0000000000179024

AUTHOR

Shan-rui Han

showing 13 related works from this author

One-step polymerase chain reaction-based typing of Helicobacter pylori vacA gene: association with gastric histopathology.

2000

Heterogeneity of the Helicobacter pylori vacA gene may be associated with bacterial virulence and presentation. In this study, the possible correlation between vacA genotypes and gastric histopathology was investigated. Using a modified one-step polymerase chain reaction (PCR)-based method, 122 of 131 H. pylori isolates obtained from 63 of 67 patients from Germany were classified into distinct vacA genotypes according to their signal sequence (s1 or s2) and their midregion alleles (m1 or m2). A possible subtype of m1, now alluded to as m3, was identified in one-third of the isolates. Signal sequence s1 was significantly associated with higher H. pylori density but not with gastric inflammat…

Microbiology (medical)AdultDNA BacterialMaleAdolescentGenotypeSpirillaceaeImmunologyPeripheral blood mononuclear cellPolymerase Chain ReactionMicrobiologylaw.inventionHelicobacter InfectionsBacterial ProteinslawGenotypemedicineImmunology and AllergyCagAHumansTypingChildPolymerase chain reactionAntigens BacterialbiologyHelicobacter pyloriGeneral MedicineHelicobacter pyloriMiddle Agedbacterial infections and mycosesbiology.organism_classificationdigestive system diseasesBacterial Typing TechniquesGastric MucosaChild PreschoolGastritisFemaleGastritismedicine.symptomMedical microbiology and immunology
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Pore-forming Staphylococcus aureus alpha-toxin triggers epidermal growth factor receptor-dependent proliferation.

2006

Staphylococcal alpha-toxin is an archetypal killer protein that homo-oligomerizes in target cells to create small transmembrane pores. The membrane-perforating beta-barrel motif is a conserved attack element of cytolysins of Gram-positive and Gram-negative bacteria. Following the recognition that nucleated cells can survive membrane permeabilization, a profile of abundant transcripts was obtained in transiently perforated keratinocytes. Several immediate early genes were found to be upregulated, reminiscent of the cellular response to growth factors. Cell cycle analyses revealed doubling of S + G2/M phase cells 26 h post toxin treatment. Determination of cell counts uncovered that after an …

KeratinocytesStaphylococcus aureusSrc Homology 2 Domain-Containing Transforming Protein 1ImmunologyCellBacterial ToxinsBlotting WesternFluorescent Antibody TechniqueTransfectionMicrobiologyCell LineHemolysin ProteinsDownregulation and upregulationNucleated cellVirologymedicineHumansGrowth factor receptor inhibitorEpidermal growth factor receptorStaphylococcus aureus alpha toxinAdaptor Proteins Signal TransducingCell Line TransformedCell ProliferationbiologyCytotoxinsReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingCell CycleCell cycleFlow CytometryTransmembrane proteinCell biologyErbB Receptorsmedicine.anatomical_structureShc Signaling Adaptor Proteinsbiology.proteinMitogensSignal TransductionCellular microbiology
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Identification of a Unique Helicobacter Species by 16S rRNA Gene Analysis in an Abdominal Abscess from a Patient with X-Linked Hypogammaglobulinemia

2000

ABSTRACT A unique Helicobacter species, MZ640285, was isolated from a patient with X-linked hypogammaglobulinemia suffering from recurrent abdominal abscesses and was identified by 16S rRNA gene sequence analysis. In the phylogenetic tree, the isolate fell into a cluster which included Flexispira rappini , Helicobacter bilis , and Helicobacter sp. strain Mainz. Helicobacters are being increasingly recognized as pathogens in immunocompromised hosts. These fastidious bacteria are not easily cultured in the routine diagnostic laboratory, and this is the first report of their identification by 16S rRNA gene sequencing performed directly from a clinical specimen.

AdultMaleMicrobiology (medical)Fastidious organismHelicobacter bilisAbdominal AbscessX ChromosomeGenetic LinkageMolecular Sequence DataBiologyPolymerase Chain ReactionHelicobacter InfectionsHypogammaglobulinemiaImmunocompromised HostAgammaglobulinemiaRecurrenceHelicobacterRNA Ribosomal 16SmedicineHumansHelicobacterRibosomal DNAPhylogenetic treeGenes rRNABacteriologySequence Analysis DNARibosomal RNA16S ribosomal RNAmedicine.diseasebiology.organism_classificationVirologyJournal of Clinical Microbiology
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Hepatic Granuloma Due to Propionibacterium acnes in a Patient with Acute Myelogenous Leukemia

2000

AdultMicrobiology (medical)Pathologymedicine.medical_specialtyMyeloidPropionibacterium acnesMyelogenousHumansMedicinePropionibacterium acnesGram-Positive Bacterial InfectionsPropionibacteriaceaeGranulomabiologybusiness.industryLiver Diseasesbiology.organism_classificationmedicine.diseaseRadiographyLeukemia Myeloid AcuteLeukemiaInfectious Diseasesmedicine.anatomical_structureGranulomaImmunologyFemalebusinessHepatic granulomaBacteriaClinical Infectious Diseases
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Persistent Legionella Infection in a Patient after Bone Marrow Transplantation

2000

ABSTRACT We report on a patient who developed Legionella pneumonia after bone marrow transplantation. Despite appropriate antibiotic treatment, disease progressed. The patient developed a lung abscess from which Legionella and Prevotella were isolated. Cure was achieved by surgical resection. The resected material was sterile, but 16S ribosomal DNA analysis revealed Legionella DNA.

MaleMicrobiology (medical)medicine.medical_specialtyPathologyLegionellaLegionella PneumoniaLung abscessCase ReportsLegionella pneumophilaLegionella pneumophilamedicineHumansLung AbscessAbscessBone Marrow Transplantationbiologybusiness.industryMiddle Agedbacterial infections and mycosesmedicine.diseasebiology.organism_classificationrespiratory tract diseasesSurgeryPneumoniamedicine.anatomical_structurebacteriaLegionnaires' diseaseBone marrowLegionnaires' DiseasebusinessJournal of Clinical Microbiology
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No association between Helicobacter pylori genotypes and antibiotic resistance phenotypes within families.

2002

Background. Triple therapy combining a proton pump inhibitor with two antibiotics, e.g. clarythromycin (CLR), metronidazole (MTZ) or amoxicillin (AMX), represents the standard in Helicobacter pylori eradication regimens. Resistance to antimicrobial agents, particularly MTZ (up to 56% in Western countries) and CLR (up to 15% in southern Europe), is frequently observed and may be associated with treatment failure [1]. Recently, several studies indicated that individual H. pylori colonies from a single anatomic site may not always yield identical genotypes, or the identical patterns of susceptibility to antibiotics [2–5]. Representative for every single patient we analyzed 27 H. pylori antrum …

Genotypemedicine.drug_classAntibioticsDrug resistanceMicrobial Sensitivity TestsPolymerase Chain ReactionMicrobiologyHelicobacter InfectionsAntibiotic resistanceDrug Resistance BacterialmedicineHelicobacterbiologyHelicobacter pyloriGastroenterologyGeneral MedicineAmoxicillinHelicobacter pyloribiology.organism_classificationAntimicrobialAnti-Bacterial AgentsElectrophoresis Gel Pulsed-FieldMetronidazoleInfectious DiseasesPhenotypePolymorphism Restriction Fragment Lengthmedicine.drugHelicobacter
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Helicobacter pylori: clonal population structure and restricted transmission within families revealed by molecular typing.

2000

ABSTRACT Helicobacter pylori infects up to 50% of the human population worldwide. The infection occurs predominantly in childhood and persists for decades or a lifetime. H. pylori is believed to be transmitted from person to person. However, tremendous genetic diversity has been reported for these bacteria. In order to gain insight into the epidemiological basis of this phenomenon, we performed molecular typing of H. pylori isolates from different families. Fifty-nine H. pylori isolates from 27 members of nine families were characterized by using restriction fragment length polymorphism analysis of five PCR-amplified genes, by pulsed-field gel electrophoresis (PFGE) of chromosomal DNA, and …

Microbiology (medical)GenotypeEpidemiologyPopulationBiologyPolymerase Chain ReactionRibotypingHelicobacter InfectionsBacterial ProteinsRNA Ribosomal 16SGenotypePulsed-field gel electrophoresisDisease Transmission InfectiousCagAHumansFamilyGenetic variabilityeducationChildGenotypingPhylogenyGeneticseducation.field_of_studyAntigens BacterialMolecular epidemiologyHelicobacter pyloriDNAbacterial infections and mycosesBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthJournal of clinical microbiology
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Possible protective role for C-reactive protein in atherogenesis: complement activation by modified lipoproteins halts before detrimental terminal se…

2004

Background—Previous work indicated that enzymatically remodeled LDL (E-LDL) might activate complement in atherosclerotic lesions via a C-reactive protein (CRP)–dependent and CRP-independent pathway. We sought to substantiate this contention and determine whether both pathways drive the sequence to completion.Methods and Results—E-LDL was prepared by sequential treatment of LDL with a protease and cholesteryl esterase. Trypsin, proteinase K, cathepsin H, or plasmin was used with similar results. Functional tests were used to assess total complement hemolytic activity, and immunoassays were used to demonstrate C3 cleavage and to quantify C3a, C4a, C5a, and C5b-9. E-LDL preparations activated …

PlasminArteriosclerosisLipoproteinsCathepsin HPhysiology (medical)EndopeptidasesmedicineHumansComplement ActivationbiologyC-reactive proteinC4ADrug SynergismComplement System ProteinsSterol EsteraseProteinase KTrypsinImmunohistochemistryComplement systemLipoproteins LDLC-Reactive ProteinBiochemistrybiology.proteinCardiology and Cardiovascular MedicineLipoproteinmedicine.drugCirculation
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vacA Genotypes and Genetic Diversity in Clinical Isolates of Helicobacter pylori

1998

ABSTRACT Genetic diversity in Helicobacter pylori strains may affect the function and antigenicity of virulence factors associated with bacterial infection and, ultimately, disease outcome. In this study, DNA diversity of H. pylori isolates was examined by analysis of vacA genotypes and by restriction fragment length polymorphism (RFLP) analysis of H. pylori -associated genes ( vacA , cagA , flaA , ureAB , and ureCD ). Thirty-seven H. pylori isolates from 26 patients were successfully classified into distinct vacA allelic genotypes. The signal sequence allele s1 (31 of 37) predominated over the s2 allele (6 of 37) and was significantly associated with the occurrence (past or present) of gas…

Microbiology (medical)Molecular Sequence DataClinical BiochemistryImmunologyArticleMicrobiologyNucleotide diversityBacterial ProteinsGenetic variationGenotypeHumansImmunology and AllergyCagAAmino Acid SequenceAlleleGeneticsGenetic diversityBase SequenceHelicobacter pyloribiologyGenetic VariationHelicobacter pyloribacterial infections and mycosesbiology.organism_classificationdigestive system diseasesGenes BacterialRestriction fragment length polymorphismClinical Diagnostic Laboratory Immunology
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Enzymatically hydrolyzed low-density lipoprotein modulates inflammatory responses in endothelial cells

2009

SummaryThere is evidence that low-density lipoprotein (LDL) is modified by hydrolytic enzymes,and that the product (E-LDL) induces selective production of interleukin 8 (IL-8) in endothelial cells. Since nuclear factor-kappaB (NF-κB) is a major regulator of IL-8 transcription, we studied its activation in endothelial cells treated with E-LDL. Unexpectedly,the modified lipoprotein not only failed to activate NF-κB, but completely blocked its activation by tumour necrosis factor-alpha (TNF-α) in EA.hy926-cells, as assessed by electrophoretic mobility shift assays and immunofluorescence. Inhibition occurred upstream of NF-κB translocation, as inhibitor of NF-κB- (IκB)-phosphorylation was suppr…

Time FactorsProto-Oncogene Proteins c-junPyridinesmedicine.medical_treatmentFatty Acids NonesterifiedBiologyp38 Mitogen-Activated Protein KinasesCell Linechemistry.chemical_compoundNF-KappaB Inhibitor alphamedicineHumansTrypsinInterleukin 8PhosphorylationPromoter Regions GeneticProtein Kinase InhibitorsTranscription factorInflammationTumor Necrosis Factor-alphaActivator (genetics)HydrolysisInterleukin-8ImidazolesTranscription Factor RelAEndothelial CellsNF-κBHematologySterol EsteraseMolecular biologyLipoproteins LDLTranscription Factor AP-1Endothelial stem cellCytokineBiochemistrychemistryLow-density lipoproteinI-kappa B ProteinsLipoproteinThrombosis and Haemostasis
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Enzymatic modification of low-density lipoprotein in the arterial wall: a new role for plasmin and matrix metalloproteinases in atherogenesis.

2004

Objective— Functionally interactive proteases of the plasminogen/plasmin and the matrix metalloproteinase (MMP) system degrade and reorganize the extracellular matrix of the vessel wall in atherosclerosis. Here we investigated whether such proteases are able to confer atherogenic properties onto low density lipoprotein by nonoxidative modification. Methods and Results— Similar to the recently described enzymatically-modified low-density lipoprotein (E-LDL), native LDL exposed to plasmin or matrix MMP-2 or MMP-9 and cholesterylester-hydrolase (CEH) showed extensive deesterification, with ratios of free cholesterol to total cholesterol rising to 0.8 compared with 0.2 in native LDL. When the …

AdultLipoprotein modificationProteasesAdolescentPlasminArteriosclerosisBlotting WesternMatrix metalloproteinaseComplement Hemolytic Activity AssayMonocyteschemistry.chemical_compoundmedicineHumansTrypsinFibrinolysinComplement ActivationCells CulturedAgedbiologyMacrophagesAntibodies MonoclonalSodium Dodecyl SulfateLipoprotein(a)Middle AgedSterol EsteraseCell biologyLipoproteins LDLC-Reactive ProteinchemistryBiochemistryMatrix Metalloproteinase 9Low-density lipoproteinbiology.proteinMatrix Metalloproteinase 2lipids (amino acids peptides and proteins)Electrophoresis Polyacrylamide GelCardiology and Cardiovascular MedicinePlasminogen activatormedicine.drugLipoproteinArteriosclerosis, thrombosis, and vascular biology
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Characterization of a Catalase-Negative Methicillin-Resistant Staphylococcus aureus Strain

2007

ABSTRACT We describe an unusual clinical strain of catalase-negative methicillin-resistant Staphylococcus aureus sensu stricto. Sequence analysis of its catalase gene showed 99.60% identities to the catalase genes of the reference strains. A 5-base deletion, however, led to a shift of the nucleotide reading frame and a loss of the enzymatic activity.

DNA BacterialMaleMicrobiology (medical)Staphylococcus aureusSequence analysisMolecular Sequence DataBiologymedicine.disease_causeStaphylococcal infectionsMicrobiologyparasitic diseasesmedicineHumansGeneAgedchemistry.chemical_classificationStrain (chemistry)BacteriologySequence Analysis DNAStaphylococcal InfectionsCatalasebacterial infections and mycosesmedicine.diseaseMethicillin-resistant Staphylococcus aureusEnzymechemistryStaphylococcus aureusCatalasebiology.proteinMethicillin ResistanceJournal of Clinical Microbiology
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Enzymatically modified LDL induces cathepsin H in human monocytes: potential relevance in early atherogenesis.

2003

Objective—Modification with proteases and cholesterylesterase transforms LDL to a moiety that resembles lipoproteins isolated from atherosclerotic lesions and possesses atherogenic properties. To identify changes in monocyte-derived foam cells laden with enzymatically modified LDL (E-LDL), we compared patterns of the most abundant transcripts in these cells after incubation with LDL or E-LDL.Methods and Results—Serial analyses of gene expression (SAGE) libraries were constructed from human monocytes after treatment with LDL or E-LDL. Several tags were differentially expressed in LDL-treated versus E-LDL–treated cells, whereby marked selective induction by E-LDL of cathepsin H was conspicuou…

ProteasesCathepsin HCoronary Artery DiseaseBiologyCathepsin HCathepsin L1medicineMacrophageHumansFoam cellGene LibraryCathepsinMonocyteGene Expression ProfilingColocalizationSterol EsteraseMolecular biologyCathepsinsLipoproteins LDLCysteine Endopeptidasesmedicine.anatomical_structureCholesterolBiochemistryGene Expression Regulationlipids (amino acids peptides and proteins)Cardiology and Cardiovascular MedicineFoam CellsArteriosclerosis, thrombosis, and vascular biology
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