Pregled bibliografske jedinice broj: 42333
Detection and identification of Mycoplasma conjunctivae in infectious keratoconjunctivitis by PCR based on the 16S rRNA gene
Detection and identification of Mycoplasma conjunctivae in infectious keratoconjunctivitis by PCR based on the 16S rRNA gene // Journal of Veterinary Medicine B, 46 (1999), 173-180 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 42333 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Detection and identification of Mycoplasma conjunctivae in infectious keratoconjunctivitis by PCR based on the 16S rRNA gene
Autori
Giacometti, Marco ; Nicolet, J. ; Johansson, K.E-, Naglić, Tomo ; Degiorgis, M. -P. ; Frey, Joachim
Izvornik
Journal of Veterinary Medicine B (0931-1793) 46
(1999);
173-180
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Mycoplasma conjunctivae; identification by PCR; infectious keratoconjunctivitis
(conjunctivae; identification by PCR; infectious keratoconjunctivitis)
Sažetak
A specific PCR assay based on unique sequences of the rrs genes (16S rRNA)of Mycoplasma conjunctivae was developed for direct detection and identification of this pathogen from clinical material. DNA from eye swabs was amplified after a simple lysis step by either a single PCR with the M. conjunctivae specific primer pair McoR1 and McoF1, or by a nested PCR with the Mycoplasma genus specific primer pair MOLIGEN1-L and16UNI-R in the first step and McoR1 and McoF1 in the second step. The specificity of the primer pair McoR1 and McoF1 was verified with purified DNA from the type strain, from 17 field isolates of M. conjunctivae and from several Mollicutes which are phylogenetically related to M. conjunctivae or which can be isolated from the same host animals. This method identified mycoplasma ioslates from goat, sheep, ibex and chamois originating from different countries as M. conjunctivae. No cross amplifications with other mycoplasmas which a related to M. conjunctivae were observed. Eye swab samples containing known numbers of M. conjunctivae cells were analysed after direct lysis of the material. The detection level was estimated to be 20 cells per swab when nested PCR procedure was used and 2 x 105 by the single PCR method. In an experimental infection model of sheep, the nested PCR method for detection of M. conjunctivae gave results which were comparable to mycoplasmal culture. These are the implications for diagnostic purposes: M. conjunctivae isolates can be identified by the one step PCR method, whereas for detection and identification of M. conjunctivae in clinical material the two-step method should be used (higher sensitivity).
Izvorni jezik
Engleski
Znanstvena područja
Veterinarska medicina
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- Biological Abstracts
- Veterinary Bulletin
- Index Veterinarius