You are here

FASEB J DOI:10.1096/fj.12-224444

Sequencing and characterization of the complete mitochondrial genomes of three Pneumocystis species provide new insights into divergence between human and rodent Pneumocystis.

Publication TypeJournal Article
Year of Publication2013
AuthorsMa, L, Huang, D-W, Cuomo, CA, Sykes, S, Fantoni, G, Das, B, Sherman, BT, Yang, J, Huber, C, Xia, Y, Davey, E, Kutty, G, Bishop, L, Sassi, M, Lempicki, RA, Kovacs, JA
JournalFASEB J
Volume27
Issue5
Pages1962-72
Date Published2013 May
ISSN1530-6860
KeywordsAmino Acid Sequence, Animals, Codon, DNA Replication, DNA, Mitochondrial, Genome, Mitochondrial, Humans, Models, Biological, Molecular Sequence Data, Phylogeny, Pneumocystis, Pneumocystis carinii, Rodentia, Sequence Analysis, DNA
Abstract

Pneumocystis jirovecii is an important opportunistic pathogen associated with AIDS and other immunodeficient conditions. Currently, very little is known about its nuclear and mitochondrial genomes. In this study, we sequenced the complete mitochondrial genome (mtDNA) of this organism and its closely related species Pneumocystis carinii and Pneumocystis murina by a combination of sequencing technologies. Our study shows that P. carinii and P. murina mtDNA share a nearly identical number and order of genes in a linear configuration, whereas P. jirovecii has a circular mtDNA containing nearly the same set of genes but in a different order. Detailed studies of the mtDNA terminal structures of P. murina and P. carinii suggest a unique replication mechanism for linear mtDNA. Phylogenetic analysis supports a close association of Pneumocystis species with Taphrina, Saitoella, and Schizosaccharomyces, and divergence within Pneumocystis species, with P. murina and P. carinii being more closely related to each other than either is to P. jirovecii. Comparative analysis of four complete P. jirovecii mtDNA sequences in this study and previously reported mtDNA sequences for diagnosing and genotyping suggests that the current diagnostic and typing methods can be improved using the complete mtDNA data. The availability of the complete P. jirovecii mtDNA also opens the possibility of identifying new therapeutic targets.

DOI10.1096/fj.12-224444
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/23392351?dopt=Abstract

Alternate JournalFASEB J.
PubMed ID23392351
PubMed Central IDPMC3633818
Grant ListU54 HG003067 / HG / NHGRI NIH HHS / United States
N0I-CO-56000 / CO / NCI NIH HHS / United States
U54HG003067 / HG / NHGRI NIH HHS / United States
/ / Intramural NIH HHS / United States