Review: Other Helicobacter species.
animal disease
animal models
genomics and evolution
human disease
non-Helicobacter pylori Helicobacter
pathogenesis
Journal
Helicobacter
ISSN: 1523-5378
Titre abrégé: Helicobacter
Pays: England
ID NLM: 9605411
Informations de publication
Date de publication:
Sep 2020
Sep 2020
Historique:
entrez:
12
9
2020
pubmed:
13
9
2020
medline:
2
7
2021
Statut:
ppublish
Résumé
This review covers the most important, accessible, and relevant literature published between April 2019 and April 2020 in the field of non-Helicobacter pylori Helicobacter species (NHPH). The initial part of the review covers new insights regarding the presence of gastric and enterohepatic NHPH in humans and animals, while the subsequent section focuses on the progress in our understanding of animal models, the pathogenicity and omics of these species. Over the last year, the clinical relevance of gastric NHPH infections in humans was highlighted. With regard to NHPH in animals, the ancestral source of Helicobacter suis was further established showing that Cynomolgus macaques are the common ancestor of the pig-associated H. suis population, and 3 novel Helicobacter species isolated from the gastric mucosa of red foxes were described. "Helicobacter burdigaliensis" sp nov. and "Helicobacter labetoulli" sp nov. were proposed as novel enterohepatic Helicobacter species associated with human digestive diseases. An analysis of Helicobacter cinaedi recurrent infections in humans proposed long-term antibiotic therapies. Several studies using rodent models further elucidated the mechanisms underlying the development of NHPH-related disease, as well as intestinal immunity in inflammatory bowel disease models. Omics approaches supported Helicobacteraceae taxonomy and unraveled the transcriptomic signatures of H. suis and Helicobacter heilmannii upon adherence to the human gastric epithelium. With regard to virulence, data showed that the nuclear remodeling promoted by cytolethal distending toxin of Helicobacters involves the MAFB oncoprotein and is associated with nucleoplasmic reticulum formation in surviving cells.
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e12744Informations de copyright
© 2020 John Wiley & Sons Ltd.
Références
Mohammadi M, Talebi Bezmin Abadi A, Rahimi F, Forootan M Helicobacter heilmannii colonization is associated with high risk for gastritis. Arch Med Res. 2019;50:423-427.
Takigawa H, Masaki S, Naito T, et al. Helicobacter suis infection is associated with nodular gastritis-like appearance of gastric mucosa-associated lymphoid tissue lymphoma. Cancer Med. 2019;8:4370-4379.
Pichon M, Broutin L, Touroult-Jupin P, et al. First detection in Helicobacter suis of a mutation conferring resistance to clarithromycin in Helicobacter pylori : case report and review of the literature. Microb. Drug Resist. 2020;26:677-680.
Augustin AD, Savio A, Nevel A, et al. Helicobacter suis is associated with mortality in Parkinson’s disease. Front Med. 2019;6:188.
Albaret G, Sifré E, Floch P, et al. Alzheimer’s disease and Helicobacter pylori infection: Inflammation from stomach to brain? JAD. 2020;73:801-809.
Ochoa S, Martínez OA, Fernández H, Collado L. Comparison of media and growth conditions for culturing enterohepatic Helicobacter species. Lett Appl Microbiol. 2019;69:190-197.
Sato H, Ogino A, Matsuzaka S, et al. Ovarian abscess caused by Helicobacter cinaedi in a patient with endometriosis. IDCases. 2019;17:e00578.
Nukui Y, Chino T, Tani C, et al. Molecular epidemiologic and clinical analysis of Helicobacter cinaedi bacteremia in Japan. Helicobacter. 2020;25(1):e12675. https://doi.org/10.1111/hel.12675
Sawada O, Gotoh Y, Taniguchi T, et al. Genome sequencing verifies relapsed Infection of Helicobacter cinaedi. Open Forum Infect Dis. 2019;6:ofz200.
Endo Y, Araoka H, Baba M, et al. Matrix-assisted laser desorption ionization-time of flight mass spectrometry can be used to identify Helicobacter cinaedi. Diagn Microbiol Infect Dis. 2020;96:114964.
Gruntar I, Papić B, Pate M, Zajc U, Ocepek M, Kušar D Helicobacter labacensis sp. nov., Helicobacter mehlei sp. nov., and Helicobacter vulpis sp. nov., isolated from gastric mucosa of red foxes (Vulpes vulpes). Intl J System Evol Microbiol. 2020;70:2395-2404.
De Witte C, Berlamont H, Smet A, Ducatelle R, Haesebrouck F. Rhesus macaques are most likely the ancestral source of Helicobacter suis infection in pigs and not Cynomolgus macaques. Helicobacter. 2020;25(3):e12689 https://doi.org/10.1111/hel.12689
Berlamont H, Smet A, De Bruykere S, et al. Antimicrobial susceptibility pattern of Helicobacter suis isolates from pigs and macaques. Vet Microbiol. 2019;239:108459.
Whary MT, Wang C, Ruff CF, et al. Effects of colonization of gnotobiotic Swiss Webster mice with Helicobacter bilis. Comp Med. 2020;70:216-232.
Mannion A, Shen Z, Feng Y, et al. Natural transmission of Helicobacter saguini causes multigenerational inflammatory bowel disease in C57/129 IL-10-/- mice. mSphere. 2020;5(2):e00011-20. https://doi.org/10.1128/mSphere.00011-20
Bostick JW, Wang Y, Shen Z, et al. Dichotomous regulation of group 3 innate lymphoid cells by nongastric Helicobacter species. Proc Natl Acad Sci USA. 2019;116:24760-24769.
Corbin AL, Gomez-Vazquez M, Berthold DL, et al. IRF5 guides monocytes toward an inflammatory CD11c + macrophage phenotype and promotes intestinal inflammation. Sci Immunol. 2020;5:eaax6085.
Cao S, Zhu C, Feng J, et al. Helicobacter hepaticus infection induces chronic hepatitis and fibrosis in male BALB/c mice via the activation of NF-κB, Stat3, and MAPK signaling pathways. Helicobacter. 2020;25:e12677.
Cao S, Zhu L, Zhu C, et al. Helicobacter hepaticus infection-induced IL-33 promotes hepatic inflammation and fibrosis through ST2 signaling pathways in BALB/c mice. Biochem Biophysl Res Comm. 2020;525:654-661.
Sun J, Liang W, Yang X, Li Q, Zhang G. Cytoprotective effects of galacto-oligosaccharides on colon epithelial cells via up-regulating miR-19b. Life Sci. 2019;231:116589.
Han X, Huang T, Han J. Cytokines derived from innate lymphoid cells assist Helicobacter hepaticus to aggravate hepatocellular tumorigenesis in viral transgenic mice. Gut Pathog. 2019;11:23.
de Sousa DA, da Silva KVGC, Cascon CM, et al. Epidermal growth factor receptor 2 immunoexpression in gastric cells of domestic cats with H. heilmannii infection. Acta Histochem. 2019;121(4):413-418.
Nakamura M, Kodama Y, Øverby A, et al. Helicobacter heilmannii infection in mouse induced not only gastric, but hepatic and pulmonary MALT lymphoma: relation to substance P. CPD. 2020;26(25):3039-3045. https://doi.org/10.2174/1381612826666200424163506
De Witte C, Demeyere K, De Bruyckere S, et al. Characterization of the non-glandular gastric region microbiota in Helicobacter suis-infected versus non-infected pigs identifies a potential role for Fusobacterium gastrosuis in gastric ulceration. Vet Res. 2019;50:39.
Chonwerawong M, Ferrand J, Chaudhry HM, et al. Innate immune molecule NLRC5 protects mice from Helicobacter-induced formation of gastric lymphoid tissue. Gastroenterology. 2020;159(1):169-182.e8.
Zhao Y, Lu F, Ye J, et al. Myeloid-derived suppressor cells and γδT17 cells contribute to the development of gastric MALT lymphoma in H felis-infected mice. Front Immunol. 2020;10:3104.
Ding L, Li Q, Chakrabarti J, et al. MiR130b from Schlafen4 + MDSCs stimulates epithelial proliferation and correlates with preneoplastic changes prior to gastric cancer. Gut. 2020; gutjnl-2019-318817.
El-Zaatari M, Bishu S, Zhang M, et al. Aim2-mediated/IFN-β-independent regulation of gastric metaplastic lesions via CD8+ T cells. JCI Insight. 2020;5:e94035.
Ji L, Qian W, Gui L, et al. Blockade of β-catenin-induced CCL28 suppresses gastric cancer progression via inhibition of Treg cell infiltration. Cancer Res. 2020;80:2004-2016.
Mejías-Luque R, Lozano-Pope I, Wanisch A, Heikenwälder M, Gerhard M, Obonyo M. Increased LIGHT expression and activation of non-canonical NF-κB are observed in gastric lesions of MyD88-deficient mice upon Helicobacter felis infection. Sci Rep. 2019;9:7030.
Esposito R, Vllahu M, Morello S, et al. Low copper availability limits Helicobacter infection in mice. FEBS J. 2020; 287(14):2948-2960.
Hong S, Shi Y, Wu NC, et al. Bacterial glycosyltransferase-mediated cell-surface chemoenzymatic glycan modification. Nat Commun. 2019;10:1799.
Javed K, Gul F, Abbasi R, et al. Prevalence and role of Type six secretion system in pathogenesis of emerging zoonotic pathogen Helicobacter pullorum from retail poultry. Avian Pathol. 2019;48:557-563.
Péré-Védrenne C, He W, Azzi-Martin L, et al. The nuclear remodeling induced by Helicobacter cytolethal distending toxin involves MAFB oncoprotein. Toxins (Basel). 2020;12:174.
Azzi-Martin L, He W, Péré-Védrenne C, et al. Cytolethal distending toxin induces the formation of transient messenger-rich ribonucleoprotein nuclear invaginations in surviving cells. PLoS Pathog. 2019;15:e1007921.
Hu X, Bai Y, Fan T-P, Zheng X, Cai Y. A novel type alanine dehydrogenase from Helicobacter aurati: molecular characterization and application. Int J Biol Macromol. 2020;161:636-642.
Rimbara E, Suzuki M, Matsui H, et al. Complete genome sequence of Helicobacter suis strain SNTW101c, originally isolated from a patient with nodular gastritis. Microbiol Resour Announc. 2020;9(1):e0134019. https://doi.org/10.1128/MRA.01340-19
Berthenet E, Bénéjat L, Ménard A, et al. Whole-genome sequencing and bioinformatics as pertinent tools to support Helicobacteracae taxonomy, based on three strains suspected to belong to novel Helicobacter species. Front Microbiol. 2019;10:2820.
Berlamont H, De Witte C, Bauwens E, et al. Distinct transcriptome signatures of Helicobacter suis and Helicobacter heilmannii strains upon adherence to human gastric epithelial cells. Vet Res. 2020;51:62.
Hortelano I, Moreno Y, Moreno-Mesonero L, Ferrús MA. Deep-amplicon sequencing (DAS) analysis to determine the presence of pathogenic Helicobacter species in wastewater reused for irrigation. Environm Poll. 2020;264:114768.