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1.
J Dairy Sci ; 95(8): 4442-6, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22818457

ABSTRACT

Prototheca zopfii causes bovine mastitis, resulting in reduced milk production and the secretion of thin watery milk with white flakes. Prototheca zopfii has been biochemically and serologically divided into at least 2 genotypes, P. zopfii genotype 1 and P. zopfii genotype 2. The latter is known to be the main causative agent of bovine protothecal mastitis. Prototheca zopfii was later reclassified into 5 varieties: var. zopfii (genotypes 1 and 2), var. 1 (formerly Prototheca blaschkeae), var. 3 (formerly P. moriformis), and var. portoricensis. In this study, the 18S ribosomal DNA sequences of diverse clinical specimens from different areas in Japan were studied to clarify the pathogenicity of P. zopfii var. zopfii. The phylogenetic tree revealed that all genotype 2 isolates were grouped in a cluster of P. zopfii var. zopfii SAG 2021(T) (type strain genotype 2), and were independent from the cluster of the genotype 1 isolates. Thus, all isolates from bovine mastitis in Japan were identified as P. zopfii genotype 2. Therefore, P. zopfii var. zopfii genotype 2 is associated with bovine mastitis.


Subject(s)
Infections/veterinary , Mastitis, Bovine/microbiology , Prototheca/classification , Animals , Cattle , DNA, Plant/chemistry , DNA, Plant/genetics , Female , Genotype , Infections/genetics , Japan , Mastitis, Bovine/genetics , Phylogeny , Polymerase Chain Reaction/veterinary , Prototheca/genetics , RNA, Ribosomal, 18S/chemistry , RNA, Ribosomal, 18S/genetics
2.
Tohoku J Exp Med ; 171(4): 277-83, 1993 Dec.
Article in English | MEDLINE | ID: mdl-8184402

ABSTRACT

A sister and a brother with 46, XX (46, XY), -21, +der (15) (q22.1; q22.1) mat were reported whose mother had a karyotype of 46, XX, t(15; 21)(q22.1; 22.1) and was phenotypically normal. Both sibs were mentally retarded and dysmorphic. Moreover, the sister had a holoprosencephaly with congenital hydrocephalus, and the brother showed congenital hydrocephalus.


Subject(s)
Chromosomes, Human, Pair 15 , Chromosomes, Human, Pair 21 , Hydrocephalus/genetics , Monosomy/genetics , Trisomy/genetics , Abnormalities, Multiple/genetics , Chromosome Deletion , Female , Holoprosencephaly/genetics , Humans , Infant, Newborn , Male , Pedigree
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