Whole genomic and randomly-cloned DNA probes for two fastidious periodontal pathogens, Porphyromonas gingivalis and Bacteroides forsythus were labeled with digoxigenin and detected by a colorimetric method. The specificity and sensitivity of the whole genomic and cloned probes were compared. The cloned probes were highly specific compared to the whole genomic probes. A significant degree of cross-reactivity with Bacteroides species. Capnocytophaga sp. and Prevotella sp. was observed with the whole genomic probes. The cloned probes were less sensitive than the whole genomic probes and required at least 106 target cells or a minimum of 10 ng of target DNA to be detected during hybridization. Although a ten-fold increase in sensitivity was obt...
Aim: Research has demonstrated that there are multiple strains of Porphyromonas gingivalis with vary...
Purpose: We aim to develop peptic nucleic acid (PNA) probes for the identification and localization ...
FISH Probes were designed by sequencing the 16S rRNA for each bacterium, identifying hypervariable r...
Oligonucleotide DNA probes complementary to the hypervariable region of the 16S rRNA of Bacteroides ...
In the present study, detection patterns of subgingival Porphyromonas gingivalis (Pg), Prevotella in...
Previous research has shown that using DNA probes to identify the presence of specific bacteria in h...
Species-specific DNA probes were used to determine the presence of Actinobacillus actinomycetemcomit...
Aggressive periodontitis is characterized by rapid attachment and bone loss with no underlying syste...
The purpose of the present study was to investigate the occurrence of Bacteroides forsythus in infec...
We developed quantitative fimA genotype assays and applied them in a pilot study investigating the f...
Porphyromonas gingivalis is a major pathogen in destructive periodontal disease in humans. Detection...
In the course of time the laboratory diagnosis of periodontal infection has been influenced by the ...
Introduction: Porphyromonas gingivalis and Tannerella forsythia are anaerobic bacteria commonly invo...
The impact of a semiquantitative commercially available test based on DNA-strip technology (microIDe...
Galassi F, Kaman WE, Anssari Moin D, van der Horst J, Wismeijer D, Crielaard W, Laine ML, Veerman EC...
Aim: Research has demonstrated that there are multiple strains of Porphyromonas gingivalis with vary...
Purpose: We aim to develop peptic nucleic acid (PNA) probes for the identification and localization ...
FISH Probes were designed by sequencing the 16S rRNA for each bacterium, identifying hypervariable r...
Oligonucleotide DNA probes complementary to the hypervariable region of the 16S rRNA of Bacteroides ...
In the present study, detection patterns of subgingival Porphyromonas gingivalis (Pg), Prevotella in...
Previous research has shown that using DNA probes to identify the presence of specific bacteria in h...
Species-specific DNA probes were used to determine the presence of Actinobacillus actinomycetemcomit...
Aggressive periodontitis is characterized by rapid attachment and bone loss with no underlying syste...
The purpose of the present study was to investigate the occurrence of Bacteroides forsythus in infec...
We developed quantitative fimA genotype assays and applied them in a pilot study investigating the f...
Porphyromonas gingivalis is a major pathogen in destructive periodontal disease in humans. Detection...
In the course of time the laboratory diagnosis of periodontal infection has been influenced by the ...
Introduction: Porphyromonas gingivalis and Tannerella forsythia are anaerobic bacteria commonly invo...
The impact of a semiquantitative commercially available test based on DNA-strip technology (microIDe...
Galassi F, Kaman WE, Anssari Moin D, van der Horst J, Wismeijer D, Crielaard W, Laine ML, Veerman EC...
Aim: Research has demonstrated that there are multiple strains of Porphyromonas gingivalis with vary...
Purpose: We aim to develop peptic nucleic acid (PNA) probes for the identification and localization ...
FISH Probes were designed by sequencing the 16S rRNA for each bacterium, identifying hypervariable r...