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Exp Anim ; 64(1): 49-56, 2015.
Article in English | MEDLINE | ID: mdl-25312507

ABSTRACT

The clone library method using PCR amplification of the 16S ribosomal RNA (rRNA) gene was used to identify pathogens from corneal scrapings of C57BL/6-corneal opacity (B6-Co) mice with bacterial keratitis. All 10 samples from the eyes with bacterial keratitis showed positive PCR results. All 10 samples from the normal cornea showed negative PCR results. In all 10 PCR-positive samples, the predominant and second most predominant species accounted for 20.9 to 40.6% and 14.7 to 26.1%, respectively, of each clone library. The predominant species were Staphylococcus lentus, Pseudomonas aeruginosa, and Staphylococcus epidermidis. The microbiota analysis detected a diverse group of microbiota in the eyes of B6-Co mice with bacterial keratitis and showed that the causative pathogens could be determined based on percentages of bacterial species in the clone libraries. The bacterial species detected in this study were mostly in accordance with results of studies on clinical bacterial keratitis in human eyes. Based on the results of our previous studies and this study, the B6-Co mouse should be considered a favorable model for studying bacterial keratitis.


Subject(s)
Disease Models, Animal , Gene Library , Keratitis/microbiology , Nucleic Acid Amplification Techniques/methods , Polymerase Chain Reaction/methods , Pseudomonas Infections , Pseudomonas aeruginosa/isolation & purification , Pseudomonas aeruginosa/pathogenicity , RNA, Bacterial/genetics , RNA, Ribosomal, 16S/genetics , Sequence Analysis/methods , Staphylococcal Infections , Staphylococcus/isolation & purification , Animals , Female , Male , Mice, Inbred C57BL , Mice, Mutant Strains , Staphylococcus epidermidis/isolation & purification , Staphylococcus epidermidis/pathogenicity
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