Pneumocystis jiroveci in Portuguese immunocompromised patients: association of specific ITS genotypes with treatment failure, bad clinical outcome and childhood

被引:21
作者
Matos, Olga [1 ]
Lee, Chao-Hung [2 ]
Jin, Shaoling [2 ]
Li, Baozheng [2 ]
Costa, Marina C. [1 ]
Goncalves, Luzia [3 ]
Antunes, Francisco [1 ,4 ]
机构
[1] Inst Higiene & Med Trop, Unidade Protozoarios Oportunistas VIH & Outras Pr, UPMM, P-1349008 Lisbon, Portugal
[2] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[3] Inst Higiene & Med Trop, Unidade Epidemiol & Bioestat, P-1349008 Lisbon, Portugal
[4] Hosp Santa Maria, Clin Doencas Infecciosas, Lisbon, Portugal
关键词
Genotyping; Portuguese immunocompromised patients; ITS regions; DHPS gene; Pneumocystis jiroveci pneumonia;
D O I
10.1016/S1567-1348(03)00092-3
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We analyzed the genetic variation among isolates of Pneumocystis jiroveci from Portuguese immunocompromised patients with PCP at the internal transcribed spacer (ITS) regions of the nuclear rRNA operon and at the dihydropteroate synthase (DHPS) gene. Pulmonary secretions from 42 patients with PCP corresponding to 43 episodes were studied. Demographic, immunological, and clinical data were obtained from all patients. By combining the two regions ITS1 and ITS2, we found 17 different ITS types of P. jiroveci, two of them were new types (Pb and Pe). The four most prevalent ITS types were Eg (23.3%), Eb and Ne (11.6% each), and Bi (9.3%). A single type was detected in 95.3% of the samples and 4.7% had mixed infections with three different ITS types. DHPS mutants were present in 17 (46%), and the wildtype was present in 20 (54%) of 37 isolates. No association was found between ITS and DHPS types and between DHPS types and therapy or response to anti-PCP treatment. Type Ne presented an association with negative response to anti-PCP treatment (P < 0.001) and with death before 120 days after PCP diagnosis (P = 0.025). Type Eb was significantly more common in children than in adults (P = 0.001). Our data suggest an association of specific ITS genotypes with treatment failure, bad clinical outcome and childhood. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:281 / 285
页数:5
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