Comparative Genomics Suggests that the Fungal Pathogen Pneumocystis Is an Obligate Parasite Scavenging Amino Acids from Its Host's Lungs

Pneumocystis jirovecii is a fungus causing severe pneumonia in immuno-compromised patients. Progress in understanding its pathogenicity and epidemiology has been hampered by the lack of a long-term in vitro culture method. Obligate parasitism of this pathogen has been suggested on the basis of various features but remains controversial. We analysed the 7.0 Mb draft genome sequence of the closely related species Pneumocystis carinii infecting rats, which is a well established experimental model of the disease. We predicted 8’085 (redundant) peptides and 14.9% of them were mapped onto the KEGG biochemical pathways. The proteome of the closely related yeast Schizosaccharomyces pombe was used as a control for the annotation procedure (4’974 genes, 14.1% mapped). About two thirds of the mapped peptides of each organism (65.7% and 73.2%, respectively) corresponded to crucial enzymes for the basal metabolism and standard cellular processes. However, the proportion of P. carinii genes relative to those of S. pombe was significantly smaller for the “amino acid metabolism” category of pathways than for all other categories taken together (40 versus 114 against 278 versus 427, P<0.002). Importantly, we identified in P. carinii only 2 enzymes specifically dedicated to the synthesis of the 20 standard amino acids. By contrast all the 54 enzymes dedicated to this synthesis reported in the KEGG atlas for S. pombe were detected upon reannotation of S. pombe proteome (2 versus 54 against 278 versus 427, P<0.0001). This finding strongly suggests that species of the genus Pneumocystis are scavenging amino acids from their host's lung environment. Consequently, they would have no form able to live independently from another organism, and these parasites would be obligate in addition to being opportunistic. These findings have implications for the management of patients susceptible to P. jirovecii infection given that the only source of infection would be other humans.

[1]  P. Hoffman,et al.  Cysteine Metabolism in Legionella pneumophila: Characterization of an l-Cystine-Utilizing Mutant , 2006, Applied and Environmental Microbiology.

[2]  P. Dhar,et al.  Genome reduction in prokaryotic obligatory intracellular parasites of humans: a comparative analysis. , 2004, International journal of systematic and evolutionary microbiology.

[3]  M. Quail,et al.  Gene Arrays at Pneumocystis carinii Telomeres , 2005, Genetics.

[4]  Ian Korf,et al.  Gene finding in novel genomes , 2004, BMC Bioinformatics.

[5]  M. Borodovsky,et al.  Gene prediction in novel fungal genomes using an ab initio algorithm with unsupervised training. , 2008, Genome research.

[6]  J. L. Davis,et al.  Respiratory infection complicating HIV infection , 2008, Current opinion in infectious diseases.

[7]  U. Reichard,et al.  Sezernierte Proteasen des Schimmelpilzes Aspergillus fumigatus , 2008 .

[8]  M. Cushion Comparative Genomics of Pneumocystis carinii with Other Protists: Implications for Life Style1 , 2004, The Journal of eukaryotic microbiology.

[9]  Y. Chung,et al.  Purification of a 68-kDa cysteine proteinase from crude extract of Pneumocystis carinii. , 2000, The Korean journal of parasitology.

[10]  E. Dei‐Cas,et al.  Phylogeny of Pneumocystis carinii from 18 Primate Species Confirms Host Specificity and Suggests Coevolution , 2001, Journal of Clinical Microbiology.

[11]  J. Andersson,et al.  Insights into the evolutionary process of genome degradation. , 1999, Current opinion in genetics & development.

[12]  L. Farinelli,et al.  The complete sequence of the smallest known nuclear genome from the microsporidian Encephalitozoon intestinalis , 2010, Nature communications.

[13]  C. Slamovits,et al.  Comparative Genomics of Microsporidia , 2022 .

[14]  L. Delhaes,et al.  Pneumocystis species, co-evolution and pathogenic power. , 2008, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

[15]  M. Nowrousian Next-Generation Sequencing Techniques for Eukaryotic Microorganisms: Sequencing-Based Solutions to Biological Problems , 2010, Eukaryotic Cell.

[16]  Geetha Kutty,et al.  Variation in the major surface glycoprotein genes in Pneumocystis jirovecii. , 2008, The Journal of infectious diseases.

[17]  J. Sugiyama Relatedness, phylogeny, and evolution of the fungi , 1998 .

[18]  A. Fonseca,et al.  Molecular systematics of the dimorphic ascomycete genus Taphrina. , 2003, International journal of systematic and evolutionary microbiology.

[19]  A. Limper,et al.  Pneumocystis pneumonia. , 2004, The New England journal of medicine.

[20]  Peer Bork,et al.  KEGG Atlas mapping for global analysis of metabolic pathways , 2008, Nucleic Acids Res..

[21]  R. Heinzen,et al.  Host cell-free growth of the Q fever bacterium Coxiella burnetii , 2009, Proceedings of the National Academy of Sciences.

[22]  A. Limper,et al.  Current insights into the biology and pathogenesis of Pneumocystis pneumonia , 2007, Nature Reviews Microbiology.

[23]  Jonathan E. Allen,et al.  Genome sequence of the human malaria parasite Plasmodium falciparum , 2002, Nature.

[24]  J. Stringer,et al.  The genome of Pneumocystis carinii. , 1998, FEMS immunology and medical microbiology.

[25]  Aleksey A. Porollo,et al.  Transcriptome of Pneumocystis carinii during Fulminate Infection: Carbohydrate Metabolism and the Concept of a Compatible Parasite , 2007, PloS one.

[26]  C. Haidaris,et al.  Pneumocystis carinii is not universally transmissible between mammalian species , 1993, Infection and immunity.

[27]  Michael Muller,et al.  HitKeeper, a generic software package for hit list management , 2007, Source Code for Biology and Medicine.

[28]  Burkhard Morgenstern,et al.  Gene prediction in eukaryotes with a generalized hidden Markov model that uses hints from external sources , 2006, BMC Bioinformatics.

[29]  J. Stringer,et al.  II. The genome of Pneumocystis carinii , 1998 .

[30]  Determination of the Copy Number of the Nuclear rDNA and Beta-tubulin Genes of Pneumocystis carinii f. sp. hominis Using PCR Multicompetitors , 2000, The Journal of eukaryotic microbiology.

[31]  E. Kaneshiro Sterol metabolism in the opportunistic pathogen Pneumocystis: Advances and new insights , 2004, Lipids.

[32]  E. Angeli,et al.  In vitro activity of human immunodeficiency virus protease inhibitors against Pneumocystis carinii. , 2000, The Journal of infectious diseases.

[33]  R. Miller,et al.  Expression and complexity of the PRT1 multigene family of Pneumocystis carinii. , 2004, Microbiology.

[34]  M. Cushion,et al.  Sterol biosynthesis and sterol uptake in the fungal pathogen Pneumocystis carinii. , 2010, FEMS microbiology letters.

[35]  J. Stringer,et al.  Genetics, metabolism and host specificity of Pneumocystis carinii. , 1998, Medical mycology.

[36]  Sofia M. C. Robb,et al.  MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomes. , 2007, Genome research.

[37]  K. Whyte,et al.  Discrimination against people with HIVinfection and AIDS , 1994, BMJ.

[38]  Samuel H. Payne,et al.  Retention and Loss of Amino Acid Biosynthetic Pathways Based on Analysis of Whole-Genome Sequences , 2006, Eukaryotic Cell.

[39]  A. E. Wakefield Re-examination of epidemiological concepts. , 1995 .

[40]  J. Stajich,et al.  De novo Assembly of a 40 Mb Eukaryotic Genome from Short Sequence Reads: Sordaria macrospora, a Model Organism for Fungal Morphogenesis , 2010, PLoS genetics.

[41]  Patricia C. Babbitt,et al.  Annotation Error in Public Databases: Misannotation of Molecular Function in Enzyme Superfamilies , 2009, PLoS Comput. Biol..

[42]  E. Kaneshiro,et al.  Uptake of the neutral amino acids glutamine, leucine, and serine by Pneumocystis carinii. , 2001, Archives of biochemistry and biophysics.

[43]  R. Durbin,et al.  GeneWise and Genomewise. , 2004, Genome research.