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Copy Number Variation of Mitochondrial DNA Genes in Pneumocystis jirovecii According to the Fungal Load in BAL Specimens

Authors :
Alexandre Alanio
Nicolas Guigue
Marion Benazra
Maud Gits-Muselli
Samia Hamane
María José Buitrago
Stéphane Bretagne
Aude Sturny-Leclère
Clara Valero
Instituto de Salud Carlos III [Madrid] (ISC)
Université Paris Diderot - Paris 7 (UPD7)
Laboratoire de Parasitologie-Mycologie [CHU Saint Louis, Paris]
Groupe Hospitalier Saint Louis - Lariboisière - Fernand Widal [Paris]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Mycologie moléculaire
Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)
Centre National de Référence des Mycoses invasives et antifongiques - Mycologie moléculaire (CNRMA)
Centre National de Référence Mycologie et Antifongiques-Mycologie Moléculaire (CNRMA)
Institut Pasteur [Paris]
This work was supported by research project PI14CIII/00045 from the Spanish Fondo de Investigaciones Sanitarias of the Instituto de Salud Carlos III. CV is supported by research fellowships from the Fondo de Investigaciones Sanitarias of the Spanish Ministry of Economy and Competitiveness (FI12/00095).
Ministerio de Economía y Competitividad (España)
Instituto de Salud Carlos III
Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)
Institut Pasteur [Paris] (IP)
Source :
Frontiers in Microbiology, Frontiers in Microbiology, Frontiers Media, 2016, 7, pp.1413. ⟨10.3389/fmicb.2016.01413⟩, Repisalud, Instituto de Salud Carlos III (ISCIII), Frontiers in Microbiology, Vol 7 (2016), Frontiers in Microbiology, 2016, 7, pp.1413. ⟨10.3389/fmicb.2016.01413⟩
Publication Year :
2016
Publisher :
Frontiers Media S.A., 2016.

Abstract

Pneumocystis jirovecii is an unculturable fungus and the causative agent of Pneumocystis pneumonia, a life-threatening opportunistic infection. Although molecular diagnosis is often based on the detection of mtLSU rRNA mitochondrial gene, the number of copies of mitochondrial genes had not been investigated. We developed and optimized six real-time PCR assays in order to determine the copy number of four mitochondrial genes (mtSSU rRNA, mtLSU rRNA, NAD1, and CYTB) in comparison to nuclear genome (DHPS and HSP70) and tested 84 bronchoalveolar fluids of patients at different stages of the infection. Unexpectedly, we found that copy number of mitochondrial genes varied from gene to gene with mtSSU rRNA gene being more represented (37 copies) than NAD1 (23 copies), mtLSU rRNA (15 copies) and CYTB (6 copies) genes compared to nuclear genome. Hierarchical clustering analysis (HCA) allowed us to define five major clusters, significantly associated with fungal load (p = 0.029), in which copy number of mitochondrial genes was significantly different among them. More importantly, copy number of mtLSU rRNA, NAD1, and CYTB but not mtSSU rRNA differed according to P. jirovecii physiological state with a decreased number of copies when the fungal load is low. This suggests the existence of a mixture of various subspecies of mtDNA that can harbor different amplification rates. Overall, we revealed here an unexpected variability of P. jirovecii mtDNA copy number that fluctuates according to P. jirovecii's physiological state, except for mtSSU that is the most stable and the most present mitochondrial gene. This work was supported by research project PI14CIII/00045 from the Spanish Fondo de Investigaciones Sanitarias of the Instituto de Salud Carlos III. CV is supported by research fellowships from the Fondo de Investigaciones Sanitarias of the Spanish Ministry of Economy and Competitiveness (FI12/00095). Sí

Details

Language :
English
ISSN :
1664302X
Volume :
7
Database :
OpenAIRE
Journal :
Frontiers in Microbiology
Accession number :
edsair.doi.dedup.....b238de1d3101710511248d16cf81ddb3
Full Text :
https://doi.org/10.3389/fmicb.2016.01413