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Indian Journal of Pathology &... Jul 1993Swabs from 112 removed intrauterine contraceptive devices (IUCD), endocervical swabs from these women and from 65 women with pelvic inflammatory disease (PID) were...
Swabs from 112 removed intrauterine contraceptive devices (IUCD), endocervical swabs from these women and from 65 women with pelvic inflammatory disease (PID) were studied for actinomyces, using direct fluorescent antibody test and culture. Endocervical swabs from 50 control subjects were also studied. Actinomyces species could be detected in 23 (20.5 percent) of IUCD wearers and 8 (12.3 percent) of patients with PID. In control cases, no actinomyces were detected. The isolation rate using a selective medium (Actino Blood Agar) was 71.4 percent. Actinomyces israelii, Actinomyces naeslundii and Actinomyces viscosus were isolated.
Topics: Actinomyces; Female; Humans; Intrauterine Devices; Pelvic Inflammatory Disease; Vaginal Smears
PubMed: 8300169
DOI: No ID Found -
Biochemical Society Transactions May 1993
Topics: Actinomyces viscosus; Arginine; Glycolysis; Streptococcus mutans
PubMed: 8359461
DOI: 10.1042/bst021210s -
Caries Research 1978
Comparative Study
Topics: Actinomyces; Carbohydrate Metabolism; Cell Wall; Fermentation; Humans; Immunoelectrophoresis; Mouth; Serotyping
PubMed: 282008
DOI: 10.1159/000260349 -
Infection and Immunity Jan 1988A lytic bacteriophage for Actinomyces viscosus T14V (the reference strain for actinomyces coaggregation group A) was isolated from raw sewage. This phage, designated...
A lytic bacteriophage for Actinomyces viscosus T14V (the reference strain for actinomyces coaggregation group A) was isolated from raw sewage. This phage, designated BF307, also lysed the T14V-derived nonfimbriated mutant PK455-2 as well as A. viscosus MG-1 and T14AV but not the other serotype 2 or serotype 1 strains of this species that were tested or any of nine Actinomyces naeslundii isolates. Phages BF307 belonged to Bradley morphological group C and was similar in appearance to the A. viscosus MG-1 phages Av-1 and Av-3, which do not productively infect A. viscosus T14V. A. viscosus MG-1 mutants selected for resistance to phage BF307, Av-3, or CT7 (a human dental plaque isolate with the same host range as BF307) were coresistant to the other two phages but sensitive to Av-1. These results indicate that the receptors on A. viscosus MG-1 for phages BF307, Av-3, and CT7 are identical or share a common precursor and that the receptor for phage Av-1 is distinct. Comparison of the genomes of BF307, Av-3, and CT7 revealed that their DNAs were similar in size but distinguishable by restriction analysis. Two altered coaggregation phenotypes were identified among the phage BF307-resistant mutants of strains MG-1, T14V, T14AV, and PK455-2. Class I mutants had lost the ability to interact with coaggregation group 1 streptococci, and class II mutants did not coaggregate with either group 1 or group 2 streptococci. These results are consistent with the proposal that the phage BF307 receptor on these A. viscosus strains is related to one of the structures that mediates coaggregation with oral streptococci. A model to delineate the various coaggregation mediators on the surface of actinomyces coaggregation group A cells is presented, and the use of these phages to probe surface components of human oral actinomyces strains is discussed.
Topics: Actinomyces; Bacterial Proteins; Bacteriophages; DNA, Viral; Lysogeny; Membrane Proteins; Receptor Aggregation; Receptors, Virus; Streptococcus sanguis
PubMed: 3335409
DOI: 10.1128/iai.56.1.54-59.1988 -
Journal of Dental Research Oct 1993Antigenic relatedness among human strains of oral Actinomyces and similar isolates from cattle has been analyzed by agglutination and immunoblotting. Whole cell...
Antigenic relationships among oral Actinomyces isolates, Actinomyces naeslundii genospecies 1 and 2, Actinomyces howellii, Actinomyces denticolens, and Actinomyces slackii.
Antigenic relatedness among human strains of oral Actinomyces and similar isolates from cattle has been analyzed by agglutination and immunoblotting. Whole cell agglutination placed A. viscosus serotype II, A. naeslundii serotypes II and III, Actinomyces NV, and strains from numerical taxomonic clusters C1, C2, C3, C4, and C6 into a single group. A. viscosus serotype I cross-reacted weakly with this group. A naeslundii serotype I strains and the cattle isolates Actinomyces denticolens and Actinomyces howellii were distinct. The agglutination results for A. slackii were equivocal. Immunoblots of cell wall extracts developed with non-absorbed sera showed cross-reactivity (23% to 90% antigenic similarity) among all of the strains tested, including A. israelii. The range of antigenic similarities among the group which included strains of A. viscosus serotype II, the A. naeslundii serotypes, and clusters C1, C2, C3, C4, and C6 was from 39% to 89%. Immunoblotting showed that A. howellii and A. denticolens were between 39% and 72% similar to A. naeslundii and A. viscosus. Absorption of antisera with A. israelii cell walls removed antibodies recognizing antigens common to Actinomyces and made the sera more specific. Immunoblotting with absorbed sera supported the grouping and separation of strains shown by agglutination. In some cases, serotypes could be included into a specific taxonomic cluster. A. naeslundii serotype II and Actinomyces NV most closely resembled cluster C1 strains, and A. naeslundii serotype III resembled cluster C1 strains, and A. naeslundii serotype I and A. viscosus serotype I were included into clusters C5 and C7, respectively. The results support a recent proposal that strains of A. viscosus serotype II, A. naeslundii serotypes II and III, and Actinomyces NV be included into A. naeslundii genospecies 2, that A. naeslundii serotype I should be designated A. naeslundii genospecies 1, and that A. viscosus serotype I should be retained distinct from A. naeslundii, as A. viscosus.
Topics: Absorption; Actinomyces; Actinomyces viscosus; Agglutination; Animals; Antigens, Bacterial; Bacterial Proteins; Cattle; Cell Wall; Cross Reactions; Humans; Immune Sera; Immunoblotting; Pronase; Rabbits; Serotyping
PubMed: 8408879
DOI: 10.1177/00220345930720100601 -
Journal of Endodontics Sep 2003Species of Actinomyces have been associated with endodontic treatment that failed to heal. In this study polymerase chain reaction was used with a pair of universal...
Species of Actinomyces have been associated with endodontic treatment that failed to heal. In this study polymerase chain reaction was used with a pair of universal primers for Actinomyces and species-specific primers to evaluate the contents of infected root canals and aspirates from abscesses or cellulitis for the presence of Actinomyces israelii, A. naeslundii, and A. viscosus. DNA was extracted from 131 clinical samples. DNA from 2 of the original 131 samples was not available for polymerase chain reaction with the universal primer for Actinomyces and A. naeslundii. DNA reacting with the universal primer for Actinomyces was detected in 72 of 129 (55.8%) clinical samples. Of those 41 of 51 (80.4%) were from infected root canals, 22 of 48 (45.8%) were from abscesses, and 9 of 30 (30%) were associated with cellulitis. A. viscosus was detected in 42 of 131 (32.1%) clinical samples. Of those 31 of 52 (59.6%) were from infected root canals, 6 of 43 (14%) were from abscesses, and 5 of 36 (13.9%) were associated with cellulitis. A. israelii was detected in 31 of 131 (23.7%) clinical samples. Of those 14 of 52 (26.9%) were from infected root canals, 11 of 43 (25.6%) were from abscesses, and 6 of 36 (16.7%) were associated with cellulitis. A. naeslundii was detected in 11 of 131 (8.5%) clinical samples. Of those 7 of 51 (13.7%) were from infected root canals, 2 of 48 (4.2%) were from abscesses, and 2 of 30 (6.7%) were associated with cellulitis.
Topics: Actinomyces; Actinomyces viscosus; Actinomycosis; Cellulitis; DNA Primers; DNA, Bacterial; Dental Pulp Diseases; Humans; Periapical Abscess; Periapical Diseases; Polymerase Chain Reaction; RNA, Ribosomal, 16S
PubMed: 14503823
DOI: 10.1097/00004770-200309000-00001 -
Infection and Immunity Aug 1995Stable transformants of Actinomyces viscosus T14V carrying heterologous DNA were obtained with the aid of integration plasmids. These plasmids contained a kanamycin...
Stable transformants of Actinomyces viscosus T14V carrying heterologous DNA were obtained with the aid of integration plasmids. These plasmids contained a kanamycin resistance (Kmr) gene flanked by A. viscosus T14V genomic DNA, including parts of the type 1 structural fimbrial subunit gene (fimP) on one or both sides of the antibiotic marker. Significantly more Kmr transformants were obtained with a plasmid carrying longer segments of homologous strain T14V DNA. Integration of this plasmid into the A. viscosus T14V genome affected the expression and function of type 1 fimbriae in the transformants. In the transformant strain designated A. viscosus MY50D, the inactivated fimP replaced the wild-type fimP via allelic replacement. A. viscosus MY51S and MY52S each contained a copy of the plasmid integrated into the genome by a Campbell-like insertion mechanism. A. viscosus MY50D and MY51S lacked type 1 fimbriae and did not bind to proline-rich proteins (the fimbrial receptors) immobilized on nitrocellulose. In contrast, strain MY52S synthesized the structural subunit protein, as detected by immunostaining with anti-A. viscosus T14V type 1 fimbria antibodies. However, the high-molecular-weight proteins observed in sodium dodecyl sulfate-polyacrylamide gels of fimbriae from the cell wall of the wild-type strain T14V were absent in cell wall preparations of this strain. Moreover, A. viscosus MY52S failed to bind, in vitro, to proline-rich proteins. Thus, these results demonstrate that insertion of heterologous DNA at specific sites of the Actinomyces genome can be facilitated with integratable plasmids and that the transformants and mutants generated will aid in the delineation of the roles and contributions of specific genes to the structure and function of any macromolecule produced by these organisms.
Topics: Actinomyces; DNA, Bacterial; Fimbriae, Bacterial; Genes, Bacterial; Genetic Vectors; Mutagenesis, Site-Directed; Plasmids; Recombination, Genetic; Structure-Activity Relationship; Transformation, Genetic
PubMed: 7622214
DOI: 10.1128/iai.63.8.2924-2930.1995 -
Archives of Oral Biology Jan 1972
Topics: Actinomyces; Agglutination Tests; Animals; Cattle; Cricetinae; Dental Plaque; Fluorescent Antibody Technique; Humans; Immunodiffusion; Rats; gamma-Globulins
PubMed: 4114782
DOI: 10.1016/0003-9969(72)90145-8 -
Advances in Clinical and Experimental... Feb 2019Actinomyces species have a low virulence and pathogenicity, but under specific circumstances they may be involved in root canal and periapical tissue infections. (Comparative Study)
Comparative Study
BACKGROUND
Actinomyces species have a low virulence and pathogenicity, but under specific circumstances they may be involved in root canal and periapical tissue infections.
OBJECTIVES
The aim of the study was to investigate the antibacterial activity of various root canal sealers on standardized strains of Actinomyces.
MATERIAL AND METHODS
The materials tested in this study included AH Plus™ Jet (AH), Apexit® Plus (AP), Endomethasone N (EN), GuttaFlow® (GF), Hybrid Root SEAL (HB), MTA Fillapex (FL), Real® Seal (RCS), Roeko Seal Automix (RSA), Sealapex™ (SP), and Tubli-Seal™ (TS). The antibacterial effect of the freshly mixed sealers on standardized strains of Actinomyces israelii NCTC 8047 and Actinomyces viscosus ATCC 15987 was evaluated with the use of the agar diffusion test (ADT). The results were obtained by measuring the diameter of the growth inhibition zone at 96 h and 1, 2, 3, and 4 weeks, and were analyzed in time using repeated measures analysis of variance (ANOVA). Statistically significant differences among the materials were determined by using one-way ANOVA and Tukey's post hoc testing. A paired Student's t-test was applied to compare the susceptibility of particular strains to each sealer. The critical level of significance for all tests was p < 0.05.
RESULTS
Most sealers demonstrated growth inhibition zones against both tested bacteria, except for RSA and GF. Actinomyces viscosus was significantly more susceptible than A. israelii to AP, RCS (p < 0.001) and TS (p = 0.012). Actinomyces israelii was significantly more susceptible than A. viscosus to EN, HB and SP (p < 0.001).
CONCLUSIONS
The antimicrobial effect of the examined materials varied considerably depending on the type of material and bacterial species tested. Most of the tested root canal sealers exhibited antibacterial activity on standardized strains of Actinomyces, with FL showing the highest antibacterial effect on both bacterial strains. Importantly, both standardized strains of Actinomyces were characterized by varied sensitivity to root canal sealers.
Topics: Actinomyces; Anti-Bacterial Agents; Colony Count, Microbial; Dental Pulp Cavity; Humans; Root Canal Filling Materials
PubMed: 30085427
DOI: 10.17219/acem/78022 -
Applied and Environmental Microbiology Sep 1987Lactobacillus casei ATCC 4646 and Actinomyces viscosus OMZ105E were found to differ markedly in acid tolerance. For example, pH profiles for glycolysis of intact cells...
Lactobacillus casei ATCC 4646 and Actinomyces viscosus OMZ105E were found to differ markedly in acid tolerance. For example, pH profiles for glycolysis of intact cells in dense suspensions indicated that glycolysis by L. casei had an optimal pH of about 6.0 and that glucose degradation was reduced by 50% at a pH of 4.2. Comparable values for A. viscosus cells were at pHs of about 7.0 and 5.6. The difference in acid tolerance appeared to depend mainly on membrane physiology, and the addition of 40 microM gramicidin to cell suspensions increased the sensitivity of the glycolytic system by as much as 1.5 pH units for L. casei and up to 0.5 pH unit for A. viscosus. L. casei cells were inherently somewhat more resistant to severe acid damage than were A. viscosus cells, in that Mg release from L. casei cells in medium with a pH of 3.0 occurred only after a lag of some 4 h, compared with rapid release from A. viscosus cells. However, the major differences pertinent to the physiology of the organisms appeared to be related to proton-translocating ATPases. Isolated membranes of L. casei had about 3.29 U of ATPase per mg of protein, compared with only about 0.06 U per mg of protein for those of A. viscosus. Moreover, the ATPase of L. casei had a pH optimum for hydrolytic activity of about 5, compared with an optimal pH of about 7 for that of A. viscosus.(ABSTRACT TRUNCATED AT 250 WORDS)
Topics: Actinomyces; Adenosine Triphosphatases; Cell Membrane; Cell Membrane Permeability; Fluorides; Glycolysis; Gramicidin; Humans; Hydrogen-Ion Concentration; Lacticaseibacillus casei; Magnesium; Protons
PubMed: 2445289
DOI: 10.1128/aem.53.9.2124-2128.1987