http://www.cnr.it/ontology/cnr/individuo/prodotto/ID288220
Simultaneous identification by multiplex PCR of major Prototheca spp. isolated from bovine and buffalo intramammary infection and bulk tank. (Articolo in rivista)
- Type
- Label
- Simultaneous identification by multiplex PCR of major Prototheca spp. isolated from bovine and buffalo intramammary infection and bulk tank. (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1111/lam.12326 (literal)
- Alternative label
Capra, E; Cremonesi, P; Cortimiglia, C; Bignoli, G; Ricchi, M; Moroni, P; Pesce, A; Luini, M; Castiglioni, B (2014)
Simultaneous identification by multiplex PCR of major Prototheca spp. isolated from bovine and buffalo intramammary infection and bulk tank.
in Letters in applied microbiology
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Capra, E; Cremonesi, P; Cortimiglia, C; Bignoli, G; Ricchi, M; Moroni, P; Pesce, A; Luini, M; Castiglioni, B (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- IBBA-CNR: Capra, Cremonesi, Bignoli, Castiglioni
IZSLER: Cortimiglia, Ricchi, Pesce, Luini
UNIMI: Moroni
Cornell University - USA: Moroni (literal)
- Titolo
- Simultaneous identification by multiplex PCR of major Prototheca spp. isolated from bovine and buffalo intramammary infection and bulk tank. (literal)
- Abstract
- Bovine mastitis caused by Prototheca spp. infection is increasing worldwide,
therefore becoming more relevant to the dairy industry. Almost all Prototheca
isolates from bovine mammary protothecosis came from P. zopfii genotype 2,
with a lower prevalence of infection due to P. blaschkeae and rarely to
P. wickerhamii. In this study, we report the development of two multiplex PCR
assays able to discriminate among the three species responsible for bovine
intramammary infection (IMI). Our assay is based on the specific amplification
of new DNA target from mitochondria and chloroplasts partial sequences, of
different Prototheca isolates. Both methods were set up using reference strains
belonging to all Prototheca species and validated by the analysis of 93 isolates
from bovine and buffalo IMI and bulk tank milk samples. The investigation
involves 70 isolates from North, 13 from Central and 10 from South Italian
regions. Isolates from bovine were most commonly identified as P. zopfii
genotype 2, and only in one case as P. blaschkeae, whereas isolates from
buffaloes belonged both to P. zopfii genotype 2 and P. wickerhamii. These
findings proved the suitability of our multiplex PCRs as a rapid test to
discriminate among pathogenic Prototheca strains. (literal)
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