyo, Osaki, Takako, Nagata, Noriyo, Shibayama, Keigo, Tokunaga, Kengo
• Format: Article
• Language: English
• Subjects: Adult; Animals; Biological Sciences; Disease Models, Animal; Female; Genome, Bacterial; Helicobacter heilmannii - genetics; Helicobacter heilmannii - isolation & purification; Helicobacter heilmannii - pathogenicity; Helicobacter Infections - genetics; Humans; Male; Mice; Mice, Inbred C57BL; Middle Aged; Stomach - microbiology; Stomach Diseases - microbiology; Swine; Type IV Secretion Systems - genetics; Virulence - genetics; Virulence Factors - genetics
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2026337118

Helicobacter suis, a bacterial species naturally hosted by pigs, can colonize the human stomach in the context of gastric diseases such as gastric mucosa-associated lymphoid tissue (MALT) lymphoma. Because H. suis has been successfully isolated from pigs, but not from humans, evidence linking human H. suis infection to gastric diseases has remained incomplete. In this study, we successfully in vitro cultured H. suis directly from human stomachs. Unlike Helicobacter pylori, the viability of H. suis decreases significantly on neutral pH; therefore, we achieved this using a low-pH medium for transport of gastric biopsies. Ultimately, we isolated H. suis from three patients with gastric diseases, including gastric MALT lymphoma. Successful eradication of H. suis yielded significant improvements in endoscopic and histopathological findings. Oral infection of mice with H. suis clinical isolates elicited gastric and systemic inflammatory responses; in addition, progression of gastric mucosal metaplasia was observed 4 mo postinfection. Because H. suis could be isolated from the stomachs of infected mice, our findings satisfied Koch’s postulates. Although further prospective clinical studies are needed, H. suis, like H. pylori, is likely a gastric pathogen in humans. Furthermore, comparative genomic analysis of H. suis using complete genomes of clinical isolates revealed that the genome of each H. suis isolate contained highly plastic genomic regions encoding putative strain-specific virulence factors, including type IV secretion system–associated genes, and that H. suis isolates from humans and pigs were genetically very similar, suggesting possible pig-to-human transmission.