An outbreak of Pneumocystis jiroveci pneumonia with 1 predominant genotype among renal transplant recipients:: Interhuman transmission or a common environmental source?

被引:121
作者
de Boer, Mark G. J.
van Coppenraet, Lesla E. S. Bruijnesteijn
Gaasbeek, Andre
Berger, Stefan P.
Gelinck, Luc B. S.
van Houwelingen, Hans C.
van den Broek, Peterhans
Kuijper, Ed J.
Kroon, Frank P.
Vandenbroucke, Jan P.
机构
[1] LUMC, Dept Infect Dis, Ctr Infect Dis, NL-2300 RC Leiden, Netherlands
[2] LUMC, Dept Med Microbiol, Ctr Infect Dis, NL-2300 RC Leiden, Netherlands
[3] LUMC, Dept Nephrol, NL-2300 RC Leiden, Netherlands
[4] LUMC, Dept Med Stat, NL-2300 RC Leiden, Netherlands
[5] LUMC, Dept Clin Epidemiol, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.1086/513198
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. An outbreak of Pneumocystis jiroveci pneumonia (PCP) occurred among renal transplant recipients attending the outpatient department at the Leiden University Medical Centre ( Leiden, The Netherlands) from 1 March 2005 through 1 February 2006. Clinical, epidemiological, and molecular data were analyzed to trace the outbreak's origin. Methods. Renal transplant recipients with a clinical suspected diagnosis of PCP were included in the study. The diagnosis had to be confirmed by direct microscopy or real-time polymerase chain reaction of the dihydropteroate synthase gene in a bronchoalveolar fluid specimen. To detect contacts between patients, a transmission map was constructed. A case-control analysis was performed to asses whether infection was associated with certain wardrooms. Genotyping of Pneumocystis isolates was performed by sequence analysis of the internal transcribed spacer ( ITS) number 1 and 2 gene regions. Results. Twenty-two confirmed PCP cases were identified; approximately 0 - 1 would have been expected over the same time period. No risk factor was predominantly present, and standard immunosuppressive regimens had not changed. Liver transplant recipients who used the same outpatient facilities had not acquired PCP. The transmission map findings were compatible with interhuman transmission on multiple occasions. The case-control study did not point to wardrooms as a common source. Genotyping by sequencing of the ITS1 and ITS2 gene regions revealed type Ne in 12 of 16 successfully typed samples. Genotype Ne was found in only 2 of 12 reference samples. Conclusions. The clinical data and genotyping results are compatible with either interhuman transmission or an environmental source of infection. More complex models may account for PCP clusters.
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页码:1143 / 1149
页数:7
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