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Pneumocystis carinii: what is it, exactly?
1Department of Molecular Genetics, Biochemistry and Microbiology, College of Medicine, University of Cincinnati, OH 45267-0524, USA. stringjr@ucbeh.san.uc.edu
Clinical Microbiology Reviews
|October 1, 1996
Summary
Pneumocystis carinii, once thought a protozoan, is now classified as a fungus. Genetic analysis reveals it is a complex group of organisms, not a single species, impacting pneumonia research.
Area of Science:
- Mycology
- Eukaryotic genetics
- Infectious disease
Background:
- The classification of Pneumocystis carinii has been historically debated due to its unique characteristics.
- Phenotypic traits, such as inability to culture and resistance to antifungals, led to its initial classification as a protozoan.
- Recent genetic analyses challenge this long-held view.
Purpose of the Study:
- To clarify the phylogenetic identity of Pneumocystis carinii.
- To investigate the genetic diversity within the Pneumocystis genus.
- To explore the implications of genetic variation for understanding Pneumocystis pneumonia.
Main Methods:
- DNA sequence analysis to determine phylogenetic relationships.
- Gene sequence analysis to assess genetic divergence among isolates.
- Comparison of genetic variation within and between host species.
Main Results:
- DNA sequence data confirm Pneumocystis carinii belongs to the fungal lineage.
- Pneumocystis is a complex group of organisms, with significant genetic divergence between host-specific isolates.
- Genetic variation exists within isolates from the same host, enabling strain identification.
- Recurrent Pneumocystis pneumonia may not solely result from reactivation.
- A genetic system for surface antigen variation has been identified.
Conclusions:
- Pneumocystis carinii is a fungus, not a protozoan.
- The genus Pneumocystis comprises diverse, genetically distinct organisms.
- Understanding genetic variation is crucial for Pneumocystis pneumonia epidemiology and treatment.
- Pneumocystis exhibits host adaptation and potential for immune evasion through antigen variation.
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