200 subgingival specimens collected from 100 healthy periodontal adults of Thanhliet, Thanhtri, Hanoi, from 100 periodontitis adults of Odonto-stomatology Departments of Dongda and Thanhnhan Hospital were cultured and isolated for Actinobacillus actinomycetemcomitans and Capnocytophaga gingivitis. The prevalence of Aa and Cg in the periodontitis group is clearly different from that in the healthy periodontal one. The higher rate of Cg compared with the rate of Aa is found in female with periodontitis. Both Aa and Cg are sensitive to ampicillin, tetracycline, and chloramphenicole. Their sensitivity to erythromycin and sulfamethoxazole/ trimethoprime changes. Cg is resistant to amikacin. TSBV medium used for culturing and isolating Aa has improved to be suitable to Laboratories in Vietnam.
Actinobacillus actinomycetemcomitans ; Gingivitis

No abstract available.
Actinobacillus* ; Aggregatibacter actinomycetemcomitans* ; Clone Cells* ; Cloning, Organism*

No abstract available.
Actinobacillus* ; Aggregatibacter actinomycetemcomitans* ; Animals ; Osteoclasts ; Rats*

No abstract available.
Actinobacillus* ; Aggregatibacter actinomycetemcomitans* ; Apoptosis* ; Humans ; Jurkat Cells*

OBJECTIVETo study the effect of Actinobacillus actinomycetem (A. actinomycetem) on the secretion and apoptosis rate of polymorphonuclear leukocytes (PMN) in type 2 diabetes patients.

METHODSPeripheral PMN from healths and type 2 diabetes patients were isolated by Percoll gradient centrifugation. The PMN were stimulated with filtrate of ultrasonic pulverization from A. actinomycetem as the experiment group. As the control group, PMN suspension was incubated with PBS. The release of interleukin-6 (IL-6) was measured at 20, 40, 60 min by enzymelinked immune sorbent assay (ELISA) technique. The apoptosis rate of PMN was tested at 6 and 12 hours by flow cytometry.

RESULTSIncubated with filtrate of ultrasonic pulverization from A. actinomycetem, the PMN of type 2 diabetes patients released significantly higher levels of IL-6 compared with the healthy subjects (P < 0.001). The apoptosis rate of PMN from the healthy subjects was higher than that from type 2 diabetes patients (P < 0.001). Regardless of body condition, interaction with filtrate of ultrasonic pulverization from A. actinomycetem could induce the seretion of IL-6 and reduce the apoptosis rate.

CONCLUSIONThe PMN of type 2 diabetes patients may possess hyper-reactive inflammatory response trait.

Actinobacillus (A.) pleuropneumoniae is the causative agent of pleuropneumonia which is one of the most important respiratory diseases in pigs worldwide. A total of 32 A. pleuropneumoniae isolates from diseased pigs during 2008 to 2010 were serotyped by polymerase chain reaction method. The susceptibility of the isolates to 13 antimicrobial agents were determined by disk diffusion test. In all the 32 isolates examined in this study, serotype 5 (16 isolates: 50%), 1 (7 isolates: 21.9%), 2 (5 isolates: 15.6%) and 12 (1 isolate: 3.1%) were found. Of all tested antimicrobial agents, resistance to oxytetracycline was found in 96.9% of isolates, followed by resistance to amikacin (81.2%), neomycin (68.7%), kanamycin (53.1%), penicillin (50.0%), gentamicin (43.7%), florfenicol (25.0%), ampicillin (18.7%), colistin (9.4%), trimethoprim/sulfamethoxazole, ceftiofur (8.3%), amoxicillin/clavulanic acid (3.1%) and enrofloxacin (0%). Oxytetracycline or florfenicol-resistant isolates were examined for the presence of resistance gene. Among the 31 oxytetracycline-resistant isolates, tetB, tetH and tetO genes were detected in 22 (71%), 8 (26%) and 1 (3%) isolates, respectively. The floR genes were detected in 8 (100%) of the 8 florfenicol-resistant A. pleuropneumoniae isolates.
Actinobacillus ; Actinobacillus pleuropneumoniae ; Amikacin ; Ampicillin ; Anti-Infective Agents ; Cephalosporins ; Colistin ; Diffusion ; Fluoroquinolones ; Gentamicins ; Kanamycin ; Korea ; Neomycin ; Oxytetracycline ; Penicillins ; Pleuropneumonia ; Polymerase Chain Reaction ; Swine ; Thiamphenicol

Actinobacillus pleuropneumoniae is a Gram-negative bacterium that resides in the respiratory tract of pigs and causes porcine respiratory disease complex, which leads to significant losses in the pig industry worldwide. The incidence of drug resistance in this bacterium is increasing; thus, identifying new protein/gene targets for drug and vaccine development is critical. In this study, we used an in silico approach, utilizing several databases including the Kyoto Encyclopedia of Genes and Genomes (KEGG), the Database of Essential Genes (DEG), DrugBank, and Swiss-Prot to identify non-homologous essential genes and prioritize these proteins for their druggability. The results showed 20 metabolic pathways that were unique and contained 273 non-homologous proteins, of which 122 were essential. Of the 122 essential proteins, there were 95 cytoplasmic proteins and 11 transmembrane proteins, which are potentially suitable for drug and vaccine targets, respectively. Among these, 25 had at least one hit in DrugBank, and three had similarity to metabolic proteins from Mycoplasma hyopneumoniae, another pathogen causing porcine respiratory disease complex; thus, they could serve as common therapeutic targets. In conclusion, we identified glyoxylate and dicarboxylate pathways as potential targets for antimicrobial therapy and tetra-acyldisaccharide 4′-kinase and 3-deoxy-D-manno-octulosonic-acid transferase as vaccine candidates against A. pleuropneumoniae.
Actinobacillus pleuropneumoniae ; Actinobacillus ; Computer Simulation ; Cytoplasm ; Databases, Protein ; Drug Resistance ; Genes, Essential ; Genome ; Genomics ; Incidence ; Metabolic Networks and Pathways ; Mycoplasma hyopneumoniae ; Pleuropneumonia ; Respiratory System ; Swine ; Transferases

Among various vaccines against Actinobacillus pleuropneumoniae, subunit vaccines using recombinant proteins of ApxI, ApxII, and ApxIII as vaccine antigens have shown good efficacy in terms of safety and protection. Therefore, subunit vaccines are being applied worldwide and the development of new subunit vaccines is actively being conducted. To evaluate the efficacy of the subunit vaccines, it is important to measure immune responses to each Apx toxin separately. However, the cross-reactivity of antibodies makes it difficult to measure specific immune reactivity to each toxin. In the present study, specific antigen regions among the toxins were identified and cloned to solve this problem. The antigenicity of each recombinant protein was demonstrated by Western blot. Using the recombinant proteins, we developed enzyme-linked immunosorbent assay (ELISA) methods that can detect specific immune responses to each Apx toxin in laboratory guinea pigs. We suggest that the ELISA method developed in this study can be an important tool in the evaluation of vaccine efficiency and vaccine development.
Actinobacillus pleuropneumoniae ; Actinobacillus ; Animals ; Antibodies ; Blotting, Western ; Clone Cells ; Enzyme-Linked Immunosorbent Assay ; Guinea Pigs ; Methods ; Recombinant Proteins ; Vaccines ; Vaccines, Subunit

Actinobacillus actinomycetemcomitans, a rare human pathogen, was repeatedly isolated from the blood of a 20-year-old male patient with patent ductus arteriosus who developed subacute bacterial endocarditis. Difficulties in isolating and identifying the organism are discussed. The bacterial isolate was found to be susceptible to various antimicrobial agents.
Actinobacillus/isolation & purification* ; Adult ; Blood/microbiology* ; Case Report ; Endocarditis, Subacute Bacterial/microbiology* ; Human ; Male ; Septicemia/microbiology

Actinobacillus pleuropneumoniae causes porcine pleuropneumoniae which is one of severe threats to the swine industry. In total, 54 strains of Actinobacillus pleuropneumoniae were isolated from 443 pigs between 2012 and 2013 in Korea. Isolates were classified into serotypes 1, 2, 5, 7, 12, and unclassified by multiplex PCR. Genotypes of isolates were divided into three groups according to the sequence of the omlA gene. The antimicrobial resistance rate of serotype 1 was slightly higher than that of serotype 5. In conclusion, to block and treat porcine pleuropneumonia, it is necessary to conduct ongoing characterization of A. pleuropneumoniae isolated from pigs.
Actinobacillus pleuropneumoniae* ; Genotype ; Korea ; Multiplex Polymerase Chain Reaction ; Pleuropneumonia ; Prevalence* ; Swine*