Characterization of Cryptococcus neoformans var. neoformans serotype A and A/D in samples from Egypt
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu hodnotící studie, časopisecké články
PubMed
12800514
DOI
10.1007/bf02930967
Knihovny.cz E-zdroje
- MeSH
- Cryptococcus neoformans klasifikace genetika izolace a purifikace MeSH
- dítě MeSH
- DNA fungální krev mozkomíšní mok MeSH
- dospělí MeSH
- kryptokoková meningitida diagnóza mikrobiologie MeSH
- kryptokokóza diagnóza mikrobiologie MeSH
- latex fixační testy MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mykologické určovací techniky MeSH
- nemoci střev diagnóza mikrobiologie MeSH
- polymerázová řetězová reakce metody MeSH
- polysacharidy krev mozkomíšní mok MeSH
- předškolní dítě MeSH
- senzitivita a specificita MeSH
- sérotypizace MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- předškolní dítě MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- Geografické názvy
- Egypt MeSH
- Názvy látek
- cryptococcal polysaccharide MeSH Prohlížeč
- DNA fungální MeSH
- polysacharidy MeSH
The cryptococcal polysaccharide antigen was detected in 10 cerebrospinal fluid (CSF) and 23 serum samples from cryptococcal meningitis and intestinal cryptococcosis by the cryptococcal antigen latex agglutination system (CALAS). CALAS titers in CSF and serum samples of cryptococcal meningitis ranged over 8-2048 and 32-2048, respectively, while in cases of intestinal cryptococcosis, serum titers ranged over 8-2048. The isolates of yeast Cryptococcus neoformans were determined to be of serotype A or of the A/D pair. The total leukocyte count and biochemical parameters in CSF were significantly increased as indicators of microbial infection. Furthermore, the in vitro change of the teleomorph (sexual state) to the anamorph (asexual state) was also detected and the teleomorph state changed in vivo to the encapsulated anamoph state which is more virulent during infection in vivo than the yeast-like noncapsulated form. Two primers for internal transcribed spacer (ITS) regions of ribosomal DNA were used for molecular detection of C. neoformans. After PCR amplification, a DNA band of 415 bp, visualized on agarose gel, indicated the presence of C. neoformans cells in the tested CSF and serum samples. The primer sensitivity was also characterized using purified yeast chromosomal DNA as template; it was about 20 pg or more chromosomal DNA which represents about 10 cells of C. neoformans. The primers were also specific for ITS regions of C. neoformans and gave negative results with Candida albicans and E. coli chromosomal DNA templates.
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