Gits-Muselli Maud, Peraldi Marie-Noelle, de Castro Nathalie, Delcey Véronique, Menotti Jean, Guigue Nicolas, Hamane Samia, Raffoux Emmanuel, Bergeron Anne, Valade Sandrine, Molina Jean-Michel, Bretagne Stéphane, Alanio Alexandre
Laboratoire de Parasitologie-Mycologie, AP-HP, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand-Widal, Paris, France.
Service de transplantation rénale, AP-HP, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand-Widal, Paris, France; Université Paris-Diderot, Sorbonne Cité, Paris, France.
PLoS One. 2015 May 1;10(5):e0125763. doi: 10.1371/journal.pone.0125763. eCollection 2015.
Pneumocystis pneumonia is a severe opportunistic infection in immunocompromised patients caused by the unusual fungus Pneumocystis jirovecii. Transmission is airborne, with both immunocompromised and immunocompetent individuals acting as a reservoir for the fungus. Numerous reports of outbreaks in renal transplant units demonstrate the need for valid genotyping methods to detect transmission of a given genotype. Here, we developed a short tandem repeat (STR)-based molecular typing method for P. jirovecii. We analyzed the P. jirovecii genome and selected six genomic STR markers located on different contigs of the genome. We then tested these markers in 106 P. jirovecii PCR-positive respiratory samples collected between October 2010 and November 2013 from 91 patients with various underlying medical conditions. Unique (one allele per marker) and multiple (more than one allele per marker) genotypes were observed in 34 (32%) and 72 (68%) samples, respectively. A genotype could be assigned to 55 samples (54 patients) and 61 different genotypes were identified in total with a discriminatory power of 0.992. Analysis of the allelic distribution of the six markers and minimum spanning tree analysis of the 61 genotypes identified a specific genotype (Gt21) in our hospital, which may have been transmitted between 10 patients including six renal transplant recipients. Our STR-based molecular typing method is a quick, cheap and reliable approach to genotype Pneumocystis jirovecii in hospital settings and is sensitive enough to detect minor genotypes, thus enabling the study of the transmission and pathophysiology of Pneumocystis pneumonia.
肺孢子菌肺炎是由罕见真菌耶氏肺孢子菌引起的免疫功能低下患者的严重机会性感染。传播途径为空气传播,免疫功能低下和免疫功能正常的个体均为该真菌的储存宿主。肾移植病房爆发的大量报告表明,需要有效的基因分型方法来检测特定基因型的传播。在此,我们开发了一种基于短串联重复序列(STR)的耶氏肺孢子菌分子分型方法。我们分析了耶氏肺孢子菌基因组,并选择了位于基因组不同重叠群上的6个基因组STR标记。然后,我们在2010年10月至2013年11月期间从91例患有各种基础疾病的患者中收集的106份耶氏肺孢子菌PCR阳性呼吸道样本中测试了这些标记。分别在34份(32%)和72份(68%)样本中观察到独特(每个标记一个等位基因)和多重(每个标记一个以上等位基因)基因型。可以为55份样本(54例患者)指定基因型,总共鉴定出61种不同基因型,鉴别力为0.992。对6个标记的等位基因分布分析以及对61种基因型的最小生成树分析在我们医院中鉴定出一种特定基因型(Gt21),该基因型可能在包括6名肾移植受者在内的10名患者之间传播。我们基于STR的分子分型方法是一种在医院环境中对耶氏肺孢子菌进行基因分型的快速、廉价且可靠的方法,并且灵敏度足以检测到次要基因型,从而能够研究肺孢子菌肺炎的传播和病理生理学。