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Published on: February 23, 2014
Analysis of Pneumocystis Transcription Factor Evolution and Implications for Biology and Lifestyle
Ryan Ames1, Alistair J P Brown1,2, Ivana Gudelj1
1Biosciences and Living Systems Institute, University of Exeter, Exeter, United Kingdom.
Abstract:
Pneumocystis jirovecii kills hundreds of thousands of immunocompromised patients each year. Yet many aspects of the biology of this obligate pathogen remain obscure because it is not possible to culture the fungus in vitro independently of its host. Consequently, our understanding of Pneumocystis pathobiology is heavily reliant upon bioinformatic inferences. We have exploited a powerful combination of genomic and phylogenetic approaches to examine the evolution of transcription factors in Pneumocystis species. We selected protein families (Pfam families) that correspond to transcriptional regulators and used bioinformatic approaches to compare these families in the seven Pneumocystis species that have been sequenced to date with those from other yeasts, other human and plant pathogens, and other obligate parasites. Some Pfam families of transcription factors have undergone significant reduction during their evolution in the Pneumocystis genus, and other Pfam families have been lost or appear to be in the process of being lost. Meanwhile, other transcription factor families have been retained in Pneumocystis species, and some even appear to have undergone expansion. On this basis, Pneumocystis species seem to have retained transcriptional regulators that control chromosome maintenance, ribosomal gene regulation, RNA processing and modification, and respiration. Meanwhile, regulators that promote the assimilation of alternative carbon sources, amino acid, lipid, and sterol biosynthesis, and iron sensing and homeostasis appear to have been lost. Our analyses of transcription factor retention, loss, and gain provide important insights into the biology and lifestyle of Pneumocystis. IMPORTANCE Pneumocystis jirovecii is a major fungal pathogen of humans that infects healthy individuals, colonizing the lungs of infants. In immunocompromised and transplant patients, this fungus causes life-threatening pneumonia, and these Pneumocystis infections remain among the most common and serious infections in HIV/AIDS patients. Yet we remain remarkably ignorant about the biology and epidemiology of Pneumocystis due to the inability to culture this fungus in vitro. Our analyses of transcription factor retentions, losses, and gains in sequenced Pneumocystis species provide valuable new views of their specialized biology, suggesting the retention of many metabolic and stress regulators and the loss of others that are essential in free-living fungi. Given the lack of in vitro culture methods for Pneumocystis, this powerful bioinformatic approach has advanced our understanding of the lifestyle of P. jirovecii and the nature of its dependence on the host for survival.
Insights
Pneumocystis jirovecii, a pathogen causing pneumonia, has lost and gained transcription factors. This genomic study reveals its host-dependent lifestyle and specialized biology due to lack of in vitro culture.
Area of Science:
- Mycology and Infectious Diseases
- Genomics and Bioinformatics
- Evolutionary Biology
Background:
- Pneumocystis jirovecii is an obligate fungal pathogen responsible for severe pneumonia in immunocompromised individuals.
- The inability to culture Pneumocystis in vitro hinders a comprehensive understanding of its biology and pathobiology.
- Bioinformatic approaches are crucial for inferring the biology of host-dependent pathogens.
Purpose of the Study:
- To investigate the evolution of transcription factors in Pneumocystis species using genomic and phylogenetic analyses.
- To gain insights into the specialized biology and host-dependent lifestyle of Pneumocystis.
- To identify retained, lost, and expanded transcription factor families in Pneumocystis.
Main Methods:
- Comparative genomic analysis of transcription factor-encoding protein families (Pfam families) across seven sequenced Pneumocystis species.
- Phylogenetic comparisons with transcription factors from other yeasts, pathogens, and obligate parasites.
- Bioinformatic identification and analysis of transcription factor retentions, losses, and expansions.
Main Results:
- Significant reduction, loss, or apparent loss of certain transcription factor families in Pneumocystis.
- Retention and expansion of transcription factor families involved in chromosome maintenance, ribosomal gene regulation, RNA processing, and respiration.
- Loss of transcription factor families associated with alternative carbon source assimilation, amino acid/lipid/sterol biosynthesis, and iron homeostasis.
Conclusions:
- Pneumocystis species exhibit a specialized biology characterized by the loss of metabolic regulators and retention of stress and essential cellular process regulators.
- The observed transcription factor repertoire provides insights into the fungus's dependence on the host for survival and nutrient acquisition.
- Bioinformatic analysis of transcription factor evolution offers a valuable alternative to in vitro culture for understanding Pneumocystis biology.
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