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1.
Biomed Res Int ; 2017: 8682057, 2017.
Article in English | MEDLINE | ID: mdl-28540303

ABSTRACT

One of the important elements for most bacterial growth is iron, the bioavailability of which is limited in hosts. Riemerella anatipestifer (R. anatipestifer, RA), an important duck pathogen, requires iron to live. However, the genes involved in iron metabolism and the mechanisms of iron transport are largely unknown. Here, we investigated the transcriptomic effects of iron limitation condition on R. anatipestifer CH-1 using the RNA-Seq and RNA-Seq-based analysis. Data analysis revealed genes encoding functions related to iron homeostasis, including a number of putative TonB-dependent receptor systems, a HmuY-like protein-dependent hemin (an iron-containing porphyrin) uptake system, a Feo system, a gene cluster related to starch utilization, and genes encoding hypothetical proteins that were significantly upregulated in response to iron limitation. Compared to the number of upregulated genes, more genes were significantly downregulated in response to iron limitation. The downregulated genes mainly encoded a number of outer membrane receptors, DNA-binding proteins, phage-related proteins, and many hypothetical proteins. This information suggested that RNA-Seq-based analysis in iron-limited medium is an effective and fast method for identifying genes involved in iron uptake in R. anatipestifer CH-1.


Subject(s)
Iron Metabolism Disorders/genetics , Iron/metabolism , Riemerella/genetics , Transcriptome/genetics , Animals , Ducks/microbiology , High-Throughput Nucleotide Sequencing , Iron Metabolism Disorders/metabolism , Iron Metabolism Disorders/microbiology , Poultry Diseases/metabolism , Poultry Diseases/microbiology , Riemerella/metabolism , Riemerella/pathogenicity
2.
J Innate Immun ; 8(5): 517-28, 2016.
Article in English | MEDLINE | ID: mdl-27423740

ABSTRACT

Withdrawal of iron from serum (hypoferraemia) is a conserved innate immune antimicrobial strategy that can withhold this critical nutrient from invading pathogens, impairing their growth. Hepcidin (Hamp1) is the master regulator of iron and its expression is induced by inflammation. Mice lacking Hamp1 from birth rapidly accumulate iron and are susceptible to infection by blood-dwelling siderophilic bacteria such as Vibrio vulnificus. In order to study the innate immune role of hepcidin against a background of normal iron status, we developed a transgenic mouse model of tamoxifen-sensitive conditional Hamp1 deletion (termed iHamp1-KO mice). These mice attain adulthood with an iron status indistinguishable from littermate controls. Hamp1 disruption and the consequent decline of serum hepcidin concentrations occurred within hours of a single tamoxifen dose. We found that the TLR ligands LPS and Pam3CSK4 and heat-killed Brucella abortus caused an equivalent induction of inflammation in control and iHamp1-KO mice. Pam3CSK4 and B. abortus only caused a drop in serum iron in control mice, while hypoferraemia due to LPS was evident but substantially blunted in iHamp1-KO mice. Our results characterise a powerful new model of rapidly inducible hepcidin disruption, and demonstrate the critical contribution of hepcidin to the hypoferraemia of inflammation.


Subject(s)
Brucella abortus/immunology , Hepcidins/metabolism , Inflammation/immunology , Iron Metabolism Disorders/immunology , Animals , Antigens, Bacterial/immunology , Genotype , Hepcidins/genetics , Humans , Inflammation/microbiology , Iron Metabolism Disorders/microbiology , Lipopeptides/immunology , Lipopolysaccharides/immunology , Mice , Mice, Inbred C57BL , Mice, Knockout , Models, Animal , Toll-Like Receptors/metabolism
3.
Pol Merkur Lekarski ; 21(123): 235-8, 2006 Sep.
Article in Polish | MEDLINE | ID: mdl-17163184

ABSTRACT

UNLABELLED: Role of Helicobacter pylori infection in chronic gastritis and gastric and/or duodenal ulcers is well known. Simultaneously there are some articles in literature considering H. pylori as a cause of extra-gastrointestinal illnesses such as atopic dermatitis, chronic urticaria or acne rosacea, hypotrophy, Schoenlein-Henoch disease, atherosclerosis or hypochromic anaemia. The aim of the study. was to asses iron status in aspect of plasmatic transferrin receptors concentration among children and youth with chronic gastritis with or without Helicobacter pylori infection. MATERIALS AND METHODS: Forty one patients were included as a study group. Range of age was 9-18 years. All patients were diagnosed due to chronic abdominal pains. There were 13 males and 28 females. Blood was collected from every patient for blood cell count, iron, transferrin and transferrin receptors concentration (sTfR) assessment before endoscopy of upper gastrointestinal tract. RESULTS: Concentration of sTfR was higher than age norm among 29 (71%) of patients. Among patients with higher level of sTfR 20 (69%) had normal haemoglobin concentration and in this group 10 patients had H. pylori infection. During analysis of 12 patients with nornal level of sTfR normal haemoglobin concentration was found and among five of them H. pylori infection was stated. Among 21 patients without H. pylori infection 14 had normal level of sTfR and 7 had higher level of sTfR which means that 33% had hidden iron deficiency (involuntary of normal Hb concentrations). Among 15 of 20 patients with H. pylori infection level of sTfR was higher which means that 75% patients with infection had hidden iron deficiency (involuntary of normal Hb concentrations). CONCLUSION: Level of plasmatic transferrin receptors can be good and sensitive indicator of iron deficiency and can be helpful in differential diagnosis of hypochromic anaemia and anaemia caused by chronic illness including chronic gastritis with Helicobacter pylori infection.


Subject(s)
Anemia, Iron-Deficiency/blood , Anemia, Iron-Deficiency/diagnosis , Gastritis/blood , Helicobacter Infections/blood , Helicobacter pylori/isolation & purification , Iron/blood , Receptors, Transferrin/blood , Adolescent , Anemia, Iron-Deficiency/etiology , Biomarkers/blood , Child , Chronic Disease , Female , Gastritis/complications , Helicobacter Infections/complications , Hemoglobinometry , Humans , Iron Metabolism Disorders/blood , Iron Metabolism Disorders/microbiology , Male
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