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Journal of Clinical Microbiology, Feb 1997, 383-387, Vol 35, No. 2
S Latouche, E Ortona, E Mazars, P Margutti, E Tamburrini, A Siracusano, K Guyot, M Nigou and P Roux
The purpose of this study was to identify the most useful gene for the
detection of biodiversity of Pneumocystis carinii hominis isolates and to
compare samples from French and Italian subjects. We studied 20
bronchoalveolar lavage fluid specimens from 20 human immunodeficiency
virus-infected patients (10 French and 10 Italian patients) with
Pneumocystis carinii pneumonia by DNA sequencing of the thymidylate
synthase (TS), 5S rRNA, large-subunit mitochondrial rRNA (mt LSU rRNA), and
internal transcribed spacer (ITS1 and ITS2) genes. Thirteen of the 20
sequenced samples had the prototype TS gene sequence. Fourteen of the 20
samples showed the prototype sequence of the 5S rRNA gene, and 6 had
variant sequences of the 5S rRNA gene. The mt LSU rRNA gene was sequenced
for 18 of the 20 samples; all sequences were different from the prototype
sequence and were classified into four groups. Thirteen of the 20 ITS1 and
ITS2 sequences were analyzed, and all the sequences were found to be
different from the prototype sequence and were classified into 10 groups.
The internal transcribed spacer regions thus appear to be the most
discriminatory region of DNA for analysis of the biodiversity of P. carinii
hominis isolates.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Biodiversity of Pneumocystis carinii hominis: typing with different DNA regions
Laboratoire de Parasitologie-Mycologie, Centre Hospitalier Universitaire Saint-Antoine, Paris, France.
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