1.Opacity proteins of neisseria gonorrhoeae in lipooligosaccharide mutants lost ability to interact with neutrophil-restricted CEACAM3 (CD66d).
Song ZHANG ; Ya-Ting TU ; Hua-Hua CAI ; Hong-Hui DING ; Qiao LI ; Ying-Xia HE ; Xin-Xin LIU ; Xin WANG ; Feng HU ; Tie CHEN ; Hong-Xiang CHEN
Journal of Huazhong University of Science and Technology (Medical Sciences) 2016;36(3):344-349
Lipooligosacharide (LOS) of Neisseria gonorrhoeae (gonococci, GC) is involved in the interaction of GC with host cells. Deletion of the alpha-oligosaccharide (alpha-OS) moiety of LOS (lgtF mutant) significantly impairs invasion of GC into epithelial cell lines. GC opacity (Opa) proteins, such as OpaI, mediate phagocytosis and stimulate chemiluminescence responses in neutrophils in part through interaction with members of the carcinoembryonic antigen (CEA) family, which includes CEACAM3 (CD66d), a human neutrophil specific receptor for phagocytosis of bacteria. In the present work, we examined the effects of OpaI-expressing lgtF mutant on phagocytosis by HeLa-CEACAM3 cells and chemiluminescence responses in neutrophils. The results showed that lgtF mutant even expressing OpaI completely lost the ability to promote either phagocytosis mediated by CEACAM3 interaction in HeLa cells or chemiluminescence responses in neutrophils. These data indicated that Opa proteins in the lgtF mutant, which might result from the conformational change, cannot be functional.
Antigens, Bacterial
;
chemistry
;
genetics
;
immunology
;
metabolism
;
Carbohydrate Sequence
;
Carcinoembryonic Antigen
;
genetics
;
immunology
;
Gene Expression Regulation
;
HeLa Cells
;
Host-Pathogen Interactions
;
Humans
;
Lipopolysaccharides
;
chemistry
;
immunology
;
Luminescent Measurements
;
Mutation
;
Neisseria gonorrhoeae
;
genetics
;
metabolism
;
pathogenicity
;
Neutrophils
;
immunology
;
microbiology
;
Phagocytosis
2.Immunogenicity and prediction of epitopic region of antigen Ag I/II and glucosyltransferase from Streptococcus mutans.
Xi-Xi CAO ; Jian FAN ; Jiang CHEN ; Yu-Hong LI ; Ming-Wen FAN
Journal of Huazhong University of Science and Technology (Medical Sciences) 2016;36(3):416-421
The levels of Streptococcus (S.) mutans infections in saliva were evaluated and a comparison for specific antibody levels among children with different levels of S. mutans infection was made. The promising epitopic regions of antigen AgI/II (PAc) and glucosyltransferase (GTF) for potential vaccine targets related to S. mutans adherence were screened. A total of 94 children aged 3-4 years were randomly selected, including 53 caries-negative and 41 caries-positive children. The values of S. mutans and those of salivary total secretory immunoglobulin A (sIgA), anti-PAc and anti-Glucan binding domain (anti-GLU) were compared to determine the correlation among them. It was found the level of s-IgA against specific antigens did not increase with increasing severity of S. mutans infection, and the complete amino acid sequence of PAc and GTFB was analyzed using the DNAStar Protean system for developing specific anti-caries vaccines related to S. mutans adherence. A significantly positive correlation between the amount of S. mutans and children decayed, missing, and filled teeth index was observed. No significant difference was detected in specific sIgA against PAc or GLU between any two groups. No significant correlation was found between such specific sIgA and caries index. A total of 16 peptides from PAc as well as 13 peptides from GTFB were chosen for further investigation. S. mutans colonization contributed to early children caries as an important etiological factor. The level of sIgA against specific antigens did not increase with increasing severity of S. mutans infection in children. The epitopes of PAc and GTF have been screened to develop the peptide-based or protein-based anti-caries vaccines.
Antibodies, Bacterial
;
biosynthesis
;
Antigens, Bacterial
;
chemistry
;
immunology
;
Bacterial Proteins
;
chemistry
;
immunology
;
Case-Control Studies
;
Child, Preschool
;
Dental Caries
;
immunology
;
pathology
;
prevention & control
;
Epitopes
;
chemistry
;
immunology
;
Female
;
Glucosyltransferases
;
chemistry
;
immunology
;
Humans
;
Immunoglobulin A, Secretory
;
biosynthesis
;
Male
;
Peptides
;
chemistry
;
immunology
;
Saliva
;
chemistry
;
microbiology
;
Severity of Illness Index
;
Streptococcal Vaccines
;
biosynthesis
;
chemistry
;
immunology
;
Streptococcus mutans
;
chemistry
;
immunology
;
pathogenicity
;
Vaccines, Subunit
;
Virulence Factors
;
chemistry
;
immunology
3.Evaluation of adjuvant effects of fucoidan for improving vaccine efficacy.
Journal of Veterinary Science 2015;16(2):145-150
Fucoidan is a sulfated polysaccharide derived from brown seaweed, including Fucus vesiculosus. This compound is known to have immunostimulatory effects on various types of immune cells including macrophages and dendritic cells. A recent study described the application of fucoidan as a vaccine adjuvant. Vaccination is regarded as the most efficient prophylactic method for preventing harmful or epidemic diseases. To increase vaccine efficacy, effective adjuvants are needed. In the present study, we determined whether fucoidan can function as an adjuvant using vaccine antigens. Flow cytometric analysis revealed that fucoidan increases the expression of the activation markers major histocompatibility complex class II, cluster of differentiation (CD)25, and CD69 in spleen cells. In combination with Bordetella bronchiseptica antigen, fucoidan increased the viability and tumor necrosis factor-alpha production of spleen cells. Furthermore, fucoidan increased the in vivo production of antigen-specific antibodies in mice inoculated with Mycoplasma hyopneumoniae antigen. Overall, this study has provided valuable information about the use of fucoidan as a vaccine adjuvant.
Adjuvants, Immunologic/pharmacology
;
Animals
;
Antigens, Bacterial/*immunology
;
Bacterial Vaccines/administration & dosage/*immunology
;
Biomarkers/metabolism
;
Bordetella bronchiseptica/*immunology
;
Cells, Cultured
;
Cytokines/*metabolism
;
Female
;
Flow Cytometry
;
Fucus/*chemistry
;
Gene Expression Regulation/drug effects
;
Mice
;
Mice, Inbred BALB C
;
Mycoplasma hyopneumoniae/*immunology
;
Polysaccharides/*pharmacology
;
Spleen/metabolism
4.Improvement of the Diagnostic Sensitivity of Scrub Typhus Using a Mixture of Recombinant Antigens Derived from Orientia tsutsugamushi Serotypes.
Young Jin KIM ; Seon Ju YEO ; Sang Jin PARK ; Ye Ju WOO ; Min Woo KIM ; Seung Han KIM ; In Ae CHANG ; Sung Ho JEON ; Byung Jae PARK ; Gi Jun SONG ; Myoung Gu LEE ; Ik Sang KIM ; Yoon Won KIM
Journal of Korean Medical Science 2013;28(5):672-679
Diagnosis of scrub typhus is difficult because its symptoms are very similar to other acute febrile illnesses, such as leptospirosis, murine typhus, and other viral hemorrhagic fevers. To differentiate scrub typhus from other acute febrile diseases, a rapid and reliable serological diagnosis is important. We have developed a chimeric recombinant antigen cr56 and two other recombinant antigens, r21 and kr56, from various serotypes of Orientia tsutsugamushi. They were tested for the detection of antibodies against O. tsutsugamushi in the patient's serum samples using enzyme-linked immunosorbent assay (ELISA) and dot-blot analyses. As of conventional immunofluorescence assay (IFA), when the mixture of these three recombinant antigens was used, both sensitivity and specificity of the recombinant antigens were increased up to 98% in IgM and IgG at ELISA and dot blotting. Additionally, both sensitivity and specificity by detection of IgM and IgG antibodies at rapid diagnostic test (RDT), using the mixture of three antigens and gold conjugated antibodies, were 99%. Our results suggest the use of mixture of these recombinant antigen proteins in ELISA or RDT is suitable as a diagnostic test for scrub typhus.
Antibodies, Bacterial/blood/chemistry/immunology
;
Antigens, Bacterial/diagnostic use/genetics/metabolism
;
Enzyme-Linked Immunosorbent Assay
;
Fluorescent Antibody Technique, Indirect
;
Gold/chemistry
;
Humans
;
Immunoassay
;
Immunoglobulin G/blood
;
Immunoglobulin M/blood
;
Orientia tsutsugamushi/immunology/*metabolism
;
Recombinant Proteins/biosynthesis/diagnostic use/genetics
;
Scrub Typhus/*diagnosis
;
Sensitivity and Specificity
;
Serotyping
5.An Inverse Relationship between the Expression of the Gastric Tumor Suppressor RUNX3 and Infection with Helicobacter pylori in Gastric Epithelial Dysplasia.
Woo Chul CHUNG ; Sung Hoon JUNG ; Kyu Re JOO ; Min Ji KIM ; Gun Jung YOUN ; Yaeni KIM ; Joune Seup LEE ; Hyewon LEE ; Ji Han JUNG ; Yun Kyung LEE
Gut and Liver 2013;7(6):688-695
BACKGROUND/AIMS: This study was performed to determine the association between RUNX3 expression and Helicobacter pylori infection in premalignant gastric lesions. METHODS: We examined 107 patients with gastric epithelial dysplasia who had undergone endoscopic mucosal resection or submucosal dissection. All tissue samples were evaluated by RUNX3 staining and subclassified by immunophenotype. H. pylori infection in dysplastic lesions and the normal surrounding tissue was examined by silver staining, and cagA status was assessed by polymerase chain reaction. RESULTS: The loss of RUNX3 expression was observed in 62 cases (57.9%), and an association with H. pylori infection was found in 54 cases (50.5%). The infection rate with the cagA-positive H. pylori strain was 63.0%. In RUNX3-negative lesions, the rate of H. pylori infection (p=0.03) and the frequency of category 4 lesions (according to the revised Vienna classification) were high (p=0.02). In addition, the gastric mucin phenotype was predominant. In RUNX3-negative category 4 lesions, the rate of cagA-positive H. pylori infection rate was high but not significantly increased (p=0.08). CONCLUSIONS: Infection with H. pylori is associated with inactivation of RUNX3 in early gastric carcinogenesis. This mechanism was prominent in gastric cancer with a gastric mucin phenotype.
Adenoma/*chemistry
;
Aged
;
Antigens, Bacterial/genetics
;
Bacterial Proteins/genetics
;
Carcinoma/*chemistry
;
Cell Transformation, Neoplastic
;
Core Binding Factor Alpha 3 Subunit/*analysis
;
Female
;
Gastric Mucosa/*chemistry/pathology
;
Helicobacter Infections/*metabolism
;
Helicobacter pylori/*genetics
;
Humans
;
Male
;
Middle Aged
;
Mucin 5AC/analysis
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Mucin-2/analysis
;
Mucin-6/analysis
;
Neprilysin/analysis
;
Phenotype
;
Precancerous Conditions/*chemistry/pathology
;
Stomach Neoplasms/*chemistry
6.Evaluation and comparison of native and recombinant LipL21 protein-based ELISAs for diagnosis of bovine leptospirosis.
Siju JOSEPH ; Naicy THOMAS ; E THANGAPANDIAN ; Vijendra P SINGH ; Rishendra VERMA ; S K SRIVASTAVA
Journal of Veterinary Science 2012;13(1):99-101
A 21-kDa leptospiral lipoprotein (LipL21) was evaluated for its diagnostic potential to detect bovine leptospirosis by ELISA. Both native LipL21 (nLipL21) and recombinant LipL21 (rLipL21) proteins were tested and compared regarding diagnostic efficiency, and no statistically significant difference was observed. The sensitivity of rLipL21 ELISA for 62 microscopic agglutination test (MAT) positive sera was 100% and the specificity with 378 MAT negative sera was 97.09%. Thus, rLipL21 protein-based ELISA could be used as an alternative to MAT for the diagnosis of bovine leptospirosis.
Animals
;
Antibodies, Bacterial/blood
;
Antigens, Bacterial/biosynthesis/*chemistry/genetics
;
Bacterial Outer Membrane Proteins/biosynthesis/*chemistry/genetics
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Cattle
;
Cattle Diseases/blood/*microbiology
;
Enzyme-Linked Immunosorbent Assay/veterinary
;
Leptospira interrogans/*isolation & purification
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Leptospirosis/blood/microbiology/*veterinary
;
Lipoproteins/biosynthesis/*chemistry/genetics
;
Recombinant Proteins/biosynthesis/chemistry/genetics
;
Sensitivity and Specificity
7.Progress in research on molecular biology and application in dominant antigens ESAT6 and CFP10 of TB vaccine.
Journal of Biomedical Engineering 2012;29(2):392-396
As the dominant antigens, early secreted antigenic target 6 (ESAT6, E6) and culture filtrate protein 10 (CFP10, C10) had once been the focus of tuberculosis (TB) vaccine due to their capability of inducing strong cell immune response in the host. They are also endowed with promising future of prevention against and diagnosis of TB. In this review, we systematically introduce recent research progress of E6 and C10, especially in structure-function, biological characteristics, protein expression and secretion, host immunity and vaccine development, and the prospects of their application are also discussed.
Antigens, Bacterial
;
chemistry
;
genetics
;
immunology
;
Bacterial Proteins
;
chemistry
;
genetics
;
immunology
;
Humans
;
Immunodominant Epitopes
;
immunology
;
Molecular Biology
;
Peptide Fragments
;
chemistry
;
genetics
;
immunology
;
Tuberculosis Vaccines
;
genetics
;
immunology
;
Vaccines, DNA
;
immunology
8.Generation of transgenic corn-derived Actinobacillus pleuropneumoniae ApxIIA fused with the cholera toxin B subunit as a vaccine candidate.
Min Kyoung SHIN ; Myung Hwan JUNG ; Won Jung LEE ; Pil Son CHOI ; Yong Suk JANG ; Han Sang YOO
Journal of Veterinary Science 2011;12(4):401-403
Corn, one of the most important forage crops worldwide, has proven to be a useful expression vehicle due to the availability of established transformation procedures for this well-studied plant. The exotoxin Apx, a major virulence factor, is recognized as a common antigen of Actinobacillus (A.) pleuropneumoniae, the causative agent of porcine pleuropneumonia. In this study, a cholera toxin B (CTB)-ApxIIA#5 fusion protein and full-size ApxIIA expressed in corn seed, as a subunit vaccine candidate, were observed to induce Apx-specific immune responses in mice. These results suggest that transgenic corn-derived ApxIIA and CTB-ApxIIA#5 proteins are potential vaccine candidates against A. pleuropneumoniae infection.
Actinobacillus Infections/microbiology/*prevention & control
;
Actinobacillus pleuropneumoniae
;
Animals
;
Antigens, Bacterial/immunology
;
Bacterial Proteins/*immunology
;
Bacterial Vaccines/*immunology
;
Cholera Toxin/*chemistry
;
Female
;
Hemolysin Proteins/*immunology
;
Immunization, Secondary
;
Mice
;
Mice, Inbred ICR
;
Plants, Genetically Modified
;
Zea mays/*genetics
9.Mitochondrial DNA mutations in gastric endothelial cells induced by extract of helicobacter pylori in vitro.
Rui-hua LUO ; Xue-wen HUANG ; Zhong-ze SHEN ; Li-li HUANG ; Xian-yuan AN ; Lan-jing ZHAO
Chinese Journal of Medical Genetics 2010;27(4):381-386
OBJECTIVETo investigate the relationship between the helicobacter pylori (HP) infection and the genetic instability of mitochondrial DNA (mtDNA) in human gastric adenocarcinoma epithelial cells (AGS).
METHODSAfter treated with extracts of HP11638 (CagA+, VacA+) or Hp11638 mutant strain (CagA+, VacA-), AGS cells were collected, and mitochondrial DNA was extracted and Cox-I, Cox-II, Cox-III, ATPase6, ATPase8 and Cytb genes and the D-Loop region were amplified by PCR and then sequenced.
RESULTSThe mutation rates of the mtDNA in AGS cells were correlated with the extracts of the two HP strains in a concentration- and time-dependent manner. But the mtDNA mutation rate in AGS cells treated with the HP11638 extract was higher than that treated with the Hp11638 mutant extract. Total of 616 mutations in D-Loop region were detected, including 489 point mutations, 81 insertions and 46 deletions. Among them, 70.9% (437/616) belonged to GC to AT and AT to GC transition. Seventeen out of 20 (85%) AGS cells treated with extract of HP had mutations in 303PolyC, 16184PolyC and 514CA regions of mtDNA D-Loop. No mutation was detected in Cox-I, Cox-II, Cox-III, ATPase6 and ATPase8 genes, three point mutations were found in the Cytb gene.
CONCLUSIONHP can cause the accumulation of mutations in mtDNA, in particular, in the D-Loop region, and the VacA participated in the process.
Antigens, Bacterial ; pharmacology ; Base Sequence ; DNA, Mitochondrial ; drug effects ; genetics ; Endothelial Cells ; drug effects ; pathology ; Helicobacter Infections ; complications ; Helicobacter pylori ; chemistry ; Humans ; Mutation ; Stomach ; pathology
10.Association of Specific IgE to Staphylococcal Superantigens with the Phenotype of Chronic Urticaria.
Young Min YE ; Gyu Young HUR ; Han Jung PARK ; Seung Hyun KIM ; Hyun Mi KIM ; Hae Sim PARK
Journal of Korean Medical Science 2008;23(5):845-851
It has been well established that bacterial superantigens lead to the induction and aggravation of chronic inflammatory skin diseases. We investigated the clinical significance of serum specific immunoglobulin E (lgE) to the staphylococcal superantigens staphylococcal enterotoxin A (SEA), staphylococcal enterotoxin B (SEB), and toxic shock syndrome toxin (TSST)-1 in patients with chronic urticaria (CU), focusing on the differences in these prevalences between aspirin-intolerant CU (AICU) and aspirin-tolerant CU (ATCU) patients. Aspirin sensitivity was confirmed by oral aspirin provocation test. There were 66 patients AICU and 117 patients ATCU in the study. Serum IgE antibodies specific for SEA, SEB, and TSST-1 were measured by the ImmunoCAP test and the patients were compared with 93 normal controls (NC). The prevalences of serum specific IgE to staphylococcal superantigens were significantly higher in CU than in NC patients (IgE to SEA, 13.7% vs. 5.4%; IgE to SEB, 12.0% vs. 4.3%; IgE to TSST-1, 18.0% vs. 6.5%; p<0.05, respectively). The patients with specific IgE to SEA, SEB, and TSST-1 had higher serum total IgE levels and higher rates of atopy. Significant associations were noted between the prevalence of specific IgE to SEA and SEB and the HLA DQB1*0609 and DRB1*1302 alleles in the AICU group. We confirmed that a sub-population of patients with CU possesses serum IgE antibodies to SEA, SEB, and TSST- 1. Particularly, the IgE immune response to TSST-1 is associated with aspirin sensitivity in CU patients.
Adolescent
;
Adult
;
Aged
;
Anti-Inflammatory Agents, Non-Steroidal/pharmacology
;
Antigens/*chemistry
;
Aspirin/pharmacology
;
Bacterial Toxins/metabolism
;
Chronic Disease
;
Enterotoxins/metabolism
;
Female
;
Humans
;
Immunoglobulin E/*chemistry/metabolism
;
Male
;
Middle Aged
;
Phenotype
;
Staphylococcus/*genetics/immunology
;
Superantigens/metabolism
;
Urticaria/*immunology

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